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Heterocyclic quinones. XVI. Pharmacomodulation in the series of 11H-indolo[3,2-c]quinolinediones: synthesis, cytotoxicity and antitumor activity of 3-substituted 11H-pyrido[3',4':4,5]pyrrolo[3,2-c]quinoline-1,4-diones.
Chem Pharm Bull (Tokyo) ; 37(9): 2413-6, 1989 Sep.
Article en En | MEDLINE | ID: mdl-2557983
With the aim of obtaining new antitumor drugs more active than previously described 11H-indolo[3,2-c]quinoline-1,4-diones and 7,8,9,10-tetrahydro-11H-indolo[3,2-c]quinoline-1,4-diones, the synthesis and activities of a series of 3-substituted 11H-pyrido[3',4':4,5]pyrrolo[3,2-c]quinoline-1,4-diones and of 7,8,9,10-tetrahydro-11H-pyrido-[3',4':4,5]pyrrolo[3,2-c] quinoline-1,4-diones were studied. Some quinones were more cytotoxic in vitro towards L1210 leukemia cells but were not active in vivo towards murine P388 leukemia.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piridinas / Pirroles / Quinolonas / Indoles / Antineoplásicos Límite: Animals Idioma: En Revista: Chem Pharm Bull (Tokyo) Año: 1989 Tipo del documento: Article Pais de publicación: Japón
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piridinas / Pirroles / Quinolonas / Indoles / Antineoplásicos Límite: Animals Idioma: En Revista: Chem Pharm Bull (Tokyo) Año: 1989 Tipo del documento: Article Pais de publicación: Japón