The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
27777011 |
92 |
Variation of the aryl substituent on the piperazine ring within the 4-(piperazin-1-yl)-2,6-di(pyrrolidin-1-yl)pyrimidine scaffold unveils potent, non-competitive inhibitors of the inflammatory caspases. |
Depaul University |
24900651 |
50 |
Irreversible inhibitors of cysteine proteases. |
Dart Neuroscience |
19715320 |
87 |
Grassystatins A-C from marine cyanobacteria, potent cathepsin E inhibitors that reduce antigen presentation. |
University of Florida |
19908842 |
84 |
Identification and optimization of inhibitors of Trypanosomal cysteine proteases: cruzain, rhodesain, and TbCatB. |
National Human Genome Research Institute |
15686936 |
210 |
Novel pyrazinone mono-amides as potent and reversible caspase-3 inhibitors. |
Merck Frosst Centre For Therapeutic Research |
28615111 |
24 |
Synthesis and antitumor activities of 1,2,3-triazines and their benzo- and heterofused derivatives. |
Universit£ |
18308563 |
39 |
Probing the elusive catalytic activity of vertebrate class IIa histone deacetylases. |
Irbm/Merck Research Laboratories |
14698155 |
68 |
Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4: Heterocycles at C3. |
Bristol-Myers Squibb |