A series of six novel 5-fluorouracil derivatives 1-6 were synthesized and theirstructures confirmed by 1H- and 13C-NMR, MS and elemental analysis. The preliminary invitro antitumor activities against B16, K562 and CHO cells and the in vivo inhibitions ofliver cancer H22 demonstrated that some of these compounds effectively inhibit the growthof tumor cells, but the in vivo trials in mice revealed that the compounds also exhibitedserious liver and lung tissue toxicity. The hydrolysis experiments indicated that this type ofcompound did not readily liberate 5-fluorouracil, as expected
Since its synthesis by Heidelberger et al.1 more than 40years ago, fluorouracil (5-FU) has become on...
Coupling of 6-benzyl-5-hydroxymethyluracil (1) with formaldehyde acetals followed by fluorination us...
We report the design, synthesis, and evaluation of novel 5-fluorouracil (5FU) prodrugs 1a,1b that ar...
Abstract: A series of six novel 5-fluorouracil derivatives 1-6 were synthesized and their structures...
OBJECTIVE: To synthesize N1-(aryl)alkyloxyacyl-5-fluorouracil derivatives and investigate their anti...
In the present study, five derivatives have been designed to be synthesized as possible mutual prodr...
This study reports two novel 5-fluorouracil-substituted ampelopsin derivatives. The structures of tw...
ABSTRACT: The new multifunctional antitumor conjugates containing ascor-bic acid and 5-fluorouracil ...
Chemotherapy is a general treatment option for various cancers, including lung cancer. In order to f...
ABSTRACT: Derivatives of 5-flurorouracil 1-N-p-vinylbenzoyl-5-fluorouracil (VBFU) were prepared and ...
5-Fluorouracil (5-FU) is widely employed in the treatment of some of the most frequently occurring m...
The synthesis of the unsaturated 4,6-dideoxy-3-fluoro-2-keto-beta-D-glucopyranosyl nucleosides of 5-...
The present invention relates to 5-fluoropyrimidine compounds of formula I that are useful for preve...
5-Fluorouracil and 5-fluorouracil-based prodrugs have been used clinically for decades to treat canc...
Attention is increasingly being focussed on the cell cycle and apoptosis as potential targets for th...
Since its synthesis by Heidelberger et al.1 more than 40years ago, fluorouracil (5-FU) has become on...
Coupling of 6-benzyl-5-hydroxymethyluracil (1) with formaldehyde acetals followed by fluorination us...
We report the design, synthesis, and evaluation of novel 5-fluorouracil (5FU) prodrugs 1a,1b that ar...
Abstract: A series of six novel 5-fluorouracil derivatives 1-6 were synthesized and their structures...
OBJECTIVE: To synthesize N1-(aryl)alkyloxyacyl-5-fluorouracil derivatives and investigate their anti...
In the present study, five derivatives have been designed to be synthesized as possible mutual prodr...
This study reports two novel 5-fluorouracil-substituted ampelopsin derivatives. The structures of tw...
ABSTRACT: The new multifunctional antitumor conjugates containing ascor-bic acid and 5-fluorouracil ...
Chemotherapy is a general treatment option for various cancers, including lung cancer. In order to f...
ABSTRACT: Derivatives of 5-flurorouracil 1-N-p-vinylbenzoyl-5-fluorouracil (VBFU) were prepared and ...
5-Fluorouracil (5-FU) is widely employed in the treatment of some of the most frequently occurring m...
The synthesis of the unsaturated 4,6-dideoxy-3-fluoro-2-keto-beta-D-glucopyranosyl nucleosides of 5-...
The present invention relates to 5-fluoropyrimidine compounds of formula I that are useful for preve...
5-Fluorouracil and 5-fluorouracil-based prodrugs have been used clinically for decades to treat canc...
Attention is increasingly being focussed on the cell cycle and apoptosis as potential targets for th...
Since its synthesis by Heidelberger et al.1 more than 40years ago, fluorouracil (5-FU) has become on...
Coupling of 6-benzyl-5-hydroxymethyluracil (1) with formaldehyde acetals followed by fluorination us...
We report the design, synthesis, and evaluation of novel 5-fluorouracil (5FU) prodrugs 1a,1b that ar...