68377-91-3|Arotinolol hydrochloride|2-Thiophenecarboxamide, 5-(2-((3-((1,1-dimethylethyl)amino)-2-hydroxypropyl)thio)-4-thiazolyl)-, monohydrochloride, (+-)-|-范德生物科技公司

Arotinolol hydrochloride

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names：
2-Thiophenecarboxamide, 5-(2-((3-((1,1-dimethylethyl)amino)-2-hydroxypropyl)thio)-4-thiazolyl)-, monohydrochloride, (+-)-
CAS号：
68377-91-3
MDL Number：
MF(分子式)： C15H22ClN3O2S3 MW(分子量)： 407.99
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	Arotinolol hydrochloride
英文别名	Arotinolol hydrochloride; Arotinolol HCl,
CAS号	68377-91-3
Inchi	InChI=1S/C15H21N3O2S3.ClH/c1-15(2,3)17-6-9(19)7-21-14-18-10(8-22-14)11-4-5-12(23-11)13(16)20;/h4-5,8-9,17,19H,6-7H2,1-3H3,(H2,16,20);1H
InchiKey	XXDAXBZYUXLDRD-UHFFFAOYSA-N
分子式 Formula	C15H22ClN3O2S3
分子量 Molecular Weight	407.99
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Arotinolol hydrochloride(CAS:68377-91-3 ):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Arotinolol (INN, marketed under the tradename Almarl) is a medication in the class of mixed alpha/beta blockers. It also acts as a β3 receptor agonist. A 1979 publication suggests arotinolol as having first been described in the scientific literature by Sumitomo Chemical as "β-adrenergic blocking, antiarrhythmic compound S-596".
Application1
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危险性	Warning
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备注

[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. PubMed PMID: 29332839.

[2]Qian Z, Le J, Chen X, Li S, Song H, Hong Z. High-throughput LC-MS/MS method with 96-well plate precipitation for the determination of arotinolol and amlodipine in a small volume of rat plasma: Application to a pharmacokinetic interaction study. J Sep Sci. 2018 Feb;41(3):618-629. doi: 10.1002/jssc.201700784. Epub 2017 Dec 11. PubMed PMID: 29115741.

[3] Fang L, Du Y, Hu X, Luo L, Guo X, Guo X, Yu J. Carboxymethyl β-cyclodextrin as chiral selector in capillary electrophoresis: Enantioseparation of 16 basic chiral drugs and its chiral recognition mechanism associated with drugs' structural features. Biomed Chromatogr. 2017 Nov;31(11). doi: 10.1002/bmc.3991. Epub 2017 May 28. PubMed PMID: 28431453.

[4] Akiyama T, Miyahara H, Waki K, Yoshinaga H, Kobayashi K. A Japanese case of hereditary chin trembling responsive to arotinolol. Parkinsonism Relat Disord. 2016 Aug;29:133-4. doi: 10.1016/j.parkreldis.2016.04.021. Epub 2016 Apr 21. PubMed PMID: 27117562.

[5] Lee DB, Woo YS, Bahk WM. Use of Arotinolol Pharmacotherapy to Treat Drug-induced Tremor: A Report of Three Cases. Pharmacopsychiatry. 2015 Jul;48(4-5):176-8. doi: 10.1055/s-0035-1549931. Epub 2015 May 13. PubMed PMID: 25970026.

6: Tang X, Hu X, Mei C, Yu S. Improvement of resistant hypertension by nocturnal hemodialysis in a patient with end-stage kidney disease. Case Rep Nephrol Dial. 2015 Feb 17;5(1):60-5. doi: 10.1159/000377671. eCollection 2015 Jan-Apr. PubMed PMID: 25874195; PubMed Central PMCID: PMC4376926.7: 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;10

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