Compile Data Set for Download or QSAR

Found 113 hits with Last Name = 'goddard' and Initial = 'c'   

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
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4078 (6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.0...) Show SMILES Oc1cc2c3c(oc(=O)c4cc(O)c(O)c(oc2=O)c34)c1O Show InChI InChI=1S/C14H6O8/c15-5-1-3-7-8-4(14(20)22-11(7)9(5)17)2-6(16)10(18)12(8)21-13(3)19/h1-2,15-18H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4115 (9-[(4-methanesulfonylphenyl)carbonyl]-9H-carbazole...) Show SMILES CS(=O)(=O)c1ccc(cc1)C(=O)n1c2cc(O)c(O)cc2c2ccc(O)c(O)c12 Show InChI InChI=1S/C20H15NO7S/c1-29(27,28)11-4-2-10(3-5-11)20(26)21-14-9-17(24)16(23)8-13(14)12-6-7-15(22)19(25)18(12)21/h2-9,22-25H,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4117 (3-phenyl-1-(1,2,6,7-tetrahydroxy-9H-carbazol-9-yl)...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(C(=O)CCc3ccccc3)c2c1O Show InChI InChI=1S/C21H17NO5/c23-16-8-7-13-14-10-17(24)18(25)11-15(14)22(20(13)21(16)27)19(26)9-6-12-4-2-1-3-5-12/h1-5,7-8,10-11,23-25,27H,6,9H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4100 (4-[(1,2,6,7-tetrahydroxy-9H-carbazol-9-yl)methyl]b...) Show SMILES Oc1cc2n(Cc3ccc(cc3)C#N)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C20H14N2O4/c21-9-11-1-3-12(4-2-11)10-22-15-8-18(25)17(24)7-14(15)13-5-6-16(23)20(26)19(13)22/h1-8,23-26H,10H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4109 (9-(naphthalen-2-ylcarbonyl)-9H-carbazole-1,2,6,7-t...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(C(=O)c3ccc4ccccc4c3)c2c1O Show InChI InChI=1S/C23H15NO5/c25-18-8-7-15-16-10-19(26)20(27)11-17(16)24(21(15)22(18)28)23(29)14-6-5-12-3-1-2-4-13(12)9-14/h1-11,25-28H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4099 (9-(3-phenylpropyl)-9H-carbazole-1,2,6,7-tetrol | C...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(CCCc3ccccc3)c2c1O Show InChI InChI=1S/C21H19NO4/c23-17-9-8-14-15-11-18(24)19(25)12-16(15)22(20(14)21(17)26)10-4-7-13-5-2-1-3-6-13/h1-3,5-6,8-9,11-12,23-26H,4,7,10H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50286755 (8-Methoxy-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-...) Show SMILES COc1ccc2Cc3c(Nc2c1)nc[nH]c3=O Show InChI InChI=1S/C12H11N3O2/c1-17-8-3-2-7-4-9-11(15-10(7)5-8)13-6-14-12(9)16/h2-3,5-6H,4H2,1H3,(H2,13,14,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of cellular oncogene pp60 c-src				Bioorg Med Chem Lett 5: 1007-1010 (1995) Article DOI: 10.1016/0960-894X(95)00157-O BindingDB Entry DOI: 10.7270/Q2DJ5FKR
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50132155 (7,8-Dimethoxy-5,10-dihydro-1H-pyrimido[4,5-b]quino...) Show SMILES COc1cc2Cc3c(Nc2cc1OC)nc[nH]c3=O Show InChI InChI=1S/C13H13N3O3/c1-18-10-4-7-3-8-12(14-6-15-13(8)17)16-9(7)5-11(10)19-2/h4-6H,3H2,1-2H3,(H2,14,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of cellular oncogene pp60 c-src				Bioorg Med Chem Lett 5: 1007-1010 (1995) Article DOI: 10.1016/0960-894X(95)00157-O BindingDB Entry DOI: 10.7270/Q2DJ5FKR
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4099 (9-(3-phenylpropyl)-9H-carbazole-1,2,6,7-tetrol | C...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(CCCc3ccccc3)c2c1O Show InChI InChI=1S/C21H19NO4/c23-17-9-8-14-15-11-18(24)19(25)12-16(15)22(20(14)21(17)26)10-4-7-13-5-2-1-3-6-13/h1-3,5-6,8-9,11-12,23-26H,4,7,10H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4110 (9-[(3-nitrophenyl)carbonyl]-9H-carbazole-1,2,6,7-t...) Show SMILES Oc1ccc2c(c1O)n(C(=O)c1cccc(c1)[N+]([O-])=O)c1cc(O)c(O)cc21 Show InChI InChI=1S/C19H12N2O7/c22-14-5-4-11-12-7-15(23)16(24)8-13(12)20(17(11)18(14)25)19(26)9-2-1-3-10(6-9)21(27)28/h1-8,22-25H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4108 (9-[(4-phenylphenyl)carbonyl]-9H-carbazole-1,2,6,7-...) Show SMILES Oc1cc2n(C(=O)c3ccc(cc3)-c3ccccc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C25H17NO5/c27-20-11-10-17-18-12-21(28)22(29)13-19(18)26(23(17)24(20)30)25(31)16-8-6-15(7-9-16)14-4-2-1-3-5-14/h1-13,27-30H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4093 (4-bromo-9H-carbazole-1,2,6,7-tetrol | Carbazole de...) Show SMILES Oc1cc2[nH]c3c(O)c(O)cc(Br)c3c2cc1O Show InChI InChI=1S/C12H8BrNO4/c13-5-2-9(17)12(18)11-10(5)4-1-7(15)8(16)3-6(4)14-11/h1-3,14-18H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4078 (6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.0...) Show SMILES Oc1cc2c3c(oc(=O)c4cc(O)c(O)c(oc2=O)c34)c1O Show InChI InChI=1S/C14H6O8/c15-5-1-3-7-8-4(14(20)22-11(7)9(5)17)2-6(16)10(18)12(8)21-13(3)19/h1-2,15-18H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4106 (9-{[4-(benzenesulfonyl)phenyl]methyl}-9H-carbazole...) Show SMILES Oc1cc2n(Cc3ccc(cc3)S(=O)(=O)c3ccccc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C25H19NO6S/c27-21-11-10-18-19-12-22(28)23(29)13-20(19)26(24(18)25(21)30)14-15-6-8-17(9-7-15)33(31,32)16-4-2-1-3-5-16/h1-13,27-30H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4111 (9-{[4-(trifluoromethyl)phenyl]carbonyl}-9H-carbazo...) Show SMILES Oc1cc2n(C(=O)c3ccc(cc3)C(F)(F)F)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C20H12F3NO5/c21-20(22,23)10-3-1-9(2-4-10)19(29)24-13-8-16(27)15(26)7-12(13)11-5-6-14(25)18(28)17(11)24/h1-8,25-28H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4113 (9-[(4-tert-butylphenyl)carbonyl]-9H-carbazole-1,2,...) Show SMILES CC(C)(C)c1ccc(cc1)C(=O)n1c2cc(O)c(O)cc2c2ccc(O)c(O)c12 Show InChI InChI=1S/C23H21NO5/c1-23(2,3)13-6-4-12(5-7-13)22(29)24-16-11-19(27)18(26)10-15(16)14-8-9-17(25)21(28)20(14)24/h4-11,25-28H,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4092 (9H-carbazole-1,2,6,7-tetrol | Carbazole deriv. 9b) Show SMILES Oc1ccc2c([nH]c3cc(O)c(O)cc23)c1O Show InChI InChI=1S/C12H9NO4/c14-8-2-1-5-6-3-9(15)10(16)4-7(6)13-11(5)12(8)17/h1-4,13-17H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4080 (2,3,7,8-tetrahydroxy-5,6-dihydrophenanthridin-6-on...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3[nH]c(=O)c2c1O Show InChI InChI=1S/C13H9NO5/c15-8-2-1-5-6-3-9(16)10(17)4-7(6)14-13(19)11(5)12(8)18/h1-4,15-18H,(H,14,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4103 (9-[(2,6-dichlorophenyl)methyl]-9H-carbazole-1,2,6,...) Show SMILES Oc1cc2n(Cc3c(Cl)cccc3Cl)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C19H13Cl2NO4/c20-12-2-1-3-13(21)11(12)8-22-14-7-17(25)16(24)6-10(14)9-4-5-15(23)19(26)18(9)22/h1-7,23-26H,8H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4085 (2,3,8,9-tetrahydroxy-5-[(4-nitrophenyl)methyl]-5,6...) Show SMILES Oc1cc2n(Cc3ccc(cc3)[N+]([O-])=O)c(=O)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C20H14N2O7/c23-16-5-12-13-6-17(24)19(26)8-15(13)21(20(27)14(12)7-18(16)25)9-10-1-3-11(4-2-10)22(28)29/h1-8,23-26H,9H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4101 (4-[(4-bromo-1,2,6,7-tetrahydroxy-9H-carbazol-9-yl)...) Show SMILES Oc1cc2n(Cc3ccc(cc3)C#N)c3c(O)c(O)cc(Br)c3c2cc1O Show InChI InChI=1S/C20H13BrN2O4/c21-13-6-17(26)20(27)19-18(13)12-5-15(24)16(25)7-14(12)23(19)9-11-3-1-10(8-22)2-4-11/h1-7,24-27H,9H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4097 (9-benzoyl-9H-carbazole-1,2,6,7-tetrol | Carbazole ...) Show SMILES Oc1cc2n(C(=O)c3ccccc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C19H13NO5/c21-14-7-6-11-12-8-15(22)16(23)9-13(12)20(17(11)18(14)24)19(25)10-4-2-1-3-5-10/h1-9,21-24H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4079 (2,3,8,9-tetrahydroxy-5,6-dihydrophenanthridin-6-on...) Show SMILES Oc1cc2[nH]c(=O)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C13H9NO5/c15-9-1-5-6-2-10(16)12(18)4-8(6)14-13(19)7(5)3-11(9)17/h1-4,15-18H,(H,14,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4109 (9-(naphthalen-2-ylcarbonyl)-9H-carbazole-1,2,6,7-t...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(C(=O)c3ccc4ccccc4c3)c2c1O Show InChI InChI=1S/C23H15NO5/c25-18-8-7-15-16-10-19(26)20(27)11-17(16)24(21(15)22(18)28)23(29)14-6-5-12-3-1-2-4-13(12)9-14/h1-11,25-28H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50286752 (7,8-Dimethoxy-3-methyl-5,10-dihydro-3H-pyrimido[4,...) Show SMILES COc1cc2Cc3c(Nc2cc1OC)ncn(C)c3=O Show InChI InChI=1S/C14H15N3O3/c1-17-7-15-13-9(14(17)18)4-8-5-11(19-2)12(20-3)6-10(8)16-13/h5-7,16H,4H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of cellular oncogene pp60 c-src				Bioorg Med Chem Lett 5: 1007-1010 (1995) Article DOI: 10.1016/0960-894X(95)00157-O BindingDB Entry DOI: 10.7270/Q2DJ5FKR
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4087 (5-[(3,4-dichlorophenyl)methyl]-2,3,8,9-tetrahydrox...) Show SMILES Oc1cc2n(Cc3ccc(Cl)c(Cl)c3)c(=O)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C20H13Cl2NO5/c21-13-2-1-9(3-14(13)22)8-23-15-7-19(27)17(25)5-11(15)10-4-16(24)18(26)6-12(10)20(23)28/h1-7,24-27H,8H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4107 (9-[(4-bromophenyl)carbonyl]-9H-carbazole-1,2,6,7-t...) Show SMILES Oc1cc2n(C(=O)c3ccc(Br)cc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C19H12BrNO5/c20-10-3-1-9(2-4-10)19(26)21-13-8-16(24)15(23)7-12(13)11-5-6-14(22)18(25)17(11)21/h1-8,22-25H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4091 (9H-carbazole-2,3,6,7-tetrol | Carbazole deriv. 9a) Show SMILES Oc1cc2[nH]c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C12H9NO4/c14-9-1-5-6-2-10(15)12(17)4-8(6)13-7(5)3-11(9)16/h1-4,13-17H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4110 (9-[(3-nitrophenyl)carbonyl]-9H-carbazole-1,2,6,7-t...) Show SMILES Oc1ccc2c(c1O)n(C(=O)c1cccc(c1)[N+]([O-])=O)c1cc(O)c(O)cc21 Show InChI InChI=1S/C19H12N2O7/c22-14-5-4-11-12-7-15(23)16(24)8-13(12)20(17(11)18(14)25)19(26)9-2-1-3-10(6-9)21(27)28/h1-8,22-25H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4105 (9-[(3-methylphenyl)methyl]-9H-carbazole-1,2,6,7-te...) Show SMILES Cc1cccc(Cn2c3cc(O)c(O)cc3c3ccc(O)c(O)c23)c1 Show InChI InChI=1S/C20H17NO4/c1-11-3-2-4-12(7-11)10-21-15-9-18(24)17(23)8-14(15)13-5-6-16(22)20(25)19(13)21/h2-9,22-25H,10H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4095 (9-benzyl-9H-carbazole-1,2,6,7-tetrol | Carbazole d...) Show SMILES Oc1cc2n(Cc3ccccc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C19H15NO4/c21-15-7-6-12-13-8-16(22)17(23)9-14(13)20(18(12)19(15)24)10-11-4-2-1-3-5-11/h1-9,21-24H,10H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4112 (4-bromo-9-{[4-(trifluoromethyl)phenyl]carbonyl}-9H...) Show SMILES Oc1cc2n(C(=O)c3ccc(cc3)C(F)(F)F)c3c(O)c(O)cc(Br)c3c2cc1O Show InChI InChI=1S/C20H11BrF3NO5/c21-11-6-15(28)18(29)17-16(11)10-5-13(26)14(27)7-12(10)25(17)19(30)8-1-3-9(4-2-8)20(22,23)24/h1-7,26-29H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4089 (5-{[4-(benzenesulfonyl)phenyl]methyl}-2,3,8,9-tetr...) Show SMILES Oc1cc2n(Cc3ccc(cc3)S(=O)(=O)c3ccccc3)c(=O)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C26H19NO7S/c28-22-10-18-19-11-23(29)25(31)13-21(19)27(26(32)20(18)12-24(22)30)14-15-6-8-17(9-7-15)35(33,34)16-4-2-1-3-5-16/h1-13,28-31H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4117 (3-phenyl-1-(1,2,6,7-tetrahydroxy-9H-carbazol-9-yl)...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(C(=O)CCc3ccccc3)c2c1O Show InChI InChI=1S/C21H17NO5/c23-16-8-7-13-14-10-17(24)18(25)11-15(14)22(20(13)21(16)27)19(26)9-6-12-4-2-1-3-5-12/h1-5,7-8,10-11,23-25,27H,6,9H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4108 (9-[(4-phenylphenyl)carbonyl]-9H-carbazole-1,2,6,7-...) Show SMILES Oc1cc2n(C(=O)c3ccc(cc3)-c3ccccc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C25H17NO5/c27-20-11-10-17-18-12-21(28)22(29)13-19(18)26(23(17)24(20)30)25(31)16-8-6-15(7-9-16)14-4-2-1-3-5-14/h1-13,27-30H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4104 (9-[(4-bromophenyl)methyl]-9H-carbazole-1,2,6,7-tet...) Show SMILES Oc1cc2n(Cc3ccc(Br)cc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C19H14BrNO4/c20-11-3-1-10(2-4-11)9-21-14-8-17(24)16(23)7-13(14)12-5-6-15(22)19(25)18(12)21/h1-8,22-25H,9H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50286758 (7-Methoxy-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-...) Show SMILES COc1ccc2Nc3nc[nH]c(=O)c3Cc2c1 Show InChI InChI=1S/C12H11N3O2/c1-17-8-2-3-10-7(4-8)5-9-11(15-10)13-6-14-12(9)16/h2-4,6H,5H2,1H3,(H2,13,14,15,16)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of cellular oncogene pp60 c-src				Bioorg Med Chem Lett 5: 1007-1010 (1995) Article DOI: 10.1016/0960-894X(95)00157-O BindingDB Entry DOI: 10.7270/Q2DJ5FKR
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4116 (4-bromo-9-[(4-methanesulfonylphenyl)carbonyl]-9H-c...) Show SMILES CS(=O)(=O)c1ccc(cc1)C(=O)n1c2cc(O)c(O)cc2c2c(Br)cc(O)c(O)c12 Show InChI InChI=1S/C20H14BrNO7S/c1-30(28,29)10-4-2-9(3-5-10)20(27)22-13-8-15(24)14(23)6-11(13)17-12(21)7-16(25)19(26)18(17)22/h2-8,23-26H,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4096 (9-benzoyl-9H-carbazole-2,3,6,7-tetrol | Carbazole ...) Show SMILES Oc1cc2n(C(=O)c3ccccc3)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C19H13NO5/c21-15-6-11-12-7-16(22)18(24)9-14(12)20(13(11)8-17(15)23)19(25)10-4-2-1-3-5-10/h1-9,21-24H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4081 (5-ethyl-2,3,8,9-tetrahydroxy-5,6-dihydrophenanthri...) Show SMILES CCn1c2cc(O)c(O)cc2c2cc(O)c(O)cc2c1=O Show InChI InChI=1S/C15H13NO5/c1-2-16-10-6-14(20)12(18)4-8(10)7-3-11(17)13(19)5-9(7)15(16)21/h3-6,17-20H,2H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.10E+3	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4107 (9-[(4-bromophenyl)carbonyl]-9H-carbazole-1,2,6,7-t...) Show SMILES Oc1cc2n(C(=O)c3ccc(Br)cc3)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C19H12BrNO5/c20-10-3-1-9(2-4-10)19(26)21-13-8-16(24)15(23)7-12(13)11-5-6-14(22)18(25)17(11)21/h1-8,22-25H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4083 (5-(Phenylmethyl)-2,3,8,9-tetrahydroxy-6(5H)-phenan...) Show SMILES Oc1cc2n(Cc3ccccc3)c(=O)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C20H15NO5/c22-16-6-12-13-7-17(23)19(25)9-15(13)21(10-11-4-2-1-3-5-11)20(26)14(12)8-18(16)24/h1-9,22-25H,10H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.40E+3	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4101 (4-[(4-bromo-1,2,6,7-tetrahydroxy-9H-carbazol-9-yl)...) Show SMILES Oc1cc2n(Cc3ccc(cc3)C#N)c3c(O)c(O)cc(Br)c3c2cc1O Show InChI InChI=1S/C20H13BrN2O4/c21-13-6-17(26)20(27)19-18(13)12-5-15(24)16(25)7-14(12)23(19)9-11-3-1-10(8-22)2-4-11/h1-7,24-27H,9H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4094 (9-benzyl-9H-carbazole-2,3,6,7-tetrol | Carbazole d...) Show SMILES Oc1cc2n(Cc3ccccc3)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C19H15NO4/c21-16-6-12-13-7-17(22)19(24)9-15(13)20(14(12)8-18(16)23)10-11-4-2-1-3-5-11/h1-9,21-24H,10H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4112 (4-bromo-9-{[4-(trifluoromethyl)phenyl]carbonyl}-9H...) Show SMILES Oc1cc2n(C(=O)c3ccc(cc3)C(F)(F)F)c3c(O)c(O)cc(Br)c3c2cc1O Show InChI InChI=1S/C20H11BrF3NO5/c21-11-6-15(28)18(29)17-16(11)10-5-13(26)14(27)7-12(10)25(17)19(30)8-1-3-9(4-2-8)20(22,23)24/h1-7,26-29H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4090 (5-{[4-(benzenesulfonyl)phenyl]methyl}-2,3,7,8-tetr...) Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(Cc3ccc(cc3)S(=O)(=O)c3ccccc3)c(=O)c2c1O Show InChI InChI=1S/C26H19NO7S/c28-21-11-10-18-19-12-22(29)23(30)13-20(19)27(26(32)24(18)25(21)31)14-15-6-8-17(9-7-15)35(33,34)16-4-2-1-3-5-16/h1-13,28-31H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4120 (9-[(2,5-dichlorobenzene)sulfonyl]-9H-carbazole-1,2...) Show SMILES Oc1cc2n(c3c(O)c(O)ccc3c2cc1O)S(=O)(=O)c1cc(Cl)ccc1Cl Show InChI InChI=1S/C18H11Cl2NO6S/c19-8-1-3-11(20)16(5-8)28(26,27)21-12-7-15(24)14(23)6-10(12)9-2-4-13(22)18(25)17(9)21/h1-7,22-25H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4098 (9-(pyridin-3-ylmethyl)-9H-carbazole-2,3,6,7-tetrol...) Show SMILES Oc1cc2n(Cc3cccnc3)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C18H14N2O4/c21-15-4-11-12-5-16(22)18(24)7-14(12)20(13(11)6-17(15)23)9-10-2-1-3-19-8-10/h1-8,21-24H,9H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
cAMP-dependent protein kinase catalytic subunit alpha (Bos taurus (bovine))	BDBM4085 (2,3,8,9-tetrahydroxy-5-[(4-nitrophenyl)methyl]-5,6...) Show SMILES Oc1cc2n(Cc3ccc(cc3)[N+]([O-])=O)c(=O)c3cc(O)c(O)cc3c2cc1O Show InChI InChI=1S/C20H14N2O7/c23-16-5-12-13-6-17(24)19(26)8-15(13)21(20(27)14(12)7-18(16)25)9-10-1-3-11(4-2-10)22(28)29/h1-8,23-26H,9H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.40E+3	n/a	n/a	n/a	n/a	7.4	30
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4102 (9-{[4-(trifluoromethyl)phenyl]methyl}-9H-carbazole...) Show SMILES Oc1cc2n(Cc3ccc(cc3)C(F)(F)F)c3c(O)c(O)ccc3c2cc1O Show InChI InChI=1S/C20H14F3NO4/c21-20(22,23)11-3-1-10(2-4-11)9-24-14-8-17(27)16(26)7-13(14)12-5-6-15(25)19(28)18(12)24/h1-8,25-28H,9H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...				J Med Chem 37: 2224-31 (1994) Article DOI: 10.1021/jm00040a015 BindingDB Entry DOI: 10.7270/Q27M0648
					More data for this Ligand-Target Pair

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