null

SMILES: COc1cc(ccc1Nc1ncc2c(C)cc(=O)n(-c3cccc(NC(=O)C=C)c3)c2n1)N1CCN(CC1)C(=O)CCCCCCCCCCCNC(=O)CC12CC3CC(CC(C3)C1)C2

InChI Key:

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50591179   

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
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human))	BDBM50591179 (CHEMBL5181769) Show SMILES COc1cc(ccc1Nc1ncc2c(C)cc(=O)n(-c3cccc(NC(=O)C=C)c3)c2n1)N1CCN(CC1)C(=O)CCCCCCCCCCCNC(=O)CC12CC3CC(CC(C3)C1)C2 |TLB:58:59:56.57.62:63,THB:60:59:56:62.61.63,60:61:56:64.59.58,58:57:63:64.59.60| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c01246 BindingDB Entry DOI: 10.7270/Q2FX7FG8
					More data for this Ligand-Target Pair
RAC-gamma serine/threonine-protein kinase (Homo sapiens (Human))	BDBM50591179 (CHEMBL5181769) Show SMILES COc1cc(ccc1Nc1ncc2c(C)cc(=O)n(-c3cccc(NC(=O)C=C)c3)c2n1)N1CCN(CC1)C(=O)CCCCCCCCCCCNC(=O)CC12CC3CC(CC(C3)C1)C2 |TLB:58:59:56.57.62:63,THB:60:59:56:62.61.63,60:61:56:64.59.58,58:57:63:64.59.60| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c01246 BindingDB Entry DOI: 10.7270/Q2FX7FG8
					More data for this Ligand-Target Pair
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human))	BDBM50591179 (CHEMBL5181769) Show SMILES COc1cc(ccc1Nc1ncc2c(C)cc(=O)n(-c3cccc(NC(=O)C=C)c3)c2n1)N1CCN(CC1)C(=O)CCCCCCCCCCCNC(=O)CC12CC3CC(CC(C3)C1)C2 |TLB:58:59:56.57.62:63,THB:60:59:56:62.61.63,60:61:56:64.59.58,58:57:63:64.59.60| Show InChI	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a
TBA									Citation and Details Article DOI: 10.1021/acs.jmedchem.2c01246 BindingDB Entry DOI: 10.7270/Q2FX7FG8
					More data for this Ligand-Target Pair