Cefpodoxime sodiumProduct ingredient for Cefpodoxime

Name
Cefpodoxime sodium
Drug Entry
Cefpodoxime

Cefpodoxime is an oral third generation cephalosporin antibiotic with effectiveness against most Gram positive and Gram negative bacteria. Commonly used to treat acute otitis media, pharyngitis, and sinusitis, cefpodoxime proxetil is a prodrug which is absorbed and de-esterified by the intestinal mucosa to Cefpodoxime.

Accession Number
DBSALT001810
Structure
Synonyms
Not Available
UNII
3ULP5169B3
CAS Number
82619-04-3
Weight
Average: 449.43
Monoisotopic: 449.04396988
Chemical Formula
C15H16N5NaO6S2
InChI Key
JNMXSNGAMPXCDR-XYNKDNFRSA-M
InChI
InChI=1S/C15H17N5O6S2.Na/c1-25-3-6-4-27-13-9(12(22)20(13)10(6)14(23)24)18-11(21)8(19-26-2)7-5-28-15(16)17-7;/h5,9,13H,3-4H2,1-2H3,(H2,16,17)(H,18,21)(H,23,24);/q;+1/p-1/b19-8-;/t9-,13-;/m1./s1
IUPAC Name
sodium (6R,7R)-7-[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamido]-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
SMILES
[Na+].COCC1=C(N2[C@H](SC1)[C@H](NC(=O)C(=N/OC)\C1=CSC(N)=N1)C2=O)C([O-])=O
ChemSpider
7851231
Predicted Properties
PropertyValueSource
Water Solubility0.228 mg/mLALOGPS
logP0.8ALOGPS
logP-1.7Chemaxon
logS-3.3ALOGPS
pKa (Strongest Acidic)3.22Chemaxon
pKa (Strongest Basic)4.16Chemaxon
Physiological Charge-1Chemaxon
Hydrogen Acceptor Count9Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area159.27 Å2Chemaxon
Rotatable Bond Count7Chemaxon
Refractivity111.55 m3·mol-1Chemaxon
Polarizability39.94 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon