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Salidroside Sale

(Synonyms: 红景天苷; Rhodioloside) 目录号 : GN10127

红景天苷是一种具有多种生物活性的糖苷,具有抗癌、抗氧化、抗衰老、抗糖尿病、抗糖尿病、抗高血压、抗炎、免疫调节等药理作用。

Salidroside Chemical Structure

Cas No.:10338-51-9

规格 价格 库存 购买数量
10mM (in 1mL Water)
¥424.00
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5mg
¥385.00
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10mg
¥616.00
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Description

Salidroside is a tyrosol glycoside primarily found in the roots of Rhodiola species, exhibiting a wide range of biological and pharmacological properties, including anti-cancer, antioxidant, anti-aging, anti-diabetic, anti-hypertensive, anti-inflammatory, and immunomodulatory effects. Salidroside can improve muscle nutrition by increasing the expression of mTOR, p-mTOR, and MyHC[1]. It alleviates cachexia symptoms in a mouse model of cancer cachexia by activating the mTOR signaling pathway[1]. Furthermore, salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy[2]. Its anti-cancer activity is primarily due to the inhibition of the PI3K/AKT, JAK/STAT, and MEK/ERK pathways, as well as the activation of cell apoptosis and autophagy[3].

In vitro, salidroside significantly increases the expression of mTOR, p-mTOR, and MyHC in C2C12 myotubes and can effectively rescue the downregulation of mTOR, p-mTOR, and MyHC expression induced by tumor necrosis factor-alpha[1]. Salidroside (10, 25, and 50µM) significantly prevents MPP+-induced cytotoxicity and reverses the reduction in dopamine, HVA, and DOPAC levels induced by MPTP in the striatum[2]. Additionally, salidroside (100µM) inhibits the activity of prolyl endopeptidase (PEP), an enzyme associated with learning and memory, by 10.6±1.9%[4].

In vivo, salidroside (120 mg/kg/day; i.p.) significantly maintains fat mass and increases lean body mass, especially the mass of the gastrocnemius muscle, indicating a notable improvement in the main features of cancer-associated cachexia in mice[1]. Salidroside (10/20/40 mg/kg/day) also induces a mouse model of testicular damage[5].

References:
[1] Chen X, et al. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activatingmTOR signalling. J Cachexia Sarcopenia Muscle. 2016 May;7(2):225-32.
[2]Li R, et al. Salidroside Protects Dopaminergic Neurons by Enhancing PINK1/Parkin-Mediated Mitophagy. Oxid Med Cell Longev. 2019 Sep 10; 2019: 9341018.
[3] Zhifeng Z , Jing H , Jizhou Z ,et al.Pharmacological activities, mechanisms of action, and safety of salidroside in the central nervous system[J].Drug Design Development & Therapy, 2018, 12:1479-1489.
[4] Fan W, et al. Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis. Chem Pharm Bull (Tokyo). 2001 Apr;49(4):396-401.
[5] Wang Z, et al. Salidroside Ameliorates Furan-Induced Testicular Inflammation in Relation to the Gut-Testis Axis and Intestinal Apoptosis. J Agric Food Chem. 2023 Nov 9.

红景天苷是一种主要存在于红景天属植物根中的酪醇糖苷。它具有多种生物学和药理学特性,如抗癌,抗氧化,抗衰老,抗糖尿病,抗糖尿病,抗高血压,抗炎,免疫调节等。 红景天苷可以通过增加mTOR,p-mTOR和MyHC表达来改善肌肉营养[1]。红景天苷可通过激活 mTOR 信号缓解肿瘤恶病质小鼠模型中的恶病质症状[1]。红景天苷还能通过增强 PINK1/Parkin 介导的线粒体自噬来保护多巴胺能神经元[2]。红景天苷对PI 3 k/AKT、JAK/ STAT和MEK/ERK通路的抑制以及对细胞凋亡和自噬的激活是其抗癌活性的主要原因[3]

 

在体外,红景天苷不仅能明显增加C2C12肌管中mTOR、p-mTOR和MyHC的表达,而且能有效挽救肿瘤坏死因子-α诱导的mTOR、p-mTOR和MyHC表达下调[1]。红景天苷(10、25和50 μM)显著防止了MPP +诱导的细胞毒性。红景天苷还逆转了纹状体中MPTP诱导的多巴胺、HVA和DOPAC水平的降低[2]。此外,红景天苷(100 μM) 抑制脯氨酰内肽酶 (PEP) 活性 (10.6±1.9%),该酶被认为与学习和记忆有关[4]

 

在体内,红景天苷(120 mg/kg/day; i.p.)能显着地保持脂肪量并增加无肿瘤体重,尤其是腓肠肌的质量,这表明红景天苷可以明显改善小鼠CAC的主要特征[1]。红景天苷(10/20/40 mg/kg/day) 还可诱导的小鼠睾丸损伤模型[5]

实验参考方法

Cell experiment [1]:

Cell lines

MN9D cells

Preparation method

MN9D cells were cultured in RPMI medium with 10% FBS in a humidified atmosphere incubator of 5% CO2 at 37°C. The cells were pretreated with Salidroside(10, 25, and 50 μM) for 24 h and incubated with 200 μM of MPP+ for an additional 24 h based on a previous dose-effect study

Reaction Conditions

0, 25, 50 μM; 24 h

Applications

200 μM of MPP+ remarkably reduced the cell viability, and  Salidroside (10, 25, and 50 μM) markedly prevented the cell toxicity induced by MPP+.

Animal experiment [2]:

Animal models

BABL/c and C57BL/6 mice

Preparation method

BABL/c mice were inoculated with CT-26 cells (1.0×106/100 μL), while C57BL/6 mice with LLC cells (7×105/100 μL), both of them were injected s.c. into the right flank. Nine days after inoculation, tumours were palpable (about 5 mm in diameter) in BABL/c and C57BL/6 mice, respectively. Treatments were given i.p. with the control group, salidroside (60 mg/kg/day), and salidroside (120 mg/kg/day) for 25 days in BABL/c tumour model, while for 20 days in C57BL/6 model.

Dosage form

60 mg/kg/day、120 mg/kg/day; i.p.

Applications

salidroside had an effective anti-cachexia activity in CAC models in vivo, including increasing quality of life and prolonging survival time.

References:

[1]Li R, et al. Salidroside Protects Dopaminergic Neurons by Enhancing PINK1/Parkin-Mediated Mitophagy. Oxid Med Cell Longev. 2019 Sep 10; 2019: 9341018.  

[2] Chen X, et al. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activatingmTOR signalling. J Cachexia Sarcopenia Muscle. 2016 May;7(2):225-32.

化学性质

Cas No. 10338-51-9 SDF
别名 红景天苷; Rhodioloside
化学名 (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol
Canonical SMILES C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O
分子式 C14H20O7 分子量 300.3
溶解度 ≥ 30mg/mL in DMSO,≥100 mg/mL in Water.Measured 储存条件 4°C, protect from light
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1 mg 5 mg 10 mg
1 mM 3.33 mL 16.65 mL 33.3 mL
5 mM 0.666 mL 3.33 mL 6.66 mL
10 mM 0.333 mL 1.665 mL 3.33 mL
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