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Details

Stereochemistry RACEMIC
Molecular Formula C20H23N3O4
Molecular Weight 369.4143
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPANOLOL

SMILES

OC(CNCCNC(=O)CC1=CC=C(O)C=C1)COC2=C(C=CC=C2)C#N

InChI

InChIKey=YARKMNAWFIMDKV-UHFFFAOYSA-N
InChI=1S/C20H23N3O4/c21-12-16-3-1-2-4-19(16)27-14-18(25)13-22-9-10-23-20(26)11-15-5-7-17(24)8-6-15/h1-8,18,22,24-25H,9-11,13-14H2,(H,23,26)

HIDE SMILES / InChI

Molecular Formula C20H23N3O4
Molecular Weight 369.4143
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 15:59:44 UTC 2023
Edited
by admin
on Fri Dec 15 15:59:44 UTC 2023
Record UNII
9KGC55KP6A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EPANOLOL
INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
EPANOLOL [MART.]
Common Name English
epanolol [INN]
Common Name English
ICI 141,292
Code English
EPANOLOL [USAN]
Common Name English
EPANOLOL [MI]
Common Name English
ICI-141292
Code English
Epanolol [WHO-DD]
Common Name English
(±)-N-(2-((3-(O-CYANOPHENOXY)-2-HYDROXYPROPYL)AMINO)ETHYL)-2-(P-HYDROXYPHENYL)ACETAMIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
WHO-ATC C07AB10
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
WHO-VATC QC07AB10
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C72616
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
WIKIPEDIA
EPANOLOL
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
USAN
W-141
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
EVMPD
SUB06558MIG
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
INN
5654
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
PUBCHEM
72014
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
DRUG CENTRAL
4467
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
FDA UNII
9KGC55KP6A
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
DRUG BANK
DB13757
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
MERCK INDEX
m162
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID90868959
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
SMS_ID
100000080243
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
ChEMBL
CHEMBL87697
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
CAS
86880-51-5
Created by admin on Fri Dec 15 15:59:44 UTC 2023 , Edited by admin on Fri Dec 15 15:59:44 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY