535893
5-甲基尿苷
97%
别名:
胸腺嘧啶核糖核苷
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经验公式（希尔记法）:
C10H14N2O6
化学文摘社编号:
分子量:
258.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
215-973-9
MDL number:
Assay:
97%
InChI key
DWRXFEITVBNRMK-JXOAFFINSA-N
InChI
1S/C10H14N2O6/c1-4-2-12(10(17)11-8(4)16)9-7(15)6(14)5(3-13)18-9/h2,5-7,9,13-15H,3H2,1H3,(H,11,16,17)/t5-,6-,7-,9-/m1/s1
SMILES string
CC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(=O)NC1=O
assay
97%
mp
183-184 °C (lit.)
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存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Clive Persaud et al.
Biochemical and biophysical research communications, 392(2), 223-227 (2010-01-14)
Ribosomal RNAs (rRNAs) from all kingdoms contain a variety of post-transcriptional modifications and these are typically clustered in the functional centers of the ribosome. The functions of two bases in the 23S rRNA of Escherichia coli that are post-transcriptionally modified
Marcus J O Johansson et al.
RNA (New York, N.Y.), 8(3), 324-335 (2002-05-11)
A 5-methyluridine (m(5)U) residue at position 54 is a conserved feature of bacterial and eukaryotic tRNAs. The methylation of U54 is catalyzed by the tRNA(m5U54)methyltransferase, which in Saccharomyces cerevisiae is encoded by the nonessential TRM2 gene. In this study, we
Marino J E Resendiz et al.
Journal of the American Chemical Society, 134(30), 12478-12481 (2012-07-26)
Photolabile nucleotides that disrupt nucleic acid structure are useful mechanistic probes and can be used as tools for regulating biochemical processes. Previous probes can be limited by the need to incorporate multiple modified nucleotides into oligonucleotides and in kinetic studies
Pseudouridine and ribothymidine formation in the tRNA-like domain of turnip yellow mosaic virus RNA.
H F Becker et al.
Nucleic acids research, 26(17), 3991-3997 (1998-08-15)
The last 82 nucleotides of the 6.3 kb genomic RNA of plant turnip yellow mosaic virus (TYMV), the so-called 'tRNA-like' domain, presents functional, structural and primary sequence homologies with canonical tRNAs. In particular, one of the stem-loops resembles the TPsi(pseudouridine)-branch
H An et al.
The Journal of organic chemistry, 66(8), 2789-2801 (2001-04-17)
Novel 5'-O-DMT- and MMT-protected 3'-C-methylene-modified thymidine, 5-methyluridine, and 5-methylcytidine H-phosphonates 1-7 with O-methyl, fluoro, hydrogen, and O-(2-methoxyethyl) substituents at the 2'-position have been synthesized by a new effective strategy from the corresponding key intermediates 3'-C-iodomethyl nucleosides and intermediate BTSP, prepared
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