Compound 48/80 trihydrochloride C48/80 trihydrochloride|cas:848035-21-2|西域试剂

Compound 48/80 trihydrochloride C48/80 trihydrochloride,99.24%

产品编号：Bellancom-130592| CAS NO：848035-21-2| 分子式：C₃₂H₄₈Cl₃N₃O₃| 分子量：629.10

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货号	包装	价格	库存与货期	购买量	操作
Bellancom-130592		￥1100.00	杭州北京（现货）
Bellancom-130592		￥1900.00	杭州北京（现货）

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Compound 48/80 trihydrochloride C48/80 trihydrochloride

产品介绍

Compound 48/80 trihydrochloride (C48/80 trihydrochloride) 是 N-甲基对甲氧基苯乙胺与甲醛缩合产物的混合物。Compound 48/80 trihydrochloride 也是一种组胺 (histamine) 释放剂和肥大细胞 (mast cell) 脱颗粒剂。Compound 48/80 trihydrochloride 抑制人血小板磷脂酰肌醇特异性磷脂酶 C (phosphatidylinositol-specific phospholipase C) 活性。

生物活性

Compound 48/80 trihydrochloride (C48/80 trihydrochloride) is a mixture of condensation products of N-methyl-p-methoxyphenethylamine with formaldehyde. Compound 48/80 trihydrochloride is also a histamine releaser and a mast cell degranulator. Compound 48/80 inhibits phosphatidylinositol-specific phospholipase C activity from human platelets .

体外研究

Compound 48/80 trihydrochloride (C48/80 trihydrochloride) inhibits both cytosolic and particulate phosphatidylinositol-specific phospholipase C activities with a similar efficiency; IC₅₀ values are 2.1 μg/ml (supernatant) and 5.0 μg /ml (particulate fraction). The aggregation of human platelets induced by ADP and PAF-acether is inhibited by Compound 48/80.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

Compound 48/80 trihydrochloride (0.75 mg/kg; i.p.; Killed after 0.5, 3 or 6 h) increases serum serotonin, histamine and corticosterone levels at 0.5 h, but their increases were reduced thereafter.
Compound 48/80 trihydrochloride causes oxidative stress in rat adrenal gland through mast cell degranulation.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:	7-week-old Wistar male rats (fasted for 24 hours)
Dosage:	0.75 mg/kg
Administration:	Intraperitoneal injection; Killed after 0.5, 3 or 6 h
Result:	Serum histamine and serotonin concentrations significantly higher than those in untreated control rats at 0.5 h after treatment. The increased serum histamine and serotonin concentrations in rats decreased time-dependently thereafter.

体内研究

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:	7-week-old Wistar male rats (fasted for 24 hours)
Dosage:	0.75 mg/kg
Administration:	Intraperitoneal injection; Killed after 0.5, 3 or 6 h
Result:	Serum histamine and serotonin concentrations significantly higher than those in untreated control rats at 0.5 h after treatment. The increased serum histamine and serotonin concentrations in rats decreased time-dependently thereafter.

性状

Solid

溶解性数据

In Vitro:

H₂O : 25 mg/mL (39.74 mM; Need ultrasonic)

DMSO : 10 mg/mL (15.90 mM; ultrasonic and warming and heat to 60°C)

配制储备液

浓度溶剂体积质量	1 mg	5 mg	10 mg

1 mM	1.5896 mL	7.9479 mL	15.8957 mL
5 mM	0.3179 mL	1.5896 mL	3.1791 mL
10 mM	0.1590 mL	0.7948 mL	1.5896 mL

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。
储备液的保存方式和期限：-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液，再依次添加助溶剂：

——为保证实验结果的可靠性，澄清的储备液可以根据储存条件，适当保存；体内实验的工作液，建议您现用现配，当天使用；以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比；如在配制过程中出现沉淀、析出现象，可以通过加热和/或超声的方式助溶

1.

请依序添加每种溶剂： 10% DMSO 40% PEG300 5% Tween-80 45% saline
Solubility: ≥ 2.5 mg/mL (3.97 mM); Clear solution

此方案可获得 ≥ 2.5 mg/mL (3.97 mM，饱和度未知) 的澄清溶液。
以 1 mL 工作液为例，取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀；向上述体系中加入50 μL Tween-80，混合均匀；然后继续加入 450 μL生理盐水定容至 1 mL。
将 0.9 g 氯化钠，完全溶解于 100 mL ddH₂O 中，得到澄清透明的生理盐水溶液
2.

请依序添加每种溶剂： 10% DMSO 90% (20% SBE-β-CD in saline)
Solubility: ≥ 2.5 mg/mL (3.97 mM); Clear solution

此方案可获得 ≥ 2.5 mg/mL (3.97 mM，饱和度未知) 的澄清溶液。
以 1 mL 工作液为例，取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中，混合均匀。
将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中，再用生理盐水定容至 10 mL，完全溶解，澄清透明