1. Protein Tyrosine Kinase/RTK Stem Cell/Wnt MAPK/ERK Pathway
  2. SHP2 ERK
  3. SHP2-IN-44

SHP2-IN-44 (Compound 26) 是一种变构的、具有口服活性的 SHP2 抑制剂,其 IC50 为 27 nM。SHP2-IN-44 还能抑制 ERK 磷酸化 (IC50 为 299 nM),且不具有脱靶 hERG 活性。SHP2-IN-44 具有广谱抗癌活性,如治疗幼年型粒单核细胞白血病、神经母细胞瘤和乳腺癌。SHP2-IN-44 可用于努南综合征、LEOPARD 综合征和癌症研究。

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SHP2-IN-44

SHP2-IN-44 Chemical Structure

CAS No. : 2818955-47-2

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生物活性

SHP2-IN-44 (Compound 26) is an allosteric and orally active SHP2 inhibitor with an IC50 of 27  nM. SHP2-IN-44 also inhibits ERK phosphorylation (IC50 of 299  nM) without off-target hERG activity. SHP2-IN-44 has a broad-spectrum anticancer activity, such as juvenile myelomonocytic leukemia, neuroblastoma and breast cancer. SHP2-IN-44 can be used for Noonan syndrome, LEOPARD syndrome and cancers research[1].

分子量

471.98

Formula

C22H23ClFN7S

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.

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    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:
SHP2-IN-44
目录号:
HY-175803
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