Literature DB >> 16621542

Design and semisynthesis of novel fredericamycin A derivatives with an improved antitumor profile.

Ulrich Abel1, Werner Simon, Peter Eckard, Friedrich G Hansske.   

Abstract

We report the design, semisynthesis, and biological activity of a series of fredericamycin (1) derivatives. Within this series compound 1e combines low nanomolar cytotoxic potency in vitro, increased tumor cell line selectivity, and in vivo activity in a human xenograft model.

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Year:  2006        PMID: 16621542     DOI: 10.1016/j.bmcl.2006.03.029

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Synthetic Approach to the ABCD Ring System of Anticancer Agent Fredericamycin A via Claisen Rearrangement and Ring-Closing Metathesis as Key Steps.

Authors:  Sambasivarao Kotha; Subba Rao Cheekatla; Ambareen Fatma
Journal:  ACS Omega       Date:  2019-10-14
  1 in total

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