BDBM50354886 CHEMBL466465

SMILES Cc1ccc(cc1)S(=O)(=O)N[C@@H](CCCCN)C(=O)CCl

InChI Key InChIKey=RDFCSSHDJSZMTQ-UHFFFAOYSA-N

Data  5 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50354886   

TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50354886(CHEMBL466465)
Affinity DataIC50: 1.43E+8nMAssay Description:Inhibition of human acrosin using N-alpha-benzoyl-DL-arginine para-nitroanilide-HCl as substrate after 3 hrs by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50354886(CHEMBL466465)
Affinity DataIC50: 1.43E+8nMAssay Description:Inhibition of acrosin activity in human spermatozoa using N-alpha-benzoyl-DL-arginine para-nitroanilide-HCI as a substrate after 3 hrs by spectrophot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/20/2012
Entry Details Article
PubMed
TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50354886(CHEMBL466465)
Affinity DataIC50: 1.43E+8nMAssay Description:Inhibition of human acrosin using N-alpha-benzoyl-DL-arginine para-nitroanilide-HCl as substrate after 3 hrs by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50354886(CHEMBL466465)
Affinity DataIC50: 1.43E+8nMAssay Description:Inhibition of human sperm acrosin using BAPNA as substrate after 3 hrs by spectrophotometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50354886(CHEMBL466465)
Affinity DataIC50: 1.43E+8nMAssay Description:Inhibition of acrosin in human spermatozoa assessed as effect on amidase activity after 3 hrs incubation by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed