Chelidonium asiaticum

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Chelidonium asiaticum

Family: Papaveraceae Genus: Chelidonium Species: asiaticum

Synonyms: Chelidonium majus subsp. asiaticum, Chelidonium majus var. asiaticum, Chelidonium majus var. hirsutum

Western Herbalism Properties

Actions:
alterativeantispasmodicdiaphoreticdiuretic

Botanical Description

Chelidonium asiaticum is a herbaceous perennial of the Papaveraceae closely related to the European greater celandine (C. majus), distinguished mainly by leaf and capsule details and now treated as a distinct species native to eastern Asia, including parts of China, the Russian Far East, Korea, and Japan. It grows to 30-80 cm tall from a short, stout rhizome and yellow taproot, producing erect, sparsely hairy, hollow stems that exude a bright orange-yellow latex when broken. The pinnately or deeply lobed alternate leaves are glaucous below and have rounded, crenate lobes. Bright yellow four-petaled flowers about 1.5-2 cm across are borne in long-pedicelled umbel-like cymes in spring and summer, followed by slender, linear capsules 3-5 cm long that split from the base to release small black seeds bearing a white elaiosome that promotes ant dispersal.

Native Region: Amur, China North-Central, Japan, Khabarovsk, Korea, Kuril Is., Manchuria, Primorye, Sakhalin

Active Constituents

Chelidonine

Benzophenanthridine (isoquinoline) alkaloid

Concentration: Major alkaloid of the aerial parts and roots, as in the closely related C. majus

Chelidonine is the principal spasmolytic and antimitotic alkaloid of Chelidonium. It relaxes smooth muscle and disrupts microtubule assembly, giving antiproliferative activity in cell studies, but its metabolites are implicated in the plant's hepatotoxicity.

Sanguinarine

Benzophenanthridine (quaternary) alkaloid

Concentration: Present in aerial parts and the bright orange latex; higher in roots

Sanguinarine is a strongly bioactive quaternary alkaloid with antimicrobial, anti-inflammatory and cytotoxic properties. It is also the most toxic of the group (blocks hERG cardiac channels, damages DNA), so it is a key contributor to the plant's overall toxicity.

Chelerythrine

Benzophenanthridine (quaternary) alkaloid

Concentration: Minor to moderate constituent of aerial parts and latex

Chelerythrine is a protein kinase C inhibitor with antimicrobial and pro-apoptotic activity; like sanguinarine it contributes to cytotoxic and cardiotoxic potential.

Coptisine

Protoberberine alkaloid

Concentration: One of the more abundant protoberberine alkaloids in Chelidonium

Coptisine has anti-inflammatory, antimicrobial and choleretic (bile-stimulating) activity, supporting the traditional use of the herb for liver and gallbladder complaints.

Berberine

Protoberberine alkaloid

Concentration: Minor constituent

Berberine contributes antimicrobial, anti-inflammatory and metabolic (antidiabetic, hypolipidaemic) activity documented across berberine-containing plants.

Protopine

Protopine-type isoquinoline alkaloid

Concentration: Minor constituent of aerial parts

Protopine has mild spasmolytic, analgesic and sedative activity and adds to the smooth-muscle-relaxant profile of Chelidonium extracts.

⚠ Drug Interactions

Hepatotoxic drugs (e.g. paracetamol/acetaminophen, isoniazid, methotrexate, statins)

Major Evidence: Probable

Chelidonium alkaloids (notably chelidonine metabolites) can cause idiosyncratic herb-induced liver injury by forming reactive quinone species and depleting hepatic glutathione. Combining the herb with other hepatotoxic agents compounds this risk.

Clinical note: Avoid combining Chelidonium preparations with hepatotoxic medications; monitor liver enzymes if the herb is used at all, and discontinue at any sign of liver injury.

QT-prolonging / antiarrhythmic drugs

Moderate Evidence: Theoretical

Sanguinarine and chelerythrine block hERG potassium channels and can prolong cardiac action-potential duration in experimental models, which could add to the effect of QT-prolonging drugs.

Clinical note: Use caution in patients taking antiarrhythmics or other QT-prolonging medications.

CYP-metabolized drugs

Moderate Evidence: Theoretical

Isoquinoline alkaloids such as berberine and coptisine can inhibit cytochrome-P450 enzymes and drug transporters, potentially raising levels of co-administered substrates.

Clinical note: Consider the possibility of altered plasma levels of narrow-therapeutic-index drugs.

Preparation Methods

Fresh latex, topical (traditional)

Parts: fresh stem, latex

The bright orange latex from a broken stem has traditionally been dabbed directly onto warts and corns. This is a folk use only: the latex is caustic and irritant, should never be applied near the eyes or mucous membranes, and should not be ingested.

Dilute decoction / tincture (traditional, restricted)

Parts: aerial parts

In East Asian and European folk practice small, carefully controlled doses of a dilute decoction or standardized tincture were used as an antispasmodic and choleretic for biliary and cramping complaints. Because the whole plant contains toxic isoquinoline alkaloids and has caused serious liver injury, internal use is unsafe without professional supervision and is contraindicated in pregnancy, lactation, liver disease and for children.

Historical Texts

East Asian materia medica (bai qu cai, 白屈菜)

Traditional; formalized in later Chinese and Korean/Japanese pharmacopoeial literature
The East Asian Chelidonium (of which C. asiaticum is the local species) is recorded as bai qu cai, used cautiously as an antispasmodic and analgesic for cough, abdominal cramping and pain, and noted as a toxic herb requiring careful dosing.

European herbals on greater celandine (Dioscorides, Culpeper) — applied to the genus

Antiquity to 17th century
The closely related greater celandine was used from classical times for eye complaints, warts, jaundice and liver/gallbladder conditions; C. asiaticum shares this reputation and alkaloid profile.

References

  1. Li XL, Sun YP, Wang M, Wang ZB, Kuang HX. Alkaloids in Chelidonium majus L: a review of its phytochemistry, pharmacology and toxicology . Frontiers in Pharmacology (2024) [DOI]
  2. Zielińska S, Jezierska-Domaradzka A, Wójciak-Kosior M, Sowa I, Junka A, Matkowski AM. Greater Celandine's Ups and Downs—21 Centuries of Medicinal Uses of Chelidonium majus from the Viewpoint of Today's Pharmacology . Frontiers in Pharmacology (2018) [DOI]

This information is for educational purposes only and is not intended to replace professional medical advice. Always consult a qualified healthcare provider before using any herbal remedy, especially if you are pregnant, nursing, or taking medications.

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