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Praeruptorin A/白花前胡甲素A {[allProObj[0].p_purity_real_show]}

货号:A839991 同义名: 白花前胡甲素 / (+)-Praeruptorin A

Praeruptorin A是白头翁的主要生物活性成分,具有抗炎作用,主要通过抑制 NF-κB 活化发挥效果。它具有扩张血管、增强内皮一氧化氮合酶活性的特性。

Praeruptorin A/白花前胡甲素A 化学结构 CAS号:73069-27-9
Praeruptorin A/白花前胡甲素A 化学结构
CAS号:73069-27-9
Praeruptorin A/白花前胡甲素A 3D分子结构
CAS号:73069-27-9
Praeruptorin A/白花前胡甲素A 化学结构 CAS号:73069-27-9
Praeruptorin A/白花前胡甲素A 3D分子结构 CAS号:73069-27-9
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Praeruptorin A/白花前胡甲素A 纯度/质量文件 产品仅供科研

货号:A839991 标准纯度: {[allProObj[0].p_purity_real_show]}
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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。

Praeruptorin A/白花前胡甲素A 生物活性

靶点
  • Calcium Channel

描述 (+)-Praeruptorin A is a natural product isolated and purified from the roots of Peucedanum praeruptorum Dunn., which exerted distinct relaxant effects on isolated rat aorta rings, which might be mainly attributed to nitric oxide synthesis catalyzed by endothelial nitric oxide synthase.

Praeruptorin A/白花前胡甲素A 细胞实验

Cell Line
Concentration Treated Time Description References
Rat thoracic aorta rings 0.277-204 µM 10 minutes PA at concentrations as low as 2.77 × 10−7 M had a vasorelaxant effect in intact rat thoracic aorta rings; however, this effect was significantly reduced after removal of the vascular endothelium. Bioengineered. 2022 Apr;13(4):10038-10046
HEK293T cells 10 µM 2 days To evaluate the effect of Praeruptorin A on NFATc1 transcriptional activity, results showed that Praeruptorin A significantly inhibited RANKL-induced NFATc1 transcriptional activity. PLoS One. 2014 Feb 21;9(2):e88974
HeLa cells 20 µM 2 hours pretreatment, then TPA treatment for different times PA inhibited TPA-induced ERK1/2 activation, MMP-2 expression, migration and invasion of HeLa cells Int J Mol Sci. 2017 Dec 21;19(1):10
HeLa cells 20 µM 24 hours PA suppressed ERK1/2 activation and enhanced the effect of PD98059 (a specific MEK1/2 inhibitor) in downregulating MMP-2 and upregulating TIMP-2 Int J Mol Sci. 2017 Dec 21;19(1):10
HeLa cells 20 and 30 µM 24 hours PA significantly reduced MMP-2 expression and increased TIMP-2 expression Int J Mol Sci. 2017 Dec 21;19(1):10
HeLa cells 0 to 30 µM 24 hours PA induced cell cycle arrest at G0/G1 phase in HeLa cells, upregulated Rb, p16, p21 and p27 proteins, and downregulated cyclin D1 and Skp2 proteins Int J Mol Sci. 2017 Dec 21;19(1):10
SiHa cells 0 to 50 µM 24 hours PA significantly inhibited the proliferation and colony formation of SiHa cells Int J Mol Sci. 2017 Dec 21;19(1):10
HeLa cells 0 to 50 µM 24 hours PA significantly inhibited the proliferation and colony formation of HeLa cells Int J Mol Sci. 2017 Dec 21;19(1):10
H1299 cells 0, 10, 20, 30, 40, 50 µM 24 hours Evaluate the effect of Praeruptorin A on cell viability, results showed no significant effect on H1299 cells Molecules. 2020 Apr 1;25(7):1625
A549 cells 0, 10, 20, 30, 40, 50 µM 24 hours Evaluate the effect of Praeruptorin A on cell viability, results showed no significant effect on A549 cells Molecules. 2020 Apr 1;25(7):1625
SGC7901 human gastric cancer cells 10, 50, 100 µM 24 hours Evaluate the cytotoxicity of Praeruptorin A on SGC7901 cells. Results showed that Praeruptorin A at 10, 50, and 100 μM increased LDH release, with a maximum release rate of 29.7%. Molecules. 2010 Nov 9;15(11):8060-71
SGC7901 human gastric cancer cells 10, 50, 100 µM 24 hours Evaluate the inhibitory effect of Praeruptorin A on SGC7901 cell proliferation. Results showed that Praeruptorin A inhibited cell growth by 19.9%, 24.1%, and 33.7% at concentrations of 10, 50, and 100 μM, respectively. Molecules. 2010 Nov 9;15(11):8060-71
Bone marrow-derived macrophages (BMMs) 10 µM 4 days To evaluate the effect of Praeruptorin A on RANKL-induced osteoclast differentiation, results showed that Praeruptorin A significantly inhibited the formation of TRAP-positive multinucleated cells and TRAP activity. PLoS One. 2014 Feb 21;9(2):e88974

Praeruptorin A/白花前胡甲素A 参考文献

[1]Liu X, Chen DW, et al. The Inhibition of UDP-Glucuronosyltransferase (UGT) Isoforms by Praeruptorin A and B. Phytother Res. 2016 Nov;30(11):1872-1878.

[2]Yeon JT, Choi SW, et al. Praeruptorin A inhibits in vitro migration of preosteoclasts and in vivo bone erosion, possibly due to its potential to target calmodulin. J Nat Prod. 2015 Apr 24;78(4):776-82.

Praeruptorin A/白花前胡甲素A 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.59mL

0.52mL

0.26mL

12.94mL

2.59mL

1.29mL

25.88mL

5.18mL

2.59mL

Praeruptorin A/白花前胡甲素A 技术信息

CAS号73069-27-9
分子式C21H22O7
分子量 386.4
SMILES Code C/C=C(C)\C(O[C@@H]1C(C)(C)OC2=C(C3=C(C=CC(O3)=O)C=C2)[C@@H]1OC(C)=O)=O
MDL No. MFCD02752489
别名 白花前胡甲素 ;(+)-Praeruptorin A
运输蓝冰
InChI Key XGPBRZDOJDLKOT-NXIDYTHLSA-N
Pubchem ID 38347607
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: 35 mg/mL(90.58 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
方案 一
方案 二
方案 三
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