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DNA alkylation properties of yatakemycin.
Parrish, Jay P; Kastrinsky, David B; Wolkenberg, Scott E; Igarashi, Yasuhiro; Boger, Dale L.
Afiliación
  • Parrish JP; Department of Chemistry and the Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
J Am Chem Soc ; 125(36): 10971-6, 2003 Sep 10.
Article en En | MEDLINE | ID: mdl-12952479
ABSTRACT
Yatakemycin represents the newest and now most potent member of a class of naturally occurring antitumor compounds that includes CC-1065 and the duocarmycins, which derive their biological properties from a characteristic DNA alkylation reaction. Herein, the first description of the yatakemycin DNA alkylation properties is detailed, constituting the first such study of a naturally occurring "sandwiched" member of this class. Thus, the event, sequence selectivity, relative rate and efficiency, and reversibility of the DNA alkylation reaction of yatakemycin are described.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pirroles / ADN / Indoles Tipo de estudio: Prognostic_studies Idioma: En Revista: J Am Chem Soc Año: 2003 Tipo del documento: Article País de afiliación: Estados Unidos
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pirroles / ADN / Indoles Tipo de estudio: Prognostic_studies Idioma: En Revista: J Am Chem Soc Año: 2003 Tipo del documento: Article País de afiliación: Estados Unidos