受体
内皮素受体
背景(考古学)
吡咯
化学
羧酸
配体(生物化学)
药理学
生物化学
立体化学
医学
生物
有机化学
古生物学
作者
Loredana Salerno,Maria Modica,Giuseppe Romeo,Valeria Pittalà,Alfredo Cagnotto,Maria Angela Siracusa
出处
期刊:Medicinal Chemistry
日期:2014-09-19
卷期号:11 (2): 109-117
被引量:1
标识
DOI:10.2174/1573406410666140917160653
摘要
The interest of researchers for ligands of the endothelin receptors ETA and ETB is due to their extensive therapeutic potential. In particular, receptor antagonists are useful in a number of diseases such as pulmonary hypertension, acute myocardial infarction, congestive heart failure, renal failure, and atherosclerosis. In the context of our research program aimed to the development of new endothelin receptor ligands, in this paper we describe the synthesis and structure- activity relationships of a new series of 1,3,5-substituted pyrrole-2-carboxylic acid derivatives 27-40 possessing the structural features for ET receptors binding. New synthesized compounds were tested on ETA and ETB receptors stably expressed in CHO cells and some of them showed interesting affinity and selectivity towards ETA receptors. Keywords: Endothelins, cardiovascular diseases, ET receptors, binding assays, 1, 3, 5-substituted pyrroles.
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