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Retusone A, a Guaiane-Type Sesquiterpene Dimer from Wikstroemia retusa and Its Inhibitory Effects on Histone Acetyltransferase HBO1 Expression.


ABSTRACT: Retusone A (1), a new sesquiterpene dimer consisting of two guaiane-type sesquiterpenoids, and oleodaphnal (2) were isolated from heartwood of Wikstroemia retusa (Thymelaeaceae). The planar structure of 1 was elucidated on the basis of HRESIMS and NMR spectroscopic data, and the relative stereochemistry was established by X-ray diffraction analysis. The absolute configuration of 1 was determined by electronic circular dichroism. Compound 1 suppressed luciferase reporter gene expression driven by the HBO1 (histone acetyltransferase binding to ORC1) gene promoter in human breast cancer MCF7 cells. Compound 1 also decreased the expression of endogenous HBO1 mRNA and protein, and inhibited proliferation of the cells. These results suggest that retusone A (1), which has a unique dimeric sesquiterpenoid structure with inhibitory activity against HBO1 expression, may contribute to the development of a novel therapeutic candidate for the treatment of breast cancer.

SUBMITTER: Yun YS 

PROVIDER: S-EPMC9105026 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature

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Retusone A, a Guaiane-Type Sesquiterpene Dimer from <i>Wikstroemia retusa</i> and Its Inhibitory Effects on Histone Acetyltransferase HBO1 Expression.

Yun Young Sook YS   Nakano Tomomi T   Fukaya Haruhiko H   Hitotsuyanagi Yukio Y   Nakamura Miho M   Umetsu Megumi M   Matsushita Nobuko N   Miyake Katsunori K   Fuchino Hiroyuki H   Kawahara Nobuo N   Moriya Fuki F   Ito Akihiro A   Takahashi Yuji Y   Inoue Hideshi H  

Molecules (Basel, Switzerland) 20220503 9


Retusone A (<b>1</b>), a new sesquiterpene dimer consisting of two guaiane-type sesquiterpenoids, and oleodaphnal (<b>2</b>) were isolated from heartwood of <i>Wikstroemia retusa</i> (Thymelaeaceae). The planar structure of <b>1</b> was elucidated on the basis of HRESIMS and NMR spectroscopic data, and the relative stereochemistry was established by X-ray diffraction analysis. The absolute configuration of <b>1</b> was determined by electronic circular dichroism. Compound <b>1</b> suppressed luc  ...[more]

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