{"title":"利巴韦林类似物作为核苷酶抑制剂的生物自传和合成","authors":"A. Srinivas","doi":"10.1134/S1070428024604382","DOIUrl":null,"url":null,"abstract":"<p>Ribavirin analogues were synthesized starting from D-glucose through a series of reactions. The structure of the synthesized compounds was confirmed by IR, NMR, and mass spectrometry. Their nucleosidase enzyme inhibitory activity was tested using TLC bioautography. Almost all of the compounds exhibited enzyme inhibitory activity.</p>","PeriodicalId":766,"journal":{"name":"Russian Journal of Organic Chemistry","volume":"61 3","pages":"527 - 534"},"PeriodicalIF":0.8000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioautography and Synthesis of Ribavirin Analogues as Possible Nucleosidase Inhibitors\",\"authors\":\"A. Srinivas\",\"doi\":\"10.1134/S1070428024604382\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Ribavirin analogues were synthesized starting from D-glucose through a series of reactions. The structure of the synthesized compounds was confirmed by IR, NMR, and mass spectrometry. Their nucleosidase enzyme inhibitory activity was tested using TLC bioautography. Almost all of the compounds exhibited enzyme inhibitory activity.</p>\",\"PeriodicalId\":766,\"journal\":{\"name\":\"Russian Journal of Organic Chemistry\",\"volume\":\"61 3\",\"pages\":\"527 - 534\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-05-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1070428024604382\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070428024604382","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Bioautography and Synthesis of Ribavirin Analogues as Possible Nucleosidase Inhibitors
Ribavirin analogues were synthesized starting from D-glucose through a series of reactions. The structure of the synthesized compounds was confirmed by IR, NMR, and mass spectrometry. Their nucleosidase enzyme inhibitory activity was tested using TLC bioautography. Almost all of the compounds exhibited enzyme inhibitory activity.
期刊介绍:
Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.