Found 80 hits with Last Name = 'chang' and Initial = 'yl' 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 |
|---|
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328416
((Z)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)c(F)c34)cc(C)c12 Show InChI InChI=1S/C25H24F2N2O2/c1-15-13-16(14-18-23-20(28-25(18)30)10-9-19(26)24(23)27)17-7-4-5-8-21(22(15)17)31-12-6-11-29(2)3/h4-5,7-10,13-14H,6,11-12H2,1-3H3,(H,28,30)/b18-14- | 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 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328416
((Z)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)c(F)c34)cc(C)c12 Show InChI InChI=1S/C25H24F2N2O2/c1-15-13-16(14-18-23-20(28-25(18)30)10-9-19(26)24(23)27)17-7-4-5-8-21(22(15)17)31-12-6-11-29(2)3/h4-5,7-10,13-14H,6,11-12H2,1-3H3,(H,28,30)/b18-14- | 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 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328417
((Z)-4,5-difluoro-3-((3-methyl-4-(3-morpholinopropo...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ccc(F)c(F)c23)c2ccccc(OCCCN3CCOCC3)c12 Show InChI InChI=1S/C27H26F2N2O3/c1-17-15-18(16-20-25-22(30-27(20)32)8-7-21(28)26(25)29)19-5-2-3-6-23(24(17)19)34-12-4-9-31-10-13-33-14-11-31/h2-3,5-8,15-16H,4,9-14H2,1H3,(H,30,32)/b20-16- | 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 | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328417
((Z)-4,5-difluoro-3-((3-methyl-4-(3-morpholinopropo...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ccc(F)c(F)c23)c2ccccc(OCCCN3CCOCC3)c12 Show InChI InChI=1S/C27H26F2N2O3/c1-17-15-18(16-20-25-22(30-27(20)32)8-7-21(28)26(25)29)19-5-2-3-6-23(24(17)19)34-12-4-9-31-10-13-33-14-11-31/h2-3,5-8,15-16H,4,9-14H2,1H3,(H,30,32)/b20-16- | 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 | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328406
((Z)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C25H25FN2O2/c1-16-13-17(14-21-20-15-18(26)9-10-22(20)27-25(21)29)19-7-4-5-8-23(24(16)19)30-12-6-11-28(2)3/h4-5,7-10,13-15H,6,11-12H2,1-3H3,(H,27,29)/b21-14- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328406
((Z)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C25H25FN2O2/c1-16-13-17(14-21-20-15-18(26)9-10-22(20)27-25(21)29)19-7-4-5-8-23(24(16)19)30-12-6-11-28(2)3/h4-5,7-10,13-15H,6,11-12H2,1-3H3,(H,27,29)/b21-14- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328419
((Z)-3-((4-(3-(diethylamino)propoxy)-3-methylazulen...)Show SMILES CCN(CC)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)c(F)c34)cc(C)c12 Show InChI InChI=1S/C27H28F2N2O2/c1-4-31(5-2)13-8-14-33-23-10-7-6-9-19-18(15-17(3)24(19)23)16-20-25-22(30-27(20)32)12-11-21(28)26(25)29/h6-7,9-12,15-16H,4-5,8,13-14H2,1-3H3,(H,30,32)/b20-16- | 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 | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328419
((Z)-3-((4-(3-(diethylamino)propoxy)-3-methylazulen...)Show SMILES CCN(CC)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)c(F)c34)cc(C)c12 Show InChI InChI=1S/C27H28F2N2O2/c1-4-31(5-2)13-8-14-33-23-10-7-6-9-19-18(15-17(3)24(19)23)16-20-25-22(30-27(20)32)12-11-21(28)26(25)29/h6-7,9-12,15-16H,4-5,8,13-14H2,1-3H3,(H,30,32)/b20-16- | 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 | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit autophosphorylation in human Kasumi-1 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit autophosphorylation in human Kasumi-1 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 autophosphorylation in human RS4-11 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 autophosphorylation in human RS4-11 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328418
((Z)-4,5-difluoro-3-((3-methyl-4-(3-(piperidin-1-yl...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ccc(F)c(F)c23)c2ccccc(OCCCN3CCCCC3)c12 Show InChI InChI=1S/C28H28F2N2O2/c1-18-16-19(17-21-26-23(31-28(21)33)11-10-22(29)27(26)30)20-8-3-4-9-24(25(18)20)34-15-7-14-32-12-5-2-6-13-32/h3-4,8-11,16-17H,2,5-7,12-15H2,1H3,(H,31,33)/b21-17- | 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 | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328418
