中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis and antifungal evaluation of (1,2,3-triazol-4-yl)methyl nicotinate chitosan

文献类型:期刊论文

作者Qin, Yukun1; Liu, Song1; Xing, Ronge1; Li, Kecheng1,2; Yu, Huahua1; Li, Pengcheng1
刊名INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
出版日期2013-10-01
卷号61页码:58-62
关键词Chitosan 1 Click reaction Characterization Antifungal activity 2 3-Triazole
ISSN号0141-8130
通讯作者Xing, RG
中文摘要With an aim to discover novel chitosan derivatives with significant activities against crop-threatening fungi, (1,2,3-triazol-4-yl)methyl nicotinate chitosan (TAMNCS) was prepared via azide-alkyne click reaction. Its structure was characterized by FT-IR, H-1 NMR, elemental analysis, DSC, and SEM. In vitro antifungal properties of TAMNCS against Rhizoctonia solani Kuhn (R. solani), Stemphylium solani weber (S. solani), and Alternaria porri (A. porri) were studied at the concentrations ranged from 0.25 mg/mL to 1.0 mg/mL. Experiments conducted displayed the derivative had obviously enhanced antifungal activity after chemical modification compared with original chitosan. Moreover, it was shown that TAMNCS can 94.2% inhibit growth of A. pouf at 1.0 mg/mL, while dose at which the fungicide triadimefon had lower inhibitory index (62.2%). The primary antifungal results described here indicate this derivative may be a promising candidate as an antifungal agent. (C). 2013 Elsevier B.V. All rights reserved.
英文摘要With an aim to discover novel chitosan derivatives with significant activities against crop-threatening fungi, (1,2,3-triazol-4-yl)methyl nicotinate chitosan (TAMNCS) was prepared via azide-alkyne click reaction. Its structure was characterized by FT-IR, H-1 NMR, elemental analysis, DSC, and SEM. In vitro antifungal properties of TAMNCS against Rhizoctonia solani Kuhn (R. solani), Stemphylium solani weber (S. solani), and Alternaria porri (A. porri) were studied at the concentrations ranged from 0.25 mg/mL to 1.0 mg/mL. Experiments conducted displayed the derivative had obviously enhanced antifungal activity after chemical modification compared with original chitosan. Moreover, it was shown that TAMNCS can 94.2% inhibit growth of A. pouf at 1.0 mg/mL, while dose at which the fungicide triadimefon had lower inhibitory index (62.2%). The primary antifungal results described here indicate this derivative may be a promising candidate as an antifungal agent. (C). 2013 Elsevier B.V. All rights reserved.
WOS标题词Science & Technology ; Life Sciences & Biomedicine
学科主题Biochemistry & Molecular Biology
类目[WOS]Biochemistry & Molecular Biology
研究领域[WOS]Biochemistry & Molecular Biology
关键词[WOS]CLICK CHEMISTRY ; CARBOXYMETHYL CHITOSAN ; THIOUREA DERIVATIVES ; CHITIN
收录类别SCI
原文出处10.1016/j.ijbiomac.2013.05.023
语种英语
WOS记录号WOS:000326660700009
公开日期2014-07-17
源URL[http://ir.qdio.ac.cn/handle/337002/16724]  
专题海洋研究所_海洋生物技术研发中心
海洋研究所_海洋环境工程技术研究发展中心
作者单位1.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100039, Peoples R China
推荐引用方式
GB/T 7714
Qin, Yukun,Liu, Song,Xing, Ronge,et al. Synthesis and antifungal evaluation of (1,2,3-triazol-4-yl)methyl nicotinate chitosan[J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,2013,61:58-62.
APA Qin, Yukun,Liu, Song,Xing, Ronge,Li, Kecheng,Yu, Huahua,&Li, Pengcheng.(2013).Synthesis and antifungal evaluation of (1,2,3-triazol-4-yl)methyl nicotinate chitosan.INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,61,58-62.
MLA Qin, Yukun,et al."Synthesis and antifungal evaluation of (1,2,3-triazol-4-yl)methyl nicotinate chitosan".INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES 61(2013):58-62.

入库方式: OAI收割

来源:海洋研究所

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