Forsythoside B 是从传统中药植物连翘(Forsythia suspensa)叶中分离出来的苯乙烯苷类物质,可用于研究炎症性疾病和促进血液循环。Forsythoside B 抑制 TNF-alpha、IL-6、IκB 并调节 NF-κB。


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| 产品名称 | TNF-α ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Thalidomide | ✔ | E3 Ligase | 98% | ||||||||||||||||
| GSK2982772 |
++
human RIP1, IC50: 16 nM |
99%+ | |||||||||||||||||
| QNZ |
++++
TNF-α, IC50: 7 nM |
NF-κB | 99%+ | ||||||||||||||||
| Lenalidomide |
+++
TNF-α, IC50: 13 nM |
99% | |||||||||||||||||
| Pomalidomide |
+++
TNF-α, IC50: 13 nM |
98% | |||||||||||||||||
| GSK481 | ✔ | 99%+ | |||||||||||||||||
| Apremilast |
++
TNF-α, IC50: 77 nM |
98% | |||||||||||||||||
| Necrostatin-1 |
+
RIP1, EC50: 490 nM |
99%+ | |||||||||||||||||
| Acetylcysteine | ✔ | 98% | |||||||||||||||||
| Adalimumab | ✔ | 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。 | |||||||||||||||||||
| 产品名称 | NF-κB ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ammonium pyrrolidine-1-carbodithioate | ✔ | 98% | |||||||||||||||||
| QNZ |
++++
NF-κB, IC50: 11 nM |
99%+ | |||||||||||||||||
| Sodium 4-Aminosalicylate Dihydrate | ✔ | 98% | |||||||||||||||||
| Sodium Salicylate | ✔ | 95% | |||||||||||||||||
| Parthenolide | ✔ | p53 | 97% HPLC | ||||||||||||||||
| JSH-23 |
+
NF-κB, IC50: 7.1 μM |
98% | |||||||||||||||||
| Phenethyl caffeate | ✔ | 98% | |||||||||||||||||
| Andrographolide | ✔ | 98+% | |||||||||||||||||
| Curcumin | ✔ | HDAC,Nrf2 | 98% | ||||||||||||||||
| SC75741 |
+++
NF-κB, EC50: 200 nM |
99%+ | |||||||||||||||||
| CBL0137 HCl |
++
NF-κB, EC50: 0.47 μM |
p53 | 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 | Forsythoside B is a natural product isolated and purified from the fruits of Forsythia suspensa which inhibits inflammatory response,and has antioxidant properties with potent neuroprotective effects with a favorable therapeutic time-window, reduce of cerebral ischemia and reperfusion injury degree, attenuating blood-brain barrier (BBB) breakdown, and can rescue cardiac function from I/R injury. Forsythoside B has antisepsis effect, is mediated by decreasing local and systemic levels of a wide spectrum of inflammatory mediators. Its antisepsis mechanism may be that Forsythoside B binds to LPS and reduces the biological activity of serum LPS, and inhibits NF-κB activition. |
| Concentration | Treated Time | Description | References | |
| Mouse primary cortical neurons | 0.1, 1, 10 μmol/L | 24 hours | To evaluate the protective effect of Forsythoside B on oxygen-glucose deprivation/reoxygenation (OGD/R)-induced neuronal injury. Results showed that Forsythoside B significantly increased the viability of neurons after OGD/R treatment. | Acta Pharm Sin B. 2022 May;12(5):2330-2347. |
| BV-2 cells | 1μM and 2.5μM | 3 hours | FTS B significantly suppressed the release of IL-6, TNF-α, iNOs, NO, and IL-1β in LPS-induced BV-2 cells. | J Neuroinflammation. 2020 Oct 15;17(1):305. |
| Bovine Serum Albumin (BSA) | 0— 3.5×10^−5 M | Investigation of the interaction between Forsythoside B and BSA, showing that the quenching mechanism is a combination of static quenching and non-radiative energy transfer. | J Pharm Anal. 2013 Feb;3(1):61-65. |
| Administration | Dosage | Frequency | Description | References | ||
| APP/PS1 transgenic mice | Alzheimer's disease model | Intragastric administration | 10 mg/kg and 40 mg/kg | Once daily for 36 days | FTS B improved cognitive function, reduced Aβ deposition and tau protein phosphorylation, and inhibited the activation of microglia and astrocytes in APP/PS1 mice. | J Neuroinflammation. 2020 Oct 15;17(1):305. |
| KM mice | Transient middle cerebral artery occlusion (tMCAO) model | Intravenous injection | 10, 20, 40 mg/kg | Single dose at the beginning of reperfusion | To evaluate the protective effect of Forsythoside B on cerebral ischemia/reperfusion injury. Results showed that Forsythoside B significantly reduced infarct volume and neurological deficit scores. | Acta Pharm Sin B. 2022 May;12(5):2330-2347. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.32mL 0.26mL 0.13mL |
6.61mL 1.32mL 0.66mL |
13.22mL 2.64mL 1.32mL |
|
| CAS号 | 81525-13-5 |
| 分子式 | C34H44O19 |
| 分子量 | 756.7 |
| SMILES Code | OC1=C(O)C=C(/C=C/C(O[C@H]2[C@H](O[C@]3([H])O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](OCCC4=CC=C(O)C(O)=C4)O[C@@H]2CO[C@H]5[C@H](O)[C@](CO)(O)CO5)=O)C=C1 |
| MDL No. | MFCD03424245 |
| 别名 | 连翘脂苷B |
| 运输 | 蓝冰 |
| InChI Key | JMBINOWGIHWPJI-UNSOMVRXSA-N |
| Pubchem ID | 23928102 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 120 mg/mL(158.58 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 H2O: 100 mg/mL(132.15 mM),配合低频超声助溶 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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