Literature for peptidase C01.009: cathepsin V

Summary Gene structure Alignment Tree Sequences Sequence features Distribution Structure Literature Substrates Pharma

(References are filtered for relevance to Inhibitor. To remove the filter click here. See explanation.)

    2018
  1. Sarria,A.L.F., Silva,T.L., de Oliveira,J.M., de Oliveira,M.A.R., Fernandes,J.B., da Silva,M.F.D.G.F., Vieira,P.C., Venancio,T., Alves Filho,E.G., Batista JM Jr and Guido,R.V.C.
    Dimeric chalcones derivatives from Myracrodruon urundeuva act as cathepsin V inhibitors
    Phytochemistry154, 31-38. PubMed  Europe PubMed DOI  I
  2. 2015
  3. Pribis,J.P., Al-Abed,Y., Yang,H., Gero,D., Xu,H., Montenegro,M.F., Bauer,E.M., Kim,S., Chavan,S.S., Cai,C., Li,T., Szoleczky,P., Szabo,C., Tracey,K.J. and Billiar,T.R.
    The HIV protease inhibitor saquinavir inhibits HMGB1-driven inflammation by targeting the interaction of cathepsin V with TLR4/MyD88
    Mol Med21, 749-757. PubMed  Europe PubMed DOI  I
  4. 2012
  5. Marques,E.F., Bueno,M.A., Duarte,P.D., Silva,L.R., Martinelli,A.M., Dos Santos,C.Y., Severino,R.P., Bromme,D., Vieira,P.C. and Correa,A.G.
    Evaluation of synthetic acridones and 4-quinolinones as potent inhibitors of cathepsins L and V
    Eur J Med Chem54, 10-21. PubMed  Europe PubMed DOI  I
  6. 2011
  7. Severino,R.P., Guido,R.V., Marques,E.F., Bromme,D., da Silva,M.F., Fernandes,J.B., Andricopulo,A.D. and Vieira,P.C.
    Acridone alkaloids as potent inhibitors of cathepsin V
    Bioorg Med Chem19, 1477-1481. PubMed  Europe PubMed DOI  I
  8. 2010
  9. Alvim,J., Severino,R.P., Marques,E.F., Martinelli,A.M., Vieira,P.C., Fernandes,J.B., da Silva,M.F. and Correa,A.G.
    Solution phase synthesis of a combinatorial library of chalcones and flavones as potent cathepsin V inhibitors
    J Comb Chem12, 687-695. PubMed  Europe PubMed DOI  I
  10. Piovan,L., Alves,M.F.M., Juliano,L., Bromme,D., Cunha,R.L.O.R. and Andrade,L.H.
    Chemoenzymatic synthesis of organoselenium(IV) compounds and their evaluation as cysteine protease inhibitors
    J Braz Chem Soc21, 2108-2118.  I
  11. 2009
  12. Bethel,P.A., Gerhardt,S., Jones,E.V., Kenny,P.W., Karoutchi,G.I., Morley,A.D., Oldham,K., Rankine,N., Augustin,M., Krapp,S., Simader,H. and Steinbacher,S.
    Design of selective cathepsin inhibitors
    Bioorg Med Chem Lett19, 4622-4625. PubMed  Europe PubMed DOI  I
  13. 2000
  14. [YEAR:17-10-2000]Somoza,J.R., Zhan,H., Bowman,K.K., Yu,L., Mortara,K.D., Palmer,J.T., Clark,J.M. and McGrath,M.E.
    Crystal structure of human cathepsin V
    Biochemistry39, 12543-12551. PubMed  Europe PubMed DOI  S  I