Literature DB >> 1218441

Syntheses of potential antimetabolites. XX. Syntheses of 5-carbomethoxymethyl- and 5-methylaminomethyl-2-thiouridine (the "first letters" of some anticodons) and closely related nucleosides from uridine.

K Ikeda, S Tanaka, Y Mizuno.   

Abstract

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Year:  1975        PMID： 1218441     DOI： 10.1248/cpb.23.2958

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN： 0009-2363            Impact factor:   1.645


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  3 in total

1.  C5-substituents of uridines and 2-thiouridines present at the wobble position of tRNA determine the formation of their keto-enol or zwitterionic forms - a factor important for accuracy of reading of guanosine at the 3΄-end of the mRNA codons.

Authors:  Elzbieta Sochacka; Elzbieta Lodyga-Chruscinska; Justyna Pawlak; Marek Cypryk; Paulina Bartos; Katarzyna Ebenryter-Olbinska; Grazyna Leszczynska; Barbara Nawrot
Journal:  Nucleic Acids Res       Date:  2017-05-05       Impact factor: 16.971

2.  Synthesis of stable-isotope enriched 5-methylpyrimidines and their use as probes of base reactivity in DNA.

Authors:  Artur Burdzy; Katherine T Noyes; Victoria Valinluck; Lawrence C Sowers
Journal:  Nucleic Acids Res       Date:  2002-09-15       Impact factor: 16.971

3.  Efficient syntheses of [3-15N]uracil and [3-15N]thymine.

Authors:  R H Griffey; C D Poulter
Journal:  Nucleic Acids Res       Date:  1983-09-24       Impact factor: 16.971
  3 in total

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