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New sources of chemical diversity inspired by biosynthesis: rational design of a potent epothilone analogue.
Frein, Jeffrey D; Taylor, Richard E; Sackett, Dan L.
Afiliação
  • Frein JD; Department of Chemistry and Biochemistry and the Walther Cancer Research Center University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, Indiana 46556-5670, USA.
Org Lett ; 11(15): 3186-9, 2009 Aug 06.
Article em En | MEDLINE | ID: mdl-19572566
ABSTRACT
A concise total synthesis of (S)-14-methoxyepothilone D has been accomplished. (S)-14-Methoxyepothilone D represents a conceptually novel example of polyketide analogue design based on an alternative biogenetic pattern of extender units. The significant biological activity observed for this compound provides a foundation to support studies designed to prepare derivatives of this type through fermentation of genetically engineered organisms expressing the epothilone PKS gene cluster.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Macrolídeos / Epotilonas Limite: Humans Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Macrolídeos / Epotilonas Limite: Humans Idioma: En Ano de publicação: 2009 Tipo de documento: Article