Found 3 hits for monomerid = 50009224 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 2
(Homo sapiens (Human)) | BDBM50009224
(CHEMBL3233188)Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(=O)(=O)C(C)(C)C)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r| Show InChI InChI=1S/C27H40F3N3O4S/c1-17(2)32(6)21-10-11-23(19(15-21)16-38(36,37)26(3,4)5)33-13-12-22(25(33)35)31-24(34)18-8-7-9-20(14-18)27(28,29)30/h7-9,14,17,19,21-23H,10-13,15-16H2,1-6H3,(H,31,34)/t19-,21+,22-,23-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.960 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Company
Curated by ChEMBL
| Assay Description Displacement of [125I]-labeled human MCP1 from CCR2 in human PBMC |
Bioorg Med Chem Lett 24: 1843-5 (2014)
Article DOI: 10.1016/j.bmcl.2014.02.013 BindingDB Entry DOI: 10.7270/Q2FQ9Z4P |
More data for this Ligand-Target Pair | |
C-C chemokine receptor type 2
(Homo sapiens (Human)) | BDBM50009224
(CHEMBL3233188)Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(=O)(=O)C(C)(C)C)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r| Show InChI InChI=1S/C27H40F3N3O4S/c1-17(2)32(6)21-10-11-23(19(15-21)16-38(36,37)26(3,4)5)33-13-12-22(25(33)35)31-24(34)18-8-7-9-20(14-18)27(28,29)30/h7-9,14,17,19,21-23H,10-13,15-16H2,1-6H3,(H,31,34)/t19-,21+,22-,23-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.200 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Company
Curated by ChEMBL
| Assay Description Antagonist activity at CCR2 in human monocytes assessed as reduction of chemotaxis in presence of 0.1 M BSA |
Bioorg Med Chem Lett 24: 1843-5 (2014)
Article DOI: 10.1016/j.bmcl.2014.02.013 BindingDB Entry DOI: 10.7270/Q2FQ9Z4P |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50009224
(CHEMBL3233188)Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(=O)(=O)C(C)(C)C)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r| Show InChI InChI=1S/C27H40F3N3O4S/c1-17(2)32(6)21-10-11-23(19(15-21)16-38(36,37)26(3,4)5)33-13-12-22(25(33)35)31-24(34)18-8-7-9-20(14-18)27(28,29)30/h7-9,14,17,19,21-23H,10-13,15-16H2,1-6H3,(H,31,34)/t19-,21+,22-,23-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Company
Curated by ChEMBL
| Assay Description Inhibition of human ERG by FLIPR assay |
Bioorg Med Chem Lett 24: 1843-5 (2014)
Article DOI: 10.1016/j.bmcl.2014.02.013 BindingDB Entry DOI: 10.7270/Q2FQ9Z4P |
More data for this Ligand-Target Pair | |