Oxadiazole derivatives

Anti-inflammatory is the property of a substance or treatment that reduces inflammation in the body (redness, swelling, and pain) by blocking certain substances in the body that cause inflammation. They are used to treat many different conditions.

5p vimichaelfaraday 28-12-2023 4 3   Download

In this study, nine ferulic and caffeic acid-based 1,2,4 and 1,3,4 oxadiazole molecular hybrids were synthesized and their cytotoxic activity was evaluated mainly against Glioblastoma (GBM) cell lines. Compounds 1 and 5 exhibited the highest inhibitory activity against three different GBM cell lines (LN229, T98G, and U87), without toxicity to healthy human mesenchymal stem cells (hMSC). In addition, their cytotoxicity was also evaluated against three additional cancer cell lines and more inhibitory results were found than GBM cell lines.

22p lyhuyenthu 31-01-2023 7 2   Download

The reaction between salicylaldehyde and ethyl chloroacetate in DMF formed ester ethyl benzofuran-2- carboxylate 2, followed by the treatment with hydrazine hydrate to afford benzofuran-2-carbohydrazide 3, with carbon disulfide, potassium hydroxide and hydrazine hydrate formed 4-amino-5-(benzofuran-2-yl)-1,2,4- triazole-3-thiol 4a which existed in the mixture of two tautomers (thiol form 4a and thione form 4b).

3p viclerkmaxwel 16-02-2022 12 2   Download

Some novel 2-(substitutedbenzylthio)-5-((2-(4-substitutedphenyl)-1H -benzo[d]imidazol-1-yl)methyl)-1,3,4- oxadiazoles (5–12) and 2-(2-(4-chlorophenyl)-1H -benzo[d]imidazol-1-yl)-N ′ -(arylmethylene)acetohydrazide derivatives (13–22) were prepared and their in vitro antioxidant properties were investigated by determination of rat liver microsomal NADPH-dependent inhibition of lipid peroxidation (LP) levels and microsomal ethoxyresorufin O-deethylase (EROD) activity. Compound 18 was found to be the most active compound with 100% inhibition on LP level and 92% inhibition on EROD.

12p langthannam 29-12-2021 18 1   Download

The three-component reaction of benzoic acid derivatives, (N -isocyanimino)triphenylphosphorane, and trichloroacetyl isocyanate in a 1:1:1 ratio in CH3 CN occurred at room temperature, and the 5-aryl-N -(trichloroacetyl)- 1,3,4-oxadiazole-2-carboxamide derivatives produced were formed in high yields. The reaction proceeded smoothly and cleanly under mild reaction conditions and no side reactions were observed. The structures of the products were confirmed by IR, 1 H NMR, 13 C NMR, mass spectroscopy, and elemental analysis.

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Coumarinyl 1,3,4-oxadiazoles were synthesized from Schiff bases and acetic anhydride. All compounds were characterized by melting points and their structures confirmed by mass and 1H and 13C NMR spectrometry. These novel coumarinyl derivatives were subjected to antibacterial, antifungal, antaflatoxigenic, and antioxidant activity. Their activity varied depending on their structure, where 2-(3-acetyl-5-(((4-methyl-2-oxo-2 H -chromen-7-yl)oxy)methyl)- 2,3-dihydro-1,3,4-oxadiazol-2-yl)-1,4-phenylene diacetate showed significant antioxidant and antibacterial activity on B. subtilis.

25p tudichquannguyet 29-11-2021 7 1   Download

A series of novel sulfide derivatives containing 1,3,4-oxadiazole and pyridine were synthesized, characterized, and tested for their antibacterial activity against tobacco bacterial wilt and rice bacterial blight and for insecticidal activity toward diamondback moth. The results showed that some compounds had good insecticidal and bactericidal activity, e.g.

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In the present work, a library of fifteen 2-hydroxy benzothiazole-linked 1,3,4 -oxadiazole derivatives have been synthesized and confirmed using different analytical techniques. All of the synthesized compounds have been tested for antibacterial and in silico pharmacokinetic studies for the first time. From the ADME predictions, compound 4 showed the highest in silico absorption percentage (86.77%), while most of the compounds showed more than 70% absorption.

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The reaction of 3,4-dichlorophenyl-1,3,4-oxadiazole-2(3H)-thione with piperidine derivatives via Mannich reaction was used to generate eleven novel compounds in moderate to good yields. Synthesized molecules were characterized according to their structure with 1 H NMR, 13C NMR and FT-IR spectral foundations, which were compatible with literature informations. Antimicrobial activity and cytotoxicity studies were done by disc diffusion and NCI-60 sulphordamine B assay methods.

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In the present investigation, some novel S-(5-aryl-1,3,4-oxadiazol-2-yl)2-chloroethanethioate (3a–3e) derivatives were synthesized and their impact on optical properties was studied. They have also been characterized by elemental analysis and various spectroscopic methods including FTIR, 1H NMR, 13C NMR, and UV-Vis techniques. The nonlinear refractive indexes of 3a–3e were also measured in dichloromethane via Z-scan method using a continuous wave diode-pumped laser at 532 nm wavelength. The nonlinear refractive coefficient of compounds was obtained from 1011 m2/W order.

9p tudichquannguyet 29-11-2021 6 2   Download