Synthesis, Crystallization Studies, and in vitro Characterization of Cinnamic Acid Derivatives as Sm HDAC8 Inhibitors for the Treatment of Schistosomiasis

Author:

Bayer Theresa1,Chakrabarti Alokta2,Lancelot Julien3,Shaik Tajith B.4,Hausmann Kristin1,Melesina Jelena1,Schmidtkunz Karin2,Marek Martin4,Erdmann Frank1,Schmidt Matthias1,Robaa Dina1,Romier Christophe4,Pierce Raymond J.3,Jung Manfred2,Sippl Wolfgang1ORCID

Affiliation:

1. Institute of Pharmacy Martin Luther University of Halle-Wittenberg Wolfgang-Langenbeck-Str. 4 06120 Halle/Saale Germany

2. Institute of Pharmaceutical Sciences University of Freiburg 79104 Freiburg Germany

3. University of Lille CNRS Inserm, CHU Lille, Institut Pasteur de Lille, U1019—UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille 59000 Lille France

4. Département de Biologie Structurale Intégrative Institut de Génétique et Biologie Moléculaire et Cellulaire (IGBMC) Université de Strasbourg CNRS INSERM 67404 Illkirch Cedex France

Funder

Seventh Framework Programme

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Reference46 articles.

1. Epigenetic control of gene function in schistosomes: a source of therapeutic targets?

2. Structural Basis for the Inhibition of Histone Deacetylase 8 (HDAC8), a Key Epigenetic Player in the Blood Fluke Schistosoma mansoni

3. World Health Organization Weekly Epidemiological Record Vol. 84 pp. 445–452 October 23 2009 (http://www.who.int/wer/2009/wer8443/en/).

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