Joseph Sakah Kaunda , Jia Liu , Yaojun Xu , Yuansi Chen , Chenfang Yue , Xingjie Zhang , Ruihan Zhang , Muhammad Amin , Weilie Xiao , Hongliang Li , Xiaoli Li
{"title":"金刚鹦鹉叶的成分","authors":"Joseph Sakah Kaunda , Jia Liu , Yaojun Xu , Yuansi Chen , Chenfang Yue , Xingjie Zhang , Ruihan Zhang , Muhammad Amin , Weilie Xiao , Hongliang Li , Xiaoli Li","doi":"10.1016/j.chmed.2023.03.006","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To study constituents of the leaves of <em>Macaranga hemsleyana</em>, and evaluate their inhibitory effects against NOD-like receptor thermal protein domain associated protein 3 (NLRP3) inflammasome activation, and antiproliferative activity.</p></div><div><h3>Methods</h3><p>The constituents were isolated and purified by column chromatography on MCI gel CHP20P/P120, silica gel, Sephadex LH-20, and HPLC. The structures of compounds were determined by 1D, 2D NMR, and HR-ESI-MS data. The inhibitory effect of compounds on inflammasome activation was determined by lactate dehydrogenase (LDH) procedure. The antiproliferative activity was evaluated using MTT assay.</p></div><div><h3>Results</h3><p>The study led to the isolation of 23 compounds, including one new compound, identified as (2<em>Z</em>)-3-[4-(<em>β</em>-<em>D</em>-glucopyranosyloxy)-2′-hydroxy-5′-methoxyphenyl]-2-propenoic acid (<strong>1</strong>), together with 22 known compounds recognized as 1,4-dihydro-4-oxo-3-pyridinecarbonitrile (<strong>2</strong>), methyl 4-methoxynicotinate (<strong>3</strong>), 4-methoxynicotinonitrile (<strong>4</strong>), 1-(3-<em>O</em>-<em>β</em>-<em>D</em>-glucopyranosyl-4,5-dihydroxyphenyl)-ethanone (<strong>5</strong>), neoisoastilbin (<strong>6</strong>), isoastilbin (<strong>7</strong>), aromadendrin <strong>(8</strong>), neoastilbin (<strong>9</strong>), astilbin (<strong>10</strong>), quercitrin (<strong>11</strong>), neoschaftoside (<strong>12</strong>), apigenin 6,8-bis-<em>C</em>-<em>α</em>-<em>L</em>-arabinoside (<strong>13</strong>), vitexin (<strong>14</strong>), bergenin (<strong>15</strong>), scopoletin (<strong>16</strong>), glucopyranoside salicyl (<strong>17</strong>), koaburside (<strong>18</strong>), benzyl <em>β</em>-<em>D</em>-glucoside (<strong>19</strong>), icariside B5 (<strong>20</strong>), roseoside (<strong>21</strong>), loliolide (<strong>22</strong>), and adenosine (<strong>23</strong>). The tested compounds did not show LDH inhibition nor antiproliferative activity.</p></div><div><h3>Conclusion</h3><p>Compound <strong>1</strong> was a new glycoside. Compounds <strong>2</strong> and <strong>3</strong> were obtained for the first time from natural source. The 22 known compounds constituted of alkaloids (<strong>2</strong>–<strong>4</strong>, <strong>23</strong>), phenolics (<strong>5</strong>, <strong>15</strong>, <strong>17</strong>, <strong>18</strong>), flavonoids (<strong>6</strong>–<strong>14</strong>), coumarin (<strong>16</strong>), benzyl glycoside (<strong>19</strong>), and norsesquiterpenes (<strong>20</strong>–<strong>22</strong>). All the compounds, <strong>1</strong>–<strong>23</strong>, were revealed from <em>M. hemsleyana</em> for the first time. This is the initial uncovering of molecules <strong>1</strong>–<strong>10</strong>, <strong>12</strong>, <strong>13</strong>, <strong>17</strong>–<strong>19</strong>, and <strong>23</strong> from the genus <em>Macaranga</em>. The isolated compounds, <strong>11</strong>, <strong>14</strong>–<strong>16</strong>, and <strong>20</strong>–<strong>22</strong> established taxonomic classification of <em>M. hemsleyana</em> in Euphorbiaceae family. Flavonoids were outstanding as chemosystematic markers of <em>Macaranga</em> genus.</p></div>","PeriodicalId":9916,"journal":{"name":"Chinese Herbal Medicines","volume":"16 3","pages":"Pages 481-486"},"PeriodicalIF":4.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1674638423000746/pdfft?md5=fd934d08969499d988ae88f6a2d4dadf&pid=1-s2.0-S1674638423000746-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Constituents from leaves of Macaranga hemsleyana\",\"authors\":\"Joseph Sakah Kaunda , Jia Liu , Yaojun Xu , Yuansi Chen , Chenfang Yue , Xingjie Zhang , Ruihan Zhang , Muhammad Amin , Weilie Xiao , Hongliang Li , Xiaoli Li\",\"doi\":\"10.1016/j.chmed.2023.03.006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>To study constituents of the leaves of <em>Macaranga hemsleyana</em>, and evaluate their inhibitory effects against NOD-like receptor thermal protein domain associated protein 3 (NLRP3) inflammasome activation, and antiproliferative activity.</p></div><div><h3>Methods</h3><p>The constituents were isolated and purified by column chromatography on MCI gel CHP20P/P120, silica gel, Sephadex LH-20, and HPLC. The structures of compounds were determined by 1D, 2D NMR, and HR-ESI-MS data. The inhibitory effect of compounds on inflammasome activation was determined by lactate dehydrogenase (LDH) procedure. The antiproliferative activity was evaluated using MTT assay.</p></div><div><h3>Results</h3><p>The study led to the isolation of 23 compounds, including one new compound, identified as (2<em>Z</em>)-3-[4-(<em>β</em>-<em>D</em>-glucopyranosyloxy)-2′-hydroxy-5′-methoxyphenyl]-2-propenoic acid (<strong>1</strong>), together with 22 known compounds recognized as 1,4-dihydro-4-oxo-3-pyridinecarbonitrile (<strong>2</strong>), methyl 4-methoxynicotinate (<strong>3</strong>), 4-methoxynicotinonitrile (<strong>4</strong>), 1-(3-<em>O</em>-<em>β</em>-<em>D</em>-glucopyranosyl-4,5-dihydroxyphenyl)-ethanone (<strong>5</strong>), neoisoastilbin (<strong>6</strong>), isoastilbin (<strong>7</strong>), aromadendrin <strong>(8</strong>), neoastilbin (<strong>9</strong>), astilbin (<strong>10</strong>), quercitrin (<strong>11</strong>), neoschaftoside (<strong>12</strong>), apigenin 6,8-bis-<em>C</em>-<em>α</em>-<em>L</em>-arabinoside (<strong>13</strong>), vitexin (<strong>14</strong>), bergenin (<strong>15</strong>), scopoletin (<strong>16</strong>), glucopyranoside salicyl (<strong>17</strong>), koaburside (<strong>18</strong>), benzyl <em>β</em>-<em>D</em>-glucoside (<strong>19</strong>), icariside B5 (<strong>20</strong>), roseoside (<strong>21</strong>), loliolide (<strong>22</strong>), and adenosine (<strong>23</strong>). The tested compounds did not show LDH inhibition nor antiproliferative activity.</p></div><div><h3>Conclusion</h3><p>Compound <strong>1</strong> was a new glycoside. Compounds <strong>2</strong> and <strong>3</strong> were obtained for the first time from natural source. The 22 known compounds constituted of alkaloids (<strong>2</strong>–<strong>4</strong>, <strong>23</strong>), phenolics (<strong>5</strong>, <strong>15</strong>, <strong>17</strong>, <strong>18</strong>), flavonoids (<strong>6</strong>–<strong>14</strong>), coumarin (<strong>16</strong>), benzyl glycoside (<strong>19</strong>), and norsesquiterpenes (<strong>20</strong>–<strong>22</strong>). All the compounds, <strong>1</strong>–<strong>23</strong>, were revealed from <em>M. hemsleyana</em> for the first time. This is the initial uncovering of molecules <strong>1</strong>–<strong>10</strong>, <strong>12</strong>, <strong>13</strong>, <strong>17</strong>–<strong>19</strong>, and <strong>23</strong> from the genus <em>Macaranga</em>. The isolated compounds, <strong>11</strong>, <strong>14</strong>–<strong>16</strong>, and <strong>20</strong>–<strong>22</strong> established taxonomic classification of <em>M. hemsleyana</em> in Euphorbiaceae family. Flavonoids were outstanding as chemosystematic markers of <em>Macaranga</em> genus.</p></div>\",\"PeriodicalId\":9916,\"journal\":{\"name\":\"Chinese Herbal Medicines\",\"volume\":\"16 3\",\"pages\":\"Pages 481-486\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1674638423000746/pdfft?md5=fd934d08969499d988ae88f6a2d4dadf&pid=1-s2.0-S1674638423000746-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Herbal Medicines\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1674638423000746\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Herbal Medicines","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1674638423000746","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
To study constituents of the leaves of Macaranga hemsleyana, and evaluate their inhibitory effects against NOD-like receptor thermal protein domain associated protein 3 (NLRP3) inflammasome activation, and antiproliferative activity.
Methods
The constituents were isolated and purified by column chromatography on MCI gel CHP20P/P120, silica gel, Sephadex LH-20, and HPLC. The structures of compounds were determined by 1D, 2D NMR, and HR-ESI-MS data. The inhibitory effect of compounds on inflammasome activation was determined by lactate dehydrogenase (LDH) procedure. The antiproliferative activity was evaluated using MTT assay.
Results
The study led to the isolation of 23 compounds, including one new compound, identified as (2Z)-3-[4-(β-D-glucopyranosyloxy)-2′-hydroxy-5′-methoxyphenyl]-2-propenoic acid (1), together with 22 known compounds recognized as 1,4-dihydro-4-oxo-3-pyridinecarbonitrile (2), methyl 4-methoxynicotinate (3), 4-methoxynicotinonitrile (4), 1-(3-O-β-D-glucopyranosyl-4,5-dihydroxyphenyl)-ethanone (5), neoisoastilbin (6), isoastilbin (7), aromadendrin (8), neoastilbin (9), astilbin (10), quercitrin (11), neoschaftoside (12), apigenin 6,8-bis-C-α-L-arabinoside (13), vitexin (14), bergenin (15), scopoletin (16), glucopyranoside salicyl (17), koaburside (18), benzyl β-D-glucoside (19), icariside B5 (20), roseoside (21), loliolide (22), and adenosine (23). The tested compounds did not show LDH inhibition nor antiproliferative activity.
Conclusion
Compound 1 was a new glycoside. Compounds 2 and 3 were obtained for the first time from natural source. The 22 known compounds constituted of alkaloids (2–4, 23), phenolics (5, 15, 17, 18), flavonoids (6–14), coumarin (16), benzyl glycoside (19), and norsesquiterpenes (20–22). All the compounds, 1–23, were revealed from M. hemsleyana for the first time. This is the initial uncovering of molecules 1–10, 12, 13, 17–19, and 23 from the genus Macaranga. The isolated compounds, 11, 14–16, and 20–22 established taxonomic classification of M. hemsleyana in Euphorbiaceae family. Flavonoids were outstanding as chemosystematic markers of Macaranga genus.
期刊介绍:
Chinese Herbal Medicines is intended to disseminate the latest developments and research progress in traditional and herbal medical sciences to researchers, practitioners, academics and administrators worldwide in the field of traditional and herbal medicines. The journal's international coverage ensures that research and progress from all regions of the world are widely included.
CHM is a core journal of Chinese science and technology. The journal entered into the ESCI database in 2017, and then was included in PMC, Scopus and other important international search systems. In 2019, CHM was successfully selected for the “China Science and Technology Journal Excellence Action Plan” project, which has markedly improved its international influence and industry popularity. CHM obtained the first impact factor of 3.8 in Journal Citation Reports (JCR) in 2023.