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Gemfibrozil
Cat. No.:
0225LY-0905
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, HPLC, and LC-MS.
Size:
Add to basket
Product Overview
Description:
Gemfibrozil is a fibric acid derivative that lowers lipid levels by stimulating PPARalpha-mediated fatty acid oxidation and lipoprotein lipase (LPL) synthesis; this process reduces apoC-III expression, leading to lower VLDL-C serum levels and an increase in HDL-C through the stimulation of apoA-I and apoA-II.
Synonym:
CI-719; Jezil; Decrelip; Lopid; 25812-30-0; 5-(2,5-Dimethylphenoxy)-2,2-dimethylpentanoic acid; Lipur; Cholespid; Fibratol; Fibrocit; Gemfibril; Gemfibromax; Gemlipid; Hipolixan; CI-719; Gemfibrozilo; Gemfibrozilum; Renabrazin; Clearol; Elmogan; Fetinor; Gemnpid; Innogen; Ipolipid; Lanaterom; Lifibron; Lipigem; Lipizyl; Micolip; Normolip; Progemzal; Reducel; Regulip; Sinelip; Synbrozil; Taborcil; Tentroc; Brozil; Gozid; Hidil; Lipira; Gemd; Gevilon Uno; WL-Gemfibrozil; Gen-Fibro; Pentanoic acid, 5-(2,5-dimethylphenoxy)-2,2-dimethyl-; Low-Lip; Gem-S; Lipozid; 2,2-Dimethyl-5-(2,5-xylyloxy)valeric acid; 2,2-Dimethyl-5-(2,5-xylyloxy)valeriansaeure
CAS No.:
25812-30-0
Compound CID:
3463
Formula:
C15H22O3
Formula Weight:
250.33
Specification
Targets&IC50:
2C19: 24 μM(Ki); 1A2: 82 μM(Ki); CYP2C9: 5.8 μM(Ki); 2C8: 69 μM(Ki)
Relative Density:
1.044 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Gemfibrozil can be used in cardiovascular studies to explore the modulation of triglyceride levels and its impact on atherosclerosis progression.
Library Information
Target:
PPAR; Adrenergic receptor; P450
Receptor:
CYP1A2; CYP2C9; Cytochrome P450; PPARα
Pathways:
DNA damage/DNA repair; Metabolism; Neuronal signaling; GPCR/G protein signaling
Plate Number:
AOCL-12
Plate Location:
f5
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
250 mg/mL; 998.68 mM
Ethanol Max Solubility:
47 mg/mL; 187.75 mM
ALogP:
4.172
HBA_Count:
2
HBD_Count:
0
Rotatable Bond:
6





