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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cyclin-dependent kinase 5 activator 1 (Homo sapiens (Human)) | BDBM50133557 (1-[2-(2,6-Dichloro-benzyl)-thiazol-4-yl]-3-morphol...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | PubMed | 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmacia Corporation Curated by ChEMBL | Assay Description Inhibition of Tau Protein Kinase II (TPK II) | Bioorg Med Chem Lett 13: 3491-5 (2003) BindingDB Entry DOI: 10.7270/Q2XG9QHN | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cyclin-dependent kinase 5 activator 1 (Homo sapiens (Human)) | BDBM50133557 (1-[2-(2,6-Dichloro-benzyl)-thiazol-4-yl]-3-morphol...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmacia Corporation Curated by ChEMBL | Assay Description Ability to inhibit Cyclin-dependent kinase 5-p35. | Bioorg Med Chem Lett 13: 3491-5 (2003) BindingDB Entry DOI: 10.7270/Q2XG9QHN | |||||||||||
More data for this Ligand-Target Pair |