Found 3 hits for monomerid = 50372858 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 |
C-C chemokine receptor type 3
(Homo sapiens (Human)) | BDBM50372858
(CHEMBL258323)Show SMILES C[C@@H](CCN1CCC[C@@H](Cc2ccc(F)cc2)C1)NC(=O)Nc1cccc(c1)-c1nnnn1C Show InChI InChI=1S/C25H32FN7O/c1-18(12-14-33-13-4-5-20(17-33)15-19-8-10-22(26)11-9-19)27-25(34)28-23-7-3-6-21(16-23)24-29-30-31-32(24)2/h3,6-11,16,18,20H,4-5,12-15,17H2,1-2H3,(H2,27,28,34)/t18-,20-/m0/s1 | Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Company
Curated by ChEMBL
| Assay Description Displacement of [125I]eotaxin from human CCR3 receptor expressed in CHO cells |
Bioorg Med Chem Lett 18: 576-85 (2008)
Article DOI: 10.1016/j.bmcl.2007.11.067 BindingDB Entry DOI: 10.7270/Q2057GS3 |
More data for this Ligand-Target Pair | |
Cytochrome P450 2D6
(Homo sapiens (Human)) | BDBM50372858
(CHEMBL258323)Show SMILES C[C@@H](CCN1CCC[C@@H](Cc2ccc(F)cc2)C1)NC(=O)Nc1cccc(c1)-c1nnnn1C Show InChI InChI=1S/C25H32FN7O/c1-18(12-14-33-13-4-5-20(17-33)15-19-8-10-22(26)11-9-19)27-25(34)28-23-7-3-6-21(16-23)24-29-30-31-32(24)2/h3,6-11,16,18,20H,4-5,12-15,17H2,1-2H3,(H2,27,28,34)/t18-,20-/m0/s1 | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Company
Curated by ChEMBL
| Assay Description Inhibition of CYP2D6 |
Bioorg Med Chem Lett 18: 576-85 (2008)
Article DOI: 10.1016/j.bmcl.2007.11.067 BindingDB Entry DOI: 10.7270/Q2057GS3 |
More data for this Ligand-Target Pair | |
C-C chemokine receptor type 3
(Homo sapiens (Human)) | BDBM50372858
(CHEMBL258323)Show SMILES C[C@@H](CCN1CCC[C@@H](Cc2ccc(F)cc2)C1)NC(=O)Nc1cccc(c1)-c1nnnn1C Show InChI InChI=1S/C25H32FN7O/c1-18(12-14-33-13-4-5-20(17-33)15-19-8-10-22(26)11-9-19)27-25(34)28-23-7-3-6-21(16-23)24-29-30-31-32(24)2/h3,6-11,16,18,20H,4-5,12-15,17H2,1-2H3,(H2,27,28,34)/t18-,20-/m0/s1 | Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Company
Curated by ChEMBL
| Assay Description Antagonist activity at human CCR3 receptor in human eosinophil assessed as inhibition of eotaxin-induced chemotaxis |
Bioorg Med Chem Lett 18: 576-85 (2008)
Article DOI: 10.1016/j.bmcl.2007.11.067 BindingDB Entry DOI: 10.7270/Q2057GS3 |
More data for this Ligand-Target Pair | |