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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14N2O6
Molecular Weight 258.228
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THYMINE RIBOSIDE

SMILES

CC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(=O)NC1=O

InChI

InChIKey=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

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Differential effects of nucleotide analogs on scanning-dependent initiation and elongation of mammalian mRNA translation in vitro.
2010-06
Long-term AZT exposure alters the metabolic capacity of cultured human lymphoblastoid cells.
2010-05
Mutagenesis of the modified bases, m(5)U1939 and psi2504, in Escherichia coli 23S rRNA.
2010-02-05
A study on the interaction between 5-Methyluridine and human serum albumin using fluorescence quenching method and molecular modeling.
2010-02
Stereochemical mechanisms of tRNA methyltransferases.
2010-01-21
Molecularly imprinted polymer of 5-methyluridine for solid-phase extraction of pyrimidine nucleoside cancer markers in urine.
2008-10-01
Crystallization and preliminary X-ray crystallographic characterization of TrmFO, a folate-dependent tRNA methyltransferase from Thermotoga maritima.
2008-03-01
Selenium derivatization of nucleic acids for phase and structure determination in nucleic acid X-ray crystallography.
2008-03
Metabolic signature of breast cancer cell line MCF-7: profiling of modified nucleosides via LC-IT MS coupling.
2007-11-29
A counterintuitive Mg2+-dependent and modification-assisted functional folding of mitochondrial tRNAs.
2006-09-29
3D-QSAR studies on antitubercular thymidine monophosphate kinase inhibitors based on different alignment methods.
2006-02-15
Temperature-dependent biosynthesis of 2-thioribothymidine of Thermus thermophilus tRNA.
2006-01-27
Synthesis and anti-viral activity of a series of d- and l-2'-deoxy-2'-fluororibonucleosides in the subgenomic HCV replicon system.
2005-03-01
Kilo-scale synthesis process for 2'-O-(2-methoxyethyl)-pyrimidine derivatives.
2005
Thymidine and thymidine-5'-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase.
2003-09-15
Three modifications in the D and T arms of tRNA influence translation in Escherichia coli and expression of virulence genes in Shigella flexneri.
2002-10
Characterization of the 23 S ribosomal RNA m5U1939 methyltransferase from Escherichia coli.
2002-03-15
Dual function of the tRNA(m(5)U54)methyltransferase in tRNA maturation.
2002-03
Acquisition of human concentrative nucleoside transporter 2 (hcnt2) activity by gene transfer confers sensitivity to fluoropyrimidine nucleosides in drug-resistant leukemia cells.
2001-11
Synthesis of novel 3'-C-methylene thymidine and 5-methyluridine/cytidine H-phosphonates and phosphonamidites for new backbone modification of oligonucleotides.
2001-04-20
Enhanced high density oligonucleotide array-based sequence analysis using modified nucleoside triphosphates.
1998-11-01
Isolation and identification of apoptosis inducing nucleosides from CD57(+)HLA-DRbright natural suppressor cell line.
1998-10-20
Purification and characterization of uridine and thymidine phosphorylase from Lactobacillus casei.
1990-09-03
Characterization of mouse and human monoclonal antibodies cross-reactive with SLE serum antibodies to guanosine.
1984-06
Specificity of anti-nucleoside antibodies in systemic lupus erythematosus.
1983-06
Patents
Name Type Language
THYMINE RIBOSIDE, (-)-
Preferred Name English
THYMINE RIBOSIDE
Common Name English
THYMINE RIBOSIDE [MI]
Common Name English
RIBOTHYMIDINE
Common Name English
PYRIMIDINEDIONE, 5-METHYL-1-.BETA.-D-RIBOFURANOSYL-
Systematic Name English
1-.BETA.-D-RIBOFURANOSYLTHYMINE 2,4(1H,3H)-PYRIMIDINEDIONE, 5-METHYL-1-.BETA.-D-RIBOFURANOSYL-
Systematic Name English
5-METHYLURIDINE
Systematic Name English
Code System Code Type Description
EVMPD
SUB197049
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
MERCK INDEX
m11839
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
WIKIPEDIA
5-Methyluridine
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
CHEBI
45996
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID20163348
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
SMS_ID
100000182769
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
FDA UNII
ZS1409014A
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
ECHA (EC/EINECS)
215-973-9
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
CAS
1463-10-1
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY
PUBCHEM
445408
Created by admin on Mon Mar 31 22:07:27 GMT 2025 , Edited by admin on Mon Mar 31 22:07:27 GMT 2025
PRIMARY