Levophencynonate hydrochlorideProduct ingredient for Levophencynonate
- Name
- Levophencynonate hydrochloride
- Drug Entry
- Levophencynonate
Levophencynonate is under investigation in clinical trial NCT02299804 (A Clinical Trial to Evaluate Efficacy and Safety of Levophencynonate Hydrochloride in Patient With Vertigo).
- Accession Number
- DBSALT003130
- Structure
Structure for Levophencynonate hydrochloride (DBSALT003130)
- Synonyms
- Levo-phencynonate HCl / Levo-phencynonate hydrochloride / Levophencynonate HCl
- UNII
- MOI46704GT
- CAS Number
- 861655-73-4
- Weight
- Average: 393.95
Monoisotopic: 393.2070716 - Chemical Formula
- C22H32ClNO3
- InChI Key
- AUKYHFFECJXLHI-FMTMECAPSA-N
- InChI
- InChI=1S/C22H31NO3.ClH/c1-23-14-16-8-7-9-17(15-23)20(16)26-21(24)22(25,19-12-5-6-13-19)18-10-3-2-4-11-18;/h2-4,10-11,16-17,19-20,25H,5-9,12-15H2,1H3;1H/t16-,17+,20?,22-;/m0./s1
- IUPAC Name
- (1R,5S)-3-methyl-3-azabicyclo[3.3.1]nonan-9-yl 2-cyclopentyl-2-hydroxy-2-phenylacetate hydrochloride
- SMILES
- Cl.[H][C@]12CCC[C@]([H])(CN(C)C1)C2OC(=O)C(O)(C1CCCC1)C1=CC=CC=C1
- External Links
- ChemSpider
- 52084815
- Predicted Properties
Property Value Source Water Solubility 0.0518 mg/mL ALOGPS logP 3.81 ALOGPS logP 3.62 Chemaxon logS -3.8 ALOGPS pKa (Strongest Acidic) 11.54 Chemaxon pKa (Strongest Basic) 9.73 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 3 Chemaxon Hydrogen Donor Count 1 Chemaxon Polar Surface Area 49.77 Å2 Chemaxon Rotatable Bond Count 5 Chemaxon Refractivity 101.66 m3·mol-1 Chemaxon Polarizability 40.28 Å3 Chemaxon Number of Rings 4 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon