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泛酸合成酶抑制剂的设计与合成

The design and synthesis of inhibitors of pantothenate synthetase.

作者信息

Tuck Kellie L, Saldanha S Adrian, Birch Louise M, Smith Alison G, Abell Chris

机构信息

University Chemical Laboratory, Lensfield Road, Cambridge, UK CB2 1EW.

出版信息

Org Biomol Chem. 2006 Oct 7;4(19):3598-610. doi: 10.1039/b609482a. Epub 2006 Aug 30.

Abstract

Pantothenate synthetase catalyses the ATP-dependent condensation of D-pantoate and beta-alanine to form pantothenate. Ten analogues of the reaction intermediate pantoyl adenylate, in which the phosphodiester is replaced by either an ester or sulfamoyl group, were designed as potential inhibitors of the enzyme. The esters were all modest competitive inhibitors, the sulfamoyls were more potent, consistent with their closer structural similarity to the pantoyl adenylate intermediate.

摘要

泛酸合成酶催化D-泛解酸和β-丙氨酸在ATP依赖下缩合形成泛酸。设计了10种反应中间体泛酰腺苷酸的类似物,其中磷酸二酯被酯或氨磺酰基取代,作为该酶的潜在抑制剂。酯类都是适度的竞争性抑制剂,氨磺酰类更有效,这与其与泛酰腺苷酸中间体更相似的结构一致。

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