null

SMILES CCOC(=O)N1CCC(CC1)Nc1cc(C)ccn1

InChI Key InChIKey=LNRMJBWADUSJTA-UHFFFAOYSA-N

PDB links: 3 PDB IDs match this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50148162   

TargetNitric oxide synthase, inducible(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 350nMpH: 7.0 T: 2°CAssay Description:Nitric oxide formation from NOS was monitored by the hemoglobin capture assay. The assay was initiated by addition of enzyme and was monitored at 401...More data for this Ligand-Target Pair
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+4nMpH: 7.0 T: 2°CAssay Description:Nitric oxide formation from NOS was monitored by the hemoglobin capture assay. The assay was initiated by addition of enzyme and was monitored at 401...More data for this Ligand-Target Pair
TargetNitric oxide synthase, brain(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMpH: 7.0 T: 2°CAssay Description:Nitric oxide formation from NOS was monitored by the hemoglobin capture assay. The assay was initiated by addition of enzyme and was monitored at 401...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SB443QPubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+4nMAssay Description:Inhibition of wild type human eNOS using L-Arg as substrate incubated for 1 hr prior to L-Arg additionMore data for this Ligand-Target Pair
TargetNitric oxide synthase, brain(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+4nMAssay Description:In vitro inhibition of human neuronal nitric oxide synthase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M656DPubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:In vitro inhibition of human endothelial nitric oxide synthase.More data for this Ligand-Target Pair
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of wild type human iNOS expressed in Escherichia coli BL21(DE3) using L-Arg as substrate incubated for 1 hr prior to L-Arg additionMore data for this Ligand-Target Pair
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
The Scripps Research Institute

LigandPNGBDBM50148162(4-(4-Methyl-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:In vitro inhibition of human Inducible nitric oxide synthase.More data for this Ligand-Target Pair