J
Jingman Ni
Researcher at Lanzhou University
Publications - 48
Citations - 857
Jingman Ni is an academic researcher from Lanzhou University. The author has contributed to research in topics: Antimicrobial & Antimicrobial peptides. The author has an hindex of 15, co-authored 39 publications receiving 527 citations. Previous affiliations of Jingman Ni include Macau University of Science and Technology.
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An organocatalytic Michael-Michael cascade for the enantioselective construction of spirocyclopentane bioxindoles: control of four contiguous stereocenters.
TL;DR: The straightforward process, catalyzed by a bifunctional chiral squaramide catalyst, serves as a powerful tool for the enantioselective construction of potentially biological bioxindoles with four contiguous chiral centers, of which two are spiro all-carbon quaternary centers on a single cyclopentane ring.
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Antimicrobial peptides conjugated with fatty acids on the side chain of D-amino acid promises antimicrobial potency against multidrug-resistant bacteria
TL;DR: The results from the outer/inner membrane permeabilization and cytoplasmic membrane depolarization assays and flow cytometry and scanning electron microscopy analyses demonstrated that the new peptides exert antimicrobial effects by typical non-receptor-mediated membrane mechanisms, as well as intracellular targets characterized by gel retardation and reactive oxygen species (ROS) generation assays.
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Lipid-lowering, hepatoprotective, and atheroprotective effects of the mixture Hong-Qu and gypenosides in hyperlipidemia with NAFLD rats.
Sanhu Gou,Haifeng Huang,Xinyue Chen,Jie Liu,Miao He,Yinyun Ma,Xiao-Ning Zhao,Yun Zhang,Jingman Ni +8 more
TL;DR: HG is beneficial for regulating the stability of blood lipids, has atheroprotective characteristics and may prevent nonalcoholic fatty liver disease (NAFLD), providing more than just a theoretical basis for drug research of cardiovascular disease (CVD) treatment.
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Design and synthesis of new N-terminal fatty acid modified-antimicrobial peptide analogues with potent in vitro biological activity.
Chao Zhong,Tianqi Liu,Sanhu Gou,Yongtao He,Ningyi Zhu,Yuewen Zhu,Li Wang,Hui Liu,Yun Zhang,Jia Yao,Jingman Ni +10 more
TL;DR: The conjugation of fatty acids at the N-terminus of peptides and dimerization are promising strategies for obtaining potent antimicrobial agents.
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The effect of halogenation on the antimicrobial activity, antibiofilm activity, cytotoxicity and proteolytic stability of the antimicrobial peptide Jelleine-I.
Fengjing Jia,Yi Zhang,Jiayi Wang,Jinxiu Peng,Ping Zhao,Lishi Zhang,Haiyan Yao,Jingman Ni,Kairong Wang +8 more
TL;DR: A series of halogenated derivatives of the antimicrobial peptide Jelleine‐I were designed and synthesized and showed that the in vitro antimicrobial activity, antibiofilm activity and in vivo antimicrobial efficacy were enhanced 1–8‐fold after halogenation.