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薯蓣皂素 /Diosgenin {[allProObj[0].p_purity_real_show]}

货号:A136414 同义名: Nitogenin;3β-hydroxy-5-Spirostene

Diosgenin是从姜黄薯 (Dioscorea zingiberensis C.H.Wright) 提取的甾体皂苷,是类固醇激素的重要天然来源。Diosgenin 抑制 STAT3 信号通路,并通过激活 Pdia3/ERp57 和调节巨噬细胞 miR-19b 的表达,显示出抗动脉粥样硬化、调节脂质代谢和改善糖尿病的作用。

Diosgenin 化学结构 CAS号:512-04-9
Diosgenin 化学结构
CAS号:512-04-9
Diosgenin 3D分子结构
CAS号:512-04-9
Diosgenin 化学结构 CAS号:512-04-9
Diosgenin 3D分子结构 CAS号:512-04-9
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Diosgenin 纯度/质量文件 产品仅供科研

货号:A136414 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 STAT1 STAT3 STAT5 其他靶点 纯度
Nifuroxazide 98%
Fludarabine 98%
Artesunate 98%
BP-1-102 +++

STAT3, Kd: 504 nM

99%+
Niclosamide ++

STAT3, IC50: 0.7 μM

98%
Napabucasin 98%
Cryptotanshinone ++

STAT3, IC50: 4.6 μM

98%
Stattic +

STAT3, IC50: 5.1 μM

98%
NSC 74859 +

STAT3, IC50: 86 μM

99%+
Ochromycinone 98%
HO-3867 97%
C188-9 ++++

STAT3, Kd: 4.7 nM

99%+
HJC0152 99%
SH5-07 97%
SH-4-54 ++++

STAT3, Kd: 300 nM

+++

STAT5, Kd: 464 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Diosgenin 生物活性

描述 Diosgenin, a steroidal saponin, inhibits the STAT3 signaling pathway[1]. It also acts as an exogenous activator of Pdia3/ERp57[2]. Diosgenin diminishes the progression of aortic atherosclerosis by decreasing macrophage miR-19b expression[5].
体内研究

Additionally, diosgenin significantly reduces fasted and refed blood glucose levels in high-fat diet-fed mice and improves glucose tolerance in the IPGTT[4].

体外研究

At 1 μM in MC65 cells, diosgenin shows protective properties and is considered a potential candidate for compounds targeting Alzheimer's disease (AD) pathology[3].

Diosgenin dose-dependently inhibits the constitutive activation of STAT3 in C3A cells, with maximum inhibition at around 100 μM[1].

At 10 μM, diosgenin significantly decreases miR-19b levels in foam cells after 24 hours[5].

Diosgenin 动物研究

Dose Rat: 50 mg/kg, 100 mg/kg[5] (i.g.); 20 mg/kg - 200 mg/kg[6] (p.o.) Mice: 1 mg/kg - 125 mg/kg[7] (p.o.)
Administration i.g., p.o.

Diosgenin 参考文献

[1]Li F, et al. Diosgenin, a steroidal saponin, inhibits STAT3 signaling pathway leading to suppression of proliferation and chemosensitization of human hepatocellular carcinoma cells. Cancer Lett. 2010 Jun 28;292(2):197-207.

[2]Tohda C, et al. Diosgenin is an exogenous activator of 1,25D₃-MARRS/Pdia3/ERp57 and improves Alzheimer's disease pathologies in 5XFAD mice. Sci Rep. 2012;2:535.

[3]Jeremy E. Chojnacki, et al. Bivalent ligands incorporating curcumin and diosgenin as multifunctional compounds against Alzheimer’s disease. Bioorganic & Medicinal Chemistry, 23 (2015) 7324–7331

[4]Wang X, et al. Effect of diosgenin on metabolic dysfunction: Role of ERβ in the regulation of PPARγ. Toxicol Appl Pharmacol. 2015 Dec 1;289(2):286-96.

[5]Yun-cheng Lv, et al. Diosgenin Inhibits Atherosclerosis via Suppressing the MiR-19b-induced Downregulation of ATP-binding Cassette Transporter A1. Atherosclerosis, 2014, 240(1), 80-89.

Diosgenin 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.41mL

0.48mL

0.24mL

12.06mL

2.41mL

1.21mL

24.12mL

4.82mL

2.41mL

Diosgenin 技术信息

CAS号512-04-9
分子式C27H42O3
分子量 414.62
别名 Nitogenin;3β-hydroxy-5-Spirostene;NSC 33396
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Keep in dark place,Sealed in dry,Room Temperature

溶解方案

无水乙醇: 3 mg/mL(7.24 mM),配合低频超声助溶,注意:无水乙醇开封后,易挥发,也会吸收空气中的水分,导致溶解能力下降,请避免使用开封较久的乙醇

动物实验配方
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