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
ChemSpider
390137
ChEBI
7810
ChEMBL
CHEMBL3989567
Predicted Properties
PropertyValueSource
Water Solubility0.118 mg/mLALOGPS
logP2.56ALOGPS
logP1.7Chemaxon
logS-3.6ALOGPS
pKa (Strongest Acidic)3.75Chemaxon
pKa (Strongest Basic)-0.12Chemaxon
Physiological Charge-1Chemaxon
Hydrogen Acceptor Count5Chemaxon
Hydrogen Donor Count1Chemaxon
Polar Surface Area115.57 Å2Chemaxon
Rotatable Bond Count4Chemaxon
Refractivity112.67 m3·mol-1Chemaxon
Polarizability38.29 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon