Compound ID | 1888
Class: Beta-lactam (cephalosporin, first generation)
Spectrum of activity: | Gram-positive & Gram-negative |
Details of activity: | Binds to bacterial penicillin-binding proteins (PBP) and interferes with bacterial cell wall integrity and synthesis. Active against Gram-positive bacteria and moderately against Enterobacteriaceae but high resistance rates in Enterobacteriaceae |
Description: | Semisynthetic Cephalosporin, derived from Cephalosporin C |
Year first mentioned: | 1976 |
Development status: | Experimental |
Chemical structure(s): | |
Canonical SMILES: | C(C(=O)N[C@@H]1C(=O)N2C(=C(CS[C@H]12)CSC3=NN=CS3)C(=O)O)N4C=NN=N4 |
Isomeric SMILES: | C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CN3C=NN=N3)C(=O)O)CSC4=NN=CS4 |
InChI: | InChI=1S/C13H12N8O4S3/c22-7(1-20-4-14-18-19-20)16-8-10(23)21-9(12(24)25)6(2-26-11(8)21)3-27-13-17-15-5-28-13/h4-5,8,11H,1-3H2,(H,16,22)(H,24,25)/t8-,11-/m1/s1 |
InChI Key: | DZMVCVMFETWNIU-LDYMZIIASA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/65755 |
External links: | |
Guide to Pharmacology: | ceftezole |
Main Source: | https://journals.asm.org/doi/10.1128/AAC.10.1.1 |