Research Radartracking 4 published studies · 1 human · 2 clinical trials · 2 cancer pages · updated Jun 2026Open the Research Map →

Black Seed Oil / Thymoquinone

Black seed oil's thymoquinone inhibits PI3K/AKT, boosts ROS/apoptosis in tumors; preclinical synergies for chemo-sensitization in ovarian cancer.

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Human-reviewed · How we review →

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🔬⭐⭐ Low to Moderate — Robust preclinical data, including ovarian synergies; limited human trials, but promising for adjunctive use.Nigella sativa oilBlack cumin seed oilKalonji oilThymoquinone-rich oil

Forms: Black seed oil capsules or liquid (500 mg–1 g per serving)

Educational only, not medical advice. OncoForge makes no claim that Black Seed Oil / Thymoquinone treats, prevents, or cures any condition, beyond what the linked studies show. Evidence levels vary; effects may not translate to people, and some compounds can cause harm. Always coordinate with your oncology team.

Simple Summary

From black cumin seed, thymoquinone turns down PI3K/AKT survival signaling, raises ROS in tumor cells, and triggers apoptosis. It shows synergy with standard drugs (e.g., cisplatin, doxorubicin) in preclinical ovarian models.

Evidence at a glance

Tier 2 · animalOvarianBreastColorectalLungProstateVarious

Low to Moderate — Robust in vitro/in vivo; early human trials for safety, but oncology efficacy needs more studies.

How it may work

Thymoquinone (TQ), the active compound in black seed oil, inhibits PI3K/Akt and STAT3 pathways, blocking cancer cell survival and proliferation. It enhances TRAIL-mediated apoptosis, increases ROS selectively in cancer cells, and induces cell cycle arrest. In ovarian cancer, TQ promotes apoptosis via p53-dependent mechanisms, reduces NF-κB activity, and sensitizes cells to chemotherapy by targeting resistance pathways.

Targets & pathways

Curated mechanistic targets reported for this agent — how it may act on cells, not proof of a clinical effect.

  • PI3K/AKTBlocks survival and proliferation
  • STAT3
  • ApoptosisEnhances TRAIL-mediated; p53-dependent
  • ROS ProductionSelective in cancer cells
  • Cell Cycle Arrest
  • NF-κB
  • Chemotherapy ResistanceSensitizes to cisplatin, doxorubicin
PI3KROSApoptosis

Often studied / combined with

Combinations reported in the literature, not a protocol or a recommendation.

Overlapping mechanisms

Safety & interactions

Severity and how well-established each signal is are shown separately. Verify everything with your oncologist or pharmacist — absence here does not mean safe.

Risk categories
Gi Upset MildAllergic ReactionsHypotension Risk MildPregnancy AvoidHypoglycemia Risk
Potential interactions
  • Anticoagulants (e.g., warfarin)MonitorModerateTheoreticalPotential additive antiplatelet effects.
  • CYP3A4 substrates (e.g., chemotherapy drugs)MonitorMinorTheoreticalTQ may inhibit CYP3A4.
  • Cisplatin / DoxorubicinConsiderBeneficialTheoreticalSynergistic in preclinical models; may enhance efficacy/reduce resistance.

Timing

References

Research

No published studies for Black Seed Oil / Thymoquinone yet

New studies appear here once they’ve been reviewed. Browse all studies.

Dose: as studied, not a recommendation

These are doses as studied or reported, never a recommendation. The right amount of Black Seed Oil / Thymoquinone depends on you, your other medicines, and your situation; decide it with your oncology team and pharmacist, not from a web page.

Ranges seen in adjunct / practice use: 1000–3000 mg (po) Divided into 2–3 doses daily. Based on human studies (1–2.5 g/day for general use; up to 3 g/day in trials); for TQ equivalent, aim for 5–50 mg/day (oil TQ content ~0.4–2.5%). Preclinical HED from mouse studies (5–20 mg/kg TQ → HED 0.4–1.6 mg/kg, ~24–96 mg TQ for 60 kg, equating to 1–24 g oil depending on TQ%). Oncology adjunct: start low under supervision., No Rx required. Choose cold-pressed, high-TQ oil; take with food for tolerance. Oncology use experimental—consult clinician; monitor for interactions..

Trials studying Black Seed Oil / Thymoquinone

No actively-recruiting trials matched right now. Recruiting is not the same as proven. Search ClinicalTrials.gov →

Inclusion here is not an endorsement. OncoForge makes no claim beyond what the linked studies show. Discuss anything on this page with your oncology team before acting on it.

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