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首页-小分子抑制剂&激动剂-PI3K/Akt/mTOR Pathway-mTOR-Deforolimus
Deforolimus

Chemical Structure : Deforolimus

CAS No.: 572924-54-0

Deforolimus (AP-23573;MK-8669;Ridaforolimus)

货号: PC-45902Not For Human Use, Lab Use Only.

Deforolimus (AP-23573, MK-8669, Ridaforolimus) potent, selective mTOR inhibitor with IC50 of 0.2 nM in HT-1080 cell line.

规格 价格 库存 数量
10 mg ¥780 In stock
25 mg ¥1280 In stock
50 mg ¥1980 In stock
100 mg ¥3280 In stock
250 mg Get quote
1 g Get quote

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Deforolimus (AP-23573, MK-8669, Ridaforolimus) potent, selective mTOR inhibitor with IC50 of 0.2 nM in HT-1080 cell line.
Deforolimus displays significant antiproliferative activity a broad panel of cell lines with EC50 of 0.2-2.3 nM.
Deforolimus potently and selectively inhibits VEGF production in a dose-dependent manner.
Deforolimus exerts significant antitumor effects in mice bearing PC-3 (prostate), HCT-116 (colon), MCF7 (breast), PANC-1 (pancreas) or A549 (lung) xenografts.

物理化学性质&存储条件

分子量 990.2061
分子式 C53H84NO14P
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

DMSO: ≥ 44 mg/mL

Chemical Name/SMILES

Rapamycin, 42-(dimethylphosphinate) (9CI)

参考文献

1. Rivera VM, et al. Mol Cancer Ther. 2011 Jun;10(6):1059-71.

2. Legrier ME, et al. Cancer Res. 2007 Dec 1;67(23):11300-8.

3. Becker MA, et al. BMC Cancer. 2016 Oct 20;16(1):814.

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