Drugs Future 23:702–706CrossRef Mazerska Z, Gorlewska K, Kraciuk A, Konopa J (1999) The relevance of enzymatic oxidation by horseradish peroxidase to antitumour potency of imidazoacridinone derivatives. Chem Biol Interact 115:1–22CrossRef Mazerska Z, Sowiński P, Konopa J (2003) Molecular mechanism of the enzymatic oxidation investigated for imidazoacridinone antitumor
drug, C-1311. Biochem Pharmacol 66:1727–1736PubMedCrossRef Mazerski J, Muchniewicz K (2000) The intercalation of imidazoacridinones into DNA induces Wortmannin order conformational changes in their side chain. Acta Biochim Pol 47:65–78PubMed Put R, Daszykowski M, Bączek T, Vander Heyden Y (2006) Retention prediction of peptides based on uninformative variable elimination by partial least
squares. J Proteome Res 5:1618–1625PubMedCrossRef Składanowski A, Konopa J (2000) Mitoxantrone and ametantrone induce interstrand cross-links in DNA of tumour cells. Br J Cancer 82:1300–1304PubMedCrossRef Składanowski A, Plisov SY, Konopa J, Larsen AK (1996) Inhibition of DNA topoisomerase AZD0156 II by imidazoacridinones, new antineoplastic agents with strong activity against solid tumor. Mol Pharmacol 49:772–780PubMed Składanowski A, Larsen AK, Konopa J, Lemke K (1999) Inhibition of DNA topoisomerase II by antitumor triazoloacridinones in vitro and in tumor cells. Proc Am Assoc Cancer Res 40:681 Skwarska A, Augustin E, Konopa J (2007) Sequential induction of mitotic catastrophe followed by apoptosis in human leukemia MOLT4 cells by imidazoacridinone C-1311. Apoptosis 12:2245–2257PubMedCrossRef Todeschini R, Consonni V, Mannhold R, Kubinyi H, Timmerman H (2000) Handbook of molecular descriptors. Wiley-VCH, WeinheimCrossRef Wesierska-Gadek J, Schloffer D, Gueorguieva M, Uhl M, Skladanowski A (2004) Increased susceptibility of poly(ADP-ribose) polymerase-1 knockout cells to antitumor triazoloacridone
C-1305 is associated with permanent G2 cell cycle arrest. Cancer Res 64:4487–4497PubMedCrossRef Zaffaroni N, De Marco C, Villa R, Riboldi S, Daidone MG, Double JA (2001) Cell growth inhibition, G2M cell cycle arrest and apoptosis induced by the imidazoacridinone C1311 in human tumour cell lines. Eur J Cancer 37:1953–1962PubMedCrossRef”
“Introduction 5-FU in vivo The carbon–carbon triple bond is one of the most important functional groups in organic chemistry and pharmacology. The structure activity relationship studies suggest that introduction of alkyne motif may significantly modify the chemical, physical, and biological properties of acetylenic compounds (Ben-Zvi and Danon, 1994). Among a large group of synthetic and natural acetylenic compounds the quinolines possessing an alkynyl moieties are of particular interest as many of them display important activities, namely antimicrobiological, anticancer, antiprotozoal, and antiretroviral (Fuita et al., 1998; Fakhfakh et al., 2003; Abele et al., 2002).