Structurally diverse diterpenoids from Euphorbia milii: Discovery and RORγt-binding evaluation.

Bibliographic Details
Title: Structurally diverse diterpenoids from Euphorbia milii: Discovery and RORγt-binding evaluation.
Authors: Dai MY; Yunnan Key Laboratory of Genetic Improvement of Herbal Oil Crops, Industrial Crops Research Institute, Yunnan Academy of Agricultural Sciences, Kunming, 650225, PR China., Hu XL; Yunnan Key Laboratory of Genetic Improvement of Herbal Oil Crops, Industrial Crops Research Institute, Yunnan Academy of Agricultural Sciences, Kunming, 650225, PR China., Li WC; Yunnan Key Laboratory of Genetic Improvement of Herbal Oil Crops, Industrial Crops Research Institute, Yunnan Academy of Agricultural Sciences, Kunming, 650225, PR China., Lu Z; Department of Pulmonary and Critical Care Medicine, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410004, PR China., Jiang BY; Department of Central laboratory, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410018, PR China., Chen HM; Department of Pulmonary and Critical Care Medicine, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410004, PR China., Zeng Y; Department of Pharmacy, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410018, PR China., Cao DH; Department of Central laboratory, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410018, PR China; Department of Pulmonary and Critical Care Medicine, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, 410004, PR China. Electronic address: caodonghua@usc.edu.cn.
Source: Phytochemistry [Phytochemistry] 2026 Sep; Vol. 249, pp. 114934. Date of Electronic Publication: 2026 Apr 23.
Publication Type: Journal Article
Language: English
Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 0151434 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3700 (Electronic) Linking ISSN: 00319422 NLM ISO Abbreviation: Phytochemistry Subsets: MEDLINE
Imprint Name(s): Publication: 2003- : London : Elsevier
Original Publication: 1961-2003: Oxford : Pergamon Press.
MeSH Terms: Euphorbia*/chemistry , Diterpenes*/chemistry , Diterpenes*/pharmacology , Diterpenes*/isolation & purification , Nuclear Receptor Subfamily 1, Group F, Member 3*/metabolism, Cell Differentiation/drug effects ; Th17 Cells/drug effects ; Molecular Structure ; Animals ; Mice
Abstract: Ten previously undescribed diterpenoids (1-10), representing four diverse architectural types, along with eight known analogs (11-18), were isolated from Euphorbia milii. Compounds 1-3 were characterized as ent-atisane diterpenoids, with 1 and 2 featuring a C-19-nor- and a 3,4-seco-19-nor-ent-atisane framework, respectively, and their plausible biosynthetic pathways were proposed. The remaining new isolates were established to be ent-pimarane (4-7), ent-abietane (8 and 9), and ent-verticillane (10) diterpenoids. Binding affinity assays revealed that compounds 6, 7, and 14 bound directly to retinoic acid-related orphan receptor γt (RORγt), of which 14 demonstrated the highest affinity (Kd = 4.2 × 10-5 M) and significantly suppressed Th17 cell differentiation.
(Copyright © 2026 Elsevier Ltd. All rights reserved.)
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Contributed Indexing: Keywords: Diterpenoids; Euphorbia milii; Euphorbiaceae; RORγt; Structure elucidation; Th17 cell differentiation
Substance Nomenclature: 0 (Diterpenes)
0 (Nuclear Receptor Subfamily 1, Group F, Member 3)
Entry Date(s): Date Created: 20260425 Date Completed: 20260610 Latest Revision: 20260610
Update Code: 20260610
DOI: 10.1016/j.phytochem.2026.114934
PMID: 42034227
Database: MEDLINE
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