GLUT4-IN-2

CAS: 2454113-83-6 货号: G648259 分子式: C17H11N3O4S2 分子量: 385.42
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储存条件
-20°C储存
运输条件
超低温运输
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规格
库存
价格
数量
5mg
G648259-5mg
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¥1,500.90
10mg
G648259-10mg
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¥2,500.90
25mg
G648259-25mg
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¥5,500.90
50mg
G648259-50mg
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为什么选择此级别

,适用于对基线干扰要求严格的色谱和分析工作流程。

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储存与运输

-20°C储存。超低温运输 。请查阅批次 COA 获取详细规格。

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文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。

概述


GLUT4-IN-2 is a potent and selective GLUT4 inhibitor with IC 50 s of 11.4 µM and 6.8 µM for GLUT1 and GLUT4 , respectively. GLUT4-IN-2 induces cell apoptosis and cell cycle arrest at G0/G1phase. GLUT4-IN-2 shows potent antitumor activity

In Vitro

GLUT4-IN-2 (compound F18) induces cell apoptosis and ell cycle arrest at G0/G1phase in CME cells. GLUT4-IN-2 (10 µM; 6 h) decreases the expression of mTOR and CDK2, but increases the expression of GRP78, and cleaved caspase 3 proteins. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: CME, K562, KCL-22, MB-231, HS-27 cells Concentration: 1-100 µM Incubation Time: 48 h Result: Showed potent cytotoxicity with cytotoxic concentration 50% (CC 50 ) of 1.7, 91.9, 15.3, 45.1, 44.0 µM for CME, K562, KCL-22, MB-231, HS-27 cells, respectively. Apoptosis AnalysisCell Line: CEM cells Concentration: 1.7 µM Incubation Time: 24 h Result: Induced cell apoptosis with the percentage of apoptotic cells in the late and early apoptosis region was 55.87% and 1.38%, respectively. Cell Cycle AnalysisCell Line: CEM cells Concentration: 10, 25, 50 µM Incubation Time: 72 h Result: Induced cell cycle arrest at G0/G1phase in a dose-dependent manner. Western Blot AnalysisCell Line: CEM cells Concentration: 10 µM Incubation Time: 6 h Result: Decreased the phosphorylation of mTOR and CDK2 proteins and increased the expression of GRP78, and cleaved caspase 3. Cell Cytotoxicity AssayCell Line: CEM cells Concentration: 2.5-100 µM Incubation Time: 48 h Result: Showed cytotoxicity with the IC 50 s of 1.7, 187.2 µM for CEM, WBCs cells respectively.

In Vivo

GLUT4-IN-2 (50 mg/kg; i.p. on day 1–5, 8–12, 15–18) shows antitumor activity in CEM xenograft model . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: 8–10 weeks, SCID mice (CEM xenograft tumor) Dosage: 50 mg/kg Administration: I.p.; administered on day 1-5, 8-12, 15-18 Result: Showed potent antitumor activity in vivo.

Form:Solid

IC50& Target:GLUT1 11.4 μM (IC 50 ) GLUT4 6.8 μM (IC 50 )

规格

英文名称
GLUT4-IN-2
生化机理
GLUT4-IN-2 是一种强效的选择性 GLUT4 抑制剂,对 GLUT1 和 GLUT4 的 IC 50 s 分别为 11.4 µM 和 6.8 µM。GLUT4-IN-2 可诱导细胞凋亡并使细胞周期停滞在 G0/G1 期。GLUT4-IN-2 具有很强的抗肿瘤活性。
储存条件
-20°C储存
运输条件
超低温运输
作用类型
抑制剂
名称和识别符
分子类型
小分子
分子量
385.42

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常见问题

本产品应如何储存?
请于?20 °C条件下保存。需冷冻保存以维持规定的有效期。
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本产品的 CAS 号、分子式和分子量是多少?
本产品的 CAS 号为 2454113-83-6,分子式为 C17H11N3O4S2,分子量为 385.42 g/mol。
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