FENOFIBRATE

Fenofibrate activates PPAR‑α to lower triglycerides and increase HDL cholesterol. Side effects include liver enzyme elevation, muscle pain, and gastrointestinal upset.

SKU: 3806e22b35c2 Category: Tag:

Product Description


Mechanism of Action

This compound (ID 26118) acts through multi-pathway biochemical modulation, influencing cellular signalling, enzyme regulation, and structural protein dynamics. Its mechanistic profile includes receptor-level interactions, post‑translational modification control and targeted metabolic pathway influence.

Benefits and Advantages

Applications include advanced research modelling, pathway‑specific modulation, validation of pharmacodynamic targets, and high-precision experimental development in biochemical and clinical pre‑formulation environments.

Side Effects and Risks

Potential risks may include cellular stress responses, metabolic burden imbalance, receptor overstimulation or suppression, and dose‑dependent toxicity. Use under controlled laboratory conditions only.

Datasheet


Molecular Formula

C20H21ClO4

Molecular Weight

360.8 g/mol

CAS Number

49562-28-9

Storage Condition

Store at 25 °C (77 °F); excursions permitted to 15-30 °C (59-86 °F). … Protect from moisture.

Solubility

Practically insoluble in water; slightly soluble in methanol, ethanol; soluble in acetone, ether, benzene, chloroform

Purity

Purity information is available upon request (COA).

Synonym

fenofibrate; 49562-28-9; Procetofen; Tricor; Lipantil

IUPAC/Chemical Name

propan-2-yl 2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoate

InChl Key

YMTINGFKWWXKFG-UHFFFAOYSA-N

InChl Code

InChI=1S/C20H21ClO4/c1-13(2)24-19(23)20(3,4)25-17-11-7-15(8-12-17)18(22)14-5-9-16(21)10-6-14/h5-13H,1-4H3

References

https://pubchem.ncbi.nlm.nih.gov/compound/3339;

3D Conformer.

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