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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H27NO4.ClH
Molecular Weight 381.8943
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BEVANTOLOL HYDROCHLORIDE, (R)-

SMILES

Cc1cccc(c1)OC[C@@]([H])(CNCCc2ccc(c(c2)OC)OC)O.Cl

InChI

InChIKey=FJTKCFSPYUMXJB-UNTBIKODSA-N
InChI=1S/C20H27NO4.ClH/c1-15-5-4-6-18(11-15)25-14-17(22)13-21-10-9-16-7-8-19(23-2)20(12-16)24-3;/h4-8,11-12,17,21-22H,9-10,13-14H2,1-3H3;1H/t17-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C20H27NO4
Molecular Weight 345.4334
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.4609
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Use of thallium-201 myocardial scintigraphy for the prediction of the response to beta-blocker therapy in patients with dilated cardiomyopathy.
2002 Dec
Atypical cardiostimulant beta-adrenoceptor in the rat heart: stereoselective antagonism by bupranolol but lack of effect by some bupranolol analogues.
2003 Aug
Effect of beta-blocker therapy on myocardial perfusion defects in thallium-201 scintigraphy in patients with dilated cardiomyopathy.
2005
Chiral purity test of bevantolol by capillaryelectrophoresis and high performance liquid chromatography.
2006 Sep
Determination of bevantolol in human plasma by high performance liquid chromatography using solid phase extraction technique.
2007 Jul
Determination of bevantolol enantiomers in human plasma by coupled achiral-chiral high performance-liquid chromatography.
2007 Jul
Patents
Substance Class Chemical
Created
by admin
on Fri Jun 25 20:40:31 UTC 2021
Edited
by admin
on Fri Jun 25 20:40:31 UTC 2021
Record UNII
0G8M9F6QA4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BEVANTOLOL HYDROCHLORIDE, (R)-
Common Name English
2-PROPANOL, 1-((2-(3,4-DIMETHOXYPHENYL)ETHYL)AMINO)-3-(3-METHYLPHENOXY)-, HYDROCHLORIDE, (R)-
Systematic Name English
Code System Code Type Description
CAS
152510-36-6
Created by admin on Fri Jun 25 20:40:31 UTC 2021 , Edited by admin on Fri Jun 25 20:40:31 UTC 2021
PRIMARY
PUBCHEM
45266838
Created by admin on Fri Jun 25 20:40:31 UTC 2021 , Edited by admin on Fri Jun 25 20:40:31 UTC 2021
PRIMARY
FDA UNII
0G8M9F6QA4
Created by admin on Fri Jun 25 20:40:31 UTC 2021 , Edited by admin on Fri Jun 25 20:40:31 UTC 2021
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER