Academic Journal

Two new compounds from euphorbia fischeriana steud. and their antitumor activity.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Two new compounds from euphorbia fischeriana steud. and their antitumor activity.
Συγγραφείς: Sun Y; Qiqihar Medical University, Qiqihar, China., Ma T; Qiqihar Medical University, Qiqihar, China., Hong Y; Qiqihar Medical University, Qiqihar, China., Zhang J; Qiqihar Medical University, Qiqihar, China., Sun J; Qiqihar Medical University, Qiqihar, China., Liu Q; Qiqihar Medical University, Qiqihar, China., Guo L; Qiqihar Medical University, Qiqihar, China., Ma Y; Qiqihar Medical University, Qiqihar, China.
Πηγή: Natural product research [Nat Prod Res] 2026 Aug; Vol. 40 (15), pp. 4435-4444. Date of Electronic Publication: 2025 Jun 27.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Taylor & Francis Health Sciences Country of Publication: England NLM ID: 101167924 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1478-6427 (Electronic) Linking ISSN: 14786419 NLM ISO Abbreviation: Nat Prod Res Subsets: MEDLINE
Imprint Name(s): Original Publication: Milton Park, UK : Taylor & Francis Health Sciences, c2003-
Ιατρικοί όροι (MeSH): Euphorbia*/chemistry , Antineoplastic Agents, Phytogenic*/chemistry , Antineoplastic Agents, Phytogenic*/pharmacology , Antineoplastic Agents, Phytogenic*/isolation & purification, Apoptosis/drug effects ; Proto-Oncogene Proteins c-bcl-2/metabolism ; Plant Roots/chemistry ; bcl-2-Associated X Protein/metabolism ; Humans ; Molecular Structure ; Hep G2 Cells ; Drug Screening Assays, Antitumor ; HeLa Cells ; MCF-7 Cells ; Inhibitory Concentration 50 ; Animals ; Mice
Περίληψη: Extraction from Euphorbia fischeriana Steud roots yielded twelve compounds, including two novel compounds 1 (15,16-dihydroxy-ent-abieta-8,11,13-triene) and 2 (methyl-12,14-dimethoxy-8-((5R,8R,9S,10R)-9-methoxy-4,4,10-trimethyldecahydronaphthalen-8yl)benzoate) along with ten previously documented compounds (3-12). Spectral analyses (1D-NMR, 2D-NMR and HR-ESI-MS) enabled the determination of their structural frameworks, supported by validation against published literature data. When tested in vitro, these compounds exhibited distinct potencies in suppressing the growth of Hela, HepG2, MCF-7 and C2C12 cells. Notably, compound 3 exerted significant inhibitory effects on all tested cell lines, showing IC50 values between 5.53 and 21.28 μM. Further analysis indicated that compound 3 induced apoptosis in HepG2 cells by modulating the protein expression, specifically by reducing Bcl-2 and enhancing Bax levels.
Contributed Indexing: Keywords: Euphorbia fischeriana diterpenoids; antitumor activity; apoptosis; bcl-2/bax modulation
Substance Nomenclature: 0 (Antineoplastic Agents, Phytogenic)
0 (Proto-Oncogene Proteins c-bcl-2)
0 (bcl-2-Associated X Protein)
Entry Date(s): Date Created: 20250627 Date Completed: 20260730 Latest Revision: 20260730
Update Code: 20260730
DOI: 10.1080/14786419.2025.2521383
PMID: 40577107
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1478-6427
DOI:10.1080/14786419.2025.2521383