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Details

Stereochemistry RACEMIC
Molecular Formula C16H26N2O4.ClH
Molecular Weight 346.85
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CETAMOLOL HYDROCHLORIDE

SMILES

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

InChI

InChIKey=CRYTUFSEASFGMP-UHFFFAOYSA-N
InChI=1S/C16H26N2O4.ClH/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);1H

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 ( + / - )

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

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
Cetamolol: a new cardioselective beta-adrenoceptor blocking agent without membrane-stabilizing activity.
1984 Mar
Effect of cetamolol on epinephrine-induced hypokalemia.
1988 Aug
Comparison of the effects of cetamolol and atenolol on epinephrine- and isoproterenol-induced hypokalemia in anesthetized dogs.
1989 Jan
Patents

Patents

Sample Use Guides

15 mg/day
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:07:24 GMT 2023
Edited
by admin
on Fri Dec 15 15:07:24 GMT 2023
Record UNII
5UNK5C6QM5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CETAMOLOL HYDROCHLORIDE
MART.   MI   USAN  
USAN  
Official Name English
CETAMOLOL HYDROCHLORIDE [MI]
Common Name English
CETAMOLOL HYDROCHLORIDE [MART.]
Common Name English
(±)-2-(O-(3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXY)PHENOXY)-N-METHYLACETAMIDE MONOHYDROCHLORIDE
Common Name English
AI-27,303
Code English
CETAMOLOL HCL
Common Name English
CETAMOLOL HYDROCHLORIDE [USAN]
Common Name English
AI-27303
Code English
ACETAMIDE, 2-(2-(3-((1,1-DIMETHYLETHYL)AMINO)-2-HYDROXYPROPOXY)PHENOXY)-N-METHYL-, MONOHYDROCHLORIDE, (±)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
Code System Code Type Description
MERCK INDEX
m1066
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY Merck Index
ChEMBL
CHEMBL156885
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID30998805
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY
FDA UNII
5UNK5C6QM5
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY
NCI_THESAURUS
C81652
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY
ECHA (EC/EINECS)
278-729-0
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY
PUBCHEM
53697
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY
CAS
77590-95-5
Created by admin on Fri Dec 15 15:07:24 GMT 2023 , Edited by admin on Fri Dec 15 15:07:24 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY