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Details

Stereochemistry RACEMIC
Molecular Formula C12H19NO3.C2H4O2
Molecular Weight 285.3361
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of COLTEROL ACETATE

SMILES

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

InChI

InChIKey=SVYBIDRTCKRNFA-UHFFFAOYSA-N
InChI=1S/C12H19NO3.C2H4O2/c1-12(2,3)13-7-11(16)8-4-5-9(14)10(15)6-8;1-2(3)4/h4-6,11,13-16H,7H2,1-3H3;1H3,(H,3,4)

HIDE SMILES / InChI

Molecular Formula C2H4O2
Molecular Weight 60.052
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 ( + / - )

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

Targets

Targets

Primary TargetPharmacologyConditionPotency
600.0 nM [Kd]
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:30:27 GMT 2023
Edited
by admin
on Fri Dec 15 16:30:27 GMT 2023
Record UNII
CUY1XO9278
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
COLTEROL ACETATE
Common Name English
1,2-BENZENEDIOL, 4-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-, ACETATE (1:1)
Systematic Name English
Code System Code Type Description
CAS
10255-14-8
Created by admin on Fri Dec 15 16:30:27 GMT 2023 , Edited by admin on Fri Dec 15 16:30:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID50907691
Created by admin on Fri Dec 15 16:30:27 GMT 2023 , Edited by admin on Fri Dec 15 16:30:27 GMT 2023
PRIMARY
FDA UNII
CUY1XO9278
Created by admin on Fri Dec 15 16:30:27 GMT 2023 , Edited by admin on Fri Dec 15 16:30:27 GMT 2023
PRIMARY
PUBCHEM
25103
Created by admin on Fri Dec 15 16:30:27 GMT 2023 , Edited by admin on Fri Dec 15 16:30:27 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY