• 13585831301
  • 021-59541103 021-60443211
  • 3004967995

Tamoxifen

  • 產(chǎn)品貨號:CS-01Y65980
  • 產(chǎn)品價(jià)格:電議
  • 產(chǎn)品產(chǎn)地:進(jìn)口、國產(chǎn)
  • 包裝類型:5g 10g
  • 采購熱度:180
  • 庫存:100
  • CAS號:10540-29-1
  • 方法:
  • 含量:>98.00%
  • 品牌名稱:莼試
  • 分子式:C26H29NO
  • 分子量:371.51

簡介內(nèi)容:質(zhì)量保證、價(jià)格優(yōu)惠

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標(biāo)簽:Tamoxifen 

產(chǎn)品目錄

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聯(lián)系人:高小姐

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詳細(xì)地址:上海市嘉定區(qū)澄瀏公路52號中科院技術(shù)轉(zhuǎn)移中心24號樓

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 化學(xué)性質(zhì):                                                                                                             

規(guī)格

5g 10g

CAS

10540-29-1

別名

N/A

化學(xué)名

2-[4-[(1Z)-1,2-diphenyl-1-buten-1-yl]phenoxy]-N,N-dimethyl-ethanamine

分子式

C26H29NO

分子量

371.51

溶解度

18.6mg/mL in DMSO

儲存條件

4°C, protect from light

General tips

For obtaining a higher solubility , please warm the tube at 37 and shake it in the ultrasonic bath for a while.

Shipping Condition

Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request

 

產(chǎn)品描述:                                                                                                             

IC50: 5.5–10 μM

Transforming growth factor-β (TGF-β) is a growth factor which is capable of inhibiting prostate cell growth in vitro, and has apparent prostate cell growth regulatory roles in vivo. A second element of potential importance in regulating the growth of prostate cancer cells is the serine/threonine kinase, protein kinase C (PKC). PKC is a signaling enzyme of known importance in regulating the growth and/or differentiation of a variety of cell types; inhibition of its kinase activity is associated with loss of regulatory function. Tamoxifen is a drug known to have TGF-β modulatory and PKC inhibitory effects.

In vitro: IC50s for growth inhibition ranged from 5.5–10 μM, and were not affected by estrogen. Tamoxifen-mediated growth inhibition was not associated with induction of TGF-β. However, tamoxifen treatment was associated with inhibition of PKC, which was followed by induction of p21waf1/cip1, Rb dephosphorylation, and G1/S phase cell cycle arrest [1].

In vivo: The tumor cell kinetics of MCF-7 human breast carcinoma xenografts grown in nude mice can be significantly altered by hormonal manipu lation. Tamoxifen treatment or E2 deprivation resulted in an approximate doubling of the Tpol and an approximately 40% reduction in labeling index as compared to E2-stimulated tumors. An increase in cell loss rate was calculated for both tamoxifen treatment and E2 deprivation [2].

Clinical trial: Tamoxifen reduces the risk of recurrence and death from breast cancer when given as adjuvant therapy, and it provides effective palliation for metastatic breast cancer. Its use is therefore indicated for both premenopausal and postmenopausal women having estrogen-receptor–positive invasive breast cancer [3].

 
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原創(chuàng)作者:上海莼試生物技術(shù)有限公司

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