INHIBITION OF UREASE ACTIVITY BY DIPEPTIDYL HYDROXAMIC ACIDS

被引:29
作者
ODAKE, S
NAKAHASHI, K
MORIKAWA, T
TAKEBE, S
KOBASHI, K
机构
[1] FUJI CHEM IND CO LTD, RES INST, 530 CHOKEIJI, TOYAMA 933, JAPAN
[2] TOYAMA MED & PHARMACEUT UNIV, FAC PHARMACEUT SCI, TOYAMA, TOYAMA 93001, JAPAN
关键词
UREASE; HYDROXAMIC ACID; INHIBITOR; DIPEPTIDE;
D O I
10.1248/cpb.40.2764
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of dipeptidyl hydroxamic acids (H-X-Cly-NHOH: X = amino acid residues) was synthesized, and the inhibitory activity against Jack bean and Proteus mirabilis ureases [EC 3.5.1.5] was examined. A number of H-X-Gly-NHOH inhibited Jack bean urease with an I50 of the order of 10(-6) m and inhibited Proteus mirabilis urease with an I50 of the order of 10(-5) m. The inhibition against Jack bean urease was more potent than that with the corresponding aminoacyl hydroxamic acids (H-X-NHOH).
引用
收藏
页码:2764 / 2768
页数:5
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