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Synthesis and biological activity of hydroxy- substituted N-benzimidazole carboxamides (CROSBI ID 722989)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Beč, Anja ; Kralj, Marijeta ; Zlatić, Katarina ; Starčević, Kristina ; Bertoša, Branimir ; Hranjec, Marijana Synthesis and biological activity of hydroxy- substituted N-benzimidazole carboxamides // 8th EuChemS Chemistry Congress : book of abstracts / Silva, Artur M. S. ; Galvão, Adelino M. ; Machado, Bruno F. et al. (ur.). Lisabon: Sociedade Portuguesa de Química, 2022. str. 607-607

Podaci o odgovornosti

Beč, Anja ; Kralj, Marijeta ; Zlatić, Katarina ; Starčević, Kristina ; Bertoša, Branimir ; Hranjec, Marijana

engleski

Synthesis and biological activity of hydroxy- substituted N-benzimidazole carboxamides

It has been widely demonstrated that oxidative stress participates in all stages of chemical carcinogenesis. Since antioxidants are known by their function in protecting the human body against damage by reactive oxygen species (ROS) as well as by inhibiting ROS-relayed reactions, there has been tremendous and constant growing interest for the searching of novel natural or synthetic organic molecules as potential antioxidants. Being one of the well-known privileged building substructures in medicinal chemistry, benzimidazoles derivatives can be promising candidates as antioxidants. Among versatile pharmacological features, the most important ones for the rational design of novel bioactive compounds are antitumor, antimicrobial, antiviral, antioxidative and anti-inflammatory activities [1, 2]. All compounds were prepared by conventional reactions of organic synthesis as well as by microwave assisted reactions [3]. Targeted benzimidazole-2-carboxamides were synthesized by removal of methoxy protecting groups by using BBr3 in absolute dichloromethane at −75 °C, or by removal of benzyloxy protecting groups by Pd/C catalytic hydrogenation in methanol to afford the corresponding deprotected derivatives. All newly prepared compounds were screened for their antioxidant capacity using several spectroscopic methods as well as antiproliferative activity on several human cancer cells in vitro. To explore the antioxidative potency of benzimidazole-2- carboxamides we developed 3D-QSAR models and used them for computational prediction of antioxidative activity of the presented compounds.

benzimidazoles ; carboxamides ; antioxidants

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Podaci o prilogu

607-607.

2022.

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objavljeno

978-989-8124-35-7

Podaci o matičnoj publikaciji

8th EuChemS Chemistry Congress : book of abstracts

Silva, Artur M. S. ; Galvão, Adelino M. ; Machado, Bruno F. ; Faria, Joaquim L.

Lisabon: Sociedade Portuguesa de Química

Podaci o skupu

8th EuChemS Chemistry Congress (ECC8)

poster

28.08.2022-01.09.2022

Lisabon, Portugal

Povezanost rada

Kemija

Poveznice