 
        
        
        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。
 
                                 
                                
                            

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| 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 | 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]. | 
| Concentration | Treated Time | Description | References | |
| HASMCs | 10 µM | 7 days | To evaluate the effect of Ganoderic acid A on vascular smooth muscle cell calcification. Results showed that Ganoderic acid A significantly reduced calcium deposition. | Theranostics. 2023 Feb 21;13(4):1325-1341. | 
| RAW264.7 cells | 10 µM | 24 hours | To evaluate the effect of Ganoderic acid A on foam cell formation. Results showed that Ganoderic acid A significantly reduced the number of foam cells. | Theranostics. 2023 Feb 21;13(4):1325-1341. | 
| Embryonic kidney cells | 100μM | 6 days | Assess the inhibitory effect of GA-A on embryonic kidney cysts, showing significant reduction in cyst number and size. | Acta Pharmacol Sin. 2020 Jun;41(6):782-790. | 
| MDCK cells | 6.25-100μM | 24 hours | Evaluate the inhibitory effect of GA-A on cyst growth in MDCK cells, showing significant inhibition without cytotoxicity. | Acta Pharmacol Sin. 2020 Jun;41(6):782-790. | 
| Primary B-cell lymphomas (TB#2759, TB#2952, TB#3284) | 5-40μM | 24 hours | To evaluate the anti-proliferative activity of GA-A, results showed that GA-A significantly reduced cell viability in primary B-cell lymphomas with less effect on healthy B-cells. | J Cell Biochem. 2015 Jan;116(1):102-14. | 
| Non-Hodgkin’s lymphoma cells (DB, Toledo) | 5-40μM | 24 hours | To evaluate the anti-proliferative activity of GA-A, results showed that GA-A significantly reduced cell viability with an IC50 of approximately 15μM. | J Cell Biochem. 2015 Jan;116(1):102-14. | 
| Human pre-B acute lymphocytic leukemia cells (NALM-6) | 5-40μM | 24 hours | To evaluate the anti-proliferative activity of GA-A, results showed that GA-A significantly reduced cell viability with an IC50 of approximately 15-22μM. | J Cell Biochem. 2015 Jan;116(1):102-14. | 
| BV2 microglial cells | 20 μM | 6 hours | Increases phosphorylation of Axl and Pak1, activating autophagy | Int J Mol Sci. 2021 May 24;22(11):5559. | 
| BV2 microglial cells | 50 μg/ml | 24 hours | To evaluate the inhibitory effect of GAA on LPS-induced proliferation and activation of BV2 microglial cells. Results showed that GAA significantly suppressed LPS-induced BV2 microglial cells proliferation and activation, and promoted their conversion from M1 to M2 status. | Neurochem Res. 2021 Jul;46(7):1725-1736. | 
| SNU719 cells | 0.49 mM | 48 hours | To evaluate the cytotoxic and apoptosis-inducing effects of GAA and QCT co-treatment on SNU719 cells. Results showed that the co-treatment significantly enhanced QCT-mediated cytotoxicity and apoptosis. | Molecules. 2019 Oct 24;24(21):3834. | 
| Administration | Dosage | Frequency | Description | References | ||
| Mice | KPKD mouse model | Subcutaneous injection | 50 mg/kg/d | Once daily for 4 days | Evaluate the inhibitory effect of GA-A on renal cysts in kPKD mice, showing significant reduction in cyst area and kidney index. | Acta Pharmacol Sin. 2020 Jun;41(6):782-790. | 
| C57BL/6 mice | EL4 syngeneic mouse lymphoma model | Intraperitoneal injection | 60, 50 and 50 mg/kg body weight | Injected once on days 10, 14, and 18 | To evaluate the effect of GA-A on lymphoma growth and metastasis, results showed that GA-A significantly prolonged survival, reduced liver metastasis, and decreased the number of MDSCs. | J Cell Biochem. 2015 Jan;116(1):102-14. | 
| C57BL/6J mice | Alzheimer's disease mouse model | Oral gavage | 100 mg/kg/d | Once daily for 16 days | Ameliorates cognitive deficiency, reduces Aβ42 levels in hippocampus, upregulates LC3B expression | Int J Mol Sci. 2021 May 24;22(11):5559. | 
| BALB/c mice | OVA-induced asthma model | Intraperitoneal injection | 20, 40 mg/kg | Once daily for 7 days | Ganoderic acid A alleviates OVA-induced asthma inflammation in mice by inhibiting the TLR/NF-κB signaling pathway. | Inflammation. 2021 Oct;44(5):1908-1915 | 
| BALB/c mice | LPS-induced acute lung injury model | Intraperitoneal injection | 10 mg/kg and 20 mg/kg | Single dose, lasted for 6 hours | To investigate the protective effects of ganoderic acid A (GAA) on LPS-induced acute lung injury and its mechanism. The results showed that GAA significantly reduced lung wet-to-dry weight ratio, lung myeloperoxidase activity, attenuated pathological damages, increased superoxide dismutase activity, and decreased malondialdehyde content and proinflammatory cytokine levels in bronchoalveolar lavage fluid. Mechanistically, GAA inhibited LPS-induced inflammation by suppressing the Rho/ROCK/NF-κB pathway. | Biosci Rep. 2019 May 23;39(5):BSR20190301 | 
| 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 | |
| CAS号 | 81907-62-2 | 
| 分子式 | C30H44O7 | 
| 分子量 | 516.67 | 
| SMILES Code | CC1(C)C(CC[C@]2(C)C3=C([C@@]4([C@@H](O)C[C@@H]([C@]4(CC3=O)C)[C@H](C)CC(C[C@@H](C)C(O)=O)=O)C)[C@@H](O)C[C@@]12[H])=O | 
| MDL No. | MFCD26131275 | 
| 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 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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