Compile Data Set for Download or QSAR
Report error Found 33 Enz. Inhib. hit(s) with all data for entry = 50036486
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049252BDBM50049252(2-Amino-5-(N-nitro-guanidino)-pentanoic acid | CHE...)
Affinity DataIC50: 500nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049252BDBM50049252(2-Amino-5-(N-nitro-guanidino)-pentanoic acid | CHE...)
Affinity DataIC50: 500nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049255BDBM50049255(Piperidin-(2E)-ylideneamine | Piperidin-(2Z)-ylide...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049255BDBM50049255(Piperidin-(2E)-ylideneamine | Piperidin-(2Z)-ylide...)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049258BDBM50049258([1,3]Oxazinan-(2E)-ylideneamine | CHEMBL161118)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049257BDBM50049257(CHEMBL543752 | CHEMBL315857 | Azepan-(2Z)-ylidenea...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049250BDBM50049250([1,3]Thiazinan-(2E)-ylideneamine | [1,3]Thiazinan-...)
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049250BDBM50049250([1,3]Thiazinan-(2E)-ylideneamine | [1,3]Thiazinan-...)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049257BDBM50049257(CHEMBL543752 | CHEMBL315857 | Azepan-(2Z)-ylidenea...)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049258BDBM50049258([1,3]Oxazinan-(2E)-ylideneamine | CHEMBL161118)
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50063300BDBM50063300(l-NIL | CHEMBL1744034 | (L-N6-1-iminoethyl)lysine ...)
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049255BDBM50049255(Piperidin-(2E)-ylideneamine | Piperidin-(2Z)-ylide...)
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049254BDBM50049254(N(5)-carbamimidoyl-N(5)-methyl-L-ornithine | N(5)-...)
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049256BDBM50049256(Azonan-(2Z)-ylideneamine | CHEMBL158641)
Affinity DataIC50: 6.80E+3nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049250BDBM50049250([1,3]Thiazinan-(2E)-ylideneamine | [1,3]Thiazinan-...)
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049252BDBM50049252(2-Amino-5-(N-nitro-guanidino)-pentanoic acid | CHE...)
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049258BDBM50049258([1,3]Oxazinan-(2E)-ylideneamine | CHEMBL161118)
Affinity DataIC50: 8.20E+3nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049256BDBM50049256(Azonan-(2Z)-ylideneamine | CHEMBL158641)
Affinity DataIC50: 9.80E+3nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049249BDBM50049249(Azocan-(2Z)-ylideneamine | CHEMBL329431)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049249BDBM50049249(Azocan-(2Z)-ylideneamine | CHEMBL329431)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049254BDBM50049254(N(5)-carbamimidoyl-N(5)-methyl-L-ornithine | N(5)-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049254BDBM50049254(N(5)-carbamimidoyl-N(5)-methyl-L-ornithine | N(5)-...)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049257BDBM50049257(CHEMBL543752 | CHEMBL315857 | Azepan-(2Z)-ylidenea...)
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049248BDBM50049248(Tetrahydro-pyrimidin-2-ylideneamine | CHEMBL158626)
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049251BDBM50049251(CHEMBL161318 | CHEMBL543888 | Pyrrolidin-(2Z)-ylid...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049248BDBM50049248(Tetrahydro-pyrimidin-2-ylideneamine | CHEMBL158626)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, inducible(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049251BDBM50049251(CHEMBL161318 | CHEMBL543888 | Pyrrolidin-(2Z)-ylid...)
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibitory activity against human inducible nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049249BDBM50049249(Azocan-(2Z)-ylideneamine | CHEMBL329431)
Affinity DataIC50: 5.90E+4nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50063300BDBM50063300(l-NIL | CHEMBL1744034 | (L-N6-1-iminoethyl)lysine ...)
Affinity DataIC50: 6.10E+4nMAssay Description:Inhibitory activity against human Neuronal nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049248BDBM50049248(Tetrahydro-pyrimidin-2-ylideneamine | CHEMBL158626)
Affinity DataIC50: 8.70E+4nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049256BDBM50049256(Azonan-(2Z)-ylideneamine | CHEMBL158641)
Affinity DataIC50: 9.00E+4nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049251BDBM50049251(CHEMBL161318 | CHEMBL543888 | Pyrrolidin-(2Z)-ylid...)
Affinity DataIC50: 9.30E+4nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetNitric oxide synthase, endothelial(Human)
G. D. Searle Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50063300BDBM50063300(l-NIL | CHEMBL1744034 | (L-N6-1-iminoethyl)lysine ...)
Affinity DataIC50: 1.38E+5nMAssay Description:Inhibitory activity against human Endothelial nitric oxide synthaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed