null

SMILES Clc1ccc(cc1Cl)C1(CCCN2CCC(CC2)n2c3ccccc3[nH]c2=O)CCC(=O)N(Cc2ccccc2)C1

InChI Key InChIKey=ADXFJIYJEFFOSY-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50070353   

TargetSubstance-K receptor(Homo sapiens (Human))
Merck Sharp Laboratory

Curated by ChEMBL
LigandPNGBDBM50070353(1-(1-{3-[1-Benzyl-3-(3,4-dichloro-phenyl)-6-oxo-pi...)copy SMILEScopy InChI
Affinity DataIC50: 6.40nMAssay Description:Compound was evaluated for affinity towards human Neurokinin NK2 receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QV3N16PubMed
TargetC-C chemokine receptor type 5(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50070353(1-(1-{3-[1-Benzyl-3-(3,4-dichloro-phenyl)-6-oxo-pi...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Displacement of [125I]MIP-1beta from human CCR5 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WS8VG8PubMed
TargetNeuromedin-K receptor(Homo sapiens (Human))
Merck Sharp Laboratory

Curated by ChEMBL
LigandPNGBDBM50070353(1-(1-{3-[1-Benzyl-3-(3,4-dichloro-phenyl)-6-oxo-pi...)copy SMILEScopy InChI
Affinity DataIC50: 539nMAssay Description:Compound was evaluated for affinity towards human Neurokinin NK3 receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QV3N16PubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Merck Sharp Laboratory

Curated by ChEMBL
LigandPNGBDBM50070353(1-(1-{3-[1-Benzyl-3-(3,4-dichloro-phenyl)-6-oxo-pi...)copy SMILEScopy InChI
Affinity DataIC50: 743nMAssay Description:Compound was evaluated for affinity towards human Neurokinin NK1 receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QV3N16PubMed