Pentacyclic and hexacyclic cucurbitacins from Elaeocarpus petiolatus

Cho, Eun-Seon and Krishnan, Premanand and Loh, Hwei-San and Daly, Janet M. and Leong, Chee-Onn and Mai, Chun-Wai and Low, Yun-Yee and Yong, Kien-Thai and Lim, Kuan-Hon (2022) Pentacyclic and hexacyclic cucurbitacins from Elaeocarpus petiolatus. Phytochemistry, 193. ISSN 0031-9422, DOI https://doi.org/10.1016/j.phytochem.2021.112988.

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Abstract

Four undescribed cucurbitacins, designated as petiolaticins A-D, and four known cucurbitacins were isolated from the bark and leaves of Elaeocarpus petiolatus (Jack) Wall. Their chemical structures were elucidated based on detailed analyses of the NMR and MS data. The absolute configuration of petiolaticin A was also determined by X-ray diffraction analysis. Petiolaticin A represents a cucurbitacin derivative incorporating a 3,4-epoxyfuranylbearing side chain, while petiolaticin B possesses a furopyranyl unit fused to the tetracyclic cucurbitane core structure. Petiolaticins A, B, and D were evaluated in vitro against a panel of human breast, pancreatic, and colorectal cancer cell lines. Petiolaticin A exhibited the greatest cytotoxicity against the MDA-MB-468, MDA-MB-231, MCF-7, and SW48 cell lines (IC50 7.4, 9.2, 9.3, and 4.6 mu M, respectively). Additionally, petiolaticin D, 16 alpha,23 alpha-epoxy-3 beta,20 beta-dihydroxy-10 alpha H,23 beta H-cucurbit-5,24-dien-11-one, and 16 alpha,23 alpha-epoxy-3 beta,20 beta-dihydroxy-10 alpha H,23 beta H-cucurbit-5,24-dien-11-one 3-O-beta-D-glucopyranoside were tested for their ability to inhibit cell entry of a pseudotyped virus bearing the hemagglutinin envelope protein of a highly pathogenic avian influenza virus. Petiolaticin D showed the highest inhibition (44.3%), followed by 16 alpha,23 alpha-epoxy-3 beta,20 beta-dihydroxy-10 alpha H,23 beta H-cucurbit-5,24-dien-11-one (21.0%), and 16 alpha,23 alpha-epoxy-3 beta,20 beta-dihydroxy-10 alpha H,23 beta H-cucurbit-5,24-dien-11-one 3-O-beta-D-glucopyranoside showed limited inhibition (9.0%). These preliminary biological assays have demonstrated that petiolaticins A and D possess anticancer and antiviral properties, respectively, which warrant for further investigations.

Item Type: Article
Funders: None
Uncontrolled Keywords: Elaeocarpus petiolatus; Elaeocarpaceae; Cucurbitacins; Triterpenoids; X-ray crystallography; Cytotoxicity; Viral entry inhibition
Subjects: Q Science > Q Science (General)
Q Science > QH Natural history > QH301 Biology
Divisions: Faculty of Science
Depositing User: Ms. Juhaida Abd Rahim
Date Deposited: 19 Jul 2022 10:10
Last Modified: 19 Jul 2022 10:10
URI: http://eprints.um.edu.my/id/eprint/33714

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