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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Chem.</journal-id>
<journal-title>Frontiers in Chemistry</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Chem.</abbrev-journal-title>
<issn pub-type="epub">2296-2646</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1363066</article-id>
<article-id pub-id-type="doi">10.3389/fchem.2024.1363066</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Chemistry</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Chemical structures, biological activities, and medicinal potentials of amine compounds detected from <italic>Aloe</italic> species</article-title>
<alt-title alt-title-type="left-running-head">Yadeta</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fchem.2024.1363066">10.3389/fchem.2024.1363066</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Yadeta</surname>
<given-names>Adamu Tizazu</given-names>
</name>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<xref ref-type="fn" rid="fn1">
<sup>&#x2020;</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1859999/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/methodology/"/>
<role content-type="https://credit.niso.org/contributor-roles/software/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
</contrib-group>
<aff>
<institution>Department of Chemistry, College of Natural and Computational Sciences, Mekdela Amba University</institution>, <addr-line>Tulu Awuliya</addr-line>, <country>Ethiopia</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1366916/overview">Ghasem Sargazi</ext-link>, Bam University of Medical Sciences and Health Services, Iran</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1107769/overview">Ahmed A. Zaky</ext-link>, National Research Centre, Egypt</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1714134/overview">Mar&#xed;a Del Rayo Camacho Corona</ext-link>, Autonomous University of Nuevo Le&#xf3;n, Mexico</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Adamu Tizazu Yadeta, <email>adamutizazu1@gmail.com</email>
</corresp>
<fn fn-type="other" id="fn1">
<label>
<sup>&#x2020;</sup>
</label>
<p>ORCID: Adamu Tizazu Yadeta, <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0002-8670-613X">orcid.org/0000-0002-8670-613X</ext-link>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>01</day>
<month>03</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>12</volume>
<elocation-id>1363066</elocation-id>
<history>
<date date-type="received">
<day>29</day>
<month>12</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>19</day>
<month>02</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2024 Yadeta.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Yadeta</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Unrestricted interest in <italic>Aloe</italic> species has grown rapidly, and a lot of research is currently being done to learn more about the properties of the various <italic>Aloe</italic> constituents. Organic compounds containing amine as functional group are present in a vivid variety of compounds, namely, amino acids, hormones, neurotransmitters, DNA, alkaloids, dyes, etc. These compounds have amine functional groups that have various biological activities, which make them responsible for medicinal potential in the form of pharmaceutical, nutraceutical, and cosmeceutical applications. Consequently, the present review work provides an indication of the amines investigated in <italic>Aloe</italic> species and their therapeutic uses. Various amine compounds of the <italic>Aloe</italic> species have effective biological properties to treat diseases. Generally, the genus <italic>Aloe</italic> has various active amine-containing compounds to combat diseases when humans use them in various forms.</p>
</abstract>
<kwd-group>
<kwd>
<italic>Aloe</italic> species</kwd>
<kwd>nitrogen</kwd>
<kwd>amines</kwd>
<kwd>biological activities</kwd>
<kwd>medicinal potentials</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Organic Chemistry</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Unrestricted interest in <italic>Aloe</italic> species has grown rapidly and a lot of research is currently being done to learn more about the properties of the various <italic>Aloe</italic> constituents (<xref ref-type="bibr" rid="B104">Singab et al., 2015</xref>). <italic>Aloe</italic> plants are a unique source of phytochemicals because they can tolerate hot, dry weather. As a result, they store water and vital chemical components in their swollen, succulent leaves (<xref ref-type="bibr" rid="B123">W&#xf3;jcik et al., 2021</xref>). Numerous studies conducted both <italic>in vitro</italic> and <italic>in vivo</italic> have confirmed the biological properties of <italic>Aloe</italic> species, including wound healing, anti-tumoral, anti-inflammatory, antimicrobial, antimalarial, anticancer, etc. properties. Mostly, these characteristics could not be ascribed to a single class of compounds, but rather to a variety of compounds found in the phytochemical profile of <italic>Aloe</italic> extracts (<xref ref-type="bibr" rid="B44">Hamman, 2008</xref>; <xref ref-type="bibr" rid="B103">Sharrif Moghaddasi and Res, 2011</xref>; <xref ref-type="bibr" rid="B10">Andrea et al., 2020</xref>). Alkaloids, amino acids, vitamins, hormones, proteins, polyphenols, saccharides, organic acids, and other naturally occurring phytochemicals are abundant in <italic>Aloe species</italic> (<xref ref-type="bibr" rid="B127">Zayed et al., 2012</xref>; <xref ref-type="bibr" rid="B117">Ufnal et al., 2015</xref>; <xref ref-type="bibr" rid="B97">S&#xe1;nchez et al., 2020</xref>). Most of these phytochemicals have the functional group amine. Amines are present in large amounts in all living things (<xref ref-type="bibr" rid="B53">Kaur et al., 2018</xref>).</p>
<p>Amines are nitrogen-containing functional groups of organic chemistry that arise from the substitution of an alkyl or aryl group for one or more hydrogen atoms in ammonia (NH<sub>3</sub>) (<xref ref-type="bibr" rid="B61">Lawrence, 2004</xref>). Amines are categorized as primary (RNH<sub>2</sub>), secondary (R<sub>2</sub>NH), or tertiary (R<sub>3</sub>N) depending on whether one, two, or three of the hydrogen atoms in ammonia have been substituted out for organic groups (<xref ref-type="bibr" rid="B40">Graton et al., 2005</xref>). Quaternary ammonium compounds fall into a fourth category. They are created by substituting all four hydrogen atoms in the ammonium ion, NH<sub>4</sub>
<sup>&#x2b;</sup>; an anion (R<sub>4</sub>N<sup>&#x2b;</sup>X<sup>&#x2212;</sup>) is required in this case (<xref ref-type="bibr" rid="B42">Grossman and Grossman, 2003</xref>). When nitrogen is part of the ring, the compound is known as heterocyclic amine; each heterocyclic ring system has a unique parent name. Always, the nitrogen atom is assigned to position 1 in heterocyclic amines (<xref ref-type="bibr" rid="B49">Jacobi, 2018</xref>). Compounds such as pyridine, pyrrole, quinoline, imidazole, indole, pyrimidine, pyrrolidine, and piperidine are examples of commonly known heterocyclic amines. These amines are used as parent names for their substituents (<xref ref-type="bibr" rid="B64">Li, 2013</xref>). Generally, amines have two broad categories: cyclic amines and acyclic amines. Cyclic amines are heterocyclic amines that have one or more nitrogen as heteroatoms. Heterocyclic amines have no primary amines due to their rings. Cyclic amines are further classified into saturated and unsaturated amines. Unsaturated amines which have C<sup>_</sup>N double bonds cannot be primary, secondary, etc. In another way, acyclic amines have nitrogen out of the ring. Moreover, any amine falls into the categories of heterocyclic amine, primary amine, secondary amine, tertiary amine, or quaternary ammonium salt (<xref ref-type="fig" rid="F1">Figure 1</xref>).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Classification of amines.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g001.tif"/>
</fig>
<p>Organic compounds containing amine as functional group are present in a vivid variety of compounds, namely, amino acids, hormones, neurotransmitters, DNA, alkaloids, dyes, etc. Drugs such as morphine, nicotine, codeine, and heroin, etc., that have physiological properties in humans also contain amino groups in one form or another. Amines are basic because of the presence of a lone pair of electrons on nitrogen (<xref ref-type="bibr" rid="B32">El-Sakka, 2010</xref>; <xref ref-type="bibr" rid="B85">Otimenyin, 2022</xref>). Amine-containing compounds have unique properties that make them biologically active molecules. A lone pair of electrons on nitrogen dominates the chemistry of amines, making them both bases and nucleophiles (<xref ref-type="bibr" rid="B79">Morgenthaler et al., 2007</xref>; <xref ref-type="bibr" rid="B121">Vedejs and Denmark, 2016</xref>). Due to these properties, the compounds that have amine functional groups have various biological activities that are responsible for pharmaceutical, nutraceutical, and cosmeceutical applications. Using amines for a variety of applications needs attention currently. However, to the best of my knowledge, no comprehensive work was done regarding the amine-containing compounds detected in the <italic>Aloe</italic> species for their medicinal potential. Consequently, the present work summarizes amine-containing compounds investigated from <italic>Aloe</italic> species and their therapeutic uses. More generally, the core point of the current review is to describe the chemical structure of the detected amine compounds from <italic>Aloe</italic> species and relate them to the studied medicinal activities of the plants.</p>
</sec>
<sec id="s2">
<title>2 The review methodology</title>
<p>The relevant sources for this study were retrieved using search engines including Google Scholar, PubMed, and Science Direct. For the purpose of finding relevant sources, several combinations of terms and phrases such as amines, alkaloids, amino acids, vitamins, hormones, <italic>Aloe</italic> species, <italic>Aloe</italic> species phytochemicals, <italic>Aloe</italic> species applications, and medicinal activities of <italic>Aloe</italic> extracts and compounds were utilized. This review covered studies on chemical structures of amines analyzed from <italic>Aloe</italic> species, the medicinal potential of <italic>Aloe</italic> extracts, and amine compounds. Reports on such activities based on other than amine compounds were excluded. Studies that were published in languages other than English were not at all taken into account. Following the collection of all sources, a rapid study of the sources&#x2019; titles, abstracts, and conclusions was done to determine which ones met the qualifying requirements. The chosen sources were then carefully examined in order to prepare this review paper. The chemical structures of the compounds were depicted using ChemDraw Ultra 8.0 software, while citations and checking references were provided using Mendeley Desktop software.</p>
</sec>
<sec id="s3">
<title>3 Structures of amines detected from <italic>Aloe</italic> species</title>
<sec id="s3-1">
<title>3.1 Alkaloids</title>
<p>The name alkaloid (&#x201c;alkali-like&#x201d;) was originally applied to the substances because, like the inorganic alkalis, they react with acids to form salts (<xref ref-type="bibr" rid="B7">Alamgir, 2018</xref>). Alkaloids are small organic molecules that contain nitrogen, usually in a ring. Therefore, alkaloids are one of the heterocyclic amine compounds having nitrogen as a heteroatom (<xref ref-type="bibr" rid="B19">Bhardwaj et al., 2021</xref>). Alkaloids are an important group of biologically active amines that are mostly synthesized by plants to protect them from being eaten by insects and other animals. Alkaloids in nature are vast, so we need to classify them into specific groups. Compounds such as nucleosides, vitamins, hormones, some amino acids, etc. are alkaloids. For instance, pyridoxine is a vitamin as well as an alkaloid; proline is &#x3b1;-amino acid as well as an alkaloid. However, such compounds are together called amines (Wade, 2013; <xref ref-type="bibr" rid="B72">Mcmurry, 2016</xref>).</p>
<p>Alkaloids have been analyzed from <italic>Aloe</italic> species quantitatively and qualitatively (<xref ref-type="bibr" rid="B106">Sonam and Archana, 2016</xref>; <xref ref-type="bibr" rid="B119">Usman et al., 2020</xref>). Phytochemical screening showed the presence of alkaloids in various <italic>Aloe</italic> species such as <italic>A. adigratana</italic>, <italic>A. barbadensis</italic>, <italic>A. calidophila</italic>, <italic>A. ferox</italic>, <italic>A. vera</italic>, <italic>A. turkanensis</italic>, and <italic>A. Gilbertii</italic> from the leaves of plants such as gel, latex, skin, whole leaf (<xref ref-type="bibr" rid="B96">Salehi et al., 2018</xref>), roots (<xref ref-type="bibr" rid="B50">Jemal et al., 2018</xref>), and flowers (<xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al., 2020</xref>). Also, a number of alkaloid compounds have been isolated from <italic>Aloe</italic> species (<xref ref-type="bibr" rid="B96">Salehi et al., 2018</xref>). The detected alkaloids from the <italic>Aloe</italic> species are heterocyclic amines, and they are derivatives of the base heterocyclic amines (<xref ref-type="table" rid="T1">Table 1</xref>). The nomenclatures of some alkaloids were not copied directly from the names reported in the literature. Because some names of alkaloids are complex to write. For instance, the compound 23, which was obtained from GC-MS analysis of ethanolic extract <italic>A. vera</italic> was written in the literature as phenol, 4-[(5,6,7,8-tetrahydro-1,3-dioxolo [4,5-g]isoquinolin-5yl)methyl]. This name is too long; instead, &#x2018;norcinnamolaurine&#x2019;, the other name of the compound, was used in the current work (<xref ref-type="table" rid="T1">Table 1</xref>; <xref ref-type="fig" rid="F2">Figure 2</xref>).</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Alkaloids of <italic>Aloe</italic> species.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">No</th>
<th align="left">Name</th>
<th align="left">Detection method used</th>
<th align="left">Molecular formula</th>
<th align="center">Molecular weight (g/mol)</th>
<th align="left">
<italic>Aloe</italic> species</th>
<th align="left">References</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left" style="color:#1A1A1A">1</td>
<td align="left" style="color:#1A1A1A">(2-aziridinylethyl) amine</td>
<td align="left">GC-MS analysis</td>
<td align="left">C<sub>4</sub>H<sub>10</sub>N<sub>2</sub>
</td>
<td align="left">86.14</td>
<td align="left" style="color:#1A1A1A">
<italic>A.vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B8">Alghamdi et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">2</td>
<td align="left" style="color:#1A1A1A">Hydantoinpropionic acid</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>6</sub>H<sub>8</sub>N<sub>2</sub>O<sub>4</sub>
</td>
<td align="left">172.14</td>
<td align="left" style="color:#1A1A1A">
<italic>A. greatheadii</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B21">Botes et al. (2008)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">3</td>
<td align="left" style="color:#1A1A1A">Coniine</td>
<td align="left">Phytochemical investigations and GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>8</sub>H<sub>17</sub>N</td>
<td align="left">127.23</td>
<td align="left">
<italic>A. sabaea, A. globuligemma, and A. viguieri</italic>
</td>
<td align="left" style="color:#1A1A1A">
<xref ref-type="bibr" rid="B20">Blitzke et al., 2000</xref>; <xref ref-type="bibr" rid="B47">Hotti et al., 2017</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">4</td>
<td align="left" style="color:#1A1A1A">
<italic>N</italic>-methylconiine</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>9</sub>H<sub>19</sub>N</td>
<td align="left">141.25</td>
<td align="left" style="color:#1A1A1A">
<italic>A. globuligemma</italic> and <italic>A. viguieri</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B47">Hotti et al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">5</td>
<td align="left" style="color:#1A1A1A">N,N-dimethylconiine</td>
<td align="left">Phytochemical investigations</td>
<td align="left" style="color:#1A1A1A">C<sub>10</sub>H<sub>22</sub>N</td>
<td align="left">156.24</td>
<td align="left" style="color:#1A1A1A">
<italic>A. sabaea</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B20">Blitzke et al. (2000)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">6</td>
<td align="left" style="color:#1A1A1A">conhydrine</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>8</sub>H<sub>15</sub>NO</td>
<td align="left">141.21</td>
<td align="left" style="color:#1A1A1A">
<italic>A. ballyii</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B47">Hotti et al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">7</td>
<td align="left" style="color:#1A1A1A">Pseudoconhydrine</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>8</sub>H<sub>17</sub>NO</td>
<td align="left">143.23</td>
<td align="left" style="color:#1A1A1A">
<italic>A. deltoideodonta</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B47">Hotti et al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">8</td>
<td align="left" style="color:#1A1A1A">1-(phenylthioxomethyl) piperidine</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>12</sub>H<sub>15</sub>NS</td>
<td align="left">205.32</td>
<td align="left" style="color:#1A1A1A">
<italic>A. vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B16">Bawankar et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">9</td>
<td align="left" style="color:#1A1A1A">2-methyl-5-phenyl-pyrrole</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>11</sub>H<sub>11</sub>N</td>
<td align="left">157.21</td>
<td align="left" style="color:#1A1A1A">
<italic>A.vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B8">Alghamdi et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">10</td>
<td align="left" style="color:#1A1A1A">&#x3b3;-coniceine</td>
<td align="left">Phytochemical investigations and GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>8</sub>H<sub>15</sub>N</td>
<td align="left">125.21</td>
<td align="left">
<italic>A. sabaea, A. globuligemma, and A. viguieri</italic>
</td>
<td align="left" style="color:#1A1A1A">
<xref ref-type="bibr" rid="B20">Blitzke et al., 2000</xref>; <xref ref-type="bibr" rid="B47">Hotti et al., 2017</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">11</td>
<td align="left" style="color:#1A1A1A">Isonicotinic acid</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>6</sub>H<sub>5</sub>NO<sub>2</sub>
</td>
<td align="left">123.11</td>
<td align="left" style="color:#1A1A1A">
<italic>A. greatheadii</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B21">Botes et al. (2008)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">12</td>
<td align="left" style="color:#1A1A1A">Picolinic acid</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>6</sub>H<sub>5</sub>NO<sub>2</sub>
</td>
<td align="left">123.11</td>
<td align="left" style="color:#1A1A1A">
<italic>A. vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B82">Nejatzadeh-Barandozi (2013)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">13</td>
<td align="left" style="color:#1A1A1A">3-hydroxypicolinic acid</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>6</sub>H<sub>5</sub>NO<sub>3</sub>
</td>
<td align="left">139.12</td>
<td align="left" style="color:#1A1A1A">
<italic>A. greatheadii</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B21">Botes et al. (2008)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">14</td>
<td align="left" style="color:#1A1A1A">Trigonelline</td>
<td align="left">
<sup>1</sup>H NMR</td>
<td align="left" style="color:#1A1A1A">C<sub>7</sub>H<sub>7</sub>NO<sub>2</sub>
</td>
<td align="left">137.14</td>
<td align="left" style="color:#1A1A1A">
<italic>A. vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez, et al. (2020)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">15</td>
<td align="left" style="color:#1A1A1A">Hexahydrobenzoindole</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>12</sub>H<sub>13</sub>N</td>
<td align="left">171.24</td>
<td align="left" style="color:#1A1A1A">
<italic>A. greatheadii</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B21">Botes et al. (2008)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">16</td>
<td align="left" style="color:#1A1A1A">Indole-5-acetic acid</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>10</sub>H<sub>9</sub>NO<sub>2</sub>
</td>
<td align="left">180.21</td>
<td align="left" style="color:#1A1A1A">
<italic>A. greatheadii and A ferox</italic>
</td>
<td align="left" style="color:#1A1A1A">
<xref ref-type="bibr" rid="B21">Botes et al., 2008</xref>; <xref ref-type="bibr" rid="B66">Loots et al., 2007</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">17</td>
<td align="left" style="color:#1A1A1A">Pyrrolo [3,2-d]pyrimidin-2,4 (1H,3H)-dione</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>6</sub>H<sub>5</sub>N<sub>3</sub>O<sub>2</sub>
</td>
<td align="left">151.12</td>
<td align="left" style="color:#1A1A1A">
<italic>A. vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B8">Alghamdi et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">18</td>
<td align="left" style="color:#1A1A1A">Hypoxanthine</td>
<td align="left">GC-MS analysis and HPLC</td>
<td align="left" style="color:#1A1A1A">C<sub>5</sub>H<sub>4</sub>N<sub>4</sub>O</td>
<td align="left">136.11</td>
<td align="left" style="color:#1A1A1A">
<italic>A. greatheadii</italic>
</td>
<td align="left" style="color:#1A1A1A">
<xref ref-type="bibr" rid="B21">Botes et al., 2008</xref>; <xref ref-type="bibr" rid="B96">Salehi et al., 2018</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">19</td>
<td align="left" style="color:#1A1A1A">Xanthine</td>
<td align="left">HPLC</td>
<td align="left" style="color:#1A1A1A">C<sub>5</sub>H<sub>4</sub>N<sub>4</sub>O<sub>2</sub>
</td>
<td align="left">152.11</td>
<td align="left" style="color:#1A1A1A">
<italic>A. ferox</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B96">Salehi et al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">20</td>
<td align="left" style="color:#1A1A1A">Uric acid</td>
<td align="center">-</td>
<td align="left" style="color:#1A1A1A">C<sub>5</sub>H<sub>4</sub>N<sub>4</sub>O<sub>3</sub>
</td>
<td align="left">168.11</td>
<td align="left" style="color:#1A1A1A">
<italic>A. vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B44">Hamman (2008)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">21</td>
<td align="left" style="color:#1A1A1A">Bumetrizole</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>17</sub>H<sub>18</sub>ClN<sub>3</sub>O</td>
<td align="left">315.80</td>
<td align="left" style="color:#1A1A1A">
<italic>A. jucunda</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B30">Dey et al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">22</td>
<td align="left" style="color:#1A1A1A">4,7-dichloroquinoline</td>
<td align="left">UV, NMR, and MS analyses</td>
<td align="left" style="color:#1A1A1A">C<sub>9</sub>H<sub>5</sub>Cl<sub>2</sub>N</td>
<td align="left">198.05</td>
<td align="left" style="color:#1A1A1A">
<italic>A. hijazensis</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B1">Abd-Alla et al. (2009)</xref>
</td>
</tr>
<tr>
<td align="left" style="color:#1A1A1A">23</td>
<td align="left" style="color:#1A1A1A">Norcinnamolaurine</td>
<td align="left">GC-MS analysis</td>
<td align="left" style="color:#1A1A1A">C<sub>17</sub>H<sub>17</sub>NO<sub>3</sub>
</td>
<td align="left">283.32</td>
<td align="left" style="color:#1A1A1A">
<italic>A. vera</italic>
</td>
<td align="left">
<xref ref-type="bibr" rid="B8">Alghamdi et al. (2023)</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>&#x201c; -&#x201d; Unspecified.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Structure of alkaloids detected from <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g002.tif"/>
</fig>
</sec>
<sec id="s3-2">
<title>3.2 Vitamins</title>
<p>Vitamins are organic compounds required by humans as nutrients in small amounts known as micronutrients. They are very important compounds for the activities of enzyme cofactors and coenzymes. The term vitamin is derived from the Latin words &#x2018;vital&#x2019; and &#x2018;amine&#x2019;, combined as &#x201c;vital amines&#x201d; or &#x201c;vitamines&#x201d;. The &#x201c;e" at the end of &#x201c;vitamine&#x201d; was later removed when it was realized that vitamins need not be nitrogen-containing amines. Therefore, not all vitamins are amines (<xref ref-type="bibr" rid="B73">Menon et al., 2008</xref>; <xref ref-type="bibr" rid="B76">Miodownik and Lerner, 2010</xref>; <xref ref-type="bibr" rid="B39">Godswill et al., 2020</xref>). Among the vitamins detected from <italic>Aloe</italic> species are choline, folic acid (B<sub>9</sub>), vitamin B<sub>1</sub> (thiamine), niacin (nicotinic acid, also known as vitamin B<sub>3</sub>), vitamin B<sub>2</sub> (riboflavin), vitamin B<sub>6</sub> (pyridoxine), and vitamin B<sub>12</sub> (cyanocobalamin). Although vitamin B<sub>6</sub> is a collective term for pyridoxine, pyridoxal, and pyridoxamine, pyridoxine occurs predominantly in plants, whereas pyridoxal and pyridoxamine are found in foods obtained from animals (<xref ref-type="bibr" rid="B45">Hellmann and Mooney, 2010</xref>; <xref ref-type="bibr" rid="B29">Dewangan and Bhatia, 2023</xref>). Therefore, the B<sub>6</sub> detected in <italic>Aloe</italic> plants is pyridoxine (<bold>compound 28</bold>). Choline is not strictly a vitamin but is an essential nutritional quaternary ammonium salt form of amine. However, it is known in the literature by means of vitamin B<sub>4</sub> (<xref ref-type="bibr" rid="B90">Rakkar and Hillier, 2007</xref>). In <italic>Aloe</italic> species, it has been reported as a vitamin. Being mostly studied and known by various names, <italic>A. vera</italic> is the species for which these vitamins are reported (<xref ref-type="bibr" rid="B6">Akaberi et al., 2016</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, 2016</xref>; <xref ref-type="bibr" rid="B68">Maan et al., 2018</xref>; <xref ref-type="bibr" rid="B88">Pegu and Sharma, 2019</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al., 2020</xref>; <xref ref-type="bibr" rid="B2">Adlakha et al., 2022</xref>).</p>
<p>The majority of vitamin studies omitted information about the analytical techniques used to detect them. <xref ref-type="bibr" rid="B80">Munoz et al. (2015)</xref> have reported that the Association of Official Analytical Chemists (AOAC) is utilized for the purpose of detecting vitamins in <italic>A. vera</italic>. Furthermore, choline from <italic>A. vera</italic> has been detected using <sup>1</sup>H NMR (<xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al., 2020</xref>). Since nitrogen is a structural component of all these vitamins, they are all amine compounds (<xref ref-type="fig" rid="F3">Figure 3</xref>). Because of this nitrogen, the vitamin&#x2019;s amines can be classified as primary, secondary, tertiary, quaternary ammonium salts, and/or heterocyclic amines (<xref ref-type="table" rid="T2">Table 2</xref>).</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Amine containing vitamins detected from <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g003.tif"/>
</fig>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Vitamins detected in <italic>Aloe</italic> species.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">No</th>
<th align="left">Common names</th>
<th align="left">Vitamin type</th>
<th align="left">Amine type</th>
<th align="left">Molecular formula</th>
<th align="left">Molecular weight (g/mol)</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">24</td>
<td align="left">Choline</td>
<td align="left">Vitamin B<sub>4</sub>
</td>
<td align="left">Quaternary ammonium salts</td>
<td align="left">C<sub>5</sub>H<sub>14</sub>NO<sup>&#x2b;</sup>
</td>
<td align="left">104.17</td>
</tr>
<tr>
<td align="left">25</td>
<td align="left">Folic acid</td>
<td align="left">Vitamin B<sub>9</sub>
</td>
<td align="left">1&#x00B0;, 2&#x00B0; and pteridine</td>
<td align="left">C<sub>19</sub>H<sub>19</sub>N<sub>7</sub>O<sub>6</sub>
</td>
<td align="left">441.4</td>
</tr>
<tr>
<td align="left">26</td>
<td align="left">Thiamin</td>
<td align="left">Vitamin B<sub>1</sub>
</td>
<td align="left">More than one type</td>
<td align="left">C<sub>12</sub>H<sub>17</sub>N<sub>4</sub>OS<sup>&#x2b;</sup>
</td>
<td align="left">265.36</td>
</tr>
<tr>
<td align="left">27</td>
<td align="left">Nicotinic acid</td>
<td align="left">Vitamin B<sub>3</sub>
</td>
<td align="left">Pyridine</td>
<td align="left">C<sub>6</sub>H<sub>5</sub>NO<sub>2</sub>
</td>
<td align="left">123.11</td>
</tr>
<tr>
<td align="left">28</td>
<td align="left">Pyridoxine</td>
<td align="left">Vitamin B<sub>6</sub>
</td>
<td align="left">Pyridine</td>
<td align="left">C<sub>8</sub>H<sub>11</sub>NO<sub>3</sub>
</td>
<td align="left">169.18</td>
</tr>
<tr>
<td align="left">29</td>
<td align="left">Riboflavin</td>
<td align="left">Vitamin B<sub>2</sub>
</td>
<td align="left">Pteridine</td>
<td align="left">C<sub>17</sub>H<sub>20</sub>N<sub>4</sub>O<sub>6</sub>
</td>
<td align="left">376.4</td>
</tr>
<tr>
<td align="left">30</td>
<td align="left">Cyanocobalamin</td>
<td align="left">Vitamin B<sub>12</sub>
</td>
<td align="left">More than one type</td>
<td align="left">C<sub>63</sub>H<sub>88</sub>CoN<sub>14</sub>O<sub>14</sub>P</td>
<td align="left">1355.4</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s3-3">
<title>3.3 Hormones and neurotransmitters</title>
<p>Auxins are a group of naturally occurring plant hormones (<xref ref-type="bibr" rid="B3">Agboola et al., 2014</xref>), and they are one of the two hormones repeatedly reported from <italic>Aloe</italic> species such as <italic>A. vera</italic> (<xref ref-type="bibr" rid="B44">Hamman, 2008</xref>). In other studies, indole-3-acetic acid (<xref ref-type="fig" rid="F4">Figure 4</xref>; Compound 31) was detected in <italic>A. vera (</italic>
<xref ref-type="bibr" rid="B82">Nejatzadeh-Barandozi, 2013</xref>) and <italic>A ferox</italic> (<xref ref-type="bibr" rid="B66">Loots et al., 2007</xref>). This indole-3-acetic acid is one of the auxin compounds (<xref ref-type="bibr" rid="B98">Santos et al., 2021</xref>). However, the works of literature that reported the presence of auxins from <italic>Aloe</italic> species have not mentioned indole-3-acetic acid presence as well, and the literature that reported indole-3-acetic acid has not explained it as one of auxin hormones. Therefore, the current work combines the literature to clarify the auxin hormones present in the <italic>Aloe</italic> species in the form of indole-3-acetic acid. The newly reported amine-containing hormone from <italic>Aloe</italic> species is noradrenaline (32, <xref ref-type="fig" rid="F4">Figure 4</xref>). It was analyzed from <italic>A. barbadensis</italic> Mill. (<xref ref-type="bibr" rid="B5">Ahluwalia et al., 2022</xref>). Noradrenaline, also called norepinephrine, is an organic chemical in the catecholamine family that functions in the brain and body as both a hormone and neurotransmitter (<xref ref-type="bibr" rid="B99">Savaliya and Georrge, 2020</xref>). Hence, it is important to understand the two amine hormones of <italic>Aloe</italic> species, both, namely, and structurally.</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>Amine hormones detected from <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g004.tif"/>
</fig>
</sec>
<sec id="s3-4">
<title>3.4 Nucleobases, nucleosides, and nucleotides</title>
<p>Nucleobases (nitrogenous bases or simply bases) are nitrogen-containing biological compounds that form nucleosides, which, in turn, are components of nucleotides, with all of these monomers constituting the basic building blocks of nucleic acids (<xref ref-type="bibr" rid="B9">Al-hayali, 2022</xref>). Among the five nucleobases, thymine and uracil (<xref ref-type="fig" rid="F5">Figure 5</xref>) were detected in <italic>A. vera</italic> (<xref ref-type="bibr" rid="B82">Nejatzadeh-Barandozi, 2013</xref>), <italic>A. ferox</italic> (<xref ref-type="bibr" rid="B66">Loots et al., 2007</xref>), and <italic>A. greatheadii</italic> (<xref ref-type="bibr" rid="B21">Botes et al., 2008</xref>). These bases are pyrimidine bases because they are derived from pyrimidine. The main distinction between thymine (T) and uracil (U) lies in their chemical structure. Thymine <bold>(33)</bold> has a methyl group (CH<sub>3</sub>) attached to its ring structure, whereas uracil (<bold>34</bold>) does not have this methyl group. This structural difference is responsible for the various roles of thymine in DNA and uracil in RNA (<xref ref-type="bibr" rid="B84">Ono et al., 2011</xref>; <xref ref-type="bibr" rid="B65">Lippert and Sanz Miguel, 2016</xref>). In addition to nucleobases, nucleoside and nucleotide have been detected in <italic>Aloe</italic> species. Adenosine (nucleoside, <bold>36</bold>) and adenosine monophosphate (nucleotide, <bold>37</bold>) have been detected quantitatively from the flower of <italic>A. vera</italic> (<xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al., 2020</xref>).</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>Nucleobases detected from <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g005.tif"/>
</fig>
</sec>
<sec id="s3-5">
<title>3.5 Amino sugars and related amines</title>
<p>Amino sugars are chemical compounds with a sugar backbone where an amine group has taken the place of one of the hydroxyl groups (<xref ref-type="bibr" rid="B87">Parsons, 2021</xref>). Glucosamine (<bold>35</bold>) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids (<xref ref-type="bibr" rid="B27">Dalirfardouei et al., 2016</xref>). A sugar in which an amino group replaces the anomeric OH is called a glycosylamine. Adenosine (<bold>36</bold>) is glycosylamine, in which the amino component is a purine. The molecule consists of an adenine attached to a ribose via a &#x3b2;-N<sub>9</sub>-glycosidic bond. Adenosine is one of the four nucleoside building blocks of RNA (and its derivative, deoxyadenosine, is a building block of DNA), which are essential for all life on earth (<xref ref-type="bibr" rid="B120">V&#xe1;zquez-Salazar et al., 2018</xref>; <xref ref-type="bibr" rid="B92">Rodrigues, 2021</xref>). A nucleotide consists of a sugar molecule (either ribose in RNA or deoxyribose in DNA) attached to a phosphate group and a nitrogen-containing base (<xref ref-type="bibr" rid="B116">Tripathi et al., 2023</xref>). Adenosine monophosphate (AMP), also known as 5&#x2032;-adenylic acid, is a nucleotide. AMP (<bold>37</bold>) consists of a phosphate group, the sugar ribose, and the nucleobase adenine (<xref ref-type="bibr" rid="B81">Najeeb et al., 2023</xref>). Glucosamine, adenosine, and AMP have been detected in <italic>Aloe</italic> species (<xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al., 2020</xref>; <xref ref-type="bibr" rid="B5">Ahluwalia et al., 2022</xref>). These compounds have amine and sugar in their structure, which makes them similar to one another (<xref ref-type="fig" rid="F6">Figure 6</xref>).</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption>
<p>Glucosamine, adenosine, and AMP detected from <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g006.tif"/>
</fig>
</sec>
<sec id="s3-6">
<title>3.6 Amino acids</title>
<p>Amino acid is any of a group of organic molecules that consist of a basic amino group (NH<sub>2</sub>), an acidic carboxyl group (COOH), and an organic side chain <italic>(R</italic> group, unique to each amino acid) (<xref ref-type="bibr" rid="B113">Taniguchi, 2010</xref>). Amino acids are primary amines (<xref ref-type="bibr" rid="B72">Mcmurry, 2016</xref>)<bold>.</bold> Amino acids are essential plant compounds serving as the building blocks of proteins, the predominant forms of nitrogen (N) distribution, and signaling molecules (<xref ref-type="bibr" rid="B78">Moe, 2013</xref>). The amino acids of <italic>Aloe</italic> plants have been reported by many authors in both quantitative and qualitative analyses. Although there are a number of methods to detect amino acids, many of the amino acids (<xref ref-type="table" rid="T3">Table 3</xref>) detected in <italic>Aloe</italic> species were using an amino acid analyzer equipped with an HPLC and UV detector (<xref ref-type="bibr" rid="B56">Kim et al., 2013</xref>; <xref ref-type="bibr" rid="B22">Chandra Sekhar Singh et al., 2018</xref>). In addition to that, HPLC and <sup>1</sup>H NMR were used for the detection of amino acids in <italic>Aloe</italic> species (<xref ref-type="bibr" rid="B46">Hendrawati et al., 2019</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al., 2020</xref>). The analyzed amino acids from <italic>Aloe</italic> species are the twenty standard &#x3b1;-amino acids and their derivatives, which differ only in side chain (R) groups (<xref ref-type="fig" rid="F7">Figure 7</xref>: structures 38&#x2013;60). The noncyclic &#x3b1;-amino acids have an amino group in their C<sub>2</sub>, which &#x2018;2-amino&#x2019; is common for all. In addition to &#x3b1;-amino acids, &#x3b2;-amino acids (<bold>61</bold> and <bold>62</bold>) and &#x3b3;-amino acids (63) have been analyzed from <italic>Aloe</italic> species (<xref ref-type="fig" rid="F7">Figure 7</xref>). Totally, the amino acids detected from <italic>Aloe</italic> species have been summarized in <xref ref-type="table" rid="T3">Table 3</xref>; <xref ref-type="fig" rid="F7">Figure 7</xref>.</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Amino acids detected from <italic>Aloe</italic> species.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">&#x2116;</th>
<th align="center">Original/source common name</th>
<th align="center">IUPAC name</th>
<th align="left">Molecular formula</th>
<th align="center">Molecular weight (g/mol)</th>
<th align="left">
<italic>Aloe</italic> species</th>
<th align="center">References</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">38</td>
<td align="center">Glycine</td>
<td align="center">2-aminoethanoic acid</td>
<td align="left">C<sub>2</sub>H<sub>5</sub>NO<sub>2</sub>
</td>
<td align="left">75.07</td>
<td align="left">
<italic>A. vera, A. saponaria, A. arborescens</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, (2016)</xref>
</td>
</tr>
<tr>
<td align="center">39</td>
<td align="center">Alanine</td>
<td align="center">2-aminopropanoic acid</td>
<td align="left">C<sub>3</sub>H<sub>7</sub>NO<sub>2</sub>
</td>
<td align="left">89.09</td>
<td align="left">
<italic>A. vera, A. saponaria,</italic> <italic>A. arborescens</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>
</td>
</tr>
<tr>
<td align="center">40</td>
<td align="center">Valine</td>
<td align="center">2-amino-3-methylbutanoic acids</td>
<td align="left">C<sub>5</sub>H<sub>11</sub>NO<sub>2</sub>
</td>
<td align="left">117.15</td>
<td align="left">
<italic>A. vera, A. saponaria,</italic> and <italic>A. arborescens</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>
</td>
</tr>
<tr>
<td align="center">41</td>
<td align="center">Leucine</td>
<td align="center">2-amino-4-methylpentanoic acid</td>
<td align="left">C<sub>6</sub>H<sub>13</sub>NO<sub>2</sub>
</td>
<td align="left">131.17</td>
<td align="left">
<italic>A. vera</italic> and <italic>A. saponaria</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B15">Bajpai, (2018)</xref>
</td>
</tr>
<tr>
<td align="center">42</td>
<td align="center">Isoleucine</td>
<td align="center">2-amino-3-methylpentanoic acid</td>
<td align="left">C<sub>6</sub>H<sub>13</sub>NO<sub>2</sub>
</td>
<td align="left">131.17</td>
<td align="left">
<italic>A. vera, A. saponaria, and</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>
</td>
</tr>
<tr>
<td align="center">43</td>
<td align="center">Phenylalanine</td>
<td align="center">2-amino-3-phenylpropanoic acid</td>
<td align="left">C<sub>9</sub>H<sub>12</sub>NO<sub>2</sub>
</td>
<td align="left">165.19</td>
<td align="left">
<italic>A. vera,</italic> and <italic>A. saponaria</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>
</td>
</tr>
<tr>
<td align="center">44</td>
<td align="center">Serine</td>
<td align="center">2-amino-3-hydroxypropanoic acid</td>
<td align="left">C<sub>3</sub>H<sub>7</sub>NO<sub>3</sub>
</td>
<td align="left">105.09</td>
<td align="left">
<italic>A. vera, A. saponaria,</italic> and <italic>A. arborescens</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, (2016)</xref>
</td>
</tr>
<tr>
<td align="center">45</td>
<td align="center">Threonine</td>
<td align="center">2-amino-3-hydroxybutanoic acid</td>
<td align="left">C<sub>4</sub>H<sub>9</sub>NO<sub>3</sub>
</td>
<td align="left">119.12</td>
<td align="left">
<italic>A. vera</italic> and <italic>A. saponaria</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>
</td>
</tr>
<tr>
<td align="center">46</td>
<td align="center">Tyrosine</td>
<td align="center">2-amino-3-(4-hydroxyphenyl)propanoic acid</td>
<td align="left">C<sub>9</sub>H<sub>11</sub>NO<sub>3</sub>
</td>
<td align="left">181.19</td>
<td align="left">
<italic>A. vera</italic> and <italic>A. saponaria</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>
</td>
</tr>
<tr>
<td align="center">47</td>
<td align="center">Cysteine</td>
<td align="center">2-amino-3-mercaptopropanoic acid</td>
<td align="left">C<sub>3</sub>H<sub>7</sub>NO<sub>2</sub>S</td>
<td align="left">121.16</td>
<td align="left">
<italic>A.vera</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B69">Mahor and Ali (2016)</xref>
</td>
</tr>
<tr>
<td align="center">48</td>
<td align="center">Methionine</td>
<td align="center">2-amino-4-(methylthio)butanoic acid</td>
<td align="left">C<sub>5</sub>H<sub>11</sub>NO<sub>2</sub>S</td>
<td align="left">149.21</td>
<td align="left">
<italic>A. vera</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B15">Bajpai, (2018)</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, (2016)</xref>
</td>
</tr>
<tr>
<td align="center">49</td>
<td align="center">Asparagine</td>
<td align="center">2-amino-3-carbamoylpropanoic acid</td>
<td align="left">C<sub>4</sub>H<sub>8</sub>N<sub>2</sub>O<sub>3</sub>
</td>
<td align="left">132.12</td>
<td align="left">
<italic>A.vera</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B69">Mahor and Ali (2016)</xref>
</td>
</tr>
<tr>
<td align="center">50</td>
<td align="center">Glutamine</td>
<td align="center">2-amino-4-carbamoylbutanoic acid</td>
<td align="left">C<sub>5</sub>H<sub>10</sub>N<sub>2</sub>O<sub>3</sub>
</td>
<td align="left">146.14</td>
<td align="left">
<italic>A. vera</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B69">Mahor and Ali (2016)</xref>
</td>
</tr>
<tr>
<td align="center">51</td>
<td align="center">Tryptophan</td>
<td align="center">2-amino-3-(1H-indol-3-yl)propanoic acid</td>
<td align="left">C<sub>11</sub>H<sub>12</sub>N<sub>2</sub>O<sub>2</sub>
</td>
<td align="left">204.22</td>
<td align="left">
<italic>A. vera</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>; <xref ref-type="bibr" rid="B107">Sotelo et al. (2007)</xref>
</td>
</tr>
<tr>
<td align="center">52</td>
<td align="center">Aspartic acid</td>
<td align="center">2-aminosuccinic acid</td>
<td align="left">C<sub>4</sub>H<sub>7</sub>NO<sub>4</sub>
</td>
<td align="left">133.10</td>
<td align="left">
<italic>A. vera, A. saponaria, A. arborescens</italic> and <italic>A. barbadensis</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="center">53</td>
<td align="center">Glutamic acid</td>
<td align="center">2-aminopentanedioic acid</td>
<td align="left">C<sub>5</sub>H<sub>9</sub>NO<sub>4</sub>
</td>
<td align="left">147.13</td>
<td align="left">
<italic>A. vera, A. saponaria, A. arborescens</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, (2016)</xref>
</td>
</tr>
<tr>
<td align="center">54</td>
<td align="center">Lysine</td>
<td align="center">2,6-diaminohexanoic acid</td>
<td align="left">C<sub>6</sub>H<sub>14</sub>N<sub>2</sub>O<sub>2</sub>
</td>
<td align="left">146.19</td>
<td align="left">
<italic>A. vera, A. saponaria</italic> and <italic>A. arborescens</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, (2016)</xref>
</td>
</tr>
<tr>
<td align="center">55</td>
<td align="center">Arginine</td>
<td align="center">2-amino-5-guanidinopentanoic acid</td>
<td align="left">C<sub>6</sub>H<sub>14</sub>N<sub>4</sub>O<sub>2</sub>
</td>
<td align="left">174.20</td>
<td align="left">
<italic>A. vera</italic> and <italic>A. saponaria</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, (2016)</xref>
</td>
</tr>
<tr>
<td align="center">56</td>
<td align="center">Histidine</td>
<td align="center">2-amino-3-(1H-imidazole-4-yl) propanoic acid</td>
<td align="left">C<sub>6</sub>H<sub>9</sub>N<sub>3</sub>O<sub>2</sub>
</td>
<td align="left">155.15</td>
<td align="left">
<italic>A. vera</italic> and <italic>A. saponaria</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B69">Mahor and Ali, (2016)</xref>
</td>
</tr>
<tr>
<td align="center">57</td>
<td align="center">Proline</td>
<td align="center">pyrrolidine-2-carboxylic acid</td>
<td align="left">C<sub>5</sub>H<sub>9</sub>NO<sub>2</sub>
</td>
<td align="left">115.13</td>
<td align="left">
<italic>A. vera. A. saponaria</italic> and <italic>A. arborescens</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="center">58</td>
<td align="center">Hydroxyproline</td>
<td align="center">3-hydroxypyrrolidine-2-carboxylic acid</td>
<td align="left">C<sub>5</sub>H<sub>9</sub>NO<sub>3</sub>
</td>
<td align="left">131.13</td>
<td align="left">
<italic>A. vera</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B15">Bajpai (2018)</xref>
</td>
</tr>
<tr>
<td align="center">59</td>
<td align="center">Pyroglutamic acid</td>
<td align="center">5-oxopyrrolidine-2-carboxylic acid</td>
<td align="left">C<sub>5</sub>H<sub>7</sub>NO<sub>3</sub>
</td>
<td align="left">129.11</td>
<td align="left">
<italic>A. barbadensis</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B5">Ahluwalia et al., 2022</xref>
</td>
</tr>
<tr>
<td align="center">60</td>
<td align="center">&#x3b1;-amino butyric acid</td>
<td align="center">2-aminobutanoic acid</td>
<td align="left">C<sub>4</sub>H<sub>9</sub>NO<sub>2</sub>
</td>
<td align="left">103.12</td>
<td align="left">
<italic>A. vera</italic> and <italic>A. arborescens</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="center">61</td>
<td align="center">&#x3b2;-alanine</td>
<td align="center">3-aminopropanoic acid</td>
<td align="left">C<sub>3</sub>H<sub>8</sub>N<sub>2</sub>O<sub>4</sub>
</td>
<td align="left">136.11</td>
<td align="left">
<italic>A. vera, A. saponaria</italic> and <italic>A. arborescens</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="center">62</td>
<td align="center">&#x3b2;-amino isobutyric acid</td>
<td align="center">3-amino-2-methylpropanoic acid</td>
<td align="left">C<sub>4</sub>H<sub>9</sub>NO<sub>2</sub>
</td>
<td align="left">103.12</td>
<td align="left">
<italic>A. vera</italic> and <italic>A. saponaria</italic>
</td>
<td align="center">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="center">63</td>
<td align="center">&#x3b3;-aminobutyric acid (GABA)</td>
<td align="center">4-aminobutanoic acid</td>
<td align="left">C<sub>4</sub>H<sub>9</sub>NO<sub>2</sub>
</td>
<td align="left">103.12</td>
<td align="left">
<italic>A. vera, A. saponaria, A. arborescens,</italic> and <italic>A. barbadensis</italic>
</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>; <xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>; <xref ref-type="bibr" rid="B71">Mart&#xed;nez-S&#xe1;nchez et al. (2020)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>Amino acids detected from <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g007.tif"/>
</fig>
</sec>
<sec id="s3-7">
<title>3.7 Other amines of <italic>Aloe</italic> species</title>
<p>Compounds 64&#x2013;72 were reported from <italic>Aloe</italic> species (<xref ref-type="fig" rid="F8">Figure 8</xref>). These compounds have a good sense if kept as amines rather than grouping them into other organic compounds such as alkloids. For instance, compounds (67) and (68) were reported as alkaloids from <italic>Aloe</italic> species (<xref ref-type="bibr" rid="B26">Dagne et al., 2000</xref>; <xref ref-type="bibr" rid="B25">Cock, 2015</xref>). The amine called 2-phenylethanamine (69) is a precursor for many compounds, including noradrenaline (Solomons, 2011), the hormone reported from <italic>A. barbadensis</italic> Mill. Regarding the amines detected from <italic>Aloe</italic> species, any amine may be monoamine or polyamine such as diamines, triamines, tetramines, or, etc., based on the number of nitrogens present in the structure (<xref ref-type="table" rid="T4">Table 4</xref>; <xref ref-type="fig" rid="F8">Figure 8</xref>). Monoamines have one nitrogen in their structure, while polyamines have two or more ntrogens in their structures. The quantities of putresine, spermidine, and spermine polyamines have been analyzed from the leaf gels of <italic>A. arborescens</italic> Mill., <italic>A. aristata</italic> Haw., <italic>A. claviflora</italic> Str., <italic>A. ferox</italic> Mill., <italic>A. mitriformis</italic> Mill., <italic>A. saponaria</italic> Ait., <italic>A. striata</italic> Haw., and <italic>A. vera</italic> L, <italic>A. barbadensis</italic> Mill. (<xref ref-type="bibr" rid="B18">Beppu et al., 2004</xref>; <xref ref-type="bibr" rid="B126">Zapata et al., 2013</xref>; <xref ref-type="bibr" rid="B5">Ahluwalia et al., 2022</xref>). These polyamines have biochemical relationships. They also have specific odors, which make amines have unique odors, such as rotting fish. For instance, 1,4-butanediamine (<bold>71</bold>) has the appalling odors that might be expected from its common name, &#x2018;putrescine&#x2019; derived from odor. Biologically, putrescine is synthesised from the catabolism of proteins (<xref ref-type="bibr" rid="B72">Mcmurry, 2016</xref>).</p>
<fig id="F8" position="float">
<label>FIGURE 8</label>
<caption>
<p>Amines of <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g008.tif"/>
</fig>
<table-wrap id="T4" position="float">
<label>TABLE 4</label>
<caption>
<p>Amines detected from <italic>Aloe</italic> species.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">No</th>
<th align="center">Name</th>
<th align="center">Detection methods</th>
<th align="center">Amine type based on number of N</th>
<th align="center">Molecular formula</th>
<th align="center">Molecular wight (g/mol)</th>
<th align="center">References</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">64</td>
<td align="center">Cyclopropanamine</td>
<td align="left">GC-MS</td>
<td align="center">monoamine</td>
<td align="center">C<sub>3</sub>H<sub>7</sub>N</td>
<td align="center">57.09</td>
<td align="center">
<xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="center">65</td>
<td align="center">2-aminoethanol</td>
<td align="left">GC-MS</td>
<td align="center">monoamine</td>
<td align="center">C<sub>2</sub>H<sub>7</sub>NO</td>
<td align="center">61.08</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>; <xref ref-type="bibr" rid="B56">Kim et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="center">66</td>
<td align="center">2-amino-2-methylpropan-1-ol</td>
<td align="left">GC-MS</td>
<td align="center">monoamine</td>
<td align="center">C<sub>4</sub>H<sub>11</sub>NO</td>
<td align="center">89.14</td>
<td align="center">
<xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="center">67</td>
<td align="center">4-(2-(methylamino)ethyl) Phenol</td>
<td align="center">-</td>
<td align="center">monoamine</td>
<td align="center">C<sub>9</sub>H<sub>13</sub>NO</td>
<td align="center">151.21</td>
<td align="center">
<xref ref-type="bibr" rid="B26">Dagne et al. (2000)</xref>
</td>
</tr>
<tr>
<td align="center">68</td>
<td align="center">2-(4-methoxyphenyl)-N-methylethanamine</td>
<td align="center">-</td>
<td align="center">monoamine</td>
<td align="left">C<sub>10</sub>H<sub>15</sub>NO</td>
<td align="center">165.24</td>
<td align="center">
<xref ref-type="bibr" rid="B26">Dagne et al. (2000)</xref>
</td>
</tr>
<tr>
<td align="center">69</td>
<td align="center">2-phenylethanamine</td>
<td align="left">GC-MS</td>
<td align="center">monoamine</td>
<td align="center">C<sub>8</sub>H<sub>11</sub>N</td>
<td align="center">121.18</td>
<td align="center">
<xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="center">70</td>
<td align="center">Putrescine</td>
<td align="left">HPLC-DAD, Spectrofluorometric detector fitted to HPLC</td>
<td align="center">diamines</td>
<td align="center">C<sub>4</sub>H<sub>12</sub>N<sub>2</sub>
</td>
<td align="center">90.14</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>; <xref ref-type="bibr" rid="B126">Zapata et al. (2013)</xref>; <xref ref-type="bibr" rid="B18">Beppu et al. (2004)</xref>
</td>
</tr>
<tr>
<td align="center">71</td>
<td align="center">Spermidine</td>
<td align="left">HPLC-DAD, Spectrofluorometric detector fitted to HPLC</td>
<td align="center">triamines</td>
<td align="center">C<sub>7</sub>H<sub>19</sub>N<sub>3</sub>
</td>
<td align="center">145.25</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B126">Zapata et al. (2013)</xref>; <xref ref-type="bibr" rid="B18">Beppu et al. (2004)</xref>
</td>
</tr>
<tr>
<td align="center">72</td>
<td align="center">Spermine</td>
<td align="left">HPLC-DAD, Spectrofluorometric detector fitted to HPLC</td>
<td align="center">tetraamines</td>
<td align="center">C<sub>10</sub>H<sub>26</sub>N<sub>4</sub>
</td>
<td align="center">202.34</td>
<td align="center" style="color:#FF0000">
<xref ref-type="bibr" rid="B126">Zapata et al. (2013)</xref>; <xref ref-type="bibr" rid="B18">Beppu et al. (2004)</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>&#x201c;-&#x201d; unspecified.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
</sec>
<sec id="s4">
<title>4 Biological activities of <italic>Aloe</italic> amines</title>
<p>Traditionally, people use various parts of <italic>Aloe</italic> species such as leaf gel, leaf latex, fresh leaf, root, flowers, etc. solely or by incorporating them into other substances for impotency in men, wounds, malaria, ticks, bloat and fire burn, caught, stomach ache, gonorrhea, swollen foot, strain, ascariasis, anthrax, internal parasite, weaning a child from breastfeeding, psychiatric disease, sprain, diabetes, liver disease, eye aliments, used as a poison, abdominal cramp, pasterlosis, black leg, skin softening, tuberculosis, and antiworms (<xref ref-type="bibr" rid="B83">Oda and Erena, 2017</xref>; <xref ref-type="bibr" rid="B17">Belayneh et al., 2020</xref>). These applications of <italic>Aloe</italic> species arise from the biologically active properties of the plants, which are due to their compounds (<xref ref-type="bibr" rid="B89">Radha and Laxmipriya, 2015</xref>; <xref ref-type="bibr" rid="B74">Mikayoulou et al., 2021</xref>). In modern days, the <italic>in vivo</italic> and <italic>in vitro</italic> bioactivities of <italic>Aloe</italic> species have been investigated. antioxidants (<xref ref-type="bibr" rid="B48">Hu et al., 2003</xref>; <xref ref-type="bibr" rid="B62">Lee et al., 2012</xref>; <xref ref-type="bibr" rid="B100">Sazhina et al., 2016</xref>), anti-inflammatory (<xref ref-type="bibr" rid="B43">Hajhashemi et al., 2012</xref>), antibacterial (<xref ref-type="bibr" rid="B86">Pandey and Mishra, 2010</xref>; <xref ref-type="bibr" rid="B63">Leitgeb et al., 2021</xref>), antifungal (<xref ref-type="bibr" rid="B126">Zapata et al., 2013</xref>), antiviral (<xref ref-type="bibr" rid="B38">Glatthaar-Saalm&#xfc;ller et al., 2015</xref>), antimalarial (<xref ref-type="bibr" rid="B124">Yadeta, 2022</xref>), anticancer (<xref ref-type="bibr" rid="B52">Karpagam et al., 2019</xref>), antidiabetic (<xref ref-type="bibr" rid="B54">Kazeem et al., 2022</xref>), wound healing (<xref ref-type="bibr" rid="B36">Fox et al., 2017</xref>), and etc. (<xref ref-type="bibr" rid="B96">Salehi et al., 2018</xref>).</p>
<p>In most of the <italic>Aloe</italic> species, the synergistic effects of amine compounds were investigated. In the literature, amine compounds were one of the compounds detected by GC-MS in <italic>A. vera</italic> for antibacterial activities and antioxidant capacity (<xref ref-type="bibr" rid="B82">Nejatzadeh-Barandozi, 2013</xref>). The study is similar to the work of <xref ref-type="bibr" rid="B21">Botes et al. (2008)</xref> on <italic>A. greatheadii</italic> var. <italic>davyana</italic>. These studies show the biological activities of the <italic>Aloe</italic> plants and the synergistic effect of the compounds, which indicate that amines have a vital role in the biological activities of <italic>Aloe</italic> extracts. In another way, <xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref> tested compounds of <italic>A. barbadensis</italic> Miller including amines by correlating them to the effect of human blood T cells. The amine compounds, such as glucosamine single effect was identified from <italic>A. barbadensis</italic> Miller. Such tests identify the highly effective components of the plant extracts as well as the amine compounds such as glucosamine. The biological activities of amines in <italic>Aloe</italic> species have been summarized in <xref ref-type="table" rid="T5">Table 5</xref>. Generally, researchers use three approaches to determine the biological activities of <italic>Aloe</italic> species. These are: (i) using the extracts of the plant without identifying the active constituents when testing the medicinal potential of the plant is necessary; (ii) testing the bioactivities of the plants&#x2019; compounds synergistically; and (iii) identifying the bioactivities of the plants&#x2019; compounds specifically.</p>
<table-wrap id="T5" position="float">
<label>TABLE 5</label>
<caption>
<p>Biological activities of <italic>Aloe</italic> species amines.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Amine compound</th>
<th align="center">Biological activities</th>
<th align="center">References</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">Pyrrolo [3,2-d] pyrimidin-2,4 (1H,3H)-dione</td>
<td align="center">anti-inflammatory, antitumor, antioxidant, antiviral, anti-HIV agents, antiasthmatic, and anticoagulant</td>
<td align="center">
<xref ref-type="bibr" rid="B8">Alghamdi et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="center">2-methyl-5-phenyl- pyrrole</td>
<td align="center">Antimicrobial, inti-inflammatory, and antitumor</td>
<td align="center">
<xref ref-type="bibr" rid="B8">Alghamdi et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="center">Polyamines</td>
<td align="center">Antifungal activities</td>
<td align="center">
<xref ref-type="bibr" rid="B126">Zapata et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="center">Glucosamine</td>
<td align="center">Human blood T cell activity</td>
<td align="center">
<xref ref-type="bibr" rid="B5">Ahluwalia et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="center">Vitamin B<sub>6</sub>
</td>
<td align="center">Antioxidant</td>
<td align="center">
<xref ref-type="bibr" rid="B70">Malik and Zarnigar (2013)</xref>
</td>
</tr>
<tr>
<td align="center">Vitamin B<sub>12</sub>
</td>
<td align="center">Production of red blood cells, antioxidants</td>
<td align="center">
<xref ref-type="bibr" rid="B37">Gajendra and Shaique, (2016)</xref>; <xref ref-type="bibr" rid="B35">Ezzat et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="center">Folic acid</td>
<td align="center">Develop new blood cells, antioxidants</td>
<td align="center">
<xref ref-type="bibr" rid="B37">Gajendra and Shaique, (2016)</xref>; <xref ref-type="bibr" rid="B35">Ezzat et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="center">Choline</td>
<td align="center">Production of energy, amino acid metabolism and developing muscle mass, antioxidants</td>
<td align="center">
<xref ref-type="bibr" rid="B37">Gajendra and Shaique, (2016)</xref>; <xref ref-type="bibr" rid="B35">Ezzat et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="center">Amino acids</td>
<td align="center">Wound healing, moisturizing effect, Anti-inflammatory, antitumor, and basic building blocks of proteins in the body and muscle tissues</td>
<td align="center">
<xref ref-type="bibr" rid="B68">Maan et al. (2018)</xref>; <xref ref-type="bibr" rid="B60">Laneri et al. (2020)</xref>; <xref ref-type="bibr" rid="B118">Upadhyay, (2018)</xref>; <xref ref-type="bibr" rid="B95">Sahu et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="center">Hormones</td>
<td align="center">Wound healing and anti-inflammatory</td>
<td align="center">
<xref ref-type="bibr" rid="B95">Sahu et al. (2013)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s5">
<title>5 Medicinal applications</title>
<sec id="s5-1">
<title>5.1 Pharmaceutical applications</title>
<p>The traditional uses of <italic>Aloe</italic> species have transformed into modern pharmaceutical applications. These days, studies on the biological activities of <italic>Aloe</italic> species both <italic>in vivo</italic> and <italic>in vitro</italic> verify the plant&#x2019;s potential for particular mammalian body systems, including the brain, pancreas, liver, portal vein, intestine, muscles, tissues, lymphatic systems, and so on (<xref ref-type="fig" rid="F9">Figure 9</xref>). In the literature, the therapeutic activities of <italic>Aloe</italic> species for the liver and kidney, gastrointestinal system, upper respiratory tract, reproductive (genital) organs, central and peripheral nervous systems, skin, eyes, hair, joints, and muscles have been reported (<xref ref-type="bibr" rid="B6">Akaberi et al., 2016</xref>). Other studies have used the healing properties of <italic>Aloe</italic> species to treat a variety of cancer diseases, including liver, colon, duodenal, skin, pancreatic, intestinal, lung, and kidney cancers (<xref ref-type="bibr" rid="B104">Singab et al., 2015</xref>). In addition, the metabolic disease Diabetes Mellitus (DM), commonly known as diabetes, has been treated by the medicinal effects of various <italic>Aloe</italic> species (<xref ref-type="bibr" rid="B58">Kumar et al., 2011</xref>; <xref ref-type="bibr" rid="B24">Chen et al., 2012</xref>). Based on these and other medicinal potentials of <italic>Aloe</italic> species, studies have shown that <italic>A. vera</italic> is used to make pharmaceutical products like ointments, tablets, and capsules (<xref ref-type="bibr" rid="B34">Eshun and He, 2004</xref>; <xref ref-type="bibr" rid="B14">Babu and Noor, 2020</xref>).</p>
<fig id="F9" position="float">
<label>FIGURE 9</label>
<caption>
<p>Specific mammalian body systems treated by therapeutic activities <italic>Aloe</italic> species.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g009.tif"/>
</fig>
<p>A large number of medically and biologically important compounds are amines. Because of their high degree of biological activity, many amines are used as drugs and medicines (<xref ref-type="bibr" rid="B105">Solomons and Fryhle, 2008</xref>; <xref ref-type="bibr" rid="B122">Wade, 2008</xref>). Alkaloids, amino acids, vitamins, and other amine compounds are biologically active compounds of <italic>Aloe</italic> species that are used in their medicinal applications and may lead to drug synthesis. For instance, 2-phenylethylamine, noradrenaline, and vitamins are mostly known amine compounds detected in <italic>Aloe</italic> species. Many phenylethylamine compounds have powerful physiological and psychological effects. Noradrenaline is a derivative of 2-phenylethylamine. Norepinephrine is hormone that is released into the bloodstream in response to stress. Recent evidence has elucidated significant changes in cerebral neurotransmitters in mice treated with <italic>A. vera</italic> extract, of which diminished levels of norepinephrine and serotonin are conspicuous (<xref ref-type="bibr" rid="B105">Solomons and Fryhle, 2008</xref>; <xref ref-type="bibr" rid="B109">Sultana and Najam, 2012</xref>). Norepinephrine is both a neurotransmitter and a hormone. It plays an important role in your body&#x2019;s &#x201c;fight-or-flight&#x201d; response. As a medication, norepinephrine is used to increase and maintain blood pressure in limited, short-term, serious health situations (<xref ref-type="bibr" rid="B77">Mittal et al., 2017</xref>). Vitamins are essential for bodily functions such as helping to fight infection because of their biological properties such as wound healing, making our bones strong, and regulating hormones (<xref ref-type="bibr" rid="B39">Godswill et al., 2020</xref>). All vitamins detected in the <italic>Aloe</italic> species are water-soluble vitamins and function as coenzymes.</p>
</sec>
<sec id="s5-2">
<title>5.2 Nutraceutical applications</title>
<p>Several species of <italic>Aloes</italic> are mentioned in the literature for their applications as cooked vegetables, snack foods, famine foods, and preserve ingredients (<xref ref-type="bibr" rid="B108">Steenkamp and Stewart, 2007</xref>; <xref ref-type="bibr" rid="B13">Azaroual et al., 2012</xref>). <italic>Aloes</italic> are also utilized as food products and beverage ingredients due to their nutritional components combined to produce beneficial and biological effects (<xref ref-type="bibr" rid="B110">Sun et al., 2015</xref>). Owing to its advantageous characteristics in managing conditions like constipation, coughs, diabetes, headaches, arthritis, and immune system deficiencies, <italic>Aloe</italic> species gel is applicable in the food industry for functional foods (<xref ref-type="bibr" rid="B75">Minjares-Fuentes et al., 2016</xref>). Famous healthy foods developed from <italic>A. vera</italic> include dahi (a fermented South Asian dairy product) by replacing skim milk with <italic>A. vera</italic> gel, <italic>A. vera</italic> gel-enriched beverages, ice cream, lassi (a traditional fermented dairy beverage of South Asia), mango nectar, and carbonated beverages. Researchers have investigated the presence of bioactive compounds in such foods and beverages (<xref ref-type="bibr" rid="B31">Elbandy et al., 2014</xref>; <xref ref-type="bibr" rid="B67">Luo et al., 2022</xref>).</p>
<p>
<italic>A. vera</italic> gel is used in the nutraceutical industry as a supplement in other food products and as a mineral source for a range of functional foods that are used to make different health drinks and beverages (<xref ref-type="bibr" rid="B93">Rodr&#xed;guez et al., 2010</xref>; <xref ref-type="bibr" rid="B91">Ray et al., 2013</xref>). The food industry uses <italic>A. vera</italic> to make health drinks, jam, jelly, yogurt, cranberry, orange, grape, raspberry, pineapple, and strawberry beverages, among other functional goods (<xref ref-type="bibr" rid="B51">Kahramano&#x11f;lu et al., 2019</xref>; <xref ref-type="bibr" rid="B33">El-Sayed and El-Sayed, 2020</xref>). The <italic>A. vera</italic> plant has been reported for its antioxidant activities of nitrogen-containing vitamins and amino acids. Thus, the consumption of such dietary antioxidants from the <italic>Aloe</italic> species is beneficial in preventing cardiovascular diseases (<xref ref-type="bibr" rid="B55">Khanam and Sharma, 2013</xref>). Dried <italic>A. vera</italic> gel powder reduces body fat mass in diet-induced obesity rats, while its gel protects the liver from oxidative stress-induced damage in an experimental rat model. <italic>A. vera</italic> juice is marketed to support the health of the digestive system. <italic>A. vera</italic> is a good nutrition supplement for diabetic wound healing, while processed <italic>Aloe</italic> food products contain ingredients that show cancer prevention (<xref ref-type="bibr" rid="B118">Upadhyay, 2018</xref>).</p>
<p>Amino acids are required for the synthesis of body proteins and other important nitrogen-containing compounds (<xref ref-type="bibr" rid="B125">Yu and Fukagawa, 2020</xref>). Amino acid deficiency causes a number of disease states, nutritional deficiencies, fatigue, accelerated aging, and even premature death. Many pathological conditions, like a depressed immune system, weight loss, pressure sores, diarrhea, hair and skin depigmentation, and muscle weakness, are related to an amino acid deficiency (<xref ref-type="bibr" rid="B102">Shakerzadeh, 2016</xref>). Therefore, consuming <italic>Aloe</italic>-based products has nutraceutical applications. Especially essential amino acids can be obtained from food only. In another way, amino acid deficiency causes a number of disease states, nutritional deficiencies, fatigue, accelerated aging, and even premature death (<xref ref-type="bibr" rid="B12">Awuchi et al., 2020</xref>). Vitamins are other dietary nitrogen-containing compounds. Every nutrient that humans eat is on a mission to provide health benefits that support the pursuit of wellness. Vitamins work hard to keep our bodies functioning properly, and they help drive essential processes needed in our everyday lives (<xref ref-type="bibr" rid="B115">Tardy et al., 2020</xref>).</p>
<p>In another way, nutritional diseases such as <ext-link ext-link-type="uri" xlink:href="https://www.britannica.com/science/cardiovascular-disease">cardiovascular disease</ext-link>, <ext-link ext-link-type="uri" xlink:href="https://www.britannica.com/science/hypertension">hypertension</ext-link>, <ext-link ext-link-type="uri" xlink:href="https://www.britannica.com/science/cancer-disease">cancer</ext-link>, and <ext-link ext-link-type="uri" xlink:href="https://www.britannica.com/science/diabetes-mellitus">diabetes mellitus</ext-link> may arise from a nutrition deficiency like vitamins (<xref ref-type="bibr" rid="B12">Awuchi et al., 2020</xref>). In order to overcome the deficiencies of vitamins and health problems, consuming nutrition rich in vitamins plays a crucial role. Many diseases were treated with <italic>Aloe</italic> species (<xref ref-type="bibr" rid="B96">Salehi et al., 2018</xref>) since these plants have nutraceutical components like vitamins. Indirectly, people prevent and treat diseases and abnormal conditions when they consume these plants. This is because amine vitamins detected in <italic>Aloe</italic> species are among the water-soluble vitamins that are required for performing specific cellular functions, such as being precursors for coenzymes in the enzymes of intermediary metabolism (<xref ref-type="bibr" rid="B7">Alamgir, 2018</xref>). <xref ref-type="table" rid="T6">Table 6</xref> summarizes the deficiency of amine vitamins (<xref ref-type="bibr" rid="B57">Kraemer et al., 2012</xref>; <xref ref-type="bibr" rid="B41">Griffiths, 2020</xref>; <xref ref-type="bibr" rid="B112">Taguchi, 2023</xref>) and treated diseases due to the presence of these vitamins, which have various biological effects (<xref ref-type="bibr" rid="B23">Channa et al., 2014</xref>; <xref ref-type="bibr" rid="B6">Akaberi et al., 2016</xref>; <xref ref-type="bibr" rid="B17">Belayneh et al., 2020</xref>; <xref ref-type="bibr" rid="B4">Ahluwalia et al., 2021</xref>; <xref ref-type="bibr" rid="B94">Sabbaghzadegan et al., 2021</xref>; <xref ref-type="bibr" rid="B114">Taqui et al., 2022</xref>).</p>
<table-wrap id="T6" position="float">
<label>TABLE 6</label>
<caption>
<p>Amine containing vitamins from <italic>Aloe</italic> species and their nutraceutical applications.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Vitamins</th>
<th align="left">Functions</th>
<th align="left">Deficiency diseases</th>
<th align="left">Symptoms</th>
<th align="left">Diseases treated by <italic>Aloe</italic> species</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Vitamin B<sub>1</sub>
</td>
<td align="left">Important in function of nervous system, helps release energy from foods, promotes normal appetite</td>
<td align="left">Beriberi, Wernicke-Korsakoff syndrome</td>
<td align="left">Anorexia, weight loss, weakness, peripheral neuropathy, gait ataxia, ophthalmoplegia, encephalopathy, dementia, and memory loss</td>
<td align="left">Increasing appetite, central and peripheral nervous systems, treating tonsillitis, hematopoetic and immunomodulatory</td>
</tr>
<tr>
<td align="left">Vitamin B<sub>2</sub>
</td>
<td align="left">Helps with vision, release energy from foods; healthy skin</td>
<td align="left">Ariboflavinosis</td>
<td align="left">Glossitis, cheilosis, dermatitis, growth retardation, conjunctivitis, and neuropathy</td>
<td align="left">Anti-inflammatory, wound healing, central and peripheral nervous systems</td>
</tr>
<tr>
<td align="left">Vitamin B<sub>3</sub>
</td>
<td align="left">Promotes healthy nerves, skin. Energy production from foods; aids digestion, and promotes normal appetite</td>
<td align="left">Pellagra</td>
<td align="left">Diarrhea, dematitis, dementia, and death</td>
<td align="left">Treating diarrhea, wound healing, central and peripheral nervous systems</td>
</tr>
<tr>
<td align="left">Vitamin B<sub>6</sub>
</td>
<td align="left">Aids in protein metabolism, absorption; aids in red blood cell formation; helps body use fats</td>
<td align="left">dermatitis, anemia</td>
<td align="left">Dermatitis, anemia, seizure, depression, encephalopathy, decline in immune function</td>
<td align="left">Wound healing, hematopoetic and immunomodulatory effects</td>
</tr>
<tr>
<td align="left">Vitamin B<sub>9</sub>
</td>
<td align="left">single carbon transfers</td>
<td align="left">Anemia, neural tube defects</td>
<td align="left">Diarrhea, depression, impaired cognition, and elevated risks of heart disease and stroke</td>
<td align="left">Treating diarrhea, anti-fibrotic, anti-hypertensive, and anti-atherosclerotic</td>
</tr>
<tr>
<td align="left">Vitamin B<sub>12</sub>
</td>
<td align="left">Metabolism of amino acids and fatty acids, DNA synthesis</td>
<td align="left">Anemia</td>
<td align="left">cognitive decline, Alzheimer&#x2019;s disease, and vascular dementia</td>
<td align="left">Treating of&#xa0;alzheimer&#x2019;s&#xa0;disease, central and peripheral nervous systems</td>
</tr>
<tr>
<td align="left">Choline</td>
<td align="left">Helps brain and nervous system need it to regulate memory, mood, and muscle control</td>
<td align="left">liver and muscle damage and increases in homocysteine</td>
<td align="left">Liver disease, growth stunting, and immune dysfunction</td>
<td align="left">Cardio protective effect, immunomodulatory effect</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s5-3">
<title>5.3 Cosmeceutical applications</title>
<p>
<italic>Aloe</italic> species are used in the preparation of traditional hair washing shampoos, which are transformed into industrial products in cosmetic and personal care (<xref ref-type="bibr" rid="B101">Sbhatu et al., 2020</xref>). <italic>Aloes</italic> ability to penetrate the epidermis, dermis, and hypodermis, expelling grease and bacteria from pores and inducing new cell production, which speeds up healing, is why they are used in cosmetics (<xref ref-type="bibr" rid="B28">de Rodriguez et al., 2006</xref>). Because of their medicinal potentials, <italic>Aloe</italic> species are incorporated into cosmetics and body care products such as soap, shampoo, <italic>Aloe</italic> bath gel, body wash, lotion, deodorant, lip balm, tooth gel, mouthwash, <italic>Aloe</italic> hand sanitizer, skin-replenishing agent, aloetic herbal beard oil, aloetic hair oil, under eye cream, conditioning face mask, skin toning cream, face scrub, shower gel, activator, exfoliator, detox capsules, and joint and muscle creams (<xref ref-type="bibr" rid="B2">Adlakha et al., 2022</xref>). One benefit of <italic>Aloe</italic>-based soaps is that they do not irritate skin or leave it feeling parched. <italic>Aloe</italic> extracts are also included in some shaving lotions and creams in the USA and Asia to speed up the healing of shaving wounds. In shaving creams, <italic>A. vera</italic> gel&#x2019;s mucilaginous quality aids in its ability to act as a barrier of defense between the skin and beard (<xref ref-type="bibr" rid="B59">Lad and Murthy, 2013</xref>; <xref ref-type="bibr" rid="B68">Maan et al., 2018</xref>). Because of its high nutritional content and antioxidant qualities, <italic>A. vera</italic> is well known for its potent healing activity, even at the epithelial level of the skin. This results in the skin having a protective layer that speeds up healing. Ayurvedic medications for persistent skin conditions like psoriasis, acne, and eczema contain A. vera (<xref ref-type="bibr" rid="B11">Arunkumar and Muthuselvam, 2009</xref>; Aburjai and Natsheh, 2003). <italic>Aloe</italic> materials have been investigated for cosmeceutical applications due to their antioxidant activity of the polyphenols, indoles, alkaloids, amino acids like leucine and isoleucine, vitamins such as choline, cyanocobalamin, and folic acid that provide cleansing action and protection of photo-damages (<xref ref-type="bibr" rid="B111">Svitina et al., 2019</xref>; <xref ref-type="bibr" rid="B35">Ezzat et al., 2021</xref>). Some <italic>Aloe</italic>-based cosmetics are given in <xref ref-type="fig" rid="F10">Figure 10</xref>.</p>
<fig id="F10" position="float">
<label>FIGURE 10</label>
<caption>
<p>Some of <italic>Aloe</italic>-based cosmetics.</p>
</caption>
<graphic xlink:href="fchem-12-1363066-g010.tif"/>
</fig>
</sec>
</sec>
<sec sec-type="conclusion" id="s6">
<title>6 Conclusion</title>
<p>Knowing the abundant components of <italic>Aloe</italic> species, one means of identification is very important, especially the components detected in a quantitative manner like amino acids and vitamins. The genus <italic>Aloe</italic> has various active compounds to prevent diseases when humans consume them since they have nutritional values and are used in cosmetics for their cosmeceutical values. In addition to these, various extracts of the <italic>Aloe</italic> have effective biological properties to treat diseases. For these reasons, the bioactive compounds of <italic>Aloe</italic> species should be studied in a comprehensive manner to provide direction for their medicinal potential. Especially identifications of medicinally active compounds like amine compounds have a great role in the development of drugs. Therefore, this trend is important for further studies on related topics. As a result, understanding the structure of amine compounds found in <italic>Aloe</italic> species provides scientific guidance for using the plants&#x2019; medicinal potential.</p>
</sec>
</body>
<back>
<sec id="s7">
<title>Author contributions</title>
<p>ATY: Conceptualization, Methodology, Software, Writing&#x2013;original draft, Writing&#x2013;review and editing.</p>
</sec>
<sec sec-type="funding-information" id="s8">
<title>Funding</title>
<p>The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of interest</title>
<p>The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s10">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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