Compile Data Set for Download or QSAR
Found 36 with Last Name = 'forgo' and Initial = 'p'
TargetCannabinoid receptor 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048063(CHEMBL3314943)copy SMILEScopy InChI
Affinity DataKi:  310nMAssay Description:Displacement of [3H]CP55,940 from human CB1 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438783(CHEMBL2415106)copy SMILEScopy InChI
Affinity DataKi:  480nMAssay Description:Displacement of [3H]CP55,940 from human CB1 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048063(CHEMBL3314943)copy SMILEScopy InChI
Affinity DataKi:  1.21E+3nMAssay Description:Displacement of [3H]CP55,940 from human CB2 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438783(CHEMBL2415106)copy SMILEScopy InChI
Affinity DataKi:  4.11E+3nMAssay Description:Displacement of [3H]CP55,940 from human CB2 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048065(CHEMBL3314941)copy SMILEScopy InChI
Affinity DataKi:  8.60E+3nMAssay Description:Displacement of [3H]CP55,940 from human CB1 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)copy SMILEScopy InChI
Affinity DataKi:  8.67E+3nMAssay Description:Displacement of [3H]CP55,940 from human CB1 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438779(CHEMBL2413161)copy SMILEScopy InChI
Affinity DataKi:  8.88E+3nMAssay Description:Displacement of [3H]CP55,940 from human CB1 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048065(CHEMBL3314941)copy SMILEScopy InChI
Affinity DataKi:  9.18E+3nMAssay Description:Displacement of [3H]CP55,940 from human CB2 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048064(CHEMBL3314942)copy SMILEScopy InChI
Affinity DataKi: >2.00E+4nMAssay Description:Displacement of [3H]CP55,940 from human CB1 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048064(CHEMBL3314942)copy SMILEScopy InChI
Affinity DataKi:  2.26E+4nMAssay Description:Displacement of [3H]CP55,940 from human CB2 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438779(CHEMBL2413161)copy SMILEScopy InChI
Affinity DataKi:  4.40E+4nMAssay Description:Displacement of [3H]CP55,940 from human CB2 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Displacement of [3H]CP55,940 from human CB2 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetG protein-activated inward rectifier potassium channel 4(Homo sapiens (Human))
Rytmion Ltd.

Curated by ChEMBL
LigandPNGBDBM50202477(CHEMBL3955249)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of GTPgammaS-induced activation of GIRK1/4 (unknown origin) expressed in HEK293 cells assessed as decrease in channel current after 2 mins...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC12NJPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438783(CHEMBL2415106)copy SMILEScopy InChI
Affinity DataIC50: 4.07E+3nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetG protein-activated inward rectifier potassium channel 4(Homo sapiens (Human))
Rytmion Ltd.

Curated by ChEMBL
LigandPNGBDBM50202479(CHEBI:69714 | Euphorbiaproliferin C)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of GTPgammaS-induced activation of GIRK1/4 (unknown origin) expressed in HEK293 cells assessed as decrease in channel current after 2 mins...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC12NJPubMed
TargetG protein-activated inward rectifier potassium channel 4(Homo sapiens (Human))
Rytmion Ltd.

Curated by ChEMBL
LigandPNGBDBM50202481(CHEMBL3901192)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of GTPgammaS-induced activation of GIRK1/4 (unknown origin) expressed in HEK293 cells assessed as decrease in channel current after 2 mins...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC12NJPubMed
TargetG protein-activated inward rectifier potassium channel 4(Homo sapiens (Human))
Rytmion Ltd.

Curated by ChEMBL
LigandPNGBDBM50202478(CHEMBL3899370)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of GTPgammaS-induced activation of GIRK1/4 (unknown origin) expressed in HEK293 cells assessed as decrease in channel current after 2 mins...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC12NJPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50107607((5Z,8Z)-Icosa-5,8,11,14-tetraenoic acid (furan-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 7.24E+3nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetG protein-activated inward rectifier potassium channel 4(Homo sapiens (Human))
Rytmion Ltd.

Curated by ChEMBL
LigandPNGBDBM50202480(CHEMBL3961215)copy SMILEScopy InChI
Affinity DataIC50: 9.70E+3nMAssay Description:Inhibition of GTPgammaS-induced activation of GIRK1/4 (unknown origin) expressed in HEK293 cells assessed as decrease in channel current after 2 mins...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC12NJPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438779(CHEMBL2413161)copy SMILEScopy InChI
Affinity DataIC50: 1.15E+4nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048064(CHEMBL3314942)copy SMILEScopy InChI
Affinity DataIC50: 1.23E+4nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048065(CHEMBL3314941)copy SMILEScopy InChI
Affinity DataIC50: 1.78E+4nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)copy SMILEScopy InChI
Affinity DataIC50: 1.91E+4nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048063(CHEMBL3314943)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048066(CHEMBL1316265 | OMDM2 | US10300048, Compound OMDM-...)copy SMILEScopy InChI
Affinity DataIC50: 2.33E+4nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetMonoglyceride lipase(Mus musculus (mouse))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048064(CHEMBL3314942)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of mouse brain MAGL-mediated [glycerol-1,2,3-3H]-2-OG hydrolysis preincubated for 15 mins measured 15 mins post 2-OG addition by liquid sc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetMonoglyceride lipase(Mus musculus (mouse))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048063(CHEMBL3314943)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of mouse brain MAGL-mediated [glycerol-1,2,3-3H]-2-OG hydrolysis preincubated for 15 mins measured 15 mins post 2-OG addition by liquid sc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetMonoglyceride lipase(Mus musculus (mouse))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of mouse brain MAGL-mediated [glycerol-1,2,3-3H]-2-OG hydrolysis preincubated for 15 mins measured 15 mins post 2-OG addition by liquid sc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetMonoglyceride lipase(Mus musculus (mouse))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438779(CHEMBL2413161)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of mouse brain MAGL-mediated [glycerol-1,2,3-3H]-2-OG hydrolysis preincubated for 15 mins measured 15 mins post 2-OG addition by liquid sc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetMonoglyceride lipase(Mus musculus (mouse))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438783(CHEMBL2415106)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of mouse brain MAGL-mediated [glycerol-1,2,3-3H]-2-OG hydrolysis preincubated for 15 mins measured 15 mins post 2-OG addition by liquid sc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetMonoglyceride lipase(Mus musculus (mouse))
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50048065(CHEMBL3314941)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of mouse brain MAGL-mediated [glycerol-1,2,3-3H]-2-OG hydrolysis preincubated for 15 mins measured 15 mins post 2-OG addition by liquid sc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q269757FPubMed
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50368315(PROSTRATIN)copy SMILEScopy InChI
Affinity DataEC50:  910nMAssay Description:Activation of PKC in human platelet assessed as induction of platelet aggregation measured within 15 mins by tribidimetric methodMore data for this Ligand-Target Pair
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50470108(AGN 204332 | Ingenol Mebutate | PEP-005 | PEP005 |...)copy SMILEScopy InChI
Affinity DataEC50:  73nMAssay Description:Activation of PKC in human platelet assessed as induction of platelet aggregation measured within 15 mins by tribidimetric methodMore data for this Ligand-Target Pair
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50470109(CHEMBL4104319)copy SMILEScopy InChI
Affinity DataEC50:  6.08E+3nMAssay Description:Activation of PKC in human platelet assessed as induction of platelet aggregation measured within 15 mins by tribidimetric methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N3MPubMed
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50470110(CHEMBL4071723)copy SMILEScopy InChI
Affinity DataEC50:  5.04E+3nMAssay Description:Activation of PKC in human platelet assessed as induction of platelet aggregation measured within 15 mins by tribidimetric methodMore data for this Ligand-Target Pair
Ligand InfoMCE
PC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N3MPubMed
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50099066(CHEMBL279115 | phorbol 13-acetate 12-myristate)copy SMILEScopy InChI
Affinity DataEC50:  9.5nMAssay Description:Activation of PKC in human platelet assessed as induction of platelet aggregation measured within 15 mins by tribidimetric methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N3MPubMed