null

SMILES O=c1n(cnc2c1sc1ncnc(NCC#C)c21)-c1ccc2OCOc2c1

InChI Key InChIKey=ZWGHMVXHXRTKNE-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 3 hits for monomerid = 50345926   

TargetMetabotropic glutamate receptor 1(RAT)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50345926(3-Benzo[1,3]dioxol-5-yl-9-prop-2-ynylamino-3H-thie...)copy SMILEScopy InChI
Affinity DataKi:  997nMAssay Description:Antagonist activity at rat mGluR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081SJPubMed
TargetMetabotropic glutamate receptor 1(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50345926(3-Benzo[1,3]dioxol-5-yl-9-prop-2-ynylamino-3H-thie...)copy SMILEScopy InChI
Affinity DataIC50: 137nMAssay Description:Antagonist activity at human mGluR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081SJPubMed
TargetMetabotropic glutamate receptor 5(Homo sapiens (Human))
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50345926(3-Benzo[1,3]dioxol-5-yl-9-prop-2-ynylamino-3H-thie...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Antagonist activity at human mGluR5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081SJPubMed