null

SMILES Cc1ccc(CN2CCC(CNC(=O)C3CCN(CC3)c3ccc(nn3)-c3cccs3)C2)cc1

InChI Key InChIKey=JTDVOOWYOMRNCY-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50205734   

TargetC-C chemokine receptor type 5(Homo sapiens (Human))
CNRS UMR 7175-LC1

Curated by ChEMBL
LigandPNGBDBM50205734(1-(6-thiophen-2-yl-pyridazin-3-yl)-piperidine-4-ca...)copy SMILEScopy InChI
Affinity DataEC50:  1.10E+3nMAssay Description:Agonist activity at CCR5 expressed in CHO-K1 cells in aqeuorin based assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KD1XK6PubMed
TargetC-C chemokine receptor type 5(Homo sapiens (Human))
CNRS UMR 7175-LC1

Curated by ChEMBL
LigandPNGBDBM50205734(1-(6-thiophen-2-yl-pyridazin-3-yl)-piperidine-4-ca...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+3nMAssay Description:Displacement of [125I]MIP1beta from CCR5 expressed in CHO-K1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KD1XK6PubMed