Lulu Wu, Lijun Shi, Liangxin Fan, Zhenliang Pan, Zhonglin Zhao, Hui Su, Caixia Wang, Nan Yang, Cuilian Xu, Guoyu Yang
{"title":"封面图片:氨基葡萄糖芳香衍生物的合成及其对四种作物植物病原真菌的抗真菌活性(化学.)","authors":"Lulu Wu, Lijun Shi, Liangxin Fan, Zhenliang Pan, Zhonglin Zhao, Hui Su, Caixia Wang, Nan Yang, Cuilian Xu, Guoyu Yang","doi":"10.1002/cbdv.202471102","DOIUrl":null,"url":null,"abstract":"<p><b>Cover Feature</b>. A series of diversified glucosamine derivatives was synthesized and their antifungal activity was examined against crop phytopathogens. One of compounds showed remarkable antifungal activity against <i>Fusarium graminearum</i> with EC<sub>50</sub> value of 3.96 μg/mL. 3D-QSAR model with the statistically recommended values (r<sup>2</sup>=0.915, q<sup>2</sup>=0.872) showed that positive charge group or bulky group in the benzyl ring was favorable for the antifungal activity. More details can be found in article number e202401052 by Guoyu Yang and co-workers (see 10.1002/cbdv.202401052).\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":9878,"journal":{"name":"Chemistry & Biodiversity","volume":"21 11","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cbdv.202471102","citationCount":"0","resultStr":"{\"title\":\"Cover Picture: Synthesis and Antifungal Activities of Glucosamine Aromatic Derivatives Against Four Phytopathogenic Fungi of Crops (Chem. Biodiversity 11/2024)\",\"authors\":\"Lulu Wu, Lijun Shi, Liangxin Fan, Zhenliang Pan, Zhonglin Zhao, Hui Su, Caixia Wang, Nan Yang, Cuilian Xu, Guoyu Yang\",\"doi\":\"10.1002/cbdv.202471102\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>Cover Feature</b>. A series of diversified glucosamine derivatives was synthesized and their antifungal activity was examined against crop phytopathogens. One of compounds showed remarkable antifungal activity against <i>Fusarium graminearum</i> with EC<sub>50</sub> value of 3.96 μg/mL. 3D-QSAR model with the statistically recommended values (r<sup>2</sup>=0.915, q<sup>2</sup>=0.872) showed that positive charge group or bulky group in the benzyl ring was favorable for the antifungal activity. More details can be found in article number e202401052 by Guoyu Yang and co-workers (see 10.1002/cbdv.202401052).\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":9878,\"journal\":{\"name\":\"Chemistry & Biodiversity\",\"volume\":\"21 11\",\"pages\":\"\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-11-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cbdv.202471102\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry & Biodiversity\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cbdv.202471102\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry & Biodiversity","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cbdv.202471102","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Cover Picture: Synthesis and Antifungal Activities of Glucosamine Aromatic Derivatives Against Four Phytopathogenic Fungi of Crops (Chem. Biodiversity 11/2024)
Cover Feature. A series of diversified glucosamine derivatives was synthesized and their antifungal activity was examined against crop phytopathogens. One of compounds showed remarkable antifungal activity against Fusarium graminearum with EC50 value of 3.96 μg/mL. 3D-QSAR model with the statistically recommended values (r2=0.915, q2=0.872) showed that positive charge group or bulky group in the benzyl ring was favorable for the antifungal activity. More details can be found in article number e202401052 by Guoyu Yang and co-workers (see 10.1002/cbdv.202401052).
期刊介绍:
Chemistry & Biodiversity serves as a high-quality publishing forum covering a wide range of biorelevant topics for a truly international audience. This journal publishes both field-specific and interdisciplinary contributions on all aspects of biologically relevant chemistry research in the form of full-length original papers, short communications, invited reviews, and commentaries. It covers all research fields straddling the border between the chemical and biological sciences, with the ultimate goal of broadening our understanding of how nature works at a molecular level.
Since 2017, Chemistry & Biodiversity is published in an online-only format.