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Merck
CN

F8883

2′-Fluoro-2′-deoxycytidine

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关于此项目

经验公式(希尔记法):
C9H12FN3O4
化学文摘社编号:
分子量:
245.21
UNSPSC Code:
12352204
MDL number:
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storage temp.

2-8°C

SMILES string

NC1=NC(=O)N(C=C1)C2OC(CO)C(O)C2F

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

此项目有


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Lieven J Stuyver et al.
Antimicrobial agents and chemotherapy, 48(2), 651-654 (2004-01-27)
2'-Deoxy-2'-fluorocytidine (FdC) is a potent inhibitor of the hepatitis C virus RNA replicon in culture, and FdC-5'-triphosphate is an effective inhibitor of the NS5B polymerase. Dynamic profiling of cell growth in an antiviral assay showed that FdC caused cytostasis due
Jeffrey J Bajramovic et al.
Antimicrobial agents and chemotherapy, 48(4), 1422-1425 (2004-03-30)
Borna disease virus (BDV) causes neurological diseases in a variety of warm-blooded animal species, possibly including humans. To date, there is no effective treatment against BDV infection. Recently, we reported on the antiviral activity of 1-beta-D-arabinofuranosylcytosine (Ara-C). However, Ara-C's cytotoxic
Frank C Richardson et al.
Chemical research in toxicology, 15(7), 922-926 (2002-07-18)
Apatmers are synthesized using 2'-fluoropyrimdines in place of normal pyrmidines to stabilize them against enzymatic degradation, and thereby improve their therapeutic efficacy. Despite this stabilizing effect, the apatmers can still be degraded by nucleases in the blood. Primer template extension
S Schmidt et al.
Biochimica et biophysica acta, 1130(1), 41-46 (1992-02-28)
Protected 2'-deoxy-2'-fluorouridine and 2'-deoxy-2'-fluorocytidine suitable for incorporation into oligonucleotides via the phosphoramidite approach have been prepared. Five modified and two unmodified oligonucleotides have been synthesized to investigate the regiospecific cleavage of a 5S RNA from Escherichia coli by RNase H.
S Helmling et al.
Nucleosides, nucleotides & nucleic acids, 22(5-8), 1035-1038 (2003-10-21)
Synthesis of 2'-fluoro-nucleosides from L-arabinose in order to perform the synthesis of 2'-fluoro-Spiegelmers binding to a neuropeptide.

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