布呋洛尔，一种新型β-肾上腺素能受体阻滞剂。 - Suppr

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Bufuralol, a new beta-adrenoceptor blocking agent.

作者信息

Fothergill G A, Francis R J, Hamilton T C, Osbond J M, Parkes M W

出版信息

Experientia. 1975 Nov 15;31(11):1322-3. doi: 10.1007/BF01945806.

DOI:10.1007/BF01945806

PMID:1287

Abstract

摘要

相似文献

Bufuralol, a new beta-adrenoceptor blocking agent.布呋洛尔，一种新型β-肾上腺素能受体阻滞剂。

Experientia. 1975 Nov 15;31(11):1322-3. doi: 10.1007/BF01945806.

Bufuralol, a new beta-adrenoceptor blocking agent. Part 1: synthesis and structure-activity studies in a series of benzofuran-2-ethanolamines.布呋洛尔，一种新型β-肾上腺素能受体阻滞剂。第1部分：一系列苯并呋喃-2-乙醇胺的合成与构效关系研究。

Arzneimittelforschung. 1977;27(5):978-81. doi: 10.1002/chin.197737180.

Bufuralol, a new beta-adrenoceptor blocking agent in a series of benzofuran-2-ethanolamines. Part 2: pharmacology.布呋洛尔，苯并呋喃 - 2 - 乙醇胺系列中的一种新型β - 肾上腺素能受体阻滞剂。第2部分：药理学。

Arzneimittelforschung. 1977 Jul;27(7):1410-7.

Decrease of peripheral resistance after acute intravenous application of a new beta-receptor blocking agents, bufuralol HCl.

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Proceedings: Preliminary studies of Ro 3-3528, a beta-adrenoceptor-blocking agent, in man.论文：β-肾上腺素受体阻滞剂Ro 3-3528在人体中的初步研究。

Br J Pharmacol. 1972 Feb;44(2):377P-378P.

Hemodynamic characterization of bufuralol-HCl and pindolol based on the competitive effects of isoproterenol.

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[Effects of tolamolol and bufuralol on the arterial blood pressure and plasma renin activity. Contribution to the study of beta-blocking agents action mechanisms (author's transl)].托拉洛尔和丁呋洛尔对动脉血压及血浆肾素活性的影响。对β受体阻滞剂作用机制研究的贡献（作者译）

Schweiz Rundsch Med Prax. 1978 Jan 3;67(1):27-35.

Beta-adrenoceptor activity of the stereoisomers of the bufuralol alcohol and ketone metabolites.

J Med Chem. 1985 Nov;28(11):1648-51. doi: 10.1021/jm00149a018.

Beta-adrenergic blocking agents. 19. 1-Phenyl-2-[[(substituted-amido)alkyl]amino]ethanols.

J Med Chem. 1980 Feb;23(2):112-7. doi: 10.1021/jm00176a002.

-Adrenergic blocking agents. 11. Heterocyclic analogs of pronethalol (2-isopropylamino-1-(2-naphthyl)ethanol).

J Med Chem. 1972 Jan;15(1):49-57. doi: 10.1021/jm00271a014.

引用本文的文献

Pharmacodynamic and pharmacokinetic studies on bufuralol in man.布呋洛尔在人体中的药效学和药代动力学研究。

Br J Clin Pharmacol. 1986 Nov;22(5):527-34. doi: 10.1111/j.1365-2125.1986.tb02931.x.

A comparison of the influence of N-isopropyl and N-tert butyl substituents on the affinity of ligands for sinoatrial beta-adrenoceptors in rat atria and beta-adrenoceptors coupled to the adenylyl cyclase in kitten ventricle.N-异丙基和N-叔丁基取代基对大鼠心房窦房结β-肾上腺素能受体及小猫心室中与腺苷酸环化酶偶联的β-肾上腺素能受体配体亲和力影响的比较。

Naunyn Schmiedebergs Arch Pharmacol. 1979 May;307(1):1-8. doi: 10.1007/BF00506545.

本文引用的文献

Structure-activity relationships in the adrenergic-blocking agents.肾上腺素能阻滞剂的构效关系。

J Pharm Sci. 1969 May;58(5):511-38. doi: 10.1002/jps.2600580502.

Comparison of some properties of pronethalol and propranolol.丙萘洛尔和普萘洛尔某些性质的比较。

Br J Pharmacol Chemother. 1965 Dec;25(3):577-91. doi: 10.1111/j.1476-5381.1965.tb01782.x.

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