11 <i>α</i> -hydroxydysobinin: a new limonoid from <i>Chisocheton macrophyllus</i> seeds (Meliaceae)

A new limonoid compound 11<i>α</i>-hydroxydisobinin (<b>1</b>), along with a known limonoid compound (<b>2</b>), was isolated from ethyl acetate extract of <i>Chisocheton macrophyllus</i> (Meliaceae) seeds. The structure and stereochemical configuration of compound <b>1</b> was characterized by HR-ESI-MS, UV, IR, NMR, and ECD analysis through quantum chemical calculations (TD-DFT analysis and DP4+ NMR). Both limonoids were tested for their cytotoxic activities against MCF-7 breast cancer cells with IC<sub>50</sub> values of 112.5 and 51.7 µM.

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Journal
Journal of Asian Natural Products Research
Published
2025-07-16
DOI
https://doi.org/10.1080/10286020.2025.2525332
Primary Topic
Phytochemical compounds biological activities
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article
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article

11 α -hydroxydysobinin: a new limonoid from Chisocheton macrophyllus seeds (Meliaceae)

Kindi Farabi, Unang Supratman, Rani Maharani, Desi Harneti et al.
Journal of Asian Natural Products Research
Phytochemical compounds biological activities
article

11 α -hydroxydysobinin: a new limonoid from Chisocheton macrophyllus seeds (Meliaceae)

Kindi Farabi, Unang Supratman, Rani Maharani, Desi Harneti, Tri Mayanti, Wahyu Safriansyah, Muhammad Badrul Huda, Lulu Wilden Azzahra
article en

Abstract

A new limonoid compound 11<i>α</i>-hydroxydisobinin (<b>1</b>), along with a known limonoid compound (<b>2</b>), was isolated from ethyl acetate extract of <i>Chisocheton macrophyllus</i> (Meliaceae) seeds. The structure and stereochemical configuration of compound <b>1</b> was characterized by HR-ESI-MS, UV, IR, NMR, and ECD analysis through quantum chemical calculations (TD-DFT analysis and DP4+ NMR). Both limonoids were tested for their cytotoxic activities against MCF-7 breast cancer cells with IC<sub>50</sub> values of 112.5 and 51.7 µM.

Journal of Asian Natural Products ResearchVol. 28(4)
Diponegoro University (ID), Padjadjaran University (ID)
Zero hunger
Openalex Percentile: Top 84%
Phytochemical compounds biological activities
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