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Schaftoside/夏佛塔苷 {[allProObj[0].p_purity_real_show]}

货号:A556269 同义名: Apigenin 6-C-glucoside-8-C-arabinoside

Schaftoside是一种在多种中草药中发现的黄酮类化合物。它具有抑制TLR4和Myd88表达的能力。此外,Schaftoside还能降低Drp1的表达和磷酸化水平,并减少线粒体分裂

Schaftoside/夏佛塔苷 化学结构 CAS号:51938-32-0
Schaftoside/夏佛塔苷 化学结构
CAS号:51938-32-0
Schaftoside/夏佛塔苷 3D分子结构
CAS号:51938-32-0
Schaftoside/夏佛塔苷 化学结构 CAS号:51938-32-0
Schaftoside/夏佛塔苷 3D分子结构 CAS号:51938-32-0
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Schaftoside/夏佛塔苷 纯度/质量文件 产品仅供科研

货号:A556269 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Dynamin 其他靶点 纯度
Dynasore ++

Dynamin1/2, IC50: ~15 μM

98%
Mdivi-1 99%+
Hydroxy-Dynasore ++++

DynI (brain), IC50: 0.38 μM

DynI (rec), IC50: 2.3 μM

99%+
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。
产品名称 Autophagy 其他靶点 纯度
SBI-0206965 +++

ULK1, IC50: 108 nM

ULK2, IC50: 711 nM

95%
Hydroxychloroquine sulfate 99%
Valproic acid sodium HDAC 97%
PFK-015 ++

PFKFB3, IC50: 207 nM

99%+
MRT68921 HCl ++++

ULK1, IC50: 2.9 nM

ULK2, IC50: 1.1 nM

99%+
ROC-325 99%+
Autophinib +++

Autophagy, IC50: 40 nM

99%
Lys05 99%+
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。

Schaftoside/夏佛塔苷 生物活性

描述 Schaftoside is a natural product isolated and purified from the herbs of Desmodium styracifolium (Osh.) Merr. with antioxidant and anticancer activities.

Schaftoside/夏佛塔苷 细胞实验

Cell Line
Concentration Treated Time Description References
Human liver microsomes 1 µM, 10 µM 1.5 hours To evaluate the metabolic stability of schaftoside in human liver microsomes. Results showed that after 1.5 h incubation, the remaining amounts of schaftoside were 100.25 ± 1.04% (1μM) and 98.36 ± 1.34% (10 μM) of the initial amounts, indicating poor metabolism of schaftoside in human liver microsomes. Front Pharmacol. 2022 Dec 14;13:1073535
Rat liver microsomes 1 µM, 10 µM 1.5 hours To evaluate the metabolic stability of schaftoside in rat liver microsomes. Results showed that after 1.5 h incubation, the remaining amounts of schaftoside were 102.66 ± 2.41% (1μM) and 97.66 ± 3.30% (10 μM) of the initial amounts, indicating poor metabolism of schaftoside in rat liver microsomes. Front Pharmacol. 2022 Dec 14;13:1073535
Vero E6 cells 11.83 ± 3.23 µM (EC50) 24 hours Evaluate the inhibitory effect of Schaftoside on SARS-CoV-2 virus, showing significant antiviral activity Acta Pharm Sin B. 2022 Nov;12(11):4154-4164
Caco-2 cells 10 µM and 100 µM 3 hours and 5 hours Investigate the metabolism of Schaftoside, results showed that Schaftoside underwent poor metabolism, with only hydroxylated/methoxylated C-glycosides observed as metabolites, and no phase II conjugates containing glucuronic acid or sulfates were detectable. Int J Mol Sci. 2021 Jun 18;22(12):6566

Schaftoside/夏佛塔苷 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Nilaparvata lugens (brown planthopper) 2-3 instar nymphs of BPH Artificial diet 0.05, 0.1, and 0.15 mg/mL Diet renewed daily, duration of 15 days To investigate the effect of Schaftoside on the survival rate of BPH, results showed that Schaftoside significantly inhibited the survival rate of BPH in a dose-dependent manner. Front Plant Sci. 2018 May 29;9:710
Rats Healthy rats Intravenous injection and oral administration 1.2 mg/kg (iv), 50, 100, 200 mg/kg TFDS (po) Single dose To investigate the pharmacokinetics and excretion pathways of schaftoside in rats. Results showed that after intravenous injection, schaftoside was quickly eliminated from blood circulation (t1/2=0.64 h) and extensively excreted into urine (54.59 ± 9.11%) and bile (24.78 ± 3.07%) as unchanged form. After oral administration of TFDS, plasma exposure of schaftoside was dose-proportional. Front Pharmacol. 2022 Dec 14;13:1073535
BALB/c mice LPS-induced acute lung injury model Intragastric administration 10 and 20 mg/kg Single dose, lasting 8 hours Evaluate the anti-inflammatory effect of Schaftoside, showing significant alleviation of lung inflammation and reduction of pro-inflammatory cytokine levels Acta Pharm Sin B. 2022 Nov;12(11):4154-4164
Root-knot nematode (Meloidogyne incognita) Root-knot nematode (Meloidogyne incognita) Aqueous solution 114.66 μg/mL (LC50) 72 hours To evaluate the nematicidal activity of Schaftoside against root-knot nematodes, showing an LC50 value of 114.66 μg/mL. Molecules. 2011 Jun 20;16(6):5079-86

Schaftoside/夏佛塔苷 参考文献

[1]Sun D, Dong L, et al. Simultaneous determination of four flavonoids and one phenolic acid in rat plasma by LC-MS/MS and its application to a pharmacokinetic study after oral administration of the Herba Desmodii Styracifolii extract. J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Aug 1;932:66-73.

Schaftoside/夏佛塔苷 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.77mL

0.35mL

0.18mL

8.86mL

1.77mL

0.89mL

17.72mL

3.54mL

1.77mL

Schaftoside/夏佛塔苷 技术信息

CAS号51938-32-0
分子式C26H28O14
分子量 564.49
SMILES Code O=C1C=C(C2=CC=C(O)C=C2)OC3=C1C(O)=C([C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)C(O)=C3[C@H]5[C@H](O)[C@@H](O)[C@@H](O)CO5
MDL No. MFCD21333256
别名 Apigenin 6-C-glucoside-8-C-arabinoside
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Keep in dark place, sealed in dry, 2-8°C

溶解方案

DMSO: 120 mg/mL(212.58 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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