Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 50118377   

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
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human))	BDBM50118377 (CHEMBL3612515) Show SMILES Cc1ccc(cc1S(=O)(=O)n1ccc(n1)-c1cnn2ccc(Cl)nc12)[N+]([O-])=O Show InChI InChI=1S/C16H11ClN6O4S/c1-10-2-3-11(23(24)25)8-14(10)28(26,27)22-7-4-13(20-22)12-9-18-21-6-5-15(17)19-16(12)21/h2-9H,1H3	PDB 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	1.30	n/a	n/a	n/a	n/a	n/a	n/a
The University of Melbourne Curated by ChEMBL					Assay Description Inhibition of FLT3 (unknown origin) using biotin-Glu-Gly-Pro-Trp-Leu-Glu-Glu-Glu-Glu-Glu-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH2 as substrate after 90 mins b...				Bioorg Med Chem 23: 6280-96 (2015) Article DOI: 10.1016/j.bmc.2015.08.035 BindingDB Entry DOI: 10.7270/Q2KK9DM6
					More data for this Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform (Homo sapiens (Human))	BDBM50118377 (CHEMBL3612515) Show SMILES Cc1ccc(cc1S(=O)(=O)n1ccc(n1)-c1cnn2ccc(Cl)nc12)[N+]([O-])=O Show InChI InChI=1S/C16H11ClN6O4S/c1-10-2-3-11(23(24)25)8-14(10)28(26,27)22-7-4-13(20-22)12-9-18-21-6-5-15(17)19-16(12)21/h2-9H,1H3	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	1.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
The University of Melbourne Curated by ChEMBL					Assay Description Inhibition of PI3Kalpha (unknown origin) by radiometric assay				Bioorg Med Chem 23: 6280-96 (2015) Article DOI: 10.1016/j.bmc.2015.08.035 BindingDB Entry DOI: 10.7270/Q2KK9DM6
					More data for this Ligand-Target Pair
Cyclin-T1/Cyclin-dependent kinase 9 (Homo sapiens (Human))	BDBM50118377 (CHEMBL3612515) Show SMILES Cc1ccc(cc1S(=O)(=O)n1ccc(n1)-c1cnn2ccc(Cl)nc12)[N+]([O-])=O Show InChI InChI=1S/C16H11ClN6O4S/c1-10-2-3-11(23(24)25)8-14(10)28(26,27)22-7-4-13(20-22)12-9-18-21-6-5-15(17)19-16(12)21/h2-9H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
The University of Melbourne Curated by ChEMBL					Assay Description Inhibition of recombinant human CDK9/cyclin-T1 using H-YSPTSPSYSPTSPSYSPTSPS-KKKK-OH as substrate after 90 mins by luminescence assay				Bioorg Med Chem 23: 6280-96 (2015) Article DOI: 10.1016/j.bmc.2015.08.035 BindingDB Entry DOI: 10.7270/Q2KK9DM6
					More data for this Ligand-Target Pair