Compound Monograph
Taraxasterol
Taraxasterol is a taraxastane-type pentacyclic triterpene of dandelion and other Asteraceae, with a coherent preclinical anti-inflammatory literature (NF-κB/MAPK suppression across arthritis, colitis, lung-injury and dermatitis models) but no human trials; as a highly lipophilic triterpene its poor oral bioavailability is a key limitation.
Sources · 4
Where Does It Come From?
Taraxasterol is a naturally occurring triterpene (taraxastane-type), found in Dandelion, Calendula, Wild lettuce and 1 other source. It is well tolerated orally (low toxicity).
Concentration
Content by Source
Concentrations not reported. No percent-dry-weight or mg/g figures have been published for this compound in its source plants.
Taraxasterol at a Glance
Taraxasterol is a taraxastane-type pentacyclic triterpene of dandelion and other Asteraceae, and one of the compounds that gives dandelion a pharmacological identity beyond its diuretic reputation.
Its preclinical anti-inflammatory literature is unusually coherent for a plant triterpene: NF-kB and MAPK suppression demonstrated consistently across arthritis, colitis, lung-injury and dermatitis models, rather than in one model only.
What It's Used For
Taraxasterol is a taraxastane-type pentacyclic triterpene, a characterizing constituent of the dandelion (Taraxacum officinale) triterpene fraction where it co-occurs with lupeol. Its literature has a clear, consistent shape: a well-replicated preclinical anti-inflammatory signal — NF-κB and MAPK suppression across rodent arthritis, colitis, lung-injury and dermatitis models 1,
Support is an experimental score — weighted by study type (human > animal > in vitro) and volume. A beta, not a validated metric. Every application is preclinical, so scores stay low by design. Each application links to its write-up.
The marquee, and the most replicated. Taraxasterol reduced paw swelling and cytokines in rat adjuvant-induced arthritis 1Reference 1AnimalAnti-inflammatory and anti-arthritic effects of taraxasterol on adjuvant-induced arthritis in ratsView study →, limited inflammation and apoptosis in ulcerative colitis 2Reference 2In vitroAnti-inflammatory and anti-apoptotic activity of taraxasterol in ulcerative colitis in vitro and in vivoView study →, protected against LPS acute lung injury 3Reference 3AnimalProtective effect of taraxasterol on acute lung injury induced by lipopolysaccharide in miceView study →, and suppressed macrophage hyperactivation in sepsis-induced ARDS 4Reference 4AnimalTaraxasterol inhibits hyperactivation of macrophages to alleviate the sepsis-induced inflammatory response of ARDS ratsView study → — converging on NF-κB p65, MAPK, COX-2 and iNOS.
Gap: every model is rodent or cell-based, with no human inflammatory-disease data and no head-to-head against a standard anti-inflammatory at an achievable oral exposure 1,
Taraxasterol dampened Th2 cytokines and eosinophilia in an ovalbumin allergic-asthma model 6Reference 6AnimalEffects of taraxasterol on ovalbumin-induced allergic asthma in miceView study → and suppressed macrophage hyperactivation in sepsis/ARDS 4Reference 4AnimalTaraxasterol inhibits hyperactivation of macrophages to alleviate the sepsis-induced inflammatory response of ARDS ratsView study → — reading as broad innate plus Th2-axis damping.
Gap: no adaptive-immunity dose-response or immune-competence data, entirely preclinical, with mechanism inferred from downstream cytokines 6,
Taraxasterol protected against acetaminophen-induced liver injury via Nrf2/HO-1 with JNK and Bax/Bcl-2 modulation 10,
Gap: all acute chemical-injury models, with no chronic-liver-disease or human data, and the effect is largely secondary to the general anti-inflammatory/antioxidant mechanism 10,
Taraxasterol stabilized p53 via MDM2 degradation in pancreatic cancer 7Reference 7Taraxasterol regulates p53 transcriptional activity to inhibit pancreatic cancer by inducing MDM2 ubiquitination degradationView study →, enhanced bladder-cancer radiosensitivity through COX-2/PGE2/JAK2/STAT3 inhibition 8Reference 8Taraxasterol enhanced bladder-cancer cell radiosensitivity via inhibiting the COX-2/PGE2/JAK2/STAT3/MMP pathwayView study →, and showed a dual anti-aging/anti-cancer effect in lung cells 9Reference 9Taraxasterol exhibits dual biological effects on anti-aging and anti-cancer in lung cellsView study →.
Gap: heterogeneous, mostly single-lab cell-line/xenograft studies with non-overlapping mechanisms, no consistent signaling story and no clinical signal — the weakest ranked set despite the volume 7,
Taraxasterol attenuated a 2,4-dinitrochlorobenzene atopic-dermatitis model via MAPK and NF-κB inactivation 5Reference 5AnimalTaraxasterol attenuates inflammatory responses in a 2,4-dinitrochlorobenzene-induced atopic-dermatitis mouse model via inactivation of MAPK and NF-κBView study → and reduced ovalbumin-induced allergic asthma 6Reference 6AnimalEffects of taraxasterol on ovalbumin-induced allergic asthma in miceView study →.
