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GDC-0425
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。
GDC-0425图片
CAS NO:1200129-48-1
包装与价格:
包装价格(元)
10 mM * 1 mL in Water电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品名称
RG-7602
产品介绍
GDC-0425 (RG-7602) 是一种有效的、具有口服活性的、高选择性的ChK1抑制剂。GDC-0425 可用于多种恶性肿瘤的研究。
生物活性

GDC-0425 (RG-7602) is an orally available, highly selective small moleculeChK1inhibitor. GDC-0425 can be used for the research of various malignancies[1][2].

IC50& Target[1]

Chk1

 

体外研究
(In Vitro)

MEK inhibition either by pharmacologic inhibitors or RNAi-mediated gene silencing significantly protected cells from reduced viability upon GDC-0425 treatment[3].
GDC-0425 (3 μM; 24 hours) treatment results the hyperphosphorylation of Chk1[3].

Cell Viability Assay[3]

Cell Line:Chk1-positive breast cancer cell lines
Concentration:0.001, 0.01, 0.1, 1, 10 mM
Incubation Time:72 hours
Result:Reduced cell proliferation.

Cell Viability Assay[3]

Cell Line:U-2 OS cells
Concentration:3 μM
Incubation Time:24 hours
Result:Led to hyperphosphorylation of Chk1.
体内研究
(In Vivo)

GDC-0425 exhibits partial suppression of tumor growth. The Gemcitabine/GDC-0425 combination results in significant tumor regression in all tested models[3].

Animal Model:NCr nude mice bearing xenografts of both osteosarcoma and triple-negative breast cancer models (143B PML BK TK, HCC1806, and HCC70 cell lines)[3]
Dosage:For the 4-arm study, mice were treated with vehicle, Gemcitabine 120 mg/kg, GDC-0425 75 mg/kg alone, or Gemcitabine and GDC-0425 combination for 15 days. For 6-arm studies of HCC1806 and HCC70 models, mice were treated with vehicle, Gemcitabine 120 mg/kg, GDC-0425 50 mg/kg, GDC-0425 75 mg/kg alone, or Gemcitabine and GDC-0425 combination.
Administration:Orally administrated at 24, 48, and 72 hours after gemcitabine administration by intraperitoneal injection.
Result:Exhibited partial suppression of tumor growth upon treatment with either Gemcitabine or GDC-0425 alone. Notably, the Gemcitabine/GDC-0425 combination resulted in significant tumor regression in all tested models.
Clinical Trial
分子量

321.38

性状

Solid

Formula

C18H19N5O

CAS 号

1200129-48-1

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: 

H2O : 25 mg/mL(77.79 mM;ultrasonic and adjust pH to 3 with HCl)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.1116 mL15.5579 mL31.1158 mL
5 mM0.6223 mL3.1116 mL6.2232 mL
10 mM0.3112 mL1.5558 mL3.1116 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。