null

SMILES N(c1nc(-c2ccccc2)[n+](s1)-c1ccccc1)c1ccccc1

InChI Key InChIKey=MWKGMZRDURKJEZ-UHFFFAOYSA-O

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 47033   

TargetPhosphoethanolamine/phosphocholine phosphatase(Homo sapiens (Human))
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM47033((2,3-diphenyl-1,2,4-thiadiazol-2-ium-5-yl)-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 4.99E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27S7M52PCBioAssay
TargetHistone acetyltransferase GCN5(Saccharomyces cerevisiae S288c)
Mayo Clinic College of Medicine

Curated by ChEMBL
LigandPNGBDBM47033((2,3-diphenyl-1,2,4-thiadiazol-2-ium-5-yl)-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of Vps75-stimulated recombinant Saccharomyces cerevisiae histone acetyltransferase Rtt109 using Asf1-dH3-H4 as substrate assessed as coenz...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M38J9PubMed
TargetHistone acetyltransferase GCN5(Saccharomyces cerevisiae S288c)
Mayo Clinic College of Medicine

Curated by ChEMBL
LigandPNGBDBM47033((2,3-diphenyl-1,2,4-thiadiazol-2-ium-5-yl)-phenyl-...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of Vps75-stimulated recombinant Saccharomyces cerevisiae histone acetyltransferase Rtt109 using Asf1-dH3-H4 as substrate assessed as coenz...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M38J9PubMed