Ganoderic acid A

製品コードS4753 バッチS475301

印刷

化学情報

 Chemical Structure Synonyms N/A Storage
(From the date of receipt)
3 years -20°C powder
1 years -80°C in solvent
化学式

C30H44O7

分子量 516.67 CAS No. 81907-62-2
Solubility (25°C)* 体外 DMSO 100 mg/mL (193.54 mM)
Ethanol (warmed with 50ºC water bath) 100 mg/mL (193.54 mM)
Water Insoluble
体内 (毎回新しく調製した物を用意してください)
Homogeneous suspension
CMC-NA
≥5mg/ml Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Ganoderic Acid A (GAA) is an active triangle compound in Ganoderma Lucidum. It can inhibit the JAK-STAT3 signal pathway and inhibit cell proliferation, vitality, and ROS. Ganoderic Acid A has analgesic, antioxidant, cytotoxicity, protecting liver and anti -tumor activity.
in vitro GAA exhibits antitumor activity on human osteosarcoma, lymphoma, meningioma and breast cancer cells through suppressing growth and invasive behavior and/or inducing apoptosis of cancer cells. GAA could also enhance chemosensitivity of HepG2 cells to Cisplatin[1]. GA-A treatment induces caspase-dependent apoptotic cell death characterized by a dose-dependent increase in active caspases 9 and 3, up-regulation of pro-apoptotic BIM and BAX proteins, and a subsequent loss of mitochondrial membrane potential with release of cytochrome c. Lower doses of GA-A enhance HLA class II-mediated antigen presentation and CD4+ T cell recognition of lymphoma in vitro[2].
in vivo GAA can significantly prolong the survival of EL4 syngeneic mice and decrease tumor metastasis to the liver, and enhance cell-mediated immune responses by attenuating myeloid-derived suppressor cells. GAA could undergo extensive metabolism, including reduction, oxidation, and hydroxylation phase I metabolism, and glucuronidation and sulfation phase II metabolism[1].

プロトコル(参考用のみ)

細胞アッセイ 細胞株 Human pre-B acute lymphocytic leukemia (NALM-6), Burkitt lymphoma (Ramos, GA-10, CA-46 and Daudi) and non-Hodgkin
濃度 5, 10, 20, and 40μM
反応時間 24 h
実験の流れ

Cells are seeded at 1×104 cells/well in 100μl of appropriate culture medium in a flat-bottom 96-well plate. GA-A is added to appropriate wells for final concentrations of 5, 10, 20, and 40μM. Following 24h of GA-A treatment, cell viability is measured using the CellTiter 96 AQueous One Solution Cell Proliferation Assay (MTS).

動物実験 動物モデル Male Sprague-Dawley rats
投薬量 20 mg/kg
投与方法 i.v.

参考

  • https://pubmed.ncbi.nlm.nih.gov/28326038/
  • https://pubmed.ncbi.nlm.nih.gov/25142864/

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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