Bradykinin (Synonyms: 缓激肽)
目录号: PC61700 纯度: ≥99%
CAS No. :58-82-2
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中文名称
Bradykinin
中文别名
3-环己基-6-(二甲基氨基)-1-甲基-1,3,5-三嗪-2,4-二酮;缓激肽;舒缓激肽
英文名称
Bradykinin
英文别名
Bradykinin;Bradykinin (1-3);BRADYZIDE;brs640;Callideic;Callidin I;H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH;H-RPPGFSPFR-OH;H-RPPGFSRPFR-OH;prs640;RPPGFSPFR;RPPGFSPFR-OH
Cas No.
58-82-2
分子式
C57H81N13O12.C2Ho2F3
分子量
1254.36
包装储存
sealed storage and away from moisture;Powder; -80°C; 2 years; -20°C; 1 year;
生物活性
Bradykinin is an active peptide that is generated by the kallikrein-kinin system. It is a inflammatory mediator and also recognized as a neuromediator and regulator of several vascular and renal functions.
性状
Solid
IC50 & Target[1][2]
Bradykinin B2 Receptor (B2R)
 Human Endogenous Metabolite
 
体外研究(In Vitro)
Bradykinin is a potent vasodilator peptide that exerts its vasodilatory action through stimulation of specific endothelial B2 receptors, thereby causing the release of prostacyclin, NO, and EDHF. Bradykinin has been reported to be involved in the progression of many types of cancer. Bradykinin treatment promotes the invasion and migration of colorectal cancer cells. Bradykinin treatment stimulates ERK1/2 activation and IL-6 production. Exogenous bradykinin markedly inhibits TF expression in mRNA and protein level induced by LPS in a dose-dependent manner. The NO synthase antagonist L-NAME and PI3K inhibitor LY294002 dramatically abolish the inhibitory effects of bradykinin on tissue factor expression.Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Application of 1 μM bradykinin to the ovary produces significant decreases in heart rate and mean arterial pressure. In vagotomized animals, application of 1 μM bradykinin to the ovary produces bradycardia and hypotension similar to the responses evoked when vagal innervation is intact. Vascular bradykinin can improve pancreatic microcirculation and hemorheology in rats with severe acute pancreatitis. The pancreatic microcirculatory blood flow volume and velocity in the vascular bradykinin treatment group increases gradually after 48 h. PI3K/Akt signaling pathway activation induced by bradykinin administration reduces the activity of GSK-3β and MAPK, and reduces NF-x03BA;B level in the nucleus, thereby inhibiting TF expression. Consistent with this, intraperitoneal injection of C57/BL6 mice with bradykinin also inhibits the thrombus formation induced by ligation of inferior ve
运输条件
Room temperature or refrigerated transport.
储存方式
sealed storage and away from moisture;Powder; -80°C; 2 years; -20°C; 1 year;
ClinicalTrial
SequenceShortening

RPPGFSPFR

Sequence

Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg

结构分类
Others
溶解度数据
体外研究:
H2O : ≥ 100 mg/mL(94.32 mM)
*≥ means soluble, but saturation unknown.
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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