Design, synthesis and biological evaluation of indole-2-carboxylic acid derivatives as novel HIV-1 integrase strand transfer inhibitors

• Published in: RSC advances Vol. 14; no. 13; pp. 92 - 931
• Main Authors: Zhang, Rong-Hong, Chen, Guo-Qi, Wang, Weilin, Wang, Yu-Chan, Zhang, Wen-Li, Chen, Ting, Xiong, Qian-Qian, Zhao, Yong-Long, Liao, Shang-Gao, Li, Yong-Jun, Yan, Guo-Yi, Zhou, Meng
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 14.03.2024; The Royal Society of Chemistry
• Subjects: Benzene; Carboxylic acids; Chemistry; Inhibitors
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/d3ra08320a

Integrase plays an important role in the life cycle of HIV-1, and integrase strand transfer inhibitors (INSTIs) can effectively impair the viral replication. However, drug resistance mutations have been confirmed to decrease the efficacy of INSTI during the antiviral therapy. Herein, indole-2-carboxylic acid ( 1 ) was found to inhibit the strand transfer of integrase, and the indole nucleus of compound 1 was observed to chelate with two Mg 2+ ions within the active site of integrase. Through optimization of compound 1 , a series of indole-2-carboxylic acid derivatives were designed and synthesized, and compound 17a was proved to markedly inhibit the effect of integrase, with IC 50 value of 3.11 μM. Binding mode analysis of 17a demonstrated that the introduced C6 halogenated benzene ring could effectively bind with the viral DNA (dC20) through π-π stacking interaction. These results indicated that indole-2-carboxylic acid is a promising scaffold for the development of integrase inhibitors. Integrase plays an important role in the life cycle of HIV-1, and indole-2-carboxylic acid derivative 17a can effectively inhibit the strand transfer of integrase.