RHC 80267 (Synonyms: U-57908)
目录号: PL06885 纯度: ≥98%
CAS No. :83654-05-1
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中文名称
RHC 80267
中文别名
1,6-双(环己基脒基羰基氨基)己烷
英文名称
RHC 80267
英文别名
Cyclohexanone,1,1'-[O,O'-[1,6-hexanediylbis(iminocarbonyl)]dioxime];(cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate;1,6-BIS(CYCLOHEXYLOXIMINOCARBONYLAMINO)HEXANE;RHC 80267;RHC-80267;1,6-Bis-cyclohexylidenaminooxycarbonylamino-hexan;1,6-bis-cyclohexylidenaminooxycarbonylamino-hexane;O,O'-[1,6-Hexanediylbis(iMinocarbonyl)]dioxiMecyclohexanone;U 57908;U-57908;1,6-bis(Cyclohexyloximinocarbonylamino)hexane
Cas No.
83654-05-1
分子式
C20H34N4O4
分子量
394.51
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
RHC 80267 (U-57908) 是一种有效的选择性二酰基甘油脂酶 (DAGL) 抑制剂 (对犬血小板的 IC50 为 4 μM)。RHC 80267 抑制胆碱酯酶活性,IC50 为 4 μM,从而增强了乙酰胆碱引起的松弛。RHC 80267 还抑制 COX 活性和磷脂酰胆碱的水解。
生物活性
RHC 80267 (U-57908) is a potent and selective inhibitor of diacylglycerol lipase (DAGL) (with IC 50 of 4 μM in canine platelets). RHC-80267 inhibits cholinesterase activity with an IC 50 of 4 μM, thereby enhancing the relaxation evoked by acetylcholine. RHC 80267 also inhibits COX and the hydrolysis of phosphatidylcholine (PC).
性状
Solid
IC50 & Target[1][2]
IC50: 4 μM (Canine diacylglycerol lipase), 4 μM (Cholinesterase);
COX;
Phosphatidylcholine
体外研究(In Vitro)
The potentiation by RHC 80267 of the relaxation to acetylcholine could be caused by the inhibition of cholinesterase: (1) RHC 80267 does not affect the responses to carbachol, the carbamyl derivative of acetylcholine which only differs from acetylcholine by its resistance to hydrolysis by cholinesterase, and (2) the effect of RHC 80267 is mimicked by the inhibitor of cholinesterase neostigmine, RHC 80267 showing no additional effect in the presence of a maximally effective concentration of neostigmine. The determination of the effect of RHC 80267 on the cholinesterase activity of brain homogenate confirmed that RHC 80267 inhibits this enzyme in the same range of concentrations increasing the relaxation to acetylcholine, namely at 1-10 μM. has not independently confirmed the accuracy of these methods. They are for refere
体内研究(In Vivo)
RHC 80267 (40 μM) enhances contractions induced by U46619 (a thromboxane A2 analog) in human and rat pulmonary arteries (hPAs and rPAs, respectively) and by angiotensin II (ANG II) in rPAs in an endothelium-dependent manner. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Sutherland CA, et al. Relative activities of rat and dog platelet phospholipase A2 and diglyceride lipase. Selective inhibition of diglyceride lipase by RHC 80267. J Biol Chem. 1982 Dec 10;257(23):14006-10.
[2]. Ghisdal P, et al. The diacylglycerol lipase inhibitor RHC-80267 potentiates the relaxation to acetylcholine in rat mesenteric artery by anti-cholinesterase action. Eur J Pharmacol. 2005 Jul 4;517(1-2):97-102.
溶解度数据
In Vitro: DMSO : 25 mg/mL (63.37 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

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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