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PubMed code 26164189

Compile data set for download or QSAR
Found 21 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50436459
PNG
(CHEMBL2396661)
Show SMILES Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1
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n/an/a 5n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110alpha (unknown origin) by Kinase-Glo assay


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50113952
PNG
(CHEMBL3605177)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc2COc3cnc(cc3-c2s1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H22F3N5O3S/c1-9-4-5-28(14(9)16(24)29)18(30)27-17-26-11-8-31-12-7-25-13(6-10(12)15(11)32-17)19(2,3)20(21,22)23/h6-7,9,14H,4-5,8H2,1-3H3,(H2,24,29)(H,26,27,30)/t9-,14+/m1/s1
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n/an/a 5n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110alpha (unknown origin) by Kinase-Glo assay


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50113952
PNG
(CHEMBL3605177)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc2COc3cnc(cc3-c2s1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H22F3N5O3S/c1-9-4-5-28(14(9)16(24)29)18(30)27-17-26-11-8-31-12-7-25-13(6-10(12)15(11)32-17)19(2,3)20(21,22)23/h6-7,9,14H,4-5,8H2,1-3H3,(H2,24,29)(H,26,27,30)/t9-,14+/m1/s1
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n/an/a 11n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110alpha expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analy...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50113951
PNG
(CHEMBL3605178)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc(C)c(s1)-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H24F3N5O2S/c1-10-6-8-28(14(10)16(24)29)18(30)27-17-26-11(2)15(31-17)12-5-7-25-13(9-12)19(3,4)20(21,22)23/h5,7,9-10,14H,6,8H2,1-4H3,(H2,24,29)(H,26,27,30)/t10-,14+/m1/s1
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n/an/a 19n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110alpha expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analy...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50113951
PNG
(CHEMBL3605178)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc(C)c(s1)-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H24F3N5O2S/c1-10-6-8-28(14(10)16(24)29)18(30)27-17-26-11(2)15(31-17)12-5-7-25-13(9-12)19(3,4)20(21,22)23/h5,7,9-10,14H,6,8H2,1-4H3,(H2,24,29)(H,26,27,30)/t10-,14+/m1/s1
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n/an/a 19n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110alpha (unknown origin) by Kinase-Glo assay


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50436459
PNG
(CHEMBL2396661)
Show SMILES Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1
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n/an/a 74n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110alpha expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analy...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50113952
PNG
(CHEMBL3605177)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc2COc3cnc(cc3-c2s1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H22F3N5O3S/c1-9-4-5-28(14(9)16(24)29)18(30)27-17-26-11-8-31-12-7-25-13(6-10(12)15(11)32-17)19(2,3)20(21,22)23/h6-7,9,14H,4-5,8H2,1-3H3,(H2,24,29)(H,26,27,30)/t9-,14+/m1/s1
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n/an/a 200n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110gamma (unknown origin) using PI or PIP2:PS as substrate measured for 15 to 60 mins by TR-FRET analysis


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50113952
PNG
(CHEMBL3605177)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc2COc3cnc(cc3-c2s1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H22F3N5O3S/c1-9-4-5-28(14(9)16(24)29)18(30)27-17-26-11-8-31-12-7-25-13(6-10(12)15(11)32-17)19(2,3)20(21,22)23/h6-7,9,14H,4-5,8H2,1-3H3,(H2,24,29)(H,26,27,30)/t9-,14+/m1/s1
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n/an/a 220n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110delta (unknown origin) using PI or PIP2:PS as substrate measured for 15 to 60 mins by TR-FRET analysis


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50113951
PNG
(CHEMBL3605178)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc(C)c(s1)-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H24F3N5O2S/c1-10-6-8-28(14(10)16(24)29)18(30)27-17-26-11(2)15(31-17)12-5-7-25-13(9-12)19(3,4)20(21,22)23/h5,7,9-10,14H,6,8H2,1-4H3,(H2,24,29)(H,26,27,30)/t10-,14+/m1/s1
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n/an/a 230n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110gamma (unknown origin) using PI or PIP2:PS as substrate measured for 15 to 60 mins by TR-FRET analysis


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50436459
PNG
(CHEMBL2396661)
Show SMILES Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1
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n/an/a 250n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110gamma (unknown origin) using PI or PIP2:PS as substrate measured for 15 to 60 mins by TR-FRET analysis


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50436459
PNG
(CHEMBL2396661)
Show SMILES Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1
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n/an/a 290n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110delta (unknown origin) using PI or PIP2:PS as substrate measured for 15 to 60 mins by TR-FRET analysis


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50113951
PNG
(CHEMBL3605178)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc(C)c(s1)-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H24F3N5O2S/c1-10-6-8-28(14(10)16(24)29)18(30)27-17-26-11(2)15(31-17)12-5-7-25-13(9-12)19(3,4)20(21,22)23/h5,7,9-10,14H,6,8H2,1-4H3,(H2,24,29)(H,26,27,30)/t10-,14+/m1/s1
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n/an/a 390n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110delta (unknown origin) using PI or PIP2:PS as substrate measured for 15 to 60 mins by TR-FRET analysis


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50113952
PNG
(CHEMBL3605177)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc2COc3cnc(cc3-c2s1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H22F3N5O3S/c1-9-4-5-28(14(9)16(24)29)18(30)27-17-26-11-8-31-12-7-25-13(6-10(12)15(11)32-17)19(2,3)20(21,22)23/h6-7,9,14H,4-5,8H2,1-3H3,(H2,24,29)(H,26,27,30)/t9-,14+/m1/s1
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n/an/a 540n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110delta expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analy...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50113951
PNG
(CHEMBL3605178)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc(C)c(s1)-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H24F3N5O2S/c1-10-6-8-28(14(10)16(24)29)18(30)27-17-26-11(2)15(31-17)12-5-7-25-13(9-12)19(3,4)20(21,22)23/h5,7,9-10,14H,6,8H2,1-4H3,(H2,24,29)(H,26,27,30)/t10-,14+/m1/s1
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n/an/a 616n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110delta expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analy...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform


(Homo sapiens (Human))
BDBM50113952
PNG
(CHEMBL3605177)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc2COc3cnc(cc3-c2s1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H22F3N5O3S/c1-9-4-5-28(14(9)16(24)29)18(30)27-17-26-11-8-31-12-7-25-13(6-10(12)15(11)32-17)19(2,3)20(21,22)23/h6-7,9,14H,4-5,8H2,1-3H3,(H2,24,29)(H,26,27,30)/t9-,14+/m1/s1
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n/an/a 670n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110beta (unknown origin) by Kinase-Glo assay


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform


(Homo sapiens (Human))
BDBM50113951
PNG
(CHEMBL3605178)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc(C)c(s1)-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H24F3N5O2S/c1-10-6-8-28(14(10)16(24)29)18(30)27-17-26-11(2)15(31-17)12-5-7-25-13(9-12)19(3,4)20(21,22)23/h5,7,9-10,14H,6,8H2,1-4H3,(H2,24,29)(H,26,27,30)/t10-,14+/m1/s1
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n/an/a 1.04E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110beta (unknown origin) by Kinase-Glo assay


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform


(Homo sapiens (Human))
BDBM50113952
PNG
(CHEMBL3605177)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc2COc3cnc(cc3-c2s1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H22F3N5O3S/c1-9-4-5-28(14(9)16(24)29)18(30)27-17-26-11-8-31-12-7-25-13(6-10(12)15(11)32-17)19(2,3)20(21,22)23/h6-7,9,14H,4-5,8H2,1-3H3,(H2,24,29)(H,26,27,30)/t9-,14+/m1/s1
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n/an/a 1.11E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110beta expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analys...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform


(Homo sapiens (Human))
BDBM50436459
PNG
(CHEMBL2396661)
Show SMILES Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1
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n/an/a 1.20E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of P110beta (unknown origin) by Kinase-Glo assay


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50436459
PNG
(CHEMBL2396661)
Show SMILES Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1
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n/an/a 1.20E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110delta expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analy...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform


(Homo sapiens (Human))
BDBM50113951
PNG
(CHEMBL3605178)
Show SMILES C[C@@H]1CCN([C@@H]1C(N)=O)C(=O)Nc1nc(C)c(s1)-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C20H24F3N5O2S/c1-10-6-8-28(14(10)16(24)29)18(30)27-17-26-11(2)15(31-17)12-5-7-25-13(9-12)19(3,4)20(21,22)23/h5,7,9-10,14H,6,8H2,1-4H3,(H2,24,29)(H,26,27,30)/t10-,14+/m1/s1
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n/an/a 2.00E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110beta expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analys...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform


(Homo sapiens (Human))
BDBM50436459
PNG
(CHEMBL2396661)
Show SMILES Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(c1)C(C)(C)C(F)(F)F |r|
Show InChI InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1
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PubMed
n/an/a 2.20E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of myristoylated human P110beta expressed in Rat1 cells assessed as inhibition of Akt phosphorylation at Serine 473 by Western blot analys...


Bioorg Med Chem Lett 25: 3582-4 (2015)


Article DOI: 10.1016/j.bmcl.2015.06.077
BindingDB Entry DOI: 10.7270/Q2G73GJG
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%