Synthesis and antimicrobial evaluation of Histidine Cinnamaldehyde Schiff base containing structural feature of 1, 3, 4-thiadiazole heterocyclic moiety

Authors

  • Doaa Mahmood Ibrahim Department of Pharmaceutical Chemistry, College of Pharmacy, Mustansiriyah University, Baghdad-Iraq
  • Karima Fadhil Ali Department of Pharmaceutical Chemistry, College of Pharmacy, Mustansiriyah University, Baghdad-Iraq
  • Mayada Hadi Abd_alwahab Department of Pharmaceutical Chemistry, College of Pharmacy, Mustansiriyah University, Baghdad-Iraq

Abstract

Reaction of aqueous solution of amino acid Histidine with ethanolic solution Cinnamaldehyde to synthesize the desired Schiff base. Then, the derivative of 1, 3, 4-thiadiazole ring have been synthesized by reaction of the imine derivative with Thiosemicarbazide in presence of POCL3.

The entire intermediate and final compound characterized and identified by elemental microanalysis as melting point, FT-IR spectra, 1H-NMR spectroscopy. Agar Well Diffusion method evaluated the antimicrobial activity on gram positive bacteria such as Staphylococcus aureus and Streptococcus pneumonia and gram-negative bacteria such as E coli & Acinetobacter species and also antifungal activity had been studied on one type of fungi (candida albicans).

References

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Published

2024-05-12

How to Cite

Doaa Mahmood Ibrahim, Karima Fadhil Ali, & Mayada Hadi Abd_alwahab. (2024). Synthesis and antimicrobial evaluation of Histidine Cinnamaldehyde Schiff base containing structural feature of 1, 3, 4-thiadiazole heterocyclic moiety. Al Mustansiriyah Journal of Pharmaceutical Sciences, 20(1), 1–12. Retrieved from https://ajps.uomustansiriyah.edu.iq/index.php/AJPS/article/view/1185

Issue

Vol. 20 No. 1 (2020): volume20,Issue1.2020

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Articles

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