Germain Revelant

发表

Aminobenzosuberone Scaffold as a Modular Chemical Tool for the Inhibition of Therapeutically Relevant M1 Aminopeptidases

C. Tarnus, E. Salomon, I. Florent, 2018, Molecules.

Stereoselective synthesis of enantiopure N-protected-3-arylpiperazines from keto-esters

G. Laconde, B. Déprez, R. Deprez-Poulain, 2012 .

Microwave-Assisted Synthesisof 5-Substituted 2-Aminothiophenes Starting from Arylacetaldehydes

G. Kirsch, S. Hesse, Germain Revelant, 2011 .

Synthesis and antiproliferative studies of 5-aryl-2-(3-thienylamino)-1,3,4-thiadiazoles.

V. Mathieu, G. Kirsch, S. Hesse, 2014, Bioorganic & medicinal chemistry letters.

2-(Thienothiazolylimino)-1,3-thiazolidin-4-ones inhibit cell division cycle 25 A phosphatase.

G. Kirsch, S. Hesse, P. Chaimbault, 2016, Bioorganic & medicinal chemistry.

Synthesis of novel 2-aminothieno[3,2- d]thiazoles and selenolo[3,2- d]thiazoles

G. Kirsch, S. Hesse, Germain Revelant, 2011 .

4-Bromo-2-(piperidin-1-yl)thiazol-5-yl-phenyl methanone (12b) inhibits Na+/K(+)-ATPase and Ras oncogene activity in cancer cells.

R. Kiss, V. Mathieu, G. Kirsch, 2013, European journal of medicinal chemistry.

Synthesis and biological evaluation of novel 2-heteroarylimino-1,3-thiazolidin-4-ones as potential anti-tumor agents.

G. Kirsch, S. Hesse, H. Schohn, 2015, European journal of medicinal chemistry.

Synthesis and antiproliferative studies of 5-aryl-2-(3-thienylamino)-1,3,4-thiadiazoles.

V. Mathieu, G. Kirsch, Charlène Gadais, 2014 .

Exploring S1 plasticity and probing S1' subsite of mammalian aminopeptidase N/CD13 with highly potent and selective aminobenzosuberone inhibitors.

C. Tarnus, Nadège Schifano-Faux, S. Albrecht, 2015, Bioorganic & medicinal chemistry.