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Academic Journal of Second Military Medical University ; (12)1982.
Artigo em Chinês | WPRIM | ID: wpr-550461

RESUMO

In order to search for a more potent and less toxic antifungal agent, five novel sulconazole analogues were synthesized by changing 1-imidazolyl and p-chlorobenzyl in sulconazole structure. The results of preliminary biological tests show that analogues Ⅰ and Ⅱ possess more potent antifungal activities and wider antifungal spectra than sulconazole.

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