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E 64

Known as: E-64, Oxiranecarboxylic acid, 3-(((1-(((4-((aminoiminomethyl)amino)butyl)amino)carbonyl)-3-methylbutyl)amino)carbonyl)-, (2S-(2alpha,3beta(R*)))- 
National Institutes of Health

Related topics

Related topics

4 relations

Broader (3)

AntimalarialsCysteine Proteinase InhibitorsLeucine
analogs & derivatives

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Carboxypeptidase cathepsin X mediates beta2-integrin-dependent adhesion of differentiated U-937 cells.
Highly Cited
1997
Highly Cited
1997
Degradation of connexin43 gap junctions involves both the proteasome and the lysosome.
Intercellular communication may be modulated by the rather rapid turnover and degradation of gap junction proteins, since many… 
Highly Cited
1996
Highly Cited
1996
Autolysis of human erythrocyte calpain produces two active enzyme forms with different cell localization
Highly Cited
1994
Highly Cited
1994
Purification and characterization of a collagen-degrading protease from Porphyromonas gingivalis.
Highly Cited
1992
Highly Cited
1992
Evidence for a nonsecretory, acidic degradation pathway for amyloid precursor protein in 293 cells. Identification of a novel, 22-kDa, beta-peptide-containing intermediate.
Highly Cited
1991
Highly Cited
1991
Isolation and complete amino acid sequence of two fibrinolytic proteinases from the toxic Saturnid caterpillar Lonomia achelous.
Highly Cited
1991
Highly Cited
1991
The selective role of cathepsins B and D in the lysosomal degradation of endogenous and exogenous proteins
Highly Cited
1990
Highly Cited
1990
Some kinetic properties of a cysteine proteinase (cruzipain) from Trypanosoma cruzi.
Highly Cited
1989
Highly Cited
1989
Plasmodium falciparum: inhibitors of lysosomal cysteine proteinases inhibit a trophozoite proteinase and block parasite development.
Highly Cited
1981
Highly Cited
1981
Papain inhibitions by optically active E-64 analogs.
Modification of E-64 focused on the terminal agmatine for practical use led to some potent analogs which were successfully… 
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