Oxacillin sodiumProduct ingredient for Oxacillin
- Name
- Oxacillin sodium
- Drug Entry
- Oxacillin
An antibiotic similar to flucloxacillin used in resistant staphylococci infections.
- Accession Number
- DBSALT000248
- Structure
Structure for Oxacillin sodium (DBSALT000248)
- Synonyms
- Anhydrous oxacillin sodium / Oxacillin sodium anhydrous / Sodium oxacillin
- UNII
- 4TWD2995UP
- CAS Number
- 1173-88-2
- Weight
- Average: 423.42
Monoisotopic: 423.08648615 - Chemical Formula
- C19H18N3NaO5S
- InChI Key
- VDUVBBMAXXHEQP-SLINCCQESA-M
- InChI
- InChI=1S/C19H19N3O5S.Na/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);/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
- SMILES
- [Na+].[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)C1=C(C)ON=C1C1=CC=CC=C1)C([O-])=O
- External Links
- 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 38.18 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