BDBM50234164 CHEMBL4100450

SMILES: Cn1nc(nc1CN1CCOCC1)-c1cnc(N)c(n1)-n1nnc2ccccc12

InChI Key: InChIKey=REPKZIYHWKNJBG-UHFFFAOYSA-N

Data: 4 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50234164   

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
p110α/p85α (Homo sapiens (Human))	BDBM50234164 (CHEMBL4100450) Show SMILES Cn1nc(nc1CN1CCOCC1)-c1cnc(N)c(n1)-n1nnc2ccccc12 Show InChI InChI=1S/C18H20N10O/c1-26-15(11-27-6-8-29-9-7-27)22-17(24-26)13-10-20-16(19)18(21-13)28-14-5-3-2-4-12(14)23-25-28/h2-5,10H,6-9,11H2,1H3,(H2,19,20)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of recombinant human His6-tagged PI3K p110alpha/p85alpha using DiC8-PIP2 as substrate preincubated for 15 mins followed by substrate addit...				Bioorg Med Chem Lett 27: 679-687 (2017) BindingDB Entry DOI: 10.7270/Q2TF00MM
					More data for this Ligand-Target Pair
p110β/p85α (Homo sapiens (Human))	BDBM50234164 (CHEMBL4100450) Show SMILES Cn1nc(nc1CN1CCOCC1)-c1cnc(N)c(n1)-n1nnc2ccccc12 Show InChI InChI=1S/C18H20N10O/c1-26-15(11-27-6-8-29-9-7-27)22-17(24-26)13-10-20-16(19)18(21-13)28-14-5-3-2-4-12(14)23-25-28/h2-5,10H,6-9,11H2,1H3,(H2,19,20)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	631	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of recombinant human His6-tagged PI3K p110beta/p85alpha using DiC8-PIP2 as substrate preincubated for 15 mins followed by substrate additi...				Bioorg Med Chem Lett 27: 679-687 (2017) BindingDB Entry DOI: 10.7270/Q2TF00MM
					More data for this Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform (Homo sapiens (Human))	BDBM50234164 (CHEMBL4100450) Show SMILES Cn1nc(nc1CN1CCOCC1)-c1cnc(N)c(n1)-n1nnc2ccccc12 Show InChI InChI=1S/C18H20N10O/c1-26-15(11-27-6-8-29-9-7-27)22-17(24-26)13-10-20-16(19)18(21-13)28-14-5-3-2-4-12(14)23-25-28/h2-5,10H,6-9,11H2,1H3,(H2,19,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	398	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of recombinant human His6-tagged PI3Kgamma (144 to 1102 residues) using DiC8-PIP2 as substrate preincubated for 15 mins followed by substr...				Bioorg Med Chem Lett 27: 679-687 (2017) BindingDB Entry DOI: 10.7270/Q2TF00MM
					More data for this Ligand-Target Pair
Phosphoinositide 3-Kinase (PI3K), delta (Homo sapiens (Human))	BDBM50234164 (CHEMBL4100450) Show SMILES Cn1nc(nc1CN1CCOCC1)-c1cnc(N)c(n1)-n1nnc2ccccc12 Show InChI InChI=1S/C18H20N10O/c1-26-15(11-27-6-8-29-9-7-27)22-17(24-26)13-10-20-16(19)18(21-13)28-14-5-3-2-4-12(14)23-25-28/h2-5,10H,6-9,11H2,1H3,(H2,19,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	63	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of recombinant human His6-tagged PI3K p110delta/p85alpha using DiC8-PIP2 as substrate preincubated for 15 mins followed by substrate addit...				Bioorg Med Chem Lett 27: 679-687 (2017) BindingDB Entry DOI: 10.7270/Q2TF00MM
					More data for this Ligand-Target Pair