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


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