Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C40H42ClN5O7 |
Molecular Weight | 740.244 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(CNC[C@H](O)C2=CC=C(O)C3=C2C=CC(=O)N3)C=C(Cl)C(NC(=O)CCN4CCC(CC4)OC(=O)NC5=CC=CC=C5C6=CC=CC=C6)=C1
InChI
InChIKey=URWYQGVSPQJGGB-DHUJRADRSA-N
InChI=1S/C40H42ClN5O7/c1-52-36-22-33(31(41)21-26(36)23-42-24-35(48)29-11-13-34(47)39-30(29)12-14-37(49)45-39)43-38(50)17-20-46-18-15-27(16-19-46)53-40(51)44-32-10-6-5-9-28(32)25-7-3-2-4-8-25/h2-14,21-22,27,35,42,47-48H,15-20,23-24H2,1H3,(H,43,50)(H,44,51)(H,45,49)/t35-/m0/s1
Batefenterol, previously known as GSK961081, a bifunctional muscarinic (M2 and M3 receptors) antagonist β2-agonist that is developed for chronic obstructive pulmonary disease (COPD). The drug has successfully completed phase II clinical trials with clinically significant improvements in lung function. No new or unexpected safety signals were observed in this COPD population. The conclusion from the trial was following that batefenterol 300 µg might represent the optimal dose for Phase III studies.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Long-acting muscarinic receptor antagonists for the treatment of respiratory disease. | 2013 Jun |
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A new class of bronchodilator improves lung function in COPD: a trial with GSK961081. | 2013 Oct |
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Randomized dose-finding study of batefenterol via dry powder inhaler in patients with COPD. | 2019 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/30880951
once-daily batefenterol 37.5, 75, 150, 300, or 600 µg for 42 days administered via dry powder inhaler
Route of Administration:
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300000034123
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CHEMBL3039518
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)