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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H30F2N2O4
Molecular Weight 460.5135
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ABEDITEROL

SMILES

O[C@@H](CNCCCCCCOCC(F)(F)C1=CC=CC=C1)C2=CC=C(O)C3=C2C=CC(=O)N3

InChI

InChIKey=SFYAXIFVXBKRPK-QFIPXVFZSA-N
InChI=1S/C25H30F2N2O4/c26-25(27,18-8-4-3-5-9-18)17-33-15-7-2-1-6-14-28-16-22(31)19-10-12-21(30)24-20(19)11-13-23(32)29-24/h3-5,8-13,22,28,30-31H,1-2,6-7,14-17H2,(H,29,32)/t22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C25H30F2N2O4
Molecular Weight 460.5135
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

Abediterol, a fast and long-acting β2-adrenoceptor agonist (LABA), is being developed by AstraZeneca, for the treatment of asthma and chronic obstructive pulmonary disease. The investigational drug is a long-acting beta2-agonist (LABA) that has a bronchodilator effect, relaxing the muscles around the airways. It is currently under development and is in Phase II clinical trials.

Originator

Approval Year

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
The first Phase 2 study of abediterol as a COPD treatment was completed in 2012. It evaluate four single doses of inhaled abediterol at 0.625, 2.5, 5 or 10 ug. Results showed that all doses significantly improved bronchodilation when compared to a placebo. Doses of 2.5, 5, and 10 ug also showed improvements when compared to the active comparator.
Route of Administration: Respiratory
In Vitro Use Guide
The potency and onset of action that abediterol shows in isolated human bronchi (EC(50) = 1.9 ± 0.4 nM; t½ onset = 7-10 min)
Substance Class Chemical
Record UNII
QXA167CM6F
Record Status Validated (UNII)
Record Version