Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 476.6 BDBM50258669

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 4 hits in this display   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Caspase-3 (Homo sapiens (Human))	BDBM50258669 ((S)-5-[1-(2-Methoxymethylpyrrolidinyl)sulfonyl]-1-...) Show SMILES COC[C@@H]1CCCN1S(=O)(=O)c1ccc2N(CCCCCCCCCC=C)C(=O)C(=O)c2c1 |r| Show InChI InChI=1S/C25H36N2O5S/c1-3-4-5-6-7-8-9-10-11-16-26-23-15-14-21(18-22(23)24(28)25(26)29)33(30,31)27-17-12-13-20(27)19-32-2/h3,14-15,18,20H,1,4-13,16-17,19H2,2H3/t20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	74	n/a	n/a	n/a	n/a	n/a	n/a
Westfalische Wilhelms-Universitat Curated by ChEMBL					Assay Description Inhibition of human recombinant caspase 3 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 mins				J Med Chem 52: 3484-95 (2009) Article DOI: 10.1021/jm8015014 BindingDB Entry DOI: 10.7270/Q2FN163D
					More data for this Ligand-Target Pair
Caspase-7 (Homo sapiens (Human))	BDBM50258669 ((S)-5-[1-(2-Methoxymethylpyrrolidinyl)sulfonyl]-1-...) Show SMILES COC[C@@H]1CCCN1S(=O)(=O)c1ccc2N(CCCCCCCCCC=C)C(=O)C(=O)c2c1 |r| Show InChI InChI=1S/C25H36N2O5S/c1-3-4-5-6-7-8-9-10-11-16-26-23-15-14-21(18-22(23)24(28)25(26)29)33(30,31)27-17-12-13-20(27)19-32-2/h3,14-15,18,20H,1,4-13,16-17,19H2,2H3/t20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	111	n/a	n/a	n/a	n/a	n/a	n/a
Westfalische Wilhelms-Universitat Curated by ChEMBL					Assay Description Inhibition of human recombinant caspase 7 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 mins				J Med Chem 52: 3484-95 (2009) Article DOI: 10.1021/jm8015014 BindingDB Entry DOI: 10.7270/Q2FN163D
					More data for this Ligand-Target Pair
Caspase-6 (Homo sapiens (Human))	BDBM50258669 ((S)-5-[1-(2-Methoxymethylpyrrolidinyl)sulfonyl]-1-...) Show SMILES COC[C@@H]1CCCN1S(=O)(=O)c1ccc2N(CCCCCCCCCC=C)C(=O)C(=O)c2c1 |r| Show InChI InChI=1S/C25H36N2O5S/c1-3-4-5-6-7-8-9-10-11-16-26-23-15-14-21(18-22(23)24(28)25(26)29)33(30,31)27-17-12-13-20(27)19-32-2/h3,14-15,18,20H,1,4-13,16-17,19H2,2H3/t20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Westfalische Wilhelms-Universitat Curated by ChEMBL					Assay Description Inhibition of human recombinant caspase 6 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 mins				J Med Chem 52: 3484-95 (2009) Article DOI: 10.1021/jm8015014 BindingDB Entry DOI: 10.7270/Q2FN163D
					More data for this Ligand-Target Pair
Caspase-1 (Homo sapiens (Human))	BDBM50258669 ((S)-5-[1-(2-Methoxymethylpyrrolidinyl)sulfonyl]-1-...) Show SMILES COC[C@@H]1CCCN1S(=O)(=O)c1ccc2N(CCCCCCCCCC=C)C(=O)C(=O)c2c1 |r| Show InChI InChI=1S/C25H36N2O5S/c1-3-4-5-6-7-8-9-10-11-16-26-23-15-14-21(18-22(23)24(28)25(26)29)33(30,31)27-17-12-13-20(27)19-32-2/h3,14-15,18,20H,1,4-13,16-17,19H2,2H3/t20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Westfalische Wilhelms-Universitat Curated by ChEMBL					Assay Description Inhibition of human recombinant caspase 1 assessed as accumulation of cleaved fluorogenic 7-amino-4-methylcoumarin after 10 mins				J Med Chem 52: 3484-95 (2009) Article DOI: 10.1021/jm8015014 BindingDB Entry DOI: 10.7270/Q2FN163D
					More data for this Ligand-Target Pair