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

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H29Cl2N3O2
Molecular Weight 426.38
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PICUMETEROL

SMILES

NC1=C(Cl)C=C(C=C1Cl)[C@@H](O)CNCCCCCCOCCC2=NC=CC=C2

InChI

InChIKey=NUBLQEKABJXICM-FQEVSTJZSA-N
InChI=1S/C21H29Cl2N3O2/c22-18-13-16(14-19(23)21(18)24)20(27)15-25-9-4-1-2-6-11-28-12-8-17-7-3-5-10-26-17/h3,5,7,10,13-14,20,25,27H,1-2,4,6,8-9,11-12,15,24H2/t20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H29Cl2N3O2
Molecular Weight 426.38
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Picumeterol (GR114297A) is a potent and highly selective beta2-adrenoceptor agonist with a longer duration of action than salbutamol, but shorter than salmeterol. Picumeterol is the (R)-isomer of the racemic entity GR63411B, and picumeterol has been shown to be about 40 times more potent than the (S)-isomer (GR114744A) in various in vitro pharmacological models of beta2-agonist activity. Picumeterol is of potential value in the treatment of asthma and related diseases in man following inhalation administration. In the clinical studies, the bronchodilator potencies of picumeterol and GR 63411B were similar. However, both drugs were short-acting, which is at odds with their activity in vitro. These compounds display dissociation between bronchodilator activity and protection against methacholine-induced bronchoconstriction.

Approval Year

PubMed

PubMed

TitleDatePubMed
Kinetics and disposition of picumeterol in animals.
1995 Sep
Picumeterol: dissociation of improvement in lung function and reduction of airways hyperresponsiveness in asthmatics.
1997 Feb
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:36:43 GMT 2023
Edited
by admin
on Fri Dec 15 16:36:43 GMT 2023
Record UNII
86WEQ311WF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PICUMETEROL
INN  
INN  
Official Name English
GR-114297X (PICUMETEROL)
Code English
GR-114297X
Code English
BENZENEMETHANOL, 4-AMINO-3,5-DICHLORO-.ALPHA.-(((6-(2-(2-PYRIDINYL)ETHOXY)HEXYL)AMINO)METHYL)-, (R)-
Systematic Name English
(-)-(R)-4-AMINO-3,5-DICHLORO-.ALPHA.-(((6-(2-(2-PYRIDYL)ETHOXY)HEXYL)AMINO)METHYL)BENZYL ALCOHOL
Systematic Name English
GR 114297X
Code English
picumeterol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
Code System Code Type Description
INN
6726
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
NCI_THESAURUS
C76543
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
CAS
130641-36-0
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110947
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID20156659
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
FDA UNII
86WEQ311WF
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
EVMPD
SUB09822MIG
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
MESH
C097635
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
PUBCHEM
131251
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
SMS_ID
100000081923
Created by admin on Fri Dec 15 16:36:43 GMT 2023 , Edited by admin on Fri Dec 15 16:36:43 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY