Literature DB >> 16986962

Synthesis of macrosphelides with a thiazole side chain: new antitumor candidates having apoptosis-inducing property.

Yuji Matsuya1, Takanori Kawaguchi, Kentaro Ishihara, Kanwal Ahmed, Qing-Li Zhao, Takashi Kondo, Hideo Nemoto.   

Abstract

Hybrid compounds of macrosphelides and epothilones, both of which are natural macrolides having a 16-membered skeleton, were designed and synthesized using a ring-closing metathesis (RCM) strategy. Some of these hybrids were found to exhibit notable apoptosis-inducing activity against human lymphoma cells with higher potency than parent natural macrosphelides, and to be a promising lead compound for development of a new antitumor agent.

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Year:  2006        PMID: 16986962     DOI: 10.1021/ol061922v

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


  3 in total

1.  Development of an advanced synthetic route to macrosphelides and its application to the discovery of a more potent macrosphelide derivative.

Authors:  Yu Mi Heo; Hunseok Lee; Young Kee Shin; Seung-Mann Paek
Journal:  Molecules       Date:  2014-09-29       Impact factor: 4.411

2.  Synthetic studies on bioactive natural polyketides: intramolecular nitrile oxide-olefin cycloaddition approach for construction of a macrolactone skeleton of macrosphelide B.

Authors:  Seung-Mann Paek; Young-Ger Suh
Journal:  Molecules       Date:  2011-06-10       Impact factor: 4.411

Review 3.  Design and Synthesis of Anti-Cancer Chimera Molecules Based on Marine Natural Products.

Authors:  Min Woo Ha; Bo Reum Song; Hye Jin Chung; Seung-Mann Paek
Journal:  Mar Drugs       Date:  2019-08-27       Impact factor: 5.118

  3 in total

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