Sultopride hydrochlorideProduct ingredient for Sultopride
- Name
- Sultopride hydrochloride
- Drug Entry
- Sultopride
Sultopride is used in Japan, Hong Kong, and Europe to treat schizophrenia. It is of the drug class atypical antipsychotics 1.
- Accession Number
- DBSALT002916
- Structure
Structure for Sultopride hydrochloride (DBSALT002916)
- Synonyms
- Sultopride HCl / Sultopride hydrochloride
- UNII
- 8Q6926T32J
- CAS Number
- 23694-17-9
- Weight
- Average: 390.92
Monoisotopic: 390.1380062 - Chemical Formula
- C17H27ClN2O4S
- InChI Key
- IGOWMQPOGQYFFM-UHFFFAOYSA-N
- InChI
- InChI=1S/C17H26N2O4S.ClH/c1-4-19-10-6-7-13(19)12-18-17(20)15-11-14(24(21,22)5-2)8-9-16(15)23-3;/h8-9,11,13H,4-7,10,12H2,1-3H3,(H,18,20);1H
- IUPAC Name
- 5-(ethanesulfonyl)-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-methoxybenzamide hydrochloride
- SMILES
- Cl.CCN1CCCC1CNC(=O)C1=CC(=CC=C1OC)S(=O)(=O)CC
- External Links
- ChemSpider
- 37852
- ChEMBL
- CHEMBL3182384
- Predicted Properties
Property Value Source Water Solubility 0.201 mg/mL ALOGPS logP 1.65 ALOGPS logP 1.08 Chemaxon logS -3.2 ALOGPS pKa (Strongest Acidic) 13.22 Chemaxon pKa (Strongest Basic) 8.22 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 5 Chemaxon Hydrogen Donor Count 1 Chemaxon Polar Surface Area 75.71 Å2 Chemaxon Rotatable Bond Count 7 Chemaxon Refractivity 95.14 m3·mol-1 Chemaxon Polarizability 38.07 Å3 Chemaxon Number of Rings 2 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon