BDBM50139853 CHEMBL3764143::US10577361, E14

SMILES Cn1c(SCCCN2CCOC(C2)c2ccc(cc2)C(F)(F)F)nnc1-c1ccc(cc1)-c1ncco1

InChI Key InChIKey=PMZOPKCHYGDQPO-UHFFFAOYSA-N

Data  14 KI  6 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 20 hits for monomerid = 50139853   

TargetCytochrome P450 3A4(Human)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human CYP3A4 expressed in bactosome using 7BQ as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetCytochrome P450 1A2(Human)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human CYP1A2 expressed in bactosomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human CYP2C9 expressed in bactosomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetCytochrome P450 2C19(Human)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human CYP2C19 expressed in bactosomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetCytochrome P450 2D6(Human)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human CYP2D6 expressed in bactosomeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of human CYP3A4 expressed in bactosome using DBOMF as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(3) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  4.90nMAssay Description:[3H]-Spiperone Binding Assay at hD3 and hD4 recombinant receptors CHO cells transiently transfected with human dopamine type 3 or 4 receptors (CHO-hD...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2020
Entry Details
Go to US Patent

TargetD(3) dopamine receptor(Rat)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  5nMAssay Description:Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D3 receptor after 45 mins by microplate scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(3) dopamine receptor(Rat)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  5.01nMAssay Description:Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D3 receptor after 45 mins by microplate scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(3) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  10nMAssay Description:Antagonist activity at human dopamine D3 receptor expressed in CHO cells after 90 mins by [35S]-GTPgamma S assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(3) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  10nMAssay Description:Antagonist activity at human dopamine D3 receptor expressed in CHO cells after 90 mins by [35S]-GTPgamma S assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(3) dopamine receptor(Rat)
Aptuit

Curated by ChEMBL
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  398nMAssay Description:Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D3 receptor after 45 mins by microplate scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  999nMAssay Description:Displacement of [3H]-dofetilide from human ERG potassium channel by scintillation proximity assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  1.00E+3nMAssay Description:Displacement of [3H]-dofetilide from human ERG potassium channel by scintillation proximity assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(2) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  1.48E+3nMAssay Description:CHO cells stably expressing human dopamine receptor type 2, long variant (hD2L), coupled to Gα16 protein (CHO-Gα16-hD2L) were re-suspended ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2020
Entry Details
Go to US Patent

TargetD(2) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  1.58E+3nMAssay Description:Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D2 receptor after 45 mins by microplate scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(2) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  1.59E+3nMAssay Description:Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D2 receptor after 45 mins by microplate scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(3) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi: <1.00E+4nMAssay Description:Agonist activity at human dopamine D3 receptor expressed in CHO cells after 90 mins by [35S]-GTPgamma S assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(3) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi: <1.00E+4nMAssay Description:Antagonist activity at human dopamine D3 receptor expressed in CHO cells after 90 mins by [35S]-GTPgamma S assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed
TargetD(2) dopamine receptor(Human)
Indivior

US Patent
LigandPNGBDBM50139853(CHEMBL3764143 | US10577361, E14)
Affinity DataKi:  1.58E+4nMAssay Description:Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D2 receptor after 45 mins by microplate scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2017
Entry Details Article
PubMed