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A direct comparison of oral treatments with BAY-n-7133, BAY-1-9139 and ketoconazole in experimental murine coccidioidomycosis.

作者信息

Levine H B

出版信息

Sabouraudia. 1984;22(1):37-46. doi: 10.1080/00362178485380071.

DOI:10.1080/00362178485380071
PMID:6322362
Abstract

Two new experimental antifungal azole drugs were compared with ketoconazole for the management of experimental murine coccidioidomycosis. The first, BAY-n-7133, a triazole, was superior to the second, BAY-1-9139, an imidazole derivative. Neither BAY drug was as effective as ketoconazole in early fulminant coccidioidomycosis of mice, in later disseminated disease and in deep-seated chronic disease. A possible limitation of BAY-n-7133 in the mouse model was its reported capacity to induce enzyme changes that accelerated its clearance from serum. Induction of such an enzyme response in human beings has been reported not to occur.

摘要

相似文献

1
A direct comparison of oral treatments with BAY-n-7133, BAY-1-9139 and ketoconazole in experimental murine coccidioidomycosis.
Sabouraudia. 1984;22(1):37-46. doi: 10.1080/00362178485380071.
2
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引用本文的文献

1
Activity of BAY n 7133 and BAY 1 9139 in vitro and in experimental murine coccidioidomycosis.BAY n 7133和BAY 1 9139在体外及实验性小鼠球孢子菌病中的活性
Eur J Clin Microbiol. 1985 Aug;4(4):400-3. doi: 10.1007/BF02148692.
2
Overview of medically important antifungal azole derivatives.医学上重要的抗真菌唑类衍生物概述。
Clin Microbiol Rev. 1988 Apr;1(2):187-217. doi: 10.1128/CMR.1.2.187.