Cefprozil Anhydrous, (E)-
The anhydrous E-isomer form of cefprozil is an oral second-generation cephalosporin used for mild to moderate upper and lower respiratory tract infections, otitis media, and skin infections. It contains a propenyl side chain that exists in E and Z geometric isomers. The clinical formulation is predominantly the E-isomer.
Molekularmasse
389,4000 g/mol
LogP
-1,40
TPSA
158,00 Ų
Lipinski-Regel der Fünf
Bestanden
Wirkmechanismus
Disrupts bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), inhibiting the final transpeptidation step of peptidoglycan synthesis. The resulting cell wall defects cause osmotic instability and bacteriolysis.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Disrupts bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), inhibiting the final transpeptidation step of peptidoglycan synthesis. The resulting cell wall defects cause osmotic instability and bacteriolysis.
2D-Struktur
Cite this structure
Embed this structure
SMILES
C/C=C/C1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)c3ccc(O)cc3)[C@H]2SC1
InChI
InChI=1S/C18H19N3O5S/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)/b3-2+/t12-,13-,17-/m1/s1
Molecular Formula
C18H19N3O5S
HBD / HBA
4 / 7
Rotierbare Bindungen
5
Schwere Atome
27
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Häufig gestellte Fragen
The anhydrous E-isomer form of cefprozil is an oral second-generation cephalosporin used for mild to moderate upper and lower respiratory tract infections, otitis media, and skin infections. It contains a propenyl side chain that exists in E and Z geometric isomers. The clinical formulation is predominantly the E-isomer.
Disrupts bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), inhibiting the final transpeptidation step of peptidoglycan synthesis. The resulting cell wall defects cause osmotic instability and bacteriolysis.
Yes, Cefprozil Anhydrous, (E)- is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL276568. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5281006. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
Medizinischer Haftungsausschluss
This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
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