BDBM50230418 CHEMBL260629::N(gamma)-hydroxy-L-arginine::N-OMEGA-HYDROXY-L-ARGININE::Nomega-hydroxy-L-arginine

SMILES NC(NO)=NCCC[C@H]([NH3+])C([O-])=O

InChI Key InChIKey=FQWRAVYMZULPNK-BYPYZUCNSA-N

Data  2 KI  5 IC50  2 Kd

  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 9 hits for monomerid = 50230418   

TargetArginase-2, mitochondrial(Homo sapiens (Human))
Oncoarendi Therapeutics

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataKi:  1.60E+3nMAssay Description:Inhibition of human Arg2 at pH 7.5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetArginase-1(Bos taurus)
Christian-Albrechts-University Of Kiel

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataKi:  3.00E+4nMAssay Description:Inhibition of bovine liver arginaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB

TargetArginase-1(Rattus norvegicus)
Oncoarendi Therapeutics

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of rat Arg1 at pH 7.4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB

TargetArginase-1(Homo sapiens (Human))
Oncoarendi Therapeutics

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataKd:  3.60E+3nMAssay Description:Binding affinity to human Arg1 at pH 8.5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB

TargetArginase-2, mitochondrial(Homo sapiens (Human))
Oncoarendi Therapeutics

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataIC50:  1.60E+3nMAssay Description:Binding affinity to human ARG2 assessed as inhibition constantMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetArginase-1(Homo sapiens (Human))
Oncoarendi Therapeutics

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataIC50:  150nMAssay Description:Inhibition of recombinant human ARG1 expressed in Escherichia coli using L-arginine hydrochloride as substrate incubated for 1 hr by colorimetric ass...More data for this Ligand-Target Pair
In DepthDetails PubMedMMDB

TargetArginase-1(Rattus norvegicus)
Oncoarendi Therapeutics

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of rat ARG1More data for this Ligand-Target Pair
In DepthDetails PubMedMMDB

TargetArginase-1(Homo sapiens (Human))
Oncoarendi Therapeutics

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataIC50:  3.60E+3nMAssay Description:Binding affinity to human ARG1 assessed as dissociation constantMore data for this Ligand-Target Pair
In DepthDetails PubMedMMDB

TargetNitric oxide synthase, inducible(Homo sapiens (Human))
University Of Utrecht

Curated by ChEMBL
LigandPNGBDBM50230418(CHEMBL260629 | N(gamma)-hydroxy-L-arginine | N-OME...)
Affinity DataKd:  5.10E+3nMAssay Description:Binding affinity to iNOS with heme domain construct (unknown origin) assessed as spectral binding constant by spectral assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB