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Sennoside A/番泻苷A {[allProObj[0].p_purity_real_show]}

货号:A559275 同义名: 番泻叶苷A / NSC 112929

Sennoside A是一种从大黄根茎提取的刺激性泻药,能够引起肠道通便作用。它也抑制HIV-1逆转录酶和核糖核酸酶 H,IC50分别为1.9 μM和5.3 μM。

Sennoside A/番泻苷A 化学结构 CAS号:81-27-6
Sennoside A/番泻苷A 化学结构
CAS号:81-27-6
Sennoside A/番泻苷A 3D分子结构
CAS号:81-27-6
Sennoside A/番泻苷A 化学结构 CAS号:81-27-6
Sennoside A/番泻苷A 3D分子结构 CAS号:81-27-6
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Sennoside A/番泻苷A 纯度/质量文件 产品仅供科研

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Sennoside A/番泻苷A 生物活性

靶点
  • MAO

    MAO, IC50:17 μM

描述 Sennoside A (SA) is a natural dianthrone glycoside mainly from medicinal plants of Senna and Rhubarb. SA possesses numerous pharmacological properties, such as laxative, anti-obesity, hypoglycemic, hepatoprotective, anti-fibrotic, anti-inflammatory, anti-tumor, anti-bacterial, anti-fungal, anti-viral, and anti-neurodegenerative activities[3]. Sennoside A is a new scaffold for the development of HIV-1 dual RT (Reverse Transcriptase) inhibitors. Sennoside A also affected HIV-1 IN activity in vitro and HIV-1 replication in cell-based assays[4]. Plasma GLP-1 (Glucagon-like peptide-1) and insulin were markedly elevated by SA (Sennoside A) at the dosage of 45 mg/kg/day. Meanwhile, the increased phosphorylation status of EKR1/2 and prohormone convertase 1/3 (PC1/3) proteins were observed in the colon of SA-treated mice[5]. Sennoside A administration markedly improved the indices in T2D mice and obesity-related traits including blood glucose level, body weight, lipid metabolism disorder, and insulin resistance. Sennoside A also reduced inflammation and increased tight junction proteins in the ileum in gene-deficient mice via gut microbiota alteration[6].

Sennoside A/番泻苷A 参考文献

[1]Kobayashi M, Yamaguchi T, et al. Regionally differential effects of sennoside A on spontaneous contractions of colon in mice. Basic Clin Pharmacol Toxicol. 2007 Aug;101(2):121-6.

[2]Hiraoka A, Koike S, et al. The sennoside constituents of rhei rhizoma and sennae folium as inhibitors of serum monoamine oxidase. Chem Pharm Bull (Tokyo). 1989 Oct;37(10):2744-6.

[3]Le J, Ji H, Zhou X, Wei X, Chen Y, Fu Y, Ma Y, Han Q, Sun Y, Gao Y, Wu H. Pharmacology, Toxicology, and Metabolism of Sennoside A, A Medicinal Plant-Derived Natural Compound. Front Pharmacol. 2021 Oct 26;12:714586

[4]Esposito F, Carli I, Del Vecchio C, Xu L, Corona A, Grandi N, Piano D, Maccioni E, Distinto S, Parolin C, Tramontano E. Sennoside A, derived from the traditional chinese medicine plant Rheum L., is a new dual HIV-1 inhibitor effective on HIV-1 replication. Phytomedicine. 2016 Nov 15;23(12):1383-1391

[5]Ma L, Cao X, Ye X, Ye J, Sun Y. Sennoside A Induces GLP-1 Secretion Through Activation of the ERK1/2 Pathway in L-Cells. Diabetes Metab Syndr Obes. 2020 Apr 29;13:1407-1415

[6]Wei Z, Shen P, Cheng P, Lu Y, Wang A, Sun Z. Gut Bacteria Selectively Altered by Sennoside A Alleviate Type 2 Diabetes and Obesity Traits. Oxid Med Cell Longev. 2020 Jun 25;2020:2375676

Sennoside A/番泻苷A 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.16mL

0.23mL

0.12mL

5.80mL

1.16mL

0.58mL

11.59mL

2.32mL

1.16mL

Sennoside A/番泻苷A 技术信息

CAS号81-27-6
分子式C42H38O20
分子量 862.74
SMILES Code O=C(C(C=C1[C@H]([C@@H]2C3=C(C(O[C@H]4[C@@H]([C@H]([C@@H]([C@@H](CO)O4)O)O)O)=CC=C3)C(C5=C(O)C=C(C(O)=O)C=C25)=O)C6=C7C(O[C@H]8[C@@H]([C@H]([C@@H]([C@@H](CO)O8)O)O)O)=CC=C6)=CC(O)=C1C7=O)O
MDL No. MFCD00151527
别名 番泻叶苷A ;NSC 112929
运输蓝冰
InChI Key IPQVTOJGNYVQEO-KGFNBKMBSA-N
Pubchem ID 73111
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, 2-8°C

溶解方案

DMSO: 120 mg/mL(139.09 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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