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Merck
CN

47580

Sigma-Aldrich

5-氟脲嘧啶

≥99.0% (HPLC)

别名:

5-氟尿嘧啶 1β-D-呋喃核苷, 皮毛

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关于此项目

经验公式(希尔记法):
C9H11FN2O6
化学文摘社编号:
分子量:
262.19
Beilstein:
33662
EC 号:
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
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生物来源

synthetic

方案

≥99.0% (HPLC)

旋光性

[α]20/D +18±1°, c = 1% in H2O

mp

182-184 °C

储存温度

2-8°C

SMILES字符串

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

InChI

1S/C9H11FN2O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2H2,(H,11,16,17)/t4-,5-,6-,8-/m1/s1

InChI key

FHIDNBAQOFJWCA-UAKXSSHOSA-N

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储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

法规信息

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分析证书(COA)

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Kara L Vine et al.
Bioorganic & medicinal chemistry letters, 20(9), 2908-2911 (2010-04-07)
A urokinase targeting conjugate of 2'-deoxy-5-fluorouridine (5-FUdr) was synthesized and tested for tumor-cell selective cytotoxicity in vitro. The 5-FUdr prodrug 2'-deoxy-5-fluoro-3'-O-(3-carboxypropanoyl)uridine (5-FUdrsuccOH) containing an ester-labile succinate linker was attached to the specific urokinase inhibitor plasminogen activator inhibitor type II (PAI-2)
Olaf H Temmink et al.
The international journal of biochemistry & cell biology, 39(3), 565-575 (2006-11-14)
Thymidine phosphorylase (TP) and uridine phosphorylase (UP) are often upregulated in solid tumors and catalyze the phosphorolysis of natural (deoxy)nucleosides and a wide variety of fluorinated pyrimidine nucleosides. Because the relative contribution of each of the two enzymes to these
Stephen Hanessian et al.
Bioorganic & medicinal chemistry, 16(6), 2921-2931 (2008-01-30)
Superparamagnetic iron oxide nanoparticles (SPIONs) are in clinical use for disease detection by MRI. A major advancement would be to link therapeutic drugs to SPIONs in order to achieve targeted drug delivery combined with detection. In the present work, we
Mingjie Chen et al.
The Plant cell, 23(8), 2991-3006 (2011-08-11)
Nucleotides are synthesized from de novo and salvage pathways. To characterize the uridine salvage pathway, two genes, UKL1 and UKL2, that tentatively encode uridine kinase (UK) and uracil phosphoribosyltransferase (UPRT) bifunctional enzymes were studied in Arabidopsis thaliana. T-DNA insertions in
Rita Humeniuk et al.
Molecular cancer therapeutics, 8(5), 1037-1044 (2009-04-23)
5-Fluorouracil (5-FU) continues to be widely used for treatment of gastrointestinal cancers. Because many tumors show primary or acquired resistance, it is important to understand the molecular basis underlying the mechanism of resistance to 5-FU. In addition to its effect

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