mTOR inhibitor-7

目录号: GC61100纯度: >98.00%
mTOR inhibitor-7 是一种雷帕霉素衍生物,是一种有效的、选择性的、具有口服活性的脑渗透性 mTOR 抑制剂,IC50 和 Ki 分别为 5 nM 和 3.6 nM。

mTOR inhibitor-7
Cas No.: 1927857-98-4
规格价格库存数量操作
5mg¥3,690.00现货
1
10mg¥6,390.00现货
1
25mg¥9,900.00现货
1
50mg¥18,000.00现货
1
100mg¥27,900.00现货
1
10mM (in 1mL DMSO)¥4,059.00现货
1

文献被引

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    Nature
    641, 529–536 (2025)
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    628, 630–638 (2024)
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    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    Science
    387(6739) (2025)
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    Science
    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    Cell Research
    31, 1291–1307 (2021)

产品描述 Description

mTOR inhibitor-7 is an orally available, and brain-penetrant mTOR inhibitor extracted from patent WO2017198346A1, compound example 44, has an IC50 of 5 nM for mTOR. mTOR inhibitor-7 can be used for the research of neurological disorder[1].

mTOR inhibitor-7 (0.04-5 μμ; 1 hour) has IC50s of 197 nM and 87 nM for pPKB S473 and pS6 S235/S236, respectively, in-cell western blot. S6 kinase (S6K), S6 ribosomal protein (S6rP) and 4E-binding protein (4E-BP) are prominent downstream effectors of mTOR[1]. Western Blot Analysis[1] Cell Line: A2058 cells

[1]. Denise RAGEOT, et al. Treatment of neurological disorders. WO2017198346A1.

产品文档 Product Documents

Purity:>98.00%

化学性质Chemical Properties

CAS 号
1927857-98-4
SMILES
NC1=NC=C(C2=NC(N3[C@H](C)COC[C@@H]3C)=NC(N4[C@H](C)COCC4)=N2)C(C(F)F)=C1
分子式
C20H27F2N7O2
分子量
435.47 g/mol
溶解性
DMSO: 100 mg/mL (229.64 mM)
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol