Bupranolol structure, CAS 14556-46-8

Bupranolol

CAS Number14556-46-8

SynonymsOphtorenin; Bupranol

Molecular FormulaC14H22O2N1Cl1

Molecular Weight271.79

Purity98.00%

Density1.098g/cm3

Boiling Point396.3ºC at 760mmHg

Melting Point

Flash Point

Appearance

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Cat. No.: 2A-9009492 Purity: 98.00%
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Quality Control of [ 14556-46-8 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number14556-46-8
Catalog No.2A-9009492
Chinese Name布拉洛尔
SynonymsOphtorenin; Bupranol
Molecular FormulaC14H22O2N1Cl1
Molecular Weight271.79
Purity98.00
Density1.098g/cm3
Boiling Point396.3ºC at 760mmHg
Storage Condition2-8°C, sealed, dry
ApplicationBuparol is an orally active, competitive and non-selective beta-adrenoceptor antagonist with no intrinsic sympathomimetic activity [1].
HTC2922509090
MDL NumberMFCD00864591
SMILESCc1ccc(Cl)c(OCC(O)CNC(C)(C)C)c1
InChIInChI=1S/C14H22ClNO2/c1-10-5-6-12(15)13(7-10)18-9-11(17)8-16-14(2,3)4/h5-7,11,16-17H,8-9H2,1-4H3
InChI KeyHQIRNZOQPUAHHV-UHFFFAOYSA-N
MSDSmsds/9492_1_14556_46_8.pdf
Use ofBupranolol is an orally active, competitive and non-selective β-adrenoceptor antagonist without intrinsic sympathomimetic activity[1]. Properties Name Bupranolol Synonym More Synonyms Bupranolol Biological Activity Description Bupranolol is an orally active, competitive and non-selective β-adrenoceptor antagonist without intrinsic sympathomimetic activity[1]. Related Catalog Research Areas >> Cancer Signaling Pathways >> GPCR/G Protein >> Adrenergic Receptor Research Areas >> Inflammation/Immunology β-adrenoceptor In Vitro Bupranolol (1~3 μM) shifts isoprenaline-induced relaxation in the presence of 30 μM propranolol. Bupranolol acts as a competitive antagonist of isoprenaline-induced relaxation in the presence of 300 nM propranolol, with a pA2 value of 5.90. Bupranolol antagonizes β1- and β2-ARs with pA2 values of ≈9.0, and also antagonizes β3-AR with a pA2 value of 6.0[1]. References [1]. Chino D, et al. Pharmacological identification of β-adrenoceptor subtypes mediating isoprenaline-induced relaxation of guinea pig colonic longitudinal smooth muscle. J Smooth Muscle Res. 2018;54(0):13-27. [2]. Babu RJ, et al. Effect of cyclodextrins on the complexation and transdermal delivery of bupranolol through rat skin. Int J Pharm. 2004;271(1-2):155-165. Chemical & Physical Properties Exact Mass 271.13400 PSA 41.49000 LogP 3.16710 Index of Refraction 1.522 InChIKey HQIRNZOQPUAHHV-UHFFFAOYSA-N Toxicological Information CHEMICAL IDENTIFICATION RTECS NUMBER : CHEMICAL NAME : 2-Propanol, 1-(tert-butylamino)-3-(2-chloro-5-methylphenoxy)- CAS REGISTRY NUMBER : 14556-46-8 LAST UPDATED : DATA ITEMS CITED : MOLECULAR FORMULA : C14-H22-Cl-N-O2 MOLECULAR WEIGHT : WISWESSER LINE NOTATION : 1X1&1&M1YQ1OR BG E1 HEALTH HAZARD DATA ACUTE TOXICITY DATA TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intravenous SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 27,1022,1977 Safety Information HS Code 2922509090
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