Novel 1,3,4-Thiadiazole-2-yl-pyrimidine Derivatives In Vitro and the Etymology of Antifungal Activity

An array of 5-(5-amino-1,3,4-thiadiazole-2-yl)-3,4-dihydro-6-methyl-4-phenyl-pyrimidin-2(1H)-one derivatives (3a–3j) were synthesized. The synthesized chemicals effectively suppressed fungus activities. IR, 1H, 13C NMR, GC-MS, and Elemental analysis techniques were used to analyze the structures of the newly synthesized compounds. The majority of substances, compared to standard Amphotericin-B, have demonstrated promising antifungal activity.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2024-12-01
DOI
https://doi.org/10.1134/s1070428024130037
Citations
1
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.25
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article

Novel 1,3,4-Thiadiazole-2-yl-pyrimidine Derivatives In Vitro and the Etymology of Antifungal Activity

S. Sudarsan, Anita Durairaj, B. Andrews
1 citations
Russian Journal of Organic Chemistry
Synthesis and biological activity
0.25
article

Novel 1,3,4-Thiadiazole-2-yl-pyrimidine Derivatives In Vitro and the Etymology of Antifungal Activity

S. Sudarsan, Anita Durairaj, B. Andrews
article en
1 citations

Abstract

An array of 5-(5-amino-1,3,4-thiadiazole-2-yl)-3,4-dihydro-6-methyl-4-phenyl-pyrimidin-2(1H)-one derivatives (3a–3j) were synthesized. The synthesized chemicals effectively suppressed fungus activities. IR, 1H, 13C NMR, GC-MS, and Elemental analysis techniques were used to analyze the structures of the newly synthesized compounds. The majority of substances, compared to standard Amphotericin-B, have demonstrated promising antifungal activity.

Russian Journal of Organic ChemistryVol. 60(S1)
South Ural State University (RU), Anna University, Chennai (IN)
Zero hunger
Openalex Percentile: Top 45%
Synthesis and biological activity
0.25
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