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吡唑和吡唑啉作为神经型和诱导型一氧化氮合酶(nNOS和iNOS)的潜在抑制剂(III)。

Pyrazoles and pyrazolines as neural and inducible nitric oxide synthase (nNOS and iNOS) potential inhibitors (III).

作者信息

Carrión M Dora, López Cara Luisa C, Camacho M Encarnación, Tapias Víctor, Escames Germaine, Acuña-Castroviejo Darío, Espinosa Antonio, Gallo Miguel A, Entrena Antonio

机构信息

Departamento de Química Farmacéutica y Orgánica, Facultad de Farmacia, Universidad de Granada, Campus de Cartuja s/n, 18071 Granada, Spain.

出版信息

Eur J Med Chem. 2008 Nov;43(11):2579-91. doi: 10.1016/j.ejmech.2008.01.014. Epub 2008 Jan 26.

Abstract

We have previously described a series of 4,5-dihydro-1H-pyrazole as moderately potent nNOS inhibitors. As a follow up of these studies, we report here the preparation and the preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1H-pyrazole and 1-alkyl-3-benzoyl-1H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS). None of the reported compounds exhibited significant iNOS or nNOS inhibition, although the 1-benzyl-3-(2-amino-5-chlorobenzoyl)-1H-pyrazole-5-carboxylic acid ethyl ester derivative (10l), which shows an inhibition of 50% versus iNOS at a 1mM final concentration and no activity against nNOS, is potentially amenable of further optimization. The reasons for the inactivity of the reported series are discussed on the basis of docking studies.

摘要

我们之前曾描述过一系列4,5-二氢-1H-吡唑作为中等强度的nNOS抑制剂。作为这些研究的后续,我们在此报告一系列1-烷基-3-苯甲酰基-4,5-二氢-1H-吡唑和1-烷基-3-苯甲酰基-1H-吡唑作为神经元型和诱导型一氧化氮合酶(nNOS和iNOS)潜在抑制剂的制备及初步评估。尽管1-苄基-3-(2-氨基-5-氯苯甲酰基)-1H-吡唑-5-羧酸乙酯衍生物(10l)在终浓度为1mM时对iNOS的抑制率为50%且对nNOS无活性,但所报道的化合物均未表现出显著的iNOS或nNOS抑制作用,不过该衍生物仍有可能进行进一步优化。基于对接研究对所报道系列化合物无活性的原因进行了讨论。

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