Cefuroxime sodiumProduct ingredient for Cefuroxime

Name
Cefuroxime sodium
Drug Entry
Cefuroxime

Broad-spectrum cephalosporin antibiotic resistant to beta-lactamase. It has been proposed for infections with gram-negative and gram-positive organisms, gonorrhea, and haemophilus.

Accession Number
DBSALT001160
Structure
Synonyms
Not Available
UNII
R8A7M9MY61
CAS Number
56238-63-2
Weight
Average: 446.37
Monoisotopic: 446.05082891
Chemical Formula
C16H15N4NaO8S
InChI Key
URDOHUPGIOGTKV-JTBFTWTJSA-M
InChI
InChI=1S/C16H16N4O8S.Na/c1-26-19-9(8-3-2-4-27-8)12(21)18-10-13(22)20-11(15(23)24)7(5-28-16(17)25)6-29-14(10)20;/h2-4,10,14H,5-6H2,1H3,(H2,17,25)(H,18,21)(H,23,24);/q;+1/p-1/b19-9-;/t10-,14-;/m1./s1
IUPAC Name
sodium (6R,7R)-3-[(carbamoyloxy)methyl]-7-[(2Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
SMILES
[Na+].CO\N=C(/C(=O)N[C@H]1[C@H]2SCC(COC(N)=O)=C(N2C1=O)C([O-])=O)C1=CC=CO1
KEGG Compound
C08108
ChemSpider
5013196
ChEBI
3517
ChEMBL
CHEMBL2146124
Wikipedia
Cefuroxime
Predicted Properties
PropertyValueSource
Water Solubility0.437 mg/mLALOGPS
logP0.56ALOGPS
logP-0.9Chemaxon
logS-3ALOGPS
pKa (Strongest Acidic)3.15Chemaxon
pKa (Strongest Basic)-1.1Chemaxon
Physiological Charge-1Chemaxon
Hydrogen Acceptor Count7Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area176.59 Å2Chemaxon
Rotatable Bond Count8Chemaxon
Refractivity108 m3·mol-1Chemaxon
Polarizability38.77 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon