Synthesis, Characterization of 2-Methylthio-1, 4-dihydropyrimidines for its Antibacterial potential

Label one rack set I- Control (blank), Gram positive Set IIStaphylococcus aureus, Set III- Bacillus Subtilis and gram negative Set IV-Escherichia coli, Set VProteus vulgaris. 2) Using a sterile 1 mL glass syringe, add 0.8 mL of DMSO in labeled 1 and 0.5 mL of DMSO labeled 2 through labeled 8 in Set...

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Veröffentlicht in:Research journal of pharmacy and technology 2019-04, Vol.12 (4), p.1585-1589
Hauptverfasser: Sarode, Varsha I., Bhole, Ritesh P.
Format: Artikel
Sprache:eng
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Zusammenfassung:Label one rack set I- Control (blank), Gram positive Set IIStaphylococcus aureus, Set III- Bacillus Subtilis and gram negative Set IV-Escherichia coli, Set VProteus vulgaris. 2) Using a sterile 1 mL glass syringe, add 0.8 mL of DMSO in labeled 1 and 0.5 mL of DMSO labeled 2 through labeled 8 in Set I-V. 3) With a sterile 1 mL glass syringe, add 0.2 mL test compounds solution in labeled 1 test tube and mix it. 4) Using a sterile 1 mL glass syringe, transfer test compounds solution 0.5 mL from tube 1 to tube 2. C-2 modified dihydropyrimidine derivatives of type II was synthesized by alkylation reaction. [...]2-methylthio-1, 4-dihydropyrimidine derivatives were synthesized from the respective tetrahydropyrimidine-2-thiones by reaction with methyl iodide in the presence of pyridine (Scheme 1). The result suggests that the antibacterial activities are markedly influenced by the aromatic substituent. [...]compounds IIe, IIf, IIi, and IIj with electron withdrawing substituents in the aromatic ring, show greater antibacterial activity. [...]these compounds may be further exploited for other pharmacological activities.
ISSN:0974-3618
0974-360X
0974-306X
DOI:10.5958/0974-360X.2019.00263.4