Xihan Wu

发表

Identification of a novel aminotetralin class of HDAC6 and HDAC8 selective inhibitors.

J. Wong, J. Wu, N. Zhang, 2014, Journal of medicinal chemistry.

Molecular modeling of the three-dimensional structure of dopamine 3 (D3) subtype receptor: discovery of novel and potent D3 ligands through a hybrid pharmacophore- and structure-based database searching approach.

Xueliang Fang, Xueliang Fang, Shaomeng Wang, 2003, Journal of medicinal chemistry.

In vitro Effects of the BH3 Mimetic, (−)-Gossypol, on Head and Neck Squamous Cell Carcinoma Cells

Shaomeng Wang, T. Carey, C. Bradford, 2004, Clinical Cancer Research.

Nonpeptidic Small-Molecule Inhibitor of Bcl-2 and Bcl-XL, (−)-Gossypol, Enhances Biological Effect of Genistein Against BxPC-3 Human Pancreatic Cancer Cell Line

Sanjeev Banerjee, F. Sarkar, Shaomeng Wang, 2005, Pancreas.

Preclinical studies of a nonpeptidic small-molecule inhibitor of Bcl-2 and Bcl-X(L) [(-)-gossypol] against diffuse large cell lymphoma.

Shaomeng Wang, R. Mohammad, Jianyong Chen, 2005, Molecular cancer therapeutics.

A novel Bcl-2 small molecule inhibitor 4-(3-methoxy-phenylsulfannyl)-7-nitro-benzofurazan-3-oxide (MNB)-induced apoptosis in leukemia cells

Shaomeng Wang, R. Mohammad, Renxiao Wang, 2007, Annals of Hematology.

A FACILE AND DIRECT SYNTHESIS OF ALENDRONATE FROM PYRROLIDONE

Xihan Wu, Guangyu Xu, Yuyuan Xie, 2004 .

Novel indole α-methylene-γ-lactones as potent inhibitors for AKT-mTOR signaling pathway kinases

Jian Ding, Xiongwen Zhang, Xihan Wu, 2005 .

Syntheses of quinolone hydrochloride enantiomers from synthons (R)- and (S)-2-methylpiperazine.

J. Cui, Xihan Wu, Chunhao Yang, 2005, Bioorganic & medicinal chemistry.

IMPROVED SYNTHESIS OF TADALAFIL

Xihan Wu, Qian He, Yuyuan Xie, 2005 .

Improved Synthesis of Tadalafil.

Xihan Wu, Qian He, Yuyuan Xie, 2005 .

A Novel and Facile Method to Synthesize (R)‐ and (S)‐2‐methylpiperazine

Xihan Wu, Chunhao Yang, Guangyu Xu, 2004 .

Design, synthesis and structure-activity relationship studies of hexahydropyrazinoquinolines as a novel class of potent and selective dopamine receptor 3 (D3) ligands.

Shaomeng Wang, Ke Ding, Jianyong Chen, 2005, Bioorganic & medicinal chemistry letters.

Benzothieno[3,2-b]indole derivatives as potent selective estrogen receptor modulators.

Ming-Wei Wang, Xihan Wu, Chunhao Yang, 2005, Bioorganic & medicinal chemistry letters.

Benzothiophenes containing a piperazine side chain as selective ligands for the estrogen receptor alpha and their bioactivities in vivo.

Ming-Wei Wang, Xihan Wu, Chunhao Yang, 2005, Bioorganic & medicinal chemistry letters.

Antitumor activity of TY-011 against gastric cancer by inhibiting Aurora A, Aurora B and VEGFR2 kinases

Yan-fen Fang, T. Zhu, Xiongwen Zhang, 2016, Journal of Experimental & Clinical Cancer Research.

In vitro Effects of the BH 3 Mimetic , ( )-Gossypol , on Head and Neck Squamous Cell Carcinoma Cells

Shaomeng Wang, T. Carey, C. Bradford, 2004 .

DNA topoisomerase I inhibitors from Rinorea anguifera.

S. Hecht, Xihan Wu, Ji Ma, 2005, Bioorganic & medicinal chemistry letters.

Pharmacokinetic optimization of class-selective histone deacetylase inhibitors and identification of associated candidate predictive biomarkers of hepatocellular carcinoma tumor response.

J. Wong, Tai-guang Jin, N. Zhang, 2012, Journal of medicinal chemistry.

Deglycobleomycin: solid-phase synthesis and DNA cleavage by the resin-bound ligand.

Z. Tao, S. Hecht, Xihan Wu, 2002, Organic letters.

Impact of Sequence Length and Copying on Clause-Level Inflection

Garrett Nicolai, Miikka Silfverberg, Xihan Wu, 2022, MRL.

Catechol–bisphosphonate conjugates: New types of chelators for metal intoxication therapy

Xihan Wu, Junbo Wang, Guangyu Xu, 2004 .

Synthesis of new potential chelating agents: Catechol–bisphosphonate conjugates for metal intoxication therapy

Xihan Wu, Chunhao Yang, Guangyu Xu, 2004 .

Synthesis of New Potential Chelating Agents: Catechol—Bisphosphonate Conjugates for Metal Intoxication Therapy.

Xihan Wu, Chunhao Yang, Guangyu Xu, 2004 .

Alteration of the selectivity of DNA cleavage by a deglycobleomycin analogue containing a trithiazole moiety.

Z. Tao, S. Hecht, Xihan Wu, 2002, Journal of the American Chemical Society.

Small Molecule R1498 as a Well-Tolerated and Orally Active Kinase Inhibitor for Hepatocellular Carcinoma and Gastric Cancer Treatment via Targeting Angiogenesis and Mitosis Pathways

Taiping Chen, Meifang Zhang, Xiongwen Zhang, 2013, PloS one.

Design and synthesis of orally bioavailable aminopyrrolidinone histone deacetylase 6 inhibitors.

J. Wong, Wenming Chen, Sheng Zhong, 2015, Journal of medicinal chemistry.

Antitumor activity of TY-011 against gastric cancer by inhibiting Aurora A, Aurora B and VEGFR2 kinases

Xiao Liu, Yan-fen Fang, T. Zhu, 2016, Journal of experimental & clinical cancer research : CR.

Enantiomerically pure hexahydropyrazinoquinolines as potent and selective dopamine 3 subtype receptor ligands.

J. Deschamps, Shaomeng Wang, Yipin Lu, 2005, Journal of medicinal chemistry.