n ω-硝基- n ω'-取代胍:一类简单的一氧化氮合酶抑制剂。

Christophe D Guillon, David D Wisnoski, Jaya Saxena, Ned D Heindel, Diane E Heck, Donald J Wolff, Jeffrey D Laskin
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引用次数: 2

摘要

制备了一系列n ω-硝基-n ω-取代胍类化合物,作为人一氧化氮合酶(NOS)亚型的潜在抑制剂。氨基胍和硝基精氨酸在iNOS抑制中的应用表明了硝基胍类似物的潜在应用。化合物文库对三种一氧化氮合酶亚型(eNOS、iNOS和nNOS)进行了检测。几个候选物对nNOS表现出良好的活性和选择性。一种特殊的化合物甚至对iNOS表现出良好的选择性。讨论了这种选择性抑制剂的潜在用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

<i>N</i><sup>ω</sup>-NITRO-<i>N</i><sup>ω'</sup>-SUBSTITUTED GUANIDINES: A SIMPLE CLASS OF NITRIC OXIDE SYNTHASE INHIBITORS.

Nω-NITRO-Nω'-SUBSTITUTED GUANIDINES: A SIMPLE CLASS OF NITRIC OXIDE SYNTHASE INHIBITORS.

A series of Nω-nitro-Nω'-substituted guanidines has been prepared as potential inhibitors of the human Nitric Oxide Synthase (NOS) isoforms. The reported utility of aminoguanidine and nitroarginine in iNOS inhibition points to a potential similar utility for analogs of nitro-guanidine. The compound library was tested against the three isoforms of Nitric Oxide Synthase (eNOS, iNOS and nNOS). Several candidates showed excellent activity and good selectivity for nNOS. One particular compound even demonstrated good selectivity for iNOS. The potential usefulness of such selective inhibitors is discussed.

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