Synthesis of functionalized new conjugates of batracylin with tuftsin/ retro-tuftsin derivatives and their biological evaluation - Publikacja - MOST Wiedzy

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Synthesis of functionalized new conjugates of batracylin with tuftsin/ retro-tuftsin derivatives and their biological evaluation

Abstrakt

New batracylin conjugates with tuftsin/retro-tuftsin derivatives were designed and synthesized using T3P as a coupling agent. The conjugates possess an amide bond formed between the carboxyl group of heterocyclic molecule and the N-termini of the tuftsin/retro-tuftsin chain. The in vitro cytotoxic activity of the new analogues and their precursors was evaluated using a series of human and murine tumor cells. BAT conjugates containing retro-tuftsin with branched side aminoacid chain, in particular with leucine or isoleucine, were about 10-fold more cytotoxic toward two human tumor cell lines (lung adenocarcinoma (A549) and myeloblastic leukemia (HL-60)). These compounds showed about 10-fold increased cytotoxicity against the two types of tumor cells compared to parent BAT. We have not observed important differences in the mechanism of action between BAT and its cytotoxic tuftsin/retrotuftsin conjugates.We propose that high biological activity of the most active BAT conjugates is a result of their greatly increased intracellular accumulation.

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Kategoria:
Publikacja w czasopiśmie
Typ:
artykuł w czasopiśmie wyróżnionym w JCR
Opublikowano w:
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY nr 106, strony 85 - 94,
ISSN: 0223-5234
Język:
angielski
Rok wydania:
2015
Opis bibliograficzny:
Januchta W., Serocki M., Dzierzbicka K., Cholewiński G., Składanowski A.: Synthesis of functionalized new conjugates of batracylin with tuftsin/ retro-tuftsin derivatives and their biological evaluation// EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. -Vol. 106, (2015), s.85-94
DOI:
Cyfrowy identyfikator dokumentu elektronicznego (otwiera się w nowej karcie) 10.1016/j.ejmech.2015.10.012
Weryfikacja:
Politechnika Gdańska

wyświetlono 106 razy

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