跳转至内容

Dear Customer:

The current international situation is complex and volatile, and uncertain tariff policies may potentially impact our product prices. Given these uncertainties, we value your understanding regarding order-related matters.

If you decide to place an order during this period, we reserve the right to adjust the price based on the evolving situation. We understand that market changes may cause inconvenience. We will negotiate with you if there’s a significant price fluctuation due to tariff policy changes before the order’s actual delivery, and in such cases we may adjust or cancel the order as necessary.

For important updates on recent policy changes, please click here for more details.

Merck
CN
所有图片(4)

主要文件

F0503

Sigma-Aldrich

5-氟-2′-脱氧尿嘧啶核苷

thymidylate synthase inhibitor

别名:

2′-脱氧-5-氟脲苷, FUDR, 氟脲苷

登录查看公司和协议定价

选择尺寸

500 MG
¥1,861.34

¥1,861.34


国内现货,预计发货时间2025年4月23日详情


获取大包装报价

选择尺寸

变更视图
500 MG
¥1,861.34

About This Item

经验公式(希尔记法):
C9H11FN2O5
CAS号:
分子量:
246.19
Beilstein:
90221
EC 号:
MDL编号:
UNSPSC代码:
12352202
PubChem化学物质编号:
NACRES:
NA.77

¥1,861.34


国内现货,预计发货时间2025年4月23日详情


获取大包装报价

生物来源

synthetic (organic)

质量水平

方案

≥99% (HPLC)

表单

powder

mp

148 °C (lit.)

溶解性

water: 50 mg/mL, clear, colorless to faintly yellow

储存温度

room temp

SMILES字符串

OC[C@H]1O[C@H](C[C@@H]1O)N2C=C(F)C(=O)NC2=O

InChI

1S/C9H11FN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)/t5-,6+,7+/m0/s1

InChI key

ODKNJVUHOIMIIZ-RRKCRQDMSA-N

正在寻找类似产品? 访问 产品对比指南

比较类似商品

查看完整比较结果

显示差异

1 of 4

此商品
32029341620803071
Quality Level

200

Quality Level

200

Quality Level

-

Quality Level

-

bp

188 °C (lit.)

bp

188 °C (lit.)

bp

188 °C (lit.)

bp

188.5 °C/1013 hPa (decomposition)

mp

−32 °C (lit.)

mp

−32 °C (lit.)

mp

−32 °C (lit.)

mp

-31.8 °C

form

liquid

form

liquid

form

-

form

liquid

refractive index

n20/D 1.386 (lit.)

refractive index

n20/D 1.386 (lit.)

refractive index

n20/D 1.386 (lit.), n20/D 1.387

refractive index

-

一般描述

5-氟-2′-脱氧脲核苷,也称为氟脲苷,可在癌细胞中引起DNA介导的细胞毒性作用。[1]氟脲苷可有效治疗肝癌[2] 并且能够清除金黄色葡萄球菌( Staphylococcus aureus)的毒性。[3]氟脲苷与吉西他滨的二肽前药组合具有更强的细胞渗透性和抗增殖活性。[4]氟脲苷能够有效治疗实体瘤和晚期癌症。[5]

应用

5-氟-2′-脱氧脲核苷已被用作施旺(schwann)细胞增殖[6]、胶质细胞增殖[7][8] 和背根神经节培养物中非神经细胞的有丝分裂抑制剂。[9]

生化/生理作用

一种抗肿瘤药物,是胸苷酸合成酶的有效抑制剂 通过低水平支原体感染,可使癌细胞培养物产生FUdR耐受性。

象形图

Skull and crossbones

警示用语:

Danger

危险声明

预防措施声明

危险分类

Acute Tox. 3 Oral

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

    没有发现合适的版本?

    如果您需要特殊版本,可通过批号或批次号查找具体证书。

    已有该产品?

    在文件库中查找您最近购买产品的文档。

    访问文档库

    Enhanced absorption and growth inhibition with amino acid monoester prodrugs of floxuridine by targeting hPEPT1 transporters
    Tsume Y, et al.
    Molecules (Basel), 13(7), 1441-1454 (2008)
    J A van Laar et al.
    European journal of cancer (Oxford, England : 1990), 34(3), 296-306 (1998-06-26)
    Despite more than 30 years of intensive studies on new drugs against advanced colorectal cancer, the fluoropyrimidines remain the drugs of choice for systemic treatment and for hepatic artery infusion (HAI). This overview describes new developments in advanced colorectal cancer
    The Dipeptide Monoester Prodrugs of Floxuridine and Gemcitabine?Feasibility of Orally Administrable Nucleoside Analogs
    Tsume Y, et al.
    Pharmaceuticals (Basel, Switzerland), 7(2), 169-191 (2014)
    Iron deficiency impairs developing hippocampal neuron gene expression, energy metabolism, and dendrite complexity
    Bastian TW, et al.
    Developmental Neuroscience, 38(4), 264-276 (2016)
    Elite Possik et al.
    PLoS genetics, 10(4), e1004273-e1004273 (2014-04-26)
    Dysregulation of AMPK signaling has been implicated in many human diseases, which emphasizes the importance of characterizing AMPK regulators. The tumor suppressor FLCN, responsible for the Birt-Hogg Dubé renal neoplasia syndrome (BHD), is an AMPK-binding partner but the genetic and

    我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

    联系客户支持