4.6 Article

Novel Pyrimidine-based Ferrocenyl substituted Organometallic Compounds: Synthesis, Characterization and Biological Evaluation

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APPLIED ORGANOMETALLIC CHEMISTRY
卷 32, 期 4, 页码 -

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WILEY
DOI: 10.1002/aoc.4261

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antiprotozoal assay; ferrocenyl unit; HM1: IMSS strain of Entamoeba histolytica; new leads in amoebic chemotherapy; novel pyrimidine-based organometallics

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  1. Deanship of Scientific Research (DSR), University of Tabuk, Kingdom of Saudi Arabia [S-0117-1438]

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Some novel pyrimidine-based ferrocenyl substituted organometallic compounds were synthesized via multistep reactions, well characterized by different spectroscopic techniques and elemental analyses and evaluated for in vitro antiprotozoal susceptibility against HM1: IMSS strain of Entamoeba histolytica. The results of antiprotozoal susceptibility unveiled these compounds, as new leads in protozoal chemotherapy as most of the organometallics displayed an exceptionally higher antiamoebic activity (IC50 = 0.055 M - 0.815 M) than the reference drug metronidazole which gave IC50 (50% inhibitory concentration) value 1.781 M in our experiments, concluding that newly synthesized organometallic compounds have potential to be employed as effective antiamoebic agents and these organometallics can be very useful for further optimization work on amoebic chemotherapy.

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