Erastin愛拉斯?。ㄨF死亡激活劑)
產(chǎn)品編號 | 產(chǎn)品名稱 | 包裝規(guī)格 | 價格 |
NBS5879-1mg | Erastin愛拉斯?。ㄨF死亡激活劑) | 1mg | 850 |
NBS5879-5mg | Erastin愛拉斯?。ㄨF死亡激活劑) | 5mg | 1688 |
NBS5879-10mg | Erastin愛拉斯?。ㄨF死亡激活劑) | 10mg | 2938 |
NBS5879-50mg | Erastin愛拉斯汀(鐵死亡激活劑) | 50mg | 7938 |
產(chǎn)品簡介:
鐵死亡(Ferroptosis)是一種鐵依賴形式的非凋亡性細胞死亡。愛拉斯?。?span>Erastin)是一種鐵死亡激活劑(誘導(dǎo)劑)。體外誘導(dǎo)鐵死亡性細胞壞死,這一效應(yīng)可被鐵死亡抑制劑(比如:Ferrostatin-1、Trolox、環(huán)匹羅司乙醇胺、放線菌酮和β-巰基乙醇)所阻斷。HT-1080纖維肉瘤和Calu-1肺腫瘤細胞中,愛拉斯?。?span>5 μM)通過谷氨酸-胱氨酸反向轉(zhuǎn)運體(System Xc-)抑制胱氨酸攝??;以及在酶結(jié)合的熒光分析實驗中抑制谷氨酸釋放。在表達Ras和SV40小T腫瘤蛋白的細胞中選擇性誘導(dǎo)細胞死亡(IC50s = 1.25-5 μg/ml)。
產(chǎn)品特性:
1) 化學(xué)名:2-[1-[4-[2-(4-chlorophenoxy)acetyl]-1-piperazinyl]ethyl]-3-(2
-ethoxyphenyl)-4(3H)-quinazolinone
2) CAS NO:571203-78-6
3) 分子式:C30H31ClN4O4
4) 分子量:547.04
5) 外觀:固體
6) 純度:≥98%
7) 溶解性:溶于DMSO(≥5mg/ml,需要溫育助溶)、不溶于乙醇、不溶于水
保存條件:
-20oC干燥保存,至少2年有效。
儲存液制備:
質(zhì)量 溶劑體積 濃度 | 1mg | 5mg | 10mg |
1mM | 1.8280 mL | 9.1401 mL | 18.2802 mL |
5mM | 0.3656 mL | 1.8280 mL | 3.6560 mL |
10mM | 0.1828 mL | 0.9140 mL | 1.8280 mL |
【溫馨提示】:請根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;本品在溶液狀態(tài)不穩(wěn)定,建議現(xiàn)配現(xiàn)用。
產(chǎn)品使用: 【源自文獻,僅作參考】
文獻1,Liang, Z., Wu, Q., Wang, H. et al. Silencing of lncRNA MALAT1 facilitates erastin-induced ferroptosis in endometriosis through miR-145-5p/MUC1 signaling. Cell Death Discov. 8, 190 (2022). https://doi.org /10.1038/s41420-022-00975-w
體內(nèi)研究(動物模型):
動物模型(Animal Model):Endometriosis mouse model
實驗方法(Assay):Seven-to-8-week-old C57BL/6 female mice were obtained and 17-β-estradiol-3-benzoate (30μg/kg) was administered to each mouse every day for 3 days. We removed uterine horns from the donor mice and added them to saline. Endometrium was cut into 1mm2 fragments. The endometrial fragments from each uterine horn were suspended in 0.3ml saline and injected into the peritoneal cavities of recipient mice with an 18-gauge needle. At 8 days (5 days after the operation), endometrial-like lesions were established, and they were randomly divided into two groups (each group contained 12 mice).In the experimental group, each mouse received erastin (20mg/kg/day) by intraperitoneal injection over a 7-day period. In the control group, DMSO was used instead of erastin.At 15 days, the mice were sacrificed and endometriotic lesions were collected.
文獻2,Huo H, Zhou Z, Qin J, Liu W, Wang B, Gu Y. Erastin Disrupts Mitochondrial Permeability Transition Pore (mPTP) and Induces Apoptotic Death of Colorectal Cancer Cells. PLoS One. 2016 May 12;11(5):
e0154605. doi: 10.1371/journal.pone.0154605. PMID: 27171435; PMCID: PMC4865238.
體內(nèi)研究(動物模型):
動物模型(Animal Model):HT-29 tumor bearing SCID mice
實驗方法(Assay):Briefly, 2×106viable HT-29 cells in 100 μL of growth medium (per mouse) were subcutaneously inoculated, and mice bearing ~100 mm3tumors were randomly divided into three groups with 10 mice per group.Mice were treated daily with 10 or 30 mg/kg body weight of erastin (intraperitoneal injection, for 4 weeks) or vehicle control (Saline).
注意事項:
1. 針對溶解性比較差的化合物,可通過37℃孵育以及超聲的方式來促進其溶解。
2. 本品并非商業(yè)化的臨床藥物,僅用作科研用途,不得用作臨床診斷或治療,不得用于食品或藥品,絕對禁止用在人身上。
3. 為了您的安全和健康,請穿實驗服并戴一次性手套操作。
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