All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Filters

201 (0,161s)

Result

Design and synthesis of 5,6-disubstituted uracil derivatives as potent inhibitors of thymidine phosphorylase

We report on a series of novel 5,6-disubstituted uracils with significant inhibitory activity against human and Escherichia coli thymidine phosphorylases....

CC - Organická chemie

  • 2005
  • D
Result

Comparative analysis of thymidylate synthase, thymidine phosphorylase and dihydropyrimidine dehydrogenase expression in colorectal cancer and surrounding normal tissue

thymidylate synthase, thymidine phosphorylase...

ED - Fyziologie

  • 2005
  • Jx
Result

Inhibition of thymidine phosphorylase (PD-ECGF) from SD-lymphoma by phosphonomethoxyalkyl thymines

A series of thymine phosphonomethoxyalkyl derivatives were evaluated for their ability to inhibit thymidine phosphorylase (dThdPase) purified from rat spontaneous T-cell lymphoma....

CC - Organická chemie

  • 2005
  • Jx
Result

Novel nucleoside phosphonic acids-based inhibitors of thymidine phosphorylase

Several sugar-modified thymine-containing nucleoside phosphonic acids were found as a strong inhibitors of thymidine phosphorylase purified from spontaneous T-cell lymphomas of an inbred Sprague-Dawley rat strain....

CC - Organická chemie

  • 2005
  • D
Result

Syntheses of N3-substituted thymine acyclic nucleoside phosphonates and a comparison of their inhibitory effect towards thymidine phosphorylase

for their ability to inhibit the human thymidine phosphorylase expressed in V79 Chinese hamster cells,as well as thymidine phosphorylase from SD-lymphoma, Escherichia coli a considerable inhibitory activity toward...

CC - Organická chemie

  • 2008
  • Jx
Result

Design and synthesis of novel 5,6-disubstituted uracil derivatives as potent inhibitors of thymidine phosphorylase

We report on a series of novel 5,6-disubstituted uracils with significant inhibitory activity against human and Escherichia coli thymidine phosphorylases. Bis-uracil conjugates were identified as the most potent inhibitors of TPs in...

CC - Organická chemie

  • 2006
  • Jx
Result

Discovery of 5-substituted-6-chlorouracils as efficient inhibitors of human thymidine phosphorylase

We have discovered that 6-halouracils substituted at position C5 by certain hydrophobic groups exhibit significant inhibitory activity against human thymidine phosphorylase. The most potent compounds bear a five- or six-membered cyc...

CC - Organická chemie

  • 2007
  • Jx
Result

Nucleoside phosphonic acids in thymidine phosphorylase inhibition: Structure - activity relationship

A number of structurally diverse nucleosides phosphonic acids have been tested against human recombinant thymidine phosphorylase and human platelets supernatant using 2'-deoxy-5-nitrouridine as the substrate. We have selected severa...

CC - Organická chemie

  • 2008
  • Jx
Result

Syntheses of base and side-chain modified pyrimidine 1-[2-(phosphonomethoxy)propyl] derivatives as potent inhibitors of thymidine phosphorylase (PD-ECGF) from SD-lymphoma

aspotent inhibitors of thymidine phosphorylase. While the 5-fluorouracil derivatives toward thymidine phosphorylase from rat spontaneous T-cell lymphoma....

CC - Organická chemie

  • 2006
  • Jx
Result

Syntheses of pyrimidine acyclic nucleoside phosphonates as potent inhibitors of thymidine phosphorylase (PD-ECGF) from SD-lymphoma

. The obtained compounds exhibit a considerable inhibitory potency of thymidine phosphorylase inhibitors of E. coli and human thymidine phosphorylase....

CC - Organická chemie

  • 2007
  • Jx
  • 1 - 10 out of 201