null

SMILES CC1CCN=C(N)C1

InChI Key InChIKey=GGDLOMFAKKVDPT-UHFFFAOYSA-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 8 hits for monomerid = 50062133   

TargetNitric oxide synthase, inducible(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of human Inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GM86D2PubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GM86D2PubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GM86D2PubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Inhibitory activity against human Inducible nitric oxide synthase (iNOS)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8F3MPubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibitory activity against endothelial nitric oxide synthase (eNOS)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2319V30PubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthase (nNOS)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8F3MPubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 146nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthase (eNOS)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8F3MPubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
G. D. Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50062133(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibitory activity against inducible nitric oxide synthase (iNOS)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2319V30PubMed