N,2,6-Trisubstituted 1H-benzimidazole derivatives as a new scaffold of antimicrobial and anticancer agents: design, synthesis, in vitro evaluation, and in silico studies

Author:

Pham Em Canh1ORCID,Le Thi Tuong Vi23,Ly Hong Huong Ha4,Vo Thi Bich Ngoc4,Vong Long B.56,Vu Thao Thanh7,Vo Duy Duc8,Tran Nguyen Ngoc Vi3,Bao Le Khanh Nguyen3,Truong Tuyen Ngoc3ORCID

Affiliation:

1. Department of Medicinal Chemistry, Faculty of Pharmacy, Hong Bang International University, 700000 Ho Chi Minh City, Vietnam

2. Department of Pharmacology – Clinical Pharmacy, Faculty of Pharmacy, City Children's Hospital, 700000 Ho Chi Minh City, Vietnam

3. Department of Organic Chemistry, Faculty of Pharmacy, University of Medicine and Pharmacy at Ho Chi Minh City, 700000 Ho Chi Minh City, Vietnam

4. Department of Pharmacognosy & Botany, Faculty of Pharmacy, Hong Bang International University, 700000 Ho Chi Minh City, Vietnam

5. School of Biomedical Engineering, International University, 700000 Ho Chi Minh City, Vietnam

6. Vietnam National University Ho Chi Minh City (VNU-HCM), Ho Chi Minh 700000, Vietnam

7. Department of Microbiology – Parasitology, Faculty of Pharmacy, University of Medicine and Pharmacy at Ho Chi Minh City, 700000 Ho Chi Minh City, Vietnam

8. Uppsala University, Sweden, Tra Vinh University, Vietnam

Abstract

The purpose of this study is to synthesize novel N,2,6-trisubstituted 1H-benzimidazole derivatives and evaluation of their antibacterial, antifungal, and anticancer activities as well as to study their mechanism of action.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

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