PMDTT

PMDTT
Names
	IUPAC name ({[(3R,5R)-5-(5-Methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)oxolan-3-yl]oxy}methyl)phosphonic acid
Identifiers
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3976812;
ChemSpider	4440846;
PubChem CID	5276920;
	InChI InChI=1S/C10H15N2O7P/c1-6-3-12(10(14)11-9(6)13)8-2-7(4-18-8)19-5-20(15,16)17/h3,7-8H,2,4-5H2,1H3,(H,11,13,14)(H2,15,16,17)/t7-,8-/m1/s1 Key: ICGMUOZWOCLUNS-HTQZYQBOSA-N; InChI=1/C10H15N2O7P/c1-6-3-12(10(14)11-9(6)13)8-2-7(4-18-8)19-5-20(15,16)17/h3,7-8H,2,4-5H2,1H3,(H,11,13,14)(H2,15,16,17)/t7-,8-/m1/s1 Key: ICGMUOZWOCLUNS-HTQZYQBOBH;
	SMILES CC1=CN(C(=O)NC1=O)[C@H]2C[C@H](CO2)OCP(=O)(O)O;
Properties
Chemical formula	C10H15N2O7P
Molar mass	306.211 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

PMDTT is an antiviral phosphonate nucleoside.^[1]

References[edit]

^ Wu, Tongfei; Froeyen, Matheus; Kempeneers, Veerle; Pannecouque, Christophe; Wang, Jing; Busson, Roger; De Clercq, Erik; Herdewijn, Piet (13 April 2005). "Deoxythreosyl phosphonate nucleosides as selective anti-HIV agents". Journal of the American Chemical Society. 127 (14): 5056–5065. doi:10.1021/ja043045z. ISSN 0002-7863. PMID 15810840.