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Details

Stereochemistry RACEMIC
Molecular Formula C12H19NO3.ClH
Molecular Weight 261.745
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of COLTEROL HYDROCHLORIDE

SMILES

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

InChI

InChIKey=GWQNMEFTYFDDKD-UHFFFAOYSA-N
InChI=1S/C12H19NO3.ClH/c1-12(2,3)13-7-11(16)8-4-5-9(14)10(15)6-8;/h4-6,11,13-16H,7H2,1-3H3;1H

HIDE SMILES / InChI
Molecular Formula C12H19NO3
Molecular Weight 225.2842
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

Description

Colterol is a beta-2 adrenoreceptor agonist. Bitolterol, a diester prodrug of colterol, was marketed by Elan Pharmaceuticals for the treatment of reversible bronchospasm associated with asthma or chronic obstructive pulmonary diseases.

Approval Year

Unknown
149124
Targets

Targets

Primary TargetPharmacologyConditionPotency
Agonist
2752
 600.0 nM [Kd]
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:42:17 GMT 2025
Edited
by admin
on Mon Mar 31 23:42:17 GMT 2025
Record UNII
E61IGY13UF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2-BENZENEDIOL, 4-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-, HYDROCHLORIDE
Preferred Name English
COLTEROL HYDROCHLORIDE
Common Name English
1,2-BENZENEDIOL, 4-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
3,4-DIHYDROXY-.BETA.-HYDROXYPHENETHYL-TERT-BUTYLAMINE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
FDA UNII
E61IGY13UF
Created by admin on Mon Mar 31 23:42:17 GMT 2025 , Edited by admin on Mon Mar 31 23:42:17 GMT 2025
PRIMARY
CAS
52872-37-4
Created by admin on Mon Mar 31 23:42:17 GMT 2025 , Edited by admin on Mon Mar 31 23:42:17 GMT 2025
PRIMARY
PUBCHEM
71314579
Created by admin on Mon Mar 31 23:42:17 GMT 2025 , Edited by admin on Mon Mar 31 23:42:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID20747304
Created by admin on Mon Mar 31 23:42:17 GMT 2025 , Edited by admin on Mon Mar 31 23:42:17 GMT 2025
PRIMARY
NIH
NCATS
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