Constituents from leaves of Macaranga hemsleyana
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. The constituents were isolated and purified by column chromatograp...
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description | 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.
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.
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.
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. |
doi_str_mv | 10.1016/j.chmed.2023.03.006 |
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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.
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.
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.</description><identifier>ISSN: 1674-6384</identifier><identifier>ISSN: 2589-3610</identifier><identifier>EISSN: 2589-3610</identifier><identifier>DOI: 10.1016/j.chmed.2023.03.006</identifier><identifier>PMID: 39072199</identifier><language>eng</language><publisher>Singapore: Elsevier B.V</publisher><subject>antiproliferative activity ; chemotaxonomic significance ; flavonoids ; glycoside ; Macaranga hemsleyana Pax et Hoffm ; NLRP3 inflammasome ; Original</subject><ispartof>Chinese herbal medicines, 2024-07, Vol.16 (3), p.481-486</ispartof><rights>2023 Tianjin Press of Chinese Herbal Medicines</rights><rights>2023 Tianjin Press of Chinese Herbal Medicines. Published by ELSEVIER B.V.</rights><rights>2023 Tianjin Press of Chinese Herbal Medicines. Published by ELSEVIER B.V. 2023 Tianjin Press of Chinese Herbal Medicines</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c410t-3a5f04c6d2cf8190fe4d0d2ba87f10652c4392bc2d7ebffddb999b0d6ade0b6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11283217/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11283217/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27911,27912,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39072199$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaunda, Joseph Sakah</creatorcontrib><creatorcontrib>Liu, Jia</creatorcontrib><creatorcontrib>Xu, Yaojun</creatorcontrib><creatorcontrib>Chen, Yuansi</creatorcontrib><creatorcontrib>Yue, Chenfang</creatorcontrib><creatorcontrib>Zhang, Xingjie</creatorcontrib><creatorcontrib>Zhang, Ruihan</creatorcontrib><creatorcontrib>Amin, Muhammad</creatorcontrib><creatorcontrib>Xiao, Weilie</creatorcontrib><creatorcontrib>Li, Hongliang</creatorcontrib><creatorcontrib>Li, Xiaoli</creatorcontrib><title>Constituents from leaves of Macaranga hemsleyana</title><title>Chinese herbal medicines</title><addtitle>Chin Herb Med</addtitle><description>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.
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.
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.
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.</description><subject>antiproliferative activity</subject><subject>chemotaxonomic significance</subject><subject>flavonoids</subject><subject>glycoside</subject><subject>Macaranga hemsleyana Pax et Hoffm</subject><subject>NLRP3 inflammasome</subject><subject>Original</subject><issn>1674-6384</issn><issn>2589-3610</issn><issn>2589-3610</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1rGzEQhkVJaYzrX1Aoe8xlnZG0q10dSggmHwWXXtqz0EojW2Z3lUhrQ_59ldox6aXDwBzmnXdmHkK-UFhSoOJ6tzTbAe2SAeNLyAniA5mxupUlFxQuyIyKpioFb6tLskhpBzkEZZxVn8gll9AwKuWMwCqMafLTHscpFS6GoehRHzAVwRU_tNFRjxtdbHFIPb7oUX8mH53uEy5OdU5-39_9Wj2W658P31e369JUFKaS69pBZYRlxrVUgsPKgmWdbhtHQdTMVFyyzjDbYOectZ2UsgMrtEXohOVzcnP0fdp3-VGT74u6V0_RDzq-qKC9-rcz-q3ahIOilLWc0SY7XJ0cYnjeY5rU4JPBvtcjhn1SHNpatJLVPEv5UWpiSCmiO--hoF55q536y1u98laQE0Se-vr-xPPMG90s-HYUYAZ18BhVMh5Hg9ZHNJOywf93wR_WBZNa</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Kaunda, Joseph Sakah</creator><creator>Liu, Jia</creator><creator>Xu, Yaojun</creator><creator>Chen, Yuansi</creator><creator>Yue, Chenfang</creator><creator>Zhang, Xingjie</creator><creator>Zhang, Ruihan</creator><creator>Amin, Muhammad</creator><creator>Xiao, Weilie</creator><creator>Li, Hongliang</creator><creator>Li, Xiaoli</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240701</creationdate><title>Constituents from leaves of Macaranga hemsleyana</title><author>Kaunda, Joseph Sakah ; Liu, Jia ; Xu, Yaojun ; Chen, Yuansi ; Yue, Chenfang ; Zhang, Xingjie ; Zhang, Ruihan ; Amin, Muhammad ; Xiao, Weilie ; Li, Hongliang ; Li, Xiaoli</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-3a5f04c6d2cf8190fe4d0d2ba87f10652c4392bc2d7ebffddb999b0d6ade0b6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>antiproliferative activity</topic><topic>chemotaxonomic significance</topic><topic>flavonoids</topic><topic>glycoside</topic><topic>Macaranga hemsleyana Pax et Hoffm</topic><topic>NLRP3 inflammasome</topic><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaunda, Joseph Sakah</creatorcontrib><creatorcontrib>Liu, Jia</creatorcontrib><creatorcontrib>Xu, Yaojun</creatorcontrib><creatorcontrib>Chen, Yuansi</creatorcontrib><creatorcontrib>Yue, Chenfang</creatorcontrib><creatorcontrib>Zhang, Xingjie</creatorcontrib><creatorcontrib>Zhang, Ruihan</creatorcontrib><creatorcontrib>Amin, Muhammad</creatorcontrib><creatorcontrib>Xiao, Weilie</creatorcontrib><creatorcontrib>Li, Hongliang</creatorcontrib><creatorcontrib>Li, Xiaoli</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chinese herbal medicines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaunda, Joseph Sakah</au><au>Liu, Jia</au><au>Xu, Yaojun</au><au>Chen, Yuansi</au><au>Yue, Chenfang</au><au>Zhang, Xingjie</au><au>Zhang, Ruihan</au><au>Amin, Muhammad</au><au>Xiao, Weilie</au><au>Li, Hongliang</au><au>Li, Xiaoli</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Constituents from leaves of Macaranga hemsleyana</atitle><jtitle>Chinese herbal medicines</jtitle><addtitle>Chin Herb Med</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>16</volume><issue>3</issue><spage>481</spage><epage>486</epage><pages>481-486</pages><issn>1674-6384</issn><issn>2589-3610</issn><eissn>2589-3610</eissn><abstract>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.
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.
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.
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.</abstract><cop>Singapore</cop><pub>Elsevier B.V</pub><pmid>39072199</pmid><doi>10.1016/j.chmed.2023.03.006</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | antiproliferative activity chemotaxonomic significance flavonoids glycoside Macaranga hemsleyana Pax et Hoffm NLRP3 inflammasome Original |
title | Constituents from leaves of Macaranga hemsleyana |
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