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)) | BDBM476709 (2-((5-chloro-4-(6-methyl-1H-indole-3-yl)pyrimidine...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM546731 ((3-(5-chloro-2-((3-cyclopropyl-5-(((3R, 5S)-3,5-di...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.400 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476709 (2-((5-chloro-4-(6-methyl-1H-indole-3-yl)pyrimidine...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.400 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476704 ( (3-(5-chloro-2-((3-cyclopropyl-5-(((3R,5S)-3,5-di...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.400 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM546731 ((3-(5-chloro-2-((3-cyclopropyl-5-(((3R, 5S)-3,5-di...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476704 ( (3-(5-chloro-2-((3-cyclopropyl-5-(((3R,5S)-3,5-di...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.5 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476700 (5-chloro-N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethyl...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase MCE PC cid PC sid UniChem | US Patent | n/a | n/a | 1.10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476700 (5-chloro-N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethyl...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase MCE PC cid PC sid UniChem | US Patent | n/a | n/a | 1.10 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476702 (N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethylpiperazin...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.20 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476702 (N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethylpiperazin...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476711 ( ((2R,6R)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3-...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476695 (5-chloro-4-(6-chloro-1H-indole-3-yl)-N-(3-cyclopro...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.5 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476711 ( ((2R,6R)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3-...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.5 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476695 (5-chloro-4-(6-chloro-1H-indole-3-yl)-N-(3-cyclopro...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476699 ((R)-5-chloro-N-(3-cyclopropyl-5-((3-methylpiperazi...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476700 (5-chloro-N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethyl...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase MCE PC cid PC sid UniChem | US Patent | n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476699 ((R)-5-chloro-N-(3-cyclopropyl-5-((3-methylpiperazi...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476700 (5-chloro-N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethyl...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase MCE PC cid PC sid UniChem | US Patent | n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476695 (5-chloro-4-(6-chloro-1H-indole-3-yl)-N-(3-cyclopro...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.90 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476695 (5-chloro-4-(6-chloro-1H-indole-3-yl)-N-(3-cyclopro...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.90 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476710 ((R)-5-chloro-N-(3-cyclopropyl-5-((3,3,5-trimethylp...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476711 ( ((2R,6R)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3-...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476711 ( ((2R,6R)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3-...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476710 ((R)-5-chloro-N-(3-cyclopropyl-5-((3,3,5-trimethylp...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476708 (3-(5-chloro-2-((3-cyclopropyl-5-(((3R,5S)-3,5-dime...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476708 (3-(5-chloro-2-((3-cyclopropyl-5-(((3R,5S)-3,5-dime...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.40 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476702 (N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethylpiperazin...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.5 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476702 (N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethylpiperazin...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 2.5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Epidermal growth factor receptor (Homo sapiens (Human)) | BDBM50384888 (CHEMBL2035810) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 3.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Hanmi Research Center Curated by ChEMBL | Assay Description Inhibition of wild-type EGFR preincubated for 10 mins followed by incubation for 30 mins by fluorescence polarization assay | J Med Chem 55: 2846-57 (2012) Article DOI: 10.1021/jm201758g BindingDB Entry DOI: 10.7270/Q23T9J8F | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476697 (2-((2R,6S)-4-(3-((5-chloro-4-(1H-indole-3-yl)pyrim...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 3.60 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476701 (US10870639, Example 10 | US11292786, Example 10 | ...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 3.60 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476701 (US10870639, Example 10 | US11292786, Example 10 | ...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 3.60 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476697 (2-((2R,6S)-4-(3-((5-chloro-4-(1H-indole-3-yl)pyrim...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 3.60 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476706 (3-(5-chloro-2-((3-cyclopropyl-5-(((3R,5S)-3,5-dime...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 3.70 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476706 (3-(5-chloro-2-((3-cyclopropyl-5-(((3R,5S)-3,5-dime...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 3.70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor tyrosine-protein kinase erbB-4 (Homo sapiens (Human)) | BDBM50384888 (CHEMBL2035810) | PDB MMDB UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Hanmi Research Center Curated by ChEMBL | Assay Description Inhibition of HER4 preincubated for 10 mins followed by incubation for 30 mins by fluorescence polarization assay | J Med Chem 55: 2846-57 (2012) Article DOI: 10.1021/jm201758g BindingDB Entry DOI: 10.7270/Q23T9J8F | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476712 ((2R,6S)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3-yl...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 6.90 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476712 ((2R,6S)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3-yl...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 6.90 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476698 (2-((2R,6S)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 7.20 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476698 (2-((2R,6S)-4-(3-((5-chloro-4-(6-methyl-1H-indole-3...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 7.20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mitogen-activated protein kinase kinase kinase 7/TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Homo sapiens (Human)) | BDBM50187114 (CHEMBL3823303) | PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem | Article PubMed | n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Chung-Ang University Curated by ChEMBL | Assay Description Inhibition of N-terminal His-tagged human TAK1 (1 to 303 amino acids)/human TAB1 (437 to 504 amino acids) expressed in baculovirus expression system ... | Eur J Med Chem 163: 660-670 (2019) Article DOI: 10.1016/j.ejmech.2018.12.025 BindingDB Entry DOI: 10.7270/Q2280C2F | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mitogen-activated protein kinase kinase kinase 7/TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Homo sapiens (Human)) | BDBM50187114 (CHEMBL3823303) | PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem | Article PubMed | n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Chung-Ang University Curated by ChEMBL | Assay Description Inhibition of N-terminal His-tagged human TAK1 (1 to 303 amino acids)/human TAB1 (437 to 504 amino acids) expressed in baculovirus expression system ... | Eur J Med Chem 163: 660-670 (2019) Article DOI: 10.1016/j.ejmech.2018.12.025 BindingDB Entry DOI: 10.7270/Q2280C2F | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mitogen-activated protein kinase kinase kinase 7 (Homo sapiens (Human)) | BDBM50187114 (CHEMBL3823303) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem | Article PubMed | n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Chung-Ang University Curated by ChEMBL | Assay Description Inhibition of recombinant FLAG-tagged TAK1 (unknown origin) co-expressed with TAB (unknown origin) in baculovirus using BT-MKK as substrate after 1 h... | Eur J Med Chem 163: 660-670 (2019) Article DOI: 10.1016/j.ejmech.2018.12.025 BindingDB Entry DOI: 10.7270/Q2280C2F | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mitogen-activated protein kinase kinase kinase 7 (Homo sapiens (Human)) | BDBM50187114 (CHEMBL3823303) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem | Article PubMed | n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Chung-Ang University Curated by ChEMBL | Assay Description Inhibition of recombinant FLAG-tagged TAK1 (unknown origin) co-expressed with TAB (unknown origin) in baculovirus using BT-MKK as substrate after 1 h... | Eur J Med Chem 163: 660-670 (2019) Article DOI: 10.1016/j.ejmech.2018.12.025 BindingDB Entry DOI: 10.7270/Q2280C2F | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476696 (2-((2R,6S)-4-(3-((5-chloro-4-(6-fluoro-1H-indole-3...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 8.10 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476696 (2-((2R,6S)-4-(3-((5-chloro-4-(6-fluoro-1H-indole-3...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 8.10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476703 (N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethylpiperazin...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 8.70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured. Th... | Citation and Details BindingDB Entry DOI: 10.7270/Q2VX0KQ4 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Dimer of Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM476703 (N-(3-cyclopropyl-5-(((3R,5S)-3,5-dimethylpiperazin...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 8.70 | n/a | n/a | n/a | n/a | n/a | n/a |
HANMI PHARM. CO.. LTD. US Patent | Assay Description The inhibitory activity of some of the compounds described above against FLT3-ITD, FLT3 wild type (WT), VEGFR2 (KDR), and SYK kinase was measured.The... | US Patent US10870639 (2020) BindingDB Entry DOI: 10.7270/Q20G3P70 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Mitogen-activated protein kinase kinase kinase 7/TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Homo sapiens (Human)) | BDBM50042034 ((5Z)-7-Oxozeaenol | 5Z-7-Oxozeaenol | CHEBI:67559 ...) | PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars | PDB Article PubMed | n/a | n/a | 9 | n/a | n/a | n/a | n/a | n/a | n/a |
Chung-Ang University Curated by ChEMBL | Assay Description Inhibition of full length TAK1/TAB1 (unknown origin) using biotin-MKK6 as substrate by AlphaScreen assay | Eur J Med Chem 163: 660-670 (2019) Article DOI: 10.1016/j.ejmech.2018.12.025 BindingDB Entry DOI: 10.7270/Q2280C2F | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) | ||||||||||||
Mitogen-activated protein kinase kinase kinase 7/TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (Homo sapiens (Human)) | BDBM50042034 ((5Z)-7-Oxozeaenol | 5Z-7-Oxozeaenol | CHEBI:67559 ...) | PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars | PDB Article PubMed | n/a | n/a | 9 | n/a | n/a | n/a | n/a | n/a | n/a |
Chung-Ang University Curated by ChEMBL | Assay Description Inhibition of full length TAK1/TAB1 (unknown origin) using biotin-MKK6 as substrate by AlphaScreen assay | Eur J Med Chem 163: 660-670 (2019) Article DOI: 10.1016/j.ejmech.2018.12.025 BindingDB Entry DOI: 10.7270/Q2280C2F | |||||||||||
More data for this Ligand-Target Pair | 3D Structure (crystal) |
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