New azetidine-3-carbonyl-N-methyl-hydrazino derivatives of fluoroquinolones: synthesis and evaluation of antibacterial and anticancer properties
| dc.contributor.author | Govinda Rajulu, G. | |
| dc.contributor.author | Bhojya Naik, Halehatty S. | |
| dc.contributor.author | Charan Kumar, G. | |
| dc.contributor.author | Ramaraj, S. | |
| dc.contributor.author | Sambasivam, Ganesh | |
| dc.contributor.author | Poonimangadu Koppolu, Kesavan | |
| dc.date.accessioned | 2023-07-12T16:20:31Z | |
| dc.date.available | 2023-07-12T16:20:31Z | |
| dc.date.issued | 2014 | |
| dc.description.abstract | A series of nine new N-(substituted azetidine-3 -carbonyl)-N-methyl-hydrazino derivatives at C-7 position of fluoroquinolones were designed and synthesized through multistep synthesis. The synthesized compounds were characterized by 1H NMR, 13C NMR, ESI–MS and IR. The new compounds were tested for their in vitro antimicrobial and anti-proliferative activity. Out of the nine derivatives, compound 6i exhibited good antibacterial activity by inhibiting the growth of Methicillin-sensitive Staphylococcus aureus, Methicillin-resistant S. aureus and ATCC 35218 Escherichia coli (MIC: 0.25–16.00 lg/mL). Compounds 6c, 6g–h are displayed good growth inhibition against MCF-7 Breast carcinoma, HCT-116 Colon carcinoma and A549 Lung adenocarcinoma cell lines. Compound 6h is the most active against MCF-7 cell line with superior growth inhibition compared to ciprofloxacin and reference anticancer drug SAHA. | en_US |
| dc.identifier.citation | Rajulu, G. G., Naik, H. S. B., Kumar, G. C., Ramaraj, S., Sambasivam, G., & Koppolu, K. P. (2014). New azetidine-3-carbonyl-N-methyl-hydrazino derivatives of fluoroquinolones: synthesis and evaluation of antibacterial and anticancer properties. Medicinal Chemistry Research, 23, 2856-2868. 10.1007/s00044-013-0873-0 | en_US |
| dc.identifier.uri | 10.1007/s00044-013-0873-0 | |
| dc.identifier.uri | https://nru.uncst.go.ug/handle/123456789/9064 | |
| dc.language.iso | en | en_US |
| dc.publisher | Medicinal Chemistry Research | en_US |
| dc.subject | Synthesis | en_US |
| dc.subject | Reductive amination | en_US |
| dc.subject | Fluoroquinolones | en_US |
| dc.subject | Antibacterial activity | en_US |
| dc.subject | Anticancer activity | en_US |
| dc.title | New azetidine-3-carbonyl-N-methyl-hydrazino derivatives of fluoroquinolones: synthesis and evaluation of antibacterial and anticancer properties | en_US |
| dc.type | Article | en_US |
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