null

SMILES Clc1ccc2[nH]c3[C@@H](CCCc3c2c1)NC(=O)c1ccccn1

InChI Key InChIKey=WJQBOBGVBBZLJU-OAHLLOKOSA-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 = 50295257   

TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Homo sapiens (Human))
University of Turin (UniTo)

Curated by ChEMBL
LigandPNGBDBM50295257((R)-N-(6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-y...)copy SMILEScopy InChI
Affinity DataKi:  203nMAssay Description:Inhibition of human DHODHMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MK0PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
GlaxoSmithKline Research& Development

Curated by ChEMBL
LigandPNGBDBM50295257((R)-N-(6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27944RXPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
GlaxoSmithKline Research& Development

Curated by ChEMBL
LigandPNGBDBM50295257((R)-N-(6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27944RXPubMed