((Z)-4,5-difluoro-3-((3-methyl-4-(3-(piperidin-1-yl...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ccc(F)c(F)c23)c2ccccc(OCCCN3CCCCC3)c12 Show InChI InChI=1S/C28H28F2N2O2/c1-18-16-19(17-21-26-23(31-28(21)33)11-10-22(29)27(26)30)20-8-3-4-9-24(25(18)20)34-15-7-14-32-12-5-2-6-13-32/h3-4,8-11,16-17H,2,5-7,12-15H2,1H3,(H,31,33)/b21-17- | 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 | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
Article
PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of PDGFRbeta autophosphorylation by cell based western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
Article
PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of PDGFRbeta autophosphorylation by cell based western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328415
((Z)-3-((4-(2-(4-(dimethylamino)piperidin-1-yl)etho...)Show SMILES CN(C)C1CCN(CCOc2ccccc3c(\C=C4/C(=O)Nc5ccc(F)cc45)cc(C)c23)CC1 Show InChI InChI=1S/C29H32FN3O2/c1-19-16-20(17-25-24-18-21(30)8-9-26(24)31-29(25)34)23-6-4-5-7-27(28(19)23)35-15-14-33-12-10-22(11-13-33)32(2)3/h4-9,16-18,22H,10-15H2,1-3H3,(H,31,34)/b25-17- | 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 | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328415
((Z)-3-((4-(2-(4-(dimethylamino)piperidin-1-yl)etho...)Show SMILES CN(C)C1CCN(CCOc2ccccc3c(\C=C4/C(=O)Nc5ccc(F)cc45)cc(C)c23)CC1 Show InChI InChI=1S/C29H32FN3O2/c1-19-16-20(17-25-24-18-21(30)8-9-26(24)31-29(25)34)23-6-4-5-7-27(28(19)23)35-15-14-33-12-10-22(11-13-33)32(2)3/h4-9,16-18,22H,10-15H2,1-3H3,(H,31,34)/b25-17- | 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 | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328403
((Z)-5-fluoro-3-((3-methyl-4-(2-morpholinoethoxy)az...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCOCC3)c12 Show InChI InChI=1S/C26H25FN2O3/c1-17-14-18(15-22-21-16-19(27)6-7-23(21)28-26(22)30)20-4-2-3-5-24(25(17)20)32-13-10-29-8-11-31-12-9-29/h2-7,14-16H,8-13H2,1H3,(H,28,30)/b22-15- | 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 | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328403
((Z)-5-fluoro-3-((3-methyl-4-(2-morpholinoethoxy)az...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCOCC3)c12 Show InChI InChI=1S/C26H25FN2O3/c1-17-14-18(15-22-21-16-19(27)6-7-23(21)28-26(22)30)20-4-2-3-5-24(25(17)20)32-13-10-29-8-11-31-12-9-29/h2-7,14-16H,8-13H2,1H3,(H,28,30)/b22-15- | 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 | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328401
((Z)-5-fluoro-3-((3-fluoroazulen-1-yl)methylene)ind...)Show InChI InChI=1S/C19H11F2NO/c20-12-6-7-18-15(10-12)16(19(23)22-18)8-11-9-17(21)14-5-3-1-2-4-13(11)14/h1-10H,(H,22,23)/b16-8- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 23 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328401
((Z)-5-fluoro-3-((3-fluoroazulen-1-yl)methylene)ind...)Show InChI InChI=1S/C19H11F2NO/c20-12-6-7-18-15(10-12)16(19(23)22-18)8-11-9-17(21)14-5-3-1-2-4-13(11)14/h1-10H,(H,22,23)/b16-8- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 23 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328405
((E)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3\C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C25H25FN2O2/c1-16-13-17(14-21-20-15-18(26)9-10-22(20)27-25(21)29)19-7-4-5-8-23(24(16)19)30-12-6-11-28(2)3/h4-5,7-10,13-15H,6,11-12H2,1-3H3,(H,27,29)/b21-14+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328405
((E)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3\C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C25H25FN2O2/c1-16-13-17(14-21-20-15-18(26)9-10-22(20)27-25(21)29)19-7-4-5-8-23(24(16)19)30-12-6-11-28(2)3/h4-5,7-10,13-15H,6,11-12H2,1-3H3,(H,27,29)/b21-14+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | 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 | 28 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of PDGFRbeta autophosphorylation by cell based western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | 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 | 28 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of PDGFRbeta autophosphorylation by cell based western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328407
((E)-3-((4-(3-(diethylamino)propoxy)-3-methylazulen...)Show SMILES CCN(CC)CCCOc1ccccc2c(\C=C3\C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C27H29FN2O2/c1-4-30(5-2)13-8-14-32-25-10-7-6-9-21-19(15-18(3)26(21)25)16-23-22-17-20(28)11-12-24(22)29-27(23)31/h6-7,9-12,15-17H,4-5,8,13-14H2,1-3H3,(H,29,31)/b23-16+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328407
((E)-3-((4-(3-(diethylamino)propoxy)-3-methylazulen...)Show SMILES CCN(CC)CCCOc1ccccc2c(\C=C3\C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C27H29FN2O2/c1-4-30(5-2)13-8-14-32-25-10-7-6-9-21-19(15-18(3)26(21)25)16-23-22-17-20(28)11-12-24(22)29-27(23)31/h6-7,9-12,15-17H,4-5,8,13-14H2,1-3H3,(H,29,31)/b23-16+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328408
((Z)-3-((4-(3-(diethylamino)propoxy)-3-methylazulen...)Show SMILES CCN(CC)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C27H29FN2O2/c1-4-30(5-2)13-8-14-32-25-10-7-6-9-21-19(15-18(3)26(21)25)16-23-22-17-20(28)11-12-24(22)29-27(23)31/h6-7,9-12,15-17H,4-5,8,13-14H2,1-3H3,(H,29,31)/b23-16- | 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 | 39 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328408
((Z)-3-((4-(3-(diethylamino)propoxy)-3-methylazulen...)Show SMILES CCN(CC)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)cc34)cc(C)c12 Show InChI InChI=1S/C27H29FN2O2/c1-4-30(5-2)13-8-14-32-25-10-7-6-9-21-19(15-18(3)26(21)25)16-23-22-17-20(28)11-12-24(22)29-27(23)31/h6-7,9-12,15-17H,4-5,8,13-14H2,1-3H3,(H,29,31)/b23-16- | 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 | 39 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit autophosphorylation in human Kasumi-1 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit autophosphorylation in human Kasumi-1 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
PDB
Article
PubMed
| n/a | n/a | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of KDR autophosphorylation in HUVEC by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM4814
(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)Show SMILES CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C Show InChI InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12- | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
PDB
Article
PubMed
| n/a | n/a | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of KDR autophosphorylation in HUVEC by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328399
((E)-5-fluoro-3-((3-methylazulen-1-yl)methylene)ind...)Show InChI InChI=1S/C20H14FNO/c1-12-9-13(16-6-4-2-3-5-15(12)16)10-18-17-11-14(21)7-8-19(17)22-20(18)23/h2-11H,1H3,(H,22,23)/b18-10+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328399
((E)-5-fluoro-3-((3-methylazulen-1-yl)methylene)ind...)Show InChI InChI=1S/C20H14FNO/c1-12-9-13(16-6-4-2-3-5-15(12)16)10-18-17-11-14(21)7-8-19(17)22-20(18)23/h2-11H,1H3,(H,22,23)/b18-10+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | 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 | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 autophosphorylation in human RS4-11 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | 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 | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 autophosphorylation in human RS4-11 cells by Western blot analysis |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328411
((Z)-5-bromo-3-((3-methyl-4-(3-morpholinopropoxy)az...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ncc(Br)cc23)c2ccccc(OCCCN3CCOCC3)c12 Show InChI InChI=1S/C26H26BrN3O3/c1-17-13-18(14-22-21-15-19(27)16-28-25(21)29-26(22)31)20-5-2-3-6-23(24(17)20)33-10-4-7-30-8-11-32-12-9-30/h2-3,5-6,13-16H,4,7-12H2,1H3,(H,28,29,31)/b22-14- | 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 | 86 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328411
((Z)-5-bromo-3-((3-methyl-4-(3-morpholinopropoxy)az...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ncc(Br)cc23)c2ccccc(OCCCN3CCOCC3)c12 Show InChI InChI=1S/C26H26BrN3O3/c1-17-13-18(14-22-21-15-19(27)16-28-25(21)29-26(22)31)20-5-2-3-6-23(24(17)20)33-10-4-7-30-8-11-32-12-9-30/h2-3,5-6,13-16H,4,7-12H2,1H3,(H,28,29,31)/b22-14- | 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 | 86 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328410
((Z)-5-fluoro-3-((3-methyl-4-(3-morpholinopropoxy)a...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ncc(F)cc23)c2ccccc(OCCCN3CCOCC3)c12 Show InChI InChI=1S/C26H26FN3O3/c1-17-13-18(14-22-21-15-19(27)16-28-25(21)29-26(22)31)20-5-2-3-6-23(24(17)20)33-10-4-7-30-8-11-32-12-9-30/h2-3,5-6,13-16H,4,7-12H2,1H3,(H,28,29,31)/b22-14- | 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 | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328410
((Z)-5-fluoro-3-((3-methyl-4-(3-morpholinopropoxy)a...)Show SMILES Cc1cc(\C=C2/C(=O)Nc3ncc(F)cc23)c2ccccc(OCCCN3CCOCC3)c12 Show InChI InChI=1S/C26H26FN3O3/c1-17-13-18(14-22-21-15-19(27)16-28-25(21)29-26(22)31)20-5-2-3-6-23(24(17)20)33-10-4-7-30-8-11-32-12-9-30/h2-3,5-6,13-16H,4,7-12H2,1H3,(H,28,29,31)/b22-14- | 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 | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | 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 | 98 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328414
(CHEMBL1258603 | E/Z-(S)-5-fluoro-3-((4-(2-(2-(hydr...)Show SMILES Cc1cc(C=C2C(=O)Nc3ccc(F)cc23)c2ccccc(OCCN3CCC[C@H]3CO)c12 |r,w:4.3| Show InChI InChI=1S/C27H27FN2O3/c1-17-13-18(14-23-22-15-19(28)8-9-24(22)29-27(23)32)21-6-2-3-7-25(26(17)21)33-12-11-30-10-4-5-20(30)16-31/h2-3,6-9,13-15,20,31H,4-5,10-12,16H2,1H3,(H,29,32)/t20-/m0/s1 | 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 | 98 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328400
((Z)-5-fluoro-3-((3-methylazulen-1-yl)methylene)ind...)Show InChI InChI=1S/C20H14FNO/c1-12-9-13(16-6-4-2-3-5-15(12)16)10-18-17-11-14(21)7-8-19(17)22-20(18)23/h2-11H,1H3,(H,22,23)/b18-10- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 128 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328400
((Z)-5-fluoro-3-((3-methylazulen-1-yl)methylene)ind...)Show InChI InChI=1S/C20H14FNO/c1-12-9-13(16-6-4-2-3-5-15(12)16)10-18-17-11-14(21)7-8-19(17)22-20(18)23/h2-11H,1H3,(H,22,23)/b18-10- | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 128 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328413
((E)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3\C(=O)Nc4c3cccc4F)cc(C)c12 Show InChI InChI=1S/C25H25FN2O2/c1-16-14-17(15-20-19-9-6-10-21(26)24(19)27-25(20)29)18-8-4-5-11-22(23(16)18)30-13-7-12-28(2)3/h4-6,8-11,14-15H,7,12-13H2,1-3H3,(H,27,29)/b20-15+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 177 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50328413
((E)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...)Show SMILES CN(C)CCCOc1ccccc2c(\C=C3\C(=O)Nc4c3cccc4F)cc(C)c12 Show InChI InChI=1S/C25H25FN2O2/c1-16-14-17(15-20-19-9-6-10-21(26)24(19)27-25(20)29)18-8-4-5-11-22(23(16)18)30-13-7-12-28(2)3/h4-6,8-11,14-15H,7,12-13H2,1-3H3,(H,27,29)/b20-15+ | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 177 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 by time resolved fluorescence method |
Bioorg Med Chem Lett 20: 6129-32 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.025
BindingDB Entry DOI: 10.7270/Q2N29X51 |
More data for this
Ligand-Target Pair | |
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