Compound ID | 2603
Synonym(s): Q-35
Class: Fluoroquinolone
Spectrum of activity: | Gram-positive & Gram-negative |
Details of activity: | For use against urinary (approved) and respiratory tract infections; inhibits DNA gyrase and topoisomerase IV enzymes |
Description: | Synthetic compound; a fourth generation fluoroquinolone |
Institute where first reported: | Choongwae Pharma (Korea) |
Year first mentioned: | 2005 |
Highest developmental phase: | Phase 3 (Korea) |
Development status: | Approved in Korea |
Chemical structure(s): | |
Canonical SMILES: | CNC1CCCN(C1)C2=C(C3=C(C=C2F)C(=O)C(=CN3C4CC4)C(=O)O)OC |
Isomeric SMILES: | CNC1CCCN(C1)C2=C(C=C3C(=C2OC)N(C=C(C3=O)C(=O)O)C4CC4)F |
InChI: | InChI=1S/C20H24FN3O4/c1-22-11-4-3-7-23(9-11)17-15(21)8-13-16(19(17)28-2)24(12-5-6-12)10-14(18(13)25)20(26)27/h8,10-12,22H,3-7,9H2,1-2H3,(H,26,27) |
InChI Key: | MGQLHRYJBWGORO-UHFFFAOYSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/65958 |
External links: | |
Guide to Pharmacology: | balofloxacin |
Main Source: | https://www.sciencedirect.com/science/article/pii/S0731708518313025 |