Found 148 hits Enz. Inhib. hit(s) with all data for entry = 50039827 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 |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384877
![PNG](/data/jpeg/tenK5038/BindingDB_50384877.png) (CHEMBL2035183)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)s3 |t:28| Show InChI InChI=1S/C26H30N4O3S/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.30 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384868
![PNG](/data/jpeg/tenK5038/BindingDB_50384868.png) (CHEMBL2035049)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc4ccn(C\C=C\COCc1c2)c4c3 |t:29| Show InChI InChI=1S/C29H31N5O2/c1-2-13-33(12-1)16-18-36-28-8-7-25-19-24(28)21-35-17-4-3-14-34-15-10-22-5-6-23(20-27(22)34)26-9-11-30-29(31-25)32-26/h3-11,15,19-20H,1-2,12-14,16-18,21H2,(H,30,31,32)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.90 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384874
![PNG](/data/jpeg/tenK5038/BindingDB_50384874.png) (CHEMBL2035055)Show SMILES CN1C\C=C\COCc2ccc(s2)-c2ccnc(Nc3ccc(OCCN4CCCC4)c(C1)c3)n2 |t:3| Show InChI InChI=1S/C27H33N5O2S/c1-31-12-4-5-16-33-20-23-7-9-26(35-23)24-10-11-28-27(30-24)29-22-6-8-25(21(18-22)19-31)34-17-15-32-13-2-3-14-32/h4-11,18H,2-3,12-17,19-20H2,1H3,(H,28,29,30)/b5-4+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384872
![PNG](/data/jpeg/tenK5038/BindingDB_50384872.png) (CHEMBL2035053)Show SMILES Cc1cnc2Nc3ccc(OCCN4CCCC4)c(COC\C=C\CCOc4cc(ccn4)-c1n2)c3 |t:23| Show InChI InChI=1S/C28H33N5O3/c1-21-19-30-28-31-24-7-8-25(35-16-13-33-11-3-4-12-33)23(17-24)20-34-14-5-2-6-15-36-26-18-22(9-10-29-26)27(21)32-28/h2,5,7-10,17-19H,3-4,6,11-16,20H2,1H3,(H,30,31,32)/b5-2+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384878
![PNG](/data/jpeg/tenK5038/BindingDB_50384878.png) (CHEMBL2035184)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3csc(COC\C=C\COCc1c2)c3 |t:28| Show InChI InChI=1S/C26H30N4O3S/c1-2-10-30(9-1)11-14-33-25-6-5-22-15-20(25)17-31-12-3-4-13-32-18-23-16-21(19-34-23)24-7-8-27-26(28-22)29-24/h3-8,15-16,19H,1-2,9-14,17-18H2,(H,27,28,29)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384869
![PNG](/data/jpeg/tenK5038/BindingDB_50384869.png) (CHEMBL2035050)Show SMILES Cc1cnc2Nc3ccc(OCCN4CCCC4)c(COC\C=C\Cn4ccc5ccc(cc45)-c1n2)c3 |t:23| Show InChI InChI=1S/C30H33N5O2/c1-22-20-31-30-32-26-8-9-28(37-17-15-34-11-2-3-12-34)25(18-26)21-36-16-5-4-13-35-14-10-23-6-7-24(19-27(23)35)29(22)33-30/h4-10,14,18-20H,2-3,11-13,15-17,21H2,1H3,(H,31,32,33)/b5-4+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384871
![PNG](/data/jpeg/tenK5038/BindingDB_50384871.png) (CHEMBL2035052)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccnc(OCC\C=C\COCc1c2)c3 |t:29| Show InChI InChI=1S/C27H31N5O3/c1-4-15-33-20-22-18-23(6-7-25(22)34-17-14-32-12-2-3-13-32)30-27-29-11-9-24(31-27)21-8-10-28-26(19-21)35-16-5-1/h1,4,6-11,18-19H,2-3,5,12-17,20H2,(H,29,30,31)/b4-1+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384876
![PNG](/data/jpeg/tenK5038/BindingDB_50384876.png) (CHEMBL2035182)Show SMILES COCCOc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\CN(C)Cc1c2)s3 |t:24| Show InChI InChI=1S/C24H28N4O3S/c1-28-11-3-4-12-30-17-20-6-8-23(32-20)21-9-10-25-24(27-21)26-19-5-7-22(18(15-19)16-28)31-14-13-29-2/h3-10,15H,11-14,16-17H2,1-2H3,(H,25,26,27)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50384882
![PNG](/data/jpeg/tenK5038/BindingDB_50384882.png) (CHEMBL2035044)Show SMILES CN1C\C=C\CCOc2cc(ccn2)-c2ccnc(Nc3cccc(C1)c3)n2 |t:3| Show InChI InChI=1S/C22H23N5O/c1-27-12-3-2-4-13-28-21-15-18(8-10-23-21)20-9-11-24-22(26-20)25-19-7-5-6-17(14-19)16-27/h2-3,5-11,14-15H,4,12-13,16H2,1H3,(H,24,25,26)/b3-2+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant CDK2 using RbING as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384877
![PNG](/data/jpeg/tenK5038/BindingDB_50384877.png) (CHEMBL2035183)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)s3 |t:28| Show InChI InChI=1S/C26H30N4O3S/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384871
![PNG](/data/jpeg/tenK5038/BindingDB_50384871.png) (CHEMBL2035052)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccnc(OCC\C=C\COCc1c2)c3 |t:29| Show InChI InChI=1S/C27H31N5O3/c1-4-15-33-20-22-18-23(6-7-25(22)34-17-14-32-12-2-3-13-32)30-27-29-11-9-24(31-27)21-8-10-28-26(19-21)35-16-5-1/h1,4,6-11,18-19H,2-3,5,12-17,20H2,(H,29,30,31)/b4-1+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384871
![PNG](/data/jpeg/tenK5038/BindingDB_50384871.png) (CHEMBL2035052)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccnc(OCC\C=C\COCc1c2)c3 |t:29| Show InChI InChI=1S/C27H31N5O3/c1-4-15-33-20-22-18-23(6-7-25(22)34-17-14-32-12-2-3-13-32)30-27-29-11-9-24(31-27)21-8-10-28-26(19-21)35-16-5-1/h1,4,6-11,18-19H,2-3,5,12-17,20H2,(H,29,30,31)/b4-1+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384872
![PNG](/data/jpeg/tenK5038/BindingDB_50384872.png) (CHEMBL2035053)Show SMILES Cc1cnc2Nc3ccc(OCCN4CCCC4)c(COC\C=C\CCOc4cc(ccn4)-c1n2)c3 |t:23| Show InChI InChI=1S/C28H33N5O3/c1-21-19-30-28-31-24-7-8-25(35-16-13-33-11-3-4-12-33)23(17-24)20-34-14-5-2-6-15-36-26-18-22(9-10-29-26)27(21)32-28/h2,5,7-10,17-19H,3-4,6,11-16,20H2,1H3,(H,30,31,32)/b5-2+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384877
![PNG](/data/jpeg/tenK5038/BindingDB_50384877.png) (CHEMBL2035183)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)s3 |t:28| Show InChI InChI=1S/C26H30N4O3S/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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 |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384876
![PNG](/data/jpeg/tenK5038/BindingDB_50384876.png) (CHEMBL2035182)Show SMILES COCCOc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\CN(C)Cc1c2)s3 |t:24| Show InChI InChI=1S/C24H28N4O3S/c1-28-11-3-4-12-30-17-20-6-8-23(32-20)21-9-10-25-24(27-21)26-19-5-7-22(18(15-19)16-28)31-14-13-29-2/h3-10,15H,11-14,16-17H2,1-2H3,(H,25,26,27)/b4-3+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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 |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 9
(Homo sapiens (Human)) | BDBM50384879
![PNG](/data/jpeg/tenK5038/BindingDB_50384879.png) (CHEMBL2035185)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)o3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 36 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of CDK9 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384874
![PNG](/data/jpeg/tenK5038/BindingDB_50384874.png) (CHEMBL2035055)Show SMILES CN1C\C=C\COCc2ccc(s2)-c2ccnc(Nc3ccc(OCCN4CCCC4)c(C1)c3)n2 |t:3| Show InChI InChI=1S/C27H33N5O2S/c1-31-12-4-5-16-33-20-23-7-9-26(35-23)24-10-11-28-27(30-24)29-22-6-8-25(21(18-22)19-31)34-17-15-32-13-2-3-14-32/h4-11,18H,2-3,12-17,19-20H2,1H3,(H,28,29,30)/b5-4+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 41 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384878
![PNG](/data/jpeg/tenK5038/BindingDB_50384878.png) (CHEMBL2035184)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3csc(COC\C=C\COCc1c2)c3 |t:28| Show InChI InChI=1S/C26H30N4O3S/c1-2-10-30(9-1)11-14-33-25-6-5-22-15-20(25)17-31-12-3-4-13-32-18-23-16-21(19-34-23)24-7-8-27-26(28-22)29-24/h3-8,15-16,19H,1-2,9-14,17-18H2,(H,27,28,29)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 45 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384879
![PNG](/data/jpeg/tenK5038/BindingDB_50384879.png) (CHEMBL2035185)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)o3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 46 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384878
![PNG](/data/jpeg/tenK5038/BindingDB_50384878.png) (CHEMBL2035184)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3csc(COC\C=C\COCc1c2)c3 |t:28| Show InChI InChI=1S/C26H30N4O3S/c1-2-10-30(9-1)11-14-33-25-6-5-22-15-20(25)17-31-12-3-4-13-32-18-23-16-21(19-34-23)24-7-8-27-26(28-22)29-24/h3-8,15-16,19H,1-2,9-14,17-18H2,(H,27,28,29)/b4-3+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 47 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384880
![PNG](/data/jpeg/tenK5038/BindingDB_50384880.png) (CHEMBL2035186)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3coc(COC\C=C\COCc1c2)c3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-10-30(9-1)11-14-33-25-6-5-22-15-21(25)17-31-12-3-4-13-32-19-23-16-20(18-34-23)24-7-8-27-26(28-22)29-24/h3-8,15-16,18H,1-2,9-14,17,19H2,(H,27,28,29)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 48 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384879
![PNG](/data/jpeg/tenK5038/BindingDB_50384879.png) (CHEMBL2035185)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)o3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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 |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384870
![PNG](/data/jpeg/tenK5038/BindingDB_50384870.png) (CHEMBL2035051)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3cncc(COC\C=C\COCc1c2)c3 |t:29| Show InChI InChI=1S/C27H31N5O3/c1-2-10-32(9-1)11-14-35-26-6-5-24-16-23(26)20-34-13-4-3-12-33-19-21-15-22(18-28-17-21)25-7-8-29-27(30-24)31-25/h3-8,15-18H,1-2,9-14,19-20H2,(H,29,30,31)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 63 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384868
![PNG](/data/jpeg/tenK5038/BindingDB_50384868.png) (CHEMBL2035049)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc4ccn(C\C=C\COCc1c2)c4c3 |t:29| Show InChI InChI=1S/C29H31N5O2/c1-2-13-33(12-1)16-18-36-28-8-7-25-19-24(28)21-35-17-4-3-14-34-15-10-22-5-6-23(20-27(22)34)26-9-11-30-29(31-25)32-26/h3-11,15,19-20H,1-2,12-14,16-18,21H2,(H,30,31,32)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 63 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384882
![PNG](/data/jpeg/tenK5038/BindingDB_50384882.png) (CHEMBL2035044)Show SMILES CN1C\C=C\CCOc2cc(ccn2)-c2ccnc(Nc3cccc(C1)c3)n2 |t:3| Show InChI InChI=1S/C22H23N5O/c1-27-12-3-2-4-13-28-21-15-18(8-10-23-21)20-9-11-24-22(26-20)25-19-7-5-6-17(14-19)16-27/h2-3,5-11,14-15H,4,12-13,16H2,1H3,(H,24,25,26)/b3-2+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 65 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384880
![PNG](/data/jpeg/tenK5038/BindingDB_50384880.png) (CHEMBL2035186)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3coc(COC\C=C\COCc1c2)c3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-10-30(9-1)11-14-33-25-6-5-22-15-21(25)17-31-12-3-4-13-32-19-23-16-20(18-34-23)24-7-8-27-26(28-22)29-24/h3-8,15-16,18H,1-2,9-14,17,19H2,(H,27,28,29)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 67 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50384879
![PNG](/data/jpeg/tenK5038/BindingDB_50384879.png) (CHEMBL2035185)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)o3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 69 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of c-fms |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384872
![PNG](/data/jpeg/tenK5038/BindingDB_50384872.png) (CHEMBL2035053)Show SMILES Cc1cnc2Nc3ccc(OCCN4CCCC4)c(COC\C=C\CCOc4cc(ccn4)-c1n2)c3 |t:23| Show InChI InChI=1S/C28H33N5O3/c1-21-19-30-28-31-24-7-8-25(35-16-13-33-11-3-4-12-33)23(17-24)20-34-14-5-2-6-15-36-26-18-22(9-10-29-26)27(21)32-28/h2,5,7-10,17-19H,3-4,6,11-16,20H2,1H3,(H,30,31,32)/b5-2+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 72 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384885
![PNG](/data/jpeg/tenK5038/BindingDB_50384885.png) (CHEMBL2035043)Show SMILES C1OCc2cccc(Nc3nccc(n3)-c3ccc4ccn(C\C=C\1)c4c3)c2 |t:24| Show InChI InChI=1S/C23H20N4O/c1-2-13-28-16-17-4-3-5-20(14-17)25-23-24-10-8-21(26-23)19-7-6-18-9-12-27(11-1)22(18)15-19/h1-10,12,14-15H,11,13,16H2,(H,24,25,26)/b2-1+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 73 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50384884
![PNG](/data/jpeg/tenK5038/BindingDB_50384884.png) (CHEMBL2035042)Show SMILES CN1C\C=C\CCn2ccc3ccc(cc23)-c2ccnc(Nc3cccc(C1)c3)n2 |t:3| Show InChI InChI=1S/C25H25N5/c1-29-13-3-2-4-14-30-15-11-20-8-9-21(17-24(20)30)23-10-12-26-25(28-23)27-22-7-5-6-19(16-22)18-29/h2-3,5-12,15-17H,4,13-14,18H2,1H3,(H,26,27,28)/b3-2+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 77 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant CDK2 using RbING as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50384885
![PNG](/data/jpeg/tenK5038/BindingDB_50384885.png) (CHEMBL2035043)Show SMILES C1OCc2cccc(Nc3nccc(n3)-c3ccc4ccn(C\C=C\1)c4c3)c2 |t:24| Show InChI InChI=1S/C23H20N4O/c1-2-13-28-16-17-4-3-5-20(14-17)25-23-24-10-8-21(26-23)19-7-6-18-9-12-27(11-1)22(18)15-19/h1-10,12,14-15H,11,13,16H2,(H,24,25,26)/b2-1+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 83 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant CDK2 using RbING as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384874
![PNG](/data/jpeg/tenK5038/BindingDB_50384874.png) (CHEMBL2035055)Show SMILES CN1C\C=C\COCc2ccc(s2)-c2ccnc(Nc3ccc(OCCN4CCCC4)c(C1)c3)n2 |t:3| Show InChI InChI=1S/C27H33N5O2S/c1-31-12-4-5-16-33-20-23-7-9-26(35-23)24-10-11-28-27(30-24)29-22-6-8-25(21(18-22)19-31)34-17-15-32-13-2-3-14-32/h4-11,18H,2-3,12-17,19-20H2,1H3,(H,28,29,30)/b5-4+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384884
![PNG](/data/jpeg/tenK5038/BindingDB_50384884.png) (CHEMBL2035042)Show SMILES CN1C\C=C\CCn2ccc3ccc(cc23)-c2ccnc(Nc3cccc(C1)c3)n2 |t:3| Show InChI InChI=1S/C25H25N5/c1-29-13-3-2-4-14-30-15-11-20-8-9-21(17-24(20)30)23-10-12-26-25(28-23)27-22-7-5-6-19(16-22)18-29/h2-3,5-12,15-17H,4,13-14,18H2,1H3,(H,26,27,28)/b3-2+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 93 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384881
![PNG](/data/jpeg/tenK5038/BindingDB_50384881.png) (CHEMBL2035181)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3cc(COC\C=C\COCc1c2)co3 |t:27| Show InChI InChI=1S/C26H30N4O4/c1-2-10-30(9-1)11-14-33-24-6-5-22-16-21(24)19-32-13-4-3-12-31-17-20-15-25(34-18-20)23-7-8-27-26(28-22)29-23/h3-8,15-16,18H,1-2,9-14,17,19H2,(H,27,28,29)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| 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 |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384873
![PNG](/data/jpeg/tenK5038/BindingDB_50384873.png) (CHEMBL2035054)Show SMILES CN1C\C=C\COCc2ccc(o2)-c2ccnc(Nc3ccc(OCCN4CCCC4)c(C1)c3)n2 |t:3| Show InChI InChI=1S/C27H33N5O3/c1-31-12-4-5-16-33-20-23-7-9-26(35-23)24-10-11-28-27(30-24)29-22-6-8-25(21(18-22)19-31)34-17-15-32-13-2-3-14-32/h4-11,18H,2-3,12-17,19-20H2,1H3,(H,28,29,30)/b5-4+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384880
![PNG](/data/jpeg/tenK5038/BindingDB_50384880.png) (CHEMBL2035186)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3coc(COC\C=C\COCc1c2)c3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-10-30(9-1)11-14-33-25-6-5-22-15-21(25)17-31-12-3-4-13-32-19-23-16-20(18-34-23)24-7-8-27-26(28-22)29-24/h3-8,15-16,18H,1-2,9-14,17,19H2,(H,27,28,29)/b4-3+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384885
![PNG](/data/jpeg/tenK5038/BindingDB_50384885.png) (CHEMBL2035043)Show SMILES C1OCc2cccc(Nc3nccc(n3)-c3ccc4ccn(C\C=C\1)c4c3)c2 |t:24| Show InChI InChI=1S/C23H20N4O/c1-2-13-28-16-17-4-3-5-20(14-17)25-23-24-10-8-21(26-23)19-7-6-18-9-12-27(11-1)22(18)15-19/h1-10,12,14-15H,11,13,16H2,(H,24,25,26)/b2-1+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384885
![PNG](/data/jpeg/tenK5038/BindingDB_50384885.png) (CHEMBL2035043)Show SMILES C1OCc2cccc(Nc3nccc(n3)-c3ccc4ccn(C\C=C\1)c4c3)c2 |t:24| Show InChI InChI=1S/C23H20N4O/c1-2-13-28-16-17-4-3-5-20(14-17)25-23-24-10-8-21(26-23)19-7-6-18-9-12-27(11-1)22(18)15-19/h1-10,12,14-15H,11,13,16H2,(H,24,25,26)/b2-1+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK1
(Homo sapiens (Human)) | BDBM50384882
![PNG](/data/jpeg/tenK5038/BindingDB_50384882.png) (CHEMBL2035044)Show SMILES CN1C\C=C\CCOc2cc(ccn2)-c2ccnc(Nc3cccc(C1)c3)n2 |t:3| Show InChI InChI=1S/C22H23N5O/c1-27-12-3-2-4-13-28-21-15-18(8-10-23-21)20-9-11-24-22(26-20)25-19-7-5-6-17(14-19)16-27/h2-3,5-11,14-15H,4,12-13,16H2,1H3,(H,24,25,26)/b3-2+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK1 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384876
![PNG](/data/jpeg/tenK5038/BindingDB_50384876.png) (CHEMBL2035182)Show SMILES COCCOc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\CN(C)Cc1c2)s3 |t:24| Show InChI InChI=1S/C24H28N4O3S/c1-28-11-3-4-12-30-17-20-6-8-23(32-20)21-9-10-25-24(27-21)26-19-5-7-22(18(15-19)16-28)31-14-13-29-2/h3-10,15H,11-14,16-17H2,1-2H3,(H,25,26,27)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50384881
![PNG](/data/jpeg/tenK5038/BindingDB_50384881.png) (CHEMBL2035181)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3cc(COC\C=C\COCc1c2)co3 |t:27| Show InChI InChI=1S/C26H30N4O4/c1-2-10-30(9-1)11-14-33-24-6-5-22-16-21(24)19-32-13-4-3-12-31-17-20-15-25(34-18-20)23-7-8-27-26(28-22)29-23/h3-8,15-16,18H,1-2,9-14,17,19H2,(H,27,28,29)/b4-3+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 180 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 using poly(Glu,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50384865
![PNG](/data/jpeg/tenK5038/BindingDB_50384865.png) (CHEMBL2035046)Show SMILES C1OCc2cccc(Nc3nccc(n3)-c3cncc(COC\C=C\1)c3)c2 |t:24| Show InChI InChI=1S/C21H20N4O2/c1-2-9-27-15-17-10-18(13-22-12-17)20-6-7-23-21(25-20)24-19-5-3-4-16(11-19)14-26-8-1/h1-7,10-13H,8-9,14-15H2,(H,23,24,25)/b2-1+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant CDK2 using RbING as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK1
(Homo sapiens (Human)) | BDBM50384874
![PNG](/data/jpeg/tenK5038/BindingDB_50384874.png) (CHEMBL2035055)Show SMILES CN1C\C=C\COCc2ccc(s2)-c2ccnc(Nc3ccc(OCCN4CCCC4)c(C1)c3)n2 |t:3| Show InChI InChI=1S/C27H33N5O2S/c1-31-12-4-5-16-33-20-23-7-9-26(35-23)24-10-11-28-27(30-24)29-22-6-8-25(21(18-22)19-31)34-17-15-32-13-2-3-14-32/h4-11,18H,2-3,12-17,19-20H2,1H3,(H,28,29,30)/b5-4+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK1 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384867
![PNG](/data/jpeg/tenK5038/BindingDB_50384867.png) (CHEMBL2035048)Show SMILES C1OCc2ccc(o2)-c2ccnc(Nc3cccc(COC\C=C\1)c3)n2 |t:23| Show InChI InChI=1S/C20H19N3O3/c1-2-11-25-14-17-6-7-19(26-17)18-8-9-21-20(23-18)22-16-5-3-4-15(12-16)13-24-10-1/h1-9,12H,10-11,13-14H2,(H,21,22,23)/b2-1+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 220 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50384868
![PNG](/data/jpeg/tenK5038/BindingDB_50384868.png) (CHEMBL2035049)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc4ccn(C\C=C\COCc1c2)c4c3 |t:29| Show InChI InChI=1S/C29H31N5O2/c1-2-13-33(12-1)16-18-36-28-8-7-25-19-24(28)21-35-17-4-3-14-34-15-10-22-5-6-23(20-27(22)34)26-9-11-30-29(31-25)32-26/h3-11,15,19-20H,1-2,12-14,16-18,21H2,(H,30,31,32)/b4-3+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant CDK2 using RbING as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384879
![PNG](/data/jpeg/tenK5038/BindingDB_50384879.png) (CHEMBL2035185)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccc(COC\C=C\COCc1c2)o3 |t:28| Show InChI InChI=1S/C26H30N4O4/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384882
![PNG](/data/jpeg/tenK5038/BindingDB_50384882.png) (CHEMBL2035044)Show SMILES CN1C\C=C\CCOc2cc(ccn2)-c2ccnc(Nc3cccc(C1)c3)n2 |t:3| Show InChI InChI=1S/C22H23N5O/c1-27-12-3-2-4-13-28-21-15-18(8-10-23-21)20-9-11-24-22(26-20)25-19-7-5-6-17(14-19)16-27/h2-3,5-11,14-15H,4,12-13,16H2,1H3,(H,24,25,26)/b3-2+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 260 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50384871
![PNG](/data/jpeg/tenK5038/BindingDB_50384871.png) (CHEMBL2035052)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3ccnc(OCC\C=C\COCc1c2)c3 |t:29| Show InChI InChI=1S/C27H31N5O3/c1-4-15-33-20-22-18-23(6-7-25(22)34-17-14-32-12-2-3-13-32)30-27-29-11-9-24(31-27)21-8-10-28-26(19-21)35-16-5-1/h1,4,6-11,18-19H,2-3,5,12-17,20H2,(H,29,30,31)/b4-1+ | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant CDK2 using RbING as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase JAK2
(Homo sapiens (Human)) | BDBM50384870
![PNG](/data/jpeg/tenK5038/BindingDB_50384870.png) (CHEMBL2035051)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3cncc(COC\C=C\COCc1c2)c3 |t:29| Show InChI InChI=1S/C27H31N5O3/c1-2-10-32(9-1)11-14-35-26-6-5-24-16-23(26)20-34-13-4-3-12-33-19-21-15-22(18-28-17-21)25-7-8-29-27(30-24)31-25/h3-8,15-18H,1-2,9-14,19-20H2,(H,29,30,31)/b4-3+ | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of recombinant JAK2 using poly(Glu,Ala,Tyr) as substrate after 2 hrs by luminometric assay |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |
Non-receptor tyrosine-protein kinase TYK2
(Homo sapiens (Human)) | BDBM50384881
![PNG](/data/jpeg/tenK5038/BindingDB_50384881.png) (CHEMBL2035181)Show SMILES C(CN1CCCC1)Oc1ccc2Nc3nccc(n3)-c3cc(COC\C=C\COCc1c2)co3 |t:27| Show InChI InChI=1S/C26H30N4O4/c1-2-10-30(9-1)11-14-33-24-6-5-22-16-21(24)19-32-13-4-3-12-31-17-20-15-25(34-18-20)23-7-8-27-26(28-22)29-23/h3-8,15-16,18H,1-2,9-14,17,19H2,(H,27,28,29)/b4-3+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 310 | n/a | n/a | n/a | n/a | n/a | n/a |
S BIO Pte. Ltd.
Curated by ChEMBL
| Assay Description Inhibition of TYK2 |
J Med Chem 55: 2623-40 (2012)
Article DOI: 10.1021/jm201454n BindingDB Entry DOI: 10.7270/Q2CC11RG |
More data for this Ligand-Target Pair | |