(Family Euphorbiaceae) is an annual aromatic plant endemic to Yunnan Province, China, which yields an aromatic, spicy oil used as a flavoring and fragrance. The aim of the present study was to acquire secondary metabolites from the leaves and twigs of and to evaluate their cytotoxic activity. Five new diterpenoids, croyanhuins A-E (-), and one new C nor-isoprenoid, croyanhuin F (), were isolated from the leaves and twigs of . Their structures and absolute configurations were determined by extensive spectroscopic methods (1D and 2D NMR, IR, and HRESIMS) and confirmed by electronic circular dichroism (ECD) spectra or single-crystal X-ray diffraction analysis. Among the new terpenoids, compounds and inhibited cell proliferation and viability in a dose- and time-dependent manner, whereas both induced cleavage of either caspase-3 or PARP-1 in the SW480 cell line. Additionally, we observed that Z-YVAD-FMK and Z-VAD-FMK, two caspase inhibitors, inhibited the compound-dependent cell viability loss, suggesting that either of them can induce pyroptosis and caspase-dependent apoptosis. These biological assay results revealed that compounds and induce different kinds of programmed cell death in SW480 cells.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8996330PMC
http://dx.doi.org/10.3389/fchem.2022.861278DOI Listing

Publication Analysis

Top Keywords

leaves twigs
12
diterpenoids nor-isoprenoid
4
nor-isoprenoid identified
4
identified leaves
4
twigs activating
4
activating apoptosis
4
apoptosis pyroptosis
4
pyroptosis family
4
family euphorbiaceae
4
euphorbiaceae annual
4

Similar Publications

Alkaloids and Iridoids from Phlogacanthus curviflorus.

Chem Biodivers

December 2024

University of Jinan, School of Biological Science and Technology, 336 West Road of Nanxinzhuang, 250022, Jinan, CHINA.

Four unreported pyridine alkaloids, curviflorines A-D (1-4), two undescribed iridoids, curviridoids A and B (5 & 6), and one known iridoid glycoside (7), were isolated from the twigs and leaves of Phlogacanthus curviflorus. The structures of these compounds were established by detailed interpretation of MS and NMR data, with the absolute configurations being assigned via comparison of experimental and calculated electronic circular dichroism spectra. Notably, it is the first report of alkaloidal constituents (1-4) from the genus Phlogacanthus.

View Article and Find Full Text PDF

Premise: Tree structure and function are constrained by and acclimate to climatic conditions. Drought limits plant growth and carbon acquisition and can result in "legacy" effects that last beyond the period of water stress. Leaf and twig-level legacy effects of past water abundance, such as that experienced by trees that established under wetter conditions are unknown.

View Article and Find Full Text PDF

Identification of 3-hydroxy-3-methylglutaryl monoacyl-coenzyme A reductase (HMGR) associated with the synthesis of terpenoids in Santalum album L.

Gene

December 2024

Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, The Chinese Academy of Sciences, Guangzhou 510650, China. Electronic address:

Santalum album is an economically important plant in the craft, spices and medicine industries. The main chemical constituents found in sandalwood essential oils are sesquiterpenes. 3-Hydroxy-3-methylglutaryl monoacyl-coenzyme A reductase (HMGR) is one of the rate-limiting enzymes required for the synthesis of sandal sesquiterpenes, but there are no studies on the HMGR gene in S.

View Article and Find Full Text PDF

Browsers are animals that consume significant proportions of leaves, twigs, and bark from woody plants. These species have evolved morphological, physiological, and behavioral adaptations to subsist on a specialized diet. In zoos and other managed care facilities, the provision of browse in appropriate amounts helps promote positive animal welfare.

View Article and Find Full Text PDF

Two new sesquiterpene eudesmanolides from the Raeusch.

Nat Prod Res

December 2024

State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, People's Republic of China.

Two new sesquiterpene eudesmanolides, 5-hydroxy-eudesman-7(11)-en-8(12)-olide (), and 5-hydroxy-7(11)-en-8-oxo-eudesmane (), along with six known sesquiterpene eudesmanolides, were isolated from the leaves and twigs of Raeusch. The structures of these compounds were established basis on NMR and MS spectroscopic analyses. The cytotoxic activities of the isolated compounds were evaluated.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!