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替米沙坦及其类似物的合成和生物活性研究 被引量:7

Synthesis of Telmisartan and Its Derivatives and Evaluation of Their Biological Activities
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摘要 设计合成了替米沙坦及其类似物,改进了替米沙坦的合成工艺.用邻苯二胺与相应的有机羧酸缩合,所得产物苯并咪唑衍生物与4'-溴甲基联苯-2-甲酸甲酯通过N-烷基化得到相应的目标化合物,合成了替米沙坦和9种未见文献报道的苯并咪唑联苯化合物,其结构经1HNMR,IR,MS和元素分析确证.用体外动脉环的方法,研究目标化合物的初步体外抗高血压活性,试验结果表明其中部分化合物具有一定的抗高血压活性. The synthetic route of telmisartan and its derivatives was developed and improved. The condensation of o-phenylenediamine with various carboxylic acids gave benzimidazole derivatives, which were N-alkylated with methyl 4'-(bromomethyl)biphenyl-2-carboxylate to afford the corresponding title compounds. Nine novel title compounds were synthesized, and their structures were confirmed by ^1H NMR, IR, MS spectra and elemental analyses. And the in vitro preliminary antihypertensive activity was evaluated by the method of aortic ring. Biological screening results demonstrated that some of the compounds displayed potential antihypertensive activity.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2006年第3期318-323,共6页 Chinese Journal of Organic Chemistry
关键词 非肽类血管紧张素Ⅱ受体拮抗剂 替米沙坦 合成 衍生物 生物活性 angiotensin Ⅱ receptor antagonist telmisartan synthesis derivative bioactivity
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  • 1Gravert DJ, Jamda KD. Telmisartan antihypertensive angiotensin Ⅱ antagonist [J]. Drugs Future, 1997, 22(10):1112-1116.
  • 2Ries UJ, Mihm G, Narr B, et al. 6-Substituted benzimidazoles as new nonpeptide angiotensin Ⅱ receptor antagonists: synthesis, biological activity, and structure-activity relationships[J]. J Med Chem, 1993, 36(25) :4040-4051.
  • 3Nouet S, Dodey PR, Bondoux XR, et al.. Specific nonpeptide photoprobes as tool for the structure study of the angiotensin Ⅱ AT1 receptor [J]. J Med Chem,1999,42(22) :4572-4583,.
  • 4Carini DJ, Duncia JV, Aldrich PE, et al. Noneptide angiotensin Ⅱ receptor antagonists:the discovery of a series of N-(biphenylylmethyl) imidazoles as potent,orally active antihypertensives[J]. J Med Chem, 1991,34(8) : 2525-2544.

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