Drug-like molecules with anti-trypanothione synthetase activity identified by high throughput screening

Author:

Benítez Diego1,Franco Jaime1,Sardi Florencia1,Leyva Alejandro2,Durán Rosario2,Choi Gahee3,Yang Gyongseon3,Kim Taehee4,Kim Namyoul4,Heo Jinyeong4,Kim Kideok5,Lee Honggun5,Choi Inhee6,Radu Constantin5,Shum David4,No Joo Hwan3,Comini Marcelo A.1

Affiliation:

1. Laboratory Redox Biology of Trypanosomes, Institut Pasteur de Montevideo, Montevideo, Uruguay

2. Analytical Biochemistry and Proteomics Unit, Institut Pasteur de Montevideo, Instituto de Investigaciones Biológicas Clemente Estable, Montevideo, Uruguay

3. Host-Parasite Research Laboratory, Institut Pasteur Korea, Gyeonggi-do, Republic of Korea

4. Assay Development and Screening, Institut Pasteur Korea, Gyeonggi-do, Republic of Korea

5. Automation and Logistics Management, Institut Pasteur Korea, Gyeonggi-do, Republic of Korea

6. Medicinal Chemistry, Institut Pasteur Korea, Gyeonggi-do, Republic of Korea

Funder

Le Réseau International des Instituts Pasteur (RIIP)”, "Actions Concertees Internacionales Pasteuriennes

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Reference69 articles.

1. WHO. Research priorities for Chagas disease, Human African Trypanosomiasis and Leishmaniasis. Technical report of the TDR disease reference group on Chagas disease, Human African Trypanosomiasis and Leishmaniasis. Technical Report 2012. https://apps.who.int/iris/handle/10665/77472

2. Trypanothione-Based Redox Metabolism of Trypanosomatids

3. The ATP-grasp enzymes

4. Biosynthesis of Polyamine–Glutathione Derivatives in Enterobacteria and Kinetoplastida

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