Thymidine monophosphate

Thymidine monophosphate
	IUPAC name 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 , 3288718
ChEBI	CHEBI:26999
ChEMBL	CHEMBL394429
Beilstein Reference	3916216
Jmol-3D images	Image 1
	SMILES Cc1cn(C2CC(O)C(COP([O-])([O-])=O)O2)c(:o)[nH]c1:o ;
	InChI InChI=1S/C10H15N2O8P/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(20-8)4-19-21(16,17)18/h3,6-8,13H,2,4H2,1H3,(H,11,14,15)(H2,16,17,18)/p-2 ; Key: GYOZYWVXFNDGLU-UHFFFAOYSA-L ;
Properties
Molecular formula	C10H13N2O8P2-
Molar mass	320.1926 g mol-1
Exact mass	320.040951914 g mol-1
	(verify) (what is: /?); 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-.

[edit] See also

^ 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.

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