Found 70 hits with Last Name = 'lv' and Initial = 'xh' 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 |
Cyclin-dependent kinase 6
(Homo sapiens (Human)) | BDBM50440135
(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) | 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 | 29 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 33 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 42 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 43 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 50 | n/a | n/a | n/a | n/a | n/a | n/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
((2Z,3Z)-2,3-bis(amino(2-aminophenylthio)methylene)...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL MMDB PC cid PC sid UniChem
Patents
Similars
| MMDB Article PubMed
| n/a | n/a | 89 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 91 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | 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 | 280 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 522 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 569 | n/a | n/a | n/a | n/a | n/a | n/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
((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 | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| Purchase
MCE KEGG MMDB PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 570 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 571 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 584 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 610 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 610 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 1.09E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 1.18E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.18E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | 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 | 1.26E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(CHEMBL2058568)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 | 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 | 1.34E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 1.36E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | 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 | 1.42E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.42E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.64E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank 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 |
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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.74E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.79E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.88E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(CHEMBL2058569)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 | 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 | 2.87E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | 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 | 3.12E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.12E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.74E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(CHEMBL2058567)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 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.48E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.57E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one |...)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 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank PDB Article PubMed
| n/a | n/a | 7.20E+3 | n/a | n/a | n/a | n/a | n/a | n/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 Structure (crystal) |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Mus musculus (Mouse)) | BDBM50137851
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.22E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(CHEMBL2058304)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 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.41E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.03E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 8.30E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 9.08E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 9.36E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.04E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.05E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.08E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | 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 | 1.24E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | 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 | 1.38E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.56E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.68E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(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+ | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.76E+4 | n/a | n/a | n/a | n/a | n/a | n/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 | |