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以血管紧张素受体为靶点的药物研究进展 被引量:4

Progress in angiotensin receptor as drug targets
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摘要 血管紧张素Ⅱ受体共有4种亚型(AT1、AT2、AT3和AT4)。血管紧张素Ⅱ受体拮抗剂是临床上常用的高血压治疗药物,以AT1受体拮抗剂和AT2受体拮抗剂应用较多。近年来,随着对血管紧张素Ⅱ受体拮抗剂研究的深入,涌现出诸多具有良好药理活性的选择性AT1受体拮抗剂、双重作用靶点的非选择性AT1受体拮抗剂和选择性AT2受体拮抗剂。本文对近年来报道的血管紧张素Ⅱ受体拮抗剂进行简要综述。 There are four subtypes of angiotensin ]] receptor ( AT1, AT2, AT3 and AT4 ). Angiotensin II re- ceptor antagonists have been used as common antihypertensive drugs clinically. AT1 and AT2 receptor an- tagonists have been used as the common drugs in clinic. In recent years, many drugs based on the progress of research on the angiotensin II receptor antagonists, such as selective AT1 ~eceptor antagonists, non-selective AT1 receptor antagonists with two targets and selective AT2 receptor antagonists have been launched. The angiotensin I1 receptor antagonists reported recently were reviewed in this article.
出处 《中国药物化学杂志》 CAS CSCD 2012年第5期442-451,共10页 Chinese Journal of Medicinal Chemistry
关键词 高血压症 血管紧张素Ⅱ受体拮抗剂 AT1受体拮抗剂 AT2受体拮抗剂 hypertension angiotensinlIreceptor antagonist AT1 receptor antagonist AT2 receptor antagonist
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  • 1王鲁雁,孙宁玲.血管紧张素Ⅱ受体拮抗剂(ARB)氯沙坦在高血压治疗中的作用及地位[J].中华高血压杂志,2007,15(z1):11-13. 被引量:8
  • 2陈清江,王瑞淦.替米沙坦治疗高血压临床研究进展[J].国外医学(老年医学分册),2004,25(5):225-228. 被引量:11
  • 3Schiffrin E L. Vascular endothelin in hypertension[J].Vascul Pharmacol, 2005,43( 1 ) : 19-29.
  • 4Hong H J, Chan P, Liu J C, et al. Angiotensin Ⅱ induces endothelin-1 gene expression via extracellular signal-regulated kinase pathway in rat aortic smooth muscle cells [J].Cardiovasc Res,2004, 61(1): 159-168.
  • 5Jesmin S, Sakuma I, Togashi H, et al. Effects of endothelin receptor antagonist on expression of AT1 and AT2 receptors in the heart of SHR-SP[J]. J Cardiovasc Pharmacol, 2004,44:S59-S63.
  • 6Cappelli A, Pericot Mohr G, Gallelli A, et al. Design, synthesis, structural Studies, biological evaluation and computational simulations of novel potent AT1 angiotensin Ⅱ receptor antagonists based on the 4-Phenylquinoline structure[J]. J Med Chem, 2004, 47(10),2574-2586.
  • 7Bolli M H, Marfurt J, Grisostomi C, et al. Novel benzo[1,4 ] diazepin-2-one derivatives as endothelin receptor antagonists[J]. J Med Chem,2004,47(11) : 2776-2795.
  • 8Imai T, Hirata Y, Emori T, et al. Induction of endothelin-1 gene by angiotensin and vasopressin in endothehal cells[J].Hypertension, 1992, 19(6) :753-757.
  • 9Murugesan N, Tellew J E, Gu Z, et al. Discovery of N-isoxazolyl biphenylsulfonamides as potent dual angiotensin Ⅱ and endothelin A receptor antagonists [J]. J Med Chem,2002,45(18): 3829-3835.
  • 10Pliquett R U, Paschke R, Koch C A.Hormones of the cardiovascular system [EB/OL].[ 2005-05-03 ]. http://www. endotext. com/adrenal/adrena125/adrena125.htm.

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  • 1张碧玫,余文博.作用于RAAS的抗高血压药研究进展[J].药学进展,2005,29(3):136-141. 被引量:5
  • 2魏臻,徐进宜,吴晓明,华维一.新型血管紧张素Ⅱ受体和内皮素受体双重拮抗剂研究进展[J].药学进展,2006,30(5):193-199. 被引量:5
  • 3ZHANG Y C,ZHOU J P, PAN W H, et al. Synthesis and bio- logical study of 3-butyl-1 - (2,6-dichlorophenyl) -1 H- [ 1,2,41 tri- azol-5 (4H) -one derivatives as anti-hypertension Drugs [ J ]. Lett Drug Design Discovery, 2010, 7 : 18-22.
  • 4BAI R R, YANG X, ZHU Y, et al. Novel nitric oxide-releasing isochroman-4-one derivatives : Synthesis and evaluation of antihy- pertensive activity [ J] . Bioorg Med Chem, 2012, 20 (23) : 6848-6855.
  • 5LI Y Q, JI H, ZHANG Y H, et al. WBll06, a novel nitric ox- ide-releasing derivative of telmisartan, inhibits hypertension and improves glucose metabolism in rats [ J]. Bioorg Med Chem Lett, 2007, 577(1-3) : 2979-2982.
  • 6BRESCH M C, CALDERONE V, DIGIACOMO M, et al. New NO-releasing pharmacodynamic hybrids of losartan and its active metabolite: Design, synthesis, and biopharmacological properties [J]. JMed Chem, 2006, 49(8) : 2628-2639.
  • 7GAOL. Studies on design and synthesis of nonpeptide angioten- sin Ⅱ receptor antagonists 1,4-substituted indoles compounds [ D]. Shanghai: East China University, 2009.
  • 8ZHANG Y C, XU J Y, LI Y M, et al. Design, synthesis and pharmacological evaluation of novel NO-releasing benzimidazole hybrids as potential antihypertensive candidate [ J ]. Chem Bio Drng Design, 2015, 85(5) : 541-548.
  • 9WU X M. The preparation of N-phenyl pyrrolyl-2-tetrazole deriv- atives. China [P]. 2003-10-10.
  • 10BovY P R, REITZ J D, COLLINS J T, et al. Nonpeptide agio- tensin Ⅱ antagonists: N-phenyl-1H-pyrrole derivatives are angio- tensin Ⅱ receptor antagonists [J]. J Med Chem, 1993, 36( 1 ) : 101-110.

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