CAS: 68377-91-3; Arotinolol Hcl

该化合物是一种制药化合物,主要因其作为非选择性乙醇-肾上腺激素对抗物的作用而得到承认,具有额外的甲型肾上腺阻塞特性,经常用于治疗高血压和某些心血管疾病,其特征是能够通过抑制三联苯胺对心脏和血管血管的影响来降低血压,导致心率和血管抗药性下降.盐酸甲醇通常以盐的形式施用,这增加了其溶性与生物利用率.该化合物已知具有中度半衰期,允许有效的剂量疗法.在安全和副作用方面,它可能造成典型的阻塞性反应,如疲劳,眩晕或心肌炎.与许多药品一样,它的使用应当由保健专业人员加以监测,以便有效地管理潜在的相互作用和抗药性.

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欧盟法规

C&L通报

上下游产品

tert-butylaminetert-butylamine 5-(2-mercapto-1,3-thiazol-4-yl)-2-thiophene carboxamide arotinolol 5-acetylthiophene-2-carboxylic acid

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    主要参考文献


    1: Wang Z, Zhang X, Jiang S, Guo X. Magnetic solid-phase extraction based on magnetic multiwalled carbon nanotubes for the simultaneous enantiomeric analysis of five β-blockers in the environmental samples by chiral liquid chromatography coupled with tandem mass spectrometry. Talanta. 2018 Apr 1;180:98-107. doi: 10.1016/j.talanta.2017.12.034. Epub 2017 Dec 14. doi: 10.1002/jssc.201700784. Epub 2017 Dec 11. doi: 10.1002/bmc.3991. Epub 2017 May 28. doi: 10.1016/j.parkreldis.2016.04.021. Epub 2016 Apr 21. doi: 10.1055/s-0035-1549931. Epub 2015 May 13. doi: 10.1159/000377671. eCollection 2015 Jan-Apr.
    7: Qian Z, Xu Y, Zheng L, Zhang J, Hong Z, Shen X. Enantiospecific determination of arotinolol in rat plasma by LC-MS/MS: application to a stereoselective pharmacokinetic study. J Pharm Biomed Anal. 2015 Jan;102:299-304. doi: 10.1016/j.jpba.2014.09.034. Epub 2014 Oct 2. doi: 10.1159/000360976. Epub 2014 Apr 11.
    9: Fang H, Chen W, Liu X, Xu W. The efficacy and safety of arotinolol combined with a different calcium channel blocker in the treatment of Chinese patients with essential hypertension: a one-year follow-up study. Clin Exp Hypertens. 2014;36(8):590-5. doi: 10.3109/10641963.2014.897714. Epub 2014 Mar 28. doi: 10.1371/journal.pone.0088722. eCollection 2014.

    合成参考文献


    摘要:Drugs of the Future., 4(442), 1979
    摘要:Iyakuhin Kenkyu. Study of Medical Supplies., 17(365), 1986
    参考文献:10.1186/s12876-021-01874-7
    摘要:He Y, Qin MZ, Chen YW. Liver injury caused by fenofibrate within 48 h after first administration: a case report. BMC Gastroenterol. 2021 Jul 29;21(1):298.
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