Comparison

Gemfibrozil European Partner

Item no. TMO-T1415-10mM
Manufacturer TargetMol
CASRN 25812-30-0
Amount 1 mL x 10 mM (in DMSO)
Quantity options 100 mg 1 mL x 10 mM (in DMSO) 10 mg 1 mL 200 mg 25 mg 2 mg 50 mg
Category
Type Molecules
Specific against other
Purity 0,98
Smiles CC1=CC(OCCCC(C)(C)C(O)=O)=C(C)C=C1
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias Lopid,Decrelip,Jezil,CI-719
Shipping Condition Cool pack
Available
Manufacturer - Targets
PPAR|||Cytochromes P450|||Adrenergic Receptor
Shipping Temperature
Cool pack
Storage Conditions
-20
Molecular Weight
250.33
Description
Gemfibrozil (CI-719) interacts with peroxisome proliferator-activated receptors (PPARalpha) resulting in PPARalpha-mediated stimulation of fatty acid oxidation and an increase in lipoprotein lipase (LPL) synthesis. Gemfibrozil is a fibric acid derivative with hypolipidemic effects. This enhances triglyceride-rich lipoprotein clearance and reduces the expression of apolipoprotein C-III (apoC-III). The reduction in hepatic production of apoC-III result in the subsequent reduction of serum levels of very-low-density-lipoprotein cholesterol (VLDL-C). In addition, gemfibrozil-mediated PPARalpha stimulation of apoA-I and apoA-II expression results in an increase in high-density lipoprotein cholesterol (HDL-C).
Pathways
Metabolism|||DNA Damage/DNA Repair|||GPCR/G Protein|||Neuroscience
Formulate
C15H22O3

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 mL x 10 mM (in DMSO)
Available: In stock
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