Elafibranor(GFT505) (DC10727) chemical structure
Chemical structureResearch use only
CAT. NO. DC10727Featured

Elafibranor(GFT505)

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Product overview

Description & Application

Elafibranor (GFT505) is a dual PPARα/δ agonist used in hepatic lipid metabolism, inflammation and fibrosis research.

ParameterValue
Chemical NameElafibranor
CAS No.923978-27-2
SynonymsGFT505; elafibranor E; GFT-505; Elafibranor(GFT505); Elafibranor; Elafibranor [USAN]; 2J3H5C81A5; Elafibranor (USAN); (E)-2-(2,6-dimethyl-4-(3-(4-(methylthio)phenyl)-3-oxoprop-1-enyl)phenoxy)-2-methylpropanoic acid; Elafibranor [INN]; GFT 505; 2-[2,6-dimethyl-4-[(E)-3-(4-methylsulfanylphenyl)-3-oxoprop-1-enyl]phenoxy]-2-methylpropanoic acid; BCP19067; s3720; DB05187; SB16790; (E)-2-(2,6-dimethyl-4-(3-(4-(methylthio)phenyl)-3-oxoprop-1-en-1-yl)phenoxy)-2-methylpropanoic acid; 2-{2,6-dimethyl-4-[(1E)-3-[4-(methylsulfanyl)phenyl]-3-oxoprop-1-en-1-yl]phenoxy}-2-methylpropanoic acid; SureCN815512; S; 2-[2,6-Dimethyl-4-[(1E)-3-[4-(methylthio)phenyl]-3-oxo-1-propen-1-yl]phenoxy]-2-methylpropanoic acid (ACI); (E)-1-[4-(Methylthio)phenyl]-3-[3,5-dimethyl-4-[(carboxydimethylmethyl)oxy]phenyl]prop-2-en-1-one
FormulaC22H24O4S
M.Wt384.488565444946
SMILESO(C1C(C)=CC(/C=C/C(C2C=CC(SC)=CC=2)=O)=CC=1C)C(C)(C)C(=O)O
PurityOn request
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
PPARα / PPARδ · Literature evidence

Biological Activity

Elafibranor (GFT505) is a dual PPARα/δ agonist used in hepatic lipid metabolism, inflammation and fibrosis research. Triglyceride content and Oil Red O staining evaluated the lipid response. The retrieved methods do not specify the subsequent GFT505 incubation duration.

In Vitro

EndpointModel / conditions / sourceReported result
Cellular lipid accumulationLO2 hepatic cells loaded with oleate/palmitate (0.8 mM total, 2:1) for 24 h, then exposed to GFT505 7.5 or 15 µM. [1], MethodsTriglyceride content and Oil Red O staining evaluated the lipid response. The retrieved methods do not specify the subsequent GFT505 incubation duration.

In Vivo

EndpointModel / conditions / sourceReported result
Diet-induced liver diseaseMale C57BL/6J mice on CDAHFD; GFT505 3, 10 or 30 mg/kg from weeks 5–12; n=10 per group. [1]The paper assessed established diet-induced steatosis, inflammation and fibrosis. Route and dosing frequency were not explicit in the reviewed methods.
Histology and biomarkersLiver histology, α-SMA/collagen-I and serum biochemistry. [1]Elafibranor improved steatosis, inflammatory changes and fibrosis-related measurements.
Transcriptomic responseTreated mouse liver RNA sequencing. [1]Broad changes in metabolic and inflammatory pathways accompanied histological responses; pathway enrichment is not a direct binding assay.

Interpretation

These model-specific responses do not establish equivalent effects in all steatohepatitis models.

Original studies

References

  1. Liu L, et al. The pharmacodynamic and differential gene expression analysis of PPAR α/δ agonist GFT505 in CDAHFD-induced NASH model. PloS one (2020).

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

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