null

SMILES Fc1ccc(cc1)[C@H](CCN1CCC(CC1)c1ccccc1)C(=O)NCc1cc(cc(c1)C(F)(F)F)C(F)(F)F

InChI Key InChIKey=TWDSSLGDUOHXCF-MHZLTWQESA-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 3 hits for monomerid = 50192278   

TargetSubstance-P receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50192278((2S)-N-(3,5-bis(trifluoromethyl)benzyl)-2-(4-fluor...)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:Inhibition of NK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ329MPubMed
TargetC-C chemokine receptor type 5(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50192278((2S)-N-(3,5-bis(trifluoromethyl)benzyl)-2-(4-fluor...)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibition of CCR5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ329MPubMed
TargetC-C chemokine receptor type 2(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50192278((2S)-N-(3,5-bis(trifluoromethyl)benzyl)-2-(4-fluor...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of [125I]MCP1 binding to CCR2 expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ329MPubMed