Thymidine
Identifiers
CAS number	50-89-5 Y
PubChem	1134
MeSH	Thymidine
SMILES	CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O
Properties
Molecular formula	C10H14N2O5
Y (what is this?)  (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Thymidine (more precisely called deoxythymidine; can also be labelled deoxyribosylthymine, and thymine deoxyriboside) is a chemical compound, more precisely a pyrimidine deoxynucleoside. Deoxythymidine is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. In cell biology it is used to synchronize the cells in S phase.

Before the boom in thymidine use caused by the need for thymidine for the production of the antiretroviral drug azidothymidine (AZT), much of the world's thymidine production came from herring sperm.^[1]

Contents 1 Structure and properties 2 Modified analogs of thymidine 3 References 4 External links

[edit] Structure and properties

In its composition, deoxythymidine is a nucleoside composed of deoxyribose (a pentose sugar) joined to the pyrimidine base thymine.

Deoxythymidine can be phosphorylated with one, two or three phosphoric acid groups, creating respectively dTMP, dTDP or dTTP ((deoxy)thymidine mono- di- or triphosphate).

It exists in solid form as small white crystals or white crystalline powder, has a molecular weight of 242.229 u, and has a melting point of 185 °C. The stability of deoxythymidine under standard temperature and pressure (STP) is very high.

Deoxythymidine is non-toxic and as part of one of the four nucleotides in DNA it is a naturally occurring compound that exists in all living organisms and DNA viruses. RNA has uridine (uracil joined to ribose) instead. Uracil is chemically very similar to thymine, the latter being 5-methyluracil. Since thymine nucleotides are precursors of DNA, not RNA, the prefix "deoxy" is often left out, i.e., deoxythymidine is often just called thymidine.

[edit] Modified analogs of thymidine

Iododeoxyuridine is a radiosensitizer and increases the amount of DNA damage received from ionizing radiation.

Azidothymidine (AZT) - used in the treatment of HIV infection. AZT inhibits the process of reverse transcription, a critical step in the viral life cycle.

Tritiated thymidine is commonly used in cell proliferation assays. The thymidine is incorporated into dividing cells and the level of this incorporation, measured using a liquid scintillation counter, is proportional to the amount of cell proliferation.

Bromodeoxyuridine (BrdU) is another thymidine analog that is often used for the detection of proliferating cells in living tissues.

[edit] References

[edit] External links

• http://money.cnn.com/magazines/fortune/fortune_archive/1990/11/05/74308/index.htm

v • d • e Nucleobases, nucleosides, and nucleotides Nucleobases Purine (Adenine, Guanine, Purine analogue) · Pyrimidine (Uracil, Thymine, Cytosine, Pyrimidine analogue) Nucleosides/ (NB+pentose) Ribonucleosides Adenosine · Guanosine · Uridine · Cytidine Deoxyribonucleosides Deoxyadenosine · Deoxyguanosine · Thymidine · Deoxyuridine · Deoxycytidine Nucleotides/ (NS+phosphate) Ribonucleotide monophosphates (AMP, GMP, UMP, CMP) · diphosphates (ADP, GDP, UDP, CDP) · triphosphates (ATP, GTP, UTP, CTP) Deoxyribonucleotides monophosphates (dAMP, dGMP, dUMP, TMP, dCMP) · diphosphates (dADP, dGDP, TDP, dCDP) · triphosphates (dATP, dGTP, TTP, dCTP) Cyclic cAMP, cGMP, c-di-GMP, cADPR Major families of biochemicals Saccharides/Carbohydrates/Glycosides · Amino acids/Peptides/Proteins/Glycoproteins · Lipids/Terpenes/Steroids/Carotenoids · Alkaloids/Nucleobases/Nucleic acids · Cofactors/Phenylpropanoids/Polyketides/Tetrapyrroles