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Acipimox

SKU: orb1224877

Description

Acipimox is a niacin derivative used as a hypolipidemic agent. It is used in low doses and may have less marked adverse effects, although it is unclear whether the recommended dose is as effective as are standard doses of nicotinic acid. Acipimox inhibits the production of triglycerides by the liver and the secretion of VLDL, which leads indirectly to a modest reduction in LDL and increase in HDL. Long-term administration is associated with reduced mortality, but unwanted effects limit its clinical use. (In Vitro):Acipimox (0-100 μM; 0-4 hours) enhances leptin release from adipocytes isolated from Sprague-Dawley rats in a time- and dose- dependent manner.Acipimox (10 mM) stimulats leptin release in adipocytes from Streptozotocin (STZ)-treated and Zucker diabetic fat (ZDF) rats.(In Vivo):Acipimox (50 mg/kg; i.p.) significantly lowers circulating free fatty acid (FFA) and glucose in high-fat fed mice.

Research Area

Pharmacology & Drug Discovery

Images & Validation

Key Properties

CAS Number51037-30-0
MW154.13
Purity>98% (HPLC)
FormulaC6H6N2O3
SMILESO=C(C1=C[N+]([O-])=C(C)C=N1)O
Targettriglycerides production
SolubilityDMSO: 31 mg/mL (201.14 mM)

Bioactivity

In Vivo
Acipimox (50 mg/kg; i.p.) significantly lowers circulating free fatty acid (FFA) and glucose in high-fat fed mice. Animal model: Female C57BL/6J mice. Dosage: 50 mg/kg. Administration: Intraperitoneal injection. Result: Reduced circulating levels of FFA and glucose after 3 h.
In Vitro
Acipimox (0-100 μM; 0-4 hours) enhances leptin release from adipocytes isolated from Sprague-Dawley rats in a time- and dose- dependent manner. Acipimox (10 mM) stimulats leptin release in adipocytes from Streptozotocin (STZ)-treated and Zucker diabetic fat (ZDF) rats.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Acipimox | K-9321 | K9321 | K 9321 | Olbemox | Olbetam

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Protocol Information

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