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Details

Stereochemistry RACEMIC
Molecular Formula C20H27NO4
Molecular Weight 345.4327
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BEVANTOLOL

SMILES

COC1=CC=C(CCNCC(O)COC2=CC(C)=CC=C2)C=C1OC

InChI

InChIKey=HXLAFSUPPDYFEO-UHFFFAOYSA-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

HIDE SMILES / InChI

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 17:19:56 UTC 2023
Edited
by admin
on Fri Dec 15 17:19:56 UTC 2023
Record UNII
34ZXW6ZV21
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BEVANTOLOL
INN   MI   WHO-DD  
INN  
Official Name English
NSC-132348
Code English
2-PROPANOL, 1-((2-(3,4-DIMETHOXYPHENYL)ETHYL)AMINO)-3-(3-METHYLPHENOXY)-, (±)-
Systematic Name English
BEVANTOLOL [MI]
Common Name English
(±)-1-((3,4-DIMETHOXYPHENETHYL)AMINO)-3-(M-TOLYLOXY)-2-PROPANOL
Systematic Name English
bevantolol [INN]
Common Name English
Bevantolol [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC C07AB06
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
WHO-VATC QC07BB06
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
WHO-ATC C07BB06
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
FDA ORPHAN DRUG 822821
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
WHO-VATC QC07AB06
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL314010
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
PUBCHEM
2372
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
CHEBI
238698
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
DRUG BANK
DB01295
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
MESH
C021148
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
SMS_ID
100000085893
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
EVMPD
SUB05808MIG
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
NSC
132348
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID70860597
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
NCI_THESAURUS
C79556
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
CAS
59170-23-9
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
DRUG CENTRAL
360
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
WIKIPEDIA
BEVANTOLOL
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
INN
4115
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
FDA UNII
34ZXW6ZV21
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY
MERCK INDEX
m2465
Created by admin on Fri Dec 15 17:19:56 UTC 2023 , Edited by admin on Fri Dec 15 17:19:56 UTC 2023
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY