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| Content Provider | Springer Nature Link |
|---|---|
| Author | Agrawal, Kapil M. Talele, Gokul S. |
| Copyright Year | 2012 |
| Abstract | The present study deals with the synthesis of some novel fluoroquinolone derivatives as antibacterial and antitubercular agents. The titled compounds 7a–g and 8a–g were found to possess comparable or more potent activity than the reference compounds ciprofloxacin, norfloxacin, isoniazid and rifampicin. The synthesized compounds showed activity against S. aureus and C. bacterium, whereas poor activity was observed against P. aeruginosa and E. coli. These compounds were subjected to in vitro cytotoxicity study by MTT assay, and their selectivity index was calculated. Compound 7d was found to be the most efficient antimycobacterial agent amongst the series. Molecular docking revealed that synthesized derivatives and target proteins were actively involved in a binding pattern and had significant correlation with biological activity.Novel N-piperazinyl fluoroquinolone derivatives were synthesized and evaluated for their in vitro antibacterial, antimycobacterial and cytotoxic properties. Activity results were compared with the docking results. |
| Starting Page | 818 |
| Ending Page | 831 |
| Page Count | 14 |
| File Format | |
| ISSN | 10542523 |
| Journal | Medicinal Chemistry Research |
| Volume Number | 22 |
| Issue Number | 2 |
| e-ISSN | 15548120 |
| Language | English |
| Publisher | Springer-Verlag |
| Publisher Date | 2012-05-11 |
| Publisher Place | New York |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Fluoroquinolone (FQ) Antibacterial Antimycobacterial Cytotoxicity Docking study Pharmacology/Toxicology Biochemistry Cell Biology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry Pharmacology, Toxicology and Pharmaceutics |
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