BDBM50185084 2-(3,4-dimethoxybenzamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide::2-(3,4-dimethoxybenzamido)-5-methyl-4-propylthiophene-3-carboxamide::CHEMBL210833
SMILES: COc1ccc(cc1OC)C(=O)Nc1sc2CCCCc2c1C(N)=O
InChI Key: InChIKey=FSPQCTGGIANIJZ-UHFFFAOYSA-N
Data: 2 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/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)) | BDBM50185084 (2-(3,4-dimethoxybenzamido)-4,5,6,7-tetrahydrobenzo...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 2.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Duquesne University Curated by ChEMBL | Assay Description Inhibition of Flt3 activity in human MV 3:11 cells by phosphotyrosine cell-based ELISA | J Med Chem 53: 1563-78 (2010) Article DOI: 10.1021/jm9011142 BindingDB Entry DOI: 10.7270/Q2SX6F6D | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM50185084 (2-(3,4-dimethoxybenzamido)-4,5,6,7-tetrahydrobenzo...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 42 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL | Assay Description Inhibition of FLT3 | Bioorg Med Chem Lett 16: 3282-6 (2006) Article DOI: 10.1016/j.bmcl.2006.03.032 BindingDB Entry DOI: 10.7270/Q2R49QCV | |||||||||||
More data for this Ligand-Target Pair |