NOVEL INHIBITORS OF PROLYL 4-HYDROXYLASE .3. INHIBITION BY THE SUBSTRATE-ANALOG N-OXALOGLYCINE AND ITS DERIVATIVES

被引:86
作者
CUNLIFFE, CJ [1 ]
FRANKLIN, TJ [1 ]
HALES, NJ [1 ]
HILL, GB [1 ]
机构
[1] ICI PLC,PHARMACEUT,RES DEPT I,MERESIDE,ALDERLEY PK,MACCLESFIELD SK10 4TG,CHESHIRE,ENGLAND
关键词
D O I
10.1021/jm00092a016
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
N-Oxaloglycine (3) is an alpha-ketoglutarate (1) analogue that is a competitive inhibitor of prolyl 4-hydroxylase (EC 1.14.11.2). A study of the structure-activity relationships of some other oxalo derivatives shows that substitution on the glycine moiety modulates activity stereoselectively and that if the omega-carboxylate is homologated or replaced by either acylsulfonamides or anilide, then activity is sharply reduced. This sensitivity to these changes is contrasted with the relative insensitivity of another putative alpha-ketoglutarate analogue, pyridine-2,5-dicarboxylic acid (2), and the implication is discussed that compounds of both series are unlikely to bind to prolyl hydroxylase in the same way even though both inhibit the enzyme competitively.
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页码:2652 / 2658
页数:7
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