{"title":"新型1,2,4-三唑类5-吲哚吡啶-4-噻唑烷酮衍生物的合成","authors":"T. Khan, R. Yadav","doi":"10.14233/ajomc.2019.ajomc-p214","DOIUrl":null,"url":null,"abstract":"A series of 1,2,4-triazolyl-4-(5-indolylidene)-thiazolidinone derivatives were synthesized and screened\nfor their antifungal and antioxidant activity. Among these synthesized compounds 3d, 3g showing\ngood antifungal activity and compounds 3b, 3d, 3f and 3h have high % antioxidant activity with lower\nIC50 value of 11.21, 20.89, 17.51 and 14.05 respectively. We report the antioxidant potential of the said\nclass of compound in which free radical is generated by methelenic and 2nd carbon of thiazolidinone\nring. The antifungal activity reported against A. niger, C. albicans and A. flavus. The antioxidant\nactivity of all the synthesized compounds was screened by H2O2, DPPH scavenging and by\nphosphomolybdenum method with respect to ascorbic acid.","PeriodicalId":8846,"journal":{"name":"Asian Journal of Organic & Medicinal Chemistry","volume":"305 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of Some New 5-Indolylidene-4-thiazolidinone Derivatives of\\n1,2,4-triazole as Potent Antioxidant and Antifungal Agents\",\"authors\":\"T. Khan, R. Yadav\",\"doi\":\"10.14233/ajomc.2019.ajomc-p214\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A series of 1,2,4-triazolyl-4-(5-indolylidene)-thiazolidinone derivatives were synthesized and screened\\nfor their antifungal and antioxidant activity. Among these synthesized compounds 3d, 3g showing\\ngood antifungal activity and compounds 3b, 3d, 3f and 3h have high % antioxidant activity with lower\\nIC50 value of 11.21, 20.89, 17.51 and 14.05 respectively. We report the antioxidant potential of the said\\nclass of compound in which free radical is generated by methelenic and 2nd carbon of thiazolidinone\\nring. The antifungal activity reported against A. niger, C. albicans and A. flavus. The antioxidant\\nactivity of all the synthesized compounds was screened by H2O2, DPPH scavenging and by\\nphosphomolybdenum method with respect to ascorbic acid.\",\"PeriodicalId\":8846,\"journal\":{\"name\":\"Asian Journal of Organic & Medicinal Chemistry\",\"volume\":\"305 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-p214\",\"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-p214","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of Some New 5-Indolylidene-4-thiazolidinone Derivatives of
1,2,4-triazole as Potent Antioxidant and Antifungal Agents
A series of 1,2,4-triazolyl-4-(5-indolylidene)-thiazolidinone derivatives were synthesized and screened
for their antifungal and antioxidant activity. Among these synthesized compounds 3d, 3g showing
good antifungal activity and compounds 3b, 3d, 3f and 3h have high % antioxidant activity with lower
IC50 value of 11.21, 20.89, 17.51 and 14.05 respectively. We report the antioxidant potential of the said
class of compound in which free radical is generated by methelenic and 2nd carbon of thiazolidinone
ring. The antifungal activity reported against A. niger, C. albicans and A. flavus. The antioxidant
activity of all the synthesized compounds was screened by H2O2, DPPH scavenging and by
phosphomolybdenum method with respect to ascorbic acid.