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Inhibitors of angiotensin-converting enzyme containing a tetrahedral arsenic atom.

机译:含有四面体砷原子的血管紧张素转换酶抑制剂。

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摘要

A series of tetrahedral oxo acids of Group VA and VIA elements and of silicon and boron were examined as inhibitors of angiotensin-converting enzyme. Arsenate is a competitive inhibitor with a Ki of 27 +/- 1 mM, at least 10-fold more potent than phosphate. Dimethylarsinate is a competitive inhibitor with a Ki of 70 +/- 9 mM, 2-fold more potent than dimethylphosphinate. Oxo acids of boron, silicon, antimony, sulphur and selenium are not inhibitors. On the basis of these results and the strong inhibition of this zinc metallopeptidase by substrate analogues containing a tetrahedral phosphorus atom, two substrate analogues containing a tetrahedral arsenic atom were prepared. 2-Arsonoacetyl-L-proline is a competitive inhibitor with a Ki of 18 +/- 7 mM, more than 2000-fold weaker than that of its phosphorus analogue 2-phosphonoacetyl-L-proline. 4-Arsono-2-benzylbutanoic acid is a mixed inhibitor with a Ki of 0.5 +/- 0.2 mM, indistinguishable in potency from its phosphorus analogue 2-benzyl-4-phosphonobutanoic acid.
机译:研究了一系列VA和VIA族元素以及硅和硼的四面体含氧酸作为血管紧张素转化酶的抑制剂。砷酸盐是一种竞争性抑制剂,Ki为27 +/- 1 mM,效力至少是磷酸盐的10倍。砷化二甲酯是一种竞争性抑制剂,Ki为70 +/- 9 mM,比次膦酸二甲酯强2倍。硼,硅,锑,硫和硒的含氧酸不是抑制剂。基于这些结果,并且通过含有四面体磷原子的底物类似物对这种锌金属肽酶的强抑制作用,制备了两种含有四面体砷原子的底物类似物。 2-Arsonoacetyl-L-脯氨酸是一种竞争性抑制剂,Ki为18 +/- 7 mM,比其磷类似物2-phosphonoacetyl-L-脯氨酸弱2000倍以上。 4-Arsono-2-苄基丁酸是一种混合抑制剂,Ki为0.5 +/- 0.2 mM,在效力上与它的磷类似物2-苄基-4-膦基丁酸没有区别。

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