Wuying Yang
Jiangxi Agricultural University
11 Papers
4 Citations
Wuying Yang is an academic researcher from Jiangxi Agricultural University. The author has contributed to research in topics: Chemistry & Maslinic acid. The author has an hindex of 3, co-authored 5 publications.
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Papers
Nanobody@Biomimetic mineralized MOF as a sensing immunoprobe in detection of aflatoxin B1.
TL;DR: In this article , the authors proposed an immunoprobe integration of nanobody and biomimetic mineralized metal-organic frameworks (MOF), in which plenty of succinylated horseradish peroxidase (sHRP) were encapsulated within a single MOF and the Nb was assembled on the biomimic mineralized MOF.
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Dye-sensitized solar cells based on (D−π−A)3L2 phenothiazine dyes containing auxiliary donors and flexible linkers with different length of carbon chain
Wuying Yang,Derong Cao,Hai Zhang,Xiaoli Yin,Xiaoning Liao,Jianping Huang,Guoqiang Wu,Li Liyu,Yanping Hong +8 more
TL;DR: In this article, the effect of both auxiliary donors and linkers with different length of carbon chains upon the photophysical, electrochemical as well as photovoltaic properties of the (D−π−A)3L2 dyes were further investigated.
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Synthesis of water soluble pentacyclic dihydroxyterpene carboxylic acid derivatives coupled amino acids and their inhibition activities on α-glucosidase.
TL;DR: All of the derivatives possess lower inhibitory properties of α-glucosidase than those of the parent compounds in the measurement system of DMSO solution, even if the derivatives exhibit better water solubility than that of theparent compounds.
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Semi-synthesis of C28-modified triterpene acid derivatives from maslinic acid or corosolic acid as potential α-glucosidase inhibitors
Xiaoqin Liu,Xufeng Zang,Xiaoli Yin,Wuying Yang,Jinxiang Huang,Jianping Huang,Chunxian Yu,Chunshan Ke,Yanping Hong +8 more
TL;DR: The result of enzyme kinetics study reveals that the inhibitory mechanism of the compound 12b is non-competitive inhibition and the inhibition constant Ki is 570 µM, and the binding interaction between compounds with α-glucosidase are predicted by molecular docking simulation.
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Pentacyclic triterpene carboxylic acids derivatives integrated piperazine-amino acid complexes for α-glucosidase inhibition in vitro
TL;DR: In this paper, the piperazine complex of l -amino acids at the C-28 site of the parent compounds was evaluated in vitro and the α-glucosidase inhibitory activities of the pristine derivatives were evaluated.
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