5-Ethyluracil

For research use only. Not for therapeutic Use.

  • CAT Number: M008447
  • CAS Number: 4212-49-1
  • Molecular Formula: C6H8N2O2
  • Molecular Weight: 140.142
  • Purity: ≥95%
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Catalog Number M008447
CAS Number 4212-49-1
Synonyms

HOMOTHYMINE;AURORA KA-580;5-ETHYLURACIL;2,4-DIHYDROXY-5-ETHYLPYRIMIDINE;5-Ethyl-1H-pyrimidine-2,4-dione;2,4(1H,3H)-Pyrimidinedione, 5-ethyl- (9CI);DIHYDROXY-5-ETHYLPYRIMIDINE;5-ethvluracil

Molecular Formula C6H8N2O2
Purity ≥95%
Storage room temp
IUPAC Name 5-ethyl-1H-pyrimidine-2,4-dione
InChI InChI=1S/C6H8N2O2/c1-2-4-3-7-6(10)8-5(4)9/h3H,2H2,1H3,(H2,7,8,9,10)
InChIKey RHIULBJJKFDJPR-UHFFFAOYSA-N
SMILES CCC1=CNC(=O)NC1=O
Reference

1: Mansuri MM, Ghazzouli I, Chen MS, Howell HG, Brodfuehrer PR, Benigni DA,
Martin JC. 1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-ethyluracil. A highly
selective antiherpes simplex agent. J Med Chem. 1987 May;30(5):867-71. PubMed
PMID: 3033244.
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2: Swierkowski M, Shugar D. A new thymine base analogue, 5-ethyluracil:
5-ethyluridine-5/’-pyrophosphate and poly-5-ethyluridylic acid. Acta Biochim Pol.
1969;16(3):263-77. PubMed PMID: 4904852.

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3: Piechowska M, Shugar D. Replacement of 5-methyluracil (thymine) by
5-ethyluracil in bacterial DNA. Biochem Biophys Res Commun. 1965 Sep
22;20(6):768-73. PubMed PMID: 5324103.
<br>

4: Kaul R, Kiefer G, Erhardt S, Hempel B.
2-14C-1-(2/’-deoxy-beta-D-ribofuranosyl)-5-ethyluracil: synthesis and
biotransformation in rats. J Pharm Sci. 1980 May;69(5):531-4. PubMed PMID:
7381737.
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5: Kulikowski T, Zawadzki Z, Shugar D, Descamps J, De Clercq E. Synthesis and
antiviral activities of arabinofuranosyl-5-ethylpyrimidine nucleosides. Selective
antiherpes activity of 1-(beta-D-arabinofuranosyl)-5-ethyluracil. J Med Chem.
1979 Jun;22(6):647-53. PubMed PMID: 222908.

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