Li-hong Hu

Shanghai, 201203, China

Last Updated: 09/26/2026

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Found 22 publications

Author Correction: Small molecule LX2343 ameliorates cognitive deficits in AD model mice by targeting both amyloid β production and clearance.

Author Correction: Small molecule LX2343 ameliorates cognitive deficits in AD model mice by targeting both amyloid β production and clearance.

Journal: Acta pharmacologica Sinica

Published: April 29, 2024

Correction notice to: Alleviative effects from boswellic acid on acetaminophen-induced hepatic injury - Biomedicine (Taipei). 2016 Jun; 6 (2): 9. DOI: 10.7603/s40681-016-0009-1.

Correction notice to: Alleviative effects from boswellic acid on acetaminophen-induced hepatic injury - Biomedicine (Taipei). 2016 Jun; 6 (2): 9. DOI: 10.7603/s40681-016-0009-1.

Journal: BioMedicine

Published: May 06, 2017

LX2343 alleviates cognitive impairments in AD model rats by inhibiting oxidative stress-induced neuronal apoptosis and tauopathy.

LX2343 alleviates cognitive impairments in AD model rats by inhibiting oxidative stress-induced neuronal apoptosis and tauopathy.

Journal: Acta pharmacologica Sinica

Published: June 20, 2016

Alleviative effects from boswellic acid on acetaminophen-induced hepatic injury - Corrected and republished from: Biomedicine (Taipei). 2016 Jun; 6 (2): 9. doi: 10.7603/s40681-016-0009-1PMCID: PMC4864770.

Alleviative effects from boswellic acid on acetaminophen-induced hepatic injury - Corrected and republished from: Biomedicine (Taipei). 2016 Jun; 6 (2): 9. doi: 10.7603/s40681-016-0009-1PMCID: PMC4864770.

Journal: BioMedicine

Published: March 29, 2016

Alleviative effects from boswellic acid on acetaminophen-induced hepatic injury.

Alleviative effects from boswellic acid on acetaminophen-induced hepatic injury.

Journal: BioMedicine

Published: March 29, 2016

Thamnolia vermicularis extract improves learning ability in APP/PS1 transgenic mice by ameliorating both Aβ and Tau pathologies.

Thamnolia vermicularis extract improves learning ability in APP/PS1 transgenic mice by ameliorating both Aβ and Tau pathologies.

Journal: Acta pharmacologica Sinica

Published: March 09, 2016

Small molecule LX2343 ameliorates cognitive deficits in AD model mice by targeting both amyloid β production and clearance.

Small molecule LX2343 ameliorates cognitive deficits in AD model mice by targeting both amyloid β production and clearance.

Journal: Acta pharmacologica Sinica

Published: March 02, 2016

Bufalin derivative BF211 inhibits proteasome activity in human lung cancer cells in vitro by inhibiting β1 subunit expression and disrupting proteasome assembly.

Bufalin derivative BF211 inhibits proteasome activity in human lung cancer cells in vitro by inhibiting β1 subunit expression and disrupting proteasome assembly.

Journal: Acta pharmacologica Sinica

Published: January 04, 2016

Possible target-related proteins and signal network of bufalin in A549 cells suggested by both iTRAQ-based and label-free proteomic analysis.

Possible target-related proteins and signal network of bufalin in A549 cells suggested by both iTRAQ-based and label-free proteomic analysis.

Journal: Proteomics

Published: October 28, 2015

A Novel Bufalin Derivative Exhibited Stronger Apoptosis-Inducing Effect than Bufalin in A549 Lung Cancer Cells and Lower Acute Toxicity in Mice.

A Novel Bufalin Derivative Exhibited Stronger Apoptosis-Inducing Effect than Bufalin in A549 Lung Cancer Cells and Lower Acute Toxicity in Mice.

Journal: PloS one

Published: October 09, 2015

Inhibition on Proteasome β1 Subunit Might Contribute to the Anti-Cancer Effects of Fangchinoline in Human Prostate Cancer Cells.

Inhibition on Proteasome β1 Subunit Might Contribute to the Anti-Cancer Effects of Fangchinoline in Human Prostate Cancer Cells.

Journal: PloS one

Published: March 20, 2015

Structural Basis for Small Molecule NDB (N-Benzyl-N-(3-(tert-butyl)-4-hydroxyphenyl)-2,6-dichloro-4-(dimethylamino) Benzamide) as a Selective Antagonist of Farnesoid X Receptor α (FXRα) in Stabilizing the Homodimerization of the Receptor.

Structural Basis for Small Molecule NDB (N-Benzyl-N-(3-(tert-butyl)-4-hydroxyphenyl)-2,6-dichloro-4-(dimethylamino) Benzamide) as a Selective Antagonist of Farnesoid X Receptor α (FXRα) in Stabilizing the Homodimerization of the Receptor.

Journal: The Journal of biological chemistry

Published: December 17, 2014

Showing 1-12 of 22

Last Updated: 09/26/2026