Potent and selective inhibition of cysteine proteases from Plasmodium falciparum and Trypanosoma brucei.

Publication Year: 2010

DOI:
10.1002/cmdc.201000449

PMCID:
PMC7162187

PMID:
21275051

Journal Information

Full Title: ChemMedChem

Abbreviation: ChemMedChem

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Pharmacology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
2/6
0.0% Transparent
Transparency Indicators
Click on green indicators to view evidence text
Core Indicators
Evidence found in paper:

"we began our investigations based on the first x-ray crystal structures of falcipain-2 available since 2006 (protein data bank (pdb) codes: 1yvb 2ghu 3bpf) - and of rhodesain published only recently in 2009 and 2010 (pdb codes: 2p7u 2p86) both falcipain-2 and rhodesain share the common features of clan ca cysteine proteases with the classical papain fold consisting of two distinct domains."

Code Sharing
COI Disclosure
Evidence found in paper:

"<~ErrTag=I>V.E. is grateful for a Kekulé fellowship from the German Fonds der Chemischen Industrie. Financial support by the Deutsche Forschungsgemeinschaft (DFG, SFB 630, TP A4 to T.S.) and the Swiss National Science Foundation is gratefully acknowledged. We thank Jennifer Rath and Svetlana Sologub for performing the Trypanosoma brucei brucei and macrophages assays, Dr. Daniel Bur (Actelion Pharmaceuticals Ltd.) for helpful discussions, and Dr. Valentina Aureggi and Laura Salonen for reviewing the manuscript.<~ErrTag=/I> "

Protocol Registration
Open Access
Additional Indicators
Replication
Novelty Statement
Assessment Info

Tool: rtransparent

OST Version: N/A

Last Updated: Aug 05, 2025