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Rapamycin (Sirolimus) 雷帕黴素(西(xī)羅莫司)
目錄号 MZ0201-10MG 售價 248.00元
規格 10mg 運輸溫度 室溫運輸
其他名稱 Sirolimus, Antibiotic AY 22989, AY 22989, Cypher, RAPA, NSC-226080, Rapamune, SILA 9268A 保存溫度 -20ºC幹燥保存
CAS号 53123-88-9 有效期 至少2年(nián)
應用 mTOR抑制劑 訂購數量
産品簡介:

Rapamycin (Sirolimus) 雷帕黴素(西(xī)羅莫司)

 

産品标簽

Rapamycin 雷帕黴素;Sirolimus 西(xī)羅莫司;3-MA 3-甲基腺嘌呤;自(zì)吞噬抑制劑 Autophagy inhibitor;mTOR;CAS:53123-88-9;


産品信息                                                                                    

産品名稱

産品編号

CAS NO.

規格            

價格(元) 

Rapamycin (Sirolimus) 雷帕黴素(西(xī)羅莫司)  

MZ0201-10MG        

53123-88-9    

10mg

248

Rapamycin (Sirolimus) 雷帕黴素(西(xī)羅莫司)

MZ0201-50MG

53123-88-9

50mg

480

Rapamycin (Sirolimus) 雷帕黴素(西(xī)羅莫司)

MZ0201-100MG

53123-88-9

100mg

680

Rapamycin (Sirolimus) 雷帕黴素(西(xī)羅莫司)

MZ0201-500MG

53123-88-9

500mg

2680

Rapamycin (Sirolimus) 雷帕黴素(西(xī)羅莫司)

MZ0201-1000MG

53123-88-9

1g

3980

【溫馨提示】:見(jiàn)我司的小(xiǎo)分子化合物(wù)常見(jiàn)問題-懋康生(shēng)物(wù)


産品描述

雷帕黴素(Rapamycin),也稱西(xī)羅莫司(Sirolimus),AY 22989,一(yī)種分離自(zì)細菌的大環内酯化合物(wù),抗真菌劑和免疫抑制劑。雷帕黴素是一(yī)種特異性的mTOR抑制劑,IC50為(wèi)~0.1nM(HEK293細胞)。與細胞内受體FKBP-12結合形成複合物(wù),之後作用于mTOR中的FRB結構域從(cóng)而抑制蛋白(bái)活性。雷帕黴素處理細胞引起p70 S6激酶的去磷酸化和功能(néng)失活(IC50= 50 pM)。還(hái)能(néng)引起4E-BP1/PHAS1去磷酸化,進而促使其結合并失活eIF4E。雷帕黴素能(néng)夠阻斷蛋白(bái)合成和誘導細胞周期停滞在G1期。還(hái)能(néng)誘導酵母和哺乳動物(wù)細胞的自(zì)吞噬現象。能(néng)驅使人多(duō)能(néng)幹細胞(hPSC)分化成中内胚層和血液祖細胞。


産品特性

1)CAS NO:53123-88-9

2)化學名:(3S,6R,7E,9R,10R,12R,14S,15E,17E,19E,21S,23S,26R,27R,34aS)-9,10,12,13,14,21,22,23,24,25, 26,27,32,33,34,34a-Hexadecahydro-9,27-dihydroxy-3-[(1R)-2-[(1S,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylethyl]-10,21-dimethoxy-6,8,12,14,20,26-hexamethyl-23,27-epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclohentriacontine-1,5,11,28,29(4H,6H,31H)-pentone

3)同義名:Sirolimus, Antibiotic AY 22989, AY 22989, Cypher, RAPA, NSC-226080,Rapamune, SILA 9268A

4)分子式:C51H79NO13

5)分子量:914.18

6)純度:≥98%

7)外觀:白(bái)色至類白(bái)色固體

8)溶解性:溶于DMSO(25mg/ml),乙醇(15mg/ml),幾乎不溶于水(shuǐ)

9)化學結構圖:


保存與運輸方法

保存:-20ºC幹燥保存,至少2年(nián)有效。

運輸:室溫運輸。


使用方法【源自(zì)文獻,僅作參考】

文獻1,Iwamaru A et al. Silencing mammalian target of rapamycin signaling by small interfering RNA enhances rapamycin-induced autophagy in malignant glioma cells. Oncogene. 2007 Mar 22; 26(13):1840-51. PMID: 17001313

體外研究:

細胞類型(Cell type):Human malignant glioma U87-MG and A172 cells

藥物(wù)配制(Preparation):Rapamycin was dissolved in DMSO to make 1mM stock solution and stored at -20℃.

實驗方法(Assay):Tumor cells were exposed to rapamycin (1, 10 or 100 nm) for 24 or 48 h. The cytotoxic effect of rapamycin was determined using a WST-1 cell proliferation assay.

文獻2,Caramés B et al. Autophagy activation by rapamycin reduces severity of experimental osteoarthritis. Ann Rheum Dis. 2012 Apr;71(4):575-81. PMID: 22084394

體内研究:

動物(wù)模型(Animal Model):Experimental osteoarthritis was induced in 2-month-old male C57Bl/6J mice

藥物(wù)配制(Preparation):Rapamycin was dissolved in DMSO at 25mg/ml and stored at -20℃. For injection, the stock solution was diluted in phosphate buffered saline (PBS).

注射劑量(Dosages):Mice received daily intraperitoneal injections of rapamycin at 1 mg/kg body weight/dose in a total injection volume of 0.3 ml for 10 weeks and control animals received the DMSO vehicle at 0.4% in a total injection volume of 0.3 ml.

給藥途徑(Administration):Intraperitoneal (i.p.) injection

文獻3,Eshleman JS et al. Inhibition of the Mammalian Target of Rapamycin Sensitizes U87 Xenografts to Fractionated Radiation Therapy. Cancer Res. 2002 Dec 15;62(24):7291-7. PMID: 12499272

體外研究:

細胞類型(Cell type):A172, U87, and U118 malignant glioma cell lines

藥物(wù)配制(Preparation):Rapamycin (NSC 226080) was dissolved in ethanol to yield a 5 mg/ml stock solution, which was stored at −20°C.

實驗方法(Assay):Tumor cells were incubated with 0 or 100 nM rapamycin at 37°C for 72 h and then processed in a MTS assay.

體内研究:

動物(wù)模型(Animal Model):8-10-week-old female athymic nude mice by s.c. injection of 2-5 million U87 cells

藥物(wù)配制(Preparation):For rapamycin injections, stock rapamycin was diluted first in sterile 10% PEG400/8% ethanol and then in an equal volume of sterile 10% Tween 80 for a final concentration of 20 μg rapamycin/100 μl. Rapamycin was delivered by i.p. injection, and the doses of rapamycin were calculated assuming that all mice weighed 20 g. 

給藥途徑(Administration):Intraperitoneal (i.p.) injection


注意事(shì)項

1)雷帕黴素幾乎不溶于水(shuǐ)(文獻報(bào)道僅2.6µg/ml)。[Simamora P et al. Int J Pharm. 2001 Feb 1;213(1-2):25-9.]

2)本品不是臨床藥物(wù),隻能(néng)用于科研用途,不能(néng)用于診斷或臨床用途。

3)為(wèi)了您的安全和健康,請穿實驗服并戴一(yī)次性手套操作。


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