Ganoderic Acid A

目录号: GN10109纯度: >98.00%同义词: 灵芝酸 A
Ganoderic Acid A是一种来源于灵芝(Ganoderma lucidum)的三萜类化合物,具有多种生物活性。

Ganoderic Acid A
Cas No.: 81907-62-2
规格价格库存数量操作
1mg¥350.00现货
1
5mg¥875.00现货
1
10mg¥1,400.00现货
1
25mg¥2,240.00现货
1
10mM (in 1mL DMSO)¥966.00现货
1

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产品描述 Description

Ganoderic Acid A is a triterpenoid compound derived from Ganoderma lucidumand exhibits multiple biological activities[1-2]. Ganoderic Acid A possesses inhibitory effects against cancer, oxidation, and aging, among others[3-4].

In vitro, concurrent treatment of BV2 microglial cells with Ganoderic Acid A (50μg/ml) and LPS (0.5μg/ml) for 24 hours significantly suppressed LPS-induced proliferation and activation of BV2 microglia, and promoted the polarization of microglia from the pro-inflammatory M1 phenotype to the anti-inflammatory M2 phenotype[5]. Treatment of MC3T3-E1 cells (induced with 1mM H₂O₂) and primary osteoblasts (induced with 250μM H₂O₂) with Ganoderic Acid A (5–80μM) for 24 hours significantly promoted osteogenic differentiation and mineralization nodule formation, and upregulated the protein expression of osteogenesis-related markers RUNX2, OPN, and β-catenin[6].

In vivo, intraperitoneal administration of Ganoderic Acid A (20–40mg/kg) 1 hour before Ovalbumin (0.1g) challenge in OVA-sensitized BALB/c mice significantly alleviated airway hyperresponsiveness and reduced the total number of inflammatory cells in bronchoalveolar lavage fluid[7]. Daily administration of Ganoderic Acid A (20mg/kg/d) via intraperitoneal injection or topical application for 6 days in Imiquimod (62.5mg per mouse)-induced psoriasiform dermatitis BALB/c mice significantly ameliorated skin erythema, thickening, and scaling, and lowered the Psoriasis Area and Severity Index (PASI) score[8].

References:
[1] Sui Q, Zhu C, Shi S, et al. Ganoderic acid A: an in-depth review of pharmacological effects and molecular docking analysis. J Ethnopharmacol. 2025 Jun 12;349:119868.
[2] Ma F, Wang J, Jiang W, et al. Ganoderic Acid A: A Potential Natural Neuroprotective Agent for Neurological Disorders: A Review. Int J Med Mushrooms. 2024;26(2):11-23.
[3] Zhang X, Huang S, Xu H, et al. Research progress on plant-derived natural compounds regulating the MAPK signaling pathway for the prevention and therapy of Alzheimer's disease. Front Pharmacol. 2025 Sep 19;16:1666082.
[4] Song Z, Wang C, Ding F, et al. Ganoderic Acid A Enhances Tumor Suppression Function of Oxaliplatin via Inducing the Cytotoxicity of T Cells. Anticancer Agents Med Chem. 2023;23(7):832-838.
[5] Jia Y, Zhang D, Yin H, et al. Ganoderic Acid A Attenuates LPS-Induced Neuroinflammation in BV2 Microglia by Activating Farnesoid X Receptor. Neurochem Res. 2021 Jul;46(7):1725-1736.
[6] Zhao J, Fan Y, Li H, et al. Ganoderic Acid A Prevented Osteoporosis by Modulating the PIK3CA/p-Akt/TWIST1 Signaling Pathway. Food Sci Nutr. 2025 Apr 14;13(4):e70177.
[7] Lu X, Xu C, Yang R, et al. Ganoderic Acid A Alleviates OVA-Induced Asthma in Mice. Inflammation. 2021 Oct;44(5):1908-1915.
[8] Xiao C, Chen J, Zhou X, et al. Ganoderic acid A alleviate psoriasis by inhibiting GSDMD-mediated pyroptosis. Tissue Cell. 2025 Dec;97:103078.

