Loading…
Trigohowilols A–G, Degraded Diterpenoids from the Stems of Trigonostemon howii
Two new degraded diterpenoids, trigohowilols A (1) and B (2), four new heterodimers, trigohowilols C–F (3–6), one new homodimer, trigohowilol G (7), and three known degraded diterpenoids (8–10) were isolated from the methanol extract of the stems of Trigonostemon howii. Compounds 1–7 were evaluated...
Saved in:
Published in: | Journal of natural products (Washington, D.C.) D.C.), 2012-11, Vol.75 (11), p.1962-1966 |
---|---|
Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a315t-1cf3bdbfeb5bc7daf7e7cd6e102c2ae7f9eaf0a186970ee38931b03e04ddd6543 |
---|---|
cites | cdi_FETCH-LOGICAL-a315t-1cf3bdbfeb5bc7daf7e7cd6e102c2ae7f9eaf0a186970ee38931b03e04ddd6543 |
container_end_page | 1966 |
container_issue | 11 |
container_start_page | 1962 |
container_title | Journal of natural products (Washington, D.C.) |
container_volume | 75 |
creator | Tang, Gui-Hua Zhang, Yu Yuan, Chun-Mao Li, Yan Gu, Yu-Cheng Di, Ying-Tong Wang, Yue-Hu Zuo, Guo-Ying Li, Shi-Fei Li, Shun-Lin He, Hong-Ping Hao, Xiao-Jiang |
description | Two new degraded diterpenoids, trigohowilols A (1) and B (2), four new heterodimers, trigohowilols C–F (3–6), one new homodimer, trigohowilol G (7), and three known degraded diterpenoids (8–10) were isolated from the methanol extract of the stems of Trigonostemon howii. Compounds 1–7 were evaluated for their cytotoxic activity against five human tumor cell lines by an MTT assay, and trigohowilols E (5) and F (6) exhibited inhibitory activity with IC50 values ranging from 2.33 to 12.57 μM. Moreover, compounds 1–6 showed weak antimicrobial activities (MIC values: 6.25–25 μg/mL) against Staphylococcus aureus, Pseudomonas aeruginosa, MRSA 92#, and MRSA 98# using a 2-fold dilution method. |
doi_str_mv | 10.1021/np3006315 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1499117716</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1499117716</sourcerecordid><originalsourceid>FETCH-LOGICAL-a315t-1cf3bdbfeb5bc7daf7e7cd6e102c2ae7f9eaf0a186970ee38931b03e04ddd6543</originalsourceid><addsrcrecordid>eNptkMFKw0AQhhdRbK0efAHZi6BgdDabbJJjabUKgoL1HDbZ2TYlycbdBPHmO_iGPomprT15Gga--Zn_I-SUwTUDn93UDQcQnIV7ZMhCHzwBfrhPhsAE93gsggE5cm4FAByS8JAMfM6CWETBkDzPbbEwS_NelKZ0dPz9-TW7olNcWKlQ0WnRom2wNoVyVFtT0XaJ9KXFylGj6e9xbVy_m5quU4pjcqBl6fBkO0fk9e52Prn3Hp9mD5Pxoyf7P1uP5ZpnKtOYhVkeKakjjHIlsO-T-xIjnaDUIFkskggQeZxwlgFHCJRSIgz4iFxschtr3jp0bVoVLseylDWazqUsSBLGoqhXMCKXGzS3xjmLOm1sUUn7kTJI1wLTncCePdvGdlmFakf-GeuB8w0gc5euTGfrvuU_QT9oSHhy</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1499117716</pqid></control><display><type>article</type><title>Trigohowilols A–G, Degraded Diterpenoids from the Stems of Trigonostemon howii</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Tang, Gui-Hua ; Zhang, Yu ; Yuan, Chun-Mao ; Li, Yan ; Gu, Yu-Cheng ; Di, Ying-Tong ; Wang, Yue-Hu ; Zuo, Guo-Ying ; Li, Shi-Fei ; Li, Shun-Lin ; He, Hong-Ping ; Hao, Xiao-Jiang</creator><creatorcontrib>Tang, Gui-Hua ; Zhang, Yu ; Yuan, Chun-Mao ; Li, Yan ; Gu, Yu-Cheng ; Di, Ying-Tong ; Wang, Yue-Hu ; Zuo, Guo-Ying ; Li, Shi-Fei ; Li, Shun-Lin ; He, Hong-Ping ; Hao, Xiao-Jiang</creatorcontrib><description>Two new degraded diterpenoids, trigohowilols A (1) and B (2), four new heterodimers, trigohowilols C–F (3–6), one new homodimer, trigohowilol G (7), and three known degraded diterpenoids (8–10) were isolated from the methanol extract of the stems of Trigonostemon howii. Compounds 1–7 were evaluated for their cytotoxic activity against five human tumor cell lines by an MTT assay, and trigohowilols E (5) and F (6) exhibited inhibitory activity with IC50 values ranging from 2.33 to 12.57 μM. Moreover, compounds 1–6 showed weak antimicrobial activities (MIC values: 6.25–25 μg/mL) against Staphylococcus aureus, Pseudomonas aeruginosa, MRSA 92#, and MRSA 98# using a 2-fold dilution method.