Tiazoles fluorados útiles para el tratamiento del cáncer
Los compuestos de fórmula (I) o sus sales farmacéuticamente aceptables, o sus estereoisómeros o mezcla de estereoisómeros, donde: R Compounds of formula (I) or their pharmaceutically acceptable salts, or their stereoisomers or mixtures of stereoisomers, where: R 1 is selected from the group consisti...
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creator | IGLESIAS SERRET, DANIEL RAMON ALBALATE, ROSARIO GIL SANTANO, JOAN ALBERICIO PALOMERA, FERNANDO LAVILLA GRIFOLS, RODOLFO GONZALEZ GIRONÈS, DIANA Mª PEREZ PERARNAU, ALBA PRECIADO GALLEGO, SARA |
description | Los compuestos de fórmula (I) o sus sales farmacéuticamente aceptables, o sus estereoisómeros o mezcla de estereoisómeros, donde: R
Compounds of formula (I) or their pharmaceutically acceptable salts, or their stereoisomers or mixtures of stereoisomers, where: R 1 is selected from the group consisting of: phenyl, and phenyl mono-, di-, or tri-substituted by a radical independently selected from the group consisting of F, Cl, Br, I, (C 1 -C 6 )-alkyl, COO-(C 1 -C 6 )-alkyl, and (C 1 -C 6 )-alkoxy; and R 2 is a radical selected from the same group as R 1 , further including a phenyl substituted in 4-position by a radical independently selected from the group consisting of - O(CH 2 )CONH(CH 2 ) 3 CH 3 and OCH 2 COOC(CH 3 ) 3 , a biphenyl-4-yl, thiazol-2-yl, and a thiazol-2-yl mono- or di-substituted by a radical selected from F and phenyl; inhibit cell proliferation of tumor cells independently of p53 protein and may also induce apoptosis in several tumor cells independently of p53 protein, being useful for the treatment of several types of cancer. |
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Compounds of formula (I) or their pharmaceutically acceptable salts, or their stereoisomers or mixtures of stereoisomers, where: R 1 is selected from the group consisting of: phenyl, and phenyl mono-, di-, or tri-substituted by a radical independently selected from the group consisting of F, Cl, Br, I, (C 1 -C 6 )-alkyl, COO-(C 1 -C 6 )-alkyl, and (C 1 -C 6 )-alkoxy; and R 2 is a radical selected from the same group as R 1 , further including a phenyl substituted in 4-position by a radical independently selected from the group consisting of - O(CH 2 )CONH(CH 2 ) 3 CH 3 and OCH 2 COOC(CH 3 ) 3 , a biphenyl-4-yl, thiazol-2-yl, and a thiazol-2-yl mono- or di-substituted by a radical selected from F and phenyl; inhibit cell proliferation of tumor cells independently of p53 protein and may also induce apoptosis in several tumor cells independently of p53 protein, being useful for the treatment of several types of cancer.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Tiazoles fluorados útiles para el tratamiento del cáncer |
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