01 Identity and provenance
- Accepted binomial
- Eucalyptus globulus
- Common names
- Eucalyptus
- Family (APG IV)
- Myrtaceae
- Part used
- Leaf
- Verification tier
- Tier 2 · Verified Clinical columns reviewed and a source is on record.
- Reviewer note (2026 audit)
- Reference not supplied - claim unverified against primary literature.
02 Constituent chemistry
| Chemical class | Marker compound | Synthetic analogue in use |
|---|---|---|
| Essential oil | 1,8-Cineole
Leaf
|
Eucalyptol |
The analogue column is what makes the interaction reasoning tractable: where a constituent has a marketed structural counterpart, the counterpart's interaction profile is the starting hypothesis for the plant.
03 Stated application
- Reported activity
- Expectorants
- Marketed in
- Cough syrup ,Lozenges
- Reported adverse effects
- Nausea
04 Interaction matrix
Source column, verbatim: CNS depressants
Normalised onto 1 canonical drug class below.
Curated from the reviewed source
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Sedatives, hypnotics and benzodiazepines
CNS
|
3Major | PD-additive | curated B | Excess sedation, psychomotor and driving impairment, falls, respiratory d… | why ▾ |
Class mechanism. Valepotriate, kavalactone, apigenin, sesquiterpene and alkaloid constituents act at GABA-A, adenosine and histamine sites, summating with prescribed CNS depression. Some also inhibit CYP3A4 and raise benzodiazepine exposure.
| |||||
Predicted from constituent chemistry
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Antiepileptics
CNS
|
3Major | PK-CYP induction + PD-antagonistic | predicted D | Breakthrough seizures, status epilepticus, or additive sedation and ataxi… | why ▾ |
Chemistry of this pair. Volatile monoterpenes are GABA-A antagonists at higher exposure, lowering seizure threshold, and are metabolised to reactive intermediates. Class mechanism. Enzyme-inducing botanicals lower plasma anticonvulsant concentrations, while GABAergic constituents add sedation and a few (thujone, camphor, beta-asarone, pinene-rich oils) are directly proconvulsant and lower seizure threshold.
| |||||
|
Hepatotoxic drugs
Organ toxicity
|
3Major | Organ-toxicity additive | predicted D | Transaminase elevation, cholestasis, sinusoidal obstruction syndrome, acu… | why ▾ |
Chemistry of this pair. Volatile monoterpenes are GABA-A antagonists at higher exposure, lowering seizure threshold, and are metabolised to reactive intermediates. Class mechanism. Pyrrolizidine alkaloids, high-dose anthraquinones, kava constituents and germander-type diterpenes cause hepatocellular or sinusoidal injury that adds to the risk from paracetamol, isoniazid, methotrexate, azoles and statins.
| |||||
|
Topical antiseptics, keratolytics and irritants
Dermatology
|
3Major | PD-additive local | predicted D | Contact dermatitis, chemical burn, photoirritation, unexpected systemic a… | why ▾ |
Chemistry of this pair. Volatile monoterpenes are GABA-A antagonists at higher exposure, lowering seizure threshold, and are metabolised to reactive intermediates. Class mechanism. Essential-oil terpenes, capsaicinoids and phorbol-type diterpenes add to the barrier disruption caused by topical antiseptics, retinoids and keratolytics, and increase percutaneous absorption of anything applied with them.
| |||||
05 Hazard register
The audit recorded no hazard beyond the interaction profile. The controlled-vocabulary field reads not assessed, which means the assessment has not been done rather than that it came back clear.
06 Confusable material
No same-genus or shared-common-name entry in the corpus.
07 Mechanism map
Chemistry sorts to the left, pharmacology to the right. Dashed edges are predicted. Drag nodes, scroll to zoom, export at 3× for a figure.
08 Open literature
Abstract-scoped query built from this binomial, its common names and its marker compounds, run live against Europe PMC, PubMed and OpenAlex, then ranked locally against an evidence hierarchy.
09 Isomechanistic neighbours
Species whose interaction profile overlaps this one, ranked by shared severity weight rather than by count — a shared contraindication counts for more than a shared minor signal. Practical use: these are the plants you should not stack with this one, because the mechanisms summate.
| Species | Family | Shared classes | Weight | Jaccard |
|---|---|---|---|---|
| Achillea millefolium
Yarrow |
Asteraceae | 4 | 0.33 | |
| Acorus calamus
Vacha |
Acoraceae | 4 | 0.57 | |
| Melaleuca alternifolia
Tea Tree |
Myrtaceae | 3 | 0.60 | |
| Amomum subulatum
Black Cardamom |
Zingiberaceae | 3 | 0.60 | |
| Salvia rosmarinus
Rosemary |
Lamiaceae | 3 | 0.60 | |
| Salvia officinalis
Sage |
Lamiaceae | 3 | 0.60 |
10 References and notes
No citation is on record for this entry. That is itself the finding: the audit flagged it, and it is why the entry does not carry an A evidence grade.
Curator notes
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