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Details

Stereochemistry RACEMIC
Molecular Formula C13H19Cl2NO2
Molecular Weight 292.201
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLORANOLOL

SMILES

CC(C)(C)NCC(O)COC1=C(Cl)C=CC(Cl)=C1

InChI

InChIKey=XYCMOTOFHFTUIU-UHFFFAOYSA-N
InChI=1S/C13H19Cl2NO2/c1-13(2,3)16-7-10(17)8-18-12-6-9(14)4-5-11(12)15/h4-6,10,16-17H,7-8H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C13H19Cl2NO2
Molecular Weight 292.201
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Cloranolol is a specific beta-adrenergic antagonist. It is used as an antiarrhythmic agent. Its antiarrhythmic effectiveness stronger than propranol and equal or surpass the effectivity of pindolol. It has a negligible cardiodepressant activity as compared to other beta-adrenergic antagonists. Cloranolol has mainly cardiorespiratory side effects judging from the beta-blocker characteristics

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacology of GYKI-41 099 (chlorpropanol, Tobanum) a new potent beta-adrenergic antagonist.
1980 Dec
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010 Dec

Sample Use Guides

Single dose - 10 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:01:58 GMT 2023
Edited
by admin
on Sat Dec 16 18:01:58 GMT 2023
Record UNII
Q3U058H86V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLORANOLOL
INN   MI   WHO-DD  
INN  
Official Name English
1-(TERT-BUTYLAMINO)-3-(2,5-DICHLOROPHENOXY)-2-PROPANOL
Systematic Name English
cloranolol [INN]
Common Name English
TOBANUM
Brand Name English
CLORANOLOL [MI]
Common Name English
CHLORANOLOL
Common Name English
Cloranolol [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC C07AA27
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
NCI_THESAURUS C29576
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
WHO-VATC QC07AA27
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
Code System Code Type Description
SMS_ID
100000084023
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
ChEMBL
CHEMBL156791
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
CAS
39563-28-5
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
EVMPD
SUB06752MIG
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
WIKIPEDIA
Cloranolol
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
MERCK INDEX
m1083
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB13508
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID30865962
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
INN
4646
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
FDA UNII
Q3U058H86V
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
PUBCHEM
65814
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
MESH
C025725
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
NCI_THESAURUS
C81658
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
DRUG CENTRAL
710
Created by admin on Sat Dec 16 18:01:58 GMT 2023 , Edited by admin on Sat Dec 16 18:01:58 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY