Modification of Gemifloxacin Drug Antibacterial to Promising Anti-Prostate Cancer PC3 Azomethine Compounds: Synthesis and in Vitro Studies

Authors

  • Rand Thair Abdulkader Al- Karkh University of Science
  • Reyam H. Marah Al- Karkh University of Science
  • Aqeel Mohamed Department of Medical Lab Technique
  • Abbas K. Abbas Ministry of Agriculture

DOI:

https://doi.org/10.61132/obat.v2i5.665

Keywords:

Antibacterial, Antibiotic, Gemifloxacin, Cancer

Abstract

In this study, we report a novel azomethine derivatives synthesis (H and G) by reacting pure Gemifloxacin drugs with 2-aminobenzaldehyde and 2-methylbenzaldehyde. Spectroscopic techniques, such as FT‐IR spectroscopy, characterized the derivatives (G and H). All the synthesized derivatives (G and H) were evaluated in vitro against microorganisms such as Bacillus subtilis and E. coli by zone inhibition method and screened for antimicrobial activities and anti-Prostate cancer PC3 cell viability cell lines.

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Published

2024-08-15

How to Cite

Rand Thair Abdulkader, Reyam H. Marah, Aqeel Mohamed, & Abbas K. Abbas. (2024). Modification of Gemifloxacin Drug Antibacterial to Promising Anti-Prostate Cancer PC3 Azomethine Compounds: Synthesis and in Vitro Studies. OBAT: Jurnal Riset Ilmu Farmasi Dan Kesehatan, 2(5), 145–152. https://doi.org/10.61132/obat.v2i5.665

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