01 Identity and provenance
- Accepted binomial
- Astragalus membranaceus
- Common names
- Astragalus
- Family (APG IV)
- Fabaceae
- Part used
- Root
- Verification tier
- Tier 1 · chemistry only Taxonomy, plant part and marker chemistry are populated and stable. The clinical columns are deliberately empty because no primary source has been retrieved for them yet. Interactions shown below are rule predictions from the constituent chemistry, not clinical findings.
- Reviewer note (2026 audit)
- TIER 1 populated (name, family, part, constituent class, marker) - stable taxonomic/phytochemical facts. TIER 2 columns (analogue, application, brand, interactions, side effects) left blank BY DESIGN - populate only from retrieved primary literature. Do not use clinically until Tier 2 is filled and a reference is recorded.
02 Constituent chemistry
| Chemical class | Marker compound | Synthetic analogue in use |
|---|---|---|
| Triterpenoid saponins, polysaccharides | Astragaloside IV
Root
|
none listed |
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
Left empty by design — this is a Tier 1 entry, and the clinical columns are only populated once a primary source has been retrieved for them.
04 Interaction matrix
Predicted from constituent chemistry
| Drug class | Severity | Mechanism type | Provenance | Expected effect | |
|---|---|---|---|---|---|
|
Cardiac glycosides (digoxin, digitoxin)
Cardiovascular
|
4Contraindicated | PD-additive + PK-transporter + assay interference | predicted D | Nausea, xanthopsia, bradyarrhythmia, AV block, ventricular tachycardia an… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Cardenolide- and bufadienolide-bearing plants are themselves Na+/K+-ATPase inhibitors, so co-administration is pharmacological overdose. Several also inhibit intestinal P-glycoprotein, raising digoxin exposure, and cross-react with digoxin immunoassays so that serum levels become uninterpretable.
| |||||
|
Antidiabetic drugs (insulin, sulfonylureas, biguanides, GLP-1, SGLT2)
Endocrine
|
3Major | PD-additive | predicted D | Symptomatic hypoglycaemia, sweating, tremor, confusion; severe events rep… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Hypoglycaemic botanicals act through insulin secretagogue, insulin-sensitising, alpha-glucosidase-inhibiting or glucose-transport routes. Added to a titrated pharmacological regimen the effects summate rather than plateau.
| |||||
|
Antiplatelet agents
Haemostasis
|
3Major | PD-additive | predicted D | Prolonged bleeding time, surgical and post-procedural bleeding, bruising,… | why ▾ |
Chemistry of this pair. Triterpene and steroidal saponins alter membrane permeability, inhibit platelet aggregation and show weak steroid-receptor affinity. Class mechanism. Organosulfur compounds, gingerols, salicylates, ginkgolides and eugenol inhibit thromboxane A2 synthesis, platelet aggregation and PAF-mediated activation, duplicating the pharmacology of aspirin and P2Y12 blockers.
| |||||
|
Hormonal therapy, oral contraceptives and HRT
Endocrine
|
3Major | PK-CYP3A4 induction + PD-oestrogenic | predicted D | Breakthrough bleeding and contraceptive failure; unpredictable effect in … | why ▾ |
Chemistry of this pair. Triterpene and steroidal saponins alter membrane permeability, inhibit platelet aggregation and show weak steroid-receptor affinity. Class mechanism. CYP3A4-inducing botanicals accelerate ethinylestradiol and progestin clearance. Separately, isoflavone, lignan and coumestan phyto-oestrogens bind oestrogen receptors and may add to or compete with prescribed hormones.
| |||||
|
Antibacterials and anthelmintics
Infection
|
2Moderate | PK-chelation + PK-CYP | predicted D | Treatment failure from subtherapeutic antibiotic concentrations, or raise… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Cation- and tannin-rich botanicals chelate tetracyclines and fluoroquinolones; efflux-pump-inhibiting and CYP-modulating constituents alter macrolide, rifamycin and azole exposure. Anthelmintic botanicals add to praziquantel and albendazole effect.
| |||||
|
Iron, calcium and mineral supplements
Nutrition
|
2Moderate | PK-chelation | predicted D | Failure of iron-deficiency correction, unexplained non-response to oral i… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Tannins, phytates, oxalates and mucilage form insoluble complexes with divalent and trivalent cations in the gut lumen, reducing absorption of both the mineral and any co-administered chelating drug.
| |||||
|
Thyroid hormones and antithyroid drugs
Endocrine
|
2Moderate | PK-absorption + PD-modulation | predicted D | Iatrogenic hyper- or hypothyroidism, unexplained TSH drift, loss of euthy… | why ▾ |
Chemistry of this pair. Hydrocolloids raise luminal viscosity and physically entrap co-administered drug molecules, delaying and reducing absorption. Class mechanism. Guggulsterone stimulates thyroid function and T4-to-T3 conversion; goitrogenic glucosinolates and lithospermic acid suppress it; high-fibre and cation-rich botanicals bind levothyroxine in the gut and reduce absorption.
| |||||
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.
| Astragalus gummifer
Tragacanth |
Fabaceae | Same genus (Astragalus) |
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 |
|---|---|---|---|---|
| Trigonella foenum-graecum
Fenugreek |
Fabaceae | 7 | 1.00 | |
| Panax ginseng
Ginseng |
Araliaceae | 7 | 0.70 | |
| Echinacea purpurea
Echinacea |
Asteraceae | 6 | 0.46 | |
| Linum usitatissimum
Flax (Alsi) |
Linaceae | 6 | 0.75 | |
| Phyllanthus amarus
Bhui Amla |
Phyllanthaceae | 6 | 0.46 | |
| Senegalia senegal
Gum Acacia |
Fabaceae | 5 | 0.71 |
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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