Pyrimidine acyclic nucleoside phosphonates and phosphorylated analogs. Part 2. Syntheses and investigation of their inhibitory effects towards human thymidine phosphorylase
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
Odkazy
PubMed
18776551
DOI
10.1093/nass/nrn332
PII: nrn332
Knihovny.cz E-zdroje
- MeSH
- antitumorózní látky chemická syntéza chemie farmakologie MeSH
- fosforylace MeSH
- inhibitory enzymů chemická syntéza chemie farmakologie MeSH
- lidé MeSH
- organofosfonáty chemická syntéza chemie farmakologie MeSH
- thymidinfosforylasa antagonisté a inhibitory MeSH
- thymin analogy a deriváty chemická syntéza chemie farmakologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- 1-(3-fluoro-2-(phosphonomethoxy)propyl)thymine MeSH Prohlížeč
- antitumorózní látky MeSH
- inhibitory enzymů MeSH
- organofosfonáty MeSH
- thymidinfosforylasa MeSH
- thymin MeSH
Various methods were used in the syntheses of a number of pyrimidine acyclic nucleoside phosphonates and their derivatives such as a nucleophilic fluorination, Suzuki-Miyaura coupling reactions and phosphorylation. These new compounds were further investigated for their potential biological activity. Based on results obtained the ability to inhibit human thymidine phosphorylase some of them was found.
