Thymidine monophosphate


Thymidine monophosphate
Thymidine monophosphate
Identifiers
Abbreviations TMP
PubChem 16755631 (2R,3S,5R)-3-hydrox,-5-pyrimidin,-2-yl, 25791020 (2R,3R,5R)-3-hydrox,-5-pyrimidin,-2-yl, 25791703 (2R,3R,5S)-3-hydrox,-5-pyrimidin,-2-yl, 4073694, 16755631 (2R,3S,5S)-3-hydrox,-5-pyrimidin,-2-yl
ChemSpider 10239189 (2R,3S,5R)-3-hydrox,-5-pyrimidin,-2-yl YesY, 3288718 N
ChEBI CHEBI:26999 YesY
ChEMBL CHEMBL394429 N
Beilstein Reference 3916216
Jmol-3D images Image 1
Properties
Molecular formula C10H13N2O8P2-
Molar mass 320.1926 g mol-1
Exact mass 320.040951914 g mol-1
 N (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Thymidine monophosphate, also known as 5'-thymidylate, thymidylate, or TMP, is a nucleotide that is used as a monomer in DNA. It is an ester of phosphoric acid with the nucleoside thymidine. TMP consists of a phosphate group, the pentose sugar deoxyribose, and the nucleobase thymine. Unlike the other deoxyribonucleotides, thymidine monophosphate does not contain the "deoxy" prefix in its name.[1] As a substituent, it takes the form of the prefix thymidylyl-.

See also

References

  1. ^ Coghill, Anne M.; Garson, Lorrin R., ed (2006). The ACS style guide: effective communication of scientific information (3rd ed.). Washington, D.C.: American Chemical Society. p. 244. ISBN 9780841239999. 

External links

Nucleotide
(Nucleoside monophosphate) Nucleoside diphosphate Nucleoside triphosphate biochemical families: prot · nucl · carb (glpr, alco, glys) · lipd (fata/i, phld, strd, gllp, eico) · amac/i · ncbs/i · ttpy/i

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