Light-induced primary amines and o-nitrobenzyl alcohols cyclization as a versatile photoclick reaction for modular conjugation
文献类型:期刊论文
作者 | Guo, An-Di1,2; Wei, Dan1,2; Nie, Hui-Jun2; Hu, Hao3; Peng, Chengyuan3; Li, Shao-Tong1,2; Yan, Ke-Nian1,2; Zhou, Bin-Shan2; Feng, Lei1,2; Fang, Chao2 |
刊名 | NATURE COMMUNICATIONS |
出版日期 | 2020-10-29 |
卷号 | 11期号:1页码:13 |
ISSN号 | 2041-1723 |
DOI | 10.1038/s41467-020-19274-y |
通讯作者 | Chen, Xiao-Hua(xhchen@simm.ac.cn) |
英文摘要 | The advent of click chemistry has had a profound impact on many fields and fueled a need for reliable reactions to expand the click chemistry toolkit. However, developing new systems to fulfill the click chemistry criteria remains highly desirable yet challenging. Here, we report the development of light-induced primary amines and o-nitrobenzyl alcohols cyclization (PANAC) as a photoclick reaction via primary amines as direct click handle, to rapid and modular functionalization of diverse small molecules and native biomolecules. With intrinsic advantages of temporal control, good biocompatibility, reliable chemoselectivity, excellent efficiency, readily accessible reactants, operational simplicity and mild conditions, the PANAC photoclick is robust for direct diversification of pharmaceuticals and biorelevant molecules, lysine-specific modifications of unprotected peptides and native proteins in vitro, temporal profiling of endogenous kinases and organelle-targeted labeling in living systems. This strategy provides a versatile platform for organic synthesis, bioconjugation, medicinal chemistry, chemical biology and materials science. Developing new click chemistry reactions for robust molecular assembly remains challenging. Here the authors report a light-induced primary amines and o-nitrobenzyl alcohols photoclick cyclization for rapid and modular functionalization of small molecules and native biomolecules, in vitro and in living systems. |
WOS关键词 | CLICK CHEMISTRY ; BIOCONJUGATION ; CYCLOADDITION ; STRATEGIES ; CATALYSTS ; PEPTIDES ; LIGATION ; PROBES |
资助项目 | National Science Foundation of China (NSFC)[21778062] ; National Science & Technology Major Project Key New Drug Creation and Manufacturing Program[2018ZX09711002-008] ; Science and Technology Commission of Shanghai Municipality, China[18431907100] ; Strategic Priority Research Program of the Chinese Academy of Sciences Personalized Medicines-Molecular Signature-based Drug Discovery and Development[XDA12050410] |
WOS研究方向 | Science & Technology - Other Topics |
语种 | 英语 |
出版者 | NATURE RESEARCH |
WOS记录号 | WOS:000591379900014 |
源URL | [http://119.78.100.183/handle/2S10ELR8/292628] |
专题 | 新药研究国家重点实验室 |
通讯作者 | Chen, Xiao-Hua |
作者单位 | 1.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China 2.Chinese Acad Sci, Key Lab Receptor Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 3.Chinese Acad Sci, State Key Lab Drug Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China |
推荐引用方式 GB/T 7714 | Guo, An-Di,Wei, Dan,Nie, Hui-Jun,et al. Light-induced primary amines and o-nitrobenzyl alcohols cyclization as a versatile photoclick reaction for modular conjugation[J]. NATURE COMMUNICATIONS,2020,11(1):13. |
APA | Guo, An-Di.,Wei, Dan.,Nie, Hui-Jun.,Hu, Hao.,Peng, Chengyuan.,...&Chen, Xiao-Hua.(2020).Light-induced primary amines and o-nitrobenzyl alcohols cyclization as a versatile photoclick reaction for modular conjugation.NATURE COMMUNICATIONS,11(1),13. |
MLA | Guo, An-Di,et al."Light-induced primary amines and o-nitrobenzyl alcohols cyclization as a versatile photoclick reaction for modular conjugation".NATURE COMMUNICATIONS 11.1(2020):13. |
入库方式: OAI收割
来源:上海药物研究所
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