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Evaluation of the Antiviral Activity of Tabamide A and Its Structural Derivatives against Influenza Virus.


ABSTRACT: Influenza viruses cause severe endemic respiratory infections in both humans and animals worldwide. The emergence of drug-resistant viral strains requires the development of new influenza therapeutics. Tabamide A (TA0), a phenolic compound isolated from tobacco leaves, is known to have antiviral activity. We investigated whether synthetic TA0 and its derivatives exhibit anti-influenza virus activity. Analysis of structure-activity relationship revealed that two hydroxyl groups and a double bond between C7 and C8 in TA0 are crucial for maintaining its antiviral action. Among its derivatives, TA25 showed seven-fold higher activity than TA0. Administration of TA0 or TA25 effectively increased survival rate and reduced weight loss of virus-infected mice. TA25 appears to act early in the viral infection cycle by inhibiting viral mRNA synthesis on the template-negative strand. Thus, the anti-influenza virus activity of TA0 can be expanded by application of its synthetic derivatives, which may aid in the development of novel antiviral therapeutics.

SUBMITTER: Shin SY 

PROVIDER: S-EPMC10744247 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature

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Evaluation of the Antiviral Activity of Tabamide A and Its Structural Derivatives against Influenza Virus.

Shin Soo Yong SY   Lee Joo Hee JH   Kim Jin Woo JW   Im Wonkyun Ronny WR   Damodar Kongara K   Woo Hyung Ryeol HR   Kim Won-Keun WK   Lee Jeong Tae JT   Jeon Sung Ho SH  

International journal of molecular sciences 20231209 24


Influenza viruses cause severe endemic respiratory infections in both humans and animals worldwide. The emergence of drug-resistant viral strains requires the development of new influenza therapeutics. Tabamide A (TA0), a phenolic compound isolated from tobacco leaves, is known to have antiviral activity. We investigated whether synthetic TA0 and its derivatives exhibit anti-influenza virus activity. Analysis of structure-activity relationship revealed that two hydroxyl groups and a double bond  ...[more]

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