Misplaced Pages

PMDTT

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
PMDTT
Names
IUPAC name ({oxy}methyl)phosphonic acid
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
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/s1Key: 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/s1Key: ICGMUOZWOCLUNS-HTQZYQBOBH
SMILES
  • CC1=CN(C(=O)NC1=O)2C(CO2)OCP(=O)(O)O
Properties
Chemical formula C10H15N2O7P
Molar mass 306.211 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

PMDTT is an antiviral phosphonate nucleoside.

References

  1. 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.
Categories: