Information about Uridine

Nucleosides are glycosylamines made by attaching a nucleobase (often referred to simply as bases) to a ribose or deoxyribose ring. Examples of these include cytidine, uridine, adenosine, guanosine, thymidine and inosine. In short, a nucleoside is a base linked to sugar.
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Uracil is a pyrimidine which is common and naturally occurring.^[1] Uracil was originally discovered in 1900. It was isolated by hydrolysis of yeast nuclein that was found in bovine thymus and spleen, herring sperm, and wheat germ.
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Ribose (ɹˈaɪbəʊs [1] , ɹˈaɪbəɹʊs [2] ), primarily seen as D -ribose, is an aldopentose — a monosaccharide containing five carbon atoms, and including an aldehyde functional group in its
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Ribofuranose is the biochemical name for the 5-carbon sugar (pentose) commonly known as ribose when having the furan ring structure.

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In chemistry, a glycosidic bond is a certain type of functional group that joins a carbohydrate (sugar) molecule to an alcohol, which may be another carbohydrate. Specifically, a glycosidic bond is formed between the hemiacetal group of a saccharide (or a molecule derived from a
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Uracil is a pyrimidine which is common and naturally occurring.^[1] Uracil was originally discovered in 1900. It was isolated by hydrolysis of yeast nuclein that was found in bovine thymus and spleen, herring sperm, and wheat germ.
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Deoxyribose, also known as D -Deoxyribose and 2-deoxyribose, is an aldopentose — a monosaccharide containing five carbon atoms, and including an aldehyde functional group.
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Deoxyuridine is a compound and a nucleoside. It is similar in chemical structure to uridine, but without the 2'-hydroxyl group.

Idoxuridine and Trifluridine are variants of deoxyuridine used as antiviral drugs.
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Biochemistry is the study of the chemical processes in living organisms.^[1] The word "biochemistry" comes from the Greek word βιοχημεία biochēmeia, which means "the chemistry of life.
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Peptides (from the Greek πεπτίδια, "small digestibles") are short polymers formed from the linking, in a defined order, of α-amino acids.
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amino acid is a molecule that contains both amine and carboxyl functional groups. In biochemistry, this term refers to alpha-amino acids with the general formula H₂NCHRCOOH, where R is an organic substituent.
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A nucleic acid is a macromolecule composed of nucleotide chains. In biochemistry these molecules carry genetic information or form structures within cells. The most common nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
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Lipids can be broadly defined as any fat-soluble (hydrophobic), naturally-occurring molecules. The term is more-specifically used to refer to fatty-acids and their derivatives (including tri-, di-, and monoglycerides and phospholipids) as well as other fat-soluble sterol-containing
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Terpenes are a large and varied class of hydrocarbons, produced primarily by a wide variety of plants, particularly conifers, though also by some insects such as swallowtail butterflies, which emit terpenes from their osmeterium.
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Carotenoids are organic pigments that are naturally occurring in plants and some other photosynthetic organisms like algae, some types of fungus and some bacteria. There are over 600 known carotenoids; they are split into two classes, xanthophylls and carotenes.
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Tetrapyrroles are compounds containing four pyrrole rings. With the exception of corrin, the four pyrrole rings are interconnected through one-carbon (methine or methylene) bridges, either in a linear or cyclic fashion.
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EC1 Oxidoreductases/list - EC2 Transferases/list - EC3 Hydrolases/list - EC4 Lyases/list - EC5 Isomerases/list - EC6 Ligases/list
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flavonoid refers to a class of plant secondary metabolites. According to the IUPAC nomenclature,^[1] they can be classified into:

• flavonoids, derived from 2-phenylchromen-4-one (2-phenyl-1,4-benzopyrone) structure
• isoflavonoids

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alkaloid is, strictly speaking, a naturally occurring amine produced by a plant, but amines produced by animals and fungi are also called alkaloids^[1]. Many alkaloids have pharmacological effects on humans and other animals.
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Polyketides are secondary metabolites from bacteria, fungi, plants, and animals. Secondary metabolites seem to be unnecessary for an organism’s ontogeny, but appear to have applications such as defence and intercellular communication.
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Genin redirects here. For the Naruto ninja rank, see Genin (Naruto).

In chemistry, glycosides are certain molecules in which a sugar part is bound to some other part. Glycosides play numerous important roles in living organisms.
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A nucleic acid is a macromolecule composed of nucleotide chains. In biochemistry these molecules carry genetic information or form structures within cells. The most common nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
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Nucleobases are the parts of RNA and DNA that may be involved in pairing (see also base pairs). These include cytosine, guanine, adenine, thymine (DNA), uracil (RNA) and xanthine and hypoxanthine (mutated forms of guanine and adenine, respectively).
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Purine (1) is a heterocyclic aromatic organic compound, consisting of a pyrimidine ring fused to an imidazole ring. Purines make up one of the two groups of nitrogenous bases. Pyrimidines make up the other group.
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Adenine is a purine with a variety of roles in biochemistry including cellular respiration, in the form of both the energy-rich adenosine triphosphate (ATP) and the cofactors nicotinamide adenine
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Guanine is one of the five main nucleobases found in the nucleic acids DNA and RNA; the others being adenine, cytosine, thymine, and uracil. With the formula C₅H₅N₅
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Pyrimidine is a heterocyclic aromatic organic compound similar to benzene and pyridine, containing two nitrogen atoms at positions 1 and 3 of the six-member ring.^[1] It is isomeric with two other forms of diazine.
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Uracil is a pyrimidine which is common and naturally occurring.^[1] Uracil was originally discovered in 1900. It was isolated by hydrolysis of yeast nuclein that was found in bovine thymus and spleen, herring sperm, and wheat germ.
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