</description><identifier>ISSN: 0163-3864</identifier><identifier>EISSN: 1520-6025</identifier><identifier>DOI: 10.1021/np3006315</identifier><identifier>PMID: 23148674</identifier><language>eng</language><publisher>United States: American Chemical Society and American Society of Pharmacognosy</publisher><subject>Anti-Bacterial Agents - isolation & purification ; Anti-Bacterial Agents - metabolism ; Anti-Bacterial Agents - pharmacology ; Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - isolation & purification ; Antineoplastic Agents, Phytogenic - pharmacology ; Diterpenes - isolation & purification ; Diterpenes - metabolism ; Diterpenes - pharmacology ; Drug Screening Assays, Antitumor ; Drugs, Chinese Herbal - chemistry ; Drugs, Chinese Herbal - isolation & purification ; Drugs, Chinese Herbal - pharmacology ; Euphorbiaceae - chemistry ; Humans ; Methicillin-Resistant Staphylococcus aureus - drug effects ; Microbial Sensitivity Tests ; Molecular Structure ; Nuclear Magnetic Resonance, Biomolecular ; Plant Stems - chemistry ; Pseudomonas aeruginosa - drug effects ; Staphylococcal Infections - drug therapy ; Staphylococcus aureus - drug effects</subject><ispartof>Journal of natural products (Washington, D.C.), 2012-11, Vol.75 (11), p.1962-1966</ispartof><rights>Copyright © 2012 American Chemical Society and American Society of Pharmacognosy</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a315t-1cf3bdbfeb5bc7daf7e7cd6e102c2ae7f9eaf0a186970ee38931b03e04ddd6543</citedby><cites>FETCH-LOGICAL-a315t-1cf3bdbfeb5bc7daf7e7cd6e102c2ae7f9eaf0a186970ee38931b03e04ddd6543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23148674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tang, Gui-Hua</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Yuan, Chun-Mao</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Gu, Yu-Cheng</creatorcontrib><creatorcontrib>Di, Ying-Tong</creatorcontrib><creatorcontrib>Wang, Yue-Hu</creatorcontrib><creatorcontrib>Zuo, Guo-Ying</creatorcontrib><creatorcontrib>Li, Shi-Fei</creatorcontrib><creatorcontrib>Li, Shun-Lin</creatorcontrib><creatorcontrib>He, Hong-Ping</creatorcontrib><creatorcontrib>Hao, Xiao-Jiang</creatorcontrib><title>Trigohowilols A–G, Degraded Diterpenoids from the Stems of Trigonostemon howii</title><title>Journal of natural products (Washington, D.C.)</title><addtitle>J. Nat. Prod</addtitle><description>Two new degraded diterpenoids, trigohowilols A (1) and B (2), four new heterodimers, trigohowilols C–F (3–6), one new homodimer, trigohowilol G (7), and three known degraded diterpenoids (8–10) were isolated from the methanol extract of the stems of Trigonostemon howii. Compounds 1–7 were evaluated for their cytotoxic activity against five human tumor cell lines by an MTT assay, and trigohowilols E (5) and F (6) exhibited inhibitory activity with IC50 values ranging from 2.33 to 12.57 μM. Moreover, compounds 1–6 showed weak antimicrobial activities (MIC values: 6.25–25 μg/mL) against Staphylococcus aureus, Pseudomonas aeruginosa, MRSA 92#, and MRSA 98# using a 2-fold dilution method.</description><subject>Anti-Bacterial Agents - isolation & purification</subject><subject>Anti-Bacterial Agents - metabolism</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - isolation & purification</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Diterpenes - isolation & purification</subject><subject>Diterpenes - metabolism</subject><subject>Diterpenes - pharmacology</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Drugs, Chinese Herbal - chemistry</subject><subject>Drugs, Chinese Herbal - isolation & purification</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Euphorbiaceae - chemistry</subject><subject>Humans</subject><subject>Methicillin-Resistant Staphylococcus aureus - drug effects</subject><subject>Microbial Sensitivity Tests</subject><subject>Molecular Structure</subject><subject>Nuclear Magnetic Resonance, Biomolecular</subject><subject>Plant Stems - chemistry</subject><subject>Pseudomonas aeruginosa - drug effects</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Staphylococcus aureus - drug effects</subject><issn>0163-3864</issn><issn>1520-6025</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNptkMFKw0AQhhdRbK0efAHZi6BgdDabbJJjabUKgoL1HDbZ2TYlycbdBPHmO_iGPomprT15Gga--Zn_I-SUwTUDn93UDQcQnIV7ZMhCHzwBfrhPhsAE93gsggE5cm4FAByS8JAMfM6CWETBkDzPbbEwS_NelKZ0dPz9-TW7olNcWKlQ0WnRom2wNoVyVFtT0XaJ9KXFylGj6e9xbVy_m5quU4pjcqBl6fBkO0fk9e52Prn3Hp9mD5Pxoyf7P1uP5ZpnKtOYhVkeKakjjHIlsO-T-xIjnaDUIFkskggQeZxwlgFHCJRSIgz4iFxschtr3jp0bVoVLseylDWazqUsSBLGoqhXMCKXGzS3xjmLOm1sUUn7kTJI1wLTncCePdvGdlmFakf-GeuB8w0gc5euTGfrvuU_QT9oSHhy</recordid><startdate>20121126</startdate><enddate>20121126</enddate><creator>Tang, Gui-Hua</creator><creator>Zhang, Yu</creator><creator>Yuan, Chun-Mao</creator><creator>Li, Yan</creator><creator>Gu, Yu-Cheng</creator><creator>Di, Ying-Tong</creator><creator>Wang, Yue-Hu</creator><creator>Zuo, Guo-Ying</creator><creator>Li, Shi-Fei</creator><creator>Li, Shun-Lin</creator><creator>He, Hong-Ping</creator><creator>Hao, Xiao-Jiang</creator><general>American Chemical Society and American Society of Pharmacognosy</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20121126</creationdate><title>Trigohowilols A–G, Degraded Diterpenoids from the Stems of Trigonostemon howii</title><author>Tang, Gui-Hua ; Zhang, Yu ; Yuan, Chun-Mao ; Li, Yan ; Gu, Yu-Cheng ; Di, Ying-Tong ; Wang, Yue-Hu ; Zuo, Guo-Ying ; Li, Shi-Fei ; Li, Shun-Lin ; He, Hong-Ping ; Hao, Xiao-Jiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a315t-1cf3bdbfeb5bc7daf7e7cd6e102c2ae7f9eaf0a186970ee38931b03e04ddd6543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Anti-Bacterial Agents - isolation & purification</topic><topic>Anti-Bacterial Agents - metabolism</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antineoplastic Agents, Phytogenic - chemistry</topic><topic>Antineoplastic Agents, Phytogenic - isolation & purification</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Diterpenes - isolation & purification</topic><topic>Diterpenes - metabolism</topic><topic>Diterpenes - pharmacology</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Drugs, Chinese Herbal - chemistry</topic><topic>Drugs, Chinese Herbal - isolation & purification</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Euphorbiaceae - chemistry</topic><topic>Humans</topic><topic>Methicillin-Resistant Staphylococcus aureus - drug effects</topic><topic>Microbial Sensitivity Tests</topic><topic>Molecular Structure</topic><topic>Nuclear Magnetic Resonance, Biomolecular</topic><topic>Plant Stems - chemistry</topic><topic>Pseudomonas aeruginosa - drug effects</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcus aureus - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tang, Gui-Hua</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Yuan, Chun-Mao</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Gu, Yu-Cheng</creatorcontrib><creatorcontrib>Di, Ying-Tong</creatorcontrib><creatorcontrib>Wang, Yue-Hu</creatorcontrib><creatorcontrib>Zuo, Guo-Ying</creatorcontrib><creatorcontrib>Li, Shi-Fei</creatorcontrib><creatorcontrib>Li, Shun-Lin</creatorcontrib><creatorcontrib>He, Hong-Ping</creatorcontrib><creatorcontrib>Hao, Xiao-Jiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of natural products (Washington, D.C.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tang, Gui-Hua</au><au>Zhang, Yu</au><au>Yuan, Chun-Mao</au><au>Li, Yan</au><au>Gu, Yu-Cheng</au><au>Di, Ying-Tong</au><au>Wang, Yue-Hu</au><au>Zuo, Guo-Ying</au><au>Li, Shi-Fei</au><au>Li, Shun-Lin</au><au>He, Hong-Ping</au><au>Hao, Xiao-Jiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trigohowilols A–G, Degraded Diterpenoids from the Stems of Trigonostemon howii</atitle><jtitle>Journal of natural products (Washington, D.C.)</jtitle><addtitle>J. Nat. Prod</addtitle><date>2012-11-26</date><risdate>2012</risdate><volume>75</volume><issue>11</issue><spage>1962</spage><epage>1966</epage><pages>1962-1966</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><abstract>Two new degraded diterpenoids, trigohowilols A (1) and B (2), four new heterodimers, trigohowilols C–F (3–6), one new homodimer, trigohowilol G (7), and three known degraded diterpenoids (8–10) were isolated from the methanol extract of the stems of Trigonostemon howii. Compounds 1–7 were evaluated for their cytotoxic activity against five human tumor cell lines by an MTT assay, and trigohowilols E (5) and F (6) exhibited inhibitory activity with IC50 values ranging from 2.33 to 12.57 μM. Moreover, compounds 1–6 showed weak antimicrobial activities (MIC values: 6.25–25 μg/mL) against Staphylococcus aureus, Pseudomonas aeruginosa, MRSA 92#, and MRSA 98# using a 2-fold dilution method.</abstract><cop>United States</cop><pub>American Chemical Society and American Society of Pharmacognosy</pub><pmid>23148674</pmid><doi>10.1021/np3006315</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0163-3864 |
ispartof | Journal of natural products (Washington, D.C.), 2012-11, Vol.75 (11), p.1962-1966 |
issn | 0163-3864 1520-6025 |
language | eng |
recordid | cdi_proquest_miscellaneous_1499117716 |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Anti-Bacterial Agents - isolation & purification Anti-Bacterial Agents - metabolism Anti-Bacterial Agents - pharmacology Antineoplastic Agents, Phytogenic - chemistry Antineoplastic Agents, Phytogenic - isolation & purification Antineoplastic Agents, Phytogenic - pharmacology Diterpenes - isolation & purification Diterpenes - metabolism Diterpenes - pharmacology Drug Screening Assays, Antitumor Drugs, Chinese Herbal - chemistry Drugs, Chinese Herbal - isolation & purification Drugs, Chinese Herbal - pharmacology Euphorbiaceae - chemistry Humans Methicillin-Resistant Staphylococcus aureus - drug effects Microbial Sensitivity Tests Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plant Stems - chemistry Pseudomonas aeruginosa - drug effects Staphylococcal Infections - drug therapy Staphylococcus aureus - drug effects |
title | Trigohowilols A–G, Degraded Diterpenoids from the Stems of Trigonostemon howii |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T06%3A56%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Trigohowilols%20A%E2%80%93G,%20Degraded%20Diterpenoids%20from%20the%20Stems%20of%20Trigonostemon%20howii&rft.jtitle=Journal%20of%20natural%20products%20(Washington,%20D.C.)&rft.au=Tang,%20Gui-Hua&rft.date=2012-11-26&rft.volume=75&rft.issue=11&rft.spage=1962&rft.epage=1966&rft.pages=1962-1966&rft.issn=0163-3864&rft.eissn=1520-6025&rft_id=info:doi/10.1021/np3006315&rft_dat=%3Cproquest_cross%3E1499117716%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a315t-1cf3bdbfeb5bc7daf7e7cd6e102c2ae7f9eaf0a186970ee38931b03e04ddd6543%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1499117716&rft_id=info:pmid/23148674&rfr_iscdi=true |