1. MAPK/ERK Pathway GPCR/G Protein Immunology/Inflammation
  2. Interleukin Related Bombesin Receptor JNK
  3. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P

[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 

目录号: HY-103544
产品使用指南

[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 是 P 物质的衍生物,是神经肽和趋化因子受体的偏向激动剂。[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 激活 G12。[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 与 IL-8GRP受体 结合。[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 抑制 ERK-2 激活,激活 JNK 活性。[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 刺激中性粒细胞迁移和 Ca2+ 动员增加。[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 也是一种 bombesin 拮抗剂,并抑制小细胞肺癌的生长。

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[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P Chemical Structure

[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P Chemical Structure

CAS No. : 96736-12-8

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P, a Substance P derivative, is a biased agonist toward neuropeptide and chemokine receptors. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P activates G12. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P binds to IL-8 and GRP receptors. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P inhibits ERK-2 activation, activates JNK activity. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P stimulates an increase in neutrophil migration and Ca2+ mobilization. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P is also a bombesin antagonist, and inhibits the growth of small cell lung cancer[1][2][3]

分子量

1516.83

Formula

C79H109N19O12

CAS 号
Sequence

{d-Arg}-Pro-Lys-Pro-{d-Phe}-Gln-{d-Trp}-Phe-{d-Trp}-Leu-Leu-NH2

Sequence Shortening

{d-Arg}-PKP-{d-Phe}-Q-{d-Trp}-F-{d-Trp}-LL-NH2

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

[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P 相关分类

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产品名称:
[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P
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