作者:Sanne D. J. Magnan、Frances N. Shirota、Herbert T. Nagasawa
DOI:10.1021/jm00351a003
日期:1982.9
The N-gamma-glutamyl derivatives of L-thiazolidine-4-carboxylic acid, 4-aminobutyric acid, 1-aminocyclopentanecarboxylic acid, 2-aminophenol, and p-fluoro-L-phenylalanine (compounds 6, 8, 9, 10, and 12, respectively) were synthesized using the synthon phthaloylglutamic anhydride. Their relative rates of cleavage by the enzyme gamma-glutamyl transpeptidase (gamma-GT) were determined in order to evaluate
L-噻唑烷-4-羧酸,4-氨基丁酸,1-氨基环戊烷羧酸,2-氨基苯酚和对氟-L-苯丙氨酸的N-γ-谷氨酰基衍生物(化合物6、8、9、10和使用间苯二甲酰谷氨酸酐合成12)。确定了它们被γ-谷氨酰转肽酶(γ-GT)切割的相对速率,以便评估在某些病理条件下该酶选择性释放的可能性。化合物6、8和9不易被γ-GT溶剂化,但是化合物10和12以及3-和4-氨基苯酚的N-γ-谷氨酰化衍生物易于裂解。