Pregled bibliografske jedinice broj: 1254945
Synthesis and antiproliferative activity of nitro and amino substituted benzimidazoles and benzothiazoles
Synthesis and antiproliferative activity of nitro and amino substituted benzimidazoles and benzothiazoles // Book of proceedings: international scientific conference/XIV Conference of Chemists, Technologists and Environmentalists of Republic of Srpska / Malinović, Borislav (ur.).
Banja Luka: University in Banja Luka, Faculty of Technology, 2023. str. 6-14 (poster, međunarodna recenzija, cjeloviti rad (in extenso), znanstveni)
CROSBI ID: 1254945 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and antiproliferative activity of nitro
and amino substituted benzimidazoles and
benzothiazoles
Autori
Hranjec, Marijana ; Racané, Livio ; Boček, Ida ; Persoons, Leentije ; Dealmans, Dirk
Vrsta, podvrsta i kategorija rada
Radovi u zbornicima skupova, cjeloviti rad (in extenso), znanstveni
Izvornik
Book of proceedings: international scientific conference/XIV Conference of Chemists, Technologists and Environmentalists of Republic of Srpska
/ Malinović, Borislav - Banja Luka : University in Banja Luka, Faculty of Technology, 2023, 6-14
ISBN
978-99938-54-98-2
Skup
XIV Conference of chemists, technologists and environmentalists of Republic of Srpska
Mjesto i datum
Banja Luka, Bosna i Hercegovina, 21.10.2022. - 22.10.2022
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
antiproliferative activity, benzimidazoles, benzothiazoles, synthesis
Sažetak
Nowadays heterocyclic compounds become unavoidable structural motifs and building blocks in organic and medicinal chemistry. Since benzimidazoles and benzothiazoles as one of the most important nitrogen heterocycles have great and versatile biological activities, these benzazoles become important structural scaffolds in the rational design of novel drugs in medicinal and pharmaceutical chemistry. These nitrogen scaffolds could be found in a variety of bioactive natural and synthetic medical and biochemical agents, which possess different chemical and pharmacological features. Within this work we present the synthesis, structural characterization and biological evaluation of methoxy and hydroxy substituted 2-benzimidazole and 2-benzothiazole derivatives bearing either nitro or protonated amino group at the benzazole scaffold (Figure 1). The targeted compounds were prepared by using conventional and well-optimized reactions of organic chemistry for the synthesis and cyclocondensation of benzimidazole and benzothiazole nuclei. All synthesized compounds were structurally characterized by means of 1H and 13C NMR spectroscopy. The antiproliferative activity was evaluated on the panel of human cancer cells in vitro. Some of tested compounds showed prominent antiproliferative activity. Obtained results revealed the strong influence of the substituents placed at the phenyl as well as on the benzazole nuclei on biological activity.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Projekti:
HRZZ-IP-2018-01-4379 - Istraživanje antioksidativnog djelovanja benzazolskog skeleta u dizajnu novih antitumorskih agensa (AntioxPot) (Hranjec, Marijana, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Tekstilno-tehnološki fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb