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J Exp Ther Oncol ; 1(2): 95-108, 1996 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-9414393

RESUMO

Cryptophycin-8 was prepared by the conversion of the epoxide group on cryptophycin-1 to a chlorohydrin. In the studies reported here, cryptophycin-8 was evaluated for preclinical activity against subcutaneous tumors of both mouse and human origin. At the highest non-toxic single course treatment, the following results were obtained (Table A). Cryptophycin-8 was less potent than cryptophycin-1 by approximately 4-fold; however, it was both more water soluble and had greater therapeutic efficacy, as demonstrated by % T/C, tumor cell log kill values, range of dose effectiveness and host cures.


Assuntos
Antineoplásicos/uso terapêutico , Depsipeptídeos , Lactamas/uso terapêutico , Lactonas/uso terapêutico , Neoplasias Experimentais/tratamento farmacológico , Animais , Antineoplásicos/toxicidade , Resistência a Múltiplos Medicamentos , Resistencia a Medicamentos Antineoplásicos , Humanos , Lactamas/toxicidade , Lactonas/toxicidade , Dose Letal Mediana , Camundongos , Camundongos Endogâmicos , Transplante de Neoplasias , Neoplasias Experimentais/patologia
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