Huixiong Chen

发表

Ontogenic and adult whole body distribution of aminopeptidase N in rat investigated by in vitro autoradiography.

B. Roques, W. Rostène, F. Noble, 2004, Biochimie.

Design, Synthesis, and Biological Evaluation of Covalent Inhibitors of Focal Adhesion Kinase (FAK) against Human Malignant Glioblastoma.

X. Coumoul, D. Lietha, Yongliang Li, 2020, Journal of medicinal chemistry.

α-Monoarylation and tandem arylation–insertion of malonates with arynes

Z. Du, Kun Zhang, Qian Chen, 2015 .

Microwave-assisted synthesis of 2,5-disubstituted pyrimidine derivatives via Buchwald-Hartwig amination

C. Garbay, M. Ethève-Quelquejeu, Huixiong Chen, 2020 .

An Efficient and Enantioselective Synthesis of Suitably Protected β‐[1‐(4‐Malonyl)naphthyl]‐L‐alanine and β‐[1‐(4‐Malonylmethyl)naphthyl]‐L‐alanine: Novel Fluorescent and Non‐Hydrolysable Phosphotyrosine Mimetics

N. Gresh, C. Garbay, Huixiong Chen, 2006 .

Synthesis of N-pyrimidin[1,3,4]oxadiazoles and N-pyrimidin[1,3,4]-thiadiazoles from 1,3,4-oxadiazol-2-amines and 1,3,4-thiadiazol-2-amines via Pd-catalyzed heteroarylamination

C. Dong, Yongliang Li, Z. Du, 2019, Tetrahedron Letters.

High yielding microwave-assisted synthesis of tri-substituted 1,3,5-triazines using Pd-catalyzed aryl and heteroarylamination

C. Garbay, P. Dao, Huixiong Chen, 2012 .

Interactions of a new alpha-aminophosphinic derivative inside the active site of TLN (thermolysin): a model for zinc-metalloendopeptidase inhibition.

T. Prangé, B. Roques, M. Fournié-Zaluski, 2003, Acta crystallographica. Section D, Biological crystallography.

Regioselective synthesis of imidazo[1,2-a][1,3,5]triazines and 3,4-dihydroimidazo[1,2-a][1,3,5]triazines from [1,3,5]triazin-2,4-diamines

C. Garbay, P. Dao, Huixiong Chen, 2013 .

Pain management by a new series of dual inhibitors of enkephalin degrading enzymes: long lasting antinociceptive properties and potentiation by CCK2 antagonist or methadone

B. Roques, R. Maldonado, F. Noble, 2003, Pain.

Synthesis and bioevaluation of 1-phenyl-pyrazole-4-carboxylic acid derivatives as potent xanthine oxidoreductase inhibitors.

Jing Li, Lei Zhang, Zheng Li, 2017, European journal of medicinal chemistry.

Inhibition of both focal adhesion kinase and fibroblast growth factor receptor 2 pathways induces anti-tumor and anti-angiogenic activities.

J. Herbeuval, D. Lietha, C. Garbay, 2014, Cancer letters.

Design, synthesis, and evaluation of novel imidazo[1,2-a][1,3,5]triazines and their derivatives as focal adhesion kinase inhibitors with antitumor activity.

X. Coumoul, J. Herbeuval, D. Lietha, 2015, Journal of medicinal chemistry.

Structure-Based Design, Synthesis, and Characterization of the First Irreversible Inhibitor of Focal Adhesion Kinase.

John C. Dawson, X. Coumoul, M. Frame, 2018, ACS chemical biology.

Synthesis of novel 1,2,4-triazine scaffold as FAK inhibitors with antitumor activity.

D. Lietha, C. Garbay, M. Ethève-Quelquejeu, 2017, Bioorganic & medicinal chemistry letters.

Binding properties of a highly potent and selective iodinated aminopeptidase N inhibitor appropriate for radioautography

M. Fournié-Zaluski, B. Roques, N. Luciani, 2000, FEBS Letters.

High yielding microwave-assisted synthesis of 2-(arylmethyl)amino-4-arylamino-6-alkyl-1,3,5-triazines

C. Garbay, P. Dao, Huixiong Chen, 2010 .

Synthesis of novel diarylamino-1,3,5-triazine derivatives as FAK inhibitors with anti-angiogenic activity.

D. Lietha, C. Garbay, Y. Lepelletier, 2013, Bioorganic & medicinal chemistry letters.

High-Yielding Microwave-Assisted Synthesis of 2-(Arylmethyl)amino-4-arylamino-6-alkyl-1,3,5-triazines.

C. Garbay, P. Dao, Huixiong Chen, 2010 .

Is N-Carbamoyl Putrescine, the Decarboxylation Derivative of Citrulline, a Regulator of Muscle Protein Metabolism in Rats?

C. Garbay, L. Cynober, N. Neveux, 2019, Nutrients.

Grb14 inhibits FGF receptor signaling through the regulation of PLCγ recruitment and activation

K. Cailliau, T. Issad, A. Burnol, 2010, FEBS letters.

Restoration of TRAIL-induced apoptosis in resistant human pancreatic cancer cells by a novel FAK inhibitor, PH11.

D. Scott‐Algara, J. Herbeuval, C. Garbay, 2015, Cancer letters.

Synthesis of novel 1,2,4-triazine scaffold as FAK inhibitors with antitumor activity.

D. Lietha, C. Garbay, M. Ethève-Quelquejeu, 2017, Bioorganic & medicinal chemistry letters.