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灵芝酸 A /Ganoderic acid A {[allProObj[0].p_purity_real_show]}

货号:A684127

Ganoderic acid A是一种从灵芝(Ganoderma lucidum)中提取的天然三萜类化合物,具有抗肿瘤活性,能够抑制 JAK-STAT3 信号通路,抑制细胞增殖并保护肝脏。

Ganoderic acid A 化学结构 CAS号:81907-62-2
Ganoderic acid A 化学结构
CAS号:81907-62-2
Ganoderic acid A 3D分子结构
CAS号:81907-62-2
Ganoderic acid A 化学结构 CAS号:81907-62-2
Ganoderic acid A 3D分子结构 CAS号:81907-62-2
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Ganoderic acid A 纯度/质量文件 产品仅供科研

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SBI-0206965 +++

ULK2, IC50: 711 nM

ULK1, IC50: 108 nM

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

PFKFB3, IC50: 207 nM

99%+
MRT68921 hydrochloride ++++

ULK2, IC50: 1.1 nM

ULK1, IC50: 2.9 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。

Ganoderic acid A 生物活性

描述 Ganoderic acid A (GAA), a representative active triterpenoid from Ganoderma lucidum, has been reported to exhibit antinociceptive, antioxidative, cytotoxic, hepatoprotective and anticancer activities[3]. GA-A (6.25-100 μM) significantly inhibited cyst growth in MDCK cyst model and embryonic kidney cyst model in vitro, and the inhibitory effect was reversible. In kidney-specific Pkd1 knockout (kPKD) mice displaying severe cystic kidney disease, administration of GA-A (50 mg· kg-1 ·d-1, sc) significantly attenuated renal cyst development[4]. Pretreatment with GA A (10 μM) significantly attenuated SNP(sodium nitroprusside)-induced cytotoxicity and NO (nitric oxide) increase in SH-SY5Y cells, but not in PC12 cells. Furthermore, pretreatment with GA A caused significantly higher adrenaline content in SH-SY5Y cells than in PC12 cells[5]. GAA attenuates acute lung injury in mouse model via the inhibition of Rho/ROCK/NF-κB pathway[6].

Ganoderic acid A 细胞研究

细胞系 浓度 检测类型 检测时间 活动说明 数据源
Bel7402 cells Cytotoxicity assay Cytotoxicity against human Bel7402 cells, IC50=7.25 μM 23092389
HepG2 cells Function assay 48 h Anticancer activity against human HepG2 cells assessed as cell viability after 48 hrs by MTT assay, IC50=38.7 μM 24974349
P388 cells Cytotoxicity assay Cytotoxicity against mouse P388 cells, IC50=7.25 μM 23092389
SGC7901 cells Cytotoxicity assay Cytotoxicity against human SGC7901 cells, IC50=7.25 μM 23092389

Ganoderic acid A 参考文献

[1]Radwan FF, Hossain A, et al. Reduction of myeloid-derived suppressor cells and lymphoma growth by a natural triterpenoid. J Cell Biochem. 2015 Jan;116(1):102-14.

[2]Yao X, Li G, et al. Inhibition of the JAK-STAT3 signaling pathway by ganoderic acid A enhances chemosensitivity of HepG2 cells to cisplatin. Planta Med. 2012 Nov;78(16):1740-8.

[3]Cao FR, Feng L, Ye LH, Wang LS, Xiao BX, Tao X, Chang Q. Ganoderic Acid A Metabolites and Their Metabolic Kinetics. Front Pharmacol. 2017 Mar 7;8:101

[4]Meng J, Sai-Zhen Wang, He JZ, Zhu S, Huang BY, Wang SY, Li M, Zhou H, Lin SQ, Yang BX. Ganoderic acid A is the effective ingredient of Ganoderma triterpenes in retarding renal cyst development in polycystic kidney disease. Acta Pharmacol Sin. 2020 Jun;41(6):782-790

[5]Yu ZR, Jia WH, Liu C, Wang HQ, Yang HG, He GR, Chen RY, Du GH. Ganoderic acid A protects neural cells against NO stress injury in vitro via stimulating β adrenergic receptors. Acta Pharmacol Sin. 2020 Apr;41(4):516-522

[6]Wan B, Li Y, Sun S, Yang Y, Lv Y, Wang L, Song M, Chen M, Wu C, Pan H, Zhang X. Ganoderic acid A attenuates lipopolysaccharide-induced lung injury in mice. Biosci Rep. 2019 May 23;39(5):BSR20190301

Ganoderic acid A 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.94mL

0.39mL

0.19mL

9.68mL

1.94mL

0.97mL

19.35mL

3.87mL

1.94mL

Ganoderic acid A 技术信息

CAS号81907-62-2
分子式C30H44O7
分子量 516.666
别名
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry,Store in freezer, under -20°C

溶解方案

DMSO: 60 mg/mL(116.13 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

无水乙醇: 50 mg/mL(96.77 mM),注意:无水乙醇开封后,易挥发,也会吸收空气中的水分,导致溶解能力下降,请避免使用开封较久的乙醇

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
动物实验配方
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