null

SMILES CC1(C)[C@H]2C[C@@H]1C(C[N+](C)(C)Cc1ccc(cc1)-c1ccccc1I)=CC2

InChI Key InChIKey=FKUOVGQOKVAIAV-FYYLOGMGSA-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 2 hits for monomerid = 50399981   

TargetC-X-C chemokine receptor type 3(Homo sapiens (Human))
VU University Amsterdam

Curated by ChEMBL
LigandPNGBDBM50399981(CHEMBL2181450)copy SMILEScopy InChI
Affinity DataKi:  50.1nMAssay Description:Displacement of [125I]CXCL10 from CXCR3 expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27P90J8PubMed
TargetC-X-C chemokine receptor type 3(Homo sapiens (Human))
VU University Amsterdam

Curated by ChEMBL
LigandPNGBDBM50399981(CHEMBL2181450)copy SMILEScopy InChI
Affinity DataEC50:  631nMAssay Description:Agonist activity at CXCR3 expressed in HEK293 cells by [35S]GTPgamma binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27P90J8PubMed