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ChemicalBook--->CAS DataBase List--->1613439-56-7

1613439-56-7

1613439-56-7 Structure

1613439-56-7 Structure
IdentificationBack Directory
[Name]

(±)-1-Isopropyl-d7-amino-3-(1-naphthyloxy)-2-propanol hydrochloride
[CAS]

1613439-56-7
[Synonyms]

D7-Propranolol hydrochloride
(±)-Propranolol-(isopropyl-d7) hydrochloride
(±)-1-Isopropyl-d7-amino-3-(1-naphthyloxy)-2-propanol hydrochloride
[Molecular Formula]

C16H15ClD7NO2
[MDL Number]

MFCD11983489
[MOL File]

1613439-56-7.mol
[Molecular Weight]

302.848
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[form ]

Solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Propranolol-d7 (hydrochloride) is a deuterium labeled Propranolol hydrochloride. Propranolol hydrochloride is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively[1]. Propranolol hydrochloride inhibits [3H]-DHA binding to rat brain membrane preparation with an IC50 of 12 nM[2]. Propranolol hydrochloride is used for the study of hypertension, pheochromocytoma, myocardial infarction, cardiac arrhythmias, angina pectoris, and hypertrophic cardiomyopathy[3].
[IC 50]

β adrenergic receptor
[storage]

Store at -20°C
[References]

[1] Galandrin S, et al. Distinct signaling profiles of beta1 and beta2 adrenergic receptor ligands toward adenylyl cyclase and mitogen-activated protein kinase reveals the pluridimensionality of efficacy. Mol Pharmacol. 2006 Nov;70(5):1575-84. DOI:10.1124/mol.106.026716
[2] Briley M, et al. Evidence against beta-adrenoceptor blocking activity of diltiazem, a drug with calcium antagonist properties. Br J Pharmacol. 1980 Aug;69(4):669-73. DOI:10.1111/j.1476-5381.1980.tb07920.x
[3] Al-Majed AA, et al. Propranolol. Profiles Drug Subst Excip Relat Methodol. 2017;42:287-338. DOI:10.1016/bs.podrm.2017.02.006
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