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Three New Pregnane Alkaloids from Pachysandra terminalis
Three new pregnane alkaloids, pachystermine C (1), pachysanamine A (2), and pachysanamine B (3), together with four known ones, pachystermine B (4), pachysamine A (5), (20S)‐20‐(dimethylamino)‐16α‐hydroxy‐3β‐(3′α‐isopropyl)lactam‐5α‐pregnan‐4‐one (6), and E‐salignone (7), were isolated from Pachysan...
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Published in: | Helvetica chimica acta 2016-07, Vol.99 (7), p.513-517 |
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container_title | Helvetica chimica acta |
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creator | Sun, Yun Chen, Jin-Xiong Chen, Jian-Chao Li, Zhong-Rong Zhou, Lin Li, Yan Qiu, Ming-Hua |
description | Three new pregnane alkaloids, pachystermine C (1), pachysanamine A (2), and pachysanamine B (3), together with four known ones, pachystermine B (4), pachysamine A (5), (20S)‐20‐(dimethylamino)‐16α‐hydroxy‐3β‐(3′α‐isopropyl)lactam‐5α‐pregnan‐4‐one (6), and E‐salignone (7), were isolated from Pachysandra terminalis. The chemical structures of the new alkaloids were elucidated by spectroscopic methods. All the compounds were evaluated for their inhibitory activities against HL‐60, SMMC‐7721, A‐549, MCF‐7, and SW480 cell lines, some of the compounds showed stronger cytotoxicity for the test cell lines, especially compounds 2, 3, and 7. |
doi_str_mv | 10.1002/hlca.201600016 |
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The chemical structures of the new alkaloids were elucidated by spectroscopic methods. All the compounds were evaluated for their inhibitory activities against HL‐60, SMMC‐7721, A‐549, MCF‐7, and SW480 cell lines, some of the compounds showed stronger cytotoxicity for the test cell lines, especially compounds 2, 3, and 7.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.201600016</identifier><language>eng</language><publisher>Zürich: Blackwell Publishing Ltd</publisher><subject>Buxaceae ; Cytotoxicity ; Pachysandra terminalis ; Pregnane alkaloids</subject><ispartof>Helvetica chimica acta, 2016-07, Vol.99 (7), p.513-517</ispartof><rights>2016 Wiley‐VHCA AG, Zürich</rights><rights>Copyright © 2016 Wiley-VHCA AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3556-43eb31e96b5cb0883f2b171f007a6e92b6afff28d40529f8f3d14ed0e2cbfe333</citedby><cites>FETCH-LOGICAL-c3556-43eb31e96b5cb0883f2b171f007a6e92b6afff28d40529f8f3d14ed0e2cbfe333</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></links><search><creatorcontrib>Sun, Yun</creatorcontrib><creatorcontrib>Chen, Jin-Xiong</creatorcontrib><creatorcontrib>Chen, Jian-Chao</creatorcontrib><creatorcontrib>Li, Zhong-Rong</creatorcontrib><creatorcontrib>Zhou, Lin</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Qiu, Ming-Hua</creatorcontrib><title>Three New Pregnane Alkaloids from Pachysandra terminalis</title><title>Helvetica chimica acta</title><addtitle>Helv. 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subjects | Buxaceae Cytotoxicity Pachysandra terminalis Pregnane alkaloids |
title | Three New Pregnane Alkaloids from Pachysandra terminalis |
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