Auriculasin
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Auriculasin is an anticancer agent that inhibits VEGFR2, PI3K/AKT/mTOR, MAPK. Auriculasin can inhibit cell proliferation, induce cell apoptosis, and inhibit angiogenesis, and promotes mitochondrial oxidative stress and ferroptosis. Auriculasin is also active at the cannabinoid receptor CB1 with an IC50 of 8.92 μM. Auriculasin can be used in cancer research, especially related diseases such as prostate cancer and non-small cell lung cancer, as well as research on the development of anti-angiogenic drugs.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 98.54%
- CAS 番号: 60297-37-2
- 分子式: C25H24O6
- 分子量:420.45
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保管条件:
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
VEGFR アイソフォーム固有の製品をすべて表示
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生物活性
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CB1 8.92 μM (IC50) |
VEGFR2 |
Auriculasin (2.5-10 μM; 6-24 h) inhibits the proliferation of human umbilical vein endothelial cells (HUVECs) in a dose- and time-dependent manner[1].
Auriculasin (5-10 μM; 12 h) inhibits VEGF-induced migration and invasion of HUVECs[1].
Auriculasin (5-10 μM; 6 h) inhibits the formation of capillary-like structures in HUVECs[1].
Auriculasin (5-10 μM; 6 days) inhibits microvascular sprouting in rat aortic rings[1].
Auriculasin (5-10 μM; 24 h or 30 min-1 h) downregulates the expression of Bcl-2, Bcl-XL, and VEGF in HUVECs, and inhibits the phosphorylation of VEGFR2 and its downstream Akt, mTOR, etc.[1].
Auriculasin (2.5-10 μM; 24 h) inhibits the viability of RC-58T/h/SA#4 primary prostate cancer cells, and the effect is more significant when combined with TRAIL, and has low toxicity to RWPE-1 prostate epithelial cells[2].
Auriculasin (5 μM) combined with TRAIL (100 ng/mL; 24 h) induces apoptosis of RC-58T/h/SA#4 cells[2].
Auriculasin (1-10 μM; 24 h) reduces the viability of LNCa P prostate cancer cells and has no effect on RWPE-1 cells[3].
Auriculasin (1-5 μM; 24 h) induces apoptosis of LNCaP cells, which is manifested by an increase in the sub-G1 population and DNA fragmentation[3].
Auriculasin (2.5-5 μM; 12-24 h) increases ROS generation in LNCaP cells[3].
Auriculasin reduces NSCLC A549 cell viability and promotes mitochondrial oxidative stress and ferroptosis[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:HUVECs
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Concentration:5 μM, 7.5 μM, 10 μM
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Incubation Time:12 h
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Result:Inhibited VEGF-induced migration in wound-healing assay and invasion in trans-well assay.
Auriculasin (5, 10 mg/kg; oral gavage; once every 2 days; 21 days) reduces tumor size, weight and volume in the nude mouse LNCaP prostate cancer xenograft model without significant toxicity[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:5-week-old male C57BL/6 mice, Matrigel plug model[1]
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Dosage:5 μg/mL, 10 μg/mL (in Matrigel with 20 units of heparin and 150 ng/mL VEGF)
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Administration:Subcutaneous injection, single dose, 7 days
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Result:Co-treated with Matrigel plugs and VEGF, showed marked reduction of red blood cells, lighter color, significantly reduced hemoglobin concentrations, dramatically blocked VEGF-induced vasculature formation, and reduced area of VEGF-staining cells compared to the VEGF alone group.
化学情報
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CAS 番号 60297-37-2
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性状 Solid
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分子量 420.45
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分子式 C25H24O6
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Color White to off-white
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SMILES
O=C1C(C(O)=C(C=CC(C)(C)O2)C2=C3C/C=C(C)\C)=C3OC=C1C4=CC=C(O)C(O)=C4
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
純度とドキュメンテーション
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データシート (276 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Cho HD, et al. Effects of auriculasin on vascular endothelial growth factor (VEGF)-induced angiogenesis via regulation of VEGF receptor 2 signaling pathways in vitro and in vivo. Food Chem Toxicol. 2018 Nov;121:612-621. [Content Brief]
[2]. Cho HD, et al. Auriculasin sensitizes primary prostate cancer cells to TRAIL-mediated apoptosis through up-regulation of the DR5-dependent pathway. Food Chem Toxicol. 2019 Apr;126:223-232. [Content Brief]
[3]. Cho HD, et al. Auriculasin-induced ROS causes prostate cancer cell death via induction of apoptosis. Food Chem Toxicol. 2018 Jan;111:660-669. [Content Brief]
[4]. Wang X, et al. Auriculasin induces mitochondrial oxidative stress and drives ferroptosis by inhibiting PI3K/Akt pathway in non-small cell lung cancer. Naunyn Schmiedebergs Arch Pharmacol. 2025 Jan;398(1):967-977. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
Auriculasin 関連分類
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