Compound Monograph

Taraxasterol

Terpenoids Triterpenes Natural (plant-derived)

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 1,2,3Reference 1Wang S et al. · 2016AnimalAnti-inflammatory and anti-arthritic effects of taraxasterol on adjuvant-induced arthritis in ratsView study →Reference 2Che X et al. · 2019In vitroAnti-inflammatory and anti-apoptotic activity of taraxasterol in ulcerative colitis in vitro and in vivoView study →Reference 3Zhang X et al. · 2014AnimalProtective effect of taraxasterol on acute lung injury induced by lipopolysaccharide in miceView study → — and no human trials of any kind. Like its sibling lupeol, it is a highly lipophilic triterpene with poor oral bioavailability, so the in-vitro and rodent potencies are not demonstrated to be reachable from ordinary intake, and dandelion delivers only trace amounts. (Keep it distinct from the separate relatives taraxerol and ψ-taraxasterol.)

A coherent anti-inflammatory mechanism:NF-κB (p65) and MAPK suppression, lowering TNF-α/IL-1β/IL-6, COX-2 and iNOS, replicated across several independent rodent models 1,2,3Reference 1Wang S et al. · 2016AnimalAnti-inflammatory and anti-arthritic effects of taraxasterol on adjuvant-induced arthritis in ratsView study →Reference 2Che X et al. · 2019In vitroAnti-inflammatory and anti-apoptotic activity of taraxasterol in ulcerative colitis in vitro and in vivoView study →Reference 3Zhang X et al. · 2014AnimalProtective effect of taraxasterol on acute lung injury induced by lipopolysaccharide in miceView study →.
Consistent but narrow:the immunomodulatory, hepatoprotective and anti-allergic effects are all downstream of the same anti-inflammatory/antioxidant mechanism 6,10Reference 6Liu J et al. · 2013AnimalEffects of taraxasterol on ovalbumin-induced allergic asthma in miceView study →Reference 10Ge W et al. · 2023Protection of taraxasterol against acetaminophen-induced liver injury elucidated through network pharmacology and in-vitro and in-vivo experimentsView study →.
The honest headline:entirely preclinical — no human data — and poor oral bioavailability (inferred from the lipophilic triterpene class and lupeol) is the key translational limitation.
Evidence by IndicationStrength of support · Beta

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.

Mechanisms

Target / pathwayEffectRelevant 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 / MDM2p53 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.

CompletedPlannedTerminatedPreclinical
—(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.

Safety at a Glance
Low / no toxicity
  • 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 10,11Reference 10Ge W et al. · 2023Protection of taraxasterol against acetaminophen-induced liver injury elucidated through network pharmacology and in-vitro and in-vivo experimentsView study →Reference 11Lin W et al. · 2024AnimalTaraxasterol protects against acetaminophen-induced hepatotoxicity by reducing liver inflammation and ameliorating oxidative stress in miceView study →. That said, there is no dedicated toxicology package — no formal LD50, repeat-dose, genotoxicity or safety-pharmacology study — so “low toxicity” is inferred from the absence of adverse findings in efficacy studies, not from a study designed to find harm, and there is no human exposure data (dandelion, the dietary source, is a whole-herb trace-level exposure, not isolated taraxasterol).

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

  1. 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/
  2. 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/
  3. 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/
  4. 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/
  5. 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/
  6. 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/
  7. 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/
  8. 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/
  9. 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/
  10. 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/
  11. 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/
  12. 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/