DNA alkylation properties of yatakemycin.
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