聯系電話
- 聯系人:
- 曹女士
- 電話:
- 400-6111-883
- 手機:
- 售后:
- 4006-111-883
- 傳真:
- 86-21-34615995
- 地址:
- 上海市浦東新區天雄路166弄1號3樓
- 網址:
- www.yeasen.com
掃一掃訪問手機商鋪
ITL1006-Chloroquine diphosphate salt
Chloroquine diphosphate salt,>98%
【英文同義名】:Chloroquine Diphosphate, Chloroquine phosphate, Aralen phosphate, Chingamin phosphate, Arechin
【中文同義名】:二磷酸氯喹
訂購信息:(*,常備現貨)
品 牌 | 產品名稱 | 產品貨號 | 規 格 | 目錄價(元) |
Gene Operation | Chloroquine diphosphate salt | ITL1006-0001G | 1 g | ¥979.00 |
ITL1006-0005G | 5 g | ¥1,899.00 | ||
ITL1006-0500MG | 500 mg | ¥549.00 |
產品描述
Chloroquine diphosphate salt是Chloroquine的二磷酸鹽型式。Chloroquine是抗瘧疾和抗風濕劑,也是ATM活化劑 [1]。Chloroquine抑制鉀離子通道內向整流,其機制包括離子通道門控變構和阻斷 [2]。 Chloroquine能顯著增加肺動脈內皮細胞(PAEC)細胞表面BMPR-II蛋白的獨立轉錄,能顯著增加突變 BMPR-II PAEC細胞和血液增生內皮細胞BMP9-BMPR-II信號通路靶點Id1, miR21和miR27a的表達 [3]。在原位移植(U87MG)人成膠質細胞瘤小鼠模型中,Chloroquine能激活p53通路,抑制細胞生長。Chloroquine也能誘導人腦膠質瘤細胞凋亡 [4]。
靶點
靶點 | ATM |
化學特性
Cas No.: 50-63-5 | 分子量: 515.86 |
分子式: C18H26ClN3.2H3O4P | 純度: >98% |
同義名: Chloroquine Diphosphate, Chloroquine phosphate, Aralen phosphate, Chingamin phosphate, Arechin | |
化學名: 4-N-(7-chloroquinolin-4-yl)-1-N,1-N-diethylpentane-1,4-diamine;phosphoric acid | |
外觀: 白色固體 | |
溶解: 溶于DMSO (up to 100 mM) | |
保存:3年 -20℃粉狀 |
儲存液配制
儲存液 (1 ml DMSO體系) | 1 mM | 5 mM | 10 mM | 25 mM | 50 mM | 100 mM |
質量(mg) | 0.5159 | 2.5793 | 5.1586 | 12.8966 | 25.7931 | 51.5863 |
結構式
使用濃度(僅作參考)
Chloroquine diphosphate salt的具體使用濃度請參考相關文獻,并根據自身實驗條件(如實驗目的,細胞種類,培養特性等)進行摸索和優化。
參考文獻
[1] Slater AF. Chloroquine: mechanism of drug action and resistance in Plasmodium falciparum. Pharmacol Ther. 57(2-3):203-35 (1993).
[2] Ponce-Balbuena D, et al. Molecular Mechanisms of Chloroquine Inhibition of Heterologously Expressed Kir6.2/SUR2A Channels. Molecular Pharmacology. 82(5):803-813 (2012).
[3] Dunmore BJ, et al. The lysosomal inhibitor, chloroquine, increases cell surface BMPR-II levels and restores BMP9 signalling in endothelial cells harbouring BMPR-II mutations. Human Molecular Genetics. 22(18):3667-3679 (2013).
[4] Kim EL, et al. Chloroquine activates the p53 pathway and induces apoptosis in human glioma cells. Neuro-Oncology. 12(4):389-400 (2010).