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SMILES: Oc1ccc2c3cc(O)c(O)cc3n(C(=O)CCc3ccccc3)c2c1O

InChI Key: InChIKey=RCNJNRIRPVQSJH-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 4117   

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
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
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