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MBX-8025 (sodium salt) Sale

目录号 : GC46168

A PPARδ agonist

MBX-8025 (sodium salt) Chemical Structure

规格 价格 库存 购买数量
1mg
¥479.00
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5mg
¥1,559.00
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10mg
¥2,878.00
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25mg
¥5,996.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

MBX-8025 is an agonist of peroxisome proliferator-activated receptor δ (PPARδ).1 It is greater than 750- and 2,500-fold selective for PPARδ over PPARα and PPARγ. MBX-8025 (10 mg/kg per day for eight weeks) reduces increases in fasting blood glucose and serum insulin levels, and decreases insulin resistance in Alms1 mutant (foz/foz) mice fed an atherogenic diet as a model of diet-induced obesity, type 2 diabetes, and non-alcoholic steatohepatitis (NASH).2 It also decreases serum alanine transaminase (ALT), as well as serum and hepatic cholesterol and triglyceride, levels and reduces markers of NASH in the same model.

|1. Bays, H.E., Schwartz, S., Littlejohn, T., 3rd, et al. MBX-8025, a novel peroxisome proliferator receptor-δ agonist: Lipid and other metabolic effects in dyslipidemic overweight patients treated with and without atorvastatin. J. Clin. Endocrinol. Metab. 96(9), 2889-2897 (2011).|2. Haczeyni, F., Wang, H., Barn, V., et al. The selective peroxisome proliferator-activated receptor-delta agonist seladelpar reverses nonalcoholic steatohepatitis pathology by abrogating lipotoxicity in diabetic obese mice. Hepatol. Commun. 1(7), 663-674 (2017).

Chemical Properties

Cas No. N/A SDF
Canonical SMILES FC(F)(F)C1=CC=C(OC[C@@H](OCC)CSC2=CC=C(OCC([O-])=O)C(C)=C2)C=C1.[Na+]
分子式 C21H22F3O5S • Na 分子量 466.4
溶解度 Soluble in DMSO 储存条件 Store at -20°C
General tips 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.1441 mL 10.7204 mL 21.4408 mL
5 mM 0.4288 mL 2.1441 mL 4.2882 mL
10 mM 0.2144 mL 1.072 mL 2.1441 mL
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