Loading…

New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis

Two new pterosin sesquiterpenes, (2S)‐13‐hydroxypterosin A (1) and (2S,3S)‐12‐hydroxypterosin Q (2), were isolated from the whole plants of Pteris ensiformis, together with six known compounds. The structures of 1 and 2 were determined through extensive 1D/2D‐NMR and MS analyses. Compound 2 exhibite...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry & biodiversity 2013-10, Vol.10 (10), p.1903-1908
Main Authors: Chen, Jih-Jung, Wang, Tai-Chi, Yang, Chieh-Kai, Liao, Hsiang-Ruei, Sung, Ping-Jyun, Chen, Ih-Sheng, Cheng, Ming-Jen, Peng, Chien-Fang, Chen, Jinn-Fen
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-c4512-10e4c8886546914f3424fb81c94081e5a62ad82644744e62f309c2f889c9822c3
cites cdi_FETCH-LOGICAL-c4512-10e4c8886546914f3424fb81c94081e5a62ad82644744e62f309c2f889c9822c3
container_end_page 1908
container_issue 10
container_start_page 1903
container_title Chemistry & biodiversity
container_volume 10
creator Chen, Jih-Jung
Wang, Tai-Chi
Yang, Chieh-Kai
Liao, Hsiang-Ruei
Sung, Ping-Jyun
Chen, Ih-Sheng
Cheng, Ming-Jen
Peng, Chien-Fang
Chen, Jinn-Fen
description Two new pterosin sesquiterpenes, (2S)‐13‐hydroxypterosin A (1) and (2S,3S)‐12‐hydroxypterosin Q (2), were isolated from the whole plants of Pteris ensiformis, together with six known compounds. The structures of 1 and 2 were determined through extensive 1D/2D‐NMR and MS analyses. Compound 2 exhibited antitubercular activity (MIC 6.25 μg/ml) against Mycobacterium tuberculosis H37Rv in vitro.
doi_str_mv 10.1002/cbdv.201300072
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1443425316</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1443425316</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4512-10e4c8886546914f3424fb81c94081e5a62ad82644744e62f309c2f889c9822c3</originalsourceid><addsrcrecordid>eNqFkM1PwjAYhxujEUSvHs0SL17Afm3rjgiKGoIEvxIvzSjvkuLosN1U_ns7QWK8eGr75vn9-uZB6JjgDsGYnqvp7L1DMWEY45juoCaJCG0TIfDu9h7TBjpwbu55Pxf7qEF5HWCsiSYj-AjGJdjCaRPcg3urtH8twYALUjMLuqbUZTUFq6o8tUGvMK4egCldkNli8R3WLgDjdFbYhXaHaC9LcwdHm7OFHq8uH3rX7eHd4KbXHbYVD-u9MHAlhIhCHiWEZ4xTnk0FUQnHgkCYRjSdCRpxHnMOEc0YThTNhEhUIihVrIXO1r1LW7xV4ErpP1eQ56mBonKScO47Q0Yij57-QedFZY3frqYo4Yx6Gy3UWVPK23AWMrm0epHalSRY1rZlbVtubfvAyaa2mi5gtsV_9HogWQMfOofVP3Wyd9F_-l3eXme1K-Fzm03tq4xiFofyeTSQk3H_5XYYc9lnX_16mUw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1442143203</pqid></control><display><type>article</type><title>New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis</title><source>Wiley</source><creator>Chen, Jih-Jung ; Wang, Tai-Chi ; Yang, Chieh-Kai ; Liao, Hsiang-Ruei ; Sung, Ping-Jyun ; Chen, Ih-Sheng ; Cheng, Ming-Jen ; Peng, Chien-Fang ; Chen, Jinn-Fen</creator><creatorcontrib>Chen, Jih-Jung ; Wang, Tai-Chi ; Yang, Chieh-Kai ; Liao, Hsiang-Ruei ; Sung, Ping-Jyun ; Chen, Ih-Sheng ; Cheng, Ming-Jen ; Peng, Chien-Fang ; Chen, Jinn-Fen</creatorcontrib><description>Two new pterosin sesquiterpenes, (2S)‐13‐hydroxypterosin A (1) and (2S,3S)‐12‐hydroxypterosin Q (2), were isolated from the whole plants of Pteris ensiformis, together with six known compounds. The structures of 1 and 2 were determined through extensive 1D/2D‐NMR and MS analyses. Compound 2 exhibited antitubercular activity (MIC 6.25 μg/ml) against Mycobacterium tuberculosis H37Rv in vitro.</description><identifier>ISSN: 1612-1872</identifier><identifier>EISSN: 1612-1880</identifier><identifier>DOI: 10.1002/cbdv.201300072</identifier><identifier>PMID: 24130033</identifier><language>eng</language><publisher>Zürich: WILEY-VCH Verlag</publisher><subject>Antitubercular activity ; Antitubercular Agents - chemistry ; Antitubercular Agents - isolation &amp; purification ; Antitubercular Agents - pharmacology ; Indans - chemistry ; Magnetic Resonance Spectroscopy ; Microbial Sensitivity Tests ; Molecular Conformation ; Mycobacterium tuberculosis - drug effects ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Pteris - chemistry ; Pteris - metabolism ; Pteris ensiformis ; Pterosin sesquiterpenes ; Sesquiterpenes ; Sesquiterpenes - chemistry ; Sesquiterpenes - isolation &amp; purification ; Sesquiterpenes - pharmacology</subject><ispartof>Chemistry &amp; biodiversity, 2013-10, Vol.10 (10), p.1903-1908</ispartof><rights>Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich</rights><rights>Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich.</rights><rights>Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zurich</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4512-10e4c8886546914f3424fb81c94081e5a62ad82644744e62f309c2f889c9822c3</citedby><cites>FETCH-LOGICAL-c4512-10e4c8886546914f3424fb81c94081e5a62ad82644744e62f309c2f889c9822c3</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/24130033$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Jih-Jung</creatorcontrib><creatorcontrib>Wang, Tai-Chi</creatorcontrib><creatorcontrib>Yang, Chieh-Kai</creatorcontrib><creatorcontrib>Liao, Hsiang-Ruei</creatorcontrib><creatorcontrib>Sung, Ping-Jyun</creatorcontrib><creatorcontrib>Chen, Ih-Sheng</creatorcontrib><creatorcontrib>Cheng, Ming-Jen</creatorcontrib><creatorcontrib>Peng, Chien-Fang</creatorcontrib><creatorcontrib>Chen, Jinn-Fen</creatorcontrib><title>New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis</title><title>Chemistry &amp; biodiversity</title><addtitle>Chemistry &amp; Biodiversity</addtitle><description>Two new pterosin sesquiterpenes, (2S)‐13‐hydroxypterosin A (1) and (2S,3S)‐12‐hydroxypterosin Q (2), were isolated from the whole plants of Pteris ensiformis, together with six known compounds. The structures of 1 and 2 were determined through extensive 1D/2D‐NMR and MS analyses. Compound 2 exhibited antitubercular activity (MIC 6.25 μg/ml) against Mycobacterium tuberculosis H37Rv in vitro.</description><subject>Antitubercular activity</subject><subject>Antitubercular Agents - chemistry</subject><subject>Antitubercular Agents - isolation &amp; purification</subject><subject>Antitubercular Agents - pharmacology</subject><subject>Indans - chemistry</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Microbial Sensitivity Tests</subject><subject>Molecular Conformation</subject><subject>Mycobacterium tuberculosis - drug effects</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Pteris - chemistry</subject><subject>Pteris - metabolism</subject><subject>Pteris ensiformis</subject><subject>Pterosin sesquiterpenes</subject><subject>Sesquiterpenes</subject><subject>Sesquiterpenes - chemistry</subject><subject>Sesquiterpenes - isolation &amp; purification</subject><subject>Sesquiterpenes - pharmacology</subject><issn>1612-1872</issn><issn>1612-1880</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkM1PwjAYhxujEUSvHs0SL17Afm3rjgiKGoIEvxIvzSjvkuLosN1U_ns7QWK8eGr75vn9-uZB6JjgDsGYnqvp7L1DMWEY45juoCaJCG0TIfDu9h7TBjpwbu55Pxf7qEF5HWCsiSYj-AjGJdjCaRPcg3urtH8twYALUjMLuqbUZTUFq6o8tUGvMK4egCldkNli8R3WLgDjdFbYhXaHaC9LcwdHm7OFHq8uH3rX7eHd4KbXHbYVD-u9MHAlhIhCHiWEZ4xTnk0FUQnHgkCYRjSdCRpxHnMOEc0YThTNhEhUIihVrIXO1r1LW7xV4ErpP1eQ56mBonKScO47Q0Yij57-QedFZY3frqYo4Yx6Gy3UWVPK23AWMrm0epHalSRY1rZlbVtubfvAyaa2mi5gtsV_9HogWQMfOofVP3Wyd9F_-l3eXme1K-Fzm03tq4xiFofyeTSQk3H_5XYYc9lnX_16mUw</recordid><startdate>201310</startdate><enddate>201310</enddate><creator>Chen, Jih-Jung</creator><creator>Wang, Tai-Chi</creator><creator>Yang, Chieh-Kai</creator><creator>Liao, Hsiang-Ruei</creator><creator>Sung, Ping-Jyun</creator><creator>Chen, Ih-Sheng</creator><creator>Cheng, Ming-Jen</creator><creator>Peng, Chien-Fang</creator><creator>Chen, Jinn-Fen</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201310</creationdate><title>New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis</title><author>Chen, Jih-Jung ; Wang, Tai-Chi ; Yang, Chieh-Kai ; Liao, Hsiang-Ruei ; Sung, Ping-Jyun ; Chen, Ih-Sheng ; Cheng, Ming-Jen ; Peng, Chien-Fang ; Chen, Jinn-Fen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4512-10e4c8886546914f3424fb81c94081e5a62ad82644744e62f309c2f889c9822c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antitubercular activity</topic><topic>Antitubercular Agents - chemistry</topic><topic>Antitubercular Agents - isolation &amp; purification</topic><topic>Antitubercular Agents - pharmacology</topic><topic>Indans - chemistry</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Microbial Sensitivity Tests</topic><topic>Molecular Conformation</topic><topic>Mycobacterium tuberculosis - drug effects</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Pteris - chemistry</topic><topic>Pteris - metabolism</topic><topic>Pteris ensiformis</topic><topic>Pterosin sesquiterpenes</topic><topic>Sesquiterpenes</topic><topic>Sesquiterpenes - chemistry</topic><topic>Sesquiterpenes - isolation &amp; purification</topic><topic>Sesquiterpenes - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Jih-Jung</creatorcontrib><creatorcontrib>Wang, Tai-Chi</creatorcontrib><creatorcontrib>Yang, Chieh-Kai</creatorcontrib><creatorcontrib>Liao, Hsiang-Ruei</creatorcontrib><creatorcontrib>Sung, Ping-Jyun</creatorcontrib><creatorcontrib>Chen, Ih-Sheng</creatorcontrib><creatorcontrib>Cheng, Ming-Jen</creatorcontrib><creatorcontrib>Peng, Chien-Fang</creatorcontrib><creatorcontrib>Chen, Jinn-Fen</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry &amp; biodiversity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Jih-Jung</au><au>Wang, Tai-Chi</au><au>Yang, Chieh-Kai</au><au>Liao, Hsiang-Ruei</au><au>Sung, Ping-Jyun</au><au>Chen, Ih-Sheng</au><au>Cheng, Ming-Jen</au><au>Peng, Chien-Fang</au><au>Chen, Jinn-Fen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis</atitle><jtitle>Chemistry &amp; biodiversity</jtitle><addtitle>Chemistry &amp; Biodiversity</addtitle><date>2013-10</date><risdate>2013</risdate><volume>10</volume><issue>10</issue><spage>1903</spage><epage>1908</epage><pages>1903-1908</pages><issn>1612-1872</issn><eissn>1612-1880</eissn><abstract>Two new pterosin sesquiterpenes, (2S)‐13‐hydroxypterosin A (1) and (2S,3S)‐12‐hydroxypterosin Q (2), were isolated from the whole plants of Pteris ensiformis, together with six known compounds. The structures of 1 and 2 were determined through extensive 1D/2D‐NMR and MS analyses. Compound 2 exhibited antitubercular activity (MIC 6.25 μg/ml) against Mycobacterium tuberculosis H37Rv in vitro.</abstract><cop>Zürich</cop><pub>WILEY-VCH Verlag</pub><pmid>24130033</pmid><doi>10.1002/cbdv.201300072</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1612-1872
ispartof Chemistry & biodiversity, 2013-10, Vol.10 (10), p.1903-1908
issn 1612-1872
1612-1880
language eng
recordid cdi_proquest_miscellaneous_1443425316
source Wiley
subjects Antitubercular activity
Antitubercular Agents - chemistry
Antitubercular Agents - isolation & purification
Antitubercular Agents - pharmacology
Indans - chemistry
Magnetic Resonance Spectroscopy
Microbial Sensitivity Tests
Molecular Conformation
Mycobacterium tuberculosis - drug effects
Plant Extracts - chemistry
Plant Extracts - pharmacology
Pteris - chemistry
Pteris - metabolism
Pteris ensiformis
Pterosin sesquiterpenes
Sesquiterpenes
Sesquiterpenes - chemistry
Sesquiterpenes - isolation & purification
Sesquiterpenes - pharmacology
title New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T17%3A22%3A25IST&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=New%20Pterosin%20Sesquiterpenes%20and%20Antitubercular%20Constituents%20from%20Pteris%20ensiformis&rft.jtitle=Chemistry%20&%20biodiversity&rft.au=Chen,%20Jih-Jung&rft.date=2013-10&rft.volume=10&rft.issue=10&rft.spage=1903&rft.epage=1908&rft.pages=1903-1908&rft.issn=1612-1872&rft.eissn=1612-1880&rft_id=info:doi/10.1002/cbdv.201300072&rft_dat=%3Cproquest_cross%3E1443425316%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4512-10e4c8886546914f3424fb81c94081e5a62ad82644744e62f309c2f889c9822c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1442143203&rft_id=info:pmid/24130033&rfr_iscdi=true