null

SMILES CCC(OC(C)=O)C(CC(C)N(C)C)(c1ccccc1)c1ccccc1

InChI Key InChIKey=XBMIVRRWGCYBTQ-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 5 hits for monomerid = 50027391   

TargetMu-type opioid receptor(Rattus norvegicus (rat))
R.W. Johnson Pharmaceutical Research Institute

Curated by PDSP Ki Database
LigandPNGBDBM50027391(Acetic acid (1S,4S)-4-dimethylamino-1-ethyl-2,2-di...)copy SMILEScopy InChI
Affinity DataKi:  9.86nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R20ZVXPubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
R.W. Johnson Pharmaceutical Research Institute

Curated by PDSP Ki Database
LigandPNGBDBM50027391(Acetic acid (1S,4S)-4-dimethylamino-1-ethyl-2,2-di...)copy SMILEScopy InChI
Affinity DataKi:  169nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R20ZVXPubMed
TargetKappa-type opioid receptor(Rattus norvegicus (rat))
R.W. Johnson Pharmaceutical Research Institute

Curated by PDSP Ki Database
LigandPNGBDBM50027391(Acetic acid (1S,4S)-4-dimethylamino-1-ethyl-2,2-di...)copy SMILEScopy InChI
Affinity DataKi:  1.02E+3nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R20ZVXPubMed
TargetNorepinephrine transporter(RAT)
R.W. Johnson Pharmaceutical Research Institute

Curated by PDSP Ki Database
LigandPNGBDBM50027391(Acetic acid (1S,4S)-4-dimethylamino-1-ethyl-2,2-di...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R20ZVXPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Reverse proteomics research institute

Curated by ChEMBL
LigandPNGBDBM50027391(Acetic acid (1S,4S)-4-dimethylamino-1-ethyl-2,2-di...)copy SMILEScopy InChI
Affinity DataIC50: 2.19E+3nMAssay Description:Inhibitory concentration against potassium channel HERGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1S7CPubMed