Junceellolide C

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Junceellolide C 

Junceellolide C 是一种 cccDNA 转录抑制剂。Junceellolide C 能抑制 HepAD38 细胞中 HBV DNA 的复制,且能显著降低细胞上清液中的 HBV RNA 水平,其 EC50 值分别为 5.19 和 3.52 μM。Junceellolide C 具有抗乙肝病毒活性。

Junceellolide C

Junceellolide C Chemical Structure

CAS No. : 121769-82-2

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Junceellolide C 相关产品

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生物活性

Junceellolide C is a transcription inhibitor of cccDNA. Junceellolide C inhibits HBV DNA replication and significantly decreases the level of supernatant HBV RNA with EC50 values of 5.19, 3.52 μM respectively in HepAD38 cells. Junceellolide C is a potent anti-HBV agent[1].

IC50 & Target

EC50: 2.27 μM (HBV DNA replication), 3.52 μM (HBV RNA decrease) in HBeAg cells[1]

体外研究
(In Vitro)

Junceellolide C (10 μM; 72 hours) inhibits HBV DNA replication and significantly decreases the level of supernatant HBV RNA in HepAD38 cells with EC50 values of 2.27, 3.52 μM, respectively[1].
Junceellolide C (10 μM; 8 days) can capable to inhibit HBV cccDNA replenishment and also to induce the existed HBV cccDNA degradation[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Junceellolide C 相关抗体:

Cell Viability Assay[1]

Cell Line: HepAD38 cells
Concentration: 10 μM
Incubation Time: 72 h, 8 days
Result: Inhibited cccDNA transcription.

分子量

540.99

Formula

C26H33ClO10

CAS 号

121769-82-2

结构分类
  • Terpenoids
  • Diterpenoids
初始来源
  • 动物

South China Sea gorgonian Dichotella gemmacea

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
Data Sheet (538 KB) 产品使用指南 (1538 KB)

参考文献
  • [1]. Jiru Wu, et al. Briarane-type diterpenoids from a gorgonian coral Ellisella sp. with anti-HBV activities. Bioorg Chem. 2020 Dec;105:104423.  [Content Brief]

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