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SMILES: Cc1[nH]c(nc1C(=O)NC1CCCCC1)-c1cc(ccn1)-c1cncc(c1)N1CCOCC1

InChI Key:

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 557213   

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
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform (Homo sapiens (Human))	BDBM557213 (N-Cyclohexyl-5- methyl-2-(5- morpholin-4-yl-3, 4'-...) Show SMILES Cc1[nH]c(nc1C(=O)NC1CCCCC1)-c1cc(ccn1)-c1cncc(c1)N1CCOCC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<50	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The kinase reaction was conducted in polystyrene 384-well Greiner Bio-one white plate from Thermo Fisher Scientific in a final volume of 25 μL. ...				Citation and Details BindingDB Entry DOI: 10.7270/Q24T6NKW
					More data for this Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform (Homo sapiens (Human))	BDBM557213 (N-Cyclohexyl-5- methyl-2-(5- morpholin-4-yl-3, 4'-...) Show SMILES Cc1[nH]c(nc1C(=O)NC1CCCCC1)-c1cc(ccn1)-c1cncc(c1)N1CCOCC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	<50	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The kinase reaction was conducted in polystyrene 384-well Greiner Bio-one white plate from Thermo Fisher Scientific in a final volume of 25 μL. ...				Citation and Details BindingDB Entry DOI: 10.7270/Q24T6NKW
					More data for this Ligand-Target Pair