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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 ( + / - )

Epanolol has been shown in animal models to be a selective beta-adrenoceptor partial agonist with agonist activity about 20 to 25% of that of the full agonist isoprenaline. Epanolol is a once-daily agent for the treatment of angina pectoris. The pharmacodynamic consequences in man of the degree of agonist activity possessed by the beta 1-selective partial agonist epanolol include little reductions at rest in heart rate, blood pressure, various measures of cardiac haemodynamic parameters, peripheral blood flow and renal function. On exercise there is attenuation of the heart rate and systolic blood pressure responses, with less perceived exertion than with atenolol. The lack of significant accumulation of epanolol indicates that no alteration of dose is necessary when using epanolol in elderly patients with normal renal and hepatic function.

Approval Year

PubMed

PubMed

TitleDatePubMed

Sample Use Guides

Single daily dose - 200 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:59:44 GMT 2023
Edited
by admin
on Fri Dec 15 15:59:44 GMT 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 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
WHO-ATC C07AB10
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
WHO-VATC QC07AB10
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C72616
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
WIKIPEDIA
EPANOLOL
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
USAN
W-141
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
EVMPD
SUB06558MIG
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
INN
5654
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
PUBCHEM
72014
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
DRUG CENTRAL
4467
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
FDA UNII
9KGC55KP6A
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
DRUG BANK
DB13757
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
MERCK INDEX
m162
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID90868959
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
SMS_ID
100000080243
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
ChEMBL
CHEMBL87697
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
CAS
86880-51-5
Created by admin on Fri Dec 15 15:59:44 GMT 2023 , Edited by admin on Fri Dec 15 15:59:44 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY