Lei Wang

ORCID: 0000-0002-8181-5644
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Heat shock proteins research
  • Computational Drug Discovery Methods
  • Genomics, phytochemicals, and oxidative stress
  • Natural product bioactivities and synthesis
  • Cholinesterase and Neurodegenerative Diseases
  • ATP Synthase and ATPases Research
  • Bioactive Natural Diterpenoids Research
  • Toxin Mechanisms and Immunotoxins
  • Ubiquitin and proteasome pathways
  • Plant-based Medicinal Research
  • Phytochemical Studies and Bioactivities
  • Protein Structure and Dynamics
  • Click Chemistry and Applications
  • Plant biochemistry and biosynthesis
  • Glutathione Transferases and Polymorphisms
  • Protein Degradation and Inhibitors
  • Phytochemistry and Biological Activities
  • Histone Deacetylase Inhibitors Research
  • Alzheimer's disease research and treatments
  • Endoplasmic Reticulum Stress and Disease
  • DNA Repair Mechanisms
  • Nicotinic Acetylcholine Receptors Study
  • Protein Tyrosine Phosphatases
  • Cancer Mechanisms and Therapy
  • Peptidase Inhibition and Analysis

State Key Laboratory of Natural Medicine
2016-2025

China Pharmaceutical University
2016-2025

Fudan University
2025

Hebei North University
2023-2024

University of Connecticut
2024

Wuhan University
2022-2024

Changhai Hospital
2017-2024

Renmin Hospital of Wuhan University
2022-2024

Zhongyuan University of Technology
2023-2024

Binzhou University
2015-2024

Triazole demonstrates distinctive physicochemical properties, characterized by weak basicity, various dipole moments, and significant dual hydrogen bond acceptor donor capabilities. These features are poised to play a pivotal role in drug–target interactions. The inherent polarity of triazole contributes its lower logP, suggesting the potential improvement water solubility. metabolic stability adds additional value drug discovery. Moreover, metal-binding capacity nitrogen atom lone pair...

10.1021/acs.jmedchem.4c00652 article EN Journal of Medicinal Chemistry 2024-05-03

Tumor necrosis factor alpha (TNFalpha) has been used to treat certain tumors in clinic trials. However, the curative effect of TNFalpha undermined by induced-NF-kappaB activation many types tumor. Maslinic acid (MA), a pharmacological safe natural product, known for its important effects as anti-oxidant, anti-inflammatory, and anti-viral activities. The aim this study was determine whether MA potentiates anti-tumor activity though regulation NF-kappaB activation.In study, we demonstrate that...

10.1186/1476-4598-9-73 article EN cc-by Molecular Cancer 2010-04-06

// Chao Zhang 1, 2 , Hui-Jie Wang Qi-Chao Bao Lei Tian-Kun Guo Wei-Lin Chen Li-Li Xu Hai-Shan Zhou Jin-Lei Bian Ying-Rui Yang Hao-Peng Sun 2, 3 Xiao-Li Qi-Dong You 1 Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing, 210009, State Natural Medicines, Department Medicinal Chemistry, School Pharmacy, Correspondence to: Xu, email: xuxiao_li@126.com You, youqidong@gmail.com Keywords: NRF2, breast cancer, RhoA/ROCK pathway, cell proliferation,...

10.18632/oncotarget.12435 article EN Oncotarget 2016-10-04

Directly disrupting the Hsp90-Cdc37 complex can selectively down-regulate kinase clients of Hsp90 and achieve cell cycle arrest.

10.1126/sciadv.aax2277 article EN cc-by-nc Science Advances 2019-09-06

A normal phosphorylation state is essential for the function of proteins. Biased regulation frequently results in morbidity, especially hyperphosphorylation oncoproteins. The ASK1 at Thr838 leads to a persistently high activity state, which accelerates course gastric cancer. Under conditions, PP5 specifically dephosphorylates p-ASK1T838 cells, thereby weakening low-basal state. However, tumor types, shows low with self-inhibition mechanism, making remain level. Thus, we aim design...

10.1021/jacs.2c10759 article EN Journal of the American Chemical Society 2022-12-22

Herein, we report a series of selective sub-nanomolar inhibitors against butyrylcholinesterase (BChE). These compounds, bearing novel N-benzyl benzamide scaffold, inhibited BChE with IC50 from picomolar to nanomolar. The inhibitory activity was confirmed by the surface plasmon resonance assay, showing KD value, which revealed that compounds exert effect through directly binding BChE. Several showed neuroprotective effects verified oxidative damage model. Furthermore, safety S11-1014 and...

10.1021/acs.jmedchem.2c00944 article EN Journal of Medicinal Chemistry 2022-08-15

Butyrylcholinesterase (BChE) is a promising biomarker and effective therapeutic target for Alzheimer's disease (AD). Herein, we designed BChE-activated near-infrared (NIR) probe,

10.1021/acs.jmedchem.4c00355 article EN Journal of Medicinal Chemistry 2024-03-28

Introduction The 90-kDa heat shock protein (HSP90) functions as a molecular chaperone, it assumes significant role in diseases such cancer, inflammation, neurodegeneration, and infection. Therefore, the research development of HSP90 inhibitors have garnered considerable attention.

10.1080/13543776.2024.2327295 article EN Expert Opinion on Therapeutic Patents 2024-02-01
Coming Soon ...