PSN632408|cas:857652-30-3|西域试剂

PSN632408,99.64%

产品编号：Bellancom-16673| CAS NO：857652-30-3| 分子式：C₁₈H₂₄N₄O₄| 分子量：360.41

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货号	价格	库存与货期
Bellancom-16673	￥860.00	杭州北京（现货）
Bellancom-16673	￥1510.00	杭州北京（现货）
Bellancom-16673	￥6620.00	杭州北京（现货）

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PSN632408

产品介绍

PSN632408 是一种选择性的口服活性 GPR119 激动剂，在重组小鼠和人GPR119 受体上显示出与 OEA 相似的效力 (EC₅₀=5.6 和 7.9 uM)。PSN632408 可以刺激 β 细胞复制并改善胰岛移植功能。PSN632408 具有研究肥胖症和相关代谢异常的潜力。

生物活性

PSN632408, a selective, orally active GPR119 agonist, shows similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC₅₀=5.6 and 7.9 uM, respectively). PSN632408 can stimulate β-cell replication and improve islet graft function. PSN632408 has the potential for the research of obesity and related metabolic disorders.

体外研究

PSN632408 produces concentration-dependent increases in cAMP level with mean EC₅₀ value of 1.9 uM.
PSN632408 stimulates β cell replication in cultured mouse islets.

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

体内研究

PSN632408 (100 mg/kg; p.o.; daily for 14 days) suppresses food intake in rats and reduce body weight gain and white adipose tissue deposition upon subchronic oral administration to high-fat-fed rats.

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

Animal Model:	Diet-induced obese (DIO) rats
Dosage:	100 mg/kg
Administration:	P.o.; daily for 14 days
Result:	The mean daily food intake was decreased by 10% during the first week of dosing and 15% during the second week. Body weight gain was significantly attenuated from day 6 onward with some evidence of weight loss.

体内研究

PSN632408 (100 mg/kg; p.o.; daily for 14 days) suppresses food intake in rats and reduce body weight gain and white adipose tissue deposition upon subchronic oral administration to high-fat-fed rats.

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

Animal Model:	Diet-induced obese (DIO) rats
Dosage:	100 mg/kg
Administration:	P.o.; daily for 14 days
Result:	The mean daily food intake was decreased by 10% during the first week of dosing and 15% during the second week. Body weight gain was significantly attenuated from day 6 onward with some evidence of weight loss.

性状

Solid

溶解性数据

In Vitro:

DMSO : 50 mg/mL (138.73 mM; Need ultrasonic)

配制储备液

浓度溶剂体积质量	1 mg	5 mg	10 mg

1 mM	2.7746 mL	13.8731 mL	27.7462 mL
5 mM	0.5549 mL	2.7746 mL	5.5492 mL
10 mM	0.2775 mL	1.3873 mL	2.7746 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: ≥ 2.5 mg/mL (6.94 mM); Clear solution

此方案可获得 ≥ 2.5 mg/mL (6.94 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 (6.94 mM); Clear solution

此方案可获得 ≥ 2.5 mg/mL (6.94 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
3.

请依序添加每种溶剂： 10% DMSO 90% corn oil
Solubility: ≥ 2.5 mg/mL (6.94 mM); Clear solution

此方案可获得 ≥ 2.5 mg/mL (6.94 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 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中，混合均匀。