null

SMILES Nc1c2CCCc2nc2CCCCc12

InChI Key InChIKey=YLUSMKAJIQOXPV-UHFFFAOYSA-N

PDB links: 1 PDB ID matches this monomer.

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50279987   

TargetCholinesterase(Equus caballus (Horse))
Nanjing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279987(2,3,5,6,7,8-Hexahydro-1H-cyclopenta[b]quinolin-9-y...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B90TVPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279987(2,3,5,6,7,8-Hexahydro-1H-cyclopenta[b]quinolin-9-y...)copy SMILEScopy InChI
Affinity DataIC50: 658nMAssay Description:In vitro inhibition of acetylcholinesterase isolated from human erythrocytes.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G73DN0
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Nanjing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279987(2,3,5,6,7,8-Hexahydro-1H-cyclopenta[b]quinolin-9-y...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B90TVPubMed