Solifenacin hydrochlorideProduct ingredient for Solifenacin
- Name
- Solifenacin hydrochloride
- Drug Entry
- Solifenacin
Solifenacin is a competitive muscarinic receptor antagonist indicated to treat an overactive bladder with urinary incontinence, urgency, and frequency.3 It has a long duration of action as it is usually taken once daily.3
Solifenacin was granted FDA approval on 19 November 2004.3
- Accession Number
- DBSALT001640
- Structure
Structure for Solifenacin hydrochloride (DBSALT001640)
- Synonyms
- Solifenacin HCl
- UNII
- Not Available
- CAS Number
- 180468-39-7
- Weight
- Average: 398.93
Monoisotopic: 398.1761058 - Chemical Formula
- C23H27ClN2O2
- InChI Key
- YAUBKMSXTZQZEB-VROPFNGYSA-N
- InChI
- InChI=1S/C23H26N2O2.ClH/c26-23(27-21-16-24-13-10-18(21)11-14-24)25-15-12-17-6-4-5-9-20(17)22(25)19-7-2-1-3-8-19;/h1-9,18,21-22H,10-16H2;1H/t21-,22-;/m0./s1
- IUPAC Name
- (3R)-1-azabicyclo[2.2.2]octan-3-yl (1S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylate hydrochloride
- SMILES
- Cl.O=C(O[C@H]1CN2CCC1CC2)N1CCC2=CC=CC=C2[C@@H]1C1=CC=CC=C1
- External Links
- ChemSpider
- 135770
- ChEMBL
- CHEMBL2361425
- Predicted Properties
Property Value Source Water Solubility 0.0729 mg/mL ALOGPS logP 3.9 ALOGPS logP 3.96 Chemaxon logS -3.7 ALOGPS pKa (Strongest Basic) 8.88 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 2 Chemaxon Hydrogen Donor Count 0 Chemaxon Polar Surface Area 32.78 Å2 Chemaxon Rotatable Bond Count 3 Chemaxon Refractivity 106.06 m3·mol-1 Chemaxon Polarizability 40.13 Å3 Chemaxon Number of Rings 5 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule Yes Chemaxon MDDR-like Rule No Chemaxon