Gang Liu

发表

An adamantyl-substituted retinoid-derived molecule that inhibits cancer cell growth and angiogenesis by inducing apoptosis and binds to small heterodimer partner nuclear receptor: effects of modifying its carboxylate group on apoptosis, proliferation, and protein-tyrosine phosphatase activity.

T. Mustelin, M. Dawson, L. Jong, 2007, Journal of medicinal chemistry.

Adamantyl-Substituted Retinoid-Related Molecules Induce Apoptosis in Human Acute Myelogenous Leukemia Cells

R. Mohammad, M. Dawson, J. Fontana, 2010, Molecular Cancer Therapeutics.

Molecular Cancer apeutics apeutic Discovery mantyl-Substituted Retinoid-Related Molecules Induce Ther ptosis in Human Acute Myelogenous Leukemia Cells

R. Mohammad, M. Dawson, J. Fontana, 2010 .

Structure–activity relationship studies on quinoxalin-2(1H)-one derivatives containing thiazol-2-amine against hepatitis C virus leading to the discovery of BH6870

Q. Zhong, Gang Liu, Rui-Ming Liu, 2015, Molecular Diversity.

Quinoxalin-2(1H)-one derivatives as inhibitors against hepatitis C virus.

M. Murray, Zhuhui Huang, Xiaoyong Guo, 2011, Journal of medicinal chemistry.

Structure–activity relationship studies on quinoxalin-2(1H)-one derivatives containing thiazol-2-amine against hepatitis C virus leading to the discovery of BH6870

Q. Zhong, Gang Liu, Rui‐Ming Liu, 2015, Molecular Diversity.

Past, Current, and Future Developments of Therapeutic Agents for Treatment of Chronic Hepatitis B Virus Infection.

S. Yan, Chunting Wang, Gang Liu, 2017, Journal of medicinal chemistry.

Adamantyl-substituted retinoid-related molecules bind small heterodimer partner and modulate the Sin3A repressor.

D. Moore, M. Dawson, J. Fontana, 2007, Cancer research.

Determinants of retinoid X receptor transcriptional antagonism.

R. Abagyan, R. Liddington, C. Cavasotto, 2004, Journal of medicinal chemistry.

Structure-activity relationships of 3,4-dihydro-1H-quinazolin-2-one derivatives as potential CDK5 inhibitors.

V. Viswanadhan, T. Osslund, D. Powers, 2007, Bioorganic & medicinal chemistry.

Antagonist analogue of 6-[3'-(1-adamantyl)-4'-hydroxyphenyl]-2-naphthalenecarboxylic acid (AHPN) family of apoptosis inducers that effectively blocks AHPN-induced apoptosis but not cell-cycle arrest.

A. Rishi, M. Dawson, L. Jong, 2004, Journal of medicinal chemistry.

Novel p-arylthio cinnamides as antagonists of leukocyte function-associated antigen-1/intracellular adhesion molecule-1 interaction. 2. Mechanism of inhibition and structure-based improvement of pharmaceutical properties.

E B Reilly, J. R. Huth, E. Olejniczak, 2001, Journal of medicinal chemistry.

Correction to Past, Current, and Future Developments of Therapeutic Agents for Treatment of Chronic Hepatitis B Virus Infection.

S. Yan, Chunting Wang, Gang Liu, 2017, Journal of Medicinal Chemistry.