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DRB18
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
DRB18图片
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议

产品介绍
DRB18 是一种有效的葡萄糖转运蛋白 (GLUT) 泛抑制剂。DRB18 通过改变葡萄糖相关途径中代谢产物的丰度来改变 A549 细胞中的能量相关代谢。DRB18 最终可导致细胞阻滞在 G1/S 期,增加氧化应激和坏死细胞死亡。DRB18 具有抗肿瘤活性。
生物活性

DRB18 is a potent pan-classGLUTinhibitor. DRB18 alters energy-related metabolism in A549 cells by changing the abundance of metabolites in glucose-related pathways. DRB18 can eventually lead to G1/S phase arrest and increase oxidative stress and necrotic cell death. DRB18 has anti-tumor activity[1].

IC50& Target

GLUT[1]

体外研究
(In Vitro)

DRB18 (0-10 μM; 30 min) reduces glucose uptake in GLUT1-4-expressed HEK293 cell lines in a dose-dependent manner with IC50s varying from ~ 900 nM to ~ 9 μM[1].
DRB18 (5 and 10 μM; 72 hours) causes cell cycle arrest in the G1/S phase transition[1].
DRB18 (5 and 10 μM; 72 hours) increases ROS levels in A549 cells[1].
DRB18 (5 and 10 μM; 72 hours) reduces expression of glycosylated GLUT1 and GLUT2-4 in A549 cells in a dose-dependent manner[1].

Cell Proliferation Assay

Cell Line:GLUT1-4-expressed HEK293 cell lines[1]
Concentration:0-10 μM
Incubation Time:30 min
Result:Reduced glucose uptake in these cell lines in a dose-dependent manner with IC50s varying from ~ 900 nM to ~ 9 μM.

Cell Cycle Analysis

Cell Line:A549[1]
Concentration:5 and 10 μM
Incubation Time:72 hours
Result:Caused cell cycle arrest in the G1/S phase transition.

Western Blot Analysis

Cell Line:A549[1]
Concentration:5 and 10 μM
Incubation Time:72 hours
Result:Reduced expression of glycosylated GLUT1 and GLUT2-4 in A549 cells in a dose-dependent manner.

Western Blot Analysis

Cell Line:A549[1]
Concentration:5 and 10 μM
Incubation Time:72 hours
Result:Reduced expression of glycosylated GLUT1 and GLUT2-4 in A549 cells in a dose-dependent manner.
体内研究
(In Vivo)

DRB18 (10 mg/kg; IP; thrice a week for 5 weeks) inhibits tumors volume by 44% and tumors weight by 43%[1].

Animal Model:Male NU/J nude mice (3-4 weeks; tumor cell-injected)[1]
Dosage:10 mg/kg
Administration:IP; thrice a week for 5 weeks
Result:The tumors were 44% smaller by volume and 43% smaller by weight, also showed DRB18 decreased expression of GLUT1-4 (Fig. 5f) and reduced proliferative capacity within the xenografted tumor.
分子量

382.88

性状

Solid

Formula

C22H23ClN2O2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : 50 mg/mL(130.59 mM;ultrasonic and warming and heat to 60℃)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.6118 mL13.0589 mL26.1178 mL
5 mM0.5224 mL2.6118 mL5.2236 mL
10 mM0.2612 mL1.3059 mL2.6118 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℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。