Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H9ClFNO3 |
Molecular Weight | 281.667 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CN(C2CC2)C3=C(C=C(F)C(Cl)=C3)C1=O
InChI
InChIKey=ISPVACVJFUIDPD-UHFFFAOYSA-N
InChI=1S/C13H9ClFNO3/c14-9-4-11-7(3-10(9)15)12(17)8(13(18)19)5-16(11)6-1-2-6/h3-6H,1-2H2,(H,18,19)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/25705547Curator's Comment: The description was created based on several sources, including
https://www.google.com.na/patents/DE3142854 | https://www.ncbi.nlm.nih.gov/pubmed/16386005
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25705547
Curator's Comment: The description was created based on several sources, including
https://www.google.com.na/patents/DE3142854 | https://www.ncbi.nlm.nih.gov/pubmed/16386005
Fluoroquinolonic acid is major impurity present in Fluoroquinolone Antibacterial Agents such as Enrofloxacin or ciprofloxacin
of metoclopramide. Fluoroquinolonic acid shows weak antimicrobial activity.
Originator
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20210078
Antimicrobial activity of Fluoroquinolonic acid was evaluated in vitro in two Gram positive bacteria S. aureus MTCC - 96, S. pyogenes MTCC - 443 and two Gram negative bacteria E. coli MTCC - 442, P. aeruginosa MTCC - 441 and fungi C. albicans MTCC - 227, A. niger MTCC - 282 and A. clavatus MTCC - 1323 organisms by broth dilution method. DMSO was used as a diluent which not effected the growth of microbes. MIC Fluoroquinolonic acid for Gram negative and Gram positive bacteria were 100 mkg/ml, for fungi 500-1000 mkg/ml
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SUBSTANCE RECORD