null

SMILES: CCS(=O)(=O)N[C@H]1C[C@H](C1)N(C)c1ncnc2[nH]ccc12

InChI Key: InChIKey=ACEKXGRKUIQUIE-AOOOYVTPSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50243851   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Tyrosine-protein kinase JAK2 (Homo sapiens (Human))	BDBM50243851 (CHEMBL4092805) Show SMILES CCS(=O)(=O)N[C@H]1C[C@H](C1)N(C)c1ncnc2[nH]ccc12 |r,wD:8.10,6.5,(13.65,-10.72,;12.32,-9.95,;10.98,-10.72,;11.74,-12.05,;10.21,-12.04,;9.65,-9.96,;8.32,-10.73,;6.83,-10.34,;6.44,-11.83,;7.93,-12.22,;5.11,-12.61,;3.77,-11.84,;5.11,-14.15,;3.78,-14.92,;3.78,-16.46,;5.12,-17.23,;6.46,-16.45,;7.93,-16.92,;8.83,-15.67,;7.91,-14.42,;6.45,-14.91,)| Show InChI InChI=1S/C13H19N5O2S/c1-3-21(19,20)17-9-6-10(7-9)18(2)13-11-4-5-14-12(11)15-8-16-13/h4-5,8-10,17H,3,6-7H2,1-2H3,(H,14,15,16)/t9-,10+	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>3.31E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description In vitro inhibitory activity against human AchE (Acetylcholinesterase)				J Med Chem 61: 1130-1152 (2018) Article DOI: 10.1021/acs.jmedchem.7b01598 BindingDB Entry DOI: 10.7270/Q2D79DTW
					More data for this Ligand-Target Pair
Tyrosine-protein kinase JAK2 (Homo sapiens (Human))	BDBM50243851 (CHEMBL4092805) Show SMILES CCS(=O)(=O)N[C@H]1C[C@H](C1)N(C)c1ncnc2[nH]ccc12 |r,wD:8.10,6.5,(13.65,-10.72,;12.32,-9.95,;10.98,-10.72,;11.74,-12.05,;10.21,-12.04,;9.65,-9.96,;8.32,-10.73,;6.83,-10.34,;6.44,-11.83,;7.93,-12.22,;5.11,-12.61,;3.77,-11.84,;5.11,-14.15,;3.78,-14.92,;3.78,-16.46,;5.12,-17.23,;6.46,-16.45,;7.93,-16.92,;8.83,-15.67,;7.91,-14.42,;6.45,-14.91,)| Show InChI InChI=1S/C13H19N5O2S/c1-3-21(19,20)17-9-6-10(7-9)18(2)13-11-4-5-14-12(11)15-8-16-13/h4-5,8-10,17H,3,6-7H2,1-2H3,(H,14,15,16)/t9-,10+	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.59E+4	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of JAK2 in CD34+ human whole blood assessed as reduction in EOP induced STAT5 phosphorylation preincubated for 45 mins followed by EOP add...				J Med Chem 61: 1130-1152 (2018) Article DOI: 10.1021/acs.jmedchem.7b01598 BindingDB Entry DOI: 10.7270/Q2D79DTW
					More data for this Ligand-Target Pair
Non-receptor tyrosine-protein kinase TYK2 (Homo sapiens (Human))	BDBM50243851 (CHEMBL4092805) Show SMILES CCS(=O)(=O)N[C@H]1C[C@H](C1)N(C)c1ncnc2[nH]ccc12 |r,wD:8.10,6.5,(13.65,-10.72,;12.32,-9.95,;10.98,-10.72,;11.74,-12.05,;10.21,-12.04,;9.65,-9.96,;8.32,-10.73,;6.83,-10.34,;6.44,-11.83,;7.93,-12.22,;5.11,-12.61,;3.77,-11.84,;5.11,-14.15,;3.78,-14.92,;3.78,-16.46,;5.12,-17.23,;6.46,-16.45,;7.93,-16.92,;8.83,-15.67,;7.91,-14.42,;6.45,-14.91,)| Show InChI InChI=1S/C13H19N5O2S/c1-3-21(19,20)17-9-6-10(7-9)18(2)13-11-4-5-14-12(11)15-8-16-13/h4-5,8-10,17H,3,6-7H2,1-2H3,(H,14,15,16)/t9-,10+	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of recombinant human TYK2 using 5'FAM-KKSRGDYMTMQID as substrate in presence of 1 mM ATP by mobility shift assay				J Med Chem 61: 1130-1152 (2018) Article DOI: 10.1021/acs.jmedchem.7b01598 BindingDB Entry DOI: 10.7270/Q2D79DTW
					More data for this Ligand-Target Pair
Tyrosine-protein kinase JAK1 (Homo sapiens (Human))	BDBM50243851 (CHEMBL4092805) Show SMILES CCS(=O)(=O)N[C@H]1C[C@H](C1)N(C)c1ncnc2[nH]ccc12 |r,wD:8.10,6.5,(13.65,-10.72,;12.32,-9.95,;10.98,-10.72,;11.74,-12.05,;10.21,-12.04,;9.65,-9.96,;8.32,-10.73,;6.83,-10.34,;6.44,-11.83,;7.93,-12.22,;5.11,-12.61,;3.77,-11.84,;5.11,-14.15,;3.78,-14.92,;3.78,-16.46,;5.12,-17.23,;6.46,-16.45,;7.93,-16.92,;8.83,-15.67,;7.91,-14.42,;6.45,-14.91,)| Show InChI InChI=1S/C13H19N5O2S/c1-3-21(19,20)17-9-6-10(7-9)18(2)13-11-4-5-14-12(11)15-8-16-13/h4-5,8-10,17H,3,6-7H2,1-2H3,(H,14,15,16)/t9-,10+	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	178	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of recombinant human JAK1 using 5'FAM-KKSRGDYMTMQID as substrate in presence of 1 mM ATP by mobility shift assay				J Med Chem 61: 1130-1152 (2018) Article DOI: 10.1021/acs.jmedchem.7b01598 BindingDB Entry DOI: 10.7270/Q2D79DTW
					More data for this Ligand-Target Pair
Non-receptor tyrosine-protein kinase TYK2/Tyrosine-protein kinase JAK1 (Homo sapiens (Human))	BDBM50243851 (CHEMBL4092805) Show SMILES CCS(=O)(=O)N[C@H]1C[C@H](C1)N(C)c1ncnc2[nH]ccc12 |r,wD:8.10,6.5,(13.65,-10.72,;12.32,-9.95,;10.98,-10.72,;11.74,-12.05,;10.21,-12.04,;9.65,-9.96,;8.32,-10.73,;6.83,-10.34,;6.44,-11.83,;7.93,-12.22,;5.11,-12.61,;3.77,-11.84,;5.11,-14.15,;3.78,-14.92,;3.78,-16.46,;5.12,-17.23,;6.46,-16.45,;7.93,-16.92,;8.83,-15.67,;7.91,-14.42,;6.45,-14.91,)| Show InChI InChI=1S/C13H19N5O2S/c1-3-21(19,20)17-9-6-10(7-9)18(2)13-11-4-5-14-12(11)15-8-16-13/h4-5,8-10,17H,3,6-7H2,1-2H3,(H,14,15,16)/t9-,10+	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	930	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Inc. Curated by ChEMBL					Assay Description Inhibition of JAK1/TYK2 in human whole blood assessed as reduction in IFNalpha induced STAT3 phosphorylation preincubated for 45 mins followed by IFN...				J Med Chem 61: 1130-1152 (2018) Article DOI: 10.1021/acs.jmedchem.7b01598 BindingDB Entry DOI: 10.7270/Q2D79DTW
					More data for this Ligand-Target Pair