Piperoxan hydrochloride
目录号: PL14293 纯度: ≥99%
CAS No. :135-87-5
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中文名称
Piperoxan hydrochloride
英文名称
Piperoxan hydrochloride
英文别名
Piperidine,1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-, hydrochloride (1:1);1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]piperidinium chloride;dl-Piperoxan hydrochloride;piperoxan.HC;1-(1,4-Benzodioxan-2-ylmethyl)piperidine hydrochloride;1,4-Benzodioxan,2-(1-piperidylmethyl)-,hydrochloride;2-(1-Piperidylmethyl)-1,4-benzodioxan hydrochloride;2-Piperidinomethyl-1,4-benzodioxan hydrochloride;933F;933F Hydrochloride;Benodaine hydrochloride;Benzodioxane hydrochloride;piperoxan.HCl;Piperoxane hydrochloride;Piperoxan (hydrochloride);Piperoxan hydrochloride
Cas No.
135-87-5
分子式
C14H20NO2+.Cl-
分子量
269.77
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
Piperoxan (Benodaine) hydrochloride 是一种 α2 肾上腺素受体拮抗剂。Piperoxan hydrochloride 是第一代抗组胺剂。
生物活性
Piperoxan (Benodaine) hydrochloride is an α 2 adrenoceptor antagonist. Piperoxan hydrochloride is the first-generation antihistamine.
性状
Solid
IC50 & Target[1][2]
adrenoceptor
体外研究(In Vitro)
When the medulla is superfused with α2 adrenoceptor antagonist Piperoxane (50 μM; 5 min) while the pons is with artificial cerebrospinal fluid (ACSF), the three inactive preparations display rhythmic phrenic bursts at a low frequency (2-4 c/min), and the phrenic burst frequency of the 12 active ones significantly increases during the last 3 min of Piperoxane applications (163±12% of the previous mean frequency). In active medullary preparations, the effects of NA applications (25 μM; 5 min) are compared when the preparations sre superfused either by ACSF (n=8) or by the α2 adrenoceptor antagonist Piperoxane (50 μM; PIP-ACSF; n=5). NA applications either alone (NA-ACSF) or with Piperoxane (PIP-ACSF+NA) significantly increases the phrenic burst frequency. However, the blockage of the medullary α2 adrenoceptors by Piperoxane potentiates a phrenic burst frequency increa
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Viemari JC, et al. Nasal trigeminal inputs release the A5 inhibition received by the respiratory rhythm generator of the mouse neonate. J Neurophysiol. 2004 Feb;91(2):746-58.
[2]. Bentley GA, et al. The antinociceptive action of some beta-adrenoceptor agonists in mice. Br J Pharmacol. 1986 Jul;88(3):515-21.
溶解度数据
In Vitro: H2O : 50 mg/mL (185.34 mM; Need ultrasonic)DMSO : ≥ 31 mg/mL (114.91 mM)
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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