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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Adenosine kinase (Rattus norvegicus (rat)) | BDBM50100581 (7-(4-Methoxy-phenyl)-pteridin-4-ylamine | CHEMBL67...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 2.00E+3 | 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)) | BDBM50100581 (7-(4-Methoxy-phenyl)-pteridin-4-ylamine | CHEMBL67...) | 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 | >1.00E+4 | 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 |