您好,欢迎来到试剂信息网! [登录] [免费注册]
试剂信息网
位置:首页 > 产品库 > RX-3117
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
RX-3117
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。
RX-3117图片
CAS NO:865838-26-2
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
2mg电议
5mg电议
10mg电议
50mg电议

产品名称
TV-1360
fluorocyclopentenylcytosine
产品介绍
RX-3117 (TV-1360) 是一种有效的口服活性抗癌和抗代谢物药剂。RX-3117 抑制 DNA 甲基转移酶 1 (DNMT1。RX-3117 显示出抗增殖和抗肿瘤活性。RX-3117 诱导细胞周期停滞在 S 期和细胞凋亡 (apoptosis)。
生物活性

RX-3117 (TV-1360) is a potent and orally activeanticancerandantimetaboliteagent. RX-3117 inhibitsDNA methyltransferase1 (DNMT1). RX-3117 shows antiproliferative and anti-tumour activity. RX-3117 induces cell cycle arrest at S phase andapoptosis[1][2][3].

体外研究
(In Vitro)

RX-3117 causes both inhibition of DNA and RNA synthesis[1].
RX-3117 (11.7, 21 μM; 48 h) shows antiproliferative activity in A549, SW1573 cells[1].
RX-3117 is activated by uridine-cytidine kinase 2 (UCK2)[1].
RX-3117 (1-25 μM; 72 h) inhibits the growth of HCT-116, MDA-MB-231, PANC-1, Caki-1, MCF7, A549, MKN45, U251 cells with IC50s of 0.39, 0.18, 0.62, 0.84, 0.34, 0.34, 0.50, 0.83 μM, respectively[2].
RX-3117 (5, 10 μM; 4 days) induces cell cycle arrest at S phase and apoptosis[2].
RX-3117 (1-5 μM; 24 h) decreases the cellular amount of DNMT1 in a dose-dependent manner in MDA-MB-231[3].

Cell Viability Assay[1]

Cell Line:A549, SW1573 cells
Concentration:11.7, 21 μM
Incubation Time:48 h
Result:Showed antiproliferative activity in A549 (63.7% cell growth), SW1573 cells (59% cell growth).

Apoptosis Analysis[2]

Cell Line:A549, SW1573 NSCLC cells
Concentration:5 μM for A549 cells, 10 μM for SW1573 cells
Incubation Time:4 days
Result:Induced cell cycle arrest at S phase and apoptosis.
体内研究
(In Vivo)

RX-3117 (2, 10 mg/kg; i.p.; three times per week for five weeks) shows anti-tumour activity in nude mice[3].

Animal Model:Nude mice (human colon carcinoma HCT116 xenograft model)[3]
Dosage:2, 10 mg/kg
Administration:I.p.; three times per week for five weeks
Result:Caused significant inhibition of tumor growth at the doses of 2 and 10 mg/kg.
Clinical Trial
分子量

257.22

性状

Solid

Formula

C10H12FN3O4

CAS 号

865838-26-2

中文名称

氟环戊烯基胞嘧啶

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(194.39 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.8877 mL19.4386 mL38.8772 mL
5 mM0.7775 mL3.8877 mL7.7754 mL
10 mM0.3888 mL1.9439 mL3.8877 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。