1. MAPK/ERK Pathway Cell Cycle/DNA Damage
  2. SOS1 PERK
  3. SOS1-IN-22

SOS1-IN-22 是一种 非七激酶子同源物 (SOS1) 抑制剂。SOS1-IN-22 能够抑制 KRAS-G12C/SOS1 复合物的形成,其 IC50 值为 40.28 nM。SOS1-IN-22 可以降低 ERK 的磷酸化水平。SOS1-IN-22 可用于癌症研究,如胰腺癌和阑尾癌。

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SOS1-IN-22

SOS1-IN-22 Chemical Structure

CAS No. : 3092445-74-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

SOS1-IN-22 is a son of sevenless homolog 1 (SOS1) inhibitor. SOS1-IN-22 can inhibit KRAS-G12C/SOS1 complex formation with an IC50 value of 40.28 nM. SOS1-IN-22 can reduce phosphorylation ERK levels. SOS1-IN-22 can be used for the research of cancer, such as pancreatic carcinoma and appendiceal carcinoma[1].

体外研究
(In Vitro)

SOS1-IN-22 (Compound A15f) (72 h) 在 K562 细胞中显示出增殖抑制活性,其 IC50 值为 1.03 μM[1]
SOS1-IN-22 (0-10000 nM) 可抑制 KRAS-G12C/SOS1 复合物的形成[1]
SOS1-IN-22 (0-300 nM, 2 h) 以剂量依赖性方式降低 K562 细胞中的 pERK 水平[1]
SOS1-IN-22 (1-10 μM, 2 h) 与 AMG510 (HY-114277) (20 nM) 联合使用时,可显著增强对 MIAPaCa-2 细胞中 pERK 表达的抑制作用[1]
SOS1-IN-22 (0.0001-10 μM, 72 h) 在 HL-7702 和 5k 细胞中未表现出显著的细胞毒性[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: MIAPaCa-2 cells
Concentration: 1 and 10 μM
Incubation Time: 2 h, combined within AMG510 (HY-114277) (20 nM)
Result: Decreased pERK levels.
分子量

462.51

Formula

C24H29F3N4O2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
SOS1-IN-22
目录号:
HY-175560
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