Found 47 hits of Enzyme Inhibition Constant Data Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kJ/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314060
(1-(3-(2-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-7-y...)Show SMILES FC(F)(F)c1cccc(NC(=O)Nc2cccc(c2)-c2ccnc3cc(nn23)-c2ccncc2)c1 Show InChI InChI=1S/C25H17F3N6O/c26-25(27,28)18-4-2-6-20(14-18)32-24(35)31-19-5-1-3-17(13-19)22-9-12-30-23-15-21(33-34(22)23)16-7-10-29-11-8-16/h1-15H,(H2,31,32,35) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | 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 | 32 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314061
(1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(2-(py...)Show SMILES FC(F)(F)c1cc(NC(=O)Nc2cccc(c2)-c2ccnc3cc(nn23)-c2ccncc2)ccc1Cl Show InChI InChI=1S/C25H16ClF3N6O/c26-20-5-4-18(13-19(20)25(27,28)29)33-24(36)32-17-3-1-2-16(12-17)22-8-11-31-23-14-21(34-35(22)23)15-6-9-30-10-7-15/h1-14H,(H2,32,33,36) | 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 | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314062
(CHEMBL1092180 | N-(3-(2-(2-(2-(dimethylamino)ethyl...)Show SMILES CN(C)CCNc1cc(ccn1)-c1cc2nccc(-c3cccc(NC(=O)c4cccc(c4)C(F)(F)F)c3)n2n1 Show InChI InChI=1S/C29H26F3N7O/c1-38(2)14-13-34-26-17-19(9-11-33-26)24-18-27-35-12-10-25(39(27)37-24)20-5-4-8-23(16-20)36-28(40)21-6-3-7-22(15-21)29(30,31)32/h3-12,15-18H,13-14H2,1-2H3,(H,33,34)(H,36,40) | 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 | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314059
(4-chloro-N-(3-(2-(pyridin-4-yl)pyrazolo[1,5-a]pyri...)Show SMILES FC(F)(F)c1cc(ccc1Cl)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H15ClF3N5O/c26-20-5-4-17(13-19(20)25(27,28)29)24(35)32-18-3-1-2-16(12-18)22-8-11-31-23-14-21(33-34(22)23)15-6-9-30-10-7-15/h1-14H,(H,32,35) | 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 | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314069
(CHEMBL1091690 | N-(3-(2-(2-(2-(4-hydroxypiperidin-...)Show SMILES OC1CCN(CCNc2cc(ccn2)-c2cc3nccc(-c4cccc(NC(=O)c5cccc(c5)C(F)(F)F)c4)n3n2)CC1 Show InChI InChI=1S/C32H30F3N7O2/c33-32(34,35)24-5-1-4-23(17-24)31(44)39-25-6-2-3-22(18-25)28-8-12-38-30-20-27(40-42(28)30)21-7-11-36-29(19-21)37-13-16-41-14-9-26(43)10-15-41/h1-8,11-12,17-20,26,43H,9-10,13-16H2,(H,36,37)(H,39,44) | 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 | 66 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314068
(CHEMBL1091689 | N-(3-(2-(2-(3-(1H-imidazol-2-yl)pr...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccnc(NCCCc2ncc[nH]2)c1 Show InChI InChI=1S/C31H25F3N8O/c32-31(33,34)23-6-1-5-22(16-23)30(43)40-24-7-2-4-21(17-24)26-10-13-39-29-19-25(41-42(26)29)20-9-12-36-28(18-20)35-11-3-8-27-37-14-15-38-27/h1-2,4-7,9-10,12-19H,3,8,11H2,(H,35,36)(H,37,38)(H,40,43) | 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 | 66 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314065
(CHEMBL1091686 | N-(3-(2-(2-(2-(pyrrolidin-1-yl)eth...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccnc(NCCN2CCCC2)c1 Show InChI InChI=1S/C31H28F3N7O/c32-31(33,34)24-7-3-6-23(17-24)30(42)38-25-8-4-5-22(18-25)27-10-12-37-29-20-26(39-41(27)29)21-9-11-35-28(19-21)36-13-16-40-14-1-2-15-40/h3-12,17-20H,1-2,13-16H2,(H,35,36)(H,38,42) | 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 | 68 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314055
(CHEMBL1093105 | N-(3-(2-morpholinopyrazolo[1,5-a]p...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)N1CCOCC1 Show InChI InChI=1S/C24H20F3N5O2/c25-24(26,27)18-5-1-4-17(13-18)23(33)29-19-6-2-3-16(14-19)20-7-8-28-21-15-22(30-32(20)21)31-9-11-34-12-10-31/h1-8,13-15H,9-12H2,(H,29,33) | 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 | 99 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314050
(CHEMBL1088768 | N-(3-(2-(1-methyl-1H-imidazol-5-yl...)Show SMILES Cn1cncc1-c1cc2nccc(-c3cccc(NC(=O)c4cccc(c4)C(F)(F)F)c3)n2n1 Show InChI InChI=1S/C24H17F3N6O/c1-32-14-28-13-21(32)19-12-22-29-9-8-20(33(22)31-19)15-4-3-7-18(11-15)30-23(34)16-5-2-6-17(10-16)24(25,26)27/h2-14H,1H3,(H,30,34) | 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 | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314066
(CHEMBL1091687 | N-(3-(2-(2-(3-(pyrrolidin-1-yl)pro...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccnc(NCCCN2CCCC2)c1 Show InChI InChI=1S/C32H30F3N7O/c33-32(34,35)25-8-3-7-24(18-25)31(43)39-26-9-4-6-23(19-26)28-11-14-38-30-21-27(40-42(28)30)22-10-13-37-29(20-22)36-12-5-17-41-15-1-2-16-41/h3-4,6-11,13-14,18-21H,1-2,5,12,15-17H2,(H,36,37)(H,39,43) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314067
(CHEMBL1091688 | N-(3-(2-(2-(3-(2-oxopyrrolidin-1-y...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccnc(NCCCN2CCCC2=O)c1 Show InChI InChI=1S/C32H28F3N7O2/c33-32(34,35)24-7-1-6-23(17-24)31(44)39-25-8-2-5-22(18-25)27-11-14-38-29-20-26(40-42(27)29)21-10-13-37-28(19-21)36-12-4-16-41-15-3-9-30(41)43/h1-2,5-8,10-11,13-14,17-20H,3-4,9,12,15-16H2,(H,36,37)(H,39,44) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314064
(CHEMBL1091685 | N-(3-(2-(2-(3-morpholinopropylamin...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccnc(NCCCN2CCOCC2)c1 Show InChI InChI=1S/C32H30F3N7O2/c33-32(34,35)25-6-1-5-24(18-25)31(43)39-26-7-2-4-23(19-26)28-9-12-38-30-21-27(40-42(28)30)22-8-11-37-29(20-22)36-10-3-13-41-14-16-44-17-15-41/h1-2,4-9,11-12,18-21H,3,10,13-17H2,(H,36,37)(H,39,43) | 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 | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314063
(CHEMBL1091684 | N-(3-(2-(2-(2-morpholinoethylamino...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccnc(NCCN2CCOCC2)c1 Show InChI InChI=1S/C31H28F3N7O2/c32-31(33,34)24-5-1-4-23(17-24)30(42)38-25-6-2-3-22(18-25)27-8-10-37-29-20-26(39-41(27)29)21-7-9-35-28(19-21)36-11-12-40-13-15-43-16-14-40/h1-10,17-20H,11-16H2,(H,35,36)(H,38,42) | 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 | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314058
(3,4-dichloro-N-(3-(2-(pyridin-4-yl)pyrazolo[1,5-a]...)Show SMILES Clc1ccc(cc1Cl)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C24H15Cl2N5O/c25-19-5-4-17(13-20(19)26)24(32)29-18-3-1-2-16(12-18)22-8-11-28-23-14-21(30-31(22)23)15-6-9-27-10-7-15/h1-14H,(H,29,32) | 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 | 660 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314056
(3-chloro-N-(3-(2-(pyridin-4-yl)pyrazolo[1,5-a]pyri...)Show SMILES Clc1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C24H16ClN5O/c25-19-5-1-4-18(13-19)24(31)28-20-6-2-3-17(14-20)22-9-12-27-23-15-21(29-30(22)23)16-7-10-26-11-8-16/h1-15H,(H,28,31) | 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 | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314049
(CHEMBL1089411 | N-(3-(2-(1H-imidazol-5-yl)pyrazolo...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1c[nH]cn1 Show InChI InChI=1S/C23H15F3N6O/c24-23(25,26)16-5-1-4-15(9-16)22(33)30-17-6-2-3-14(10-17)20-7-8-28-21-11-18(31-32(20)21)19-12-27-13-29-19/h1-13H,(H,27,29)(H,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 | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314057
(3-methoxy-N-(3-(2-(pyridin-4-yl)pyrazolo[1,5-a]pyr...)Show SMILES COc1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H19N5O2/c1-32-21-7-3-5-19(15-21)25(31)28-20-6-2-4-18(14-20)23-10-13-27-24-16-22(29-30(23)24)17-8-11-26-12-9-17/h2-16H,1H3,(H,28,31) | 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 | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314053
(CHEMBL1092827 | N-(3-(2-(piperazin-1-yl)pyrazolo[1...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)N1CCNCC1 Show InChI InChI=1S/C24H21F3N6O/c25-24(26,27)18-5-1-4-17(13-18)23(34)30-19-6-2-3-16(14-19)20-7-8-29-21-15-22(31-33(20)21)32-11-9-28-10-12-32/h1-8,13-15,28H,9-12H2,(H,30,34) | 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 | 6.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314052
(CHEMBL1091500 | N-(3-(2-(pyridin-3-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1cccnc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-7-1-5-17(12-19)24(34)31-20-8-2-4-16(13-20)22-9-11-30-23-14-21(32-33(22)23)18-6-3-10-29-15-18/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314048
(CHEMBL1089410 | N-(3-(2-(thiophen-2-yl)pyrazolo[1,...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1cccs1 Show InChI InChI=1S/C24H15F3N4OS/c25-24(26,27)17-6-1-5-16(12-17)23(32)29-18-7-2-4-15(13-18)20-9-10-28-22-14-19(30-31(20)22)21-8-3-11-33-21/h1-14H,(H,29,32) | 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 | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314054
(CHEMBL1093104 | N-(3-(2-(4-methylpiperazin-1-yl)py...)Show SMILES CN1CCN(CC1)c1cc2nccc(-c3cccc(NC(=O)c4cccc(c4)C(F)(F)F)c3)n2n1 Show InChI InChI=1S/C25H23F3N6O/c1-32-10-12-33(13-11-32)23-16-22-29-9-8-21(34(22)31-23)17-4-3-7-20(15-17)30-24(35)18-5-2-6-19(14-18)25(26,27)28/h2-9,14-16H,10-13H2,1H3,(H,30,35) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314046
(3-(trifluoromethyl)-N-(3-(2-(3-(trifluoromethyl)ph...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C27H16F6N4O/c28-26(29,30)19-7-1-4-16(12-19)22-15-24-34-11-10-23(37(24)36-22)17-5-3-9-21(14-17)35-25(38)18-6-2-8-20(13-18)27(31,32)33/h1-15H,(H,35,38) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50314047
(CHEMBL1089412 | N-(3-(2-(4-methoxyphenyl)pyrazolo[...)Show SMILES COc1ccc(cc1)-c1cc2nccc(-c3cccc(NC(=O)c4cccc(c4)C(F)(F)F)c3)n2n1 Show InChI InChI=1S/C27H19F3N4O2/c1-36-22-10-8-17(9-11-22)23-16-25-31-13-12-24(34(25)33-23)18-4-3-7-21(15-18)32-26(35)19-5-2-6-20(14-19)27(28,29)30/h2-16H,1H3,(H,32,35) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of b-Raf |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of Fyn |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 1
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of ERK2 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of PKCalpha |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of PI3Kalpha |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Inhibitor of nuclear factor kappa-B kinase subunit beta
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of IKK-beta |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
RAC-alpha serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of PKBalpha |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of P38alpha |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of Abl1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of mTOR |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Protein kinase C beta type
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of PKCbeta |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Rho-associated protein kinase 1
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of ROCK1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of LCK |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Insulin-like growth factor 1 receptor
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of IGFR1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of CDK2 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
3-phosphoinositide-dependent protein kinase 1
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of PDK1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase PLK1
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of PLK1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
MAP kinase-activated protein kinase 2
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of MK2 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase kinase kinase kinase 2
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of GCK |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase kinase kinase 8
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of TPL2 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Serine/threonine-protein kinase Chk1
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of CHK1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of Src |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 1
(Homo sapiens (Human)) | BDBM50314051
(CHEMBL1089082 | N-(3-(2-(pyridin-4-yl)pyrazolo[1,5...)Show SMILES FC(F)(F)c1cccc(c1)C(=O)Nc1cccc(c1)-c1ccnc2cc(nn12)-c1ccncc1 Show InChI InChI=1S/C25H16F3N5O/c26-25(27,28)19-5-1-4-18(13-19)24(34)31-20-6-2-3-17(14-20)22-9-12-30-23-15-21(32-33(22)23)16-7-10-29-11-8-16/h1-15H,(H,31,34) | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Wyeth Research
Curated by ChEMBL
| Assay Description
Inhibition of CDK1 |
Bioorg Med Chem Lett 19: 6890-2 (2009)
Article DOI: 10.1016/j.bmcl.2009.10.074
BindingDB Entry DOI: 10.7270/Q2C829F3 |
More data for this
Ligand-Target Pair | |
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