Synthesis, Characterization and Biological Activities of Substituted 1-[Benzothiazol-(1H)-2-yl]-3-phenyl-prop-2-en-1-ones

C. Anuba, T. Reji
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Abstract

A series of ortho and para substituted 1-[benzothiazol-(1H)-2-yl]-3-phenyl-prop-2-en-1-one derivatives were synthesized from 2-acetyl benzothiazole and ortho and para-substituted benzaldehye using ethanol as solvent. The synthesized compounds were characterized by UV-visible, FT-IR, 1H NMR and mass spectrometry. Antioxidant activities of synthesized compounds have been evaluated by DPPH free radical scavenging activity using ascorbic acid as standard. The standard solution and 1-[benzothiazol- (1H)-2-yl]-3-phenylprop-2-en-1-ones compounds were prepared with different concentrations. Anticancer activity of 1-[benzothiazol-(1H)-2-yl]-3-phenylprop-2-en-1-one and 1-[benzothiazol-(1H)- 2-yl]-3(4-chlorophenyl)prop-2-en-1-one were assigned by MTT assays.
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取代1-[苯并噻唑-(1H)-2-基]-3-苯基-丙-2-烯-1的合成、表征及生物活性
以2-乙酰苯并噻唑和邻苯并甲醛为原料,以乙醇为溶剂合成了一系列邻苯并噻唑-(1H)-2-基]-3-苯基丙烷-2-烯-1- 1衍生物。合成的化合物通过紫外可见光谱、红外光谱、核磁共振氢谱和质谱进行了表征。以抗坏血酸为标准,通过对DPPH自由基的清除活性来评价合成化合物的抗氧化活性。制备了不同浓度的标准溶液和1-[苯并噻唑-(1H)-2-基]-3-苯基丙-2-烯-1-酮化合物。用MTT法测定了1-[苯并噻唑-(1H)-2-基]-3-苯基prop-2-en-1和1-[苯并噻唑-(1H)-2-基]-3(4-氯苯基)prop-2-en-1的抗癌活性。
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