The design and synthesis of potent benzimidazole derivatives via scaffold hybridization and evaluating their antiproliferative and proapoptotic activity against breast and lung cancer cell lines

Author:

Elgawish Mohamed Saleh12ORCID,Nafie Mohamed S.3ORCID,Yassen Asmaa S. A.4,Yamada Koji5,Ghareb Nagat4

Affiliation:

1. Medicinal Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt

2. Chemistry Department, Korea University, Seoul 02841, Republic of Korea

3. Chemistry Department, Faculty of Science, Suez Canal University, Ismailia 41522, Egypt

4. Pharmaceutical Organic Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt

5. Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan

Abstract

New series of benzimidazole bearing scaffold as powerful antiproliferative antiangiogenic compounds against breast (MCF-7) and lung (A549) cell lines cancer were designed using molecular hybridization as a new strategy for drug development.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

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