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Found 74 with Last Name = 'patricelli' and Initial = 'mp'
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073987(1,1,1-Trifluoro-9-phenyl-nonan-2-one | 1,1,1-trifl...)
Affinity DataKi:  25nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50069273((Z)-1,1,1-Trifluoro-nonadec-10-en-2-one | 1,1,1-tr...)
Affinity DataKi:  82nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073986(1,1,1-Trifluoro-8-(4-heptyl-phenyl)-octan-2-one | ...)
Affinity DataKi:  96nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073974(1,1,1-Trifluoro-8-phenyl-octan-2-one | 1,1,1-Trifl...)
Affinity DataKi:  100nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073985(1,1,1-Trifluoro-undecan-2-one | 1,1,1-trifluoround...)
Affinity DataKi:  130nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073975(1,1,1-Trifluoro-tridecan-2-one | 1,1,1-trifluorotr...)
Affinity DataKi:  140nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073984(1,1,1-Trifluoro-8-(3-hexyl-phenyl)-octan-2-one | C...)
Affinity DataKi:  140nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073973((E)-1,1,1-Trifluoro-nonadec-10-en-2-one | 1,1,1-Tr...)
Affinity DataKi:  170nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073989(1,1,1-Trifluoro-7-phenyl-heptan-2-one | 1,1,1-Trif...)
Affinity DataKi:  170nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069276(4-Bromo-3-oxo-butyric acid (Z)-tetradec-5-enyl est...)
Affinity DataKi:  190nMpH: 9.0Assay Description:Compound was tested for inhibitory potency against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073981(1,1,1-Trifluoro-nonadecan-2-one | 1,1,1-trifluoron...)
Affinity DataKi:  240nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069273((Z)-1,1,1-Trifluoro-nonadec-10-en-2-one | 1,1,1-tr...)
Affinity DataKi:  250nMpH: 9.0Assay Description:Compound was tested for inhibitory potency against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073982(1,1,1-Trifluoro-9-(2-octyl-phenyl)-nonan-2-one | C...)
Affinity DataKi:  320nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069272((Z)-1-Bromo-nonadec-10-en-2-one | CHEMBL157736)
Affinity DataKi:  390nMpH: 9.0Assay Description:Compound was tested for inhibitory potency against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073980(5-((1R,6R)-6-Butoxymethyl-cyclohex-3-enylmethoxy)-...)
Affinity DataKi:  440nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073970(1,1,1-Trifluoro-pentadecan-2-one | 1,1,1-trifluoro...)
Affinity DataKi:  490nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069270(4-Bromo-3-oxo-butyric acid heptyl ester | CHEMBL15...)
Affinity DataKi:  550nMpH: 9.0Assay Description:Inhibitory concentration against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073978(5-((1R,6S)-6-Butoxymethyl-cyclohex-3-enylmethoxy)-...)
Affinity DataKi:  570nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073990(5-((1R,2S)-2-Butoxymethyl-cyclohexylmethoxy)-1,1,1...)
Affinity DataKi:  780nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069269((R)-octan-2-yl 4-bromo-3-oxobutanoate | 4-Bromo-3-...)
Affinity DataKi:  800nMpH: 9.0Assay Description:Concentration of the compound required to inhibit fatty acid amide hydrolase (FAAH) at pH 7.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069271(4-Chloro-3-oxo-butyric acid (R)-1-methyl-heptyl es...)
Affinity DataKi:  1.10E+3nMpH: 9.0Assay Description:Concentration of the compound required to inhibit Fatty-acid amide hydrolase (FAAH) at pH 7.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069280(4-Bromo-3-oxo-butyric acid (S)-1-methyl-heptyl est...)
Affinity DataKi:  1.10E+3nMpH: 9.0Assay Description:Concentration of the compound required to inhibit fatty acid amide hydrolase (FAAH) at pH 7.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073977(1,1,1-Trifluoro-nonan-2-one | 1,1,1-trifluorononan...)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073971(5-((1R,2R)-2-Butoxymethyl-cyclohexylmethoxy)-1,1,1...)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073979(1,1,1-Trifluoro-7-(2-hexyl-phenyl)-heptan-2-one | ...)
Affinity DataKi:  2.80E+3nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073983(5-(3-Butyl-naphthalen-2-yl)-1,1,1-trifluoro-pentan...)
Affinity DataKi:  4.40E+3nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073976(1,1,1-Trifluoro-octan-2-one | 1,1,1-trifluorooctan...)
Affinity DataKi:  1.07E+4nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073988(1,1,1-Trifluoro-heptan-2-one | 1,1,1-trifluorohept...)
Affinity DataKi:  2.69E+4nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073991(3-(3-Ethyl-anthracen-2-yl)-1,1,1-trifluoro-propan-...)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073972((Z)-Nonadec-10-en-2-one | CHEMBL92219 | nonadec-10...)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM482160(BDBM50396041 | HG-10-102-01)
Affinity DataIC50:  20.3nMAssay Description:Inhibition of LRRK2 expressed in HEK293 cells using nictide as substrate and [gamma32P]ATP after 15 mins by Cerenkov counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073987(1,1,1-Trifluoro-9-phenyl-nonan-2-one | 1,1,1-trifl...)
Affinity DataIC50:  120nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073975(1,1,1-Trifluoro-tridecan-2-one | 1,1,1-trifluorotr...)
Affinity DataIC50:  130nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073974(1,1,1-Trifluoro-8-phenyl-octan-2-one | 1,1,1-Trifl...)
Affinity DataIC50:  450nMAssay Description:Inhibitory constant of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50069273((Z)-1,1,1-Trifluoro-nonadec-10-en-2-one | 1,1,1-tr...)
Affinity DataIC50:  460nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073986(1,1,1-Trifluoro-8-(4-heptyl-phenyl)-octan-2-one | ...)
Affinity DataIC50:  590nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073985(1,1,1-Trifluoro-undecan-2-one | 1,1,1-trifluoround...)
Affinity DataIC50:  600nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069276(4-Bromo-3-oxo-butyric acid (Z)-tetradec-5-enyl est...)
Affinity DataIC50:  600nMpH: 9.0Assay Description:Inhibitory concentration against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069273((Z)-1,1,1-Trifluoro-nonadec-10-en-2-one | 1,1,1-tr...)
Affinity DataIC50:  600nMpH: 9.0Assay Description:Inhibitory concentration against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMAP kinase-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM482160(BDBM50396041 | HG-10-102-01)
Affinity DataIC50:  600nMAssay Description:Inhibition of MNK2 by radiometric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069271(4-Chloro-3-oxo-butyric acid (R)-1-methyl-heptyl es...)
Affinity DataIC50:  700nMpH: 9.0Assay Description:Concentration of the compound required to inhibit fatty acid amide hydrolase (FAAH) at pH 7.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069271(4-Chloro-3-oxo-butyric acid (R)-1-methyl-heptyl es...)
Affinity DataIC50:  700nMpH: 7.0Assay Description:Compound was tested for inhibitory potency against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073984(1,1,1-Trifluoro-8-(3-hexyl-phenyl)-octan-2-one | C...)
Affinity DataIC50:  760nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073973((E)-1,1,1-Trifluoro-nonadec-10-en-2-one | 1,1,1-Tr...)
Affinity DataIC50:  780nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073989(1,1,1-Trifluoro-7-phenyl-heptan-2-one | 1,1,1-Trif...)
Affinity DataIC50:  840nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069272((Z)-1-Bromo-nonadec-10-en-2-one | CHEMBL157736)
Affinity DataIC50:  1.00E+3nMpH: 9.0Assay Description:Compound was tested for inhibitory potency against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50073981(1,1,1-Trifluoro-nonadecan-2-one | 1,1,1-trifluoron...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibitory concentration of the compound against Fatty-acid amide hydrolase (FAAH) in rat liverMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069270(4-Bromo-3-oxo-butyric acid heptyl ester | CHEMBL15...)
Affinity DataIC50:  1.50E+3nMpH: 9.0Assay Description:Inhibitory concentration against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase kinase kinase 9(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM482160(BDBM50396041 | HG-10-102-01)
Affinity DataIC50:  2.10E+3nMAssay Description:Inhibition of MLK1 by radiometric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Institute For Chemical Biology

Curated by ChEMBL
LigandPNGBDBM50069270(4-Bromo-3-oxo-butyric acid heptyl ester | CHEMBL15...)
Affinity DataIC50:  2.10E+3nMpH: 7.0Assay Description:Compound was tested for inhibitory potency against Fatty-acid amide hydrolase (FAAH) at pH 9.0More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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