货号:A907987
同义名:
ICodonolactone; 8β-Hydroxyasterolide
Atractylenolide III 是白术根茎中的主要活性成分,具有诱导肺癌细胞凋亡的作用,并表现出胃保护和神经保护潜力,适用于癌症、认知障碍及神经损伤机制研究。


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解

| 产品名称 | diphenolase ↓ ↑ | monophenolase ↓ ↑ | tyrosinase ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Hexylresorcinol |
+++
diphenolase, IC50: 0.85 μM |
++
monophenolase, IC50: 1.24 μM |
+++
diphenolase, IC50: 0.85 μM monophenolase, IC50: 0.85 μM |
99%+ | |||||||||||||||
| Aloin | ✔ | 98% (mixture of A&B) | |||||||||||||||||
| Arbutin |
+
tyrosinase, IC50: 1.09 mM |
98% | |||||||||||||||||
| Monobenzone | ✔ | 98% | |||||||||||||||||
| Deoxyarbutin |
++++
tyrosinase, IC50: 50 nM |
98% | |||||||||||||||||
| 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 | Atractylenolide III, also known as ICodonolactone, constitutes the primary active compound of the Atractylodes rhizome and exhibits the capability to induce apoptosis in lung cancer cells. It is recognized for its oral efficacy as a gastroprotective agent . |
| 体内研究 | Atractylenolide III, administered orally at doses of 5 and 10 mg/kg, demonstrates gastroprotective effects and reduces gastric ulcers induced by 70% ethanol in rats by up to 70%[2]. Atractylenolide III, when administered at 30 mg/kg through oral gavage for either 14 or 28 days, alleviates depressive- and anxiogenic-like behaviors in rat models of depression. This effect is observed in models induced by lipopolysaccharide (LPS) and chronic unpredictable mild stress (CUMS)[5]. |
| 体外研究 | Atractylenolide III, at concentrations ranging from 1 to 100 μM over 48 hours, induces apoptosis in A549 cells, as evidenced by the activation of caspase-3 and caspase-9 and the cleavage of PARP[1]. Atractylenolide III, in concentrations between 1 and 100 μM over a period of 72 hours, inhibits proliferation and angiogenesis, as indicated by tube formation, in Human Umbilical Vein Endothelial Cells (HUVECs)[1]. Atractylenolide III, at concentrations of 1-100 μM, inhibits the production of proinflammatory cytokines (IL-6, IL-1β, TNF-α, and IL-8) induced by thymic stromal lymphopoietin (TSLP) in HMC-1 cells[4]. |
| Concentration | Treated Time | Description | References | |
| HepG2 cells | 12.5, 25, 50 µg/ml | 24 h | To evaluate the effects of ATL III on lipid metabolism, ATL III treatment significantly reduced FFAs-induced lipid accumulation in HepG2 cells. | Int J Biol Sci. 2022 Jan 31;18(4):1594-1611 |
| bEnd.3 cells | 10 µM | 2 h | To evaluate the effect of Atractylenolide III combined with Atractylenolide I and Paeoniflorin on the tube formation of bEnd.3 cells. The results showed that the combination significantly promoted cell tube formation. | Chin Med. 2024 Jan 4;19(1):3 |
| bEnd.3 cells | 10 µM | 16 h | To evaluate the effect of Atractylenolide III combined with Paeoniflorin on the migration of bEnd.3 cells. The results showed that the combination significantly promoted cell migration. | Chin Med. 2024 Jan 4;19(1):3 |
| bEnd.3 cells | 10 µM | 24 h | To evaluate the effect of Atractylenolide III combined with Atractylenolide I and Paeoniflorin on the proliferation of bEnd.3 cells. The results showed that the combination significantly promoted cell proliferation. | Chin Med. 2024 Jan 4;19(1):3 |
| Rat HSC cell line T6 | 20, 30 or 40 mM | Atractylenolide III inhibits ASCT2 expression, induces HSC senescence, and reduces proinflammatory SASP production | Acta Pharm Sin B. 2022 Sep;12(9):3618-3638 |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6J mice | HFD-induced NAFLD model | Tail intravenous injection | 10 mg/kg | Every other day for 4 weeks | ATL III treatment significantly ameliorated liver injury and hepatic lipid accumulation in the HFD-induced NAFLD mouse model, reducing serum levels of ALT, AST, TG, TC, and LDL. | Int J Biol Sci. 2022 Jan 31;18(4):1594-1611 |
| ICR mice | CCl4-induced liver fibrosis model | Intraperitoneal injection | 20, 30 or 40 mg/kg | Three times a week for 8 weeks | Atractylenolide III induces HSC senescence by inhibiting ASCT2 and ameliorates liver fibrosis | Acta Pharm Sin B. 2022 Sep;12(9):3618-3638 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.03mL 0.81mL 0.40mL |
20.14mL 4.03mL 2.01mL |
40.27mL 8.05mL 4.03mL |
|
| CAS号 | 73030-71-4 |
| 分子式 | C15H20O3 |
| 分子量 | 248.32 |
| SMILES Code | O=C1C(C)=C(C[C@@]23[H])[C@@](C[C@@]3(C)CCCC2=C)(O)O1 |
| MDL No. | MFCD00238543 |
| 别名 | ICodonolactone; 8β-Hydroxyasterolide; Codonolactone; Atractylenolide β |
| 运输 | 蓝冰 |
| InChI Key | FBMORZZOJSDNRQ-GLQYFDAESA-N |
| Pubchem ID | 155948 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 50 mg/mL(201.35 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 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
|
沪公网安备 31011702889066号
沪ICP备2024050318号-1