1. Apoptosis
  2. Apoptosis
  3. Apoptosis inducer 7

Apoptosis inducer 7 (Compound 5I) 诱导癌细胞凋亡。Apoptosis inducer 7 诱导 PARP、caspases 的裂解和抗凋亡蛋白 c-Flip 的下调以及促凋亡蛋白 Noxa 的上调。Apoptosis inducer 7 具有抗肿瘤活性。

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Apoptosis inducer 7 Chemical Structure

Apoptosis inducer 7 Chemical Structure

CAS No. : 2252278-57-0

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Apoptosis inducer 7 (Compound 5I) induces apoptosis in cancer cells. Apoptosis inducer 7 inducrs cleavage of PARP, caspases, down-regulation of anti-apoptotic protein c-Flip and up regulation of pro-apoptotic protein Noxa. Apoptosis inducer 7 exhibits antitumor activity[1].

体外研究
(In Vitro)

Apoptosis inducer 7 (Compound 5I) (0.098-50 μM, 96 hours; human tumor cell lines) exerts the most potent antitumor activities against human cancer cell lines[1].
Apoptosis inducer 7 (Compound 5I) induces apoptosis in HCT-116 cells, and the apoptosis induction is related to the downregulation of anti-apoptotic protein c-Flip and upregulation of pro-apoptotic protein Noxa[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: Human breast cancer MDA-MB-231 cells, human lung cancer A549 cells, human colorectal cancer HCT-116 cells, human liver cancer HepG-2 cells and one non-tumor human breast epithelial MCF-10A cells.
Concentration: 0.098-50 μM
Incubation Time: 96 hours
Result: Inhibited with IC50 values of 0.22, 0.15, 0.42, 0.14 and 1.03 μM for MDA-MB-231, A549, HCT-116, HepG-2 and MCF-10A, respectively.

Cell Cycle Analysis[1]

Cell Line: HCT-116 cells
Concentration: 0.5, 0.75 and 1.0 μM
Incubation Time: 24 hours
Result: More than 40% of the cells were detected in the sub G1 phase.

Western Blot Analysis[1]

Cell Line: HCT-116 cells
Concentration: 0.5, 0.75 and 1.0 μM
Incubation Time: 24 hours
Result: Induced cleavage of PARP, caspases and decreased the levels of c-Flip and HDAC3 proteins.
体内研究
(In Vivo)

Apoptosis inducer 7 (Compound 5I) (5 mg/kg; i.p.; three times a week, for 14 days; LL/2 xenograft model in C57/ BL6J mice) inhibits tumor growth[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: KARPAS-422 subcutaneous xenograft in mice[1]
Dosage: 5 mg/kg
Administration: Intraperitoneal injection; three times a week, for 14 days.
Result: Inhibited the tumor growth with an inhibition rate of 62.3%, without significant body weight loss.
分子量

797.07

Formula

C49H68N2O7

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献

Apoptosis inducer 7 相关分类

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Apoptosis inducer 7
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HY-149017
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