Literature for Ep475 (C01.001 inhibitor)

Summary Structure Literature

(Topics flags: S Structure, I Inhibitor. To select only the references relevant to a single topic, click the link above. See explanation.)

    2013
  1. Radzey,H., Rethmeier,M., Klimpel,D., Grundhuber,M., Sommerhoff,C.P. and Schaschke,N.
    E-64c-hydrazide: a lead structure for the development of irreversible cathepsin C inhibitors
    ChemMedChem8, 1314-1321. PubMed  Europe PubMed DOI  I
  2. 2000
  3. [YEAR:8-12-2000]Roush,W.R., Hernandez,A.A., McKerrow,J.H., Selzer,P.M., Hansell,E. and Engel,J.C.
    Design, synthesis and evaluation of D-homophenylalanyl epoxysuccinate inhibitors of the trypanosomal cysteine protease cruzain
    Tetrahedron56, 9747-9762.  I
  4. 1996
  5. [YEAR:16-8-1996]Meara,J.P. and Rich,D.H.
    Mechanistic studies on the inactivation of papain by epoxysuccinyl inhibitors
    J Med Chem39, 3357-3366. PubMed  Europe PubMed DOI  I
  6. 1994
  7. Matsumoto,K., Murata,M., Sumiya,S., Kitamura,K. and Ishida,T.
    Clarification of substrate specificity of papain by crystal analyses of complexes with covalent-type inhibitors
    Biochim Biophys Acta1208, 268-276. PubMed  Europe PubMed DOI  I
  8. 1993
  9. Bihovsky,R., Powers,J.C., Kam,C.M., Walton,R. and Loewi,R.C.
    Further evidence for the importance of free carboxylate in epoxysuccinate inhibitors of thiol proteases
    J Enzyme Inhib7, 15-25. PubMed  Europe PubMed  I
  10. 1992
  11. [YEAR:29-5-1992]Huang,Z., McGowan,E.B. and Detwiler,T.C.
    Ester and amide derivatives of E64c as inhibitors of platelet calpains
    J Med Chem35, 2048-2054. PubMed  Europe PubMed DOI  I
  12. Kim,M.J., Yamamoto,D., Matsumoto,K., Inoue,M., Ishida,T., Mizuno,H., Sumiya,S. and Kitamura,K.
    Crystal structure of papain-E64-c complex. Binding diversity of E64-c to papain S2 and S3 subsites
    Biochem J287, 797-803. PubMed  Europe PubMed  S  I
  13. 1991
  14. Yamamoto,D., Matsumoto,K., Ohishi,H., Ishida,T., Inoue,M., Kitamura,K. and Mizuno,H.
    Refined X-ray structure of papain.E-64-c complex at 2.1-A resolution
    J Biol Chem266, 14771-14777. PubMed  Europe PubMed  S  I
  15. 1990
  16. Yamamoto,D., Matsumoto,K., Ohishi,H., Ishida,T., Inoue,M., Kitamura,K. and Hanada,K.
    The importance of Val-157 hydrophobic interaction for papain inhibitory activity of an epoxysuccinyl amino acid derivative. A structure-activity relationship based on the crystal structure of the papain-E-64-c complex
    FEBS Lett263, 134-136. PubMed  Europe PubMed DOI  S  I
  17. 1989
  18. [YEAR:13-3-1989]Matsumoto,K., Yamamoto,D., Ohishi,H., Tomoo,K., Ishida,T., Inoue,M., Sadatome,T., Kitamura,K. and Mizuno,H.
    Mode of binding of E-64-c, a potent thiol protease inhibitor, to papain as determined by X-ray crystal analysis of the complex
    FEBS Lett245, 177-180. PubMed  Europe PubMed DOI  S  I
  19. 1982
  20. Barrett,A.J., Kembhavi,A.A., Brown,M.A., Kirschke,H., Knight,C.G., Tamai,M. and Hanada,K.
    L-trans-Epoxysuccinyl-leucylamido(4-guanidino)butane (E-64) and its analogues as inhibitors of cysteine proteinases including cathepsins B, H and L
    Biochem J201, 189-198. PubMed  Europe PubMed  I
  21. 1978
  22. Hanada,K., Tamai,M., Morimoto,S., Adachi,T., Ohmura,S., Sawada,J. and Tanaka,I.
    Inhibitory activities of E-64 derivatives on papain
    Agric Biol Chem42, 537-541. DOI  I