首页> 外文期刊>Journal of Medicinal Chemistry >Design and synthesis of tricyclic compounds with enone functionalities in rings a and C: a novel class of highly active inhibitors of nitric oxide production in mouse macrophages.
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Design and synthesis of tricyclic compounds with enone functionalities in rings a and C: a novel class of highly active inhibitors of nitric oxide production in mouse macrophages.

机译:设计和合成具有环烯和环功能的三环化合物:小鼠巨噬细胞中一氧化氮生成的一类新型高效抑制剂。

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摘要

Novel tricyclic compounds with enone functionalities in rings A and C, which were designed on the basis of the structure of a synthetic triterpenoid, 2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oic acid, have been synthesized. Among them, 10 shows high inhibitory activity (IC(50) = 1 nM level) against production of nitric oxide induced by interferon-gamma in mouse macrophages and is orally active at 15 mg/kg (once) in a preliminary in vivo study using mouse peritoneal inflammation induced by thioglycollate and interferon-gamma.
机译:根据合成的三萜类化合物2-氰基-3,12-二氧代油酸酯-1,9(11)-二烯-28-油酸的结构设计了在环A和C中具有烯酮官能团的新型三环化合物,已经合成。其中10个对小鼠巨噬细胞中的干扰素-γ诱导的一氧化氮产生具有很高的抑制活性(IC(50)= 1 nM水平),并且在体内初步研究中使用15 mg / kg(一次)口服活性巯基乙酸盐和干扰素-γ诱导的小鼠腹膜炎症。

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