null

SMILES CN(CCC[C@H](N)C(O)=O)C(N)=N

InChI Key InChIKey=XKCWNEVAXQCMGP-YFKPBYRVSA-N

  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 9 hits for monomerid = 50049254   

TargetNitric oxide synthase, inducible(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataKi:  1.40E+6nMAssay Description:Binding affinity towards inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V69KBCPubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q261110MPubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q261110MPubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q261110MPubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:Inhibition of human recombinant iNOS by griess assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KW5GXNPubMed
TargetN(G),N(G)-dimethylarginine dimethylaminohydrolase 1(Homo sapiens (Human))
Christian-Albrechts-University of Kiel

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+6nMAssay Description:Inhibition of human recombinant DDAH1 expressed in Escherichia coli BL21 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KW5GXNPubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:Inhibition of human recombinant eNOS by griess assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KW5GXNPubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:Inhibition of human recombinant nNOS by griess assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KW5GXNPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
Université de Haute-Alsace

Curated by ChEMBL
LigandPNGBDBM50049254((2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Compound was evaluated for inhibitory activity against iNOS obtained from RAW 264.7 cells.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DZ07G5PubMed