Found 70 hits Enz. Inhib. hit(s) with all data for entry = 50031033 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 alpha isoform
(Homo sapiens (Human)) | BDBM50305663
((3-(1-(1-benzylpiperidin-4-yl)-4-morpholino-1H-pyr...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-20-22-7-4-8-23(17-22)26-30-27(33-13-15-36-16-14-33)25-18-29-34(28(25)31-26)24-9-11-32(12-10-24)19-21-5-2-1-3-6-21/h1-8,17-18,24,35H,9-16,19-20H2 | 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 | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305645
((3-(4-morpholino-7-(piperidin-4-yl)-7H-pyrrolo[2,3...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ccn(C3CCNCC3)c2n1 Show InChI InChI=1S/C22H27N5O2/c28-15-16-2-1-3-17(14-16)20-24-21(26-10-12-29-13-11-26)19-6-9-27(22(19)25-20)18-4-7-23-8-5-18/h1-3,6,9,14,18,23,28H,4-5,7-8,10-13,15H2 | 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 | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM35600
(pyrazolo pyrimidine, 5e)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C27H30N6O2/c34-23-8-4-7-21(17-23)25-29-26(32-13-15-35-16-14-32)24-18-28-33(27(24)30-25)22-9-11-31(12-10-22)19-20-5-2-1-3-6-20/h1-8,17-18,22,34H,9-16,19H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 32 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM35596
(pyrazolo pyrimidine, 5a)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCNCC3)c2n1 Show InChI InChI=1S/C20H24N6O2/c27-16-3-1-2-14(12-16)18-23-19(25-8-10-28-11-9-25)17-13-22-26(20(17)24-18)15-4-6-21-7-5-15/h1-3,12-13,15,21,27H,4-11H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 36 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305306
((3-(9-(1-benzylpiperidin-4-yl)-6-morpholino-9H-pur...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-19-22-7-4-8-23(17-22)26-30-27(33-13-15-36-16-14-33)25-28(31-26)34(20-29-25)24-9-11-32(12-10-24)18-21-5-2-1-3-6-21/h1-8,17,20,24,35H,9-16,18-19H2 | 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 | 45 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305307
((3-(6-morpholino-9-(piperidin-4-yl)-9H-purin-2-yl)...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCNCC3)c2n1 Show InChI InChI=1S/C21H26N6O2/c28-13-15-2-1-3-16(12-15)19-24-20(26-8-10-29-11-9-26)18-21(25-19)27(14-23-18)17-4-6-22-7-5-17/h1-3,12,14,17,22,28H,4-11,13H2 | 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 | 58 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305300
(3-(6-morpholino-9-(piperidin-4-yl)-9H-purin-2-yl)p...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCNCC3)c2n1 Show InChI InChI=1S/C20H24N6O2/c27-16-3-1-2-14(12-16)18-23-19(25-8-10-28-11-9-25)17-20(24-18)26(13-22-17)15-4-6-21-7-5-15/h1-3,12-13,15,21,27H,4-11H2 | 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 | 65 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305301
(3-(9-(1-benzylpiperidin-4-yl)-6-morpholino-9H-puri...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C27H30N6O2/c34-23-8-4-7-21(17-23)25-29-26(32-13-15-35-16-14-32)24-27(30-25)33(19-28-24)22-9-11-31(12-10-22)18-20-5-2-1-3-6-20/h1-8,17,19,22,34H,9-16,18H2 | 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 | 80 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM35600
(pyrazolo pyrimidine, 5e)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C27H30N6O2/c34-23-8-4-7-21(17-23)25-29-26(32-13-15-35-16-14-32)24-18-28-33(27(24)30-25)22-9-11-31(12-10-22)19-20-5-2-1-3-6-20/h1-8,17-18,22,34H,9-16,19H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 83 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305663
((3-(1-(1-benzylpiperidin-4-yl)-4-morpholino-1H-pyr...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-20-22-7-4-8-23(17-22)26-30-27(33-13-15-36-16-14-33)25-18-29-34(28(25)31-26)24-9-11-32(12-10-24)19-21-5-2-1-3-6-21/h1-8,17-18,24,35H,9-16,19-20H2 | 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 | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305300
(3-(6-morpholino-9-(piperidin-4-yl)-9H-purin-2-yl)p...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCNCC3)c2n1 Show InChI InChI=1S/C20H24N6O2/c27-16-3-1-2-14(12-16)18-23-19(25-8-10-28-11-9-25)17-20(24-18)26(13-22-17)15-4-6-21-7-5-15/h1-3,12-13,15,21,27H,4-11H2 | 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 | 131 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305301
(3-(9-(1-benzylpiperidin-4-yl)-6-morpholino-9H-puri...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C27H30N6O2/c34-23-8-4-7-21(17-23)25-29-26(32-13-15-35-16-14-32)24-27(30-25)33(19-28-24)22-9-11-31(12-10-22)18-20-5-2-1-3-6-20/h1-8,17,19,22,34H,9-16,18H2 | 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 |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305650
(4-(2-(1H-indol-6-yl)-9H-purin-6-yl)morpholine | CH...)Show SMILES C1CN(CCO1)c1nc(nc2nc[nH]c12)-c1ccc2cc[nH]c2c1 Show InChI InChI=1S/C17H16N6O/c1-2-12(9-13-11(1)3-4-18-13)15-21-16-14(19-10-20-16)17(22-15)23-5-7-24-8-6-23/h1-4,9-10,18H,5-8H2,(H,19,20,21,22) | 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 | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305662
(3-(9-((1-benzylpiperidin-4-yl)methyl)-6-morpholino...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(CC3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-24-8-4-7-23(17-24)26-30-27(33-13-15-36-16-14-33)25-28(31-26)34(20-29-25)19-22-9-11-32(12-10-22)18-21-5-2-1-3-6-21/h1-8,17,20,22,35H,9-16,18-19H2 | 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 | 199 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM35596
(pyrazolo pyrimidine, 5a)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCNCC3)c2n1 Show InChI InChI=1S/C20H24N6O2/c27-16-3-1-2-14(12-16)18-23-19(25-8-10-28-11-9-25)17-13-22-26(20(17)24-18)15-4-6-21-7-5-15/h1-3,12-13,15,21,27H,4-11H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 215 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305299
(3-(6-morpholino-9H-purin-2-yl)phenol | CHEMBL59351...)Show InChI InChI=1S/C15H15N5O2/c21-11-3-1-2-10(8-11)13-18-14-12(16-9-17-14)15(19-13)20-4-6-22-7-5-20/h1-3,8-9,21H,4-7H2,(H,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 | 232 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305661
((3-(9-((1-benzylpiperidin-4-yl)methyl)-6-morpholin...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(CC3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C29H34N6O2/c36-20-24-7-4-8-25(17-24)27-31-28(34-13-15-37-16-14-34)26-29(32-27)35(21-30-26)19-23-9-11-33(12-10-23)18-22-5-2-1-3-6-22/h1-8,17,21,23,36H,9-16,18-20H2 | 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 | 248 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305645
((3-(4-morpholino-7-(piperidin-4-yl)-7H-pyrrolo[2,3...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ccn(C3CCNCC3)c2n1 Show InChI InChI=1S/C22H27N5O2/c28-15-16-2-1-3-17(14-16)20-24-21(26-10-12-29-13-11-26)19-6-9-27(22(19)25-20)18-4-7-23-8-5-18/h1-3,6,9,14,18,23,28H,4-5,7-8,10-13,15H2 | 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 | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305646
(4-(6-morpholino-9H-purin-2-yl)phenol | CHEMBL59226...)Show InChI InChI=1S/C15H15N5O2/c21-11-3-1-10(2-4-11)13-18-14-12(16-9-17-14)15(19-13)20-5-7-22-8-6-20/h1-4,9,21H,5-8H2,(H,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 | 450 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305645
((3-(4-morpholino-7-(piperidin-4-yl)-7H-pyrrolo[2,3...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ccn(C3CCNCC3)c2n1 Show InChI InChI=1S/C22H27N5O2/c28-15-16-2-1-3-17(14-16)20-24-21(26-10-12-29-13-11-26)19-6-9-27(22(19)25-20)18-4-7-23-8-5-18/h1-3,6,9,14,18,23,28H,4-5,7-8,10-13,15H2 | 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 | 510 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305662
(3-(9-((1-benzylpiperidin-4-yl)methyl)-6-morpholino...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(CC3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-24-8-4-7-23(17-24)26-30-27(33-13-15-36-16-14-33)25-28(31-26)34(20-29-25)19-22-9-11-32(12-10-22)18-21-5-2-1-3-6-21/h1-8,17,20,22,35H,9-16,18-19H2 | 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 | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305660
(4-(2-(thiophen-2-yl)-9H-purin-6-yl)morpholine | CH...)Show InChI InChI=1S/C13H13N5OS/c1-2-9(20-7-1)11-16-12-10(14-8-15-12)13(17-11)18-3-5-19-6-4-18/h1-2,7-8H,3-6H2,(H,14,15,16,17) | 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 | 640 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305659
(2-(6-morpholino-9H-purin-2-yl)phenol | CHEMBL58540...)Show InChI InChI=1S/C15H15N5O2/c21-11-4-2-1-3-10(11)13-18-14-12(16-9-17-14)15(19-13)20-5-7-22-8-6-20/h1-4,9,21H,5-8H2,(H,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 | 667 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305307
((3-(6-morpholino-9-(piperidin-4-yl)-9H-purin-2-yl)...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCNCC3)c2n1 Show InChI InChI=1S/C21H26N6O2/c28-13-15-2-1-3-16(12-15)19-24-20(26-8-10-29-11-9-26)18-21(25-19)27(14-23-18)17-4-6-22-7-5-17/h1-3,12,14,17,22,28H,4-11,13H2 | 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 | 683 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305306
((3-(9-(1-benzylpiperidin-4-yl)-6-morpholino-9H-pur...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-19-22-7-4-8-23(17-22)26-30-27(33-13-15-36-16-14-33)25-28(31-26)34(20-29-25)24-9-11-32(12-10-24)18-21-5-2-1-3-6-21/h1-8,17,20,24,35H,9-16,18-19H2 | 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 | 691 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305300
(3-(6-morpholino-9-(piperidin-4-yl)-9H-purin-2-yl)p...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCNCC3)c2n1 Show InChI InChI=1S/C20H24N6O2/c27-16-3-1-2-14(12-16)18-23-19(25-8-10-28-11-9-25)17-20(24-18)26(13-22-17)15-4-6-21-7-5-15/h1-3,12-13,15,21,27H,4-11H2 | 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 | 870 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305663
((3-(1-(1-benzylpiperidin-4-yl)-4-morpholino-1H-pyr...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-20-22-7-4-8-23(17-22)26-30-27(33-13-15-36-16-14-33)25-18-29-34(28(25)31-26)24-9-11-32(12-10-24)19-21-5-2-1-3-6-21/h1-8,17-18,24,35H,9-16,19-20H2 | 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 | 975 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM35596
(pyrazolo pyrimidine, 5a)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCNCC3)c2n1 Show InChI InChI=1S/C20H24N6O2/c27-16-3-1-2-14(12-16)18-23-19(25-8-10-28-11-9-25)17-13-22-26(20(17)24-18)15-4-6-21-7-5-15/h1-3,12-13,15,21,27H,4-11H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 993 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305306
((3-(9-(1-benzylpiperidin-4-yl)-6-morpholino-9H-pur...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-19-22-7-4-8-23(17-22)26-30-27(33-13-15-36-16-14-33)25-28(31-26)34(20-29-25)24-9-11-32(12-10-24)18-21-5-2-1-3-6-21/h1-8,17,20,24,35H,9-16,18-19H2 | 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 | 1.13E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305652
(4-(2-(benzo[d][1,3]dioxol-5-yl)-9H-purin-6-yl)morp...)Show InChI InChI=1S/C16H15N5O3/c1-2-11-12(24-9-23-11)7-10(1)14-19-15-13(17-8-18-15)16(20-14)21-3-5-22-6-4-21/h1-2,7-8H,3-6,9H2,(H,17,18,19,20) | 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 | 1.21E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305661
((3-(9-((1-benzylpiperidin-4-yl)methyl)-6-morpholin...)Show SMILES OCc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(CC3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C29H34N6O2/c36-20-24-7-4-8-25(17-24)27-31-28(34-13-15-37-16-14-34)26-29(32-27)35(21-30-26)19-23-9-11-33(12-10-23)18-22-5-2-1-3-6-22/h1-8,17,21,23,36H,9-16,18-20H2 | 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 | 1.65E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305649
(4-(2-(4-(methylsulfonyl)phenyl)-9H-purin-6-yl)morp...)Show SMILES CS(=O)(=O)c1ccc(cc1)-c1nc(N2CCOCC2)c2[nH]cnc2n1 Show InChI InChI=1S/C16H17N5O3S/c1-25(22,23)12-4-2-11(3-5-12)14-19-15-13(17-10-18-15)16(20-14)21-6-8-24-9-7-21/h2-5,10H,6-9H2,1H3,(H,17,18,19,20) | 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 | 1.76E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305650
(4-(2-(1H-indol-6-yl)-9H-purin-6-yl)morpholine | CH...)Show SMILES C1CN(CCO1)c1nc(nc2nc[nH]c12)-c1ccc2cc[nH]c2c1 Show InChI InChI=1S/C17H16N6O/c1-2-12(9-13-11(1)3-4-18-13)15-21-16-14(19-10-20-16)17(22-15)23-5-7-24-8-6-23/h1-4,9-10,18H,5-8H2,(H,19,20,21,22) | 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 | 2.33E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305299
(3-(6-morpholino-9H-purin-2-yl)phenol | CHEMBL59351...)Show InChI InChI=1S/C15H15N5O2/c21-11-3-1-2-10(8-11)13-18-14-12(16-9-17-14)15(19-13)20-4-6-22-7-5-20/h1-3,8-9,21H,4-7H2,(H,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 | 2.34E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM35600
(pyrazolo pyrimidine, 5e)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2cnn(C3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C27H30N6O2/c34-23-8-4-7-21(17-23)25-29-26(32-13-15-35-16-14-32)24-18-28-33(27(24)30-25)22-9-11-31(12-10-22)19-20-5-2-1-3-6-20/h1-8,17-18,22,34H,9-16,19H2 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.37E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50305662
(3-(9-((1-benzylpiperidin-4-yl)methyl)-6-morpholino...)Show SMILES Oc1cccc(c1)-c1nc(N2CCOCC2)c2ncn(CC3CCN(Cc4ccccc4)CC3)c2n1 Show InChI InChI=1S/C28H32N6O2/c35-24-8-4-7-23(17-24)26-30-27(33-13-15-36-16-14-33)25-28(31-26)34(20-29-25)19-22-9-11-32(12-10-22)18-21-5-2-1-3-6-21/h1-8,17,20,22,35H,9-16,18-19H2 | 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 | 2.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kgamma by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305653
(4-(2-(thiophen-3-yl)-9H-purin-6-yl)morpholine | CH...)Show InChI InChI=1S/C13H13N5OS/c1-6-20-7-9(1)11-16-12-10(14-8-15-12)13(17-11)18-2-4-19-5-3-18/h1,6-8H,2-5H2,(H,14,15,16,17) | 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 | 2.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305299
(3-(6-morpholino-9H-purin-2-yl)phenol | CHEMBL59351...)Show InChI InChI=1S/C15H15N5O2/c21-11-3-1-2-10(8-11)13-18-14-12(16-9-17-14)15(19-13)20-4-6-22-7-5-20/h1-3,8-9,21H,4-7H2,(H,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 | 2.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305659
(2-(6-morpholino-9H-purin-2-yl)phenol | CHEMBL58540...)Show InChI InChI=1S/C15H15N5O2/c21-11-4-2-1-3-10(11)13-18-14-12(16-9-17-14)15(19-13)20-5-7-22-8-6-20/h1-4,9,21H,5-8H2,(H,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 | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305646
(4-(6-morpholino-9H-purin-2-yl)phenol | CHEMBL59226...)Show InChI InChI=1S/C15H15N5O2/c21-11-3-1-10(2-4-11)13-18-14-12(16-9-17-14)15(19-13)20-5-7-22-8-6-20/h1-4,9,21H,5-8H2,(H,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 | 2.54E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305660
(4-(2-(thiophen-2-yl)-9H-purin-6-yl)morpholine | CH...)Show InChI InChI=1S/C13H13N5OS/c1-2-9(20-7-1)11-16-12-10(14-8-15-12)13(17-11)18-3-5-19-6-4-18/h1-2,7-8H,3-6H2,(H,14,15,16,17) | 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 | 2.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305647
((4-(6-morpholino-9H-purin-2-yl)phenyl)methanol | C...)Show InChI InChI=1S/C16H17N5O2/c22-9-11-1-3-12(4-2-11)14-19-15-13(17-10-18-15)16(20-14)21-5-7-23-8-6-21/h1-4,10,22H,5-9H2,(H,17,18,19,20) | 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 | 2.89E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305656
(3-(6-morpholino-9H-purin-2-yl)benzonitrile | CHEMB...)Show InChI InChI=1S/C16H14N6O/c17-9-11-2-1-3-12(8-11)14-20-15-13(18-10-19-15)16(21-14)22-4-6-23-7-5-22/h1-3,8,10H,4-7H2,(H,18,19,20,21) | 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 | 2.92E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305651
(4-(2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-9H-puri...)Show SMILES C1COc2cc(ccc2O1)-c1nc(N2CCOCC2)c2[nH]cnc2n1 Show InChI InChI=1S/C17H17N5O3/c1-2-12-13(25-8-7-24-12)9-11(1)15-20-16-14(18-10-19-16)17(21-15)22-3-5-23-6-4-22/h1-2,9-10H,3-8H2,(H,18,19,20,21) | 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 | 3.48E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305655
(3-(6-(piperidin-1-yl)-9H-purin-2-yl)phenol | CHEMB...)Show InChI InChI=1S/C16H17N5O/c22-12-6-4-5-11(9-12)14-19-15-13(17-10-18-15)16(20-14)21-7-2-1-3-8-21/h4-6,9-10,22H,1-3,7-8H2,(H,17,18,19,20) | 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 | 3.77E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305654
(4-(2-(furan-3-yl)-9H-purin-6-yl)morpholine | CHEMB...)Show InChI InChI=1S/C13H13N5O2/c1-4-20-7-9(1)11-16-12-10(14-8-15-12)13(17-11)18-2-5-19-6-3-18/h1,4,7-8H,2-3,5-6H2,(H,14,15,16,17) | 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 | 3.79E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305653
(4-(2-(thiophen-3-yl)-9H-purin-6-yl)morpholine | CH...)Show InChI InChI=1S/C13H13N5OS/c1-6-20-7-9(1)11-16-12-10(14-8-15-12)13(17-11)18-2-4-19-5-3-18/h1,6-8H,2-5H2,(H,14,15,16,17) | 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 | 3.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305657
(4-(2-(3-(methylsulfonyl)phenyl)-9H-purin-6-yl)morp...)Show SMILES CS(=O)(=O)c1cccc(c1)-c1nc(N2CCOCC2)c2[nH]cnc2n1 Show InChI InChI=1S/C16H17N5O3S/c1-25(22,23)12-4-2-3-11(9-12)14-19-15-13(17-10-18-15)16(20-14)21-5-7-24-8-6-21/h2-4,9-10H,5-8H2,1H3,(H,17,18,19,20) | 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 | 3.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50305658
(CHEMBL589864 | N-(3-(6-morpholino-9H-purin-2-yl)ph...)Show SMILES CS(=O)(=O)Nc1cccc(c1)-c1nc(N2CCOCC2)c2[nH]cnc2n1 Show InChI InChI=1S/C16H18N6O3S/c1-26(23,24)21-12-4-2-3-11(9-12)14-19-15-13(17-10-18-15)16(20-14)22-5-7-25-8-6-22/h2-4,9-10,21H,5-8H2,1H3,(H,17,18,19,20) | 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 | 4.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of GST-GRP1-fused PI3Kalpha by microtiter plate based fluorescence polarization assay |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50305647
((4-(6-morpholino-9H-purin-2-yl)phenyl)methanol | C...)Show InChI InChI=1S/C16H17N5O2/c22-9-11-1-3-12(4-2-11)14-19-15-13(17-10-18-15)16(20-14)21-5-7-23-8-6-21/h1-4,10,22H,5-9H2,(H,17,18,19,20) | 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 | 4.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description Inhibition of human TOR in HEK293 cells by DELFIA |
Bioorg Med Chem Lett 20: 636-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.11.051 BindingDB Entry DOI: 10.7270/Q2V98852 |
More data for this Ligand-Target Pair | |