BDBM50621475 CHEMBL5403404
SMILES CCCN1CCN(CC1)c1ccc2CCCC(N(C)C(=O)OCc3ccccc3)c2c1
InChI Key InChIKey=PBFDUYRSNDQIDN-UHFFFAOYSA-N
Data 40 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
 Found 40 hits  for monomerid = 50621475    
Affinity DataKi:  5.5nMAssay Description:Displacement of [3H]-ditolylguanidine from sigma 2 receptor/TMEM97 in rat PC-12 cells assessed as inhibition constant in the presence of (+)-pentazoc...More data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  20nMAssay Description:Binding affinity at human Histamine H1 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  33nMAssay Description:Displacement of [3H]-ditolylguanidine from human sigma 2 receptor/TMEM97 transfected in HEK293 cells assessed as inhibition constant in the presence ...More data for this Ligand-Target Pair
Ligand InfoSimilars
TargetSigma non-opioid intracellular receptor 1(Human)
The University of Texas At Austin
Curated by ChEMBL
The University of Texas At Austin
Curated by ChEMBL
Affinity DataKi:  82nMAssay Description:Displacement of [3H](+)-pentazocine from human sigma 1 receptor transfected in HEK293 cells assessed as inhibition constant by competition binding as...More data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  100nMAssay Description:Binding affinity to human 5HT2B receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  135nMAssay Description:Binding affinity to human 5HT1D receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  156nMAssay Description:Binding affinity to human 5HT1A receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
TargetSigma non-opioid intracellular receptor 1(Guinea pig)
The University of Texas At Austin
Curated by ChEMBL
The University of Texas At Austin
Curated by ChEMBL
Affinity DataKi:  200nMAssay Description:Displacement of [3H](+)-pentazocine from sigma 1 receptor in guinea pig brain assessed as inhibition constant by competition binding assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  315nMAssay Description:Binding affinity to human 5HT2A receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  362nMAssay Description:Binding affinity to human 5HT1B receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  438nMAssay Description:Binding affinity to human dopamine D3 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  459nMAssay Description:Binding affinity to human 5HT7 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  690nMAssay Description:Binding affinity to human dopamine D1 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  762nMAssay Description:Binding affinity to human 5HT2C receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  778nMAssay Description:Binding affinity to human 5HT6 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  1.03E+3nMAssay Description:Binding affinity to human alpha 2A adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  1.35E+3nMAssay Description:Binding affinity at human Histamine H3 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  2.36E+3nMAssay Description:Binding affinity to human alpha 1A adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  2.60E+3nMAssay Description:Binding affinity to human alpha 1D adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  3.33E+3nMAssay Description:Binding affinity to human alpha 2B adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  3.96E+3nMAssay Description:Binding affinity to human dopamine D5 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  6.62E+3nMAssay Description:Binding affinity at human muscarinic M5 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  6.66E+3nMAssay Description:Binding affinity to human dopamine D4 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi:  8.33E+3nMAssay Description:Binding affinity at human PBR assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human beta 3 adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human 5HT1E receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
TargetSodium-dependent noradrenaline transporter(Human)
The University of Texas At Austin
Curated by ChEMBL
The University of Texas At Austin
Curated by ChEMBL
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human Norepinephrine transporter assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
TargetSodium-dependent serotonin transporter(Human)
The University of Texas At Austin
Curated by ChEMBL
The University of Texas At Austin
Curated by ChEMBL
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human SERT assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human dopamine D2 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human alpha 1B adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human DOR assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human alpha 2C adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human beta 1 adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity to human beta 2 adrenergic receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human KOR assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human muscarinic M1 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human muscarinic M2 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human muscarinic M3 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human muscarinic M4 receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity at human MOR assessed as inhibition constantMore data for this Ligand-Target Pair
Ligand InfoSimilars
