Found 39 hits Enz. Inhib. hit(s) with all data for entry = 50013987 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)) | BDBM50571491
(CHEMBL4868092)Show SMILES Cc1c(NC(=O)CCNC2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 0.600 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
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 | 0.700 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 0.800 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
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 | 0.800 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571484
(CHEMBL4851401)Show SMILES Cc1c(NC(=O)CCN2CCCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.30 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
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 | 1.40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 D835Y mutant (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571480
(CHEMBL4862765)Show SMILES Cc1c(NC(=O)CN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571487
(CHEMBL4877838)Show SMILES CN(C)CCC(=O)Nc1c[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571489
(CHEMBL4860305)Show SMILES CCCNCCC(=O)Nc1c[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571490
(CHEMBL4853071)Show SMILES Cc1c(NC(=O)CCNC(C)(C)C)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.90 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 D835Y mutant (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571483
(CHEMBL4866775)Show SMILES CN(C)CC(=O)Nc1c[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571486
(CHEMBL4864382)Show SMILES CCN(CC)CCC(=O)Nc1c[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571479
(CHEMBL4846119)Show SMILES Cc1c(NC(=O)C2CCCCN2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571488
(CHEMBL4862737)Show SMILES CCNCCC(=O)Nc1c[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571478
(CHEMBL4861526)Show SMILES Cc1c(NC(=O)[C@@H]2CCCN2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 |r| | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571482
(CHEMBL4868929)Show SMILES CN1CCN(CC(=O)Nc2c[nH]c(\C=C3/C(=O)Nc4ccc(F)cc34)c2C)CC1 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571481
(CHEMBL4865208)Show SMILES Cc1c(NC(=O)CC2CCCN2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
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 | 2.80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of c-KIT (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571485
(CHEMBL4857231)Show SMILES CN1CCN(CCC(=O)Nc2c[nH]c(\C=C3/C(=O)Nc4ccc(F)cc34)c2C)CC1 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
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 | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of PDGFRbeta (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 ITD mutant (unknown origin) expressed in mouse BaF3 cells assessed as antiproliferative activity incubated for 72 hrs by CCK8 assa... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 ITD/D835V double mutant (unknown origin) expressed in mouse BaF3 cells assessed as antiproliferative activity incubated for 72 hrs... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha
(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
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank Article PubMed
| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of PDGFRalpha (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of TEL-FLT3 D835V mutant (unknown origin) expressed in mouse BaF3 cells assessed as antiproliferative activity incubated for 72 hrs by CCK... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 37 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 ITD/D835Y double mutant (unknown origin) expressed in mouse BaF3 cells assessed as antiproliferative activity incubated for 72 hrs... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 37 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of TEL-FLT3 D835Y mutant (unknown origin) expressed in mouse BaF3 cells assessed as antiproliferative activity incubated for 72 hrs by CCK... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 42 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of PDGFRbeta (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of FLT3 ITD/F691L double mutant (unknown origin) expressed in mouse BaF3 cells assessed as antiproliferative activity incubated for 72 hrs... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of TEL-FLT3 D835H mutant (unknown origin) expressed in mouse BaF3 cells assessed as antiproliferative activity incubated for 72 hrs by CCK... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
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 | 76 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of VEGFR2 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Platelet-derived growth factor receptor alpha
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of PDGFRalpha (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(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 | 83 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of CSF1R (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(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
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 | 91 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of VEGFR1 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of VEGFR1 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 137 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of VEGFR2 (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 716 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of CSF1R (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50571477
(CHEMBL4869059)Show SMILES Cc1c(NC(=O)CCN2CCCC2)c[nH]c1\C=C1/C(=O)Nc2ccc(F)cc12 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description Inhibition of c-KIT (unknown origin) incubated for 30 mins in presence of ATP by mobility shift assay |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c02247 BindingDB Entry DOI: 10.7270/Q29G5RKV |
More data for this Ligand-Target Pair | |