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Cucurbitacin E

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Chemical Structure| 18444-66-1 同义名 : α-Elaterin;α-Elaterine;NSC 521775;NSC 106399
CAS号 : 18444-66-1
货号 : A513376
分子式 : C32H44O8
纯度 : 99%+
分子量 : 556.687
MDL号 : MFCD00135936
存储条件:

粉末 Sealed in dry,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 50 mg/mL(89.82 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

动物实验配方:
生物活性
描述 Cyclin-dependent kinases (CDKs) are a group of multifunctional enzymes consisting of catalytic and regulatory subunits[3]. Cucurbitacin E is a natural compound which from the climbing stem of Cucumic melo L. Cucurbitacin E significantly suppresses the activity of the cyclin B1/CDC2 complex. in vitro study is initiated in which each of the CRC cell lines is exposed to increasing doses of Cucurbitacin E (0, 2.5, 5, and 7.5 μM) over a period of 24 h. Cucurbitacin E is shown to induce morphological changes in the primary colon cancer cells. A remarkable change in morphology was observed in the period of 6 and 24 h. Cucurbitacin E inhibits tumor growth by arresting the cell cycle in the G2/M phase via GADD45γ gene expression and the blockage of cyclin B1/CDC2 complex in primary CRC cells[4]. A high fat diet mice model of metabolic syndrome (HFD-MetS) is developed to assess the role of Cucurbitacin E (CuE) on body weight and fat tissue biology. Results showed a significant decrease in body weights of mice treated with Cucurbitacin E (0.5mg/kg) and central obesity is also reduced after the treatment[5].
临床研究
NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT02858388 Otitis Media With Effusion Phase 3 Completed - Italy ... 展开 >> San Gennaro Hospital Naples, Italy, 80136 收起 <<
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

1.80mL

0.36mL

0.18mL

8.98mL

1.80mL

0.90mL

17.96mL

3.59mL

1.80mL

参考文献

[1]Li Y, Wang R, et al. The induction of G2/M cell-cycle arrest and apoptosis by cucurbitacin E is associated with increased phosphorylation of eIF2alpha in leukemia cells. Anticancer Drugs. 2010 Apr;21(4):389-400.

[2]He X, Gao Q, et al. Cucurbitacin E induces apoptosis of human prostate cancer cells via cofilin-1 and mTORC1. Oncol Lett. 2017 Jun;13(6):4905-4910.

[3]Bharat Goel,et al. Small Molecule CDK Inhibitors for the Therapeutic Management of Cancer. Curr Top Med Chem. 2020. 20(17), 1535-1563.

[4]Hsu YC, et al. Therapeutic ROS targeting of GADD45γ in the induction of G2/M arrest in primary human colorectal cancer cell lines by cucurbitacin E. Cell Death Dis. 2014. 5(4), e1198.

[5]Murtaza M, et al. Cucurbitacin E reduces obesity and related metabolic dysfunction in mice by targeting JAK-STAT5 signaling pathway. PLoS One. 2017. 12(6), e0178910.