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Pentacyclic and hexacyclic cucurbitacins from Elaeocarpuspetiolatus
Eun-Seon Cho1, Premanand Krishnan2, Hwei-San Loh1
1School of Biosciences, University of Nottingham Malaysia, Jalan Broga, 43500, Semenyih, Selangor, Malaysia.
Four new cucurbitacins, petiolaticins A-D, were isolated from Elaeocarpus petiolatus. Petiolaticin A shows potent anticancer activity, while petiolaticin D exhibits antiviral properties against avian influenza virus.
Area of Science:
- Natural Products Chemistry
- Medicinal Chemistry
- Pharmacology
Background:
- Elaeocarpus petiolatus is a plant source of bioactive compounds.
- Cucurbitacins are a class of natural products with diverse biological activities.
Purpose of the Study:
- To isolate and characterize new cucurbitacins from Elaeocarpus petiolatus.
- To evaluate the anticancer and antiviral potential of isolated compounds.
Main Methods:
- Isolation and structural elucidation of compounds using NMR and MS.
- X-ray diffraction analysis for absolute configuration determination.
- In vitro cytotoxicity assays against cancer cell lines.
- Antiviral assays against avian influenza virus.
Main Results:
- Four new cucurbitacins (petiolaticins A-D) and four known analogs were identified.
- Petiolaticin A demonstrated significant cytotoxicity against breast, pancreatic, and colorectal cancer cell lines.
- Petiolaticin D exhibited notable inhibition of avian influenza virus entry.
Conclusions:
- Petiolaticins A and D possess promising anticancer and antiviral activities, respectively.
- Elaeocarpus petiolatus is a valuable source for novel therapeutic agents.
- Further investigation is warranted to explore the therapeutic potential of petiolaticins.
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