Flomoxef SodiumProduct ingredient for Flomoxef
- Name
- Flomoxef Sodium
- Drug Entry
- Flomoxef
Flomoxef has been used in trials studying the treatment of Urinary Tract Infection.
- Accession Number
- DBSALT002108
- Structure
Structure for Flomoxef Sodium (DBSALT002108)
- Synonyms
- Not Available
- UNII
- 445HIB8XNF
- CAS Number
- 92823-03-5
- Weight
- Average: 518.44
Monoisotopic: 518.04658987 - Chemical Formula
- C15H17F2N6NaO7S2
- InChI Key
- PPPZBOLFWGINKN-YLCXCWDSSA-M
- InChI
- InChI=1S/C15H18F2N6O7S2.Na/c1-29-15(18-8(25)6-31-13(16)17)11(28)23-9(10(26)27)7(4-30-12(15)23)5-32-14-19-20-21-22(14)2-3-24;/h12-13,24H,2-6H2,1H3,(H,18,25)(H,26,27);/q;+1/p-1/t12-,15+;/m1./s1
- IUPAC Name
- sodium (6R,7R)-7-{2-[(difluoromethyl)sulfanyl]acetamido}-3-({[1-(2-hydroxyethyl)-1H-1,2,3,4-tetrazol-5-yl]sulfanyl}methyl)-7-methoxy-8-oxo-5-oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
- SMILES
- [Na+].CO[C@]1(NC(=O)CSC(F)F)[C@H]2OCC(CSC3=NN=NN3CCO)=C(N2C1=O)C([O-])=O
- External Links
- ChemSpider
- 392022
- Predicted Properties
Property Value Source Water Solubility 1.82 mg/mL ALOGPS logP 0.21 ALOGPS logP -0.11 Chemaxon logS -2.4 ALOGPS pKa (Strongest Acidic) 3.28 Chemaxon pKa (Strongest Basic) -1.5 Chemaxon Physiological Charge -1 Chemaxon Hydrogen Acceptor Count 10 Chemaxon Hydrogen Donor Count 2 Chemaxon Polar Surface Area 171.83 Å2 Chemaxon Rotatable Bond Count 11 Chemaxon Refractivity 130.5 m3·mol-1 Chemaxon Polarizability 42.87 Å3 Chemaxon Number of Rings 3 Chemaxon Bioavailability 0 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule Yes Chemaxon