Metabolite 1-hydroxymidazolam-O-glucuronide
- Name
- 1-hydroxymidazolam-O-glucuronide
- Description
- Not Available
- Structure
- Synonyms
- Not Available
- UNII
- Not Available
- CAS number
- Not Available
- Weight
- Average: 517.89
Monoisotopic: 517.1052059 - Chemical Formula
- C24H21ClFN3O7
- InChI Key
- ICIUMXQTLQXWGL-UHFFFAOYSA-N
- InChI
- InChI=1S/C24H21ClFN3O7/c25-11-5-6-16-14(7-11)18(13-3-1-2-4-15(13)26)28-9-12-8-27-17(29(12)16)10-35-24-21(32)19(30)20(31)22(36-24)23(33)34/h1-8,19-22,24,30-32H,9-10H2,(H,33,34)
- IUPAC Name
- 6-{[12-chloro-9-(2-fluorophenyl)-2,4,8-triazatricyclo[8.4.0.0^{2,6}]tetradeca-1(10),3,5,8,11,13-hexaen-3-yl]methoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid
- SMILES
- OC1C(O)C(OCC2=NC=C3CN=C(C4=CC=CC=C4F)C4=C(C=CC(Cl)=C4)N23)OC(C1O)C(O)=O
- Reactions
- Midazolam 1-hydroxymidazolam
- 1-hydroxymidazolam 1,4-dihydroxymidazolam
- 1-hydroxymidazolam 1-hydroxymidazolam-O-glucuronide
- 1-hydroxymidazolam 1-hydroxymidazolam-N-glucuronide
- Midazolam 1-hydroxymidazolam
- Spectra
- Not Available
- Chromatographic Properties
Collision Cross Sections (CCS)
Not Available- External Links
- Human Metabolome Database
- HMDB0247486
- ChemSpider
- 22378575
- Predicted Properties
Property Value Source Water Solubility 0.192 mg/mL ALOGPS logP 2.02 ALOGPS logP 0.39 Chemaxon logS -3.4 ALOGPS pKa (Strongest Acidic) 2.87 Chemaxon pKa (Strongest Basic) 4.64 Chemaxon Physiological Charge -1 Chemaxon Hydrogen Acceptor Count 9 Chemaxon Hydrogen Donor Count 4 Chemaxon Polar Surface Area 146.63 Å2 Chemaxon Rotatable Bond Count 5 Chemaxon Refractivity 133.41 m3·mol-1 Chemaxon Polarizability 49.78 Å3 Chemaxon Number of Rings 5 Chemaxon Bioavailability 1 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon