
PAR-4 Agonist Peptide, amide
CAS No. 352017-71-1
PAR-4 Agonist Peptide, amide ( PAR-4-AP; AY-NH2 )
产品货号. M29763 CAS No. 352017-71-1
PAR-4 agonist peptide stimulates thromboxane production by human platelets with the maximal response to this agonist being approximately half of that observed after maximal thrombin stimulation.
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1058 | 有现货 |
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10MG | ¥1778 | 有现货 |
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25MG | ¥3010 | 有现货 |
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50MG | ¥4291 | 有现货 |
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100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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生物学信息
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产品名称PAR-4 Agonist Peptide, amide
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述PAR-4 agonist peptide stimulates thromboxane production by human platelets with the maximal response to this agonist being approximately half of that observed after maximal thrombin stimulation.
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产品描述PAR-4 agonist peptide stimulates thromboxane production by human platelets with the maximal response to this agonist being approximately half of that observed after maximal thrombin stimulation.(In Vivo):Compared with their BALB/cBy controls, SCID mice have a significantly greater abdominal response to colorectal distension (CRD) at the distension levels of 0.04 to 0.1 mL increasing the intensity of EMG response by 384% to 132%, respectively (P<0.01; P<0.01; P<0.01; P<0.001). PAR-4 activation effectively reverses this hypersensitivity (P<0.01, P<0.05; P<0.05; P<0.05) .
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体外实验——
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体内实验Compared with their BALB/cBy controls, SCID mice have a significantly greater abdominal response to colorectal distension (CRD) at the distension levels of 0.04 to 0.1 mL increasing the intensity of EMG response by 384% to 132%, respectively (P<0.01; P<0.01; P<0.01; P<0.001). PAR-4 activation effectively reverses this hypersensitivity (P<0.01, P<0.05; P<0.05; P<0.05) .
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同义词PAR-4-AP; AY-NH2
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通路GPCR/G Protein
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靶点PAR
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受体PAR-4
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研究领域——
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适应症——
化学信息
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CAS Number352017-71-1
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分子量680.79
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分子式C34H48N8O7
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (146.89 mM)
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SMILES——
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化学全称Sequence:Ala-Tyr-Pro-Gly-Lys-Phe-NH2
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
Annaházi A, et al. Proteinase-activated receptor-4 evoked colorectal analgesia in mice: an endogenously activatedfeed-back loop in visceral inflammatory pain. Neurogastroenterol Motil. 2012 Jan;24(1):76-85, e13.
产品手册




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