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Details

Stereochemistry RACEMIC
Molecular Formula C20H27NO4.ClH
Molecular Weight 381.894
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BEVANTOLOL HYDROCHLORIDE

SMILES

Cl.COC1=C(OC)C=C(CCNCC(O)COC2=CC(C)=CC=C2)C=C1

InChI

InChIKey=FJTKCFSPYUMXJB-UHFFFAOYSA-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

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C20H27NO4
Molecular Weight 345.4327
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:10:55 UTC 2023
Edited
by admin
on Fri Dec 15 15:10:55 UTC 2023
Record UNII
4VB9HU07BC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BEVANTOLOL HYDROCHLORIDE
JAN   MART.   MI   USAN   WHO-DD  
USAN  
Official Name English
SOM3355
Code English
CL-775
Code English
BEVANTOLOL HCL
Common Name English
CALVAN
Brand Name English
SOM-3355
Code English
Bevantolol hydrochloride [WHO-DD]
Common Name English
BEVANTOLOL HYDROCHLORIDE [MI]
Common Name English
2-PROPANOL, 1-((2-(3,4-DIMETHOXYPHENYL)ETHYL)AMINO)-3-(3-METHYLPHENOXY)-, HYDROCHLORIDE, (±)-
Systematic Name English
CL 775
Code English
BEVANTOLOL HYDROCHLORIDE [JAN]
Common Name English
(±)-1-((3,4-DIMETHOXYPHENETHYL)AMINO)-3-(M-TOLYLOXY)-2-PROPANOL HYDROCHLORIDE
Systematic Name English
BEVANTOLOL HYDROCHLORIDE [USAN]
Common Name English
VANTOL
Brand Name English
BEVANTOLOL HYDROCHLORIDE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
Code System Code Type Description
DRUG BANK
DBSALT002868
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
ChEMBL
CHEMBL314010
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
NCI_THESAURUS
C142952
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
CHEBI
31282
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
CAS
42864-78-8
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
EVMPD
SUB00793MIG
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
MESH
C021148
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
PUBCHEM
39324
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
SMS_ID
100000085024
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
EPA CompTox
DTXSID5048633
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
FDA UNII
4VB9HU07BC
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY
MERCK INDEX
m2465
Created by admin on Fri Dec 15 15:10:55 UTC 2023 , Edited by admin on Fri Dec 15 15:10:55 UTC 2023
PRIMARY Merck Index
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY