Xiaofeng Min

Wuyi University — China

Medicine · Health Sciences

9h-index338citations11works32.92yr avg
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Research Topics

Phytochemicals and Antioxidant Activities(4), melanin and skin pigmentation(4), Biochemical Analysis and Sensing Techniques(4), Natural Antidiabetic Agents Studies(3), Natural product bioactivities and synthesis(3)

Publications11 total

Design, synthesis and biological evaluation of a 1,2,3-triazolyl-bearing betulinic acid derivatives as α-glucosidase inhibitors
Journal of Molecular Structure·2024· 2 cited
Insights into inhibitory action and interaction of bisdemethoxycurcumin on tyrosinase: Spectroscopic and docking analysis
International Journal of Biological Macromolecules·2024· 18 cited
Design, synthesis and biological evaluation of novel betulinic acid derivatives containing 1,2,4-triazole-derived schiff bases as α-glucosidase inhibitors
Journal of Molecular Structure·2024· 4 cited
Identification of 1,3,4-Thiadiazolyl-Containing Thiazolidine-2,4-dione Derivatives as Novel PTP1B Inhibitors with Antidiabetic Activity
Journal of Medicinal Chemistry·2024· 65 citedOpen Access
Synthesis, anti-α-glucosidase activity, inhibition interaction, and anti-diabetic activity of novel cryptolepine derivatives
Journal of Molecular Structure·2024· 42 cited
1,2,3-Triazole-based betulinic acid derivatives as α-glucosidase inhibitors: Synthesis and in vitro and in vivo biological evaluation
Journal of Molecular Structure·2024· 11 cited
Thiazolidine-2,4-dione derivatives as potential α-glucosidase inhibitors: Synthesis, inhibitory activity, binding interaction and hypoglycemic activity
Bioorganic Chemistry·2024· 56 cited
Investigation on the inhibition mechanism and binding behavior of cryptolepine to α-glucosidase and its hypoglycemic activity by multi-spectroscopic method
Journal of Luminescence·2024· 65 cited
In Vitro and In Vivo Biological Evaluation of Indole-thiazolidine-2,4-dione Derivatives as Tyrosinase Inhibitors
Molecules·2023· 17 citedOpen Access
Investigation on the inhibition mechanism and binding behavior of paeonol to tyrosinase and its anti-browning property by multi-spectroscopic and molecular docking methods
International Journal of Biological Macromolecules·2023· 34 cited
Synthesis, Anti-Tyrosinase Activity, and Spectroscopic Inhibition Mechanism of Cinnamic Acid–Eugenol Esters
Molecules·2023· 24 citedOpen Access

Frequent Co-authors

Xuetao Xu(8), Jinping Sun(6), Bingwen Liang(6), Shao‐Hua Wang(3), Xue-Tao Xu(3), Jiangyi Li(3), Zhuang Xiong(3), Wen‐Hua Chen(3), Mengyue Li(2), Yu‐Jing Lu(2), Xi Zheng(2), Yufei Zhang(2), Huiyun Li(1), Lei Xu(1), Jia Li(1), Suqin Guo(1), Jinhui Hu(1), Rihui Wu(1), Mei Feng(1), Li Lu(1)