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  3. SDZ 51641

SDZ 51641 是一种具有口服活性的脂肪酸氧化抑制剂。SDZ 51641 可通过降低脂肪酸氧化,进而剥夺糖异生过程所需的能量及辅因子,从而降低糖尿病模型的血糖水平。SDZ 51641 可用于糖尿病的研究。

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SDZ 51641

SDZ 51641 Chemical Structure

CAS No. : 91456-99-4

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

SDZ 51641 is an orally active fatty acid oxidation inhibitor. By reducing fatty acid oxidation, SDZ 51641 deprives the gluconeogenesis process of required energy and cofactors, thereby lowering blood glucose levels in diabetic models. SDZ 51641 can be used in diabetes research[1].

体内研究
(In Vivo)

SDZ 51641(70-100 μmol/kg;口服;1-11 天)在 18 小时禁食正常 Sprague‑Dawley 大鼠与 Streptozotocin (STZ) (HY-13753) 诱导糖尿病大鼠中降低脂肪酸氧化与血糖水平且无外周毒性[1]
SDZ 51641 (700 µmol/kg;口服;每日一次;持续 28 天) 可使正常 Sprague Dawley 大鼠的体重和睾丸重量较对照组降低,同时使肝脏重量升高[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Sprague‑Dawley rats treated STZ[1]
Dosage: 70 µmol/kg
Administration: p.o.; daily; 11 days
Result: Inhibited hepatic fatty acid oxidation, decreased β‑hydroxybutyrate levels, reduced blood glucose production, and lowered serum glucose levels, while avoiding toxic effects on peripheral tissues such as the testes.
分子量

220.31

Formula

C14H20O2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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This equation is commonly abbreviated as: C1V1 = C2V2

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
SDZ 51641
目录号:
HY-182438
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