Siamenoside I ( —— )

产品货号. M22822 CAS No. 126105-12-2

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

产品询价大包装询价加入购物车

产品名称

Siamenoside I
注意事项

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
产品简述

Siamenoside I是一种天然产物，是具有多种生物活性的罗汉果苷之一，具有麦芽糖酶抑制作用，IC50值为12 mM。
产品描述

Siamenoside I is a natural product,and is one of the mogrosides that has several kinds of bioactivities, it exhibits maltase inhibitory effect with the IC50 value of 12 mM.Siamenoside I is the sweetest mogroside that has several kinds of bioactivities, and it is also a constituent of Siraitiae Fructus, a fruit and herb in China.?In rats, siamenoside I was found to undergo deglycosylation, hydroxylation, dehydrogenation, deoxygenation, isomerization, and glycosylation reactions.
体外实验

——
体内实验

In rat, the metabolic reactions of siamenoside I include deglycosylation, hydroxylation, dehydrogenation, deoxygenation, isomerization, and glycosylation. Siamenoside I and its metabolites are mainly distributed to the intestines, stomach, kidneys, and brain.
同义词

——
通路

Others
靶点

Other Targets
受体

Others
研究领域

——
适应症

——

CAS Number

126105-12-2
分子量

1125.29
分子式

C54H92O24
纯度

>98% (HPLC)
溶解度

In Vitro:?DMSO : 100 mg/mL (88.87 mM)
SMILES

C[C@@]([C@@](CC[C@H](O[C@]([C@@H]([C@@H](O)[C@@H]1O)O)([H])O[C@@H]1CO)C2(C)C)([H])C2=CC3)([C@@H](C[C@@]45C)O)[C@]3([H])[C@@]4(CC[C@]5([H])[C@H](C)CC[C@H](C(C)(O)C)O[C@H](O[C@H](CO[C@@H]([C@@H]([C@@H](O)[C@@H]6O)O)O[C@@H]6CO)[C@@H](O)[C@@H]7O)[C@@H]7O[C@]([C@@H]([C@@H](O)[C@@H]8O)O)([H])O[C@@H]8CO)C
化学全称

——

1.Sweet elements of Siraitia grosvenori inhibit oxidative modification of low-density lipoprotein.J Atheroscler Thromb. 2002;9(2):114-20.

计算器

产品手册

关联产品

Ampelopsin G

Ampelopsin G is a natural product for research related to life sciences.
GRP (porcine)

Mammalian bombesin-like peptide neurotransmitter that is an agonist for the gastrin-releasing peptide receptor (GRPR). GRP has been reported to activate GABAergic interneurons in the amygdala leading to increased GABA release and fear suppression in mice in vivo. Also involved in mitogenesis, and GI tract and appetite regulation.
JG-2016

JG-2016 是一种有效的组蛋白乙酰转移酶 1 (HAT1) 抑制剂，在 HAT1 乙酰化检测中 IC50 为 14.8 μM[1]。