Bingwen Liang

Medicine · Health Sciences

16h-index996citations25works25.52yr avg
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Research Topics

Natural Antidiabetic Agents Studies(7), Carbohydrate Chemistry and Synthesis(4), Neuroinflammation and Neurodegeneration Mechanisms(4), Advancements in Transdermal Drug Delivery(3), Natural product bioactivities and synthesis(3)

Publications25 total

Corrigendum to “JLX001 Ameliorates ischemia/reperfusion injury by reducing neuronal apoptosis via downregulating JNK signaling pathway” [Neuroscience 418 (2019) 189–204]
Neuroscience·2025
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
Unlocking the Stratum Corneum Barrier to Skin Penetration for the Transdermal Delivery of Cyclovirobuxine D
Pharmaceutics·2024· 4 citedOpen Access
Novel coumarin-thiazolidine-2,4‑dione hybrids as potential α-glucosidase inhibitors: Synthesis and bioactivity evaluation
Journal of Molecular Structure·2024· 21 cited
Expert consensus on the technical specifications of the in vitro skin penetration test of cosmetic product by Franz diffusion cell
Journal of Dermatologic Science and Cosmetic Technology·2024· 1 citedOpen Access
Novel thiosemicarbazide-based β-carboline derivatives as α-glucosidase inhibitors: Synthesis and biological evaluation
European Journal of Medicinal Chemistry·2024· 75 citedOpen Access
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
Synthesis and biological evaluation of indole derivatives containing thiazolidine-2,4-dione as α-glucosidase inhibitors with antidiabetic activity
European Journal of Medicinal Chemistry·2023· 104 citedOpen Access
Identification of 1,3,4-oxadiazolyl-containing β-carboline derivatives as novel α-glucosidase inhibitors with antidiabetic activity
European Journal of Medicinal Chemistry·2023· 60 citedOpen Access
Preparation and Evaluation of Auxiliary Permeable Microneedle Patch Composed of Polyvinyl Alcohol and Eudragit NM30D Aqueous Dispersion
Pharmaceutics·2023· 6 citedOpen Access
New β-carboline derivatives as potential α-glucosidase inhibitor: Synthesis and biological activity evaluation
Journal of Molecular Structure·2023· 57 cited
JLX001 attenuates blood-brain barrier dysfunction in MCAO/R rats via activating the Wnt/β-catenin signaling pathway
Life Sciences·2020· 22 cited
JLX001 improves myocardial ischemia-reperfusion injury by activating Jak2-Stat3 pathway
Life Sciences·2020· 30 cited
JLX001 Ameliorates Ischemia/Reperfusion Injury by Reducing Neuronal Apoptosis via Down-Regulating JNK Signaling Pathway
Neuroscience·2019· 18 cited
Therapeutic effects of JLX-001 on ischemic stroke by inducing autophagy via AMPK-ULK1 signaling pathway in rats
Brain Research Bulletin·2019· 23 cited
JLX001 Modulated the Inflammatory Reaction and Oxidative Stress in pMCAO Rats via Inhibiting the TLR2/4-NF-κB Signaling Pathway
Neurochemical Research·2019· 22 cited
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Frequent Co-authors

Jinping Sun(7), Weiyang Shen(7), Zhuang Xiong(6), Xue-Tao Xu(6), Xiaofeng Min(6), Yunman Li(6), Xuetao Xu(5), Jiangyi Li(4), Shao‐Hua Wang(4), Wen‐Hua Chen(4), Xiong Zhu(4), Luyao Ao(4), Lin Zhou(4), Yunyi Yan(4), Di Xiao(3), Qiyang Yin(3), Yuxiang Fei(3), Wan-ting Li(3), Anqi Ye(3), Cheng-yuan Li(3)