{"title":"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","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":"{\"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}","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}
Synthesis, Characterization and Biological Activities of Substituted
1-[Benzothiazol-(1H)-2-yl]-3-phenyl-prop-2-en-1-ones
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.