BDBM50420356 NC 150::PHENAZOPYRIDINE HYDROCHLORIDE

SMILES Nc1ccc(\N=N\c2ccccc2)c(N)n1

InChI Key InChIKey=QPFYXYFORQJZEC-FOCLMDBBSA-N

Data  1 KI  2 IC50

  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 = 50420356   

TargetNAD(+) hydrolase SARM1(Human)
Umass Medical School

Curated by ChEMBL
LigandPNGBDBM50420356(NC 150 | PHENAZOPYRIDINE HYDROCHLORIDE)
Affinity DataKi:  7.00E+4nMAssay Description:Competitive inhibition of recombinant human SARM1 TIR domain (561 to 724 residues) expressed in Escherichia coli C43 (DE3) cells lysates assessed as ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSnake venom metalloproteinase BaP1(Terciopelo)
TBA

Curated by ChEMBL
LigandPNGBDBM50420356(NC 150 | PHENAZOPYRIDINE HYDROCHLORIDE)
Affinity DataIC50:  5.43E+4nMAssay Description:Inhibition of snake venom BaP1 using Abz-Ala-Gly-Leu-Ala-Nba as substrate incubated for 30 mins prior to substrate addition by fluorescence spectroph...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNAD(+) hydrolase SARM1(Human)
Umass Medical School

Curated by ChEMBL
LigandPNGBDBM50420356(NC 150 | PHENAZOPYRIDINE HYDROCHLORIDE)
Affinity DataIC50:  1.45E+5nMAssay Description:Inhibition of recombinant human SARM1 TIR domain (561 to 724 residues) expressed in Escherichia coli C43 (DE3) cells lysates using ENAD as substrate ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed