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Compile Data Set for Download or QSAR

Found 70 hits with Last Name = 'lv' and Initial = 'xh'   
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
Cyclin-dependent kinase 6


(Homo sapiens (Human))
BDBM50440135
PNG
(CHEMBL2426395)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(OC)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O3S/c1-31-20-12-8-17(9-13-20)23-22(16-29(28-23)19-6-4-3-5-7-19)24(30)27-25(33)26-18-10-14-21(32-2)15-11-18/h3-16H,1-2H3,(H2,26,27,30,33)
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n/an/a 29n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK6 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 6


(Homo sapiens (Human))
BDBM50440136
PNG
(CHEMBL2426391)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(F)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19FN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 33n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK6 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 6


(Homo sapiens (Human))
BDBM50440137
PNG
(CHEMBL2426387)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(Cl)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19ClN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 42n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK6 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 6


(Homo sapiens (Human))
BDBM50440138
PNG
(CHEMBL2426383)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(C)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O2S/c1-17-8-10-18(11-9-17)23-22(16-29(28-23)20-6-4-3-5-7-20)24(30)27-25(32)26-19-12-14-21(31-2)15-13-19/h3-16H,1-2H3,(H2,26,27,30,32)
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n/an/a 43n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK6 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 6


(Homo sapiens (Human))
BDBM50440139
PNG
(CHEMBL2426399)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccccc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H20N4O2S/c1-30-20-14-12-18(13-15-20)25-24(31)26-23(29)21-16-28(19-10-6-3-7-11-19)27-22(21)17-8-4-2-5-9-17/h2-16H,1H3,(H2,25,26,29,31)
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n/an/a 50n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK6 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Dual specificity mitogen-activated protein kinase kinase 1


(Homo sapiens (Human))
BDBM50072147
PNG
((2Z,3Z)-2,3-bis(amino(2-aminophenylthio)methylene)...)
Show SMILES Nc1ccccc1SC(=N)C(C#N)C(C#N)C(=N)Sc1ccccc1N
Show InChI InChI=1S/C18H16N6S2/c19-9-11(17(23)25-15-7-3-1-5-13(15)21)12(10-20)18(24)26-16-8-4-2-6-14(16)22/h1-8,11-12,23-24H,21-22H2
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n/an/a 89n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of recombinant full length human N-terminal GST-tagged C-terminal His6-tagged MEK1 expressed in Escherichia coli using myelin basic protei...


Bioorg Med Chem 24: 4652-4659 (2016)


Article DOI: 10.1016/j.bmc.2016.08.002
BindingDB Entry DOI: 10.7270/Q2MP56SS
More data for this
Ligand-Target Pair
Dual specificity mitogen-activated protein kinase kinase 1


(Homo sapiens (Human))
BDBM50536790
PNG
(CHEMBL4575118)
Show SMILES Cc1ccc(cc1)-c1nn(cc1C(=O)NOCc1ccccc1F)-c1ccccc1
Show InChI InChI=1S/C24H20FN3O2/c1-17-11-13-18(14-12-17)23-21(15-28(26-23)20-8-3-2-4-9-20)24(29)27-30-16-19-7-5-6-10-22(19)25/h2-15H,16H2,1H3,(H,27,29)
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n/an/a 91n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of recombinant full length human N-terminal GST-tagged C-terminal His6-tagged MEK1 expressed in Escherichia coli using myelin basic protei...


Bioorg Med Chem 24: 4652-4659 (2016)


Article DOI: 10.1016/j.bmc.2016.08.002
BindingDB Entry DOI: 10.7270/Q2MP56SS
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50137968
PNG
(CHEMBL3754002)
Show SMILES Fc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccccc1F)-c1ccccc1
Show InChI InChI=1S/C23H17F2N3O/c24-20-12-10-17(11-13-20)23-19(15-28(27-23)21-7-2-1-3-8-21)14-26-29-16-18-6-4-5-9-22(18)25/h1-15H,16H2/b26-14+
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n/an/a 280n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 1


(Homo sapiens (Human))
BDBM50440135
PNG
(CHEMBL2426395)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(OC)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O3S/c1-31-20-12-8-17(9-13-20)23-22(16-29(28-23)19-6-4-3-5-7-19)24(30)27-25(33)26-18-10-14-21(32-2)15-11-18/h3-16H,1-2H3,(H2,26,27,30,33)
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n/an/a 522n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK1 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 1


(Homo sapiens (Human))
BDBM50440136
PNG
(CHEMBL2426391)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(F)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19FN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 569n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK1 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50022815
PNG
((3S,6S,9S,12R,15S,18S,21S,24S,30S,33S)-30-ethyl-33...)
Show SMILES CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C |r|
Show InChI InChI=1S/C62H111N11O12/c1-25-27-28-40(15)52(75)51-56(79)65-43(26-2)58(81)67(18)33-48(74)68(19)44(29-34(3)4)55(78)66-49(38(11)12)61(84)69(20)45(30-35(5)6)54(77)63-41(16)53(76)64-42(17)57(80)70(21)46(31-36(7)8)59(82)71(22)47(32-37(9)10)60(83)72(23)50(39(13)14)62(85)73(51)24/h25,27,34-47,49-52,75H,26,28-33H2,1-24H3,(H,63,77)(H,64,76)(H,65,79)(H,66,78)/b27-25+/t40-,41+,42-,43+,44+,45+,46+,47+,49+,50+,51+,52-/m1/s1
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n/an/a 570n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 1


(Homo sapiens (Human))
BDBM50440137
PNG
(CHEMBL2426387)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(Cl)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19ClN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 571n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK1 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 1


(Homo sapiens (Human))
BDBM50440138
PNG
(CHEMBL2426383)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(C)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O2S/c1-17-8-10-18(11-9-17)23-22(16-29(28-23)20-6-4-3-5-7-20)24(30)27-25(32)26-19-12-14-21(31-2)15-13-19/h3-16H,1-2H3,(H2,26,27,30,32)
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n/an/a 584n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK1 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Dual specificity mitogen-activated protein kinase kinase 1


(Homo sapiens (Human))
BDBM50536790
PNG
(CHEMBL4575118)
Show SMILES Cc1ccc(cc1)-c1nn(cc1C(=O)NOCc1ccccc1F)-c1ccccc1
Show InChI InChI=1S/C24H20FN3O2/c1-17-11-13-18(14-12-17)23-21(15-28(26-23)20-8-3-2-4-9-20)24(29)27-30-16-19-7-5-6-10-22(19)25/h2-15H,16H2,1H3,(H,27,29)
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n/an/a 610n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of MEK1 in BRAF mutant human A549 cells assessed as reduction in ERK1/2 phosphorylation by ELISA


Bioorg Med Chem 24: 4652-4659 (2016)


Article DOI: 10.1016/j.bmc.2016.08.002
BindingDB Entry DOI: 10.7270/Q2MP56SS
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 1


(Homo sapiens (Human))
BDBM50440139
PNG
(CHEMBL2426399)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccccc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H20N4O2S/c1-30-20-14-12-18(13-15-20)25-24(31)26-23(29)21-16-28(19-10-6-3-7-11-19)27-22(21)17-8-4-2-5-9-17/h2-16H,1H3,(H2,25,26,29,31)
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n/an/a 610n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK1 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 5


(Homo sapiens (Human))
BDBM50440135
PNG
(CHEMBL2426395)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(OC)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O3S/c1-31-20-12-8-17(9-13-20)23-22(16-29(28-23)19-6-4-3-5-7-19)24(30)27-25(33)26-18-10-14-21(32-2)15-11-18/h3-16H,1-2H3,(H2,26,27,30,33)
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n/an/a 1.09E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK5 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 5


(Homo sapiens (Human))
BDBM50440136
PNG
(CHEMBL2426391)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(F)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19FN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 1.18E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK5 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50137968
PNG
(CHEMBL3754002)
Show SMILES Fc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccccc1F)-c1ccccc1
Show InChI InChI=1S/C23H17F2N3O/c24-20-12-10-17(11-13-20)23-19(15-28(27-23)21-7-2-1-3-8-21)14-26-29-16-18-6-4-5-9-22(18)25/h1-15H,16H2/b26-14+
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n/an/a 1.18E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50137851
PNG
(CHEMBL3752866)
Show SMILES Fc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccc(Cl)cc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H16Cl2FN3O/c24-19-9-6-17(22(25)12-19)15-30-27-13-18-14-29(21-4-2-1-3-5-21)28-23(18)16-7-10-20(26)11-8-16/h1-14H,15H2/b27-13+
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n/an/a 1.26E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50388726
PNG
(CHEMBL2058568)
Show SMILES COc1cc(ccc1O)-c1nnc(SCc2ccccc2)o1
Show InChI InChI=1S/C16H14N2O3S/c1-20-14-9-12(7-8-13(14)19)15-17-18-16(21-15)22-10-11-5-3-2-4-6-11/h2-9,19H,10H2,1H3
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n/an/a 1.34E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma after 4 hrs


Bioorg Med Chem 20: 4226-36 (2012)


Article DOI: 10.1016/j.bmc.2012.05.055
BindingDB Entry DOI: 10.7270/Q2MK6DXD
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 5


(Homo sapiens (Human))
BDBM50440137
PNG
(CHEMBL2426387)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(Cl)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19ClN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 1.36E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK5 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 5


(Homo sapiens (Human))
BDBM50440138
PNG
(CHEMBL2426383)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(C)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O2S/c1-17-8-10-18(11-9-17)23-22(16-29(28-23)20-6-4-3-5-7-20)24(30)27-25(32)26-19-12-14-21(31-2)15-13-19/h3-16H,1-2H3,(H2,26,27,30,32)
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n/an/a 1.42E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK5 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 7


(Homo sapiens (Human))
BDBM50440135
PNG
(CHEMBL2426395)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(OC)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O3S/c1-31-20-12-8-17(9-13-20)23-22(16-29(28-23)19-6-4-3-5-7-19)24(30)27-25(33)26-18-10-14-21(32-2)15-11-18/h3-16H,1-2H3,(H2,26,27,30,33)
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n/an/a 1.42E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK7 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 5


(Homo sapiens (Human))
BDBM50440139
PNG
(CHEMBL2426399)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccccc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H20N4O2S/c1-30-20-14-12-18(13-15-20)25-24(31)26-23(29)21-16-28(19-10-6-3-7-11-19)27-22(21)17-8-4-2-5-9-17/h2-16H,1H3,(H2,25,26,29,31)
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n/an/a 1.50E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK5 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 7


(Homo sapiens (Human))
BDBM50440136
PNG
(CHEMBL2426391)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(F)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19FN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 1.64E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK7 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 7


(Homo sapiens (Human))
BDBM50440137
PNG
(CHEMBL2426387)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(Cl)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H19ClN4O2S/c1-31-20-13-11-18(12-14-20)26-24(32)27-23(30)21-15-29(19-5-3-2-4-6-19)28-22(21)16-7-9-17(25)10-8-16/h2-15H,1H3,(H2,26,27,30,32)
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n/an/a 1.65E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK7 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50137701
PNG
(CHEMBL3752369)
Show SMILES Fc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccccc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H17ClFN3O/c24-22-9-5-4-6-18(22)16-29-26-14-19-15-28(21-7-2-1-3-8-21)27-23(19)17-10-12-20(25)13-11-17/h1-15H,16H2/b26-14+
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n/an/a 1.74E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 7


(Homo sapiens (Human))
BDBM50440138
PNG
(CHEMBL2426383)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccc(C)cc2)-c2ccccc2)cc1
Show InChI InChI=1S/C25H22N4O2S/c1-17-8-10-18(11-9-17)23-22(16-29(28-23)20-6-4-3-5-7-20)24(30)27-25(32)26-19-12-14-21(31-2)15-13-19/h3-16H,1-2H3,(H2,26,27,30,32)
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n/an/a 1.79E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK7 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 7


(Homo sapiens (Human))
BDBM50440139
PNG
(CHEMBL2426399)
Show SMILES COc1ccc(NC(=S)NC(=O)c2cn(nc2-c2ccccc2)-c2ccccc2)cc1
Show InChI InChI=1S/C24H20N4O2S/c1-30-20-14-12-18(13-15-20)25-24(31)26-23(29)21-16-28(19-10-6-3-7-11-19)27-22(21)17-8-4-2-5-9-17/h2-16H,1H3,(H2,25,26,29,31)
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n/an/a 1.88E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of CDK7 (unknown origin) using histone H1 as substrate after 10 mins in presence of [gamma-32P]-ATP


Eur J Med Chem 68: 1-9 (2013)


Article DOI: 10.1016/j.ejmech.2013.07.003
BindingDB Entry DOI: 10.7270/Q2PK0HKH
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50388727
PNG
(CHEMBL2058569)
Show SMILES COc1cccc(CSc2nnc(o2)-c2ccc(O)c(OC)c2)c1
Show InChI InChI=1S/C17H16N2O4S/c1-21-13-5-3-4-11(8-13)10-24-17-19-18-16(23-17)12-6-7-14(20)15(9-12)22-2/h3-9,20H,10H2,1-2H3
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n/an/a 2.87E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma after 4 hrs


Bioorg Med Chem 20: 4226-36 (2012)


Article DOI: 10.1016/j.bmc.2012.05.055
BindingDB Entry DOI: 10.7270/Q2MK6DXD
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50137701
PNG
(CHEMBL3752369)
Show SMILES Fc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccccc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H17ClFN3O/c24-22-9-5-4-6-18(22)16-29-26-14-19-15-28(21-7-2-1-3-8-21)27-23(19)17-10-12-20(25)13-11-17/h1-15H,16H2/b26-14+
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n/an/a 3.12E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50388728
PNG
(CHEMBL2058576)
Show SMILES COc1cc(ccc1OCc1ccccc1F)-c1nnc(SCc2ccccc2F)o1
Show InChI InChI=1S/C23H18F2N2O3S/c1-28-21-12-15(10-11-20(21)29-13-16-6-2-4-8-18(16)24)22-26-27-23(30-22)31-14-17-7-3-5-9-19(17)25/h2-12H,13-14H2,1H3
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n/an/a 5.12E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma after 4 hrs


Bioorg Med Chem 20: 4226-36 (2012)


Article DOI: 10.1016/j.bmc.2012.05.055
BindingDB Entry DOI: 10.7270/Q2MK6DXD
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50388729
PNG
(CHEMBL2058577)
Show SMILES COc1cc(ccc1OCc1c(F)cccc1F)-c1nnc(SCc2c(F)cccc2F)o1
Show InChI InChI=1S/C23H16F4N2O3S/c1-30-21-10-13(8-9-20(21)31-11-14-16(24)4-2-5-17(14)25)22-28-29-23(32-22)33-12-15-18(26)6-3-7-19(15)27/h2-10H,11-12H2,1H3
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n/an/a 5.74E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma after 4 hrs


Bioorg Med Chem 20: 4226-36 (2012)


Article DOI: 10.1016/j.bmc.2012.05.055
BindingDB Entry DOI: 10.7270/Q2MK6DXD
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50388725
PNG
(CHEMBL2058567)
Show SMILES COc1cc(ccc1O)-c1nnc(SCc2ccccc2C)o1
Show InChI InChI=1S/C17H16N2O3S/c1-11-5-3-4-6-13(11)10-23-17-19-18-16(22-17)12-7-8-14(20)15(9-12)21-2/h3-9,20H,10H2,1-2H3
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n/an/a 6.48E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma after 4 hrs


Bioorg Med Chem 20: 4226-36 (2012)


