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Design, synthesis and bioevaluation of PI3Kα-selective inhibitors as potential colorectal cancer drugs.

Guizhou Medical University
Design, synthesis and evaluation of novel 1-phenyl-pyrrolo[1,2-b]isoquinolin-3-one derivatives as antagonists for the glycine binding site of the NMDA receptor.

Guizhou Medical University
Novel carbazole-oxadiazole derivatives as anti-α-glucosidase and anti-α-amylase agents: Design, synthesis, molecular docking, and biological evaluation.

Guizhou Medical University
Advances in dual-targeting inhibitors of HDAC6 for cancer treatment.

Guizhou Medical University
Design, Synthesis, Formulation, and Bioevaluation of Trisubstituted Triazines as Highly Selective mTOR Inhibitors for the Treatment of Human Breast Cancer.

Guizhou Medical University
Serendipitous discovery of Class I HDAC inhibitors from rational design of molecular glue degraders targeting HDAC.

Guizhou Medical University
Development of the "hidden" multi-target-directed ligands by AChE/BuChE for the treatment of Alzheimer's disease.

Guizhou Medical University
Facilitated Drug Repurposing with Artemisinin-Derived PROTACs: Unveiling PCLAF as a Therapeutic Target.

Guizhou Medical University
Design, synthesis and biological evaluation of cajanonic acid A analogues as potent PPAR γ antagonists.

Guizhou Medical University
An overview of hydroxypyranone and hydroxypyridinone as privileged scaffolds for novel drug discovery.

Guizhou Medical University
Zinc-dependent deacetylases (HDACs) as potential targets for treating Alzheimer's disease.

Guizhou Medical University
Development of novel 2-aminoalkyl-6-(2-hydroxyphenyl)pyridazin-3(2H)-one derivatives as balanced multifunctional agents against Alzheimer's disease.

Guizhou Medical University
Occurrence, synthesis and biological activity of 2-(2-phenyethyl)chromones.

Guizhou Medical University
Alzheimer's disease: Updated multi-targets therapeutics are in clinical and in progress.

Guizhou Medical University
Synthesis and activity evaluation of selenazole-coupled CPI-1 irreversible bifunctional inhibitors for botulinum toxin A light chain.

Guizhou Medical University
Cysteine derivatives as acetyl lysine mimics to inhibit zinc-dependent histone deacetylases for treating cancer.

Guizhou Medical University
Synthesis and bioevaluation of diaryl urea derivatives as potential antitumor agents for the treatment of human colorectal cancer.

Guizhou Medical University
Indirubin Derivatives as Dual Inhibitors Targeting Cyclin-Dependent Kinase and Histone Deacetylase for Treating Cancer.

Guizhou Medical University
Design, synthesis, and biological evaluation of 2,4-diamino pyrimidine derivatives as potent FAK inhibitors with anti-cancer and anti-angiogenesis activities.

Guizhou Medical University
Design, synthesis and bioevaluation of novel substituted triazines as potential dual PI3K/mTOR inhibitors.

Guizhou Medical University
Design, synthesis and biological activity of novel 2,3,4,5-tetra-substituted thiophene derivatives as PI3Kα inhibitors with potent antitumor activity.

Guizhou Medical University
Novel 3-benzylidene/benzylphthalide Mannich base derivatives as potential multifunctional agents for the treatment of Alzheimer's disease.

Guizhou Medical University
Design, synthesis and evaluation of flurbiprofen-clioquinol hybrids as multitarget-directed ligands against Alzheimer's disease.

Guizhou Medical University
Design, synthesis and evaluation of phthalide alkyl tertiary amine derivatives as promising acetylcholinesterase inhibitors with high potency and selectivity against Alzheimer's disease.

Guizhou Medical University
Novel berberine-based derivatives with potent hypoglycemic activity.

Guizhou Medical University
The development of 2-acetylphenol-donepezil hybrids as multifunctional agents for the treatment of Alzheimer's disease.

Guizhou Medical University
Synthesis, pharmacological evaluation, and mechanistic study of adefovir mixed phosphonate derivatives bearing cholic acid and l-amino acid moieties for the treatment of HBV.

Guizhou Medical University
Scutellarin inhibits Hela cell growth and glycolysis by inhibiting the activity of pyruvate kinase M2.

Guizhou Medical University