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Sweroside/獐牙菜苷 {[allProObj[0].p_purity_real_show]}

货号:A308538 同义名: 1,9-trans-9,5-cis-Sweroside

Sweroside是一种从Swertia bimaculata草本植物中分离纯化的天然产物,具有强肝脏保护、抗骨质疏松、类胰岛素和创伤愈合作用。它能在300 μM时无细胞毒性地抑制Melan-a细胞中的黑色素生成,并且降低酪氨酸酶、酪氨酸酶相关蛋白1(TRP-1)和TRP-2蛋白的生成。

Sweroside/獐牙菜苷 化学结构 CAS号:14215-86-2
Sweroside/獐牙菜苷 化学结构
CAS号:14215-86-2
Sweroside/獐牙菜苷 3D分子结构
CAS号:14215-86-2
Sweroside/獐牙菜苷 化学结构 CAS号:14215-86-2
Sweroside/獐牙菜苷 3D分子结构 CAS号:14215-86-2
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Sweroside/獐牙菜苷 纯度/质量文件 产品仅供科研

货号:A308538 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 diphenolase monophenolase tyrosinase 其他靶点 纯度
Hexylresorcinol +++

diphenolase, IC50: 0.85 μM

++

monophenolase, IC50: 1.24 μM

+++

monophenolase, IC50: 0.85 μM

diphenolase, IC50: 0.85 μM

99%+
Aloin 98% (mixture of A&B)
Arbutin +

tyrosinase, IC50: 1.09 mM

98%
Monobenzone 98%
Deoxyarbutin ++++

tyrosinase, IC50: 50 nM

98%
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。

Sweroside/獐牙菜苷 生物活性

描述 Sweroside, a natural product isolated and purified from the herbs of Swertia bimaculata with strong hepatoprotective, anti-osteoporotic, insulin-mimicking, and wound-healing effects, can inhibit potent melanogenesis in melan-a cells at 300uM without cytotoxicity, also decreases tyrosinase, tyrosinase-related protein-1 (TRP-1) and TRP-2 protein production in melan a cells.

Sweroside/獐牙菜苷 细胞实验

Cell Line
Concentration Treated Time Description References
SH-SY5Y cells 302.0 ng/mL 24 h To evaluate the effect of Sweroside on the expression of CREB and GAP-43. The results showed that Sweroside significantly increased the expression of CREB and GAP-43 (P<0.01). Drug Des Devel Ther. 2019 Jul 16;13:2357-2370.
Bone marrow-derived macrophages (BMDMs) 100 µM 1 h Inhibited NLRP3 inflammasome activation, reduced IL-1β secretion and caspase-1 (p20) production Int J Mol Sci. 2020 Apr 17;21(8):2790.
H9c2 cardiomyoblast cells 2-20 μM 24 h To evaluate the protective effects of Sweroside on aconitine-induced toxicity in H9c2 cells. Results showed that Sweroside significantly increased cell viability, reduced LDH leakage, and inhibited aconitine-induced oxidative stress and intracellular ROS production. Front Pharmacol. 2018 Oct 25;9:1138.
RAW264.7 cells 20, 40, 80 μM 7 days To investigate the anti-inflammatory effect of sweroside in LPS-induced RAW264.7 cells. Results showed that sweroside significantly inhibited cell proliferation, reduced the production of NO, PGE2, and ROS, and alleviated inflammation by activating SIRT1 to suppress NF-κB and promote FOXO1 signaling pathways. Molecules. 2019 Mar 1;24(5):872.

Sweroside/獐牙菜苷 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 N mice TAC-induced heart failure model Intraperitoneal injection 15, 30, 60 mg/kg Once daily for 8 weeks Sweroside significantly improved cardiac function in TAC-induced mice, increased EF and FS, and reduced myocardial fibrosis and cardiomyocyte hypertrophy. Redox Biol. 2024 Aug;74:103223
C57BL/6J mice ANIT-induced cholestatic liver injury model Oral 120 mg/kg Once daily for 5 consecutive days To evaluate the protective effect of Sweroside on ANIT-induced cholestatic liver injury, results showed that Sweroside attenuated liver injury by restoring bile acid synthesis and transport to normal levels and suppressing pro-inflammatory responses. Acta Pharmacol Sin. 2016 Sep;37(9):1218-28
Zebrafish (Danio rerio) Scopolamine-induced memory deficits model Immersion 2.79, 8.35, and 13.95 nM Once daily for 8 days Sweroside significantly improved the Sco-induced decrease of the cholinergic system activity and brain oxidative stress. These results suggest that sweroside exerts a significant effect on anxiety and cognitive impairment, driven in part by the modulation of the cholinergic system activity and brain antioxidant action. Molecules. 2022 Sep 11;27(18):5901
C57BL/6 mice Methionine-choline-deficient (MCD) diet-induced NASH model Intraperitoneal injection 5 and 30 mg/kg Once daily for two weeks Alleviated hepatic inflammation, fat accumulation, and fibrosis, suppressed hepatic NLRP3 inflammasome activation, and reduced IL-1β and caspase-1 production Int J Mol Sci. 2020 Apr 17;21(8):2790.
Sprague-Dawley rats Aconitine-induced arrhythmia model Intraperitoneal injection 50 mg/kg Once daily for 5 days To evaluate the protective effects of Sweroside on aconitine-induced arrhythmias. Results showed that Sweroside significantly reduced the incidence of arrhythmias and lowered the risk of ventricular fibrillation and sudden death. Front Pharmacol. 2018 Oct 25;9:1138.

Sweroside/獐牙菜苷 参考文献

[1]Jeong YT, Jeong SC, et al. Modulation effects of sweroside isolated from the Lonicera japonica on melanin synthesis. Chem Biol Interact. 2015 Aug 5;238:33-9.

[2]Ozturk N, Korkmaz S, et al. Effects of gentiopicroside, sweroside and swertiamarine, secoiridoids from gentian (Gentiana lutea ssp. symphyandra), on cultured chicken embryonic fibroblasts. Planta Med. 2006 Mar;72(4):289-94.

Sweroside/獐牙菜苷 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.79mL

0.56mL

0.28mL

13.95mL

2.79mL

1.40mL

27.91mL

5.58mL

2.79mL

Sweroside/獐牙菜苷 技术信息

CAS号14215-86-2
分子式C16H22O9
分子量 358.34
SMILES Code O=C1C2=CO[C@@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)[C@H](C=C)[C@]2([H])CCO1
MDL No. MFCD09954487
别名 1,9-trans-9,5-cis-Sweroside
运输蓝冰
InChI Key VSJGJMKGNMDJCI-ZASXJUAOSA-N
Pubchem ID 161036
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Keep in dark place, inert atmosphere, store in freezer, under -20°C

溶解方案

DMSO: 105 mg/mL(293.02 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

H2O: 50 mg/mL(139.53 mM),配合低频超声助溶

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
方案 一
方案 二
方案 三
配制的工作液建议现用现配,短期内尽快用完。 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
方案 一
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