null

SMILES NC1=NC(Nc2cccc(F)c12)C1CCC1

InChI Key InChIKey=TWDKMKHCHFFGDT-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 3 hits for monomerid = 50124537   

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

Curated by ChEMBL
LigandPNGBDBM50124537(2-Cyclobutyl-5-fluoro-1,2-dihydro-quinazolin-4-yla...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay 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, inducible(Homo sapiens (Human))
AstraZeneca R& D Charnwood

Curated by ChEMBL
LigandPNGBDBM50124537(2-Cyclobutyl-5-fluoro-1,2-dihydro-quinazolin-4-yla...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay 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
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
AstraZeneca R& D Charnwood

Curated by ChEMBL
LigandPNGBDBM50124537(2-Cyclobutyl-5-fluoro-1,2-dihydro-quinazolin-4-yla...)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibitory activity against human endothelial nitiric oxide synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75H3MPubMed