Salidroside
(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。
Cas No.:10338-51-9
Sample solution is provided at 25 µL, 10mM.
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]。
Cell experiment [1]: |
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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. |
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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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
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 |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
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% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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Quality Control & SDS
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- Purity: >98.50%
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