G. F. Vafina, T. A. Sapozhnikova, S. F. Gabdrakhmanova
{"title":"马来酰亚胺的2-安替吡林-、(5-硫氧-2,5-二氢- 1h -1,2,4-三唑)-6- yl -、(1,3,4-噻二唑-2- yl)-6-羧基酰胺-、6-硫脲-和6-肼基硫醇衍生物的体外抗氧化活性","authors":"G. F. Vafina, T. A. Sapozhnikova, S. F. Gabdrakhmanova","doi":"10.1007/s10600-025-04790-4","DOIUrl":null,"url":null,"abstract":"<p>New derivatives of maleopimaric acid containing phenylthioureide fragments were synthesized. The antioxidant activity of 24 maleopimaric acid derivatives in the 2- and 6-positions was studied in three in vitro models, i.e., FRAP, reduction of DPPH radical, and reduction of ABTS radical. Methyl-, 2-isonicotinoyl-, and 2-(pyridin-3-ylcarbonyl)hydrazinocarbonothioyl derivatives of 2-allylmaleopimarimide showed antioxidant activity in vitro in the ABTS model comparable to the reference drug ascorbic acid and superior than that of Trolox.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 5","pages":"936 - 940"},"PeriodicalIF":0.9000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antioxidant Activity in vitro of 2-Antipyrine-, (5-Thioxo-2,5-Dihydro-1H-1,2,4-Triazol)-6-YL-, (1,3,4-Thiadiazol-2-YL)-6-Carboxamide-, 6-Thioureide-, and 6-Hydrazinothiol Derivatives of Maleopimarimide\",\"authors\":\"G. F. Vafina, T. A. Sapozhnikova, S. F. Gabdrakhmanova\",\"doi\":\"10.1007/s10600-025-04790-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>New derivatives of maleopimaric acid containing phenylthioureide fragments were synthesized. The antioxidant activity of 24 maleopimaric acid derivatives in the 2- and 6-positions was studied in three in vitro models, i.e., FRAP, reduction of DPPH radical, and reduction of ABTS radical. Methyl-, 2-isonicotinoyl-, and 2-(pyridin-3-ylcarbonyl)hydrazinocarbonothioyl derivatives of 2-allylmaleopimarimide showed antioxidant activity in vitro in the ABTS model comparable to the reference drug ascorbic acid and superior than that of Trolox.</p>\",\"PeriodicalId\":514,\"journal\":{\"name\":\"Chemistry of Natural Compounds\",\"volume\":\"61 5\",\"pages\":\"936 - 940\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry of Natural Compounds\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10600-025-04790-4\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Natural Compounds","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10600-025-04790-4","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Antioxidant Activity in vitro of 2-Antipyrine-, (5-Thioxo-2,5-Dihydro-1H-1,2,4-Triazol)-6-YL-, (1,3,4-Thiadiazol-2-YL)-6-Carboxamide-, 6-Thioureide-, and 6-Hydrazinothiol Derivatives of Maleopimarimide
New derivatives of maleopimaric acid containing phenylthioureide fragments were synthesized. The antioxidant activity of 24 maleopimaric acid derivatives in the 2- and 6-positions was studied in three in vitro models, i.e., FRAP, reduction of DPPH radical, and reduction of ABTS radical. Methyl-, 2-isonicotinoyl-, and 2-(pyridin-3-ylcarbonyl)hydrazinocarbonothioyl derivatives of 2-allylmaleopimarimide showed antioxidant activity in vitro in the ABTS model comparable to the reference drug ascorbic acid and superior than that of Trolox.
期刊介绍:
Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.