Literature DB >> 16805551

C-15 thiazol-4-yl analogues of (E)-9,10-didehydroepothilone D: synthesis and cytotoxicity.

Brian R Hearn1, Dan Zhang, Yong Li, David C Myles.   

Abstract

The syntheses and biological evaluation of six epothilone D analogues are reported. These side-chain variants of the (E)-9,10-didehydroepothilone scaffold contain C-15 thiazole appendages that are derived from bromomethyl ketone intermediates. Although each of these analogues is less cytotoxic than the parent (E)-9,10-didehydroepothilone D, three maintain IC(50) values in the double-digit nanomolar range against both susceptible and resistant cell lines.

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Year:  2006        PMID: 16805551     DOI: 10.1021/ol061087h

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Synthesis of a ring-expanded bryostatin analogue.

Authors:  Barry M Trost; Hanbiao Yang; Oliver R Thiel; Alison J Frontier; Cheyenne S Brindle
Journal:  J Am Chem Soc       Date:  2007-02-06       Impact factor: 15.419

2.  Total syntheses of bryostatins: synthesis of two ring-expanded bryostatin analogues and the development of a new-generation strategy to access the C7-C27 fragment.

Authors:  Barry M Trost; Hanbiao Yang; Guangbin Dong
Journal:  Chemistry       Date:  2011-07-21       Impact factor: 5.236

3.  Synthesis of thiazolo- and 7,8-dihydrothiazolo[4,5-e]benzoisoxazoles.

Authors:  M H El-Badri; Mark J Kurth
Journal:  J Comb Chem       Date:  2009-03-09
  3 in total

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