BDBM50427901 CHEMBL2326088

SMILES N[C@H](CCCCB(O)O)C(O)=O

InChI Key InChIKey=HFKKMXCOJQIYAH-UHFFFAOYSA-N

Data  3 IC50

  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 3 hits for monomerid = 50427901   

TargetArginase-1(Human)
Institutes For Pharmaceutical Discovery

Curated by ChEMBL
LigandPNGBDBM50427901(CHEMBL2326088)
Affinity DataIC50: 1.45E+3nMAssay Description:Inhibition of human recombinant full length arginase I overexpressed in Escherichia coli BL21(DE3) assessed as inhibition of urea formation after 60 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetArginase-2, mitochondrial(Human)
Institutes For Pharmaceutical Discovery

Curated by ChEMBL
LigandPNGBDBM50427901(CHEMBL2326088)
Affinity DataIC50: 1.92E+3nMAssay Description:Inhibition of human recombinant fully active truncated form of arginase 2 overexpressed in Escherichia coli BL21(DE3) assessed as inhibition of urea ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetArginase-1(Human)
Institutes For Pharmaceutical Discovery

Curated by ChEMBL
LigandPNGBDBM50427901(CHEMBL2326088)
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of human arginase 1 transfected in CHO cells assessed as inhibition of urea formation after 24 hrs by spectrophotometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed