Found 178 hits with Last Name = 'hamar' and Initial = 'p' 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)) | BDBM50300690
![PNG](/data/jpeg/tenK5030/BindingDB_50300690.png) (1-(5-Tert-Butyl-1,2-Oxazol-3-Yl)-3-(4-{7-[2-(Morph...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(cc2)-c2cn3c(n2)sc2cc(OCCN4CCOCC4)ccc32)no1 Show InChI InChI=1S/C29H32N6O4S/c1-29(2,3)25-17-26(33-39-25)32-27(36)30-20-6-4-19(5-7-20)22-18-35-23-9-8-21(16-24(23)40-28(35)31-22)38-15-12-34-10-13-37-14-11-34/h4-9,16-18H,10-15H2,1-3H3,(H2,30,32,33,36) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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| n/a | n/a | 1.10 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of human partial length FLT3 ITD mutant expressed in bacterial expression system by Kinomescan method |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50277584
![PNG](/data/jpeg/tenK5027/BindingDB_50277584.png) (CHEMBL482968 | N-(5-methyl-1H-pyrazol-3-yl)-6-(4-m...)Show SMILES CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(C=Cc2ccccc2)n1 |w:19.20| Show InChI InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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| Article PubMed
| n/a | n/a | 1.90 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50504574
![PNG](/data/jpeg/tenK5050/BindingDB_50504574.png) (CHEMBL4469622)Show SMILES [H][C@]12C[C@](C)(CO)[C@](C)(O1)n1c3ccccc3c3c4C(=O)NCc4c4c5ccccc5n2c4c13 |r| Show InChI InChI=1S/C27H23N3O3/c1-26(13-31)11-19-29-17-9-5-3-7-14(17)20-16-12-28-25(32)22(16)21-15-8-4-6-10-18(15)30(24(21)23(20)29)27(26,2)33-19/h3-10,19,31H,11-13H2,1-2H3,(H,28,32)/t19-,26-,27+/m1/s1 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 (unknown origin) autophosphorylation expressed in BaF3 cells |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50300690
![PNG](/data/jpeg/tenK5030/BindingDB_50300690.png) (1-(5-Tert-Butyl-1,2-Oxazol-3-Yl)-3-(4-{7-[2-(Morph...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(cc2)-c2cn3c(n2)sc2cc(OCCN4CCOCC4)ccc32)no1 Show InChI InChI=1S/C29H32N6O4S/c1-29(2,3)25-17-26(33-39-25)32-27(36)30-20-6-4-19(5-7-20)22-18-35-23-9-8-21(16-24(23)40-28(35)31-22)38-15-12-34-10-13-37-14-11-34/h4-9,16-18H,10-15H2,1-3H3,(H2,30,32,33,36) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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| n/a | n/a | 4.20 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of wild-type human partial length FLT3 (V592 to Y969 residues) expressed in bacterial expression system by Kinomescan method |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50355496
![PNG](/data/jpeg/tenK5035/BindingDB_50355496.png) (CHEMBL1908397)Show SMILES O=C(N1CCNCC1)c1ccc(\C=C\c2n[nH]c3ccccc23)cc1 Show InChI InChI=1S/C20H20N4O/c25-20(24-13-11-21-12-14-24)16-8-5-15(6-9-16)7-10-19-17-3-1-2-4-18(17)22-23-19/h1-10,21H,11-14H2,(H,22,23)/b10-7+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| n/a | n/a | 6.60 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of human FLT3 |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50277584
![PNG](/data/jpeg/tenK5027/BindingDB_50277584.png) (CHEMBL482968 | N-(5-methyl-1H-pyrazol-3-yl)-6-(4-m...)Show SMILES CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(C=Cc2ccccc2)n1 |w:19.20| Show InChI InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant human His-tagged FMS expressed in baculovirus expression system |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50277584
![PNG](/data/jpeg/tenK5027/BindingDB_50277584.png) (CHEMBL482968 | N-(5-methyl-1H-pyrazol-3-yl)-6-(4-m...)Show SMILES CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(C=Cc2ccccc2)n1 |w:19.20| Show InChI InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
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Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant human GST-tagged RET expressed in baculovirus expression system |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50277584
![PNG](/data/jpeg/tenK5027/BindingDB_50277584.png) (CHEMBL482968 | N-(5-methyl-1H-pyrazol-3-yl)-6-(4-m...)Show SMILES CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(C=Cc2ccccc2)n1 |w:19.20| Show InChI InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant human His-tagged VEGFR 2 expressed in baculovirus expression system |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha
(Homo sapiens (Human)) | BDBM50277584
![PNG](/data/jpeg/tenK5027/BindingDB_50277584.png) (CHEMBL482968 | N-(5-methyl-1H-pyrazol-3-yl)-6-(4-m...)Show SMILES CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(C=Cc2ccccc2)n1 |w:19.20| Show InChI InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26) | PDB
KEGG
UniProtKB/SwissProt
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| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant human GST-tagged PDGFR alpha (550 to 1089 residues) expressed in baculovirus expression system |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50277584
![PNG](/data/jpeg/tenK5027/BindingDB_50277584.png) (CHEMBL482968 | N-(5-methyl-1H-pyrazol-3-yl)-6-(4-m...)Show SMILES CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(C=Cc2ccccc2)n1 |w:19.20| Show InChI InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26) | PDB MMDB
KEGG
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Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant human full length His-tagged Src expressed in baculovirus expression system |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50177716
![PNG](/data/jpeg/tenK5017/BindingDB_50177716.png) (CHEMBL3813873 | US11679110, Compound Pexidartinib ...)Show SMILES FC(F)(F)c1ccc(CNc2ccc(Cc3c[nH]c4ncc(Cl)cc34)cn2)cn1 Show InChI InChI=1S/C20H15ClF3N5/c21-15-6-16-14(10-28-19(16)29-11-15)5-12-2-4-18(26-7-12)27-9-13-1-3-17(25-8-13)20(22,23)24/h1-4,6-8,10-11H,5,9H2,(H,26,27)(H,28,29) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant FLT3 ITD mutant (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50177716
![PNG](/data/jpeg/tenK5017/BindingDB_50177716.png) (CHEMBL3813873 | US11679110, Compound Pexidartinib ...)Show SMILES FC(F)(F)c1ccc(CNc2ccc(Cc3c[nH]c4ncc(Cl)cc34)cn2)cn1 Show InChI InChI=1S/C20H15ClF3N5/c21-15-6-16-14(10-28-19(16)29-11-15)5-12-2-4-18(26-7-12)27-9-13-1-3-17(25-8-13)20(22,23)24/h1-4,6-8,10-11H,5,9H2,(H,26,27)(H,28,29) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant FMS (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | ![3D 3D](/images/Docked_3d.png) 3D Structure (crystal) |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50277584
![PNG](/data/jpeg/tenK5027/BindingDB_50277584.png) (CHEMBL482968 | N-(5-methyl-1H-pyrazol-3-yl)-6-(4-m...)Show SMILES CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(C=Cc2ccccc2)n1 |w:19.20| Show InChI InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant full length His-tagged human aurora A using peptide substrate in presence of ATP at its Km concentration by Z-lyte kinase a... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50177716
![PNG](/data/jpeg/tenK5017/BindingDB_50177716.png) (CHEMBL3813873 | US11679110, Compound Pexidartinib ...)Show SMILES FC(F)(F)c1ccc(CNc2ccc(Cc3c[nH]c4ncc(Cl)cc34)cn2)cn1 Show InChI InChI=1S/C20H15ClF3N5/c21-15-6-16-14(10-28-19(16)29-11-15)5-12-2-4-18(26-7-12)27-9-13-1-3-17(25-8-13)20(22,23)24/h1-4,6-8,10-11H,5,9H2,(H,26,27)(H,28,29) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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| n/a | n/a | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FL3 ITD mutant in human MV4-11 cells |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50177716
![PNG](/data/jpeg/tenK5017/BindingDB_50177716.png) (CHEMBL3813873 | US11679110, Compound Pexidartinib ...)Show SMILES FC(F)(F)c1ccc(CNc2ccc(Cc3c[nH]c4ncc(Cl)cc34)cn2)cn1 Show InChI InChI=1S/C20H15ClF3N5/c21-15-6-16-14(10-28-19(16)29-11-15)5-12-2-4-18(26-7-12)27-9-13-1-3-17(25-8-13)20(22,23)24/h1-4,6-8,10-11H,5,9H2,(H,26,27)(H,28,29) | PDB
UniProtKB/SwissProt
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Similars
| Article PubMed
| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of recombinant c-kit (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50326053
![PNG](/data/jpeg/tenK5032/BindingDB_50326053.png) (CHEMBL608533 | PKC-412)Show SMILES CO[C@@H]1[C@@H](C[C@H]2O[C@]1(C)n1c3ccccc3c3c4CNC(=O)c4c4c5ccccc5n2c4c13)N(C)C(=O)c1ccccc1 |r| Show InChI InChI=1S/C35H30N4O4/c1-35-32(42-3)25(37(2)34(41)19-11-5-4-6-12-19)17-26(43-35)38-23-15-9-7-13-20(23)28-29-22(18-36-33(29)40)27-21-14-8-10-16-24(21)39(35)31(27)30(28)38/h4-16,25-26,32H,17-18H2,1-3H3,(H,36,40)/t25-,26-,32-,35+/m1/s1 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389615
![PNG](/data/jpeg/tenK38/BindingDB_389615.png) (N'-(6-chloro-2-{(E)-2-[4- (methylsulfonyl)phenyl]v...)Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(cc2)S(C)(=O)=O)nc2ccc(Cl)cc12 Show InChI InChI=1S/C21H23ClN4O2S/c1-26(2)13-12-23-21-18-14-16(22)7-10-19(18)24-20(25-21)11-6-15-4-8-17(9-5-15)29(3,27)28/h4-11,14H,12-13H2,1-3H3,(H,23,24,25)/b11-6+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50300690
![PNG](/data/jpeg/tenK5030/BindingDB_50300690.png) (1-(5-Tert-Butyl-1,2-Oxazol-3-Yl)-3-(4-{7-[2-(Morph...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(cc2)-c2cn3c(n2)sc2cc(OCCN4CCOCC4)ccc32)no1 Show InChI InChI=1S/C29H32N6O4S/c1-29(2,3)25-17-26(33-39-25)32-27(36)30-20-6-4-19(5-7-20)22-18-35-23-9-8-21(16-24(23)40-28(35)31-22)38-15-12-34-10-13-37-14-11-34/h4-9,16-18H,10-15H2,1-3H3,(H2,30,32,33,36) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM4814
![PNG](/data/jpeg/tenK0/BindingDB_4814.png) (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
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Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y mutant (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM4814
![PNG](/data/jpeg/tenK0/BindingDB_4814.png) (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
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Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) phosphorylation measured after 2 hrs by Western blot analysis |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389616
![PNG](/data/jpeg/tenK38/BindingDB_389616.png) (N'-(6-chloro-2-{(E)-2-[4- (methylsulfonyl)phenyl]v...)Show SMILES CCN(CC)CCNc1nc(\C=C\c2ccc(cc2)S(C)(=O)=O)nc2ccc(Cl)cc12 Show InChI InChI=1S/C23H27ClN4O2S/c1-4-28(5-2)15-14-25-23-20-16-18(24)9-12-21(20)26-22(27-23)13-8-17-6-10-19(11-7-17)31(3,29)30/h6-13,16H,4-5,14-15H2,1-3H3,(H,25,26,27)/b13-8+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389608
![PNG](/data/jpeg/tenK38/BindingDB_389608.png) (N'-{6-chloro-2-[(E)-2-(4- isopropylphenyl)vinyl]qu...)Show SMILES CC(C)c1ccc(\C=C\c2nc(NCCN(C)C)c3cc(Cl)ccc3n2)cc1 Show InChI InChI=1S/C23H27ClN4/c1-16(2)18-8-5-17(6-9-18)7-12-22-26-21-11-10-19(24)15-20(21)23(27-22)25-13-14-28(3)4/h5-12,15-16H,13-14H2,1-4H3,(H,25,26,27)/b12-7+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 80 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389602
![PNG](/data/jpeg/tenK38/BindingDB_389602.png) (N'-(6-chloro-2-{(E)-2-[4- (methylthio)phenyl]vinyl...)Show SMILES CSc1ccc(\C=C\c2nc(NCCN(C)C)c3cc(Cl)ccc3n2)cc1 Show InChI InChI=1S/C21H23ClN4S/c1-26(2)13-12-23-21-18-14-16(22)7-10-19(18)24-20(25-21)11-6-15-4-8-17(27-3)9-5-15/h4-11,14H,12-13H2,1-3H3,(H,23,24,25)/b11-6+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389591
![PNG](/data/jpeg/tenK38/BindingDB_389591.png) (N'-{2-[(E)-2-(4- isopropylphenyl)vinyl]quinazolin-...)Show SMILES CC(C)c1ccc(\C=C\c2nc(NCCN(C)C)c3ccccc3n2)cc1 Show InChI InChI=1S/C23H28N4/c1-17(2)19-12-9-18(10-13-19)11-14-22-25-21-8-6-5-7-20(21)23(26-22)24-15-16-27(3)4/h5-14,17H,15-16H2,1-4H3,(H,24,25,26)/b14-11+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389604
![PNG](/data/jpeg/tenK38/BindingDB_389604.png) (N,N-dimethyl-N'-(2-{(E)-2-[4- (methylsulfonyl)phen...)Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(cc2)S(C)(=O)=O)nc2ccccc12 Show InChI InChI=1S/C21H24N4O2S/c1-25(2)15-14-22-21-18-6-4-5-7-19(18)23-20(24-21)13-10-16-8-11-17(12-9-16)28(3,26)27/h4-13H,14-15H2,1-3H3,(H,22,23,24)/b13-10+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM13535
![PNG](/data/jpeg/tenK1/BindingDB_13535.png) (4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin...)Show SMILES COc1cc2c(ncnc2cc1OCCCN1CCCCC1)N1CCN(CC1)C(=O)Nc1ccc(OC(C)C)cc1 Show InChI InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of c-Kit (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50300690
![PNG](/data/jpeg/tenK5030/BindingDB_50300690.png) (1-(5-Tert-Butyl-1,2-Oxazol-3-Yl)-3-(4-{7-[2-(Morph...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(cc2)-c2cn3c(n2)sc2cc(OCCN4CCOCC4)ccc32)no1 Show InChI InChI=1S/C29H32N6O4S/c1-29(2,3)25-17-26(33-39-25)32-27(36)30-20-6-4-19(5-7-20)22-18-35-23-9-8-21(16-24(23)40-28(35)31-22)38-15-12-34-10-13-37-14-11-34/h4-9,16-18H,10-15H2,1-3H3,(H2,30,32,33,36) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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CHEMBL MCE PC cid PC sid PDB UniChem
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| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of wildtype FLT3 (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM13535
![PNG](/data/jpeg/tenK1/BindingDB_13535.png) (4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin...)Show SMILES COc1cc2c(ncnc2cc1OCCCN1CCCCC1)N1CCN(CC1)C(=O)Nc1ccc(OC(C)C)cc1 Show InChI InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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CHEMBL DrugBank MCE PC cid PC sid UniChem
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| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of PDGFR beta (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Fibroblast growth factor receptor 1/2/3/4
(Homo sapiens (Human)) | BDBM13535
![PNG](/data/jpeg/tenK1/BindingDB_13535.png) (4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin...)Show SMILES COc1cc2c(ncnc2cc1OCCCN1CCCCC1)N1CCN(CC1)C(=O)Nc1ccc(OC(C)C)cc1 Show InChI InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FGFR (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389609
![PNG](/data/jpeg/tenK38/BindingDB_389609.png) (N'-{6-chloro-2-[(E)-2-(4- isopropylphenyl)vinyl]qu...)Show SMILES CCN(CC)CCNc1nc(\C=C\c2ccc(cc2)C(C)C)nc2ccc(Cl)cc12 Show InChI InChI=1S/C25H31ClN4/c1-5-30(6-2)16-15-27-25-22-17-21(26)12-13-23(22)28-24(29-25)14-9-19-7-10-20(11-8-19)18(3)4/h7-14,17-18H,5-6,15-16H2,1-4H3,(H,27,28,29)/b14-9+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389611
![PNG](/data/jpeg/tenK38/BindingDB_389611.png) (N'-{6-fluoro-2-[(E)-2-(4- isopropylphenyl)vinyl]qu...)Show SMILES CC(C)c1ccc(\C=C\c2nc(NCCN(C)C)c3cc(F)ccc3n2)cc1 Show InChI InChI=1S/C23H27FN4/c1-16(2)18-8-5-17(6-9-18)7-12-22-26-21-11-10-19(24)15-20(21)23(27-22)25-13-14-28(3)4/h5-12,15-16H,13-14H2,1-4H3,(H,25,26,27)/b12-7+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389591
![PNG](/data/jpeg/tenK38/BindingDB_389591.png) (N'-{2-[(E)-2-(4- isopropylphenyl)vinyl]quinazolin-...)Show SMILES CC(C)c1ccc(\C=C\c2nc(NCCN(C)C)c3ccccc3n2)cc1 Show InChI InChI=1S/C23H28N4/c1-17(2)19-12-9-18(10-13-19)11-14-22-25-21-8-6-5-7-20(21)23(26-22)24-15-16-27(3)4/h5-14,17H,15-16H2,1-4H3,(H,24,25,26)/b14-11+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389613
![PNG](/data/jpeg/tenK38/BindingDB_389613.png) (N'-(6-chloro-2-{(E)-2-[4- (methylsulfonyl)phenyl]v...)Show SMILES CN(C)CCCNc1nc(\C=C\c2ccc(cc2)S(C)(=O)=O)nc2ccc(Cl)cc12 Show InChI InChI=1S/C22H25ClN4O2S/c1-27(2)14-4-13-24-22-19-15-17(23)8-11-20(19)25-21(26-22)12-7-16-5-9-18(10-6-16)30(3,28)29/h5-12,15H,4,13-14H2,1-3H3,(H,24,25,26)/b12-7+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50504565
![PNG](/data/jpeg/tenK5050/BindingDB_50504565.png) (CHEMBL4446825)Show SMILES CCN(CC)CCNc1nc(\C=C\c2ccc(cc2)C(C)C)nc2ccccc12 Show InChI InChI=1S/C25H32N4/c1-5-29(6-2)18-17-26-25-22-9-7-8-10-23(22)27-24(28-25)16-13-20-11-14-21(15-12-20)19(3)4/h7-16,19H,5-6,17-18H2,1-4H3,(H,26,27,28)/b16-13+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM13535
![PNG](/data/jpeg/tenK1/BindingDB_13535.png) (4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin...)Show SMILES COc1cc2c(ncnc2cc1OCCCN1CCCCC1)N1CCN(CC1)C(=O)Nc1ccc(OC(C)C)cc1 Show InChI InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
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CHEMBL DrugBank MCE PC cid PC sid UniChem
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| Article PubMed
| n/a | n/a | 220 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 (unknown origin) |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389612
![PNG](/data/jpeg/tenK38/BindingDB_389612.png) (N,N-diethyl-N'-{6-fluoro-2-[(E)-2-(4- isopropylphe...)Show SMILES CCN(CC)CCNc1nc(\C=C\c2ccc(cc2)C(C)C)nc2ccc(F)cc12 Show InChI InChI=1S/C25H31FN4/c1-5-30(6-2)16-15-27-25-22-17-21(26)12-13-23(22)28-24(29-25)14-9-19-7-10-20(11-8-19)18(3)4/h7-14,17-18H,5-6,15-16H2,1-4H3,(H,27,28,29)/b14-9+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389615
![PNG](/data/jpeg/tenK38/BindingDB_389615.png) (N'-(6-chloro-2-{(E)-2-[4- (methylsulfonyl)phenyl]v...)Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(cc2)S(C)(=O)=O)nc2ccc(Cl)cc12 Show InChI InChI=1S/C21H23ClN4O2S/c1-26(2)13-12-23-21-18-14-16(22)7-10-19(18)24-20(25-21)11-6-15-4-8-17(9-5-15)29(3,27)28/h4-11,14H,12-13H2,1-3H3,(H,23,24,25)/b11-6+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM4814
![PNG](/data/jpeg/tenK0/BindingDB_4814.png) (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 ![](/images/AffyNet_logo.png)
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CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
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| Article PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of wildtype FLT3 (unknown origin) phosphorylation measured after 2 hrs by Western blot analysis |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM13535
![PNG](/data/jpeg/tenK1/BindingDB_13535.png) (4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin...)Show SMILES COc1cc2c(ncnc2cc1OCCCN1CCCCC1)N1CCN(CC1)C(=O)Nc1ccc(OC(C)C)cc1 Show InChI InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| Purchase
CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM13535
![PNG](/data/jpeg/tenK1/BindingDB_13535.png) (4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin...)Show SMILES COc1cc2c(ncnc2cc1OCCCN1CCCCC1)N1CCN(CC1)C(=O)Nc1ccc(OC(C)C)cc1 Show InChI InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| Purchase
CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of wildtype FLT3 (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389604
![PNG](/data/jpeg/tenK38/BindingDB_389604.png) (N,N-dimethyl-N'-(2-{(E)-2-[4- (methylsulfonyl)phen...)Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(cc2)S(C)(=O)=O)nc2ccccc12 Show InChI InChI=1S/C21H24N4O2S/c1-25(2)15-14-22-21-18-6-4-5-7-19(18)23-20(24-21)13-10-16-8-11-17(12-9-16)28(3,26)27/h4-13H,14-15H2,1-3H3,(H,22,23,24)/b13-10+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 330 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389586
![PNG](/data/jpeg/tenK38/BindingDB_389586.png) (N,N-dimethyl-N'-(2-{(E)-2-[4- (methylthio)phenyl]v...)Show InChI InChI=1S/C21H24N4S/c1-25(2)15-14-22-21-18-6-4-5-7-19(18)23-20(24-21)13-10-16-8-11-17(26-3)12-9-16/h4-13H,14-15H2,1-3H3,(H,22,23,24)/b13-10+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 340 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389610
![PNG](/data/jpeg/tenK38/BindingDB_389610.png) (N'-{6-fluoro-2-[(E)-2-(4- isopropylphenyl)vinyl]qu...)Show SMILES CC(C)c1ccc(\C=C\c2nc(NCCCN(C)C)c3cc(F)ccc3n2)cc1 Show InChI InChI=1S/C24H29FN4/c1-17(2)19-9-6-18(7-10-19)8-13-23-27-22-12-11-20(25)16-21(22)24(28-23)26-14-5-15-29(3)4/h6-13,16-17H,5,14-15H2,1-4H3,(H,26,27,28)/b13-8+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 340 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389606
![PNG](/data/jpeg/tenK38/BindingDB_389606.png) (N'-{6-chloro-2-[(E)-2-(4- isopropylphenyl)vinyl]qu...)Show SMILES CC(C)c1ccc(\C=C\c2nc(NCCCN(C)C)c3cc(Cl)ccc3n2)cc1 Show InChI InChI=1S/C24H29ClN4/c1-17(2)19-9-6-18(7-10-19)8-13-23-27-22-12-11-20(25)16-21(22)24(28-23)26-14-5-15-29(3)4/h6-13,16-17H,5,14-15H2,1-4H3,(H,26,27,28)/b13-8+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 410 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389608
![PNG](/data/jpeg/tenK38/BindingDB_389608.png) (N'-{6-chloro-2-[(E)-2-(4- isopropylphenyl)vinyl]qu...)Show SMILES CC(C)c1ccc(\C=C\c2nc(NCCN(C)C)c3cc(Cl)ccc3n2)cc1 Show InChI InChI=1S/C23H27ClN4/c1-16(2)18-8-5-17(6-9-18)7-12-22-26-21-11-10-19(24)15-20(21)23(27-22)25-13-14-28(3)4/h5-12,15-16H,13-14H2,1-4H3,(H,25,26,27)/b12-7+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 410 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389616
![PNG](/data/jpeg/tenK38/BindingDB_389616.png) (N'-(6-chloro-2-{(E)-2-[4- (methylsulfonyl)phenyl]v...)Show SMILES CCN(CC)CCNc1nc(\C=C\c2ccc(cc2)S(C)(=O)=O)nc2ccc(Cl)cc12 Show InChI InChI=1S/C23H27ClN4O2S/c1-4-28(5-2)15-14-25-23-20-16-18(24)9-12-21(20)26-22(27-23)13-8-17-6-10-19(11-7-17)31(3,29)30/h6-13,16H,4-5,14-15H2,1-3H3,(H,25,26,27)/b13-8+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 440 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389586
![PNG](/data/jpeg/tenK38/BindingDB_389586.png) (N,N-dimethyl-N'-(2-{(E)-2-[4- (methylthio)phenyl]v...)Show InChI InChI=1S/C21H24N4S/c1-25(2)15-14-22-21-18-6-4-5-7-19(18)23-20(24-21)13-10-16-8-11-17(26-3)12-9-16/h4-13H,14-15H2,1-3H3,(H,22,23,24)/b13-10+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 480 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389574
![PNG](/data/jpeg/tenK38/BindingDB_389574.png) (N'-{2-[(E)-2-(4- fluorophenyl)vinyl]quinazolin-4-y...)Show InChI InChI=1S/C20H21FN4/c1-25(2)14-13-22-20-17-5-3-4-6-18(17)23-19(24-20)12-9-15-7-10-16(21)11-8-15/h3-12H,13-14H2,1-2H3,(H,22,23,24)/b12-9+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 560 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 D835Y (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IMAP-FP... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389602
![PNG](/data/jpeg/tenK38/BindingDB_389602.png) (N'-(6-chloro-2-{(E)-2-[4- (methylthio)phenyl]vinyl...)Show SMILES CSc1ccc(\C=C\c2nc(NCCN(C)C)c3cc(Cl)ccc3n2)cc1 Show InChI InChI=1S/C21H23ClN4S/c1-26(2)13-12-23-21-18-14-16(22)7-10-19(18)24-20(25-21)11-6-15-4-8-17(27-3)9-5-15/h4-11,14H,12-13H2,1-3H3,(H,23,24,25)/b11-6+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 620 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM389573
![PNG](/data/jpeg/tenK38/BindingDB_389573.png) (N'-{6-bromo-2-[(E)-2-(3,4- difluorophenyl)vinyl]qu...)Show SMILES CN(C)CCNc1nc(\C=C\c2ccc(F)c(F)c2)nc2ccc(Br)cc12 Show InChI InChI=1S/C20H19BrF2N4/c1-27(2)10-9-24-20-15-12-14(21)5-7-18(15)25-19(26-20)8-4-13-3-6-16(22)17(23)11-13/h3-8,11-12H,9-10H2,1-2H3,(H,24,25,26)/b8-4+ | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 740 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd
Curated by ChEMBL
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... |
Eur J Med Chem 184: (2019)
Article DOI: 10.1016/j.ejmech.2019.111710 BindingDB Entry DOI: 10.7270/Q27947ZV |
More data for this Ligand-Target Pair | |