Found 36 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 delta isoform
(Homo sapiens (Human)) | BDBM50315213
(2-(difluoromethyl)-1-(4,6-dimorpholin-4-yl-1,3,5-t...)Show SMILES FC(F)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H21F2N7O2/c20-15(21)16-22-13-3-1-2-4-14(13)28(16)19-24-17(26-5-9-29-10-6-26)23-18(25-19)27-7-11-30-12-8-27/h1-4,15H,5-12H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| MMDB
PDB
Article
PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50315213
(2-(difluoromethyl)-1-(4,6-dimorpholin-4-yl-1,3,5-t...)Show SMILES FC(F)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H21F2N7O2/c20-15(21)16-22-13-3-1-2-4-14(13)28(16)19-24-17(26-5-9-29-10-6-26)23-18(25-19)27-7-11-30-12-8-27/h1-4,15H,5-12H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50315213
(2-(difluoromethyl)-1-(4,6-dimorpholin-4-yl-1,3,5-t...)Show SMILES FC(F)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H21F2N7O2/c20-15(21)16-22-13-3-1-2-4-14(13)28(16)19-24-17(26-5-9-29-10-6-26)23-18(25-19)27-7-11-30-12-8-27/h1-4,15H,5-12H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50315213
(2-(difluoromethyl)-1-(4,6-dimorpholin-4-yl-1,3,5-t...)Show SMILES FC(F)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H21F2N7O2/c20-15(21)16-22-13-3-1-2-4-14(13)28(16)19-24-17(26-5-9-29-10-6-26)23-18(25-19)27-7-11-30-12-8-27/h1-4,15H,5-12H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 38 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50426814
(CHEMBL2323114)Show SMILES COc1ccc2nc(C(F)F)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-14-15(12-13)29(17(23-14)16(21)22)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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 | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50426815
(CHEMBL2323117)Show SMILES CC(C)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C21H27N7O2/c1-15(2)18-22-16-5-3-4-6-17(16)28(18)21-24-19(26-7-11-29-12-8-26)23-20(25-21)27-9-13-30-14-10-27/h3-6,15H,7-14H2,1-2H3 | 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 | 128 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50355706
(CHEMBL1910989)Show SMILES Cc1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H23N7O2/c1-14-20-15-4-2-3-5-16(15)26(14)19-22-17(24-6-10-27-11-7-24)21-18(23-19)25-8-12-28-13-9-25/h2-5H,6-13H2,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 187 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50426814
(CHEMBL2323114)Show SMILES COc1ccc2nc(C(F)F)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-14-15(12-13)29(17(23-14)16(21)22)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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 | 214 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50355706
(CHEMBL1910989)Show SMILES Cc1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H23N7O2/c1-14-20-15-4-2-3-5-16(15)26(14)19-22-17(24-6-10-27-11-7-24)21-18(23-19)25-8-12-28-13-9-25/h2-5H,6-13H2,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50426814
(CHEMBL2323114)Show SMILES COc1ccc2nc(C(F)F)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-14-15(12-13)29(17(23-14)16(21)22)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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 | 375 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50426815
(CHEMBL2323117)Show SMILES CC(C)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C21H27N7O2/c1-15(2)18-22-16-5-3-4-6-17(16)28(18)21-24-19(26-7-11-29-12-8-26)23-20(25-21)27-9-13-30-14-10-27/h3-6,15H,7-14H2,1-2H3 | 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 | 419 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50426817
(CHEMBL2323119)Show SMILES COc1ccc2nc(C(C)C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-5-4-16(30-3)14-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 | 423 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50426815
(CHEMBL2323117)Show SMILES CC(C)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C21H27N7O2/c1-15(2)18-22-16-5-3-4-6-17(16)28(18)21-24-19(26-7-11-29-12-8-26)23-20(25-21)27-9-13-30-14-10-27/h3-6,15H,7-14H2,1-2H3 | 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 | 431 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50426819
(CHEMBL2323116)Show SMILES COc1ccc2nc(C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-4-3-15(28-2)13-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 | 458 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50355706
(CHEMBL1910989)Show SMILES Cc1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H23N7O2/c1-14-20-15-4-2-3-5-16(15)26(14)19-22-17(24-6-10-27-11-7-24)21-18(23-19)25-8-12-28-13-9-25/h2-5H,6-13H2,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 523 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50426817
(CHEMBL2323119)Show SMILES COc1ccc2nc(C(C)C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-5-4-16(30-3)14-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 | 726 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50426819
(CHEMBL2323116)Show SMILES COc1ccc2nc(C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-4-3-15(28-2)13-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 | 823 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50426816
(CHEMBL2323113)Show SMILES COc1ccc2n(c(nc2c1)C(F)F)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-15-14(12-13)23-17(16(21)22)29(15)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50426817
(CHEMBL2323119)Show SMILES COc1ccc2nc(C(C)C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-5-4-16(30-3)14-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 | 1.05E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50426818
(CHEMBL2323118)Show SMILES COc1ccc2n(c(nc2c1)C(C)C)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-14-16(30-3)4-5-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 | 1.12E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50426819
(CHEMBL2323116)Show SMILES COc1ccc2nc(C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-4-3-15(28-2)13-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 | 1.79E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50355706
(CHEMBL1910989)Show SMILES Cc1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C19H23N7O2/c1-14-20-15-4-2-3-5-16(15)26(14)19-22-17(24-6-10-27-11-7-24)21-18(23-19)25-8-12-28-13-9-25/h2-5H,6-13H2,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.86E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50426815
(CHEMBL2323117)Show SMILES CC(C)c1nc2ccccc2n1-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C21H27N7O2/c1-15(2)18-22-16-5-3-4-6-17(16)28(18)21-24-19(26-7-11-29-12-8-26)23-20(25-21)27-9-13-30-14-10-27/h3-6,15H,7-14H2,1-2H3 | 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 | 2.53E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
(Homo sapiens (Human)) | BDBM50426820
(CHEMBL2323115)Show SMILES COc1ccc2n(c(C)nc2c1)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-13-15(28-2)3-4-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 | 2.77E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kdelta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50426816
(CHEMBL2323113)Show SMILES COc1ccc2n(c(nc2c1)C(F)F)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-15-14(12-13)23-17(16(21)22)29(15)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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 | >5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50426820
(CHEMBL2323115)Show SMILES COc1ccc2n(c(C)nc2c1)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-13-15(28-2)3-4-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 | 9.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50426816
(CHEMBL2323113)Show SMILES COc1ccc2n(c(nc2c1)C(F)F)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-15-14(12-13)23-17(16(21)22)29(15)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50426817
(CHEMBL2323119)Show SMILES COc1ccc2nc(C(C)C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-5-4-16(30-3)14-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50426818
(CHEMBL2323118)Show SMILES COc1ccc2n(c(nc2c1)C(C)C)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-14-16(30-3)4-5-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50426814
(CHEMBL2323114)Show SMILES COc1ccc2nc(C(F)F)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-14-15(12-13)29(17(23-14)16(21)22)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50426816
(CHEMBL2323113)Show SMILES COc1ccc2n(c(nc2c1)C(F)F)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H23F2N7O3/c1-30-13-2-3-15-14(12-13)23-17(16(21)22)29(15)20-25-18(27-4-8-31-9-5-27)24-19(26-20)28-6-10-32-11-7-28/h2-3,12,16H,4-11H2,1H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50426820
(CHEMBL2323115)Show SMILES COc1ccc2n(c(C)nc2c1)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-13-15(28-2)3-4-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kbeta (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50426818
(CHEMBL2323118)Show SMILES COc1ccc2n(c(nc2c1)C(C)C)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-14-16(30-3)4-5-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50426820
(CHEMBL2323115)Show SMILES COc1ccc2n(c(C)nc2c1)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-13-15(28-2)3-4-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50426818
(CHEMBL2323118)Show SMILES COc1ccc2n(c(nc2c1)C(C)C)-c1nc(nc(n1)N1CCOCC1)N1CCOCC1 Show InChI InChI=1S/C22H29N7O3/c1-15(2)19-23-17-14-16(30-3)4-5-18(17)29(19)22-25-20(27-6-10-31-11-7-27)24-21(26-22)28-8-12-32-13-9-28/h4-5,14-15H,6-13H2,1-3H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50426819
(CHEMBL2323116)Show SMILES COc1ccc2nc(C)n(-c3nc(nc(n3)N3CCOCC3)N3CCOCC3)c2c1 Show InChI InChI=1S/C20H25N7O3/c1-14-21-16-4-3-15(28-2)13-17(16)27(14)20-23-18(25-5-9-29-10-6-25)22-19(24-20)26-7-11-30-12-8-26/h3-4,13H,5-12H2,1-2H3 | 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 |
Monash Institute of Pharmaceutical Sciences
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kgamma (unknown origin) expressed in SF21 cells using phosphatidylinositol as substrate after 60 mins by Kinase-Glo assay |
Bioorg Med Chem Lett 23: 802-5 (2013)
Article DOI: 10.1016/j.bmcl.2012.11.076
BindingDB Entry DOI: 10.7270/Q2WM1FQ2 |
More data for this
Ligand-Target Pair | |
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