1. Metabolic Enzyme/Protease Apoptosis
  2. Phosphodiesterase (PDE) Apoptosis
  3. Nauclefine

Nauclefine 是一种从 Nauclea officinalis 中分离出来的吲哚类生物碱。Nauclefine 可作为一种 PDE3A 调节剂,通过 PDE3A-SLFN12 依赖的死亡途径诱导癌细胞凋亡(apoptosis)。

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Nauclefine Chemical Structure

Nauclefine Chemical Structure

CAS No. : 57103-51-2

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规格 价格 是否有货 数量
1 mg ¥2208
1 - 2 周
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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Nauclefine is an indole alkaloid isolated from Nauclea officinalis. Nauclefine acts as a PDE3A modulator to induce cancer cell apoptosis through a PDE3A-SLFN12-dependent death pathway[1].

体外研究
(In Vitro)

Nauclefine (250?nM, 48 h) 可以抑制 HeLa 细胞活力,并诱导细胞凋亡,造成细胞 PDE3A 和 SLFN12 依赖性死亡。Nauclefine 可以结合 PDE3A,但不抑制其磷酸二酯酶活性,能够促进 PDE3A 和 SLFN12 之间的相互作用,并通过增加 SLFN12 的稳定性促进细胞死亡[1]

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

体内研究
(In Vivo)

Nauclefine (5 mg/kg, intratumorally, once per day for 22 days) 在感染 HeLa 细胞的雌性裸鼠(Balb/c-nu)中,显著降低了HeLa-luc 细胞肿瘤的总体生长,特别是处理第 6 天后肿瘤体积明显减小,且没有导致小鼠体重的任何降低。其对肿瘤生长的抑制依赖于 PDE3A 和 SLFN12 的表达[1]

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

分子量

287.32

Formula

C18H13N3O

CAS 号
结构分类
初始来源
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
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Nauclefine
目录号:
HY-N10149
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