Thymidine: Difference between revisions
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'''Thymidine''' is a pyrimidine | == Thymidine == | ||
[[File:Desoxythymidin.svg|thumb|right|Chemical structure of thymidine]] | |||
'''Thymidine''' is a nucleoside composed of the [[pyrimidine]] base [[thymine]] attached to a [[deoxyribose]] sugar. It is one of the four nucleosides in [[DNA]], the others being [[adenosine]], [[cytidine]], and [[guanosine]]. Thymidine is crucial for the replication and repair of DNA, playing a vital role in the [[cell cycle]] and [[cell division]]. | |||
== Structure == | == Structure == | ||
Thymidine | |||
Thymidine consists of the base thymine linked to a deoxyribose sugar via a _-N1-glycosidic bond. The chemical formula of thymidine is C<sub>10</sub>H<sub>14</sub>N<sub>2</sub>O<sub>5</sub>. The deoxyribose sugar in thymidine lacks a hydroxyl group at the 2' position, distinguishing it from [[ribose]] found in [[RNA]] nucleosides. | |||
== Function == | == Function == | ||
Thymidine is | |||
Thymidine is incorporated into DNA during the [[S phase]] of the cell cycle. It pairs with [[adenine]] through two hydrogen bonds, maintaining the stability of the DNA double helix. Thymidine is also involved in the [[DNA repair]] process, where it helps to replace damaged or mismatched bases. | |||
== Synthesis == | == Synthesis == | ||
== Clinical | Thymidine can be synthesized in cells through the [[salvage pathway]] or the [[de novo synthesis]] pathway. In the salvage pathway, thymidine is formed from thymine and deoxyribose-1-phosphate. In the de novo pathway, thymidine is synthesized from [[deoxyuridine]] monophosphate (dUMP) through the action of the enzyme [[thymidylate synthase]]. | ||
Thymidine analogs, such as | |||
== Clinical Significance == | |||
Thymidine analogs, such as [[zidovudine]] (AZT), are used as [[antiretroviral drugs]] in the treatment of [[HIV/AIDS]]. These analogs interfere with viral DNA synthesis, inhibiting the replication of the virus. Thymidine is also used in [[thymidine labeling]] techniques to study cell proliferation. | |||
== Related pages == | |||
* [[DNA]] | |||
* [[Nucleoside]] | |||
* [[Thymine]] | |||
* [[Deoxyribose]] | * [[Deoxyribose]] | ||
* [[Cell cycle]] | * [[Cell cycle]] | ||
[[Category:Nucleosides]] | [[Category:Nucleosides]] | ||
Latest revision as of 03:47, 13 February 2025
Thymidine[edit]
Thymidine is a nucleoside composed of the pyrimidine base thymine attached to a deoxyribose sugar. It is one of the four nucleosides in DNA, the others being adenosine, cytidine, and guanosine. Thymidine is crucial for the replication and repair of DNA, playing a vital role in the cell cycle and cell division.
Structure[edit]
Thymidine consists of the base thymine linked to a deoxyribose sugar via a _-N1-glycosidic bond. The chemical formula of thymidine is C10H14N2O5. The deoxyribose sugar in thymidine lacks a hydroxyl group at the 2' position, distinguishing it from ribose found in RNA nucleosides.
Function[edit]
Thymidine is incorporated into DNA during the S phase of the cell cycle. It pairs with adenine through two hydrogen bonds, maintaining the stability of the DNA double helix. Thymidine is also involved in the DNA repair process, where it helps to replace damaged or mismatched bases.
Synthesis[edit]
Thymidine can be synthesized in cells through the salvage pathway or the de novo synthesis pathway. In the salvage pathway, thymidine is formed from thymine and deoxyribose-1-phosphate. In the de novo pathway, thymidine is synthesized from deoxyuridine monophosphate (dUMP) through the action of the enzyme thymidylate synthase.
Clinical Significance[edit]
Thymidine analogs, such as zidovudine (AZT), are used as antiretroviral drugs in the treatment of HIV/AIDS. These analogs interfere with viral DNA synthesis, inhibiting the replication of the virus. Thymidine is also used in thymidine labeling techniques to study cell proliferation.
