null

SMILES C(Nc1nc(-c2ccccc2)[n+](s1)-c1ccccc1)c1ccccc1

InChI Key InChIKey=JQPAQHRUZOUMMG-UHFFFAOYSA-O

  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 = 47034   

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

Curated by PubChem BioAssay
LigandPNGBDBM47034(2,3-diphenyl-N-(phenylmethyl)-1,2,4-thiadiazol-2-i...)copy SMILEScopy InChI
Affinity DataIC50: 2.59E+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
LigandPNGBDBM47034(2,3-diphenyl-N-(phenylmethyl)-1,2,4-thiadiazol-2-i...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+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
LigandPNGBDBM47034(2,3-diphenyl-N-(phenylmethyl)-1,2,4-thiadiazol-2-i...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+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