Iodo and diiodotyrosine epoxysuccinyl derivatives as selective inhibitors of cathepsin B
- 31 December 1993
- journal article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 28 (12) , 917-926
- https://doi.org/10.1016/0223-5234(93)90046-h
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Synthesis and inhibiting activities of 1-peptidyl-2-haloacetyl hydrazines toward cathepsin B and calpainsEuropean Journal of Medicinal Chemistry, 1993
- A comparison between the binding modes of a substrate and inhibitor to papain as observed in complex crystal structuresBiochemical and Biophysical Research Communications, 1990
- Molecular dynamics simulation of papain-E-64 (N-(N-(L-3-trans-carboxyoxirane-2-carbonyl)-L-leucyl)agmatine) complex.CHEMICAL & PHARMACEUTICAL BULLETIN, 1990
- Mode of binding of E‐64‐c, a potent thiol protease inhibitor, to papain as determined by X‐ray crystal analysis of the complexFEBS Letters, 1989
- Crystal structure and molecular conformation of E-64, a cysteine protease inhibitor.CHEMICAL & PHARMACEUTICAL BULLETIN, 1989
- Prolongation of life span of dystrophic hamster by cysteine proteinase inhibitor, loxistatin (EST).Journal of Pharmacobio-Dynamics, 1987
- Peptidsynthesen mit 3′-Iod-L-tyrosin, II Synthese von Peptiden mit 3′-Iod-L-tyrosin ohne Blockierung der PhenolfunktionEuropean Journal of Organic Chemistry, 1981
- Study on thiol protease inhibitors. Part IV. Relationship between structure and papain inhibitory activity of epoxysuccinyl amino acid derivatives.Agricultural and Biological Chemistry, 1981
- Inhibition of cathepsin B1 by E-64, a thiol proteinase inhibitor, and its derivatives.Agricultural and Biological Chemistry, 1979
- Synthese von radioaktiv markierten Bromacetyl- und Diazoacetyl-α-melanotropin-Derivaten zum Studium von kovalenten Hormon-Makromolekül-KomplexenHelvetica Chimica Acta, 1977