Carbenicillin disodiumProduct ingredient forCarbenicillin

Name
Carbenicillin disodium
Drug Entry
Carbenicillin

Broad-spectrum semisynthetic penicillin derivative used parenterally. It is susceptible to gastric juice and penicillinase and may damage platelet function.

Accession Number
DBSALT001334
Structure
Synonyms
Not Available
UNII
9TS4B3H261
CAS Number
4800-94-6
Weight
Average: 422.36
Monoisotopic: 422.05244598
Chemical Formula
C17H16N2Na2O6S
InChI Key
RTYJTGSCYUUYAL-YCAHSCEMSA-L
InChI
InChI=1S/C17H18N2O6S.2Na/c1-17(2)11(16(24)25)19-13(21)10(14(19)26-17)18-12(20)9(15(22)23)8-6-4-3-5-7-8;;/h3-7,9-11,14H,1-2H3,(H,18,20)(H,22,23)(H,24,25);;/q;2*+1/p-2/t9?,10-,11+,14-;;/m1../s1
IUPAC Name
disodium (2S,5R,6R)-6-(2-carboxylato-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
SMILES
[Na+].[Na+].[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)C(C([O-])=O)C1=CC=CC=C1)C([O-])=O
KEGG Compound
C13967
ChemSpider
19694
ChEBI
34609
ChEMBL
CHEMBL606260
Wikipedia
Carbenicillin
Predicted Properties
Property Value Source
Water Solubility 0.4 mg/mL ALOGPS
logP 1.71 ALOGPS
logP 0.82 Chemaxon
logS -3 ALOGPS
pKa (Strongest Acidic) 3.11 Chemaxon
pKa (Strongest Basic) -6.3 Chemaxon
Physiological Charge -2 Chemaxon
Hydrogen Acceptor Count 6 Chemaxon
Hydrogen Donor Count 1 Chemaxon
Polar Surface Area 129.67 Å2 Chemaxon
Rotatable Bond Count 5 Chemaxon
Refractivity 112.49 m3·mol-1 Chemaxon
Polarizability 35.15 Å3 Chemaxon
Number of Rings 3 Chemaxon
Bioavailability 1 Chemaxon
Rule of Five Yes Chemaxon
Ghose Filter Yes Chemaxon
Veber's Rule No Chemaxon
医学博士DR-like Rule No Chemaxon