Cefprozil monohydrateProduct ingredient for Cefprozil
- Name
- Cefprozil monohydrate
- Drug Entry
- Cefprozil
Cefprozil is a cephalosporin antibiotic that is commonly employed to treat a variety of bacterial infections, including those of the ear and skin, bronchitis, and others.
- Accession Number
- DBSALT001051
- Structure
Structure for Cefprozil monohydrate (DBSALT001051)
- Synonyms
- Not Available
- UNII
- 3ADV90MJVU
- CAS Number
- 121123-17-9
- Weight
- Average: 407.44
Monoisotopic: 407.115106582 - Chemical Formula
- C18H21N3O6S
- InChI Key
- ALYUMNAHLSSTOU-CIRGZYLNSA-N
- InChI
- InChI=1S/C18H19N3O5S.H2O/c1-2-3-10-8-27-17-13(16(24)21(17)14(10)18(25)26)20-15(23)12(19)9-4-6-11(22)7-5-9;/h2-7,12-13,17,22H,8,19H2,1H3,(H,20,23)(H,25,26);1H2/b3-2+;/t12-,13-,17-;/m1./s1
- IUPAC Name
- (6R,7R)-7-{[(2R)-2-amino-1-hydroxy-2-(4-hydroxyphenyl)ethylidene]amino}-8-oxo-3-[(1E)-prop-1-en-1-yl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid hydrate
- SMILES
- O.C\C=C\C1=C(N2[C@H](SC1)[C@H](N=C(O)[C@H](N)C1=CC=C(O)C=C1)C2=O)C(O)=O
- External Links
- ChemSpider
- 4941253
- Predicted Properties
Property Value Source Water Solubility 0.112 mg/mL ALOGPS logP 0.42 ALOGPS logP -1.3 Chemaxon logS -3.5 ALOGPS pKa (Strongest Acidic) 2.64 Chemaxon pKa (Strongest Basic) 8.38 Chemaxon Physiological Charge 0 Chemaxon Hydrogen Acceptor Count 7 Chemaxon Hydrogen Donor Count 4 Chemaxon Polar Surface Area 136.45 Å2 Chemaxon Rotatable Bond Count 5 Chemaxon Refractivity 101.79 m3·mol-1 Chemaxon Polarizability 38.56 Å3 Chemaxon Number of Rings 3 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon