{"title":"Synthesis, Characterization and Biological Activities of Substituted\n1-[Benzothiazol-(1H)-2-yl]-3-phenyl-prop-2-en-1-ones","authors":"C. Anuba, T. Reji","doi":"10.14233/ajomc.2019.ajomc-p181","DOIUrl":null,"url":null,"abstract":"A series of ortho and para substituted 1-[benzothiazol-(1H)-2-yl]-3-phenyl-prop-2-en-1-one derivatives\nwere synthesized from 2-acetyl benzothiazole and ortho and para-substituted benzaldehye using ethanol\nas solvent. The synthesized compounds were characterized by UV-visible, FT-IR, 1H NMR and mass\nspectrometry. Antioxidant activities of synthesized compounds have been evaluated by DPPH free\nradical scavenging activity using ascorbic acid as standard. The standard solution and 1-[benzothiazol-\n(1H)-2-yl]-3-phenylprop-2-en-1-ones compounds were prepared with different concentrations.\nAnticancer activity of 1-[benzothiazol-(1H)-2-yl]-3-phenylprop-2-en-1-one and 1-[benzothiazol-(1H)-\n2-yl]-3(4-chlorophenyl)prop-2-en-1-one were assigned by MTT assays.","PeriodicalId":8846,"journal":{"name":"Asian Journal of Organic & Medicinal Chemistry","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic & Medicinal Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14233/ajomc.2019.ajomc-p181","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.