47580
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
EC Number:
206-260-3
UNSPSC Code:
41106305
PubChem Substance ID:
Beilstein/REAXYS Number:
33662
MDL number:
InChI key
FHIDNBAQOFJWCA-UAKXSSHOSA-N
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
SMILES string
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=C(F)C(=O)NC2=O
biological source
synthetic
assay
≥99.0% (HPLC)
optical activity
[α]20/D +18±1°, c = 1% in H2O
mp
182-184 °C
storage temp.
2-8°C
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
法规信息
新产品
此项目有
Alvaro A A de Queiroz et al.
Acta biomaterialia, 2(6), 641-650 (2006-08-01)
The effect of gamma-radiation doses of 12.5-380 kGy on the infrared spectra, gel content, mechanical properties, and the release of oxobutyl-5-fluoro-2'-deoxyuridine (OfdUrd, an antitumor agent) from poly(ethylene-co-vinyl acetate) (EVA) films was studied. The results showed that the application of radiation
Erik Schleicher et al.
The FEBS journal, 272(8), 1855-1866 (2005-04-12)
Cyclobutane-type pyrimidine dimers generated by ultraviolet irradiation of DNA can be cleaved by DNA photolyase. The enzyme-catalysed reaction is believed to be initiated by the light-induced transfer of an electron from the anionic FADH- chromophore of the enzyme to the
Edward J Miracco et al.
Journal of the American Chemical Society, 133(31), 11826-11829 (2011-07-13)
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Michaela Traub et al.
The Plant journal : for cell and molecular biology, 49(5), 855-864 (2007-01-27)
The fluorouridine insensitive 1 (fur1) locus in Arabidopsis thaliana (L.) Heynh. has previously been identified in a screen for growth resistance towards the toxic compound fluorouridine. Mutation of this locus by ethylmethane sulfonate (EMS) allows mutants to grow on this
Huai Wang et al.
Journal of biotechnology, 129(4), 689-695 (2007-03-21)
For the first time, lipozyme TL IM, an inexpensive lipase from Thermomyces lanuginosa, was successfully applied to the regioselective synthesis of lipophilic 5-fluorouridine ester derivatives. The ESI-MS and (13)C NMR analysis confirmed that the end products of the acylation were
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