CCCC >
Archive >
2010,
Volume 75 >
Issue 8 >
p. 887 >
References
Collect. Czech. Chem. Commun.
2010, 75, 887-903
https://doi.org/10.1135/cccc2010048
Published online 2010-08-31 09:18:53
Glyoxyl analogs of indole phytoalexins: Synthesis and anticancer activity
Peter Kutschya,*, Andrej Sýkorab, Zuzana Čurillováa, Mária Repovskáa, Martina Pilátovác, Ján Mojžišc, Roman Mezencevd, Pavel Pazderae and Tatiana Hromjákováa
a P. J. Šafárik University, Faculty of Science, Institute of Chemical Sciences, Department of Organic Chemistry, Moyzesova 11, 040 01 Košice, Slovak Republic
b University of Prešov, Faculty of Health Care, Partizánska 1, 080 01 Prešov, Slovak Republic
c P. J. Šafárik University, Faculty of Medicine, Department of Pharmacology, SNP 1, 040 66 Košice, Slovak Republic
d Georgia Institute of Technology, College of Science, School of Biology, 315 Ferst Drive, Atlanta, GA 30332, USA
e Centre for Syntheses at Sustainable Conditions and Their Management, Department of Chemistry, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic
References
2a.
Kobayashi J., Murayama T., Ishibashi M., Kosuge S., Takamatsu M., Ohizumi Y., Kobayashi H., Ohta T., Nozoe S., Sasaki T.: Tetrahedron 1990, 46, 7699.
<
https://doi.org/10.1016/S0040-4020(01)90065-1>
3a. Bacher G., Nickel B., Emig P., Vanhoefer U., Seeber S., Shandra A., Klenner T., Beckers T.: Cancer Res. 2001, 61, 392.
3b.
Da Settimo F., Simorini F., Taliani S., La Motta C., Marini A. M., Salerno S., Bellandi M., Novellino E., Greco G., Cosimelli B., Da Pozzo E., Costa B., Simola N., Morelli M., Martini C.: J. Med. Chem. 2008, 51, 5798.
<
https://doi.org/10.1021/jm8003224>
3c.
Taliani S., Cosimelli B., Da Settimo F., Marini A. M., La Motta C., Simorini F., Salerno S., Novellino E., Greco G., Cosconati S., Marinelli L., Salvetti F., Lábbate G., Trasciatti S., Montali M., Costa B., Martini C.: J. Med. Chem. 2009, 52, 3723.
<
https://doi.org/10.1021/jm9001154>
3e.
Wang T., Yin Z., Zhang Z., Bender J. A., Yang Z., Johnson G., Yang Z., Zadjura L. M., D’Arienzo C. J., DiGiugno Parker D., Gesenberg C., Yamanaka G. A., Gong Y-F., Ho H-T., Fang H., Zhou N., McAuliffe B. V., Eggers B. J., Fan L., Nowicka-Sans B., Dicker I. B., Gao Q., Colonno R. J., Lin P-F., Meanwell N. A., Kadow J. F.: J. Med. Chem. 2009, 52, 7778.
<
https://doi.org/10.1021/jm900843g>
4a. Mezencev R., Mojžiš J., Pilátová M., Kutschy P.: Neoplasma 2003, 50, 239.
4b.
Pilátová M., Šarišský M., Kutschy P., Miroššay A., Mezencev R., Čurillová Z., Suchý M., Monde K., Miroššay L., Mojžiš J.: Leukemia Res. 2005, 29, 415.
<
https://doi.org/10.1016/j.leukres.2004.09.003>
4e.
Kutschy P., Salayová A., Čurillová Z., Kožár T., Mezencev R., Mojžiš J., Pilátová M., Balentová E., Pazdera P., Sabol M., Zburová M.: Bioorg. Med. Chem. 2009, 17, 3698.
<
https://doi.org/10.1016/j.bmc.2009.03.064>
4g. Kutschy P., Mezencev R. in: Targets in Heterocyclic Systems – Chemistry and Properties (O. A. Attanasi and D. Spinelli, Eds), Vol. 12, p. 120 (2008). Italian Society of Chemistry, Urbino 2009.
4h.
Kutschy P., Sabol M., Marušková R., Čurillová Z., Dzurilla M., Géci I., Alföldi J., Kováčik V.: Collect. Czech. Chem. Commun. 2004, 69, 850.
<
https://doi.org/10.1135/cccc20040850>
4i. Kutschy P., Čurillová Z., Mojžiš J., Pilátová M.: Unpublished results.
6b. Masataka Y., Hidekatsu H.: Synthesis 1985, 891.
7b. Kawasaki T., Kodama A., Nishida T., Shimizu K., Somei M.: Heterocycles 1991, 32, 221.
9a. Zemplén G., Gerecs A., Hadacsy J.: Ber. Dtsch. Chem. Ges. 1936, 69, 1927.
10d.
Pedemonte N., Sonawane N. D., Taddei A., Hu J., Zegerra-Moran O., Suen Y. F., Robins L. I., Dicus C. W., Willenbring D., Nantz M. H., Kurth M. J., Galietta L. J. V., Verkman A. S.: Mol. Pharmacol. 2005, 67, 1797.
<
https://doi.org/10.1124/mol.105.010959>