Article DOI: 10.1016/j.bmc.2012.05.055
BindingDB Entry DOI: 10.7270/Q2MK6DXD
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50138037
PNG
(CHEMBL3752051)
Show SMILES Fc1ccccc1CO\N=C\c1cn(nc1-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C23H18FN3O/c24-22-14-8-7-11-19(22)17-28-25-15-20-16-27(21-12-5-2-6-13-21)26-23(20)18-9-3-1-4-10-18/h1-16H,17H2/b25-15+
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n/an/a 6.57E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM12915
PNG
(2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one |...)
Show SMILES O=c1cc(oc2c(cccc12)-c1ccccc1)N1CCOCC1
Show InChI InChI=1S/C19H17NO3/c21-17-13-18(20-9-11-22-12-10-20)23-19-15(7-4-8-16(17)19)14-5-2-1-3-6-14/h1-8,13H,9-12H2
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n/an/a 7.20E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50137851
PNG
(CHEMBL3752866)
Show SMILES Fc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccc(Cl)cc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H16Cl2FN3O/c24-19-9-6-17(22(25)12-19)15-30-27-13-18-14-29(21-4-2-1-3-5-21)28-23(18)16-7-10-20(26)11-8-16/h1-14H,15H2/b27-13+
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n/an/a 7.22E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50388724
PNG
(CHEMBL2058304)
Show SMILES COc1cc(ccc1O)-c1nnc(SCc2ccc(C)cc2)o1
Show InChI InChI=1S/C17H16N2O3S/c1-11-3-5-12(6-4-11)10-23-17-19-18-16(22-17)13-7-8-14(20)15(9-13)21-2/h3-9,20H,10H2,1-2H3
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n/an/a 7.41E+3n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma after 4 hrs


Bioorg Med Chem 20: 4226-36 (2012)


Article DOI: 10.1016/j.bmc.2012.05.055
BindingDB Entry DOI: 10.7270/Q2MK6DXD
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50137967
PNG
(CHEMBL3752088)
Show SMILES Fc1ccccc1CO\N=C\c1cn(nc1-c1ccc(Cl)cc1)-c1ccccc1
Show InChI InChI=1S/C23H17ClFN3O/c24-20-12-10-17(11-13-20)23-19(15-28(27-23)21-7-2-1-3-8-21)14-26-29-16-18-6-4-5-9-22(18)25/h1-15H,16H2/b26-14+
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n/an/a 8.03E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50536790
PNG
(CHEMBL4575118)
Show SMILES Cc1ccc(cc1)-c1nn(cc1C(=O)NOCc1ccccc1F)-c1ccccc1
Show InChI InChI=1S/C24H20FN3O2/c1-17-11-13-18(14-12-17)23-21(15-28(26-23)20-8-3-2-4-9-20)24(29)27-30-16-19-7-5-6-10-22(19)25/h2-15H,16H2,1H3,(H,27,29)
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n/an/a 8.30E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of Aurora A (unknown origin)


Bioorg Med Chem 24: 4652-4659 (2016)


Article DOI: 10.1016/j.bmc.2016.08.002
BindingDB Entry DOI: 10.7270/Q2MP56SS
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50137656
PNG
(CHEMBL3753671)
Show SMILES Clc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccccc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H17Cl2N3O/c24-20-12-10-17(11-13-20)23-19(15-28(27-23)21-7-2-1-3-8-21)14-26-29-16-18-6-4-5-9-22(18)25/h1-15H,16H2/b26-14+
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n/an/a 9.08E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50137685
PNG
(CHEMBL3753973)
Show SMILES Clc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccc(Cl)cc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H16Cl3N3O/c24-19-9-6-16(7-10-19)23-18(14-29(28-23)21-4-2-1-3-5-21)13-27-30-15-17-8-11-20(25)12-22(17)26/h1-14H,15H2/b27-13+
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n/an/a 9.36E+3n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50138037
PNG
(CHEMBL3752051)
Show SMILES Fc1ccccc1CO\N=C\c1cn(nc1-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C23H18FN3O/c24-22-14-8-7-11-19(22)17-28-25-15-20-16-27(21-12-5-2-6-13-21)26-23(20)18-9-3-1-4-10-18/h1-16H,17H2/b25-15+
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n/an/a 1.04E+4n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50394210
PNG
(CHEMBL2159053)
Show SMILES COc1ccc(cc1)C1=NN(C(C1)c1ccc(Cl)cc1)C(=O)c1ccc(Cl)cc1O |t:9|
Show InChI InChI=1S/C23H18Cl2N2O3/c1-30-18-9-4-14(5-10-18)20-13-21(15-2-6-16(24)7-3-15)27(26-20)23(29)19-11-8-17(25)12-22(19)28/h2-12,21,28H,13H2,1H3
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n/an/a 1.05E+4n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of EGFR


Bioorg Med Chem Lett 22: 6596-601 (2012)


Article DOI: 10.1016/j.bmcl.2012.09.004
BindingDB Entry DOI: 10.7270/Q25M66TW
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50137685
PNG
(CHEMBL3753973)
Show SMILES Clc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccc(Cl)cc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H16Cl3N3O/c24-19-9-6-16(7-10-19)23-18(14-29(28-23)21-4-2-1-3-5-21)13-27-30-15-17-8-11-20(25)12-22(17)26/h1-14H,15H2/b27-13+
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n/an/a 1.08E+4n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50137967
PNG
(CHEMBL3752088)
Show SMILES Fc1ccccc1CO\N=C\c1cn(nc1-c1ccc(Cl)cc1)-c1ccccc1
Show InChI InChI=1S/C23H17ClFN3O/c24-20-12-10-17(11-13-20)23-19(15-28(27-23)21-7-2-1-3-8-21)14-26-29-16-18-6-4-5-9-22(18)25/h1-15H,16H2/b26-14+
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n/an/a 1.24E+4n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50137656
PNG
(CHEMBL3753671)
Show SMILES Clc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccccc1Cl)-c1ccccc1
Show InChI InChI=1S/C23H17Cl2N3O/c24-20-12-10-17(11-13-20)23-19(15-28(27-23)21-7-2-1-3-8-21)14-26-29-16-18-6-4-5-9-22(18)25/h1-15H,16H2/b26-14+
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n/an/a 1.38E+4n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3Kgamma (unknown origin) after 4 hrs


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Focal adhesion kinase 1


(Homo sapiens (Human))
BDBM50536790
PNG
(CHEMBL4575118)
Show SMILES Cc1ccc(cc1)-c1nn(cc1C(=O)NOCc1ccccc1F)-c1ccccc1
Show InChI InChI=1S/C24H20FN3O2/c1-17-11-13-18(14-12-17)23-21(15-28(26-23)20-8-3-2-4-9-20)24(29)27-30-16-19-7-5-6-10-22(19)25/h2-15H,16H2,1H3,(H,27,29)
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n/an/a 1.56E+4n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of FAK in human MCF7 cells


Bioorg Med Chem 24: 4652-4659 (2016)


Article DOI: 10.1016/j.bmc.2016.08.002
BindingDB Entry DOI: 10.7270/Q2MP56SS
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50138034
PNG
(CHEMBL3752413)
Show SMILES Clc1ccc(CO\N=C\c2cn(nc2-c2ccccc2)-c2ccccc2)c(Cl)c1
Show InChI InChI=1S/C23H17Cl2N3O/c24-20-12-11-18(22(25)13-20)16-29-26-14-19-15-28(21-9-5-2-6-10-21)27-23(19)17-7-3-1-4-8-17/h1-15H,16H2/b26-14+
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n/an/a 1.68E+4n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Mus musculus (Mouse))
BDBM50138021
PNG
(CHEMBL3752400)
Show SMILES Fc1ccc(cc1)-c1nn(cc1\C=N\OCc1ccccc1)-c1ccccc1
Show InChI InChI=1S/C23H18FN3O/c24-21-13-11-19(12-14-21)23-20(15-25-28-17-18-7-3-1-4-8-18)16-27(26-23)22-9-5-2-6-10-22/h1-16H,17H2/b25-15+
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n/an/a 1.76E+4n/an/an/an/an/an/a



Anhui Agricultural University

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma in mouse lymph node cells assessed as inhibition of ConA-stimulated T cell proliferation


Eur J Med Chem 108: 586-93 (2016)


Article DOI: 10.1016/j.ejmech.2015.12.020
BindingDB Entry DOI: 10.7270/Q2T72K8V
More data for this
Ligand-Target Pair
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