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Published in 2020 at "Clinical Pharmacokinetics"
DOI: 10.1007/s40262-020-00934-7
Abstract: Pyrimidine analogues can be considered as prodrugs, like their natural counterparts, they have to be activated within the cell. The intracellular activation involves several metabolic steps including sequential phosphorylation to its monophosphate, diphosphate and triphosphate.…
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Keywords:
pyrimidine analogues;
nucleotide concentrations;
intracellular nucleotide;
oncology ... See more keywords
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Published in 2019 at "Journal of Molecular Structure"
DOI: 10.1016/j.molstruc.2019.01.105
Abstract: Abstract A total of 66 novel heterofused pyrimidine analogues (pyrazolo[3,4-d]pyrimidine (7-43) and pyrido[2,3-d]pyrimidine (51a-l & 52a-h)) were synthesized by employing suitable methods. The desired structures of all the synthesized compounds were confirmed based on FT-IR,…
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Keywords:
design synthesis;
novel heterofused;
heterofused pyrimidine;
pyrimidine ... See more keywords
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Published in 2018 at "Journal of medicinal chemistry"
DOI: 10.1021/acs.jmedchem.8b00408
Abstract: Novel fluorinated 2-amino-4-oxo-6-substituted pyrrolo[2,3- d]pyrimidine analogues 7-12 were synthesized and tested for selective cellular uptake by folate receptors (FRs) α and β or the proton-coupled folate transporter (PCFT) and for antitumor efficacy. Compounds 8, 9,…
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Keywords:
substituted pyrrolo;
pyrimidine analogues;
folate;
pyrrolo pyrimidine ... See more keywords
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Published in 2017 at "Acta Parasitologica"
DOI: 10.1515/ap-2017-0070
Abstract: Inhibition of parasite metabolic pathways is a rationale for new chemotherapeutic strategies. The pyrimidine and purine salvage pathways are thus targets against Leishmania donovani and L. infantum, causative agents of visceral human leishmaniasis and canine…
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Keywords:
infantum;
pyrimidine analogues;
vitro effects;
effects purine ... See more keywords