Zixuan Wang

发表

Gold(I)-Catalyzed Glycosylation with Glycosyl Ynenoates as Donors.

Xiaona Li, Chenyuan Li, Rongkun Liu, 2019, Organic letters.

Selectively catalytic activity of metal–organic frameworks depending on the N-position within the pyridine ring of their building blocks

Zhen-liang Xu, Haitao Xu, Zixuan Wang, 2016 .

Screening and characterization of cyclic pentapeptide CXCR4 antagonists/inverse agonists using a pheromone responsive reporter gene in Saccharomyces cerevisiae: Utility of G protein coupled receptor constitutively active mutants

J. Broach, H. Tamamura, N. Fujii, 2007 .

EGLN1 prolyl hydroxylation of hypoxia-induced transcription factor HIF1α is repressed by SET7-catalyzed lysine methylation

Xing Liu, W. Xiao, Gang Ouyang, 2022, The Journal of biological chemistry.

Gold(I)-promoted synthesis of a β-(1,3)-glucan hexadecasaccharide via the highly convergent strategy.

Zixuan Wang, You Yang, Qingting Hua, 2019, Carbohydrate research.

Oncology clinical trials

P. Müller, T. Lai, G. Rosner, 2013 .

Physical association of GPR54 C-terminal with protein phosphatase 2A.

N. Fujii, S. Peiper, J. Navenot, 2008, Biochemical and biophysical research communications.

Synthesis and Application of Fluorescein‐ and Biotin‐Labeled Molecular Probes for the Chemokine Receptor CXCR4

G. Tsujimoto, M. Matsuoka, N. Fujii, 2008, Chembiochem : a European journal of chemical biology.

Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivatives.

J. Trent, A. Otaka, H. Tamamura, 2003, Organic & biomolecular chemistry.

Design and synthesis of downsized metastin (45-54) analogs with maintenance of high GPR54 agonistic activity.

J. Broach, A. Otaka, H. Tamamura, 2006, Bioorganic & medicinal chemistry letters.

Identification of Key Candidate Biomarkers and Pathways in Atherosclerosis

Yajing Wang, Jianli Zhao, Jimin Cao, 2020 .

Topochemical exploration of potent compounds using retro-enantiomer libraries of cyclic pentapeptides.

J. Trent, A. Otaka, H. Tamamura, 2004, Organic & biomolecular chemistry.

Development of a linear type of low molecular weight CXCR4 antagonists based on T140 analogs.

J. Trent, H. Tamamura, N. Fujii, 2006, Organic & biomolecular chemistry.

Structure-activity relationship studies on CXCR4 antagonists having cyclic pentapeptide scaffolds.

Teppei Ogawa, J. Trent, A. Otaka, 2005, Organic & biomolecular chemistry.

Rh(i)-Catalyzed intramolecular [2 + 2 + 1] cycloaddition of diynes with the N-terminal of the diazo group

Jianbo Wang, Zixuan Wang, Bo Wang, 2019, Organic Chemistry Frontiers.

Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131.

J. Trent, A. Otaka, H. Tamamura, 2005, Journal of medicinal chemistry.

Visible-Light-Promoted Ring-Opening Alkynylation, Alkenylation, and Allylation of Cyclic Hemiacetals through β-Scission of Alkoxy Radicals.

J. Wang, Rui Zhang, Jiang‐Ling Shi, 2019, Chemistry.

Design and synthesis of all diastereomers of cyclic pseudo-dipeptides as mimics of cyclic CXCR4 pentapeptide antagonists.

N. Fujii, H. Ohno, S. Oishi, 2007, Organic & biomolecular chemistry.

Enhancement of the T140-based pharmacophores leads to the development of more potent and bio-stable CXCR4 antagonists.

M. Akamatsu, J. Trent, A. Otaka, 2003, Organic & biomolecular chemistry.

Restricted variable residues in the C-terminal segment of HIV-1 V3 loop regulate the molecular anatomy of CCR5 utilization.

Stephen Taylor, J. Trent, R. Shattock, 2005, Journal of molecular biology.

Biomimetic synthesis and anti-inflammatory evaluation of violacin A analogues.

Mingguo Jiang, Zixuan Wang, Wenxi Wu, 2021, Bioorganic chemistry (Print).

Stereoselective synthesis of 3,6-disubstituted-3,6-dihydropyridin-2-ones as potential diketopiperazine mimetics using organocopper-mediated anti-SN2' reactions and their use in the preparation of low-molecule CXCR4 antagonists.

K. Kitaura, A. Otaka, H. Tamamura, 2006, The Journal of organic chemistry.

Ring-opening iodination and bromination of unstrained cycloalkanols through β-scission of alkoxy radicals.

Jianbo Wang, Jiang‐Ling Shi, Zixuan Wang, 2020, Chemical communications.

Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide scaffolds.

Stephen C Peiper, Satoshi Ueda, Shinya Oishi, 2005, Journal of medicinal chemistry.

Heat Shock Response in CHO Mammalian Cells Is Controlled by a Nonlinear Stochastic Process

Lei Huang, Zixuan Wang, Ovidiu Lipan, 2007, PLoS Comput. Biol..

Commercial SARS-CoV-2 Molecular Assays: Superior Analytical Sensitivity of cobas SARS-CoV-2 Relative to NxTAG Cov Extended Panel and ID NOW COVID-19 Test.

M. Pettengill, S. Peiper, Zixuan Wang, 2020, Archives of pathology & laboratory medicine.

Discovery of Anti-TNBC Agents Targeting PTP1B: Total Synthesis, Structure-Activity Relationship, In Vitro and In Vivo Investigations of Jamunones.

Liya Li, Zixuan Wang, Wenxi Wu, 2021, Journal of medicinal chemistry.

Screening out anti-inflammatory or anti-viral targets in Xuanfei Baidu Tang through a new technique of reverse finding target

Hongwei Gao, Jumei Zhang, Zixuan Wang, 2021, Bioorganic Chemistry.

CCR5 HIV-1 Coreceptor Activity

J. Murray, F. Bonneau, Benhur Lee, 1999, The Journal of Biological Chemistry.

Primary central nervous system Epstein–Barr virus-positive diffuse large B-cell lymphoma of the elderly: a clinicopathologic study of five cases

Shiyong Li, J. Glass, R. Bajaj, 2014, Brain Tumor Pathology.

Identification of a KRAS mutation in a patient with non-small cell lung cancer treated with chemoradiotherapy and panitumumab

P. Fortina, Nicholas G Zaorsky, A. Dicker, 2013, Cancer biology & therapy.

Expression profile of heptahelical putative membrane progesterone receptors in epithelial ovarian tumors.

J. Prat, J. Giri, S. Peiper, 2008, Human pathology.

A simple, Automated Quasi‐4D‐QSAR, Quasi‐multi Way PLS Approach to Develop Highly Predictive QSAR Models for Highly Flexible CXCR4 Inhibitor Cyclic Pentapeptide Ligands Using Scripted Common Molecular Modeling Tools

Zixuan Wang, Stephen C. Peiper, Nobutaka Fujii, 2005 .

Highly Efficient and Selective Photooxidation of Sulfur Mustard Simulant by a Triazolobenzothiadiazole-Moiety-Functionalized Metal-Organic Framework in Air.

Ke Cheng, Xinsheng Zhao, Zheng-Yuan Ma, 2018, Inorganic chemistry.

Kisspeptin-10-induced signaling of GPR54 negatively regulates chemotactic responses mediated by CXCR4: a potential mechanism for the metastasis suppressor activity of kisspeptins.

N. Fujii, S. Peiper, J. Navenot, 2005, Cancer research.

Expression of CXCR4, a G-protein-coupled receptor for CXCL12 in yeast identification of new-generation inverse agonists.

J. Broach, N. Fujii, S. Oishi, 2009, Methods in enzymology.

Silver Catalyzed Site-Selective C(sp3)−H Bond Amination of Secondary over Primary C(sp3)−H Bonds

Zixuan Wang, Dawei Teng, Guorui Cao, 2022, Molecules.

Exaggerated response to endotoxin in mice lacking the Duffy antigen/receptor for chemokines (DARC).

A. Lentsch, N. Maeda, A. Rot, 2000, Blood.