3(4)-烷基-[1,2,4]三唑并[1,5-a]嘧啶-7-胺的合成和降眼压特性

IF 1.9 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY ChemistrySelect Pub Date : 2024-11-11 DOI:10.1002/slct.202404243
Angelina A. Ushakova, Victor V. Fedotov, Roman A. Drokin, Evgeniy N. Ulomsky, Vladimir L. Rusinov, Alexander A. Spasov, Lyudmila V. Naumenko, Alyona S. Taran, Alina M. Chebanko, Dmitry S. Yakovlev, Maria S. Pshenichnikova
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引用次数: 0

摘要

青光眼是导致全球不可逆失明的主要原因之一。眼内压(IOP)升高是这种疾病发病和发展的关键因素。用于治疗青光眼的药物会影响多种生物靶点。偶氮嘧啶衍生物被认为是腺苷受体(AR)激动剂和拮抗剂的类似物,因此作为治疗青光眼的潜在药物备受关注。本研究合成了一系列新型 3(4)-烷基-[1,2,4]三唑并[1,5-a]嘧啶-7-胺,以开发有前景的眼科降压药。合成的化合物具有显著的降眼压活性,为青光眼治疗提供了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synthesis and Ocular Hypotensive Properties 3(4)-Alkyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-amines

Glaucoma is one of the major causes of irreversible blindness worldwide. Increased intraocular pressure (IOP) is a key factor in the onset and progression of this disease. The drugs used to treat glaucoma influence a variety of biological targets. Azolopyrimidine derivatives have attracted significant attention as potential agents for the treatment of glaucoma because they presumed to be analogs of adenosine receptor (AR) agonists and antagonists. In this study, a series of novel 3(4)-alkyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-amines were synthesized to develop promising ophthalmic hypotensive drugs. The synthesized compounds demonstrated significant hypotensive activity against IOP, which opens new possibilities for glaucoma therapy.

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来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
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