BDBM50037397 6-Amino-2-(3-amino-phenyl)-7-hydroxy-chromen-4-one::CHEMBL115102
SMILES: Nc1cccc(c1)-c1cc(=O)c2cc(N)c(O)cc2o1
InChI Key: InChIKey=PQNPYVSRVAECJJ-UHFFFAOYSA-N
Data: 3 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 |
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Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human)) | BDBM50037397![]() (6-Amino-2-(3-amino-phenyl)-7-hydroxy-chromen-4-one...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Purdue University Curated by ChEMBL | Assay Description Inhibition of in vitro protein-tyrosine kinase activity of p60v-src enzyme in presence of 5 uM ATP. | J Med Chem 37: 3353-62 (1994) BindingDB Entry DOI: 10.7270/Q2D21WNP | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Epidermal growth factor receptor (Homo sapiens (Human)) | BDBM50037397![]() (6-Amino-2-(3-amino-phenyl)-7-hydroxy-chromen-4-one...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Purdue University Curated by ChEMBL | Assay Description Inhibition of in vitro activity of EGFr enzyme from A431 cells in presence of 5 uM ATP | J Med Chem 37: 3353-62 (1994) BindingDB Entry DOI: 10.7270/Q2D21WNP | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Tyrosine-protein kinase Lck (Homo sapiens (Human)) | BDBM50037397![]() (6-Amino-2-(3-amino-phenyl)-7-hydroxy-chromen-4-one...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 5.02E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Purdue University Curated by ChEMBL | Assay Description In vitro inhibition of protein-tyrosine activity of p56lck enzyme in presence of 50 uM ATP | J Med Chem 37: 3353-62 (1994) BindingDB Entry DOI: 10.7270/Q2D21WNP | |||||||||||
More data for this Ligand-Target Pair |