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Found 146 with Last Name = 'spicer' and Initial = 'tp'
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50:  14nMAssay Description:Non-competitive inhibition of full-length recombinant human MMP-13 assessed as fTHP-15 substrate hydrolysisMore data for this Ligand-Target Pair
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM16596(4-N,6-N-bis[(4-fluoro-3-methylphenyl)methyl]pyrimi...)
Affinity DataIC50:  70nMAssay Description:Inhibition of full-length recombinant human MMP-13 assessed as bovine type-2 collagen hydrolysis after 18 hrs by ELISAMore data for this Ligand-Target Pair
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM16596(4-N,6-N-bis[(4-fluoro-3-methylphenyl)methyl]pyrimi...)
Affinity DataIC50:  110nMAssay Description:Non-competitive inhibition of full-length recombinant human MMP-13 assessed as fTHP-15 substrate hydrolysisMore data for this Ligand-Target Pair
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50361639(CHEMBL1371684)
Affinity DataIC50:  400nMAssay Description:Inhibition of full-length recombinant human MMP-13 assessed as bovine type-2 collagen hydrolysis after 18 hrs by ELISAMore data for this Ligand-Target Pair
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50314727(1-(thiazol-2-yl)ethanone O-cyclohexanecarbonyl oxi...)
Affinity DataIC50:  640nMAssay Description:Displacement of fluorophosphate-rhodamine from RBBP9 transfected in human HEK293T cells proteomes after 30 mins by SDS-PAGE gel fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50:  700nMAssay Description:Inhibition of full-length recombinant human MMP-13 assessed as bovine type-2 collagen hydrolysis after 18 hrs by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154536(2-(4-tert-butylphenyl)-1-(4-methylbenzenesulfonyl)...)
Affinity DataIC50:  800nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154531(2-(4-bromophenyl)-6-(4-chlorophenyl)-1-(4-methylbe...)
Affinity DataIC50:  1.10E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154529(2-(4-fluorophenyl)-1-(4-methylbenzenesulfonyl)-6-[...)
Affinity DataIC50:  1.10E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50314725(4-(cinnamoyloxyimino)-2,6-dimethylcyclohexa-2,5-di...)
Affinity DataIC50:  1.20E+3nMAssay Description:Displacement of fluorophosphate-rhodamine from RBBP9 transfected in human HEK293T cells proteomes after 30 mins by SDS-PAGE gel fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154534(2-(4-bromophenyl)-6-(3,4-dichlorophenyl)-1-(4-meth...)
Affinity DataIC50:  1.40E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50314728(4-(4-methoxybenzoyloxyimino)-2,6-dimethylcyclohexa...)
Affinity DataIC50:  1.50E+3nMAssay Description:Displacement of fluorophosphate-rhodamine from recombinant RBBP9 transfected in mouse brain membrane proteomes after 30 mins by SDS-PAGE gel fluoresc...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50314728(4-(4-methoxybenzoyloxyimino)-2,6-dimethylcyclohexa...)
Affinity DataIC50:  1.50E+3nMAssay Description:Displacement of fluorophosphate-rhodamine from RBBP9 transfected in human HEK293T cells proteomes after 30 mins by SDS-PAGE gel fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154540(2-(4-(tert-butyl)phenyl)-N-(2-methoxyethyl)-6-(p-t...)
Affinity DataIC50:  1.70E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50314729(1-(thiazol-2-yl)ethanone O-4-chlorobenzoyl oxime |...)
Affinity DataIC50:  1.90E+3nMAssay Description:Displacement of fluorophosphate-rhodamine from RBBP9 transfected in human HEK293T cells proteomes after 30 mins by SDS-PAGE gel fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154535(2-(4-fluorophenyl)-1-(4-methylbenzenesulfonyl)-6-(...)
Affinity DataIC50:  2.00E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50361640(CHEMBL1515648)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibition of full-length recombinant human MMP-13 assessed as bovine type-2 collagen hydrolysis after 18 hrs by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50361639(CHEMBL1371684)
Affinity DataIC50:  2.40E+3nMAssay Description:Non-competitive inhibition of full-length recombinant human MMP-13 assessed as fTHP-15 substrate hydrolysisMore data for this Ligand-Target Pair
TargetCytochrome P450 2C19(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP2C19 (unknown origin) using (S)-mephentoin substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP2D6 (unknown origin) using dextromethophan substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin) using diclofenac substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C8(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP2C8 (unknown origin) using amodiaquine substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2B6(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP2B6 (unknown origin) using bupropion substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP1A2 (unknown origin) using tacrin substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin) using midazolam substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50265079((4-[1-methyl-2,4-dioxo-6-(3-phenyl-prop-1-ynyl)-1,...)
Affinity DataIC50: >2.50E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin) using testosterone substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50361640(CHEMBL1515648)
Affinity DataIC50:  2.80E+3nMAssay Description:Non-competitive inhibition of full-length recombinant human MMP-13 assessed as fTHP-15 substrate hydrolysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCollagenase 3(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50:  3.40E+3nMAssay Description:Non-competitive inhibition of full-length recombinant human MMP-13 assessed as fTHP-15 substrate hydrolysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50361639(CHEMBL1371684)
Affinity DataIC50:  3.70E+3nMAssay Description:Inhibition of CYP1A2 (unknown origin) using tacrin substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154530(1-(4-methylbenzenesulfonyl)-2-(4-methylphenyl)-6-[...)
Affinity DataIC50:  4.50E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154542(5-(bromomethyl)-6-(4-(tert-butyl)phenyl)-2-(p-toly...)
Affinity DataIC50:  4.60E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50314726(1-(thiazol-2-yl)ethanone O-4-fluorobenzoyl oxime |...)
Affinity DataIC50:  5.70E+3nMAssay Description:Displacement of fluorophosphate-rhodamine from RBBP9 transfected in human HEK293T cells proteomes after 30 mins by SDS-PAGE gel fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50:  6.50E+3nMAssay Description:Inhibition of CYP2C19 (unknown origin) using (S)-mephentoin substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154541(N-allyl-2-(4-(tert-butyl)phenyl)-6-(p-tolyl)-1-tos...)
Affinity DataIC50:  7.50E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154543(N-((2-(4-(tert-butyl)phenyl)-6-(p-tolyl)-1-tosyl-1...)
Affinity DataIC50:  7.60E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50216297(6',7',10,11-tetramethoxyemetan | CHEMBL50588 | Eme...)
Affinity DataIC50:  7.80E+3nMAssay Description:Displacement of fluorophosphate-rhodamine from RBBP9 transfected in human HEK293T cells proteomes after 30 mins by SDS-PAGE gel fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50361639(CHEMBL1371684)
Affinity DataIC50:  7.90E+3nMAssay Description:Inhibition of CYP2C19 (unknown origin) using (S)-mephentoin substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154533(2-(3-chlorophenyl)-1-(4-methylbenzenesulfonyl)-6-(...)
Affinity DataIC50:  8.20E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50:  8.60E+3nMAssay Description:Inhibition of CYP1A2 (unknown origin) using tacrin substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50361639(CHEMBL1371684)
Affinity DataIC50:  8.80E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin) using diclofenac substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine hydrolase RBBP9(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50314724(1-(thiazol-2-yl)ethanone O-4-methoxybenzoyl oxime ...)
Affinity DataIC50:  9.20E+3nMAssay Description:Displacement of fluorophosphate-rhodamine from RBBP9 transfected in human HEK293T cells proteomes after 30 mins by SDS-PAGE gel fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154538(2-(4-(tert-butyl)phenyl)-N-cyclopropyl-6-(p-tolyl)...)
Affinity DataIC50:  9.30E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154532(2-(3-chlorophenyl)-6-(4-ethylphenyl)-1-(4-methylbe...)
Affinity DataIC50:  9.40E+3nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154537(2-(4-(tert-butyl)phenyl)-N-methyl-6-(p-tolyl)-1-to...)
Affinity DataIC50: >1.00E+4nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154544(Methyl-2-(4-(tert-butyl)phenyl)-6-(p-tolyl)-1-tosy...)
Affinity DataIC50: >1.00E+4nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Mus musculus (Mouse))
University Of California Berkeley

LigandPNGBDBM154539(2-(4-(tert-butyl)phenyl)-N-cyclohexyl-6-(p-tolyl)-...)
Affinity DataIC50: >1.00E+4nMpH: 7.5Assay Description:For in vitro experiments, proteomes were diluted to 1 mg/mL in PBS (pH 7.5, 50 μL total reaction volume), doped with 1 μM recombinant PAFAH...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50:  1.90E+4nMAssay Description:Inhibition of CYP2C9 (unknown origin) using diclofenac substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin) using testosterone substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C8(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of CYP2C8 (unknown origin) using amodiaquine substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2B6(Homo sapiens (Human))
Translational Research Institute

Curated by ChEMBL
LigandPNGBDBM50031314(CHEMBL473326)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of CYP2B6 (unknown origin) using bupropion substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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