Nucleoside

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Nitrogen base Ribonucleoside Desoxirribonucleoside
Estructura química de la adenina
Adenine
Estructura química de la adenosina
Adenosine
A
Estructura química de la desoxiadenosina
Desoxiadenosine
dA
Estructura química de la guanina
Guanina
Estructura química de la guanosina
Guanosina
G
Estructura química de la desoxiguanosina
Desoxiguanosine
dG
Estructura química de la timina
Timina
Estructura química de la 5-metiluridina
Timidina
T
Estructura química de la timidina
Timidina
dT
Estructura química del uracilo
Uracilo
Estructura química de la uridina
Uridina
U
Estructura química of deoxiuridina
Desoxiuridine
dU
Estructura química de la citosina
Citosina
Estructura química de la citidina
Citidina
C
Estructura química de la desoxicitidina
Desoxicitidine
dC

A nucleoside is a glusosilamide organic monomeric molecule, which integrates the nucleic acid macromolecules and results from the covalent union between a nitrogenous base and a pentose, which can be ribose or deoxyribose. Examples of nucleosides are cytidine, uridine, adenosine, guanosine, thymidine, and inosine.

They can be conceived as nucleotides that do not have the phosphate group. That is, nucleosides can be combined with a phosphoric group (phosphoric acid: H3PO4) by certain kinases in the cell, producing nucleotides, which are the basic molecular components. of DNA and RNA.

Nucleosides can be of two types, depending on the pentose they contain:

  • Ribonucleosides: the pentase is the ribose
  • Desoxirribonucleosides: the pentose is the 2-disoxirribosa

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