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Synthesis, Anticancer Evaluation and in Silico Studies of 1,4-Dihydropyridines.
Merugu, Santha Kumari; Krishnan K, V B R; Kumar K, Ravi; Ansari, Siddique Akber; Ansari, Irfan Aamer; Bollikolla, Hari Babu.
Afiliação
  • Merugu SK; Department of Chemistry, Acharya Nagarjuna University, NNagar, Guntur, 522510, AP-, India.
  • Krishnan K VBR; Department of Chemistry, Government Degree college, Rajhamundry, 533524, AP-, India.
  • Kumar K R; Department of Chemistry, Acharya Nagarjuna University, NNagar, Guntur, 522510, AP-, India.
  • Ansari SA; Department of Pharmaceutical Chemistry and Phytochemistry, Nirmala College of Pharmacy, Atmakur, Mangalagiri, Guntur, 522302, AP-, India.
  • Ansari IA; Department of Pharmaceutical chemistry, College of Pharmacy, King Saud University, PO Box.2457, Riyadh, 11451, Saudi Arabia.
  • Bollikolla HB; Department of Drug Science & Technology, University of Turin, 10124, Turin, Italy.
Chem Biodivers ; 20(8): e202201158, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37400965
An efficient 1,4-dihydropyridine synthesis under mild conditions has been developed. Numerous substrates were tested, with yields of 1,4-dihydropridines ranging from good to excellent and a wide range of functional group tolerance. A549, HT-29, and HepG2 cancer cells were used to investigate the anticancer efficacy of each of the produced compounds. Additionally, in-silico docking studies were conducted to understand the structure-based features of the anticancer mechanism with the cancer medication target of Adenosine A2A receptor as well as the molecular level interactions of the compounds.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Di-Hidropiridinas / Antineoplásicos Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Di-Hidropiridinas / Antineoplásicos Idioma: En Ano de publicação: 2023 Tipo de documento: Article