E. M. Brahmana, J. Kaban, G. Haro, J. Tarigan, B. Wirjosentono, Tamrin, M. Ginting
{"title":"化合物(E)-1-(3-溴苯基)-3-对甲基丙基-2-烯-1-on的合成、抗氧化及毒性活性","authors":"E. M. Brahmana, J. Kaban, G. Haro, J. Tarigan, B. Wirjosentono, Tamrin, M. Ginting","doi":"10.5220/0008836400050009","DOIUrl":null,"url":null,"abstract":"Halogen substituted analog compound chalcone (E)-1-(3-bromophenyl)-3-p-tolylprop-2-en-1-on was synthesized from 4-metylbenzaldehyde as aldehydes with 3bromoacetophenone, as ketones by using aldol condensation reaction. The compound resulted rendement with value of 62,38% and characterized by using UV, IR, MS, and 1HNMR. Test of antioxidant activity using DPPH method showed that those compounds have low potency as antioxidant agent LC50 with value 571, 7903 ppm. Toxicity tests using Brine Shrimp Lethality Test (BSLT) showed that those compounds have a potency as anticancer agent with LC50 value","PeriodicalId":20533,"journal":{"name":"Proceedings of the 1st International Conference on Chemical Science and Technology Innovation","volume":"88 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, Antioxidant and Toxicity Activity of Compounds (E)-1-(3-bromophenyl)-3-p tolylprop-2-en-1-on\",\"authors\":\"E. M. Brahmana, J. Kaban, G. Haro, J. Tarigan, B. Wirjosentono, Tamrin, M. Ginting\",\"doi\":\"10.5220/0008836400050009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Halogen substituted analog compound chalcone (E)-1-(3-bromophenyl)-3-p-tolylprop-2-en-1-on was synthesized from 4-metylbenzaldehyde as aldehydes with 3bromoacetophenone, as ketones by using aldol condensation reaction. The compound resulted rendement with value of 62,38% and characterized by using UV, IR, MS, and 1HNMR. Test of antioxidant activity using DPPH method showed that those compounds have low potency as antioxidant agent LC50 with value 571, 7903 ppm. Toxicity tests using Brine Shrimp Lethality Test (BSLT) showed that those compounds have a potency as anticancer agent with LC50 value\",\"PeriodicalId\":20533,\"journal\":{\"name\":\"Proceedings of the 1st International Conference on Chemical Science and Technology Innovation\",\"volume\":\"88 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the 1st International Conference on Chemical Science and Technology Innovation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5220/0008836400050009\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the 1st International Conference on Chemical Science and Technology Innovation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5220/0008836400050009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis, Antioxidant and Toxicity Activity of Compounds (E)-1-(3-bromophenyl)-3-p tolylprop-2-en-1-on
Halogen substituted analog compound chalcone (E)-1-(3-bromophenyl)-3-p-tolylprop-2-en-1-on was synthesized from 4-metylbenzaldehyde as aldehydes with 3bromoacetophenone, as ketones by using aldol condensation reaction. The compound resulted rendement with value of 62,38% and characterized by using UV, IR, MS, and 1HNMR. Test of antioxidant activity using DPPH method showed that those compounds have low potency as antioxidant agent LC50 with value 571, 7903 ppm. Toxicity tests using Brine Shrimp Lethality Test (BSLT) showed that those compounds have a potency as anticancer agent with LC50 value