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Capsaicin

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产品名称: Capsaicin
产品型号: GOY-Y2181
产品展商: 谷研
产品文档: 无相关文档
发布时间:2023-04-26

简单介绍

Capsaicin≥ 15.27 mg/mL in DMSO, ≥ 52.3 mg/mL in EtOH with gentle warming


Capsaicin  的详细介绍


性能参数

产品名称

Capsaicin

规格

10mM (in 1mL DMSO) 50mg 100mg

货号

GOY-Y2181

 含量

>98.00%

CAS

404-86-4

别名

(E)-Capsaicin;Zostrix, Qutenza, Axsain, (E)-Capsaicin, Transacin, Capsidol

 

 

化学名

(E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-8-methylnon-6-enamide

分子式

C18H27NO3

分子量

分子 305.41

溶解度

≥ 15.27 mg/mL in DMSO, ≥ 52.3 mg/mL in EtOH with gentle warming

储存条件

4°C, protect from light

General tips

 

用途

仅供科研

价格

电询

详细内容

Capsaicin is an active component of chili peppers. It selectively binds to TRPV1 which is a heat-activated calcium channel. Capsaicin causes the channel to open below 37 °C. This is why capsaicin is linked to the sensation of heat. [1] Capsaicin has been reported to possess anti-carcinogenic and anti-mutagenic activities. In human glioma A172 cells, capsaicin reduced cell viability with IC50 of ~100 μM treated for 1 day. Capsaicin inhibited cell growth and induced apoptosis through down-regulation of Bcl-2 and activation of caspase-3. Capsaicin also induced terminal differentiation, which contribute to A172 cell growth inhibition.[2] On the other hand, capsaicin reduced the basal generation of ROS, which may played a role in the induction of apoptosis by capsaicin.[3] In MCF-7 cells, Capsaicin induced cell apoptosis through the mitochondrial pathway, and subsequently caused PARP-1 cleaved by activation of caspase-7.[4] In human SCLC cell line, capsaicin displayed robust anti-proliferative activity with MTT assay. Furthermore, capsaicin (10 mg/kg body weight) significantly reduced the growth rate of established (800 mm3) H69 tumors xenotransplanted in nude mice. [5]

References:

1. M. J. Caterina, M. A. Schumacher, M. Tominaga, T. A. Rosen, J. D. Levine and D. Julius, Nature 1997, 389, 816-824.

2. Y. G. Gil and M. K. Kang, Life Sci 2008, 82, 997-1003.

3. Y. S. Lee, D. H. Nam and J. A. Kim, Cancer Lett 2000, 161, 121-130.

4. H. C. Chang, S. T. Chen, S. Y. Chien, S. J. Kuo, H. T. Tsai and D. R. Chen, Hum Exp Toxicol 2011, 30, 1657-1665.

5. K. C. Brown, T. R. Witte, W. E. Hardman, H. Luo, Y. C. Chen, A. B. Carpenter, J. K. Lau and P. Dasgupta, PLoS One 2010, 5, e10243. >

 

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