Wistin, isolated from Caragana sinica roots, is a PPARα and PPARγ agonist[1][2].
体外研究 (In Vitro)
Wistin, is a PPARγ agonist that can induce the mRNA expression of the PPARγ target gene adiponectin in mouse 3T3-L1 cells[2]. Wistin inhibits cellular triglyceride accumulation in hepatocytes (P<0.05 at 10 μg/mL) in a dose-dependent manner[2]. Wistin (10 μg/mL) results in a 2.5-, 7.2-, and 14.8-fold increase in the expression levels of CPT1a, ACO, and ACS, respectively[2]. Treatment with Wistin for 48 h significantly decreases the amount of cellular TG in mouse primary hepatocytes in a dose-dependent manner[2]. Treatment with wistin enhanced the marker of adipocyte differentiation, such as triglyceride accumulation in 3T3-L1 cells[3].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
RT-PCR[2]
Cell Line:
Mouse hepatocytes.
Concentration:
1 or 10 μg/mL.
Incubation Time:
48 h.
Result:
Significantly increased PPARα mRNA levels in a dose-dependent manner.
分子量
460.43
Formula
C23H24O10
CAS 号
19046-26-5
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.
参考文献
[1]. SeonJu Park, et al. Neuraminidase Inhibitors from the Roots of Caragana sinica. Chem Biodivers. 2020 Nov;17(11):e2000470.
[2]. Misato Suzuki, et al. 4′,6-Dimethoxyisoflavone-7-O-β-D-glucopyranoside (wistin) is a peroxisome proliferator-activated receptor α (PPARα) agonist in mouse hepatocytes. Mol Cell Biochem. 2018 Sep;446(1-2):35-41.
[3]. Matoki Sanada, et al. 4′,6-dimethoxyisoflavone-7-O-β-D-glucopyranoside (wistin) is a peroxisome proliferator-activated receptor γ (PPARγ) agonist that stimulates adipocyte differentiation. Anim Sci J. 2016 Nov;87(11):1347-1351.
Oroxin A 是 Oroxylum indicum(L.)Kurz (紫薇科) 种子提取物 (OISE) 的主要成分。Oroxin A 是 PPARγ 的部分激动剂,可激活 PPARγ 转录。Oroxin A 通过对接 PPARγ 的蛋白配体结合区域起到激活作用。Oroxin A 对 α-葡萄糖苷酶有抑制活性,具有抗氧化能力。Oroxin A 具有可用于癌症研究。
Oroxin A Chemical Structure
CAS No. : 57396-78-8
规格
价格
是否有货
数量
5 mg
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¥1680
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50 mg
询价
100 mg
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生物活性
Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2].
IC50 & Target[1]
PPARγ
体外研究 (In Vitro)
Oroxin A (0.5- 100 μM; 24 hours) significantly increases the PPARγ transcription level and exhibits the strongest activation with 50 μM in HEK-293t cells[1].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
432.38
Formula
C21H20O10
CAS 号
57396-78-8
运输条件
Room temperature in continental US; may vary elsewhere.
将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
*以上所有助溶剂都可在 MCE 网站选购。
参考文献
[1]. Sun W, et al. Oroxin A from Oroxylum indicum prevents the progression from prediabetes to diabetes in streptozotocin and high-fat diet induced mice. Phytomedicine. 2018 Jan 1;38:24-34.
[2]. He J, et al. Oroxin A inhibits breast cancer cell growth by inducing robust endoplasmic reticulum stress and senescence. Anticancer Drugs. 2016 Mar;27(3):204-15.