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dihydrouracil

Structure via PubChem · Public domain (PubChem)

EntityQ409340· pop 15· linked from 48 articles

dihydrouracil

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Also known as Dihydro-2,4(1H,3H)-pyrimidinedione, 2,4-Dioxotetrahydropyrimidine, 5,6-dihydrouracil, hexahydropyrimidine-2,4-dione, 1,3-diazinane-2,4-dione, Dihydro-pyrimidine-2,4-dione, 5,6-Dihydro-2,4(1H,3H)-pyrimidinedione, 3,4-Dihydrouracil

Dihydrouracil is an intermediate in the catabolism of uracil. The enzyme dihydrouracil dehydrogenase (NAD+) converts uracil to dihydrouracil:

In the Vinony graph

Vinony's link graph records 48 inbound references to dihydrouracil, and connects out to nicotinamide adenine dinucleotide, deoxyribonucleotide and digital object identifier.

It sits within the topics Chembox image size set, ECHA InfoCard ID from Wikidata and Nucleobases.

Vinony links it to 14 Wikipedia language editions.

Chemical data

Formula
C4H6N2O2
Molecular weight
114.1 g/mol
IUPAC name
1,3-diazinane-2,4-dione
SMILES
C1CNC(=O)NC1=O
InChIKey
OIVLITBTBDPEFK-UHFFFAOYSA-N
XLogP
-1.1
Polar surface area
58.2 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Wikidata facts

Mass
114.043
Show 6 more facts
melting point
279.0
chemical formula
C₄H₆N₂O₂
canonical SMILES
C1CNC(=O)NC1=O
Commons category
Dihydrouracil
subject has role
primary metabolite
Sources (4)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

Dihydrouracil is an intermediate in the catabolism of uracil. The enzyme dihydrouracil dehydrogenase (NAD+) converts uracil to dihydrouracil:

The enzyme uses reduced nicotinamide adenine dinucleotide (NADH) as its cofactor.

Excerpted from Wikipedia’s “dihydrouracil” article, available under the CC BY-SA 4.0 licence.

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