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doi:10.13040/ijpsr.0975-8232.4(4).1524-28

Cited by 2 publications

(2 citation statements)

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“…They reported that the compounds which are obtained by them, 4-benzylidene-6-phenyl-4,5-dihydropyridazin-3(2H)-one and 4-benzylidene-6-(4-chlorophenyl)-4,5-dihydropyridazin-3(2H)-one, showed good antimicrobial activity against S. aureus and S. epidermidis. It is also reported that the other compounds, 4-(4-chlorobenzylidene)-6-phenyl-4,5-dihydropyridazin-3(2H)-one and 4-(4-methoxybenzylidene)-6-(4-chlorophenyl)-4,5-dihydropyridazin-3(2H)one showed good antimicrobial activity against P. euroginosa and E. coli [9] (Figure 1). Nagle et al synthesized the new pyridazinone derivative compounds containing the thymol structure and evaluated the antibacterial activity against E. coli and S. aureus and antifungal activity against A. niger and P. marneffei of these compounds and thymol by agar well diffusion method.…”

Section: Introductionmentioning

confidence: 78%

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Studies on a novel series of 3(2H)-pyridazinones: Synthesis, molecular modelling, antimicrobial activity

Özdemi̇r¹,

Alagöz²,

Akdemir³

et al. 2019

jrp

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Efforts to develop new potent and effective antimicrobial compounds with lower side effects are important not only for controlling serious infections but also for cancer, surgical operations, and preventing possible infections which are related to other threats. Therefore, it is getting more important to develop new antibacterial and antifungal compounds with wide spectrum, systemic effect and lower side effects. In this study eight new 3(2H)pyridazinone derivatives were synthesized and their antimicrobial activities were evaluated by using broth microdilution method agains two Gr (+) (Staphylococcus aureus, Enterococcus faecalis), two Gr (-) bacteria (Pseudomonas aeruginosa, Escherichia coli) and three yeasts like fungi (Candida albicans, Candida krusei). Compound D2a had the best antibacterial activity among the synthesized compounds. All compounds were more effective against the fungus than the bacteria. In this study, we performed molecular modelling studies to provide in depth understanding of their CYP51 inhibition. Antifungal susceptibility tests against standard Candida spp. including C. albicans revealed D2aas highly active compound. The molecular docking studies showed similarities in binding interactions in active site gorges of the enzymes with known inhibitors, such as VT1, fluconazole.

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Section: Introductionmentioning

confidence: 78%

“…Among the pharmacophore groups which is responsible for antimicrobial activity, the 3(2H)pyridazinone skeleton is one of the important structures used in the synthesis of more effective and broad spectrum antimicrobials [7][8][9][10][11][12][13][14].…”

Section: Introductionmentioning

confidence: 99%