Ganoderic Acid A是一种来源于灵芝(Ganoderma lucidum)的三萜类化合物,具有多种生物活性[1-2]。Ganoderic Acid A具有抑制癌症、抗氧化、抗衰老等的作用[3-4]

在体外,Ganoderic Acid A(50μg/ml)与LPS(0.5μg/ml)同时处理BV2小胶质细胞24小时,显著抑制LPS诱导的BV2小胶质细胞增殖和活化,并促进小胶质细胞由促炎的M1表型向抗炎的M2表型转化[5]。Ganoderic Acid A(5–80μM)处理MC3T3-E1(经1mM H2O2诱导)细胞和原代成骨细胞(经250μM H2O2诱导)24小时,显著促进成骨分化和矿化结节形成,并上调成骨相关标志物RUNX2、OPN和β-catenin的蛋白表达[6]

在体内,Ganoderic Acid A(20–40mg/kg)于Ovalbumin(0.1g)激发前1小时腹腔注射处理OVA致敏的BALB/c小鼠,显著减轻哮喘小鼠气道高反应性,并降低支气管肺泡灌洗液中炎症细胞总数[7]。Ganoderic Acid A(20mg/kg/d)通过腹腔注射或局部外用于Imiquimod(62.5mg/只)诱导的银屑病样皮炎BALB/c小鼠6天,显著减轻皮肤红斑、增厚和鳞屑,并降低银屑病面积和严重程度指数(PASI)评分[8]

实验参考方法 Experimental Reference Method

Cell experiment [1]:

Cell lines

BV2 microglial cells (murine microglial cell line)

Preparation Method

BV2 cells were cultured in DMEM high glucose medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin at 37°C under 5% CO₂. Cells were treated with Ganoderic Acid A at 50μg/mL concurrently with LPS (0.5μg/mL) for 24 hours.

Reaction Conditions

50μg/mL; 24h

Applications

Ganoderic Acid A significantly suppressed LPS-induced BV2 microglial proliferation and activation. Ganoderic Acid A promoted the polarization of microglia from pro-inflammatory M1 to anti-inflammatory M2 phenotype.

Animal experiment [2]:

Animal models

Female BALB/c mice

Preparation Method

Mice were sensitized by intraperitoneal injection of 10mg Ovalbumin (OVA) + 1mg aluminum hydroxide in saline on days 1, 7, and 14. From day 21, they received daily OVA aerosol challenges (0.1g OVA in 10ml saline, 30min) for 7 days. Ganoderic Acid A (20 or 40mg/kg) was administered intraperitoneally 1 hour before each OVA challenge. Lung tissues and serum were collected after the final challenge for analysis.

Dosage form

20 or 40mg/kg; i.p.; Daily for 7 days.

Applications

Ganoderic Acid A significantly attenuated OVA-induced airway hyperreactivity (AHR), reduced inflammatory cell infiltration (eosinophils, lymphocytes, neutrophils) in serum and lung tissue, and decreased levels of Th2 cytokines (IL-4, IL-5, IL-13) and IgE in serum. Ganoderic Acid A also suppressed TLR4/NF-κB signaling pathway activation, as evidenced by reduced expression of TLR4, MyD88, p-NF-κB, and p-IκBα in lung tissues.

References:
[1] Jia Y, Zhang D, Yin H, et al. Ganoderic Acid A Attenuates LPS-Induced Neuroinflammation in BV2 Microglia by Activating Farnesoid X Receptor. Neurochem Res. 2021 Jul;46(7):1725-1736.
[2] Zhao J, Fan Y, Li H, et al. Ganoderic Acid A Prevented Osteoporosis by Modulating the PIK3CA/p-Akt/TWIST1 Signaling Pathway. Food Sci Nutr. 2025 Apr 14;13(4):e70177.

产品文档 Product Documents

Purity:>98.00%

化学性质Chemical Properties

CAS 号
81907-62-2
同义词
灵芝酸 A
化学名
(2R,6R)-6-[(5R,7S,10S,13R,14R,15S,17R)-7,15-dihydroxy-4,4,10,13,14-pentamethyl-3,11-dioxo-2,5,6,7,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxoheptanoic acid
SMILES
CC(CC(=O)CC(C)C(=O)O)C1CC(C2(C1(CC(=O)C3=C2C(CC4C3(CCC(=O)C4(C)C)C)O)C)C)O
分子式
C30H42O7
分子量
514.65 g/mol
溶解性
DMF: 5mg/mL,DMSO: 1 mg/mL,Ethanol: 3 mg/mL
保存条件
4°C, away from moisture and light
General tips
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
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