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Literature summary for 3.4.22.B69 extracted from

  • Akhter, M.; Saha, R.; Tanwar, O.; Mumtaz Alam, M.; Zaman, M.
    Synthesis and antimalarial activity of quinoline-substituted furanone derivatives and their identification as selective falcipain-2 inhibitors (2015), Med. Chem. Res., 24, 879-890 .
No PubMed abstract available

Crystallization (Commentary)

Crystallization (Comment) Organism
molecular docking of inhibitors Plasmodium falciparum

Inhibitors

Inhibitors Comment Organism Structure
3-((2-chloro-6-methoxyquinolin-3-yl)methylene)-5-(2,4-dimethylphenyl)furan-2(3H)-one IC50 value on parasite 0.50 microg/ml Plasmodium falciparum
3-((2-chloro-6-methoxyquinolin-3-yl)methylene)-5-(4-chlorophenyl)furan-2(3H)-one IC50 value on parasite 0.61 micro/ml Plasmodium falciparum

Organism

Organism UniProt Comment Textmining
Plasmodium falciparum Q9N6S8
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-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
benzyloxycarbonyl-Phe-Arg-7-amido-4-methylcoumarin + H2O
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Plasmodium falciparum benzyloxycarbonyl-Phe-Arg + 7-amino-4-methylcoumarin
-
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