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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

Molecular Formula C10H14N2O6
Molecular Weight 258.228
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Specificity of anti-nucleoside antibodies in systemic lupus erythematosus.
1983 Jun
Characterization of mouse and human monoclonal antibodies cross-reactive with SLE serum antibodies to guanosine.
1984 Jun
Purification and characterization of uridine and thymidine phosphorylase from Lactobacillus casei.
1990 Sep 3
Enhanced high density oligonucleotide array-based sequence analysis using modified nucleoside triphosphates.
1998 Nov 1
Isolation and identification of apoptosis inducing nucleosides from CD57(+)HLA-DRbright natural suppressor cell line.
1998 Oct 20
Acquisition of human concentrative nucleoside transporter 2 (hcnt2) activity by gene transfer confers sensitivity to fluoropyrimidine nucleosides in drug-resistant leukemia cells.
2001 Nov
Dual function of the tRNA(m(5)U54)methyltransferase in tRNA maturation.
2002 Mar
Characterization of the 23 S ribosomal RNA m5U1939 methyltransferase from Escherichia coli.
2002 Mar 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 Oct
Thymidine and thymidine-5'-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase.
2003 Sep 15
Kilo-scale synthesis process for 2'-O-(2-methoxyethyl)-pyrimidine derivatives.
2005
Synthesis and anti-viral activity of a series of d- and l-2'-deoxy-2'-fluororibonucleosides in the subgenomic HCV replicon system.
2005 Mar 1
3D-QSAR studies on antitubercular thymidine monophosphate kinase inhibitors based on different alignment methods.
2006 Feb 15
Temperature-dependent biosynthesis of 2-thioribothymidine of Thermus thermophilus tRNA.
2006 Jan 27
A counterintuitive Mg2+-dependent and modification-assisted functional folding of mitochondrial tRNAs.
2006 Sep 29
Metabolic signature of breast cancer cell line MCF-7: profiling of modified nucleosides via LC-IT MS coupling.
2007 Nov 29
Selenium derivatization of nucleic acids for phase and structure determination in nucleic acid X-ray crystallography.
2008 Mar
Crystallization and preliminary X-ray crystallographic characterization of TrmFO, a folate-dependent tRNA methyltransferase from Thermotoga maritima.
2008 Mar 1
Molecularly imprinted polymer of 5-methyluridine for solid-phase extraction of pyrimidine nucleoside cancer markers in urine.
2008 Oct 1
A study on the interaction between 5-Methyluridine and human serum albumin using fluorescence quenching method and molecular modeling.
2010 Feb
Mutagenesis of the modified bases, m(5)U1939 and psi2504, in Escherichia coli 23S rRNA.
2010 Feb 5
Stereochemical mechanisms of tRNA methyltransferases.
2010 Jan 21
Differential effects of nucleotide analogs on scanning-dependent initiation and elongation of mammalian mRNA translation in vitro.
2010 Jun
Long-term AZT exposure alters the metabolic capacity of cultured human lymphoblastoid cells.
2010 May
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:30:15 GMT 2023
Edited
by admin
on Sat Dec 16 08:30:15 GMT 2023
Record UNII
ZS1409014A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THYMINE RIBOSIDE
Common Name English
THYMINE RIBOSIDE [MI]
Common Name English
RIBOTHYMIDINE
Common Name English
THYMINE RIBOSIDE, (-)-
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 Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
MERCK INDEX
m11839
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
WIKIPEDIA
5-Methyluridine
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
CHEBI
45996
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID20163348
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
SMS_ID
100000182769
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
FDA UNII
ZS1409014A
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
ECHA (EC/EINECS)
215-973-9
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
CAS
1463-10-1
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
PUBCHEM
445408
Created by admin on Sat Dec 16 08:30:15 GMT 2023 , Edited by admin on Sat Dec 16 08:30:15 GMT 2023
PRIMARY
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ACTIVE MOIETY