Literature DB >> 11459650

Synthesis and biological evaluation of didemnin photoaffinity analogues.

M D Vera1, A J Pfizenmayer, X Ding, D Ahuja, P L Toogood, M M Joullié.   

Abstract

The synthesis of four benzophenone-containing analogues of the antiproliferative natural product didemnin B is presented. In vitro protein biosynthesis inhibition potency and antitumor activity were evaluated. The results indicate that all four analogues are biologically active and could serve as photoaffinity reagents for the study of receptor-binding interactions of didemnins. These analogues could also be useful in studying antitumor effects of didemnins.

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Year:  2001        PMID: 11459650     DOI: 10.1016/s0960-894x(01)00339-0

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


  2 in total

1.  Synthetic studies of tamandarin B side chain analogues.

Authors:  Kenneth M Lassen; Jisun Lee; Madeleine M Joullié
Journal:  J Org Chem       Date:  2010-05-07       Impact factor: 4.354

2.  Solid phase versus solution phase synthesis of heterocyclic macrocycles.

Authors:  Seong Jong Kim; Shelli R McAlpine
Journal:  Molecules       Date:  2013-01-16       Impact factor: 4.411

  2 in total

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