Perifosine

目录号: GC15680纯度: >98.00%同义词: 哌立福新; KRX-0401; NSC 639966; D21266

Perifosine 是 Akt 的抑制剂 。


Perifosine
Cas No.: 157716-52-4
规格价格库存数量操作
5mg¥431.00现货
1
25mg¥1,523.00现货
1
10mM (in 1mL Ethanol)¥630.00现货
1

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产品描述 Description

Perifosine is an inhibitor of Akt [1].

Perifosine is a synthetic antitumor alkylphospholipid. It induces cell apoptosis through inhibiting the activity of Akt. Perifosine shows antitumor activity in various cell lines including NSCLC, MM, epithelial carcinoma, prostate carcinoma and leukemia cells. In H460 cells, perifosine decreased cell survival and induced apoptosis with IC50 values of 1μM and 10 μM, respectively. The treatment of perifosine was also found to induce cleavage of caspase-8, caspase-9, caspase-3 and PARP in this cell line. In MM.1S cells, perifosine induced sub-G1 phase population increase from 15% to 57% at 10 μM and induced cleavage of caspase-8, caspase-9 and PARP in a dose-dependent manner. In mice inoculated with MM.1S cells, oral administration of perifosine significantly reduced MM tumor growth and increased survival [1, 2].

References:
[1] Elrod H A, Lin Y D, Yue P, et al. The alkylphospholipid perifosine induces apoptosis of human lung cancer cells requiring inhibition of Akt and activation of the extrinsic apoptotic pathway. Molecular cancer therapeutics, 2007, 6(7): 2029-2038.
[2] Hideshima T, Catley L, Yasui H, et al. Perifosine, an oral bioactive novel alkylphospholipid, inhibits Akt and induces in vitro and in vivo cytotoxicity in human multiple myeloma cells. Blood, 2006, 107(10): 4053-4062.

Perifosine 是 Akt 的抑制剂 [1]

Perifosine 是一种合成的抗肿瘤烷基磷脂。它通过抑制 Akt 的活性来诱导细胞凋亡。 Perifosine 在多种细胞系中表现出抗肿瘤活性,包括 NSCLC、MM、上皮癌、前列腺癌和白血病细胞。在 H460 细胞中,perifosine 降低细胞存活率并诱导细胞凋亡,IC50 值分别为 1μM 和 10 μM。还发现哌立福新处理可诱导该细胞系中 caspase-8、caspase-9、caspase-3 和 PARP 的裂解。在 MM.1S 细胞中,perifosine 在 10 μM 时诱导亚 G1 期细胞群从 15% 增加到 57%,并以剂量依赖的方式诱导 caspase-8、caspase-9 和 PARP 的裂解。在接种 MM.1S 细胞的小鼠中,口服哌立福新可显着降低 MM 肿瘤的生长并提高存活率 [1, 2]

实验参考方法 Experimental Reference Method

Cell experiment: [1]

Cell lines

CRW22RV1 cells

Preparation method

Cells (1.2×105) were seeded in 6-cm diameter dishes and incubated overnight to allow the cells to attach. Cells were then treated with perifosine and immediately thereafter with 6 Gy of radiation. To assess the effect of perifosine on radiation-induced apoptosis, the Annexin-FITC based flow cytometry analysis was used. Both nuclear fragmentations with PI staining and translocated membrane phosphatidylserine (PS) with Annexin V staining were measured.

Reaction Conditions

10 μM, 24 hours

Applications

Both perifosine and radiation induced significant apoptotic responses as shown by the increase of apoptotic cells. When radiation (6Gy) and perifosine (10 μM) were combined, the number of apoptotic cells was significantly increased. Perifosine alone did not induce cell cycle arrest at the G2/M phases and perifosine did not affect the IR-induced G2/M checkpoint.

Animal experiment: [1]

Animal models

Male Athymic Nude-Foxn1nu mice injected with CRW22RV1 cells

Dosage form

Oral administration, in a loading dose of 300 mg/kg (2 × 150 mg/kg separated by 12 hours) followed by daily maintenance doses of 35 mg/kg for 5 days

Applications

Mice were separated into 4 groups: control, perifosine, radiotherapy and combined therapy. Perifosine alone did not have a significant effect on tumor growth. However, perifosine can significantly increase radiation induced tumor growth delay. To reach the 10-fold size of tumor volume to the initial volume in the control, it took 15, 19, 41 and 59 days in control, perifosine only, radiation only and combined treatment groups, respectively. It is noted that the combined treatment led to a complete remission of the CWR22RV1 tumor.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1] Gao Y, Ishiyama H, Sun M, et al. The alkylphospholipid, perifosine, radiosensitizes prostate cancer cells both in vitro and in vivo. Radiation oncology (London, England), 2011, 6: 39.

产品文档 Product Documents

Purity:>98.00%

化学性质Chemical Properties

CAS 号
157716-52-4
同义词
哌立福新; KRX-0401; NSC 639966; D21266
化学名
(1,1-dimethylpiperidin-1-ium-4-yl) octadecyl phosphate
SMILES
CCCCCCCCCCCCCCCCCCOP(=O)([O-])OC1CC[N+](CC1)(C)C
分子式
C25H52NO4P
分子量
461.67 g/mol
溶解性
Water : ≥ 153.33 mg/mL (332.13 mM); Ethanol : 92 mg/mL (199.28 mM)
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
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
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol