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Benzimidazole - Schiff bases and their complexes: synthesis, anticancer activity and molecular modeling as Aurora kinase inhibitor.
Magd-El-Din, Asmaa A; Mousa, Hanan A; Labib, Ammar A; Hassan, Ashraf S; Abd El-All, Amira S; Ali, Mamdouh M; El-Rashedy, Ahmed A; El-Desoky, Ahmed H.
Afiliación
  • Magd-El-Din AA; Department of Natural and Microbial Product, National Research Centre, Dokki 12622, Giza, Egypt, Phone: +20233370743.
  • Mousa HA; Department of Inorganic Chemistry, National Research Centre, Dokki 12622, Giza, Egypt.
  • Labib AA; Department of Inorganic Chemistry, National Research Centre, Dokki 12622, Giza, Egypt.
  • Hassan AS; Department of Organometallic and Organometalloid Chemistry, National Research Centre, Dokki 12622, Giza, Egypt.
  • Abd El-All AS; Department of Natural and Microbial Product, National Research Centre, Dokki 12622, Giza, Egypt.
  • Ali MM; Department of Biochemistry, National Research Centre, Dokki 12622, Giza, Egypt.
  • El-Rashedy AA; Department of Natural and Microbial Product, National Research Centre, Dokki 12622, Giza, Egypt.
  • El-Desoky AH; Department of Pharmacognosy, National Research Centre, Dokki 12622, Giza, Egypt.
Z Naturforsch C J Biosci ; 73(11-12): 465-478, 2018 Nov 27.
Article en En | MEDLINE | ID: mdl-30205654
ABSTRACT
A new series of Schiff bases containing benzіmidazole moiety 11-17 were synthesized by the reaction of 4-(1H-benzо[d]іmіdazоl-2-yl)anіline (1) with different aromatic aldehydes (4-10) via conventional heating and microwave irradiation methods. The structures of the novel Schiff bases were characterized by using different spectral data. Also, metal complexes 18-21 of compound 13 were synthesized, and their structure was confirmed by spectral measurements (IR, NMR, UV), molar conductivity, magnetic susceptibility and thermo-gravimetric analysis. The novel synthesized ligand 13 and its complexes 18-21 were tested for their in vitro antitumor activities towards breast, liver and lung cancer cell lines. Also, the acute toxicity of the prepared compounds 13 and 18-21 was determined in vivo. The results showed that the newly synthesized compounds 13 and 18-21 exhibited a significant activity against cancer, especially for complex 21, compared to standard drug doxorubicin. The molecular docking of complexes 20 and 21 has been also studied as Aurora kinase inhibitors.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bencimidazoles / Inhibidores de Proteínas Quinasas / Aurora Quinasas / Antineoplásicos Límite: Animals / Humans / Male Idioma: En Revista: Z Naturforsch C J Biosci Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bencimidazoles / Inhibidores de Proteínas Quinasas / Aurora Quinasas / Antineoplásicos Límite: Animals / Humans / Male Idioma: En Revista: Z Naturforsch C J Biosci Año: 2018 Tipo del documento: Article