BDBM50339142 CHEMBL1688558::rac-7-(phenyl(pyridin-2-ylamino)methyl)quinolin-8-ol

SMILES Oc1c(ccc2cccnc12)C(Nc1ccccn1)c1ccccc1

InChI Key InChIKey=WHPVVFZPXKODBB-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50339142   

TargetBotulinum neurotoxin type A(Clostridium botulinum)
U.S. Army Medical Research Institute of Infectious Diseases

Curated by ChEMBL
LigandPNGBDBM50339142(rac-7-(phenyl(pyridin-2-ylamino)methyl)quinolin-8-...)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of protease activity of recombinant full-length Clostridium botulinum BoNT/A light chain after 5 mins by HPLC-based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2011
Entry Details Article
PubMed
TargetBotulinum neurotoxin type A(Clostridium botulinum)
U.S. Army Medical Research Institute of Infectious Diseases

Curated by ChEMBL
LigandPNGBDBM50339142(rac-7-(phenyl(pyridin-2-ylamino)methyl)quinolin-8-...)
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of protease activity of recombinant Clostridium botulinum BoNT/A (1 to 425) light chain after 5 mins by HPLC-based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/24/2011
Entry Details Article
PubMed
TargetBotulinum neurotoxin type A(Clostridium botulinum)
U.S. Army Medical Research Institute of Infectious Diseases

Curated by ChEMBL
LigandPNGBDBM50339142(rac-7-(phenyl(pyridin-2-ylamino)methyl)quinolin-8-...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of Clostridium botulinum BoNT/A LC expressed in Escherichia coli assessed as cleavage of SNAPtide preincubated for 5 mins followed by SNAP...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetBotulinum neurotoxin type A(Clostridium botulinum)
U.S. Army Medical Research Institute of Infectious Diseases

Curated by ChEMBL
LigandPNGBDBM50339142(rac-7-(phenyl(pyridin-2-ylamino)methyl)quinolin-8-...)
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of protease activity of recombinant full length Clostridium botulinum Hall BoNT/A light chain using SNAP-25 peptide (187 to 203 residues) ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/13/2019
Entry Details Article
PubMed
TargetBifunctional peptidase and (3S)-lysyl hydroxylase JMJD7(Human)
Sichuan University

Curated by ChEMBL
LigandPNGBDBM50339142(rac-7-(phenyl(pyridin-2-ylamino)methyl)quinolin-8-...)
Affinity DataIC50: 3.16E+4nMAssay Description:Inhibition of N-terminal His-tagged human JMJD7 (1 to 316 residues) expressed in Escherichia coli BL21 (DE3) luciferase based succinate-gloTM JmjC de...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed