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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'C-C chemokine receptor type 2' and Ligand = 'BDBM50359117'   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
C-C chemokine receptor type 2


(Homo sapiens (Human))
BDBM50359117
PNG
(CHEMBL1922799)
Show SMILES COc1ccc(cn1)C1CCC(CC1)NC(C1CCN(CC1)C(=O)\C=C\c1cc(F)c(F)c(F)c1)C(N)=O |(28.92,-24.66,;30.25,-23.9,;30.26,-22.36,;28.92,-21.58,;28.93,-20.04,;30.27,-19.28,;31.6,-20.05,;31.6,-21.58,;30.28,-17.74,;28.95,-16.96,;28.95,-15.43,;30.29,-14.67,;31.62,-15.43,;31.62,-16.97,;30.29,-13.13,;31.63,-12.36,;32.96,-13.14,;32.95,-14.68,;34.27,-15.45,;35.61,-14.69,;35.62,-13.15,;34.29,-12.37,;36.94,-15.47,;36.93,-17.01,;38.28,-14.71,;39.61,-15.49,;40.94,-14.73,;40.95,-13.2,;42.28,-12.43,;42.28,-10.89,;43.62,-13.21,;44.95,-12.45,;43.6,-14.75,;44.93,-15.53,;42.27,-15.51,;31.63,-10.82,;30.3,-10.05,;32.97,-10.06,)|
Show InChI InChI=1S/C28H33F3N4O3/c1-38-24-8-5-20(16-33-24)18-3-6-21(7-4-18)34-27(28(32)37)19-10-12-35(13-11-19)25(36)9-2-17-14-22(29)26(31)23(30)15-17/h2,5,8-9,14-16,18-19,21,27,34H,3-4,6-7,10-13H2,1H3,(H2,32,37)/b9-2+
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
US Patent
n/an/a 635n/an/an/an/an/a37



Janssen Pharmaceutica NV

US Patent


Assay Description
MCP-1 Receptor Binding Assay in THP-1 Cells Human monocytic cell line THP-1 cells were obtained from American Type Culture Collection (Manassas, Va.,...


US Patent US8921559 (2014)


BindingDB Entry DOI: 10.7270/Q270804M
More data for this
Ligand-Target Pair
C-C chemokine receptor type 2


(Homo sapiens (Human))
BDBM50359117
PNG
(CHEMBL1922799)
Show SMILES COc1ccc(cn1)C1CCC(CC1)NC(C1CCN(CC1)C(=O)\C=C\c1cc(F)c(F)c(F)c1)C(N)=O |(28.92,-24.66,;30.25,-23.9,;30.26,-22.36,;28.92,-21.58,;28.93,-20.04,;30.27,-19.28,;31.6,-20.05,;31.6,-21.58,;30.28,-17.74,;28.95,-16.96,;28.95,-15.43,;30.29,-14.67,;31.62,-15.43,;31.62,-16.97,;30.29,-13.13,;31.63,-12.36,;32.96,-13.14,;32.95,-14.68,;34.27,-15.45,;35.61,-14.69,;35.62,-13.15,;34.29,-12.37,;36.94,-15.47,;36.93,-17.01,;38.28,-14.71,;39.61,-15.49,;40.94,-14.73,;40.95,-13.2,;42.28,-12.43,;42.28,-10.89,;43.62,-13.21,;44.95,-12.45,;43.6,-14.75,;44.93,-15.53,;42.27,-15.51,;31.63,-10.82,;30.3,-10.05,;32.97,-10.06,)|
Show InChI InChI=1S/C28H33F3N4O3/c1-38-24-8-5-20(16-33-24)18-3-6-21(7-4-18)34-27(28(32)37)19-10-12-35(13-11-19)25(36)9-2-17-14-22(29)26(31)23(30)15-17/h2,5,8-9,14-16,18-19,21,27,34H,3-4,6-7,10-13H2,1H3,(H2,32,37)/b9-2+
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 640n/an/an/an/an/an/a



Johnson& Johnson Pharmaceutical Research and Development

Curated by ChEMBL


Assay Description
Antagonist activity at human CCR2


Bioorg Med Chem Lett 21: 7496-501 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.113
BindingDB Entry DOI: 10.7270/Q22J6C9M
More data for this
Ligand-Target Pair