Secondary Metabolites Isolated from the Methanol Extract of Pseudocyphellaria freycinetii and Their Cytotoxicity

Phytochemical study of the lichen, Pseudocyphellaria freycinetii (Lobariaceae) led to the isolation of two hopane-type triterpenoids (1 and 2), along with two phenolic compounds (3 and 4). The structures of the compounds were identified by 1D and 2D NMR, and MS experiments, as well as by comparison of their data with published values. Compounds 2-4 were isolated for the first time in this species. All the compounds were evaluated for their cytotoxicity. Among the isolates, compound 1 showed considerable inhibitory activity against the Hela cell growth.

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Publication Details

Journal
Korean Journal of Pharmacognosy
Published
2025-06-30
DOI
https://doi.org/10.22889/kjp.2025.56.2.80
Primary Topic
Natural product bioactivities and synthesis
Type
article
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article

Secondary Metabolites Isolated from the Methanol Extract of Pseudocyphellaria freycinetii and Their Cytotoxicity

Seong Hye Kim, Man Hyung Koo, Hye Ji Kim, Ui Joung Youn
Korean Journal of Pharmacognosy
Natural product bioactivities and synthesis
article

Secondary Metabolites Isolated from the Methanol Extract of Pseudocyphellaria freycinetii and Their Cytotoxicity

Seong Hye Kim, Man Hyung Koo, Hye Ji Kim, Ui Joung Youn
article en

Abstract

Phytochemical study of the lichen, Pseudocyphellaria freycinetii (Lobariaceae) led to the isolation of two hopane-type triterpenoids (1 and 2), along with two phenolic compounds (3 and 4). The structures of the compounds were identified by 1D and 2D NMR, and MS experiments, as well as by comparison of their data with published values. Compounds 2-4 were isolated for the first time in this species. All the compounds were evaluated for their cytotoxicity. Among the isolates, compound 1 showed considerable inhibitory activity against the Hela cell growth.

Korean Journal of PharmacognosyVol. 56(2)
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Openalex Percentile: Top 84%
Natural product bioactivities and synthesis
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