Found 48 hits of Enzyme Inhibition Constant Data 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 |
|---|
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50365890
(CHEMBL1957875)Show SMILES C[C@@H](Nc1ccccc1)c1cc(C)cn2c1nc(cc2=O)N1CCOCC1 |r| Show InChI InChI=1S/C21H24N4O2/c1-15-12-18(16(2)22-17-6-4-3-5-7-17)21-23-19(13-20(26)25(21)14-15)24-8-10-27-11-9-24/h3-7,12-14,16,22H,8-11H2,1-2H3/t16-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| Purchase
CHEMBL
MCE
PC cid
PC sid
PDB
UniChem
Similars
| Article
PubMed
| n/a | n/a | 49 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393999
(CHEMBL2158437)Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-3-1-2-10(14(11)17)9-18-15-19-12(8-13(22)20-15)21-4-6-23-7-5-21/h1-3,8H,4-7,9H2,(H2,18,19,20,22) | 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 | 84 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393984
(CHEMBL2158436)Show InChI InChI=1S/C19H20N4O2/c24-18-12-17(23-8-10-25-11-9-23)21-19(22-18)20-13-15-6-3-5-14-4-1-2-7-16(14)15/h1-7,12H,8-11,13H2,(H2,20,21,22,24) | 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 | 93 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50393984
(CHEMBL2158436)Show InChI InChI=1S/C19H20N4O2/c24-18-12-17(23-8-10-25-11-9-23)21-19(22-18)20-13-15-6-3-5-14-4-1-2-7-16(14)15/h1-7,12H,8-11,13H2,(H2,20,21,22,24) | 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 | 140 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of PI3K p110delta |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393996
(CHEMBL2158438)Show InChI InChI=1S/C15H17ClN4O2/c16-12-3-1-2-11(8-12)10-17-15-18-13(9-14(21)19-15)20-4-6-22-7-5-20/h1-3,8-9H,4-7,10H2,(H2,17,18,19,21) | 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 | 470 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393997
(CHEMBL2158439)Show InChI InChI=1S/C15H17ClN4O2/c16-12-4-2-1-3-11(12)10-17-15-18-13(9-14(21)19-15)20-5-7-22-8-6-20/h1-4,9H,5-8,10H2,(H2,17,18,19,21) | 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 | 570 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393998
(CHEMBL2158440)Show SMILES Clc1ccc(Cl)c(CNc2nc(cc(=O)[nH]2)N2CCOCC2)c1 Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-1-2-12(17)10(7-11)9-18-15-19-13(8-14(22)20-15)21-3-5-23-6-4-21/h1-2,7-8H,3-6,9H2,(H2,18,19,20,22) | 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 | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393989
(CHEMBL2158443)Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-3-1-2-10(14(11)17)9-18-12-8-13(20-15(22)19-12)21-4-6-23-7-5-21/h1-3,8H,4-7,9H2,(H2,18,19,20,22) | 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 | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393988
(CHEMBL2158441)Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-2-1-3-12(17)10(11)9-18-15-19-13(8-14(22)20-15)21-4-6-23-7-5-21/h1-3,8H,4-7,9H2,(H2,18,19,20,22) | 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 | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393985
(CHEMBL2158431)Show InChI InChI=1S/C16H17N5O/c17-11-15-19-14(18-12-13-4-2-1-3-5-13)10-16(20-15)21-6-8-22-9-7-21/h1-5,10H,6-9,12H2,(H,18,19,20) | 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 | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393986
(CHEMBL2158390)Show InChI InChI=1S/C15H18N4O2/c20-14-10-13(19-6-8-21-9-7-19)17-15(18-14)16-11-12-4-2-1-3-5-12/h1-5,10H,6-9,11H2,(H2,16,17,18,20) | 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 | 1.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393987
(CHEMBL2158427)Show InChI InChI=1S/C16H19N5O2/c17-15(22)13-10-14(21-6-8-23-9-7-21)20-16(19-13)18-11-12-4-2-1-3-5-12/h1-5,10H,6-9,11H2,(H2,17,22)(H,18,19,20) | 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 | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393983
(CHEMBL2158442)Show InChI InChI=1S/C19H20N4O2/c24-19-21-17(12-18(22-19)23-8-10-25-11-9-23)20-13-15-6-3-5-14-4-1-2-7-16(14)15/h1-7,12H,8-11,13H2,(H2,20,21,22,24) | 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 | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393999
(CHEMBL2158437)Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-3-1-2-10(14(11)17)9-18-15-19-12(8-13(22)20-15)21-4-6-23-7-5-21/h1-3,8H,4-7,9H2,(H2,18,19,20,22) | 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 | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393988
(CHEMBL2158441)Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-2-1-3-12(17)10(11)9-18-15-19-13(8-14(22)20-15)21-4-6-23-7-5-21/h1-3,8H,4-7,9H2,(H2,18,19,20,22) | 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 | 3.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393984
(CHEMBL2158436)Show InChI InChI=1S/C19H20N4O2/c24-18-12-17(23-8-10-25-11-9-23)21-19(22-18)20-13-15-6-3-5-14-4-1-2-7-16(14)15/h1-7,12H,8-11,13H2,(H2,20,21,22,24) | 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 | 4.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393998
(CHEMBL2158440)Show SMILES Clc1ccc(Cl)c(CNc2nc(cc(=O)[nH]2)N2CCOCC2)c1 Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-1-2-12(17)10(7-11)9-18-15-19-13(8-14(22)20-15)21-3-5-23-6-4-21/h1-2,7-8H,3-6,9H2,(H2,18,19,20,22) | 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 | 4.52E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393997
(CHEMBL2158439)Show InChI InChI=1S/C15H17ClN4O2/c16-12-4-2-1-3-11(12)10-17-15-18-13(9-14(21)19-15)20-5-7-22-8-6-20/h1-4,9H,5-8,10H2,(H2,17,18,19,21) | 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 | 4.88E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50365890
(CHEMBL1957875)Show SMILES C[C@@H](Nc1ccccc1)c1cc(C)cn2c1nc(cc2=O)N1CCOCC1 |r| Show InChI InChI=1S/C21H24N4O2/c1-15-12-18(16(2)22-17-6-4-3-5-7-17)21-23-19(13-20(26)25(21)14-15)24-8-10-27-11-9-24/h3-7,12-14,16,22H,8-11H2,1-2H3/t16-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
PC cid
PC sid
PDB
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393996
(CHEMBL2158438)Show InChI InChI=1S/C15H17ClN4O2/c16-12-3-1-2-11(8-12)10-17-15-18-13(9-14(21)19-15)20-4-6-22-7-5-20/h1-3,8-9H,4-7,10H2,(H2,17,18,19,21) | 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 | 7.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393982
(CHEMBL2158444)Show SMILES C[C@H](Nc1cc(nc(=O)[nH]1)N1CCOCC1)c1cccc2ccccc12 |r| Show InChI InChI=1S/C20H22N4O2/c1-14(16-8-4-6-15-5-2-3-7-17(15)16)21-18-13-19(23-20(25)22-18)24-9-11-26-12-10-24/h2-8,13-14H,9-12H2,1H3,(H2,21,22,23,25)/t14-/m0/s1 | 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 | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393986
(CHEMBL2158390)Show InChI InChI=1S/C15H18N4O2/c20-14-10-13(19-6-8-21-9-7-19)17-15(18-14)16-11-12-4-2-1-3-5-12/h1-5,10H,6-9,11H2,(H2,16,17,18,20) | 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 | 1.22E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50393984
(CHEMBL2158436)Show InChI InChI=1S/C19H20N4O2/c24-18-12-17(23-8-10-25-11-9-23)21-19(22-18)20-13-15-6-3-5-14-4-1-2-7-16(14)15/h1-7,12H,8-11,13H2,(H2,20,21,22,24) | 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 | 1.85E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of PI3K p110gamma |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393981
(CHEMBL2158428)Show InChI InChI=1S/C17H21N5O2/c1-18-16(23)14-11-15(22-7-9-24-10-8-22)21-17(20-14)19-12-13-5-3-2-4-6-13/h2-6,11H,7-10,12H2,1H3,(H,18,23)(H,19,20,21) | 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 | 2.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393980
(CHEMBL2158429)Show InChI InChI=1S/C18H23N5O2/c1-22(2)17(24)15-12-16(23-8-10-25-11-9-23)21-18(20-15)19-13-14-6-4-3-5-7-14/h3-7,12H,8-11,13H2,1-2H3,(H,19,20,21) | 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 | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393979
(CHEMBL2158424)Show InChI InChI=1S/C15H18N4O2/c20-15-17-13(16-11-12-4-2-1-3-5-12)10-14(18-15)19-6-8-21-9-7-19/h1-5,10H,6-9,11H2,(H2,16,17,18,20) | 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 | 2.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393978
(CHEMBL2158434)Show InChI InChI=1S/C18H21N3O3/c1-23-18(22)15-11-16(19-13-14-5-3-2-4-6-14)20-17(12-15)21-7-9-24-10-8-21/h2-6,11-12H,7-10,13H2,1H3,(H,19,20) | 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 | 3.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393977
(CHEMBL2158426)Show InChI InChI=1S/C16H19N3O2/c20-14-10-15(17-12-13-4-2-1-3-5-13)18-16(11-14)19-6-8-21-9-7-19/h1-5,10-11H,6-9,12H2,(H2,17,18,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393994
(CHEMBL2158445)Show SMILES C[C@@H](Nc1cc(nc(=O)[nH]1)N1CCOCC1)c1cccc2ccccc12 |r| Show InChI InChI=1S/C20H22N4O2/c1-14(16-8-4-6-15-5-2-3-7-17(15)16)21-18-13-19(23-20(25)22-18)24-9-11-26-12-10-24/h2-8,13-14H,9-12H2,1H3,(H2,21,22,23,25)/t14-/m1/s1 | 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 | 3.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393990
(CHEMBL2158433)Show InChI InChI=1S/C15H18N4O/c1-2-4-13(5-3-1)11-16-14-10-15(18-12-17-14)19-6-8-20-9-7-19/h1-5,10,12H,6-9,11H2,(H,16,17,18) | 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 | 3.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393985
(CHEMBL2158431)Show InChI InChI=1S/C16H17N5O/c17-11-15-19-14(18-12-13-4-2-1-3-5-13)10-16(20-15)21-6-8-22-9-7-21/h1-5,10H,6-9,12H2,(H,18,19,20) | 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 | 4.14E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393995
(CHEMBL2158435)Show InChI InChI=1S/C17H21N3O2/c21-13-15-10-16(18-12-14-4-2-1-3-5-14)19-17(11-15)20-6-8-22-9-7-20/h1-5,10-11,21H,6-9,12-13H2,(H,18,19) | 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 | 4.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393982
(CHEMBL2158444)Show SMILES C[C@H](Nc1cc(nc(=O)[nH]1)N1CCOCC1)c1cccc2ccccc12 |r| Show InChI InChI=1S/C20H22N4O2/c1-14(16-8-4-6-15-5-2-3-7-17(15)16)21-18-13-19(23-20(25)22-18)24-9-11-26-12-10-24/h2-8,13-14H,9-12H2,1H3,(H2,21,22,23,25)/t14-/m0/s1 | 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 | 5.28E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393993
(CHEMBL2158425)Show InChI InChI=1S/C15H18N4O2/c20-14-10-13(16-11-12-4-2-1-3-5-12)17-15(18-14)19-6-8-21-9-7-19/h1-5,10H,6-9,11H2,(H2,16,17,18,20) | 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 | 6.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393983
(CHEMBL2158442)Show InChI InChI=1S/C19H20N4O2/c24-19-21-17(12-18(22-19)23-8-10-25-11-9-23)20-13-15-6-3-5-14-4-1-2-7-16(14)15/h1-7,12H,8-11,13H2,(H2,20,21,22,24) | 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 | >8.33E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393991
(CHEMBL2158432)Show InChI InChI=1S/C16H21N5O/c17-11-15-19-14(18-12-13-4-2-1-3-5-13)10-16(20-15)21-6-8-22-9-7-21/h1-5,10H,6-9,11-12,17H2,(H,18,19,20) | 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 | >8.33E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393979
(CHEMBL2158424)Show InChI InChI=1S/C15H18N4O2/c20-15-17-13(16-11-12-4-2-1-3-5-12)10-14(18-15)19-6-8-21-9-7-19/h1-5,10H,6-9,11H2,(H2,16,17,18,20) | 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 | >8.33E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393990
(CHEMBL2158433)Show InChI InChI=1S/C15H18N4O/c1-2-4-13(5-3-1)11-16-14-10-15(18-12-17-14)19-6-8-20-9-7-19/h1-5,10,12H,6-9,11H2,(H,16,17,18) | 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 | >8.33E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393992
(CHEMBL2158430)Show InChI InChI=1S/C15H19N5O/c16-15-18-13(17-11-12-4-2-1-3-5-12)10-14(19-15)20-6-8-21-9-7-20/h1-5,10H,6-9,11H2,(H3,16,17,18,19) | 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 | >8.33E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393991
(CHEMBL2158432)Show InChI InChI=1S/C16H21N5O/c17-11-15-19-14(18-12-13-4-2-1-3-5-13)10-16(20-15)21-6-8-22-9-7-21/h1-5,10H,6-9,11-12,17H2,(H,18,19,20) | 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 | 8.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393989
(CHEMBL2158443)Show InChI InChI=1S/C15H16Cl2N4O2/c16-11-3-1-2-10(14(11)17)9-18-12-8-13(20-15(22)19-12)21-4-6-23-7-5-21/h1-3,8H,4-7,9H2,(H2,18,19,20,22) | 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 | 1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50393992
(CHEMBL2158430)Show InChI InChI=1S/C15H19N5O/c16-15-18-13(17-11-12-4-2-1-3-5-12)10-14(19-15)20-6-8-21-9-7-20/h1-5,10H,6-9,11H2,(H3,16,17,18,19) | 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 | 1.10E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393995
(CHEMBL2158435)Show InChI InChI=1S/C17H21N3O2/c21-13-15-10-16(18-12-14-4-2-1-3-5-14)19-17(11-15)20-6-8-22-9-7-20/h1-5,10-11,21H,6-9,12-13H2,(H,18,19) | 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 | 1.19E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM37251
(4-methyl-6-(4-morpholinyl)-N-(phenylmethyl)-2-pyri...)Show InChI InChI=1S/C16H20N4O/c1-13-11-15(20-7-9-21-10-8-20)19-16(18-13)17-12-14-5-3-2-4-6-14/h2-6,11H,7-10,12H2,1H3,(H,17,18,19) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.30E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110beta expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen ass... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393977
(CHEMBL2158426)Show InChI InChI=1S/C16H19N3O2/c20-14-10-15(17-12-13-4-2-1-3-5-13)18-16(11-14)19-6-8-21-9-7-19/h1-5,10-11H,6-9,12H2,(H2,17,18,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.42E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393994
(CHEMBL2158445)Show SMILES C[C@@H](Nc1cc(nc(=O)[nH]1)N1CCOCC1)c1cccc2ccccc12 |r| Show InChI InChI=1S/C20H22N4O2/c1-14(16-8-4-6-15-5-2-3-7-17(15)16)21-18-13-19(23-20(25)22-18)24-9-11-26-12-10-24/h2-8,13-14H,9-12H2,1H3,(H2,21,22,23,25)/t14-/m1/s1 | 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 | 1.46E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393978
(CHEMBL2158434)Show InChI InChI=1S/C18H21N3O3/c1-23-18(22)15-11-16(19-13-14-5-3-2-4-6-14)20-17(12-15)21-7-9-24-10-8-21/h2-6,11-12H,7-10,13H2,1H3,(H,19,20) | 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 | 2.40E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50393993
(CHEMBL2158425)Show InChI InChI=1S/C15H18N4O2/c20-14-10-13(16-11-12-4-2-1-3-5-12)17-15(18-14)19-6-8-21-9-7-19/h1-5,10H,6-9,11H2,(H2,16,17,18,20) | 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 | 2.83E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
AstraZeneca
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged PI3K p110alpha expressed in baculovirus using DiC8-PI(4,5)P2 as substrate after 20 mins by AlphaScreen as... |
Bioorg Med Chem Lett 22: 6665-70 (2012)
Article DOI: 10.1016/j.bmcl.2012.08.101
BindingDB Entry DOI: 10.7270/Q27H1KPB |
More data for this
Ligand-Target Pair | |
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