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TargetC-C chemokine receptor type 2
LigandBDBM141924
Substrate/Competitorn/a
Meas. Tech.Binding Assay
Temperature310.15±n/a K
IC50 150±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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BDBM141924
n/a
NameBDBM141924
Synonyms:US8921559, 16
TypeSmall organic molecule
Emp. Form.C29H34F3N5O2
Mol. Mass.541.6078
SMILESNC(=O)C(NC1CCC(CC1)c1c[nH]c2ccccc12)C1CCN(CC1)C(=O)Nc1cccc(c1)C(F)(F)F |(-.82,1.57,;-2.15,.8,;-3.48,1.57,;-2.15,-.74,;-3.48,-1.51,;-4.82,-.74,;-6.15,-1.51,;-7.48,-.74,;-7.48,.8,;-6.15,1.57,;-4.82,.8,;-8.82,1.57,;-10.28,1.1,;-11.19,2.34,;-10.28,3.59,;-10.6,5.1,;-9.46,6.13,;-7.99,5.65,;-7.67,4.14,;-8.82,3.11,;-.82,-1.51,;-.82,-3.05,;.52,-3.82,;1.85,-3.05,;1.85,-1.51,;.52,-.74,;3.19,-3.82,;3.19,-5.36,;4.52,-3.05,;5.85,-3.82,;5.85,-5.36,;7.19,-6.13,;8.52,-5.36,;8.52,-3.82,;7.19,-3.05,;9.85,-3.05,;11.19,-3.82,;9.85,-1.51,;11.19,-2.28,)|
Structure
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