Oxacillin sodium monohydrateProduct ingredient for Oxacillin
- Name
- Oxacillin sodium monohydrate
- Drug Entry
- Oxacillin
An antibiotic similar to flucloxacillin used in resistant staphylococci infections.
- Accession Number
- DBSALT000974
- Structure
- Synonyms
- Oxacillin sodium
- External IDs
- SQ 16,423 / SQ-16423
- UNII
- G0V6C994Q5
- CAS Number
- 7240-38-2
- Weight
- Average: 441.43
Monoisotopic: 441.09705083 - Chemical Formula
- C19H20N3NaO6S
- InChI Key
- ZVIYWUUZWWBNMB-VICXVTCVSA-M
- InChI
- InChI=1S/C19H19N3O5S.Na.H2O/c1-9-11(12(21-27-9)10-7-5-4-6-8-10)15(23)20-13-16(24)22-14(18(25)26)19(2,3)28-17(13)22;;/h4-8,13-14,17H,1-3H3,(H,20,23)(H,25,26);;1H2/q;+1;/p-1/t13-,14+,17-;;/m1../s1
- IUPAC Name
- sodium (2S,5R,6R)-3,3-dimethyl-6-(5-methyl-3-phenyl-1,2-oxazole-4-amido)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate hydrate
- SMILES
- O.[Na+].[H][C@@]1(NC(=O)C2=C(C)ON=C2C2=CC=CC=C2)C(=O)N2[C@]1([H])SC(C)(C)[C@]2([H])C([O-])=O
- External Links
- ChemSpider
- 390137
- ChEBI
- 7810
- ChEMBL
- CHEMBL3989567
- Predicted Properties
Property Value Source Water Solubility 0.118 mg/mL ALOGPS logP 2.56 ALOGPS logP 1.7 Chemaxon logS -3.6 ALOGPS pKa (Strongest Acidic) 3.75 Chemaxon pKa (Strongest Basic) -0.12 Chemaxon Physiological Charge -1 Chemaxon Hydrogen Acceptor Count 5 Chemaxon Hydrogen Donor Count 1 Chemaxon Polar Surface Area 115.57 Å2 Chemaxon Rotatable Bond Count 4 Chemaxon Refractivity 112.67 m3·mol-1 Chemaxon Polarizability 38.29 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