1. Anti-infection
  2. Fungal Parasite
  3. Posaconazole

Posaconazole  (Synonyms: 泊沙康唑; SCH 56592)

目录号: HY-17373 纯度: 99.94%
COA 产品使用指南

Posaconazole 是一种广谱的,二代三唑类物质,具有抗真菌作用。

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Posaconazole Chemical Structure

Posaconazole Chemical Structure

CAS No. : 171228-49-2

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规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥1218
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1 mg ¥359
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5 mg ¥790
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10 mg ¥1200
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50 mg ¥4800
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100 mg ¥8500
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200 mg   询价  
500 mg   询价  

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Other Forms of Posaconazole:

  • 生物活性

  • 实验参考方法

  • 纯度 & 产品资料

  • 参考文献

生物活性

Posaconazole is a broad-spectrum, second generation, triazole compound with antifungal activity.

体外研究
(In Vitro)

Posaconazole 具有强大的杀锥虫活性。胺碘酮与 Posaconazole 协同作用。Posaconazole 还会影响和破坏 T. cruzi 中的 Ca2+ 稳态。Posaconazole 阻断麦角固醇的生物合成,麦角固醇是寄生虫存活所必需的。Posaconazole 对上鞭毛体 (细胞外) 阶段的增殖具有明显的剂量依赖性作用,最小抑制浓度为 20 nM,IC50 为 14 nM。对于寄生虫的临床相关细胞内无鞭毛体形式,Posaconazole 甚至更有效。Posaconazole 具有最小抑制浓度和 IC50 值,分别为 3 nM 和 0.25 nM[1]。Posaconazole 对念珠菌和曲霉属的分离株有活性。对氟康唑、伏立康唑和两性霉素 B 表现出耐药性,并且比其他三唑对接合菌的活性强得多[2]

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

体内研究
(In Vivo)

仅用胺碘酮处理受感染的动物可减少寄生虫血症,增加感染后 60 天的存活率 (未处理的对照组为 0%,胺碘酮处理的动物为 40%),并且当与 Posaconazole 联合使用时,可延缓寄生虫血症的发展[1]
与在禁食状态下单独服用 Posaconazole 相比,Posaconazole 和 Boost Plus 的共同服用增加了药物暴露。食物,尤其是脂肪含量高的食物,可显著增加 Posaconazole 的生物利用度。当与高脂肪和脱脂膳食一起食用时,Posaconazole 的全身暴露量分别增加 4 倍和 2.6 倍[3]
Posaconazole 和胺碘酮可能构成有效的抗 T。cruzi 疗法,副作用小[4]
每天两次剂量≥ 15 mg/kg 体重时,Posaconazole 可延长小鼠的存活时间并减轻组织负荷[5]

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

Clinical Trial
分子量

700.78

Formula

C37H42F2N8O4

CAS 号
性状

固体

颜色

White to off-white

中文名称

泊沙康唑

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
In solvent -80°C 1 year
-20°C 6 months
溶解性数据
In Vitro: 

DMSO 中的溶解度 : 18.75 mg/mL (26.76 mM; 超声助溶 (<60°C); 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.4270 mL 7.1349 mL 14.2698 mL
5 mM 0.2854 mL 1.4270 mL 2.8540 mL
查看完整储备液配制表

* 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, 1 year; -20°C, 6 months。-80°C储存时,请在1年内使用, -20°C储存时,请在6个月内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

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

  • 方案 一

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 1.88 mg/mL (2.68 mM); 悬浊液

    此方案可获得 ≥ 1.88 mg/mL(饱和度未知)的均匀悬浊液,悬浊液可用于口服和腹腔注射。

    1 mL 工作液为例,取 100 μL 18.8 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL

    生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。
  • 方案 二

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 1.88 mg/mL (2.68 mM); 澄清溶液

    此方案可获得 ≥ 1.88 mg/mL(饱和度未知)的澄清溶液。

    1 mL 工作液为例,取 100 μL 18.8 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。

    20% SBE-β-CD in Saline 的配制(4°C,储存一周):2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。
动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
请输入您的动物体内配方组成:
%
DMSO +
+
%
Tween-80 +
%
Saline
如果您的动物是免疫缺陷鼠或者体弱鼠,建议 DMSO 中的在最后工作液体系中的占比尽量不超过 2%。
方案所需 助溶剂 包括:DMSO ,均可在 MCE 网站选购。 Tween 80,均可在 MCE 网站选购。
计算结果
工作液所需浓度 : mg/mL
储备液配制方法 : mg 药物溶于 μL  DMSO(母液浓度为 mg/mL)。
您所需的储备液浓度超过该产品的实测溶解度,以下方案仅供参考,如有需要,请与 MCE 中国技术支持联系。
动物实验体内工作液的配制方法 : 取 μL DMSO 储备液,加入 μL  μL ,混合均匀至澄清,再加 μL Tween 80,混合均匀至澄清,再加 μL 生理盐水
连续给药周期超过半月以上,请谨慎选择该方案。
请确保第一步储备液溶解至澄清状态,从左到右依次添加助溶剂。您可采用超声加热 (超声清洗仪,建议频次 20-40 kHz),涡旋吹打等方式辅助溶解。
纯度 & 产品资料

纯度: 99.94%

参考文献
Cell Assay
[1]

The epimastigote form of the parasite is cultivated in liver infusion tryptose medium,12 supplemented with 10% new born calf serum at 28°C with strong (120 rpm) agitation. Cultures are initiated at a cell density of 2×106 epimastigotes mL-1, and drugs are added at a cell density of 0.5−1.0 ×107 epimastigotes mL-1. Cell densities are measured by using an electronic particle counter as well as by direct counting with a hemocytometer. Cell viability is followed by Trypan blue exclusion, using light microscopy. Amastigotes are cultured in Vero cells maintained in minimal essential medium supplemented with 1% fetal calf serum in a humidified atmosphere (95% air−5% CO2) at 37°C, as described previously. Cells are infected with 10 tissue culture-derived trypomastigotes per cell for 2 h and then washed three times with phosphate-buffered saline (PBS) to remove nonadherent parasites. Fresh medium with and without drugs is added, and the cells are incubated for 96 h with a medium change at 48 h. The percent of infected cells and the numbers of parasites per cell are determined directly using light microscopy, and a statistical analysis of the results is carried out as described previously. IC50 values are calculated by nonlinear regression, using the program GraFit. Cytoplasmic free Ca2+ concentrations in control and drug-treated extracellular epimastigotes are determined by fluorimetric methods, using Fura-2, again as described previously. Subcellular Ca2+ levels and mitochondrial membrane potentials are monitored on individual Vero cells infected with T. cruzi amastigotes by using time-scan confocal microscopy, as described in detail elsewhere. Briefly, Vero cells heavily infected (72 h) with T. cruzi amastigotes are plated onto 22×40 mm glass coverslips (0.15 mm thickness) and incubated simultaneously with 10 μM cell-permeant Rhod-2 and 10 μg/mL Rhodamine-123 for 50 min at 37°C in culture medium and then washed and incubated with Ringer's solution, with or without amiodarone. Under the conditions used, fluorescence of Rhod-2 comes mainly from intracellular Ca2+-rich compartments, like mitochondria, since its low affinity for Ca2+ limits its fluorescence in the Ca2+-poor cytoplasm of the Vero cells or amastigotes. Rhodamine-123 is a mitochondrion-specific cationic dye, which distributes across the inner mitochondrial membranes strictly according to their membrane potential.

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

Animal Administration
[1]

In vivo studies are carried out by using the murine model of acute Chagas' disease in which female NMRI−IVIC mice (20−25 g) are infected with 105 or 103 bloodstream trypomastigotes and drug treatment is started 24 h later. Treatments are given for 30 consecutive days at 20 mg/kg/d for posaconazole (30 doses) and/or at 50 mg/kg every other day for amiodarone (15 doses). Negative controls (i.e. untreated animals) receive only the vehicle, while positive controls are treated with the anti-T. cruzi compound, nifurtimox, at 50 mg/kg/d for 30 days. Survival is followed daily and parasitemia weekly, the latter by direct microscopic examination. Animals are observed for 60 days postinfection, after which time parasitological cures are evaluated by using a combination of hemoculture, xenodiagnosis, and blood PCR tests.

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

参考文献

Posaconazole 相关分类

完整储备液配制表

* 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, 1 year; -20°C, 6 months。-80°C储存时,请在1年内使用, -20°C储存时,请在6个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.4270 mL 7.1349 mL 14.2698 mL 35.6745 mL
5 mM 0.2854 mL 1.4270 mL 2.8540 mL 7.1349 mL
10 mM 0.1427 mL 0.7135 mL 1.4270 mL 3.5675 mL
15 mM 0.0951 mL 0.4757 mL 0.9513 mL 2.3783 mL
20 mM 0.0713 mL 0.3567 mL 0.7135 mL 1.7837 mL
25 mM 0.0571 mL 0.2854 mL 0.5708 mL 1.4270 mL
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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