Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)
Found 27 hits in this display
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-7(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-9(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-2(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-1(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Ki: 1.70E+4nMAssay Description:The substrate peptides terminating in AMC/AFC are processed by caspases with or without inhibitors, and the accumulation of AMC/AFC was assessed with...More data for this Ligand-Target Pair
Caspase-6(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-4(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Ki: 3.30E+4nMAssay Description:The substrate peptides terminating in AMC/AFC are processed by caspases with or without inhibitors, and the accumulation of AMC/AFC was assessed with...More data for this Ligand-Target Pair
Caspase-8(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Ki: 4.90E+4nMAssay Description:The substrate peptides terminating in AMC/AFC are processed by caspases with or without inhibitors, and the accumulation of AMC/AFC was assessed with...More data for this Ligand-Target Pair
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
IC50: 17nMAssay Description:Inhibition of human recombinant caspase 3 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 minsMore data for this Ligand-Target Pair
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
IC50: 44nMAssay Description:Inhibition of caspase 3 in human SK-N-SH cells assessed as accumulation of fluorogenic 7-amino-4-methyl coumarin by flurometric assayMore data for this Ligand-Target Pair
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-7(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
IC50: 294nMAssay Description:Inhibition of human recombinant caspase 7 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 minsMore data for this Ligand-Target Pair
Caspase-7(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-7(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-6(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-1(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-1(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-8(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-6(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
IC50: >5.00E+5nMAssay Description:Inhibition of human recombinant caspase 6 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 minsMore data for this Ligand-Target Pair
Caspase-1(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
IC50: >5.00E+5nMAssay Description:Inhibition of human recombinant caspase 1 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 minsMore data for this Ligand-Target Pair
Caspase-8(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-6(Homo sapiens (Human))Glaxosmithkline
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)
Caspase-3(Homo sapiens (Human))University Hospital Of The WestfäLische Wilhelms-UniversitäT
Curated by ChEMBL
BDBM10318((S)-5-{1-[2-(Phenoxymethyl)pyrrolidinyl]sulfonyl}i...)