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TargetC-C chemokine receptor type 2
LigandBDBM141934
Substrate/Competitorn/a
Meas. Tech.Binding Assay
Temperature310.15±n/a K
IC50 230±n/a nM
Commentsextracted
Citation Lanter, JCMarkotan, TPSubasinghe, NSui, ZZhang, X 4-substituted-cyclohexylamino-4-piperidinyl-acetamide antagonists of CCR2 US Patent US8921559 Publication Date 12/30/2014
More Info.:Get all data from this article,  Assay Method
 
C-C chemokine receptor type 2
Name:C-C chemokine receptor type 2
Synonyms:C-C chemokine receptor type 2 (CCR2) | CCR2 | CCR2_HUMAN | CMKBR2 | Chemoattractant Cytokine Receptor 2 (CCR2) | Chemokine Receptor Type 2b (CCR2b) | Monocyte chemotactic protein-1 (MCP-1)
Type:Enzyme
Mol. Mass.:41932.32
Organism:Homo sapiens (Human)
Description:P41597
Residue:374
Sequence:
MLSTSRSRFIRNTNESGEEVTTFFDYDYGAPCHKFDVKQIGAQLLPPLYSLVFIFGFVGN
MLVVLILINCKKLKCLTDIYLLNLAISDLLFLITLPLWAHSAANEWVFGNAMCKLFTGLY
HIGYFGGIFFIILLTIDRYLAIVHAVFALKARTVTFGVVTSVITWLVAVFASVPGIIFTK
CQKEDSVYVCGPYFPRGWNNFHTIMRNILGLVLPLLIMVICYSGILKTLLRCRNEKKRHR
AVRVIFTIMIVYFLFWTPYNIVILLNTFQEFFGLSNCESTSQLDQATQVTETLGMTHCCI
NPIIYAFVGEKFRSLFHIALGCRIAPLQKPVCGGPGVRPGKNVKVTTQGLLDGRGKGKSI
GRAPEASLQDKEGA
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  Blast E-value cutoff:
BDBM141934
n/a
NameBDBM141934
Synonyms:US8921559, 27
TypeSmall organic molecule
Emp. Form.C28H32Cl2N4O3
Mol. Mass.543.485
SMILESOC(=O)C(N[C@H]1CC[C@@H](CC1)c1c[nH]c2ccccc12)C1CCN(CC1)C(=O)Nc1ccc(Cl)c(Cl)c1 |r,wU:5.4,wD:8.11,(-.13,1.59,;-1.46,.82,;-2.8,1.59,;-1.46,-.72,;-2.8,-1.49,;-4.13,-.72,;-5.47,-1.49,;-6.8,-.72,;-6.8,.82,;-5.47,1.59,;-4.13,.82,;-8.13,1.59,;-9.57,1.04,;-10.54,2.24,;-9.7,3.53,;-10.1,5.02,;-9.01,6.11,;-7.52,5.71,;-7.12,4.22,;-8.21,3.13,;-.13,-1.49,;-.13,-3.03,;1.2,-3.8,;2.54,-3.03,;2.54,-1.49,;1.2,-.72,;3.87,-3.8,;3.87,-5.34,;5.2,-3.03,;6.54,-3.8,;6.54,-5.34,;7.87,-6.11,;9.21,-5.34,;10.54,-6.11,;9.21,-3.8,;10.54,-3.03,;7.87,-3.03,)|
Structure
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