1. MAPK/ERK Pathway GPCR/G Protein Stem Cell/Wnt Protein Tyrosine Kinase/RTK
  2. Raf Ras MEK ERK VEGFR Tie c-Fms
  3. SJ-C1044

SJ-C1044 是一种口服有效的泛 RAF 抑制剂,具有免疫调节和抗肿瘤活性。SJ-C1044 分别抑制野生型 BRAF、野生型 CRAFBRAF (V600E)IC50 值分别为 331, 257 和 187 nM。SJ-C1044 通过抑制 kras 激活和 MEK-ERK 磷酸化来抑制肿瘤细胞的增殖。此外,SJ-C1044 对 VEGFR2TIE2CSF1R 也具有一定的抑制作用,IC50 值分别为 100、23 和 235 nM。SJ-C1044 通过抑制血管生成和调节巨噬细胞功能来改善肿瘤免疫微环境。SJ-C1044 可用于结直肠癌的研究。

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SJ-C1044 Chemical Structure

SJ-C1044 Chemical Structure

CAS No. : 2121503-76-0

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

SJ-C1044 is an orally available pan-RAF inhibitor with immunomodulatory and anti-tumor activities. SJ-C1044 inhibits wild-type BRAF, wild-type CRAF, and BRAF (V600E) with IC50 values ??of 331, 257, and 187 nM, respectively. SJ-C1044 inhibits tumor cell proliferation by inhibiting kras activation and MEK-ERK phosphorylation. In addition, SJ-C1044 also has a certain inhibitory effect on VEGFR2, TIE2, and CSF1R, with IC50 values ??of 100, 23, and 235 nM, respectively. SJ-C1044 improves the tumor immune microenvironment by inhibiting angiogenesis and regulating macrophage function. SJ-C1044 can be used in the study of colorectal cancer[1].

IC50 & Target[1]

VEGFR2

100 nM (IC50)

BRAFWT

331 nM (IC50)

BRafV600E

187 nM (IC50)

CRAF

257 nM (IC50)

Tie2

23 nM (IC50)

CSF1R

235 nM (IC50)

分子量

561.41

Formula

C25H14F7N7O

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
  • 摩尔计算器

  • 稀释计算器

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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Help & FAQs
  • 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:
SJ-C1044
目录号:
HY-164529
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