Pradofloxacin

Class: Fluoroquinolone

Spectrum of activity:	Gram-positive  &  Gram-negative
Details of activity:	Broad-spectrum activity including anaerobic bacteria and mycoplasmas; bacterial topoisomerase inhibitor
Description:	Synthetic compound; an 8-cyanofluoroquinolone for veterinary use
Year first mentioned:	2005
Highest developmental phase:	Approved for veterinary use
Development status:	Experimental

Chemical structure(s):
Canonical SMILES:	C1C[C@H]2CN(C[C@H]2NC1)C3=C(C#N)C4=C(C=C3F)C(=O)C(=CN4C5CC5)C(=O)O
Isomeric SMILES:	C1C[C@H]2CN(C[C@H]2NC1)C3=C(C=C4C(=C3C#N)N(C=C(C4=O)C(=O)O)C5CC5)F
InChI:	InChI=1S/C21H21FN4O3/c22-16-6-13-18(26(12-3-4-12)9-15(20(13)27)21(28)29)14(7-23)19(16)25-8-11-2-1-5-24-17(11)10-25/h6,9,11-12,17,24H,1-5,8,10H2,(H,28,29)/t11-,17+/m0/s1
InChI Key:	LZLXHGFNOWILIY-APPDUMDISA-N
Structure link:	https://pubchem.ncbi.nlm.nih.gov/compound/9802884

External links:
Main Source:	https://www.sciencedirect.com/science/article/abs/pii/S1090023314002640?via%3Dihub