1. Protein Tyrosine Kinase/RTK Apoptosis JAK/STAT Signaling Stem Cell/Wnt
  2. Bcr-Abl Apoptosis STAT
  3. CHMFL-48

CHMFL-48 是一种具有口服活性的 BCR-ABL 激酶抑制剂,包括野生型 (wt) 和多种耐受 Imatinib (HY-15463) 的突变体。CHMFL-48 对 ABL 野生型和 ABL T315I 突变体的 IC50 分别为 1 nM 和 0.8 nM。CHMFL-48 通过阻断 BCR-ABL 野生型及突变体的自磷酸化,影响下游信号传导介质,如 STAT5CRKL,进而导致细胞周期阻滞和细胞凋亡 (Apoptosis)。CHMFL-48 有望用于慢性粒细胞白血病 (CML) 的研究。

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CHMFL-48 Chemical Structure

CHMFL-48 Chemical Structure

CAS No. : 2479290-65-6

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生物活性

CHMFL-48 is an orally active BCR-ABL kinase inhibitor targeting both wild-type (wt) and various imatinib-resistant mutants. The IC50 values for CHMFL-48 against ABL wild-type and ABL T315I mutant are 1 nM and 0.8 nM, respectively. CHMFL-48 exerts its effects by blocking the autophosphorylation of BCR-ABL wild-type and mutant forms, which impacts downstream signaling mediators such as STAT5 and CRKL, leading to cell cycle arrest and induction of apoptosis. CHMFL-48 holds potential for research into chronic myeloid leukemia (CML)[1].

IC50 & Target

WT BCR-ABL

1 nM (IC50)

Bcr-AblT315I

0.8 nM (IC50)

STAT5

 

分子量

573.61

Formula

C31H30F3N7O

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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    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:
CHMFL-48
目录号:
HY-164469
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