null

SMILES CCO[N-][C+](C1CCN(CC1)C1(C)CCN(CC1)C(=O)c1c(Br)c[n+]([O-])cc1Br)c1ccc(Br)cc1

InChI Key InChIKey=GBZPWPDNOXXZSC-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50124957   

TargetC-C chemokine receptor type 5(Homo sapiens (Human))
Lindsley F. Kimball Research Institute of The New York Blood Center

Curated by ChEMBL
LigandPNGBDBM50124957((4-{(4-Bromo-phenyl)-[(Z)-ethoxyimino]-methyl}-4'-...)copy SMILEScopy InChI
Affinity DataKi:  0.700nMAssay Description:Inhibition of RANTES binding to the human C-C chemokine receptor type 5 (CCR5)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SB46GGPubMed
TargetC-C chemokine receptor type 5(Homo sapiens (Human))
Lindsley F. Kimball Research Institute of The New York Blood Center

Curated by ChEMBL
LigandPNGBDBM50124957((4-{(4-Bromo-phenyl)-[(Z)-ethoxyimino]-methyl}-4'-...)copy SMILEScopy InChI
Affinity DataKi:  0.700nMAssay Description:Inhibition of [125I]RANTES binding to CCR5 receptor.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VM4CTDPubMed