Literature DB >> 12444693

Triterpenoid constituents isolated from the bark of Abies sachalinensis.

Shun-ichi Wada1, Akira Iida, Reiko Tanaka.   

Abstract

Three new lanostane-type triterpenoids (1-3) were isolated from the bark of Abies sachalinensis along with a known compound (4). The structures of 1-4 were characterized by spectroscopic methods including NMR and MS. Compound 4 and some derivatives were tested for inhibitory effects on in vitro DNA topoisomerases I and II and found to be selective catalytic inhibitors of topoisomerase II activity with IC(50) values in the range 43-76 microM.

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Year:  2002        PMID: 12444693     DOI: 10.1021/np020282b

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  3 in total

1.  Holophyllane A: A Triterpenoid Possessing an Unprecedented B-nor-3,4-seco-17,14-friedo-lanostane Architecture from Abies holophylla.

Authors:  Chung Sub Kim; Joonseok Oh; Lalita Subedi; Sun Yeou Kim; Sang Un Choi; Kang Ro Lee
Journal:  Sci Rep       Date:  2017-03-02       Impact factor: 4.379

2.  Lanostane- and cycloartane-type triterpenoids from Abies balsamea oleoresin.

Authors:  Serge Lavoie; Charles Gauthier; Jean Legault; Sylvain Mercier; Vakhtang Mshvildadze; André Pichette
Journal:  Beilstein J Org Chem       Date:  2013-07-04       Impact factor: 2.883

3.  Inhibition of DNA-Topoisomerase I by Acylated Triterpene Saponins from Pittosporum angustifolium Lodd.

Authors:  Christian Bäcker; Malgorzata N Drwal; Robert Preissner; Ulrike Lindequist
Journal:  Nat Prod Bioprospect       Date:  2016-01-23
  3 in total

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