血管紧张素受体在GtoPdb v.2023.1

Wayne Alexander, K. Bernstein, K. Catt, M. de Gasparo, Khuraijam Dhanachandra Singh, S. Eguchi, E. Escher, T. Goodfriend, M. Horiuchi, L. Hunyady, A. Husain, T. Inagami, S. Karnik, Jacqueline R. Kemp, W. Thomas, P. Timmermans, Kalyan C. Tirupula, Hamiyet Unal, T. Unger, P. Vanderheyden
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引用次数: 0

摘要

血管紧张素II (Ang II)的作用是由AT1和AT2受体介导的(由NC-IUPHAR血管紧张素受体小组委员会商定的命名法[63,155]),它们的序列相似性约为30%。十肽血管紧张素I、八肽血管紧张素II和七肽血管紧张素III是内源性配体。临床上常用的AT1受体阻滞剂有氯沙坦、坎地沙坦、奥美沙坦、替米沙坦等。
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Angiotensin receptors in GtoPdb v.2023.1
The actions of angiotensin II (Ang II) are mediated by AT1 and AT2 receptors (nomenclature as agreed by the NC-IUPHAR Subcommittee on Angiotensin receptors [63, 155]), which have around 30% sequence similarity. The decapeptide angiotensin I, the octapeptide angiotensin II and the heptapeptide angiotensin III are endogenous ligands. losartan, candesartan, olmesartan, telmisartan, etc. are clinically used AT1 receptor blockers.
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