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Cyclosporin H {[allProObj[0].p_purity_real_show]}

货号:A219301 同义名: 5-(N-methyl-D-valine)-Cyclosporin A;Sandoz 37-839

Cyclosporin H is a potent and effective inhibitor of formyl peptide receptor (FPR) with Ki of 0.1 uM.

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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Cyclosporin H 化学结构 CAS号:83602-39-5
Cyclosporin H 化学结构
CAS号:83602-39-5
Cyclosporin H 3D分子结构
CAS号:83602-39-5
Cyclosporin H 化学结构 CAS号:83602-39-5
Cyclosporin H 3D分子结构 CAS号:83602-39-5
规格 价格 会员价 库存 数量
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Cyclosporin H 纯度/质量文件 产品仅供科研

货号:A219301 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 FPR1 FPRL1 其他靶点 纯度
HCH6-1 99%+
WRW4 +++

FPRL1, IC50: 0.23 μM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Cyclosporin H 生物活性

描述 As an initial signal in the innate immunity, the formyl peptide stimulates leukocyte chemotaxis, induces acute and chronic inflammation, and stimulates the release of a number of the cytokine storm mediators from monocytes, neutrophils and endothelial cells by acting through the formyl peptide receptor (FPR). Cyclosporin H, a potent anti-inflammatory compound, acts as a specific competitive antagonist of formyl peptides on FPR on phagocytic: leukocytes. Cyclosporin H completely blocked neutrophil chemotaxis induced by the standard formyl peptide, f-MLF, as well as the bacteria-derived or host-derived formyl peptide[1]. Cyclosporin H (8 to 800 nM) concentration-dependently inhibited histamine and leukotriene C4 release from purified and unpurified basophils activated by FMLP. Furthermore, Cyclosporin H inhibited tritiated FMLP binding to human polymorphonuclear leukocytes with a concentration required to inhibit binding by 50% of approximately 0.54 nM[2]. In vivo treatment by Cyclosporin H in the mouse model of HINI Swine flu influenza infection for 5 days markedly reduced lung inflammation and endothelial cell damage[1].

Cyclosporin H 参考文献

[1]Elgebaly SA, Elbayoumi T, Kreutzer DL. CYCLOSPORIN H: A NOVEL ANTI-INFLAMMATORY THERAPY FOR INFLUENZA FLU PATIENTS. J Egypt Soc Parasitol. 2017 Apr;47(1):25-33

[2]de Paulis A, Ciccarelli A, de Crescenzo G, Cirillo R, Patella V, Marone G. Cyclosporin H is a potent and selective competitive antagonist of human basophil activation by N-formyl-methionyl-leucyl-phenylalanine. J Allergy Clin Immunol. 1996 Jul;98(1):152-64

Cyclosporin H 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

0.83mL

0.17mL

0.08mL

4.16mL

0.83mL

0.42mL

8.32mL

1.66mL

0.83mL

Cyclosporin H 技术信息

CAS号83602-39-5
分子式C62H111N11O12
分子量 1202.611
别名 5-(N-methyl-D-valine)-Cyclosporin A;Sandoz 37-839;5-(N-methyl-D-valine)-Cyclosporin A, Cyclosporin H, Sandoz 37-839
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

溶解度

DMSO: 105 mg/mL(87.31 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

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