BDBM64836 5-chloranyl-1-methyl-3-[(E)-2-(1-methylpyridin-1-ium-4-yl)ethenyl]indole;hydroiodide::5-chloro-1-methyl-3-[(E)-2-(1-methyl-4-pyridin-1-iumyl)ethenyl]indole;hydroiodide::5-chloro-1-methyl-3-[(E)-2-(1-methylpyridin-1-ium-4-yl)ethenyl]indole;hydroiodide::5-chloro-1-methyl-3-[(E)-2-(1-methylpyridin-1-ium-4-yl)vinyl]indole;hydroiodide::MLS-0318401.0001::cid_44620976

SMILES Cn1cc(\C=C\c2cc[n+](C)cc2)c2cc(Cl)ccc12

InChI Key InChIKey=HQWXUJUGUGALEC-UHFFFAOYSA-N

Data  2 IC50

  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 = 64836   

TargetNucleotide-binding oligomerization domain-containing protein 1(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM64836(5-chloranyl-1-methyl-3-[(E)-2-(1-methylpyridin-1-i...)
Affinity DataIC50:  5.17E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics Source Affiliation: Sanford-Burnham Medical Research Institute Network: NIH Molecular Lib...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetG-protein coupled receptor 55(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM64836(5-chloranyl-1-methyl-3-[(E)-2-(1-methylpyridin-1-i...)
Affinity DataIC50:  3.42E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics(SSBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay