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1,6-双(环己基脒基羰基氨基)己烷

更新时间:2024-01-02 11:15:16

1,6-双(环己基脒基羰基氨基)己烷结构式
1,6-双(环己基脒基羰基氨基)己烷结构式
品牌特惠专场
常用名 1,6-双(环己基脒基羰基氨基)己烷 英文名 RHC-80267
CAS号 83654-05-1 分子量 394.508
密度 1.2±0.1 g/cm3 沸点 N/A
分子式 C20H34N4O4 熔点 N/A
MSDS 美版 闪点 N/A

 1,6-双(环己基脒基羰基氨基)己烷用途


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。

 1,6-双(环己基脒基羰基氨基)己烷名称

中文名 1,6-双(环己基脒基羰基氨基)己烷
英文名 (cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate
英文别名 更多

 1,6-双(环己基脒基羰基氨基)己烷生物活性

描述 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。
相关类别
靶点

IC50: 4 μM (Canine diacylglycerol lipase), 4 μM (Cholinesterase); COX; Phosphatidylcholine[1][3][4]

体外研究 RHC 80267对乙酰胆碱的舒张作用增强可能是由于胆碱酯酶的抑制作用:(1)rhc80267对乙酰胆碱的氨甲酰衍生物卡巴胆碱的反应没有影响,卡巴胆碱与乙酰胆碱的区别在于它对胆碱酯酶水解的抵抗力,并且(2)模拟了rhc80267的作用通过胆碱酯酶新斯的明抑制剂,RHC 80267在新斯的明的最大有效浓度存在下不显示额外的效果。测定RHC 80267对脑匀浆胆碱酯酶活性的影响,证实rhc80267在相同浓度范围内抑制这种酶,增加对乙酰胆碱的松弛,即在1-10μM时[2]。
体内研究 RHC 80267(40μM)以内皮依赖的方式增强U46619(血栓素A2类似物)和血管紧张素II(ANG II)在人和大鼠肺动脉(分别为hPAs和rPAs)中诱导的收缩[3]。
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.

[3]. Karpińska O, et al. Activation of CB1 receptors by 2-arachidonoylglycerol attenuates vasoconstriction induced by U46619 and angiotensin II in human and rat pulmonary arteries. Am J Physiol Regul Integr Comp Physiol. 2017 Jun 1;312(6):R883-R893.

[4]. Oglesby TD, et al. The inhibition of arachidonic acid metabolism in human platelets by RHC 80267, a diacylglycerol lipase inhibitor. Biochim Biophys Acta. 1984 Apr 18;793(2):269-77.

 1,6-双(环己基脒基羰基氨基)己烷物理化学性质

密度 1.2±0.1 g/cm3
分子式 C20H34N4O4
分子量 394.508
精确质量 394.257996
PSA 101.38000
LogP 3.12
外观性状 白色固体
折射率 1.571
储存条件 2-8°C,避光,干燥,密封

 1,6-双(环己基脒基羰基氨基)己烷MSDS

 1,6-双(环己基脒基羰基氨基)己烷安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危害码 (欧洲) Xi
安全声明 (欧洲) 22-24/25
危险品运输编码 NONH for all modes of transport

 1,6-双(环己基脒基羰基氨基)己烷合成线路

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1,6-双(环己基脒基羰基氨基)己烷结构式

1,6-双(环己基脒基羰基氨基)己烷

83654-05-1

文献:Petersen Justus Liebigs Annalen der Chemie, 1949 , vol. 562, p. 210,220

 1,6-双(环己基脒基羰基氨基)己烷上下游产品

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1,6-双(环己基脒基羰基氨基)己烷下游产品  0

 1,6-双(环己基脒基羰基氨基)己烷文献27

更多文献
Capsazepine, a vanilloid antagonist, abolishes tonic responses induced by 20-HETE on guinea pig airway smooth muscle.

Am. J. Physiol. Lung Cell. Mol. Physiol. 288(3) , L460-70, (2005)

The aim of this study was to delineate the mode of action of 20-hydroxy-eicosatetraenoic acid (20-HETE) in airway smooth muscle (ASM) cells. ASM metabolizes arachidonic acid by various enzymatic pathw...

L- and N-current but not M-current inhibition by M1 muscarinic receptors requires DAG lipase activity.

J. Cell Physiol. 216(1) , 91-100, (2008)

Stimulation of postsynaptic M(1) muscarinic receptors (M(1)Rs) increases firing rates of both sympathetic and central neurons that underlie increases in vasomotor tone, heart rate, and cognitive memor...

Brain phospholipase C-diacylglycerol lipase pathway is involved in vasopressin-induced release of noradrenaline and adrenaline from adrenal medulla in rats.

Eur. J. Pharmacol. 499(1-2) , 99-105, (2004)

Recently, we reported that intracerebroventricularly (i.c.v.) administered arginine-vasopressin evokes the release of noradrenaline and adrenaline from adrenal medulla by brain thromboxane A2-mediated...

 1,6-双(环己基脒基羰基氨基)己烷英文别名

1,6-Bis-cyclohexylidenaminooxycarbonylamino-hexan
(Hexane-1,6-diyldiimino)bis{[(cyclohexylideneamino)oxy]methanone}
Cyclohexanone, O,O'-[1,6-hexanediylbis(iminocarbonyl)]oxime
(1,6-Hexanediyldiimino)bis{[(cyclohexylideneamino)oxy]methanone}
1,6-bis-cyclohexylidenaminooxycarbonylamino-hexane
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