BDBM50226767 CHEMBL160553

SMILES [Br-].C[N+]1(CC#CCN2CCCC2=O)CC1

InChI Key InChIKey=UDOCPFRWZFCDBG-UHFFFAOYSA-N

Data  1 EC50

  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 6 hits for monomerid = 50226767   

TargetCytochrome P450 3A4(Homo sapiens (Human))
Kansas State University

Curated by ChEMBL
LigandPNGBDBM50226767(CHEMBL5267910)
Affinity DataIC50:  6.95E+3nMAssay Description:Inhibition of dihydrofolate reductase enzyme purified from Escherichia coli at 1x10E6 MMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Kansas State University

Curated by ChEMBL
LigandPNGBDBM50226767(CHEMBL5267910)
Affinity DataIC50:  6.85E+3nMAssay Description:Inhibition of dihydrofolate reductase enzyme purified from Escherichia coli at 1x10E6 MMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Kansas State University

Curated by ChEMBL
LigandPNGBDBM50226767(CHEMBL5267910)
Affinity DataIC50:  2.76E+4nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Kansas State University

Curated by ChEMBL
LigandPNGBDBM50226767(CHEMBL5267910)
Affinity DataIC50:  7.41E+3nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Kansas State University

Curated by ChEMBL
LigandPNGBDBM50226767(CHEMBL5267910)
Affinity DataIC50: >1.00E+5nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Kansas State University

Curated by ChEMBL
LigandPNGBDBM50226767(CHEMBL5267910)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of dihydrofolate reductase enzyme purified from Escherichia coli at 1x10E6 MMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed