Acipimox sodium structure
|
Common Name | Acipimox sodium | ||
---|---|---|---|---|
CAS Number | 76958-97-9 | Molecular Weight | 176.11 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C6H5N2NaO3 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Acipimox sodiumAcipimox (K-9321) sodium, a nicotinic acid analogue, is an antilipolytic compound. Acipimox sodium stimulates leptin releas, inhibits lipolysis and suppresses systemic levels of free fatty acids (FFAs) and improves insulin sensitivity[1][2][3]. |
Name | Acipimox sodium |
---|
Description | Acipimox (K-9321) sodium, a nicotinic acid analogue, is an antilipolytic compound. Acipimox sodium stimulates leptin releas, inhibits lipolysis and suppresses systemic levels of free fatty acids (FFAs) and improves insulin sensitivity[1][2][3]. |
---|---|
Related Catalog | |
In Vitro | Acipimox sodium (0-100 µM; 0-4 hours) enhances leptin release from adipocytes isolated from Sprague-Dawley rats in a time- and dose- dependent manner[2]. Acipimox sodium (10 mM) stimulats leptin release in adipocytes from Streptozotocin (STZ)-treated and Zucker diabetic fat (ZDF) rats[2]. |
In Vivo | Acipimox sodium (50 mg/kg; i.p.) significantly lowers circulating free fatty acid (FFA) and glucose in high-fat fed mice[3]. Animal Model: Acipimox sodium (50 mg/kg; i.p.) significantly lowers circulating free fatty acid (FFA) and glucose in high-fat fed mice[3]. Dosage: 50 mg/kg Administration: Intraperitoneal injection Result: Reduced circulating levels of FFA and glucose after 3 h. |
References |
Molecular Formula | C6H5N2NaO3 |
---|---|
Molecular Weight | 176.11 |