BDBM50100583 7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-pyrido[2,3-d]pyrimidin-4-ylamine::CHEMBL302938
SMILES: COc1ccc(cc1)-c1cc2c(N)ncnc2nc1-c1ccc(cc1)N(C)C
InChI Key: InChIKey=ZADGRKLNRFXWQT-UHFFFAOYSA-N
Data: 4 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Adenosine kinase (Rattus norvegicus (rat)) | BDBM50100583 (7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 91.7 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories Curated by ChEMBL | Assay Description In vitro inhibition of Adenosine kinase (AK) | J Med Chem 44: 2133-8 (2001) BindingDB Entry DOI: 10.7270/Q25D8R47 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Adenosine kinase (Homo sapiens (Human)) | BDBM50100583 (7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 92 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories Curated by ChEMBL | Assay Description Inhibitory concentration against Adenosine Kinase (enzyme) | Bioorg Med Chem Lett 15: 2803-7 (2005) Article DOI: 10.1016/j.bmcl.2005.03.098 BindingDB Entry DOI: 10.7270/Q2G160CH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Adenosine kinase (Homo sapiens (Human)) | BDBM50100583 (7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 567 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories Curated by ChEMBL | Assay Description Inhibitory concentration against Adenosine Kinase (intact cells) | Bioorg Med Chem Lett 15: 2803-7 (2005) Article DOI: 10.1016/j.bmcl.2005.03.098 BindingDB Entry DOI: 10.7270/Q2G160CH | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Adenosine kinase (Homo sapiens (Human)) | BDBM50100583 (7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 567 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories Curated by ChEMBL | Assay Description Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells. | J Med Chem 44: 2133-8 (2001) BindingDB Entry DOI: 10.7270/Q25D8R47 | |||||||||||
More data for this Ligand-Target Pair |