Literature for peptidase C01.009: cathepsin V

(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
   Phytochemistry (2018) 154, 31-38. PubMed  Europe PubMed DOI  I
2015
2. 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 Med (2015) 21, 749-757. PubMed  Europe PubMed DOI  I
2012
3. 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 Chem (2012) 54, 10-21. PubMed  Europe PubMed DOI  I
2011
4. 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 Chem (2011) 19, 1477-1481. PubMed  Europe PubMed DOI  I
2010
5. 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 Chem (2010) 12, 687-695. PubMed  Europe PubMed DOI  I
6. 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 Soc (2010) 21, 2108-2118.  I
2009
7. 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 Lett (2009) 19, 4622-4625. PubMed  Europe PubMed DOI  I
2000
8. [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
   Biochemistry (17-10-2000) 39, 12543-12551. PubMed  Europe PubMed DOI  S  I