PubMed-compiled information sheet
This sheet was compiled from PubMed (NIH) abstracts using AI assistance. Every factual claim is cited to a real PubMed article (see the source list). It has not yet been human-reviewed — confirm with a healthcare provider before use.
Compiled from 30 PubMed articles · model: gemma4:31b
Summary
Background
Traditional uses
Active compounds
Mechanism of action
Clinical evidence
Curcumenol inhibited survival of TNBC cells, enhanced sensitivity to paclitaxel, and reduced tumor growth and lung metastasis in mouse models [PMID:40377003]
C. phaeocaulis suppressed caspase-1 activation and decreased IL-1$\beta$ levels and cell infiltration in nanoparticle-induced mouse models [PMID:35408502]
$\beta$-elemene and the herbal combination Sparganium stoloniferum-Curcuma phaeocaulis inhibit endometriosis progression via MAPK, STAT3, and S1P/S1PR1-Akt axis modulation [PMID:39800242, 38277707, 40523453]
Extracts decreased prion aggregation and propagation in vitro and in vivo, preventing disease onset in some mouse models [PMID:36613636, 39274884]
Methanol extract significantly inhibited paw swelling and serum haptoglobin concentration in mice [PMID:16786056]
Safety & adverse effects
Evidence summary
PubMed sources
- 1.PMID: 40377003 (2025) — Curcumenol inhibits malignant progression and promotes ferroptosis via the SLC7A11/NF‑κB/TGF‑β pathway in triple‑negative breast cancer. · International journal of molecular medicine
- 2.PMID: 35408502 (2022) — Curcuma phaeocaulis Inhibits NLRP3 Inflammasome in Macrophages and Ameliorates Nanoparticle-Induced Airway Inflammation in Mice. · Molecules (Basel, Switzerland)
- 3.PMID: 40734908 (2025) — Curcumae Rhizoma: An anti-cancer traditional Chinese medicine. · Chinese herbal medicines
- 4.PMID: 35417150 (2022) — Asymmetric Total Synthesis of (-)-Phaeocaulisin A. · Journal of the American Chemical Society
- 5.PMID: 39800242 (2025) — β-elemene, a sesquiterpene constituent from Curcuma phaeocaulis inhibits the development of endometriosis by inducing ferroptosis via the MAPK and STAT3 signaling pathways.