Gao Xuri, Huang Jiaxin , Cai Junchao, . STUDIES ON ANTIFUNGAL AGENTS VI. SYNTHESIS AND ANTICANDIDAALBICANS ACTIVITY OF CTERMINAL CONTAINING MEDP PEPTIDESJ. Acta Pharmaceutica Sinica, 1999, 34(7): 505-509.
Citation: Gao Xuri, Huang Jiaxin , Cai Junchao, . STUDIES ON ANTIFUNGAL AGENTS VI. SYNTHESIS AND ANTICANDIDAALBICANS ACTIVITY OF CTERMINAL CONTAINING MEDP PEPTIDESJ. Acta Pharmaceutica Sinica, 1999, 34(7): 505-509.

STUDIES ON ANTIFUNGAL AGENTS VI. SYNTHESIS AND ANTICANDIDAALBICANS ACTIVITY OF CTERMINAL CONTAINING MEDP PEPTIDES

  • AIM: To search for compounds having strong antifungal activities. METHODS AND RESULTS: Twelve new peptides containing MEDP(N3-(2-R,3R)-4-methoxyepoxysuccinyl-L-2,3-diaminopropanoic acid) in Cterminus have been synthesized and evaluated in vitro against Candida albicans on the basis of “illicit transport”. CONCLUSION: Some of them have strong activities. The MMIC(molar mininum inhibitory concentrations) of ValMEDP, the most active peptide in this series, is 448 nmol·mL-1, 960 times the MMIC of MEDP. But all of the peptides showed weaker activities than the related peptides containing FMDP(N3-4-methoxyfumaryl-L-2,3-diaminopropanoic acid).
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