Compile Data Set for Download or QSAR

Found 248 hits with Last Name = 'ansideri' and Initial = 'f'   

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
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234890 (CHEMBL4077018) Show SMILES CSc1nc(c(-c2ccnc(Nc3ccc(NC(=O)c4cccc(NC(=O)C=C)c4)cc3)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C32H27FN6O2S/c1-4-28(40)36-26-7-5-6-22(18-26)31(41)37-25-14-12-24(13-15-25)35-27-19-21(16-17-34-27)30-29(38-32(42-3)39(30)2)20-8-10-23(33)11-9-20/h4-19H,1H2,2-3H3,(H,34,35)(H,36,40)(H,37,41)	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	0.300	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234889 (CHEMBL4062023) Show SMILES CSc1nc(c([nH]1)-c1ccnc(Nc2ccc(NC(=O)c3cccc(NC(=O)C=C)c3)cc2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C31H25FN6O2S/c1-3-27(39)35-25-6-4-5-21(17-25)30(40)36-24-13-11-23(12-14-24)34-26-18-20(15-16-33-26)29-28(37-31(38-29)41-2)19-7-9-22(32)10-8-19/h3-18H,1H2,2H3,(H,33,34)(H,35,39)(H,36,40)(H,37,38)	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	0.600	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50234889 (CHEMBL4062023) Show SMILES CSc1nc(c([nH]1)-c1ccnc(Nc2ccc(NC(=O)c3cccc(NC(=O)C=C)c3)cc2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C31H25FN6O2S/c1-3-27(39)35-25-6-4-5-21(17-25)30(40)36-24-13-11-23(12-14-24)34-26-18-20(15-16-33-26)29-28(37-31(38-29)41-2)19-7-9-22(32)10-8-19/h3-18H,1H2,2H3,(H,33,34)(H,35,39)(H,36,40)(H,37,38)	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	0.800	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GST-His tagged human p38alpha expressed in Escherichia coli assessed as reduction in ATF2 phosphorylation measured after 60 mins by ELI...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234886 (CHEMBL4082278) Show SMILES CSc1nc(C)c([nH]1)-c1ccnc(Nc2ccc(NC(=O)c3cccc(NC(=O)C=C)c3)cc2)c1 Show InChI InChI=1S/C26H24N6O2S/c1-4-23(33)30-21-7-5-6-18(14-21)25(34)31-20-10-8-19(9-11-20)29-22-15-17(12-13-27-22)24-16(2)28-26(32-24)35-3/h4-15H,1H2,2-3H3,(H,27,29)(H,28,32)(H,30,33)(H,31,34)	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	2	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234885 (CHEMBL4092555) Show SMILES CSc1nc(c(-c2ccnc(Nc3ccc(NC(=O)c4cccc(NC(=O)C=C)c4)cc3C)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C33H29FN6O2S/c1-5-29(41)36-25-8-6-7-23(18-25)32(42)37-26-13-14-27(20(2)17-26)38-28-19-22(15-16-35-28)31-30(39-33(43-4)40(31)3)21-9-11-24(34)12-10-21/h5-19H,1H2,2-4H3,(H,35,38)(H,36,41)(H,37,42)	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	2	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234883 (CHEMBL4069805) Show SMILES CCC(=O)Nc1cccc(c1)C(=O)Nc1ccc(Nc2cc(ccn2)-c2[nH]c(SC)nc2-c2ccc(F)cc2)cc1 Show InChI InChI=1S/C31H27FN6O2S/c1-3-27(39)35-25-6-4-5-21(17-25)30(40)36-24-13-11-23(12-14-24)34-26-18-20(15-16-33-26)29-28(37-31(38-29)41-2)19-7-9-22(32)10-8-19/h4-18H,3H2,1-2H3,(H,33,34)(H,35,39)(H,36,40)(H,37,38)	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	2	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234880 (CHEMBL4086457) Show SMILES CSc1nc(c(-c2ccnc(Nc3ccc(NC(=O)c4cccc(NC(=O)C=C)c4C)cc3)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C33H29FN6O2S/c1-5-29(41)38-27-8-6-7-26(20(27)2)32(42)37-25-15-13-24(14-16-25)36-28-19-22(17-18-35-28)31-30(39-33(43-4)40(31)3)21-9-11-23(34)12-10-21/h5-19H,1H2,2-4H3,(H,35,36)(H,37,42)(H,38,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50585185 (CHEMBL5077814) Show SMILES C#Cc1ccc2c(c1)[nH]c1ncnc(N3CCC4CCN(CCC#N)CC34)c21 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human GSK-3-beta using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by substrate addition a...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c02146 BindingDB Entry DOI: 10.7270/Q2CJ8JC4
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50585185 (CHEMBL5077814) Show SMILES C#Cc1ccc2c(c1)[nH]c1ncnc(N3CCC4CCN(CCC#N)CC34)c21 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human GSK-3-beta using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by substrate addition a...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c02146 BindingDB Entry DOI: 10.7270/Q2CJ8JC4
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50234880 (CHEMBL4086457) Show SMILES CSc1nc(c(-c2ccnc(Nc3ccc(NC(=O)c4cccc(NC(=O)C=C)c4C)cc3)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C33H29FN6O2S/c1-5-29(41)38-27-8-6-7-26(20(27)2)32(42)37-25-15-13-24(14-16-25)36-28-19-22(17-18-35-28)31-30(39-33(43-4)40(31)3)21-9-11-23(34)12-10-21/h5-19H,1H2,2-4H3,(H,35,36)(H,37,42)(H,38,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GST-His tagged human p38alpha expressed in Escherichia coli assessed as reduction in ATF2 phosphorylation measured after 60 mins by ELI...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234879 (CHEMBL4094220) Show SMILES CSc1nc(c(-c2ccnc(Nc3cccc(NC(=O)c4cccc(NC(=O)C=C)c4)c3)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C32H27FN6O2S/c1-4-28(40)36-24-8-5-7-22(17-24)31(41)37-26-10-6-9-25(19-26)35-27-18-21(15-16-34-27)30-29(38-32(42-3)39(30)2)20-11-13-23(33)14-12-20/h4-19H,1H2,2-3H3,(H,34,35)(H,36,40)(H,37,41)	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	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50503009 (CHEMBL4526183) Show SMILES NC(=O)c1nc(C2CCCCC2)c([nH]1)-c1ccnc(NC(=O)C2CC2)c1 Show InChI InChI=1S/C19H23N5O2/c20-17(25)18-23-15(11-4-2-1-3-5-11)16(24-18)13-8-9-21-14(10-13)22-19(26)12-6-7-12/h8-12H,1-7H2,(H2,20,25)(H,23,24)(H,21,22,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GSK3beta (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50234885 (CHEMBL4092555) Show SMILES CSc1nc(c(-c2ccnc(Nc3ccc(NC(=O)c4cccc(NC(=O)C=C)c4)cc3C)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C33H29FN6O2S/c1-5-29(41)36-25-8-6-7-23(18-25)32(42)37-26-13-14-27(20(2)17-26)38-28-19-22(15-16-35-28)31-30(39-33(43-4)40(31)3)21-9-11-24(34)12-10-21/h5-19H,1H2,2-4H3,(H,35,38)(H,36,41)(H,37,42)	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	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GST-His tagged human p38alpha expressed in Escherichia coli assessed as reduction in ATF2 phosphorylation measured after 60 mins by ELI...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524536 (CHEMBL4452170) Show SMILES Fc1ccc(CC(=O)Nc2cc(ccn2)-c2[nH]c(SCc3ccccc3)nc2-c2ccc(F)cc2)cc1 Show InChI InChI=1S/C29H22F2N4OS/c30-23-10-6-19(7-11-23)16-26(36)33-25-17-22(14-15-32-25)28-27(21-8-12-24(31)13-9-21)34-29(35-28)37-18-20-4-2-1-3-5-20/h1-15,17H,16,18H2,(H,34,35)(H,32,33,36)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234895 (CHEMBL4071770) Show SMILES CSc1nc(c(-c2ccnc(Nc3cccc(NC(=O)c4cccc(NC(=O)C=C)c4C)c3)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C33H29FN6O2S/c1-5-29(41)38-27-11-7-10-26(20(27)2)32(42)37-25-9-6-8-24(19-25)36-28-18-22(16-17-35-28)31-30(39-33(43-4)40(31)3)21-12-14-23(34)15-13-21/h5-19H,1H2,2-4H3,(H,35,36)(H,37,42)(H,38,41)	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	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50503017 (CHEMBL4483032) Show SMILES NC(=O)c1nc(C2CC2)c([nH]1)-c1ccnc(NC(=O)C2CC2)c1 Show InChI InChI=1S/C16H17N5O2/c17-14(22)15-20-12(8-1-2-8)13(21-15)10-5-6-18-11(7-10)19-16(23)9-3-4-9/h5-9H,1-4H2,(H2,17,22)(H,20,21)(H,18,19,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GSK3beta (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50234884 (CHEMBL4082212) Show SMILES CSc1nc(c([nH]1)-c1ccnc(Nc2ccc(NC(=O)c3ccc(NC(=O)C=C)cc3)cc2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C31H25FN6O2S/c1-3-27(39)35-24-10-6-20(7-11-24)30(40)36-25-14-12-23(13-15-25)34-26-18-21(16-17-33-26)29-28(37-31(38-29)41-2)19-4-8-22(32)9-5-19/h3-18H,1H2,2H3,(H,33,34)(H,35,39)(H,36,40)(H,37,38)	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	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GST-His tagged human p38alpha expressed in Escherichia coli assessed as reduction in ATF2 phosphorylation measured after 60 mins by ELI...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234884 (CHEMBL4082212) Show SMILES CSc1nc(c([nH]1)-c1ccnc(Nc2ccc(NC(=O)c3ccc(NC(=O)C=C)cc3)cc2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C31H25FN6O2S/c1-3-27(39)35-24-10-6-20(7-11-24)30(40)36-25-14-12-23(13-15-25)34-26-18-21(16-17-33-26)29-28(37-31(38-29)41-2)19-4-8-22(32)9-5-19/h3-18H,1H2,2H3,(H,33,34)(H,35,39)(H,36,40)(H,37,38)	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	3	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50234883 (CHEMBL4069805) Show SMILES CCC(=O)Nc1cccc(c1)C(=O)Nc1ccc(Nc2cc(ccn2)-c2[nH]c(SC)nc2-c2ccc(F)cc2)cc1 Show InChI InChI=1S/C31H27FN6O2S/c1-3-27(39)35-25-6-4-5-21(17-25)30(40)36-24-13-11-23(12-14-24)34-26-18-20(15-16-33-26)29-28(37-31(38-29)41-2)19-7-9-22(32)10-8-19/h4-18H,3H2,1-2H3,(H,33,34)(H,35,39)(H,36,40)(H,37,38)	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	4	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GST-His tagged human p38alpha expressed in Escherichia coli assessed as reduction in ATF2 phosphorylation measured after 60 mins by ELI...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234894 (CHEMBL4072555) Show SMILES CSc1nc(c(-c2ccnc(Nc3cccc(NC(=O)c4ccc(NC(=O)C=C)cc4)c3)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C32H27FN6O2S/c1-4-28(40)36-24-14-10-21(11-15-24)31(41)37-26-7-5-6-25(19-26)35-27-18-22(16-17-34-27)30-29(38-32(42-3)39(30)2)20-8-12-23(33)13-9-20/h4-19H,1H2,2-3H3,(H,34,35)(H,36,40)(H,37,41)	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	4	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50585181 (CHEMBL5089934) Show SMILES CN([C@H]1CCCN(CCC#N)C1)c1ncnc2[nH]c3cc(ccc3c12)C#C |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human GSK-3-beta using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by substrate addition a...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c02146 BindingDB Entry DOI: 10.7270/Q2CJ8JC4
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50585181 (CHEMBL5089934) Show SMILES CN([C@H]1CCCN(CCC#N)C1)c1ncnc2[nH]c3cc(ccc3c12)C#C |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of recombinant human GSK-3-beta using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by substrate addition a...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c02146 BindingDB Entry DOI: 10.7270/Q2CJ8JC4
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50503015 (CHEMBL4457174) Show SMILES Cc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)c(C)c1 Show InChI InChI=1S/C20H19FN4O/c1-11-9-14(5-6-16(11)21)18-19(24-12(2)23-18)15-7-8-22-17(10-15)25-20(26)13-3-4-13/h5-10,13H,3-4H2,1-2H3,(H,23,24)(H,22,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of P38alpha MAPK (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234893 (CHEMBL4063964) Show SMILES CSc1nc(c(-c2ccnc(Nc3ccc(NC(=O)c4ccc(NC(=O)C=C)cc4)cc3C)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C33H29FN6O2S/c1-5-29(41)36-25-12-8-22(9-13-25)32(42)37-26-14-15-27(20(2)18-26)38-28-19-23(16-17-35-28)31-30(39-33(43-4)40(31)3)21-6-10-24(34)11-7-21/h5-19H,1H2,2-4H3,(H,35,38)(H,36,41)(H,37,42)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234877 (CHEMBL4101953) Show SMILES CSc1nc(c(-c2ccnc(Nc3ccc(NC(=O)c4ccc(NC(=O)C=C)cc4)cc3)c2)n1C)-c1ccc(F)cc1 Show InChI InChI=1S/C32H27FN6O2S/c1-4-28(40)36-25-11-7-21(8-12-25)31(41)37-26-15-13-24(14-16-26)35-27-19-22(17-18-34-27)30-29(38-32(42-3)39(30)2)20-5-9-23(33)10-6-20/h4-19H,1H2,2-3H3,(H,34,35)(H,36,40)(H,37,41)	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	10	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50502999 (CHEMBL4561980) Show SMILES Cc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccccc1O Show InChI InChI=1S/C19H18N4O2/c1-11-21-17(18(22-11)14-4-2-3-5-15(14)24)13-8-9-20-16(10-13)23-19(25)12-6-7-12/h2-5,8-10,12,24H,6-7H2,1H3,(H,21,22)(H,20,23,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GSK3beta (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50503022 (CHEMBL4445449) Show SMILES Cc1nc([nH]c1-c1ccnc(NC(=O)C2CC2)c1)C(N)=O Show InChI InChI=1S/C14H15N5O2/c1-7-11(19-13(17-7)12(15)20)9-4-5-16-10(6-9)18-14(21)8-2-3-8/h4-6,8H,2-3H2,1H3,(H2,15,20)(H,17,19)(H,16,18,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GSK3beta (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524531 (CHEMBL4513323) Show SMILES COc1cc(CC(=O)Nc2cc(ccn2)-c2[nH]c(SC)nc2-c2ccc(F)cc2)cc(OC)c1OC Show InChI InChI=1S/C26H25FN4O4S/c1-33-19-11-15(12-20(34-2)25(19)35-3)13-22(32)29-21-14-17(9-10-28-21)24-23(30-26(31-24)36-4)16-5-7-18(27)8-6-16/h5-12,14H,13H2,1-4H3,(H,30,31)(H,28,29,32)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524523 (CHEMBL4446519) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NCC2CC2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C19H19FN4S/c1-25-19-23-17(13-4-6-15(20)7-5-13)18(24-19)14-8-9-21-16(10-14)22-11-12-2-3-12/h4-10,12H,2-3,11H2,1H3,(H,21,22)(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524519 (CHEMBL4434855) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NC(=O)CC2CC2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C20H19FN4OS/c1-27-20-24-18(13-4-6-15(21)7-5-13)19(25-20)14-8-9-22-16(11-14)23-17(26)10-12-2-3-12/h4-9,11-12H,2-3,10H2,1H3,(H,24,25)(H,22,23,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524518 (CHEMBL4442468) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NC(=O)[C@@H]2C[C@H]2c2ccccc2)c1)-c1ccc(F)cc1 |r| Show InChI InChI=1S/C25H21FN4OS/c1-32-25-29-22(16-7-9-18(26)10-8-16)23(30-25)17-11-12-27-21(13-17)28-24(31)20-14-19(20)15-5-3-2-4-6-15/h2-13,19-20H,14H2,1H3,(H,29,30)(H,27,28,31)/t19-,20+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50503011 (CHEMBL4461695) Show SMILES NC(=O)c1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)c(c1)C(F)(F)F Show InChI InChI=1S/C20H15F4N5O2/c21-13-4-3-10(7-12(13)20(22,23)24)15-16(29-18(28-15)17(25)30)11-5-6-26-14(8-11)27-19(31)9-1-2-9/h3-9H,1-2H2,(H2,25,30)(H,28,29)(H,26,27,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of P38alpha MAPK (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50502996 (CHEMBL4451444) Show SMILES OCc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C19H17FN4O2/c20-14-5-3-11(4-6-14)17-18(23-16(10-25)22-17)13-7-8-21-15(9-13)24-19(26)12-1-2-12/h3-9,12,25H,1-2,10H2,(H,22,23)(H,21,24,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of P38alpha MAPK (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524537 (CHEMBL4536012) Show SMILES CCc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C20H19FN4O/c1-2-16-23-18(12-5-7-15(21)8-6-12)19(24-16)14-9-10-22-17(11-14)25-20(26)13-3-4-13/h5-11,13H,2-4H2,1H3,(H,23,24)(H,22,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50234888 (CHEMBL4074524) Show SMILES CSc1nc(c([nH]1)-c1ccnc(Nc2ccc(N)cc2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C21H18FN5S/c1-28-21-26-19(13-2-4-15(22)5-3-13)20(27-21)14-10-11-24-18(12-14)25-17-8-6-16(23)7-9-17/h2-12H,23H2,1H3,(H,24,25)(H,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GST-His tagged human p38alpha expressed in Escherichia coli assessed as reduction in ATF2 phosphorylation measured after 60 mins by ELI...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50234892 (CHEMBL4085536) Show SMILES CCC(=O)Nc1ccc(cc1)C(=O)Nc1ccc(Nc2cc(ccn2)-c2c(nc(SC)n2C)-c2ccc(F)cc2)cc1 Show InChI InChI=1S/C32H29FN6O2S/c1-4-28(40)36-25-11-7-21(8-12-25)31(41)37-26-15-13-24(14-16-26)35-27-19-22(17-18-34-27)30-29(38-32(42-3)39(30)2)20-5-9-23(33)10-6-20/h5-19H,4H2,1-3H3,(H,34,35)(H,36,40)(H,37,41)	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	17	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of GST-His tagged human p38alpha expressed in Escherichia coli assessed as reduction in ATF2 phosphorylation measured after 60 mins by ELI...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 10 (Homo sapiens (Human))	BDBM50234891 (CHEMBL4066691) Show SMILES CCC(=O)Nc1cccc(C(=O)Nc2ccc(Nc3cc(ccn3)-c3c(nc(SC)n3C)-c3ccc(F)cc3)cc2)c1C Show InChI InChI=1S/C33H31FN6O2S/c1-5-29(41)38-27-8-6-7-26(20(27)2)32(42)37-25-15-13-24(14-16-25)36-28-19-22(17-18-35-28)31-30(39-33(43-4)40(31)3)21-9-11-23(34)12-10-21/h6-19H,5H2,1-4H3,(H,35,36)(H,37,42)(H,38,41)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of recombinant 6x-His-tagged JNK3 (39 to 402 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as reduction in A...				J Med Chem 60: 594-607 (2017) Article DOI: 10.1021/acs.jmedchem.6b01180 BindingDB Entry DOI: 10.7270/Q2891854
					More data for this Ligand-Target Pair
Glycogen synthase kinase-3 beta (Homo sapiens (Human))	BDBM50524514 (CHEMBL4474903) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C19H17FN4OS/c1-26-19-23-16(11-4-6-14(20)7-5-11)17(24-19)13-8-9-21-15(10-13)22-18(25)12-2-3-12/h4-10,12H,2-3H2,1H3,(H,23,24)(H,21,22,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant full length GSK3beta using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated with enzyme for 10 min...				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524538 (CHEMBL4476724) Show SMILES Fc1ccc(cc1)-c1nc(Cc2ccccc2)[nH]c1-c1ccnc(NC(=O)C2CC2)c1 Show InChI InChI=1S/C25H21FN4O/c26-20-10-8-17(9-11-20)23-24(29-22(28-23)14-16-4-2-1-3-5-16)19-12-13-27-21(15-19)30-25(31)18-6-7-18/h1-5,8-13,15,18H,6-7,14H2,(H,28,29)(H,27,30,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524529 (CHEMBL4476843) Show SMILES Fc1ccc(cc1)-c1nc([nH]c1-c1ccnc(NC(=O)C2CC2)c1)-c1ccco1 Show InChI InChI=1S/C22H17FN4O2/c23-16-7-5-13(6-8-16)19-20(27-21(26-19)17-2-1-11-29-17)15-9-10-24-18(12-15)25-22(28)14-3-4-14/h1-2,5-12,14H,3-4H2,(H,26,27)(H,24,25,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524521 (CHEMBL4446355) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NC(=O)[C@@H]2C[C@H](Cl)C2)c1)-c1ccc(F)cc1 |r,wU:15.15,17.18,(80.61,-5.18,;79.85,-6.51,;78.31,-6.51,;77.56,-5.17,;76.05,-5.47,;75.87,-7,;77.27,-7.65,;74.53,-7.76,;73.21,-6.97,;71.86,-7.72,;71.85,-9.27,;73.18,-10.05,;73.17,-11.59,;74.5,-12.37,;74.48,-13.91,;75.84,-11.61,;77.31,-12.02,;77.72,-10.54,;79.06,-9.78,;76.24,-10.13,;74.52,-9.29,;74.92,-4.44,;75.26,-2.93,;74.13,-1.89,;72.65,-2.35,;71.52,-1.31,;72.32,-3.86,;73.45,-4.9,)| Show InChI InChI=1S/C20H18ClFN4OS/c1-28-20-25-17(11-2-4-15(22)5-3-11)18(26-20)12-6-7-23-16(10-12)24-19(27)13-8-14(21)9-13/h2-7,10,13-14H,8-9H2,1H3,(H,25,26)(H,23,24,27)/t13-,14+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50502994 (CHEMBL4474740) Show SMILES Cc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)c(F)c1 Show InChI InChI=1S/C19H16F2N4O/c1-10-23-17(12-4-5-14(20)15(21)8-12)18(24-10)13-6-7-22-16(9-13)25-19(26)11-2-3-11/h4-9,11H,2-3H2,1H3,(H,23,24)(H,22,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of P38alpha MAPK (unknown origin) by ADP-Glo assay				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50502992 (CHEMBL4452444) Show SMILES NC(=O)c1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C19H16FN5O2/c20-13-5-3-10(4-6-13)15-16(25-18(24-15)17(21)26)12-7-8-22-14(9-12)23-19(27)11-1-2-11/h3-9,11H,1-2H2,(H2,21,26)(H,24,25)(H,22,23,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of P38alpha MAPK (unknown origin) by ELISA				ACS Med Chem Lett 10: 1407-1414 (2019) Article DOI: 10.1021/acsmedchemlett.9b00177 BindingDB Entry DOI: 10.7270/Q2SQ93N5
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524541 (CHEMBL4457096) Show SMILES Fc1ccc(cc1)-c1nc[nH]c1-c1ccnc(NC(=O)C2CC2)c1 Show InChI InChI=1S/C18H15FN4O/c19-14-5-3-11(4-6-14)16-17(22-10-21-16)13-7-8-20-15(9-13)23-18(24)12-1-2-12/h3-10,12H,1-2H2,(H,21,22)(H,20,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524527 (CHEMBL4455711) Show SMILES Cc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C19H17FN4O/c1-11-22-17(12-4-6-15(20)7-5-12)18(23-11)14-8-9-21-16(10-14)24-19(25)13-2-3-13/h4-10,13H,2-3H2,1H3,(H,22,23)(H,21,24,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524506 (CHEMBL4473730) Show SMILES Fc1ccc(cc1)-c1nc(CCc2ccccc2)[nH]c1-c1ccnc(NC(=O)C2CC2)c1 Show InChI InChI=1S/C26H23FN4O/c27-21-11-9-18(10-12-21)24-25(30-22(29-24)13-6-17-4-2-1-3-5-17)20-14-15-28-23(16-20)31-26(32)19-7-8-19/h1-5,9-12,14-16,19H,6-8,13H2,(H,29,30)(H,28,31,32)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524535 (CHEMBL4437018) Show SMILES Fc1ccc(cc1)-c1nc(SCc2ccccc2)[nH]c1-c1ccnc(NC(=O)C2CCCC2)c1 Show InChI InChI=1S/C27H25FN4OS/c28-22-12-10-19(11-13-22)24-25(32-27(31-24)34-17-18-6-2-1-3-7-18)21-14-15-29-23(16-21)30-26(33)20-8-4-5-9-20/h1-3,6-7,10-16,20H,4-5,8-9,17H2,(H,31,32)(H,29,30,33)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524532 (CHEMBL4458096) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NC(=O)C2CC(=O)C2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C20H17FN4O2S/c1-28-20-24-17(11-2-4-14(21)5-3-11)18(25-20)12-6-7-22-16(10-12)23-19(27)13-8-15(26)9-13/h2-7,10,13H,8-9H2,1H3,(H,24,25)(H,22,23,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524509 (CHEMBL4571942) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NC(=O)C2CCC(=O)C2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C21H19FN4O2S/c1-29-21-25-18(12-2-5-15(22)6-3-12)19(26-21)13-8-9-23-17(11-13)24-20(28)14-4-7-16(27)10-14/h2-3,5-6,8-9,11,14H,4,7,10H2,1H3,(H,25,26)(H,23,24,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	21	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50524511 (CHEMBL4555253) Show SMILES CSc1nc(c([nH]1)-c1ccnc(NC(=O)c2ccoc2)c1)-c1ccc(F)cc1 Show InChI InChI=1S/C20H15FN4O2S/c1-28-20-24-17(12-2-4-15(21)5-3-12)18(25-20)13-6-8-22-16(10-13)23-19(26)14-7-9-27-11-14/h2-11H,1H3,(H,24,25)(H,22,23,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Eberhard Karls Universit£t T£bingen Curated by ChEMBL					Assay Description Inhibition of p38alpha MAPK (unknown origin) using ATF-2 as substrate after 1 hr by ELISA				Eur J Med Chem 175: 309-329 (2019) Article DOI: 10.1016/j.ejmech.2019.04.035 BindingDB Entry DOI: 10.7270/Q29C71T1
					More data for this Ligand-Target Pair

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