2010
DOI: 10.1016/j.tet.2010.02.043
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Synthesis of functionalized 5-(3-R-1-adamantyl)uracils and related compounds

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Cited by 15 publications
(9 citation statements)
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“…Èçó÷åíèå öèòîòîêñè÷íîñòè è àíòèâèðóñíîãî äåéñòâèÿ â îòíîøåíèè âèðóñîâ ïðîñòîãî ãåðïåñà (ÂÏÃ) àíòèãåí-íîãî òèïà HSV-1 è HSV-2 â êóëüòóðå êëåòîê Vero àäàìàíòèëèðîâàííûõ ïèðèìèäèíîâ ñ ôóíêöèîíàëüíûìè çàìåñ-òèòåëÿìè â àäàìàíòàíîâîì ÿäðå (ñîåäèíåíèÿ 32 -38) [51] è àäàìàíòèëñîäåðaeàùèõ íóêëåîçèäíûõ àíàëîãîâ 39, 40 -43 áûëî ïðîâåäåíî àâòîðàìè íàñòîÿùåãî îáçîðà [23]. Èíòåðåñ ê ñèíòåçó àäàìàíòèëñîäåðaeàùèõ íóêëåîçè-äîâ â çíà÷èòåëüíîé ñòåïåíè áûë ñâÿçàí ñ óñïåøíûì ïðèìåíåíèåì ïðåïàðàòîâ ýòîãî êëàññà â òåðàïèè âèðóñíûõ è îíêîëîãè÷åñêèõ çàáîëåâàíèé.…”
Section: ïðîòèâîâèðóñíàÿ àêòèâíîñòüunclassified
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“…Èçó÷åíèå öèòîòîêñè÷íîñòè è àíòèâèðóñíîãî äåéñòâèÿ â îòíîøåíèè âèðóñîâ ïðîñòîãî ãåðïåñà (ÂÏÃ) àíòèãåí-íîãî òèïà HSV-1 è HSV-2 â êóëüòóðå êëåòîê Vero àäàìàíòèëèðîâàííûõ ïèðèìèäèíîâ ñ ôóíêöèîíàëüíûìè çàìåñ-òèòåëÿìè â àäàìàíòàíîâîì ÿäðå (ñîåäèíåíèÿ 32 -38) [51] è àäàìàíòèëñîäåðaeàùèõ íóêëåîçèäíûõ àíàëîãîâ 39, 40 -43 áûëî ïðîâåäåíî àâòîðàìè íàñòîÿùåãî îáçîðà [23]. Èíòåðåñ ê ñèíòåçó àäàìàíòèëñîäåðaeàùèõ íóêëåîçè-äîâ â çíà÷èòåëüíîé ñòåïåíè áûë ñâÿçàí ñ óñïåøíûì ïðèìåíåíèåì ïðåïàðàòîâ ýòîãî êëàññà â òåðàïèè âèðóñíûõ è îíêîëîãè÷åñêèõ çàáîëåâàíèé.…”
Section: ïðîòèâîâèðóñíàÿ àêòèâíîñòüunclassified
“…** Ïðè èçëîaeåíèè äàííûõ áèîëîãè÷åñêèõ èññëåäîâàíèé àâòîðàìè ðàáîò áûëè èñïîëüçîâàíû ñëåäóþùèå ïîêàçàòåëè [ïðèâîäèòñÿ àááðåâèàòóðà è åå ðàñøèôðîâêà (åñëè îíà èìååòñÿ), äàííàÿ â ñîîòâåòñòâóþùåé ïóáëèêàöèè]: MIC -ìèíèìàëüíàÿ èíãèáèðóþùàÿ êîíöåíòðàöèÿ [2,3,6]. MIC 50 -ìèíèìàëüíàÿ èíãèáèðóþùàÿ êîíöåíòðàöèÿ ïðåïàðàòà, ïîäàâëÿþùàÿ ðàçâèòèå âèðóñèíäóöèðîâàííîãî öèòîïàòè÷åñêîãî äåéñòâèÿ íà 50 % [23,51]. MÑC 50 -ìèíèìàëüíàÿ öèòîòîêñè÷åñêàÿ êîíöåíòðàöèÿ, âûçûâàþùàÿ 50 % èíãèáèðîâàíèå ðîñòà êëåòîê (êëåòêè VERO) [23,51].…”
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“…Uracil (2), 5-methyluracil (thymine) (3), 6-methyluracil (4), and 3,6-dimethyluracil (5) were selected as the pyrimidine bases. Betulin-uracil conjugates were synthesized via N-alkylation of 2-5 by betulin 28-(2-bromoacetate) (6). Bromoacetate 6 was prepared via acylation of 1 with bromoacetic acid in the presence of dicyclohexylcarbodiimide.…”
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confidence: 99%