In vitro antioxidant properties of new thiazole derivatives
نویسندگان
چکیده
منابع مشابه
Synthesis, Characterization, Anti-inflammatory, and Antioxidant Activities of Some New Thiazole Derivatives
A series of novel thiazole derivatives (A, A1, A2) were synthesized starting from 1-(3-methoxy phenyl) ethanone and thiourea. The compound (A) was obtained by heating 1-(3-methoxy phenyl) ethanone with thiourea in iodine. Compound (A) on treatment with 4-nitrobenzaldehyde afforded (Z)-4-(3-methoxyphenyl)-N-(4-nitrobenzylidene) thiazole-2-amine (A1). Acylation of compound (A) with 4-nitrobenzoyl...
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Background & Aims: Heterocyclic compounds are found be abundant in nature, these compounds have many biological properties, and many drugs also contain heterocyclic rings. In this study, antioxidant and anti-fungal properties of the seven pyrazolo[3,4-d]pyrimidine compounds has been studied that synthesized in Iran and their good antibacterial properties have been reported Materials & Methods:...
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In an attempt to find a new class of antimicrobial agents, a series of thiazole derivatives containing furan moiety 3, 7, 8a,b, 10a-c and 12 were prepared via the reaction of 2-cyano-N-(furan-2-ylmethyl)acetamide (1) with phenyl isothiocyanate and α-halocarbonyl compounds. Also, many bithiazolidinone and pyranothiazole derivatives were synthesized through interaction of thiazolidinone 7 with ap...
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Background: In this study, we evaluated antibacterial and antifungle activity of these derivatives against gram positive (Staphylococcus aureus, Bacillus subtilis, B. cereus), gram negative (Proteus vulgaris) bacteria and fungale (Candida albicans, C. tropicalis and C. glabrata). Methods: The broth macro dilution and well agar diffusion methods were used for determination of inhibition zoom (I...
متن کاملSynthesis and Anticandidal Activity Evaluation of New Benzimidazole-Thiazole Derivatives.
Azole-based antifungal agents constitute one of the important classes of antifungal drugs. Hence, in the present work, 12 new benzimidazole-thiazole derivatives 3a-3l were synthesized to evaluate their anticandidal activity against C.albicans, C.glabrata, C.krusei, and C.parapsilopsis. The structures of the newly synthesized compounds 3a-3l were confirmed by IR, ¹H-NMR, 13C-NMR, and ESI-MS spec...
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ژورنال
عنوان ژورنال: Journal of Saudi Chemical Society
سال: 2012
ISSN: 1319-6103
DOI: 10.1016/j.jscs.2011.02.007