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Cercosporamide from Cercosporidium henningsii

商品编号: S1203
图示 货号 库存 价格(¥) 数量

备注:

国外库存,货期2-4周,具体详情请联系销售人员。

质量文档

详细介绍

l  基本信息

产品名称

Cercosporamide from Cercosporidium henningsii

一般描述

Cercosporamide was initially identified as a phytotoxin with broad-spectrum anti-fungal activity. Studies have shown that cercosporamide is a specific, highly potent fungal inhibitor of the cell wall integrity-signaling pathway mediator, protein kinase (Pkc1) inhibitor.

别 称

4-Dibenzofurancarboxamide

纯 度

≥98%(HPLC)

CAS NO.

131436-22-1

分子式

C16H13NO7

分子量

331.28

适用范围

生物试剂,适用于细胞培养等

l  理化信息

外 观

淡黄色至黄色

溶解性(25°C)

DMSO

~5mg/mL

乙醇

Slightly soluble

l  生物学信息

生物活性/药理作用

Cercosporamide was initially identified as a phytotoxin with broad-spectrum anti-fungal activity. Studies have shown that cercosporamide is a specific, highly potent fungal inhibitor of the cell wall integrity-signaling pathway mediator, protein kinase (Pkc1) inhibitor. Semisynthetic cercosporamide analogues demonstrated hypoglycemic activity and therefore, serve as candidates for potential new anti diabetic drugs. Cercosporamide was found to block eIF4E (Eukaryotic Initiation Factor) phosphorylation in cultured cancer cells, inducing apoptosis, suppressing proliferation, and reducing soft agar colonization. Its eIF4E phosphorylation inhibitory effect was also shown when administrated orally on xenograft human tissue and mouse liver tissue. Cercosporamide is a potent and selective Mnk inhibitor. It reduces tumor growth in xenografted HCT116 tumor and suppresses the outgrowth of B16 melanoma lung metastases. Hence, blocking Mnk function and eIF4E phosphorylation may be an attractive anticancer strategy.

l  存储

存储温度

−20°C

l  注意事项及免责声明

本产品仅用于实验研究,不得作为药物使用,不得用于家用或其它用途。

l  参考文献

1.    http://www.drugbank.ca

2.    https://ncit.nci.nih.gov

3.  https://www.ncbi.nlm.nih.gov