首页> 外文期刊>Journal of ocular pharmacology and therapeutics: The official journal of the Association for Ocular Pharmacology and Therapeutics >Inhibition of interleukin-1-induced uveitis and corneal fibroblast proliferation by interleukin-1 blockers.
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Inhibition of interleukin-1-induced uveitis and corneal fibroblast proliferation by interleukin-1 blockers.

机译:白细胞介素-1阻断剂抑制白细胞介素-1诱导的葡萄膜炎和角膜成纤维细胞增殖。

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摘要

Interleukin-1 (IL-1) is known to trigger induction of inducible nitric oxide synthase (iNOS) to persistently mass produce nitric oxide (NO) to induce various diseases such as cancer, inflammation, Alzheimer's disease and eye diseases, including uveitis, retinopathy, age-related macular degeneration, glaucoma and myopia. Therefore, IL-1 blockers could become an important class of drugs to fight numerous diseases. Among the many compounds studied so far, 1-methyl hydrazino analogs are among the most promising agents to be developed. A minor structural change of 1-methyl hydrazino group into 1-methyl thiosemicarbazido group enhanced their anti-inflammatory activity but reduced their antiproliferation activity on corneal fibroblast cell growth.
机译:已知白细胞介素-1(IL-1)触发诱导型一氧化氮合酶(InOS)诱导持续的批量生产一氧化氮(NO),以诱导癌症,炎症,阿尔茨海默病和眼病等各种疾病,包括葡萄膜炎,视网膜病变 ,年龄相关的黄斑变性,青光眼和近视。 因此,IL-1阻滞剂可能成为对抗众多疾病的重要药物。 在到目前为止所研究的许多化合物中,1-甲基肼类似物是最有前途的试剂中待开发的。 1-甲基肼基的次要结构变化为1-甲基硫代喹甲毒性组增强了它们的抗炎活性,但在角膜成纤维细胞生长上降低了它们的抗溶解活性。

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