U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C16H26N2O4
Molecular Weight 310.3886
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CETAMOLOL

SMILES

CNC(=O)COC1=C(OCC(O)CNC(C)(C)C)C=CC=C1

InChI

InChIKey=UWCBNAVPISMFJZ-UHFFFAOYSA-N
InChI=1S/C16H26N2O4/c1-16(2,3)18-9-12(19)10-21-13-7-5-6-8-14(13)22-11-15(20)17-4/h5-8,12,18-19H,9-11H2,1-4H3,(H,17,20)

HIDE SMILES / InChI

Molecular Formula C16H26N2O4
Molecular Weight 310.3886
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Cetamolol is a beta adrenergic antagonist with intrinsic sympathomimetic activity, patented by Imperial Chemical Industries Ltd for cardiovascular disease treatment. The average plasma half-life of cetamolol is 6.4 hours in humans and peak serum levels are reached 1 to 2 hours after drug intake; oral doses as low as 10 mg produced significant reductions in exercise-induced tachycardia 24 hours after drug administration. Cetamolol is approximately three times as potent as atenolol in blocking exercise-induced tachycardia.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

15 mg/day
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:31:42 GMT 2023
Edited
by admin
on Sat Dec 16 16:31:42 GMT 2023
Record UNII
Z0VD1633O8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CETAMOLOL
INN   MI  
INN  
Official Name English
cetamolol [INN]
Common Name English
ACETAMIDE, 2-(2-(3-((1,1-DIMETHYLETHYL)AMINO)-2-HYDROXYPROPOXY)PHENOXY)-N-METHYL-, (±)-
Systematic Name English
CETAMOLOL [MI]
Common Name English
(±)-2-(O-(3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXY)PHENOXY)-N-METHYLACETAMIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
Code System Code Type Description
DRUG CENTRAL
3079
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
MESH
C038931
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
ChEMBL
CHEMBL156885
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
WIKIPEDIA
Cetamolol
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
SMS_ID
100000082049
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
NCI_THESAURUS
C81659
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
MERCK INDEX
m1066
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY Merck Index
EVMPD
SUB07446MIG
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
PUBCHEM
53698
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
INN
5144
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID20865739
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
CAS
34919-98-7
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
FDA UNII
Z0VD1633O8
Created by admin on Sat Dec 16 16:31:43 GMT 2023 , Edited by admin on Sat Dec 16 16:31:43 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY