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BioAssay: AID 743226

qHTS assay to identify small molecule antagonists of the peroxisome proliferator-activated receptor delta (PPARd) signaling pathway: Summary

The peroxisome proliferator-activated receptors (PPARs) are lipid-activated transcription factors of the nuclear receptor superfamily with three distinct subtypes namely PPAR alpha, PPAR delta (PPARd) and PPAR gamma. All these subtypes heterodimerizes with Retinoid X receptor (RXR) and have different physiological functions. Although the function of PPAR delta, is less well known until recently, more ..
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 Tested Compounds
 Tested Compounds
All(7343)
 
 
Active(84)
 
 
Inactive(6378)
 
 
Inconclusive(1083)
 
 
 Tested Substances
 Tested Substances
All(9315)
 
 
Active(92)
 
 
Inactive(7990)
 
 
Inconclusive(1233)
 
 
AID: 743226
Data Source: Tox21 (PPARDN146)
BioAssay Type: Summary, Candidate Probes/Leads with Supporting Evidence
Depositor Category: Other
Deposit Date: 2013-12-17

Data Table ( Complete ):           Active    All
Target
BioActive Compounds: 84
Depositor Specified Assays
AIDNameTypeComment
743215qHTS assay to identify small molecule antagonists of the peroxisome proliferator-activated receptor delta (PPARd) signaling pathwayconfirmatoryPPARd antagonist mode screen
743213qHTS assay to identify small molecule antagonists of the peroxisome proliferator-activated receptor delta (PPARd) signaling pathway - cell viability counter screenconfirmatoryCell viability counter screen
Description:
U.S. Tox21 Program

National Center for Advancing Translational Sciences [NCATS]
NIH Chemical Genomics Center [NCGC]
U.S. Environmental Protection Agency [EPA]
National Institutes of Environmental Health Sciences [NIEHS]
National Toxicology Program [NTP]
U.S. Food and Drug Administration [FDA]

Tox21 Assay Overview:

The peroxisome proliferator-activated receptors (PPARs) are lipid-activated transcription factors of the nuclear receptor superfamily with three distinct subtypes namely PPAR alpha, PPAR delta (PPARd) and PPAR gamma. All these subtypes heterodimerizes with Retinoid X receptor (RXR) and have different physiological functions. Although the function of PPAR delta, is less well known until recently, but the identification of the subtype specific synthetic ligands and the creation of animal models revealed its role in the regulation of cholesterol and lipid metabolism. To identify the compounds that inhibit PPAR-delta signaling, GeneBLAzer PPAR delta UAS-bla HEK293H cell line (Invitrogen, Carlsbad, CA, USA) containing a beta-lactamase reporter gene under the control of an Upstream Activator Sequence (UAS) was used to screen the Tox21 compound library. The cytotoxicity of the Tox21 compound library against the PPARd-bla cell line was tested in parallel by measuring the cell viability using CellTiter-Glo assay in the same wells.
Protocol
Please refer to other AIDs, 743215 and 743213, for detailed assay protocols.
Comment
This summary is written for the purposes of summarizing the compound activities from the project combining the results from both the PPARd antagonist mode assay (AID 743215) and cell viability counter screen (AID 743213). For all inactive compounds, PUBCHEM_ACTIVITY_SCORE is 0. Active compounds have PUBCHEM_ACTIVITY_SCORE between 40 and 100. Potency and efficacy were used for determining relative score. Inconclusive compounds have PUBCHEM_ACTIVITY_SCORE between 5 and 30 determined by phenotype.

Disclaimer:

Although all reasonable efforts have been made to ensure the accuracy and reliability of the data, caution should be exercised when interpreting the results as artifacts are possible from nonspecific effects such as assay signal interference. The curve fitting and activity calls presented here are based on the NCATS analysis methods. Alternative analysis methods and interpretations of the data are available at EPA (http://actor.epa.gov) and NTP (http://tools.niehs.nih.gov/cebs3/ui/).
Result Definitions
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TIDNameDescriptionHistogramTypeUnit
OutcomeThe BioAssay activity outcomeOutcome
ScoreThe BioAssay activity ranking scoreInteger
1Activity SummaryType of compound activity based on both the PPARd antagonist mode screen and the cell viability counter screens.String
2Ratio ActivityType of compound activity in the ratio readout of the PPARd antagonist mode screen.String
3Ratio Potency (uM)The concentration of sample yielding half-maximal inhibition in the ratio readout of the PPARd antagonist mode screen.FloatμM
4Ratio Efficacy (%)Percent inhibition in the ratio readout of the PPARd antagonist mode screen.Float%
5530 nm ActivityType of compound activity in the 530 nm readout of the PPARd antagonist mode screen.String
6530 nm Potency (uM)The concentration of sample yielding half-maximal inhibition in the 530 nm readout of the PPARd antagonist mode screen.FloatμM
7530 nm Efficacy (%)Percent inhibition in the 530 nm readout of the PPARd antagonist mode screen.Float%
8460 nm ActivityType of compound activity in the 460 nm readout of the PPARd antagonist mode screen.String
9460 nm Potency (uM)The concentration of sample yielding half-maximal inhibition in the 460 nm readout of the PPARd antagonist mode screen.FloatμM
10460 nm Efficacy (%)Percent inhibition in the 460 nm readout of the PPARd antagonist mode screen.Float%
11Viability ActivityType of compound activity in the cell viability counter screens.String
12Viability Potency (uM)The concentration of sample yielding half-maximal inhibition in the cell viability counter screen.FloatμM
13Viability Efficacy (%)Percent inhibition in the cell viability counter screen.Float%
14Sample SourceWhere sample was obtained.String

Data Table (Concise)
Classification
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