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设计、合成及 8-(2-氨基-1-羟乙基)-6-羟基-1,4-苯并恶嗪-3(4H)-酮衍生物作为潜在的β-肾上腺素能受体激动剂的生物评价。

Design, synthesis and biological evaluation of 8-(2-amino-1-hydroxyethyl)-6-hydroxy-1,4-benzoxazine-3(4H)-one derivatives as potent β-adrenoceptor agonists.

机构信息

Department of Medicinal Chemistry, School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China; Key Laboratory of Structure-Based Drug Design and Discovery of Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.

Department of Pharmacology, School of Life Sciences and Biopharmaceutics, Shenyang Pharmaceutical University, Shenyang 110016, China.

出版信息

Bioorg Med Chem. 2020 Jan 1;28(1):115178. doi: 10.1016/j.bmc.2019.115178. Epub 2019 Nov 11.

Abstract

A series of β-adrenoceptor agonists with an 8-(2-amino-1-hydroxyethyl)-6-hydroxy-1,4-benzoxazine-3(4H)-one moiety is presented. The stimulatory effects of the compounds on human β-adrenoceptor and β-adrenoceptor were characterized by a cell-based assay. Their smooth muscle relaxant activities were tested on isolated guinea pig trachea. Most of the compounds were found to be potent and selective agonists of the β-adrenoceptor. One of the compounds, (R)-18c, possessed a strong β-adrenoceptor agonistic effect with an EC value of 24 pM. It produced a full and potent airway smooth muscle relaxant effect same as olodaterol. Its onset of action was 3.5 min and its duration of action was more than 12 h in an in vitro guinea pig trachea model of bronchodilation. These results suggest that (R)-18c is a potential candidate for long-acting β-AR agonists.

摘要

呈现了一系列具有 8-(2-氨基-1-羟乙基)-6-羟基-1,4-苯并恶嗪-3(4H)-酮部分的β-肾上腺素受体激动剂。通过基于细胞的测定法,对化合物对人β-肾上腺素受体和β-肾上腺素受体的刺激作用进行了表征。在分离的豚鼠气管上测试了它们的平滑肌松弛活性。大多数化合物被发现是β-肾上腺素受体的有效且选择性激动剂。其中一种化合物 (R)-18c 具有强大的β-肾上腺素受体激动作用,EC 值为 24 pM。它产生了与奥达特罗相同的完全且有效的气道平滑肌松弛作用。在体外豚鼠气管扩张模型中,其作用开始时间为 3.5 分钟,作用持续时间超过 12 小时。这些结果表明 (R)-18c 是一种有前途的长效β-AR 激动剂候选物。

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