Gap: two models only, and the “anti-allergic” label is a re-framing of the same anti-inflammatory/Th2 mechanism rather than an independent evidence stream 5,
Mechanisms
| Target / pathway | Effect | Relevant to |
|---|---|---|
| NF-κB (p65) | ↓ activation / nuclear translocation | anti-inflammatoryhepatoprotectiveanti-allergic |
| MAPK (ERK/JNK/p38) | ↓ phosphorylation | anti-inflammatoryatopic dermatitis |
| COX-2 / iNOS | ↓ expression | arthritislung injurybladder-cancer radiosensitization |
| Th2 cytokines (IL-4/5/13), IgE, eosinophils | ↓ | allergic asthmaatopic dermatitis |
| Nrf2 / HO-1 | ↑ (antioxidant) | hepatoprotection |
| JAK2/STAT3 | ↓ | bladder cancerfulminant hepatitis |
| p53 / MDM2 | p53 stabilization | pancreatic cancer |
Pharmacokinetics
No dedicated human or in-vivo pharmacokinetic study of taraxasterol was located, so the profile is inferred from its structure and its sibling. Taraxasterol is a highly lipophilic pentacyclic triterpene monool (a single hydroxyl, no solubilizing sugar), so poor aqueous solubility and low oral bioavailability are the predicted, limiting property — the same constraint documented for lupeol (log P ≈ 7.7, poor oral absorption). The implication is that the in-vitro and rodent potencies above are not demonstrated to be reachable from ordinary oral intake, and dandelion delivers only trace amounts — treat all pharmacokinetics as inferred, not measured.
Clinical trials
There are no human trials of taraxasterol of any kind, interventional or observational. The entire evidence base is in-vitro and rodent, consistent with its Tier-B classification.
| Completed | Planned | Terminated | Preclinical |
|---|---|---|---|
| —(none) | — | — | Extensive |
Last checked: July 2026.
Toxicity & Safety
Taraxasterol looks clean in rodents, but “low toxicity” here is the absence of a finding rather than the result of a study designed to find harm — no toxicology package and no human exposure data exist.
- No overt toxicity in animal studies. Rodents tolerated therapeutic doses across the arthritis, colitis, lung-injury and asthma models.
- Net protective in liver-injury models. Taraxasterol reduced, rather than caused, hepatic damage.
- Avoid in pregnancy and lactation. Apoptosis- and immune-modulating activity with no reproductive data.
- No dedicated toxicology package. No LD50, repeat-dose, genotoxicity or safety-pharmacology study has been done.
- No human exposure data. Dietary dandelion is a trace whole-herb exposure, not isolated taraxasterol.
Full Safety & Interactions Detail
Taraxasterol shows low apparent toxicity in animal studies: across the anti-inflammatory, hepatoprotective, colitis and asthma models it was administered to rodents at therapeutic doses without reported overt toxicity, and in the liver-injury models it was net protective 10,
Dosage
There is no established human dose, and nothing here is a recommendation. All figures in the literature are preclinical research doses — typically oral or intraperitoneal rodent dosing in the single-digit-to-tens-of-mg/kg range — that do not translate to a human dose, and dietary dandelion supplies only trace taraxasterol.
References
- Wang S, et al. (2016). Anti-inflammatory and anti-arthritic effects of taraxasterol on adjuvant-induced arthritis in rats. Journal of Ethnopharmacology. https://pubmed.ncbi.nlm.nih.gov/27109342/
- Che X, et al. (2019). Anti-inflammatory and anti-apoptotic activity of taraxasterol in ulcerative colitis in vitro and in vivo. Experimental and Therapeutic Medicine. https://pubmed.ncbi.nlm.nih.gov/31410133/
- Zhang X, et al. (2014). Protective effect of taraxasterol on acute lung injury induced by lipopolysaccharide in mice. International Immunopharmacology. https://pubmed.ncbi.nlm.nih.gov/24548765/
- Bu C, Wang R, Wang Y, et al. (2022). Taraxasterol inhibits hyperactivation of macrophages to alleviate the sepsis-induced inflammatory response of ARDS rats. Cell Biochemistry and Biophysics. https://pubmed.ncbi.nlm.nih.gov/36070121/
- Zhang Y, Peng G, Zhang R (2025). Taraxasterol attenuates inflammatory responses in a 2,4-dinitrochlorobenzene-induced atopic-dermatitis mouse model via inactivation of MAPK and NF-κB. J Mol Histol. https://pubmed.ncbi.nlm.nih.gov/40119084/
- Liu J, Xiong H, Cheng Y, et al. (2013). Effects of taraxasterol on ovalbumin-induced allergic asthma in mice. Journal of Ethnopharmacology. https://pubmed.ncbi.nlm.nih.gov/23727181/
- Han A, Liu J, Du P, et al. (2025). Taraxasterol regulates p53 transcriptional activity to inhibit pancreatic cancer by inducing MDM2 ubiquitination degradation. Journal (2025). https://pubmed.ncbi.nlm.nih.gov/39671783/
- Wang Q, Zhang R, He Y, et al. (2024). Taraxasterol enhanced bladder-cancer cell radiosensitivity via inhibiting the COX-2/PGE2/JAK2/STAT3/MMP pathway. Journal (2024). https://pubmed.ncbi.nlm.nih.gov/38442139/
- Xie J, Ou Y, Fu Q, et al. (2024). Taraxasterol exhibits dual biological effects on anti-aging and anti-cancer in lung cells. Journal (2024). https://pubmed.ncbi.nlm.nih.gov/39005687/
- Ge W, et al. (2023). Protection of taraxasterol against acetaminophen-induced liver injury elucidated through network pharmacology and in-vitro and in-vivo experiments. Phytomedicine. https://pubmed.ncbi.nlm.nih.gov/37209606/
- Lin W, Gu B, Gu Y, et al. (2024). Taraxasterol protects against acetaminophen-induced hepatotoxicity by reducing liver inflammation and ameliorating oxidative stress in mice. Journal (2024). https://pubmed.ncbi.nlm.nih.gov/38943970/
- Wang G, Yin Y, Lv R, et al. (2025). Taraxasterol attenuated D-galactosamine/LPS-induced fulminant hepatitis by modulating JAK/STAT and TNF signalling. Journal (2025). https://pubmed.ncbi.nlm.nih.gov/39701218/
