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Anti-herpes simplex type-1 (HSV-1) activity from the roots of Jatropha multifida L

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Abstract

A new long chain, multifidione (1), together with seven known lathyrane-type diterpenes, 15-epi-4Z-jatrogrossidentadion (2), 4Z-jatrogrossidentadion (3), 2-epi-hydroxy isojatrogrossidentadion (4), 2-hydroxyisojatrogrossidentadion (5), 4E-jatrogrossidentadion (6), 15-epi-4E-jatrogrossidentadion (7), and jatrogrossidion (8), was isolated from the roots of Jatropha multifida L. The chemical structure of this new compound was elucidated by spectroscopic techniques. The known compounds were identified by comparison of the spectroscopic and physical data with those of reported values. The isolated all compounds were evaluated for herpes simplex type-1 (HSV-1). Among them, compound 6 showed the highest activity against HSV-1 (IC50 2.05 μg/mL), whereas the IC50 value of the standard drug, acyclovir, was 3.58 μg/mL. These results suggest that compound 6 may has a potential target for anti-HSV-1 drug development.

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Acknowledgements

We acknowledge financial support from University of Phayao (grant no. RD61027). Supports from the Thailand Research Fund (grant no. DBG6180030) and the Center of Excellence for Innovation in Chemistry (PERCH-CIC), Office of the Higher Education Commission are gratefully acknowledged.

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Correspondence to Ratchanaporn Chokchaisiri.

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Chokchaisiri, R., Srijun, J., Chaichompoo, W. et al. Anti-herpes simplex type-1 (HSV-1) activity from the roots of Jatropha multifida L. Med Chem Res 29, 328–333 (2020). https://doi.org/10.1007/s00044-019-02484-5

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