null

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

InChI Key InChIKey=KGIKZYZMTIMJTM-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50148166   

TargetNitric oxide synthase, brain(Homo sapiens (Human))
AstraZeneca R&D Charnwood

Curated by ChEMBL
LigandPNGBDBM50148166(4-(4-Ethoxy-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 9.60E+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, inducible(Homo sapiens (Human))
AstraZeneca R&D Charnwood

Curated by ChEMBL
LigandPNGBDBM50148166(4-(4-Ethoxy-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+3nMAssay Description:In vitro inhibition of human Inducible 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))
AstraZeneca R&D Charnwood

Curated by ChEMBL
LigandPNGBDBM50148166(4-(4-Ethoxy-pyridin-2-ylamino)-piperidine-1-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibition of human endothelial nitric oxide synthase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M656DPubMed