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
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
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
Title | Date | PubMed |
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Kinetics and disposition of picumeterol in animals. | 1995 Sep |
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Some pharmacodynamic aspects on long-acting beta-adrenoceptor agonists. | 1996 Jun |
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Picumeterol: dissociation of improvement in lung function and reduction of airways hyperresponsiveness in asthmatics. | 1997 Feb |
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Analysis of the Indacaterol-Regulated Transcriptome in Human Airway Epithelial Cells Implicates Gene Expression Changes in the Adverse and Therapeutic Effects of β(2)-Adrenoceptor Agonists. | 2018 Jul |
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NCI_THESAURUS |
C48149
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)