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Kaemtakols A-D, highly oxidized pimarane diterpenoids with potent anti-inflammatory activity from Kaempferia takensis.


ABSTRACT: Four highly oxidized pimarane diterpenoids were isolated from Kaempferia takensis rhizomes. Kaemtakols A-C possess a tetracyclic ring with either a fused tetrahydropyran or tetrahydrofuran motif. Kaemtakol D has an unusual rearranged A/B ring spiro-bridged pimarane framework with a C-10 spirocyclic junction and an adjacent 1-methyltricyclo[3.2.1.02,7]octene ring. Structural characterization was achieved using spectroscopic analysis, DP4 + and ECD calculations, as well as X-ray crystallography, and their putative biosynthetic pathways have been proposed. Kaemtakol B showed significant potency in inhibiting nitric oxide production with an IC50 value of 0.69 μM. Molecular docking provided some perspectives on the action of kaemtakol B on iNOS protein.

SUBMITTER: Jongsomjainuk O 

PROVIDER: S-EPMC10689700 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature

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Kaemtakols A-D, highly oxidized pimarane diterpenoids with potent anti-inflammatory activity from Kaempferia takensis.

Jongsomjainuk Orawan O   Boonsombat Jutatip J   Thongnest Sanit S   Prawat Hunsa H   Batsomboon Paratchata P   Charoensutthivarakul Sitthivut S   Ruchisansakun Saroj S   Chainok Kittipong K   Sirirak Jitnapa J   Mahidol Chulabhorn C   Ruchirawat Somsak S  

Natural products and bioprospecting 20231201 1


Four highly oxidized pimarane diterpenoids were isolated from Kaempferia takensis rhizomes. Kaemtakols A-C possess a tetracyclic ring with either a fused tetrahydropyran or tetrahydrofuran motif. Kaemtakol D has an unusual rearranged A/B ring spiro-bridged pimarane framework with a C-10 spirocyclic junction and an adjacent 1-methyltricyclo[3.2.1.0<sup>2,7</sup>]octene ring. Structural characterization was achieved using spectroscopic analysis, DP4 + and ECD calculations, as well as X-ray crystal  ...[more]

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