Compound ID | 562
Class: Fluoroquinolone
Spectrum of activity: | Gram-positive & Gram-negative |
Details of activity: | Activity is similar to temafloxacin against the tested K. pneumoniae, P. stuartii, MSSA, Enterococci and S. pyogenes. |
Description: | Jones RN, Barrett MS and Erwin ME. In vitro antimicrobial evaluations of a new fluoroquinolone, E-4868 (E-4). 32nd-Intersci-Conf-Antimicrobial-Agents-Chemother 1992; 238. |
Institute where first reported: | Esteve, Spain |
Year first mentioned: | 1992 |
Highest developmental phase: | Phase 1 |
Development status: | Inactive |
Chemical structure(s): | |
Canonical SMILES: | C[C@H]1[C@@H](CN1C2=CC3=C(C=C2F)C(=O)C(=CN3C4=CC=C(C=C4F)F)C(=O)O)N |
Isomeric SMILES: | C[C@H]1[C@@H](CN1C2=C(C=C3C(=C2)N(C=C(C3=O)C(=O)O)C4=C(C=C(C=C4)F)F)F)N |
InChI: | InChI=1S/C20H16F3N3O3/c1-9-15(24)8-25(9)18-6-17-11(5-14(18)23)19(27)12(20(28)29)7-26(17)16-3-2-10(21)4-13(16)22/h2-7,9,15H,8,24H2,1H3,(H,28,29)/t9-,15+/m0/s1 |
InChI Key: | LTDOHCZUKCZDEQ-BJOHPYRUSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/65995 |
External links: | |
Guide to Pharmacology: | cetefloxacin |
Main Source: | https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0031-1300058 |