Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 25002   

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
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human))	BDBM25002 (4-[7-(3-aminopropoxy)-4-(2-cyclopropylethynyl)-1-e...) Show SMILES CCn1c(nc2c(ncc(OCCCN)c12)C#CC1CC1)-c1nonc1N Show InChI InChI=1S/C18H21N7O2/c1-2-25-16-13(26-9-3-8-19)10-21-12(7-6-11-4-5-11)14(16)22-18(25)15-17(20)24-27-23-15/h10-11H,2-5,8-9,19H2,1H3,(H2,20,24)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	79	n/a	n/a	n/a	n/a	7.5	22
GlaxoSmithKline					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from radiolabeled AT...				J Med Chem 51: 5663-79 (2008) Article DOI: 10.1021/jm8004527 BindingDB Entry DOI: 10.7270/Q29G5K3H
					More data for this Ligand-Target Pair
Ribosomal protein S6 kinase alpha-1 (Homo sapiens (Human))	BDBM25002 (4-[7-(3-aminopropoxy)-4-(2-cyclopropylethynyl)-1-e...) Show SMILES CCn1c(nc2c(ncc(OCCCN)c12)C#CC1CC1)-c1nonc1N Show InChI InChI=1S/C18H21N7O2/c1-2-25-16-13(26-9-3-8-19)10-21-12(7-6-11-4-5-11)14(16)22-18(25)15-17(20)24-27-23-15/h10-11H,2-5,8-9,19H2,1H3,(H2,20,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	251	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from radiolabeled AT...				J Med Chem 51: 5663-79 (2008) Article DOI: 10.1021/jm8004527 BindingDB Entry DOI: 10.7270/Q29G5K3H
					More data for this Ligand-Target Pair
Rho-associated protein kinase 1 (Homo sapiens (Human))	BDBM25002 (4-[7-(3-aminopropoxy)-4-(2-cyclopropylethynyl)-1-e...) Show SMILES CCn1c(nc2c(ncc(OCCCN)c12)C#CC1CC1)-c1nonc1N Show InChI InChI=1S/C18H21N7O2/c1-2-25-16-13(26-9-3-8-19)10-21-12(7-6-11-4-5-11)14(16)22-18(25)15-17(20)24-27-23-15/h10-11H,2-5,8-9,19H2,1H3,(H2,20,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from radiolabeled AT...				J Med Chem 51: 5663-79 (2008) Article DOI: 10.1021/jm8004527 BindingDB Entry DOI: 10.7270/Q29G5K3H
					More data for this Ligand-Target Pair