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(D-Arg1,D-Phe5,D-Trp7.9,Leu11)-Substance P

更新时间:2024-01-02 10:59:49

(D-Arg1,D-Phe5,D-Trp7.9,Leu11)-Substance P结构式
(D-Arg1,D-Phe5,D-Trp7.9,Leu11)-Substance P结构式
品牌特惠专场
常用名 (D-Arg1,D-Phe5,D-Trp7.9,Leu11)-Substance P 英文名 (D-Arg1,D-Phe5,D-Trp7.9,Leu11)-Substance P
CAS号 96736-12-8 分子量 1516.831
密度 1.4±0.1 g/cm3 沸点 N/A
分子式 C79H109N19O12 熔点 N/A
MSDS 美版 闪点 N/A

 用途


[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-8 和 GRP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。

 名称

英文名 [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P
英文别名 更多

 生物活性

描述 [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-8 和 GRP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。
相关类别
参考文献

[1]. Jarpe MB, et al. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]Substance P acts as a biased agonist toward neuropeptide and chemokine receptors. J Biol Chem. 1998 Jan 30;273(5):3097-104.  

[2]. Woll PJ, Rozengurt E. [D-Arg1,D-Phe5,D-Trp7,9,Leu11]substance P, a potent bombesin antagonist in murine Swiss 3T3 cells, inhibits the growth of human small cell lung cancer cells in vitro. Proc Natl Acad Sci U S A. 1988 Mar;85(6):1859-63.  

 物理化学性质

密度 1.4±0.1 g/cm3
分子式 C79H109N19O12
分子量 1516.831
精确质量 1515.850342
PSA 505.12000
LogP 3.94
折射率 1.677

 安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危险品运输编码 NONH for all modes of transport

 文献30

更多文献
Effect of nanoconfinement on polymer dynamics: surface layers and interphases.

PLoS ONE 9(7) , e103118, (2014)

We present neutron spin echo experiments that address the much debated topic of dynamic phenomena in polymer melts that are induced by interacting with a confining surface. We find an anchored surface...

Intrarenal ghrelin receptor antagonism prevents high-fat diet-induced hypertension in male rats.

Endocrinology 155(7) , 2658-66, (2014)

Excess weight gain contributes up to 65% of the risk of primary hypertension, and the increase in blood pressure in response to high-fat diet (HFD) is preceded by significant increases in renal tubula...

Over-expression of the truncated ghrelin receptor polypeptide attenuates the constitutive activation of phosphatidylinositol-specific phospholipase C by ghrelin receptors but has no effect on ghrelin-stimulated extracellular signal-regulated kinase 1/2 activity.

Int. J. Biochem. Cell Biol. 39(4) , 752-64, (2007)

In addition to regulating growth hormone release from the pituitary, ghrelin receptors also influence cell proliferation and apoptosis. By studying mitogen-activated protein kinase activity in human e...

 英文别名

AntagonistD,D-Arg-Pro-Lys-Pro-D-Phe-Gln-D-Trp-Phe-D-Trp-Leu-Leu-NH2
L-Leucinamide, D-arginyl-L-prolyl-L-lysyl-L-prolyl-D-phenylalanyl-L-glutaminyl-D-tryptophyl-L-phenylalanyl-D-tryptophyl-L-leucyl-
D-Arg-L-Pro-L-Lys-L-Pro-D-Phe-L-Gln-D-Trp-L-Phe-D-Trp-L-Leu-L-Leu-NH2
M.W. 1516.85 C79H109N19O12
D-ARG-PRO-LYS-PRO-D-PHE-GLN-D-TRP-PHE-D-TRP-LEU-LEU-NH2
D-Arginyl-L-prolyl-L-lysyl-L-prolyl-D-phenylalanyl-L-glutaminyl-D-tryptophyl-L-phenylalanyl-D-tryptophyl-L-leucyl-L-leucinamide
H-D-ARG-PRO-LYS-PRO-D-PHE-GLN-D-TRP-PHE-D-TRP-LEU-LEU-NH2
DARG-PRO-LYS-PRO-DPHE-GLN-DTRP-PHE-DTRP-LEU-LEU-NH2: DA-PKP-DF-Q-DW-F-DW-LL-NH2
Substance P-[D-Arg1,D-Phe5,D-Trp7,9,Leu11]
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