Literature for peptidase C01.040: cathepsin H

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

2024
1. Jangra,S., Raghav,N., Wadhwa,D., Kumar,A., Bhattacharyya,S., Kumar,V. and Sheokand,J.
   Biological evaluation of trans-2,3-dihydrofuro[3,2-c]coumarins as potential cathepsin inhibitors and anticancer agents
   J Biomater Sci Polym Ed1-19. PubMed  Europe PubMed DOI  I
2016
2. Raghav,N., Jangra,S., Kumar,A., Bhattacharyya,S., Wadhwa,D. and Sindhu,J.
   Cathepsin B, H and L inhibitors as cell proliferating agents: design, synthesis, computational and pharmacological studies of some novel 2-(2-naphthoyl)-6,6-dimethyl-3-aryl-2,3,6,7-tetrahydrobenzofuran-4(5H)-ones
   RSC Adv6, 34588-34599. DOI  I
2015
3. Singh,M. and Raghav,N.
   2,3-Dihydroquinazolin-4(1H)-one derivatives as potential non-peptidyl inhibitors of cathepsins B and H
   Bioorg Chem59C, 12-22. PubMed  Europe PubMed DOI  I
2014
4. Raghav,N. and Garg,S.
   SAR studies of o-hydroxychalcones and their cyclized analogs and study them as novel inhibitors of cathepsin B and cathepsin H
   Eur J Pharm Sci60, 55-63. PubMed  Europe PubMed DOI  I
5. Raghav,N. and Singh,M.
   SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H
   Bioorg Med Chem22, 4233-4245. PubMed  Europe PubMed DOI  I
6. Raghav,N. and Singh,M.
   Acyl hydrazides and triazoles as novel inhibitors of mammalian cathepsin B and cathepsin H
   Eur J Med Chem77, 231-242. PubMed  Europe PubMed DOI  I
7. Raghav,N. and Singh,M.
   Design, synthesis and docking studies of bischalcones based quinazoline-2(1H)-ones and quinazoline-2(1H)-thiones derivatives as novel inhibitors of cathepsin B and cathepsin H
   Eur J Pharm Sci54, 28-39. PubMed  Europe PubMed DOI  I
8. Ravish,I. and Raghav,N.
   Curcumin as inhibitor of mammalian cathepsin B, cathepsin H, acid phosphatase and alkaline phosphatase: a correlation with pharmacological activities
   Med Chem Res23, 2847-2855. DOI  I
1989
9. [YEAR:15-8-1989]Angliker,H., Wikstrom,P., Kirschke,H. and Shaw,E.
   The inactivation of the cysteinyl exopeptidases cathepsin H and C by affinity-labelling reagents
   Biochem J262, 63-68. PubMed  Europe PubMed  I
1982
10. 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