null

SMILES CCOC(=O)N1CCC2(CC1)Nc1cccc(F)c1C(N)=N2

InChI Key InChIKey=FTNKTGJCALFVLR-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 = 50124521   

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

Curated by ChEMBL
LigandPNGBDBM50124521(CHEMBL174290 | ethyl 4'-amino-5'-fluorospiro[hexah...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibitory activity against human neuronal nitiric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75H3MPubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
AstraZeneca R& D Charnwood

Curated by ChEMBL
LigandPNGBDBM50124521(CHEMBL174290 | ethyl 4'-amino-5'-fluorospiro[hexah...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory activity against human endothelial nitiric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75H3MPubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
AstraZeneca R& D Charnwood

Curated by ChEMBL
LigandPNGBDBM50124521(CHEMBL174290 | ethyl 4'-amino-5'-fluorospiro[hexah...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibitory activity of compound against human inducible nitiric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75H3MPubMed