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  3. RG 14921

RG 14921是一种与erbstatin结构相关的化合物,通过动力学分析研究了其对表皮生长因子(EGF)受体酪氨酸激酶和CAMP依赖性激酶活性的抑制机制。这两种化合物都是EGF受体激酶的慢结合抑制剂。Erbstatin作为部分竞争性抑制剂抑制EGF受体激酶,相对于ATP和肽底物,表明它结合在酶的ATP和肽底物结合位点不同的位置,从而降低酶对两种底物的结合亲和力。相比之下,衍生物RG 14921以非竞争性抑制剂的方式抑制EGF受体激酶活性,相对于ATP和肽底物。结构上相关的化合物表现出不同的抑制模式,这表明受体激酶域的催化中心可能具有动态和可能扩展的结构。Erbstatin和RG 14921对CAMP依赖性蛋白激酶活性产生了类似的影响。在这个系统中,这两种化合物都表现出强烈的抑制作用,并且以竞争性抑制ATP和非竞争性抑制肽底物的方式起作用。

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RG 14921 Chemical Structure

RG 14921 Chemical Structure

CAS No. : 144909-21-7

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  • 生物活性

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生物活性

RG 14921, a compound structurally related to erbstatin, was investigated for its mechanism of inhibition of epidermal growth factor (EGF) receptor tyrosine kinase and CAMP-dependent kinase activity by kinetic analysis. Both compounds are slow-binding inhibitors of EGF receptor kinase. Erbstatin inhibits EGF receptor kinase as a partially competitive inhibitor relative to ATP and peptide substrates, suggesting that it binds at different positions in the enzyme's ATP- and peptide substrate-binding sites, thereby reducing the enzyme's binding affinity for both substrates. In contrast, the derivative RG 14921 inhibits EGF receptor kinase activity as a noncompetitive inhibitor relative to ATP and peptide substrates. Structurally related compounds exhibit different modes of inhibition, suggesting that the catalytic center of the receptor kinase domain may have a dynamic and possibly extended structure. Erbstatin and RG 14921 exerted similar effects on CAMP-dependent protein kinase activity. In this system, both compounds exhibited strong inhibition and acted in a competitive inhibition manner with ATP and a noncompetitive inhibition manner with peptide substrates.

分子量

203.19

Formula

C11H9NO3

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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参考文献

RG 14921 相关分类

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产品名称:
RG 14921
目录号:
HY-118175
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