# Spiro-meroterpenoids, Syzygioblanes D-H, Isolated from Indonesian Medicinal Plant Syzygium oblanceolatum
> Koga N.
URL kanonis: https://discover.unhas.ac.id/publications/pub_scopus_85212199785
Jurnal / Konferensi: Journal of Natural Products
Tahun terbit: 2024
DOI: https://doi.org/10.1021/acs.jnatprod.4c01154
ISSN: 01633864
Kuartil SJR: Q1
Citations: 1
## Authors
- Koga N.
## Abstract
Syzygioblanes A-C (1-3), isolated from the Indonesian traditional herbal medicine Syzygium oblanceolatum (S. oblanceolatum), are meroterpenoids with a spiro ring formed through a [4 + 2] cycloaddition of the flavanone desmethoxymatteucinol with cyclic sesquiterpenoids. Our ongoing phytochemical investigation of S. oblanceolatum resulted in the isolation of five additional spiro-meroterpenoids, syzygioblanes D-H (4-8), which are hybrids of the same flavanone with eudesmane/cadinane-type sesquiterpenoids. A possible biosynthetic pathway involves enzymatic dearomative hydroxylation of desmethoxymatteucinol followed by [4 + 2] cyclization of the resulting diene with a cyclic sesquiterpene containing an exocyclic methylene to form the unique spiro ring in the syzygioblane molecule. The isolated syzygioblanes F (6) and G (7) demonstrated collateral sensitivity by inhibiting the growth of multidrug-resistant tumor cell lines more than the related chemosensitive tumor cell lines.
## Keywords
- Indonesian
- Traditional medicine
- Syzygium
- Pharmacognosy
- Stereochemistry
- Terpene
- Biology
- Chemistry
- Botany
- Medicine
- Biological activity
- Biochemistry
- Philosophy
- In vitro
- Linguistics
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Sumber: Discover Unhas — RIMS Universitas Hasanuddin.
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