Groutas W C, Abrams W R, Theodorakis M C, Kasper A M, Rude S A, Badger R C, Ocain T D, Miller K E, Moi M K, Brubaker M J
J Med Chem. 1985 Feb;28(2):204-9. doi: 10.1021/jm00380a010.
Several amino acid derived azolides (I) have been synthesized and investigated for their inhibitory activity toward human leukocyte elastase and porcine pancreatic elastase. The inhibitory activity was found to be dependent on the nature of the precursor amino acid ester. Thus, compounds derived from L-valine methyl ester 3, L-norvaline methyl ester 5, DL-norleucine methyl ester 9, and L-methionine methyl ester 10 were found to inhibit irreversibly both enzymes. Compound 10 was found to be a specific and selective inhibitor of human leukocyte elastase. In contrast to these, inhibitors derived from glycine methyl ester 1, D-valine methyl ester 4, and D-norvaline methyl ester 6 were found to be inactive. The results of the present study show that latent isocyanates derived from appropriate amino acids can serve as selective inhibitors of serine proteases and are of potential pharmacological value.
已合成了几种氨基酸衍生的氮杂环内酯(I),并研究了它们对人白细胞弹性蛋白酶和猪胰弹性蛋白酶的抑制活性。发现抑制活性取决于前体氨基酸酯的性质。因此,发现源自L-缬氨酸甲酯3、L-正缬氨酸甲酯5、DL-正亮氨酸甲酯9和L-蛋氨酸甲酯10的化合物可不可逆地抑制这两种酶。发现化合物10是人白细胞弹性蛋白酶的特异性和选择性抑制剂。与此相反,发现源自甘氨酸甲酯1、D-缬氨酸甲酯4和D-正缬氨酸甲酯6的抑制剂无活性。本研究结果表明,源自适当氨基酸的潜在异氰酸酯可作为丝氨酸蛋白酶的选择性抑制剂,具有潜在的药理价值。