烷基
化学
立体化学
药物化学
药理学
医学
有机化学
作者
A. A. Ushakova,Victor V. Fedotov,Роман А. Дрокин,Evgeniy N. Ulomsky,В. Л. Русинов,А. А. Спасов,Lyudmila V. Naumenko,Alyona S. Taran,Alina M. Chebanko,D. S. Yakovlev,Maria S. Pshenichnikova
标识
DOI:10.1002/slct.202404243
摘要
Abstract 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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