AWZ1066S,98.64%

产品编号:Bellancom-114415| CAS NO:2239272-16-1| 分子式:C19H19F3N6O| 分子量:404.39

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-114415
2050.00 杭州 北京(现货)
Bellancom-114415
3500.00 杭州 北京(现货)
Bellancom-114415
8500.00 杭州 北京(现货)
Bellancom-114415
14500.00 杭州 北京(现货)

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AWZ1066S

产品介绍 AWZ1066S 是一种高效、特异的抗 Wolbachia剂,具有口服活性,EC50 值为 121 nM。AWZ1066S 也是一种弱 CYP2C9 抑制剂和弱 CYP3A4 诱导剂,IC50 值分别为 9.7 μM 和 37 μM。AWZ1066S 可用于盘尾丝虫病和淋巴丝虫病等热带疾病的研究。
生物活性

AWZ1066S is a highly potent, specific and orally active anti-Wolbachia agent with EC50 value of 121 nM. AWZ1066S also is a weak CYP2C9 inhibitor and a weak CYP3A4 inducer with IC50 values of 9.7 μM and 37 uM, respectively. AWZ1066S can be used for the research of tropical diseases such as Onchocerciasis (river blindness) and lymphatic filariasis (elephantiasis) .

体外研究

AWZ1066S has anti-Wolbachia activity with EC50 value of 121 nM.
AWZ1066S has a weak CYP2C9 inhibitory activity with an IC50 value of 9.7 μM and has a weak CYP3A4 induced activity with an IC50 value of 37 uM, but does not show any time-dependent inhibition across five majorhuman CYP450 isoforms (CYP1A, CYP2C9, CYP2C19, CYP2D6, CYP3A).

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

体内研究

AWZ1066S (oral; 50, 100 mg/kg; bid; for 7 days) has high anti-Wolbachia efficacy.
AWZ1066S (i.v or p.o; 5, 10, 85, 90 242 mg/kg) can oral delivery and has good aqueous solubility and metabolic stability.
Mouse PK profiles of AWZ1066S and its mesylate salt in BALB/c mice (n=3)

Dose(mg/kg) Cmax(μg/mL) tmax(hr) t1/2(hr) AUC0-24h(μg/mL*hr) Vss(mL/kg) CLtot(mL/hr/kg) BA(%)
5IV - - 3.5 10.7 317.3 466.7 -
10PO 16.2 0.17 - 18.0 - - 84
90PO 46.6 0.75 - 132.3 - - 91
85PO 43.4 0.83 - 119.2 - - 86
242PO 87.3 0.17 - 210.2 - - 54

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

Animal Model: SCID mice
Dosage: 50, 100 mg/kg
Administration: oral, bid, for 7 days
Result: Showed good anti-Wolbachia effects.
Animal Model: BALB/c SCID mice
Dosage: 5, 10, 85, 90 242 mg/kg
Administration: i.v or p.o
Result: Showed good aqueous solubility and metabolic stability.
体内研究

AWZ1066S (oral; 50, 100 mg/kg; bid; for 7 days) has high anti-Wolbachia efficacy.
AWZ1066S (i.v or p.o; 5, 10, 85, 90 242 mg/kg) can oral delivery and has good aqueous solubility and metabolic stability.
Mouse PK profiles of AWZ1066S and its mesylate salt in BALB/c mice (n=3)

Dose(mg/kg) Cmax(μg/mL) tmax(hr) t1/2(hr) AUC0-24h(μg/mL*hr) Vss(mL/kg) CLtot(mL/hr/kg) BA(%)
5IV - - 3.5 10.7 317.3 466.7 -
10PO 16.2 0.17 - 18.0 - - 84
90PO 46.6 0.75 - 132.3 - - 91
85PO 43.4 0.83 - 119.2 - - 86
242PO 87.3 0.17 - 210.2 - - 54

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

Animal Model: SCID mice
Dosage: 50, 100 mg/kg
Administration: oral, bid, for 7 days
Result: Showed good anti-Wolbachia effects.
Animal Model: BALB/c SCID mice
Dosage: 5, 10, 85, 90 242 mg/kg
Administration: i.v or p.o
Result: Showed good aqueous solubility and metabolic stability.
性状Solid
溶解性数据
In Vitro: 

DMSO : 125 mg/mL (309.11 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.4729 mL 12.3643 mL 24.7286 mL
5 mM 0.4946 mL 2.4729 mL 4.9457 mL
10 mM 0.2473 mL 1.2364 mL 2.4729 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。-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: ≥ 2.08 mg/mL (5.14 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (5.14 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.8 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: ≥ 2.08 mg/mL (5.14 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (5.14 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.8 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。

    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
  • 3.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.08 mg/mL (5.14 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (5.14 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 西域 网站选购。
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 6 months
-20°C 1 month
参考文献

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