Pregled bibliografske jedinice broj: 1163767
Synthesis and antitumor evaluations of novel 2-aryl substituted benzimidazole derivatives
Synthesis and antitumor evaluations of novel 2-aryl substituted benzimidazole derivatives // 27th Croatian Meeting of Chemists and Chemical Engineers with international participation ; 5th Symposium Vladimir Prelog - book of abstracts / Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2021. str. 180-180 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Synthesis and antitumor evaluations of novel 2-aryl substituted benzimidazole derivatives
Autori
Sokol, Ivana ; Rakas, Anja ; Persoons, Leentje ; Vanstreels, Els ; Daelemans, Dirk ; Raić-Malić, Silvana ; Gazivoda Kraljević, Tatjana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
27th Croatian Meeting of Chemists and Chemical Engineers with international participation ; 5th Symposium Vladimir Prelog - book of abstracts
/ Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna - Zagreb : Hrvatsko kemijsko društvo, 2021, 180-180
Skup
27. hrvatski skup kemičara i kemijskih inženjera (27HSKIKI) ; 5. simpozij Vladimir Prelog
Mjesto i datum
Veli Lošinj, Hrvatska, 05.10.2021. - 08.10.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
benzimidazol ; 1, 2, 3- triazol ; klik kemija
(benzimidazole ; 1, 2, 3- triazole ; click kemija)
Sažetak
Benzimidazole is an important pharmacophore and represents a privileged structure in medicinal chemistry.[1] Its derivatives show numerous pharmacological activities such as antituberculostatic, antimalarial, antimicrobial, antiviral, antitumor and anti- inflammatory.[2] The 1, 2, 3-triazole products are more than passive linkers, they readily associate with biological targets, through hydrogen-bonding and dipole interactions and attract a lot of attention as pharmacophores.[3] In this paper, we present ultrasonic and microwave cyclization reaction of O-alkylated benzaldehydes with variously substituted 1, 2-diaminobenzene which gave 2- arylbenzimidazole derivatives. 1, 2, 3-triazolyl benzimidazole derivatives were prepared by Huisgen 1, 3-dipolar cycloaddition reaction using copper(II) acetate as catalyst. Antitumoral evaluations of all tested compounds revealed that the 2-arylbenzimidazole derivative with N, N- diethyl substituent showed the most pronounced activity against antitumor cell lines: pancreatic adenocarcinoma (Capan-1, IC50=2.2 μM), lung carcinoma (NCI-H460, IC50=2.2 μM), acute lymphoblastic leukemia (DND-41, IC50=2.6 μM), chronic myeloid leukemia (K- 562, IC50=2.0 μM) and non-Hodgkin lymphoma (Z-138, IC50=2.0 μM).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2018-01-4682 - Novi spojevi temeljeni na bioizosterima purina za ispitivanje njihovih antitumorskih i antipatogenih djelovanja (PurBioCaPa) (Raić-Malić, Silvana, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Silvana Raić-Malić
(autor)
Anja Rakas
(autor)
Ivana Sokol
(autor)
Tatjana Gazivoda Kraljević
(autor)