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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H27NO4
Molecular Weight 345.4327
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

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

SMILES

COC1=CC=C(CCNC[C@@H](O)COC2=CC(C)=CC=C2)C=C1OC

InChI

InChIKey=HXLAFSUPPDYFEO-QGZVFWFLSA-N
InChI=1S/C20H27NO4/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/t17-/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H27NO4
Molecular Weight 345.4327
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of treatment effects of bevantolol and metoprolol on cardiac function and natriuretic peptides in patients with dilated cardiomyopathy.
2002 Dec
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
Different changes of plasma membrane beta-adrenoceptors in rat heart after chronic administration of propranolol, atenolol and bevantolol.
2007 Jul 12
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:49:02 UTC 2023
Edited
by admin
on Sat Dec 16 10:49:02 UTC 2023
Record UNII
34P43RW460
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BEVANTOLOL, (R)-
Common Name English
(+)-BEVANTOLOL
Common Name English
2-PROPANOL, 1-((2-(3,4-DIMETHOXYPHENYL)ETHYL)AMINO)-3-(3-METHYLPHENOXY)-, (2R)-
Systematic Name English
Code System Code Type Description
CAS
135531-40-7
Created by admin on Sat Dec 16 10:49:02 UTC 2023 , Edited by admin on Sat Dec 16 10:49:02 UTC 2023
PRIMARY
FDA UNII
34P43RW460
Created by admin on Sat Dec 16 10:49:02 UTC 2023 , Edited by admin on Sat Dec 16 10:49:02 UTC 2023
PRIMARY
PUBCHEM
36690919
Created by admin on Sat Dec 16 10:49:02 UTC 2023 , Edited by admin on Sat Dec 16 10:49:02 UTC 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER