01 Identity and provenance
- Accepted binomial
- Valeriana jatamansi
- Common names
- Tagar
- Family (APG IV)
- Caprifoliaceae
- Part used
- Rhizome
- 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 |
|---|---|---|
| Sesquiterpenoids, Iridoids, Essential oils | Valerenic acid, Acetoxyvalerenic acid, Hydroxyvalerenic acid, Valepotriates (Didrovaltrate, Valtrate, Acevaltrate), Bornyl acetate, Patchouli alcohol, Kessyl glycol, β-Caryophyllene
Rhizome
|
Diazepam, Clonazepam, Alprazolam, Pregabalin |
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
- Sedative, anxiolytic, insomnia, epilepsy, migraine, muscle relaxation, neuroprotective, stress disorders
- Marketed in
- Herbal sleep aids, calming capsules, stress relief tablets, essential oils, teas, Ayurvedic formulations
- Reported adverse effects
- Drowsiness, impaired concentration, headache, dizziness, gastrointestinal discomfort, vivid dreams, withdrawal symptoms after prolonged high-dose use (rare)
04 Interaction matrix
Source column, verbatim: Benzodiazepines, antidepressants, anticonvulsants, opioids, alcohol, anesthetic agents, sedative antihistamines
Normalised onto 6 canonical drug classes below.
Curated from the reviewed source
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Antidepressants (SSRI, SNRI, TCA)
CNS
|
3Major | PD-additive serotonergic + PK-CYP2D6 | curated B | Serotonin syndrome (agitation, clonus, hyperthermia, autonomic instabilit… | why ▾ |
Class mechanism. Hypericin- and hyperforin-type constituents inhibit monoamine reuptake and induce CYP3A4/2C19 and P-glycoprotein; others inhibit CYP2D6, raising tricyclic and SSRI concentrations.
| |||||
|
Antiepileptics
CNS
|
3Major | PK-CYP induction + PD-antagonistic | curated B | Breakthrough seizures, status epilepticus, or additive sedation and ataxi… | why ▾ |
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.
| |||||
|
Opioid analgesics
CNS
|
3Major | PD-additive + PK-CYP2D6/3A4 | curated B | Respiratory depression, over-sedation, constipation, ileus; unpredictable… | why ▾ |
Class mechanism. Botanical mu-agonists and CNS depressants add to opioid respiratory and sedative effect; CYP2D6 and CYP3A4 modulation alters the conversion of codeine and tramadol to active metabolites.
| |||||
|
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.
| |||||
|
Alcohol
CNS
|
2Moderate | PD-additive + organ toxicity | curated B | Excess sedation, impaired judgement, higher risk of botanical hepatotoxic… | why ▾ |
Class mechanism. Additive CNS depression plus shared hepatic injury pathways; alcohol also increases the extraction and absorption of lipophilic botanical constituents from tinctures.
| |||||
|
Antihistamines
Immunology
|
2Moderate | PD-additive | curated B | Drowsiness, impaired coordination, dry mouth, urinary hesitancy, confusio… | why ▾ |
Class mechanism. Sedating antihistamines add to botanical CNS depression, and their antimuscarinic component adds to tropane alkaloid burden.
| |||||
Predicted from constituent chemistry
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Narrow-therapeutic-index CYP3A4 substrates
Pharmacokinetic
|
4Contraindicated | PK-CYP3A4 | predicted D | Toxic accumulation or subtherapeutic failure of the co-prescribed drug, s… | why ▾ |
Chemistry of this pair. Volatile terpenes are lipophilic, cross membranes readily and induce or inhibit CYP2B6 and CYP3A4 depending on the constituent. Class mechanism. Furanocoumarins, bergamottin, piperine, glabridin and berberine inhibit CYP3A4; hyperforin, andrographolide and several diterpenes induce it through PXR. Because CYP3A4 handles roughly half of marketed drugs, the affected list is broad and the direction is product-specific.
| |||||
|
Topical antiseptics, keratolytics and irritants
Dermatology
|
2Moderate | PD-additive local | predicted D | Contact dermatitis, chemical burn, photoirritation, unexpected systemic a… | why ▾ |
Chemistry of this pair. Volatile terpenes are lipophilic, cross membranes readily and induce or inhibit CYP2B6 and CYP3A4 depending on the constituent. 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
These entries could be mistaken for this one in trade, in the herbarium, or in a prescription. Powdered material is often indistinguishable, so the check is macroscopic, microscopic and chromatographic rather than nominal.
| Valeriana officinalis
Valerian |
Caprifoliaceae | Same genus (Valeriana) |
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 |
|---|---|---|---|---|
| Nardostachys jatamansi
Jatamansi |
Caprifoliaceae | 8 | 0.89 | |
| Piper methysticum
Kava |
Piperaceae | 5 | 0.38 | |
| Mitragyna speciosa
Kratom |
Rubiaceae | 5 | 0.42 | |
| Strychnos nux-vomica
Nux Vomica |
Loganiaceae | 4 | 0.31 | |
| Achillea millefolium
Yarrow |
Asteraceae | 4 | 0.25 | |
| Cannabis sativa
Cannabis |
Cannabaceae | 3 | 0.38 |
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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