Metabolite 2-Oxoticlopidine
- Name
- 2-Oxoticlopidine
- Description
- Not Available
- Structure
- Synonyms
- Not Available
- UNII
- 23YK0YMF8U
- CAS number
- Not Available
- Weight
- Average: 279.785
Monoisotopic: 279.048462472 - Chemical Formula
- C14H14ClNOS
- InChI Key
- DJZQIXWGIZIETJ-UHFFFAOYSA-N
- InChI
- InChI=1S/C14H14ClNOS/c15-12-4-2-1-3-10(12)8-16-6-5-13-11(9-16)7-14(17)18-13/h1-4,7,13H,5-6,8-9H2
- IUPAC Name
- 5-[(2-chlorophenyl)methyl]-2H,4H,5H,6H,7H,7aH-thieno[3,2-c]pyridin-2-one
- SMILES
- ClC1=CC=CC=C1CN1CCC2SC(=O)C=C2C1
- Reactions
- Ticlopidine 2-Oxoticlopidine
- 2-Oxoticlopidine Active metabolite of Ticlopidine
- Ticlopidine 2-Oxoticlopidine
- Spectra
- Chromatographic Properties
Collision Cross Sections (CCS)
Adduct CCS Value (Å2) Source type Source [M-H]- 163.9650089 predictedDarkChem Lite v0.1.0 [M-H]- 156.95757 predictedDeepCCS 1.0 (2019) [M+H]+ 164.2678089 predictedDarkChem Lite v0.1.0 [M+H]+ 159.31557 predictedDeepCCS 1.0 (2019) [M+Na]+ 164.0626089 predictedDarkChem Lite v0.1.0 [M+Na]+ 165.5219 predictedDeepCCS 1.0 (2019) - External Links
- Human Metabolome Database
- HMDB0013923
- ChemSpider
- 118335
- ChEBI
- 185074
- ChEMBL
- CHEMBL3526246
- Predicted Properties
Property Value Source Water Solubility 0.0647 mg/mL ALOGPS logP 3.02 ALOGPS logP 2.88 Chemaxon logS -3.6 ALOGPS pKa (Strongest Acidic) 8.49 Chemaxon pKa (Strongest Basic) 6.56 Chemaxon Physiological Charge 0 Chemaxon Hydrogen Acceptor Count 2 Chemaxon Hydrogen Donor Count 0 Chemaxon Polar Surface Area 20.31 Å2 Chemaxon Rotatable Bond Count 2 Chemaxon Refractivity 77.41 m3·mol-1 Chemaxon Polarizability 28.68 Å3 Chemaxon Number of Rings 3 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule Yes Chemaxon MDDR-like Rule No Chemaxon