Found 2 hits in this display 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
(Homo sapiens (Human)) | BDBM50132275
(1-{6-[4-Amino-5-(3-bromo-phenyl)-pyrido[2,3-d]pyri...)Show SMILES [#7]-c1ncnc2nc(cc(-c3cccc(Br)c3)c12)-c1ccc(nn1)-[#7]-1-[#6]-[#6]\[#6](-[#6]-[#6]-1)=[#7]\[#8]-[#6]-1-[#6]-[#6]-[#8]-[#6]-[#6]-1 Show InChI InChI=1S/C27H27BrN8O2/c28-18-3-1-2-17(14-18)21-15-23(32-27-25(21)26(29)30-16-31-27)22-4-5-24(34-33-22)36-10-6-19(7-11-36)35-38-20-8-12-37-13-9-20/h1-5,14-16,20H,6-13H2,(H2,29,30,31,32) | 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 | 7.10 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibitory concentration against adenosine kinase was determined |
Bioorg Med Chem Lett 13: 3041-4 (2003)
BindingDB Entry DOI: 10.7270/Q2JH3KJ3 |
More data for this Ligand-Target Pair | |
Adenosine kinase
(Homo sapiens (Human)) | BDBM50132275
(1-{6-[4-Amino-5-(3-bromo-phenyl)-pyrido[2,3-d]pyri...)Show SMILES [#7]-c1ncnc2nc(cc(-c3cccc(Br)c3)c12)-c1ccc(nn1)-[#7]-1-[#6]-[#6]\[#6](-[#6]-[#6]-1)=[#7]\[#8]-[#6]-1-[#6]-[#6]-[#8]-[#6]-[#6]-1 Show InChI InChI=1S/C27H27BrN8O2/c28-18-3-1-2-17(14-18)21-15-23(32-27-25(21)26(29)30-16-31-27)22-4-5-24(34-33-22)36-10-6-19(7-11-36)35-38-20-8-12-37-13-9-20/h1-5,14-16,20H,6-13H2,(H2,29,30,31,32) | 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 | 52 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibitory concentration against adenosine kinase was determined |
Bioorg Med Chem Lett 13: 3041-4 (2003)
BindingDB Entry DOI: 10.7270/Q2JH3KJ3 |
More data for this Ligand-Target Pair | |