{"title":"1,2,3-三唑类药物改性研究进展","authors":"Adarsh Sahu, Preeti Sahu, R. Agrawal","doi":"10.2174/2212796814999200807214519","DOIUrl":null,"url":null,"abstract":"\n\nMotivated by evidence garnered from literature probing the use of triazoles in\ndrug discovery and development, we reported the utilization of bioisosteric replacement and\nmolecular hybridization in this review. Bio-isosteric replacement has played a significant\nrole in modulating rapid and versatile strategy in synthesizing molecules with multifaceted\nmedicinal properties. Molecular hybridization seeks to conjugate two molecular fragments\nwith diverse applications under very mild reaction conditions. In this regard, 1,2,3-triazole is\na well-known scaffold with widespread occurrence in medicinal compounds. It is characterized\nto have several bioactivities such as anti-microbial, anti-cancer, anti-viral, analgesic, anti-\ninflammatory effects. Furthermore, the structural features of 1,2,3-triazoles enable it to\nmimic different functional groups justifying its use as bio-isostere for the synthesis of new\nmolecules of medicinal interest, which we have reported briefly.\n","PeriodicalId":10784,"journal":{"name":"Current Chemical Biology","volume":"109 1","pages":"71-87"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":"{\"title\":\"A Recent Review on Drug Modification Using 1,2,3-triazole\",\"authors\":\"Adarsh Sahu, Preeti Sahu, R. Agrawal\",\"doi\":\"10.2174/2212796814999200807214519\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nMotivated by evidence garnered from literature probing the use of triazoles in\\ndrug discovery and development, we reported the utilization of bioisosteric replacement and\\nmolecular hybridization in this review. Bio-isosteric replacement has played a significant\\nrole in modulating rapid and versatile strategy in synthesizing molecules with multifaceted\\nmedicinal properties. Molecular hybridization seeks to conjugate two molecular fragments\\nwith diverse applications under very mild reaction conditions. In this regard, 1,2,3-triazole is\\na well-known scaffold with widespread occurrence in medicinal compounds. It is characterized\\nto have several bioactivities such as anti-microbial, anti-cancer, anti-viral, analgesic, anti-\\ninflammatory effects. Furthermore, the structural features of 1,2,3-triazoles enable it to\\nmimic different functional groups justifying its use as bio-isostere for the synthesis of new\\nmolecules of medicinal interest, which we have reported briefly.\\n\",\"PeriodicalId\":10784,\"journal\":{\"name\":\"Current Chemical Biology\",\"volume\":\"109 1\",\"pages\":\"71-87\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Chemical Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2212796814999200807214519\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Chemical Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2212796814999200807214519","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A Recent Review on Drug Modification Using 1,2,3-triazole
Motivated by evidence garnered from literature probing the use of triazoles in
drug discovery and development, we reported the utilization of bioisosteric replacement and
molecular hybridization in this review. Bio-isosteric replacement has played a significant
role in modulating rapid and versatile strategy in synthesizing molecules with multifaceted
medicinal properties. Molecular hybridization seeks to conjugate two molecular fragments
with diverse applications under very mild reaction conditions. In this regard, 1,2,3-triazole is
a well-known scaffold with widespread occurrence in medicinal compounds. It is characterized
to have several bioactivities such as anti-microbial, anti-cancer, anti-viral, analgesic, anti-
inflammatory effects. Furthermore, the structural features of 1,2,3-triazoles enable it to
mimic different functional groups justifying its use as bio-isostere for the synthesis of new
molecules of medicinal interest, which we have reported briefly.
期刊介绍:
Current Chemical Biology aims to publish full-length and mini reviews on exciting new developments at the chemistry-biology interface, covering topics relating to Chemical Synthesis, Science at Chemistry-Biology Interface and Chemical Mechanisms of Biological Systems. Current Chemical Biology covers the following areas: Chemical Synthesis (Syntheses of biologically important macromolecules including proteins, polypeptides, oligonucleotides, oligosaccharides etc.; Asymmetric synthesis; Combinatorial synthesis; Diversity-oriented synthesis; Template-directed synthesis; Biomimetic synthesis; Solid phase biomolecular synthesis; Synthesis of small biomolecules: amino acids, peptides, lipids, carbohydrates and nucleosides; and Natural product synthesis).