BDBM50346865 2-PFPA::CHEMBL1797642

SMILES NC1CC1c1c(F)c(F)c(F)c(F)c1F

InChI Key InChIKey=NZZZWLLBMMVQQY-UHFFFAOYSA-N

Data  4 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 6 hits for monomerid = 50346865   

TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Key Laboratory Of Henan Provinc

Curated by ChEMBL
LigandPNGBDBM50346865(2-PFPA | CHEMBL1797642)
Affinity DataKi:  8.30E+3nMAssay Description:Inhibition of human MAO-B expressed in expressed in baculovirus infected BTI insect cells using tyramine as substrate by peroxidase-coupled methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50346865(2-PFPA | CHEMBL1797642)
Affinity DataKi:  8.90E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50346865(2-PFPA | CHEMBL1797642)
Affinity DataKi:  1.70E+4nMAssay Description:Inhibition of hexahistidine-tagged human LSD1 (172 to 833 residues) expressed in Escherichia coli Rosetta (DE3) cells using H3K4me2 peptide as substr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Key Laboratory Of Henan Provinc

Curated by ChEMBL
LigandPNGBDBM50346865(2-PFPA | CHEMBL1797642)
Affinity DataKi:  2.70E+5nMAssay Description:Inhibition of human MAO-A expressed in expressed in baculovirus infected BTI insect cells using tyramine as substrate by peroxidase-coupled methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50346865(2-PFPA | CHEMBL1797642)
Affinity DataIC50:  8.90E+3nMAssay Description:The kinetic inhibition parameters of LSD1 demethylase inhibition were obtained using the peroxidase-coupled reaction method.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50346865(2-PFPA | CHEMBL1797642)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed