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Pregled bibliografske jedinice broj: 154216

Synthesis and evaluation of antiproliferative effect of amidino substituted heterocyclic compounds "in vitro"


Starčević, Kristina; Kralj, Marijeta; Šuman, Lidija; Pavelić, Krešimir; Karminski-Zamola, Grace
Synthesis and evaluation of antiproliferative effect of amidino substituted heterocyclic compounds "in vitro" // 2nd Central European Conference, Chemistry towards Biology / Kratky, Christoph ; Konrat, Robert (ur.).
Graz, 2004. str. 64-65 (poster, sažetak, znanstveni)


Naslov
Synthesis and evaluation of antiproliferative effect of amidino substituted heterocyclic compounds "in vitro"

Autori
Starčević, Kristina ; Kralj, Marijeta ; Šuman, Lidija ; Pavelić, Krešimir ; Karminski-Zamola, Grace

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
2nd Central European Conference, Chemistry towards Biology / Kratky, Christoph ; Konrat, Robert - Graz, 2004, 64-65

Skup
2nd Central European Conference, Chemistry towards Biology

Mjesto i datum
Seggau, Austria, 26.-29.09.2004.

Vrsta sudjelovanja
Poster

Vrsta recenzije
Neobjavljeni rad

Ključne riječi
Amidines; heterocyclic compounds; biological activity

Sažetak
Amidino substituted heterocyclic compounds are widely investigated on their biological activity1. Organic dications and monocations that bind to the DNA as intercalators or "groove binders" exibit biological activities that range from effectiveness against opportunistic infections to anticaner properties.2 The purpose of this study was to synthesized three cyclic heterocyclic compound and investigate the effects on proliferation of different human tumor cell lines, as well as on normal (diploid) human fibroblasts (control cell line). The experiments were carried out on 6 human cell lines, 5 of which are derived from 5 cancer types and one normal, fibroblast cell line. The following cell lines were used: HeLa (cervical carcinoma), MCF-7 (breast carcinoma), SW 620 (colon carcinoma), MiaPaCa-2 (pancreatic carcinoma), Hep-2 (laryngeal carcinoma) and WI 38 (diploid fibroblasts). All compounds produced markedly strong antiproliferative effect and were cytotoxic to all cell lines.3, 4 LITERATURE: 1. J.E. Hall, J.E. Kerrigan, K. Ramachandran, B.C. Bender, J.P. Stanko, S.K. Jones, D.A. Patrick, R.R. Tidwell, Antimicrob Agents Chemother, 1998, 42, 666-674 2. R.R. Tidwell and D.W. Boykin, Dicationic DNA Minor Groove Binders as Antimicrobial Agents, in Small Molecule DNA and RNA Binders ; From Synthesis to Nucleic Acid Complexes, Ed. By M. Demeunynck, C. Bailly, and W.D. Wilson, Wiley-VCH, New York, 2003, vol. 2, 416-460 3. T. Mossman, Immunol 1983, 65, 55­63. 4. M.R.Boyd, D.P. Kenneth, Drug Dev Res 1995, 34, 91-109.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
0098092
0098093
0125005

Ustanove
Fakultet kemijskog inženjerstva i tehnologije, Zagreb