2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI)

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2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI) manufacturers

  • Eniluracil
  • Eniluracil pictures
  • $31.00
  • 2026-05-26
  • CAS:59989-18-3
  • Purity: 99.91%
  • Supply Ability: 10g
2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI) Basic information
Product Name:2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI)
Synonyms:5-ethynyluracil;5-Ethynyl-2,4(1H,3H)-pyriMidinedione;NSC 687296;GW776C85;ADH-300004;GW-776;5-EthynylpyriMidine-2,4(1H,3H)-dione;5-Ethynyl-1H-pyrimidine-2,4-dione
CAS:59989-18-3
MF:C6H4N2O2
MW:136.11
EINECS:
Product Categories:Nucleotides;Pharmaceuticals;PYRIMIDINE;Bases & Related Reagents;Intermediates & Fine Chemicals
Mol File:59989-18-3.mol
2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI) Structure
2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI) Chemical Properties
Melting point 320° (dec)
density 1.527
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Soluble in DMSO
form solid
pka7.44±0.10(Predicted)
color Yellow
λmax284nm(MeOH)(lit.)
Merck 14,3584
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Safety Information
HS Code 2933.59.9500
MSDS Information
2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI) Usage And Synthesis
DescriptionEniluracil (59989-18-3) is an irreversible dihydropyrimidine dehydrogenase (DPD) inhibitor.1-3 DPD is involved in the degradation of pyrimidine-based chemotherapeutic drugs such as 5-fluorouracil (5-FU). Eniluracil has been used along with 5-FU to prolong circulating concentrations of the drug.
UsesPotent inactivator of Dihydropyrimidine dehydrogenase (DPD).
DefinitionChEBI: Eniluracil is a pyrimidone.
in vivo

Eniluracil (5-Ethynyluracil) (1 mg/kg; i.p.; single daily for 3 days) exhibits neither toxicity nor intrinsic antitumor activity, and greatly improves FUra (5-fluorouracil) therapy in rats[1].

Animal Model:Female Fischer 344/HSD rats (6 to 7-week-old; 150-200 g)[1].
Dosage:1 mg/kg
Administration:Intraperitoneal injection; single daily for 3 days (l h before FUra (5-fluorouracil) and for an additional 2 days after FUra therapy)
Result:Produced complete tumor regression that was sustained for at least 90 days posttherapy when combined with 3.5 mg/kg FUra, however, 35 mg/kg FUra alone produced partial responses in 75% of the treated animals ( the tumors regrew in all of these animals).
References[1] D J PORTER. Mechanism-based inactivation of dihydropyrimidine dehydrogenase by 5-ethynyluracil.[J]. The Journal of Biological Chemistry, 1992, 267 8: 5236-5242.
[2] D P BACCANARI. 5-Ethynyluracil (776C85): a potent modulator of the pharmacokinetics and antitumor efficacy of 5-fluorouracil.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1993, 90 23: 11064-11068. DOI:10.1073/pnas.90.23.11064
[3] R L SCHILSKY  H L K. Eniluracil: an irreversible inhibitor of dihydropyrimidine dehydrogenase.[J]. Expert opinion on investigational drugs, 2000, 9 7: 1635-1649. DOI:10.1517/13543784.9.7.1635
2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI) Preparation Products And Raw materials
Tag:2,4(1H,3H)-Pyrimidinedione, 5-ethynyl- (9CI)(59989-18-3) Related Product Information
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