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Synthesis and Biological Evaluation as a Potential Allylamine Type Antimycotics  

정병호 (전남대학교 약학대학)
조원제 (전남대학교 약학대학)
천승훈 (전남대학교 약학대학)
정순영 (전남대학교 약학대학)
유진철 (조선대학교 약학대학)
Publication Information
YAKHAK HOEJI / v.47, no.5, 2003 , pp. 293-299 More about this Journal
Abstract
Structure-activity relationship studies of allylamine type of antimycotics were carried out to evaluate the effect of naphthyl and methyl portion of naftifine. Compounds with 4-fluorophenyl(2a-5a), 2-fluorophenyl(2b-5b), 2,4-dichlorophenyl(2c-5c), 2,6-dichlorophenyl(2d-5d), 4-nitrophenyl(2e-5e), and 2,3-dihydro-benzo[1,4]dioxan-6-yl( 2f-5f) instead of naphthyl group with hydrogen(3a-3f), methyl(4a-4f), and ethyl(5a-5f) in the place of methyl in naftifine were synthesized and tested their in vitro anti-fungal activity against five different fungi. Eight compounds(3a, 5a, 3c, 4c, 4d, 5d, 5e, and 4f) showed significant antifungal activity against T. mentagrophytes. (E)-N-Ethyl-(3-phenyl-2-propenyl)-4-nitro-benzenemethaneamine(5e) displayed moderate antifungal activity against all five different fungi.
Keywords
trans-cinnamylamine; 4-fluorobenzaldehyde; 2,4-difluorobenzaldehyde; 2,4-dichlorobenzaldehyde; l,4-benzodioxan-6-carboxaldehyde;
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