Plant Comparison

Greater Celandine vs Devil's Claw

A side-by-side comparison of two medicinal plants — every documented constituent, action, use, safety note and cited source, assembled automatically from the Omnia Sana database.

First plant
Second plant
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Plant AGreater CelandineChelidonium majusPapaveraceaeFull monograph →
Plant BDevil's ClawHarpagophytum procumbensPedaliaceaeFull monograph →

At a glance

Greater Celandine and Devil's Claw: they share 6 indicated uses (arthritis / joint pain, back pain, headache, …); 2 pharmacological actions in common.

Greater CelandineDevil's Claw
Constituents32
Pharmacological actions62
Indicated uses156
Safety notes23
Cited sources1415
Indicated uses
Only Greater Celandine
BloatingCancer (anticancer research)IndigestionInfection (general)Liver supportMenstrual crampsMuscle spasmWartsWounds
Shared (6)
Arthritis / joint painBack painHeadacheInflammation (general)Pain (general)Skin irritation
Only Devil's Claw
none
Pharmacological actions
Only Greater Celandine
Anticancer (preclinical)AntimicrobialAntispasmodicCholeretic / cholagogue (bile flow)
Shared (2)
Analgesic (pain relief)Anti-inflammatory
Only Devil's Claw
none

Evidence face-off — shared uses

ConditionGreater CelandineDevil's ClawVerdict
Arthritis / joint pain1/108/10Stronger for Devil's Claw
Back pain1/109/10Stronger for Devil's Claw
Headache1/108/10Stronger for Devil's Claw
Inflammation (general)1/108/10Stronger for Devil's Claw
Pain (general)1/109/10Stronger for Devil's Claw
Skin irritation1/108/10Stronger for Devil's Claw

Evidence scores (1–10) are computed from the tier of each cited source. “Comparable” means the two scores are within one point. Follow a score to its detailed sources.

Key Constituents

Isoquinoline alkaloids (chelidonine, coptisine, berberine, sanguinarine, chelerythrine)[4]

The biologically active and toxicologically important constituents.

AlkaloidsBerberine
Flavonoids and phenolic acids[4]

Antioxidant constituents.

Phenolic acidsFlavonoids
Orange latex (alkaloid-rich sap)[4]

The caustic sap used traditionally on warts.

Alkaloids
Iridoid glycosides (harpagoside, harpagide, procumbide)[12, 13, 14]

Harpagoside is the main marker compound and anti-inflammatory principle; effective extracts are standardised to it, with the better-quality clinical evidence using preparations delivering roughly 50-60 mg harpagoside per day.

Iridoid glycosidesHarpagosideGlycosides
Phenylethanoids (acteoside/verbascoside) and flavonoids[13]

Antioxidant supporting constituents.

Verbascoside (acteoside)Flavonoids

Pharmacological Actions

Analgesic (pain relief)[4]

Anti-inflammatory, antimicrobial and analgesic (preclinical)

Anti-inflammatory[1, 4, 8]

Anti-inflammatory, antimicrobial and analgesic (preclinical)

Anticancer (preclinical)[6, 7, 12]
Antimicrobial[1, 3, 4, 10]

Anti-inflammatory, antimicrobial and analgesic (preclinical)

Antispasmodic[4]

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Choleretic / cholagogue (bile flow)[4]

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Analgesic (pain relief)[1, 2, 4, 6, 7, 9, 10, 12, 13]

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain

Anti-inflammatory[1, 3, 4, 5, 6, 8, 9, 11, 12, 13]

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain

Traditional & Indicated Uses

Arthritis / joint pain[4]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Arthritis / joint pain
Back pain[4]Traditional · 1/10

inferred from analgesic action

Evidence: 1
Label: Back pain
Bloating[4]Traditional · 1/10

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Evidence: 1
Label: Bloating
Cancer (anticancer research)[6, 7, 12]Traditional · 2/10

inferred from anticancer action

Evidence: 2
Label: Cancer (anticancer research)
Headache[4]Traditional · 1/10

inferred from analgesic action

Evidence: 1
Label: Headache
Indigestion[4]Traditional · 1/10

Antispasmodic / choleretic bitter for upper-abdominal and biliary dyspepsia (indigestion, bloating, cramping) - oral use now restricted for safety

Evidence: 1
Label: Indigestion
Infection (general)[4]Traditional · 1/10

inferred from antimicrobial action

Evidence: 1
Label: Infection (general)
Inflammation (general)[4]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Inflammation (general)
Liver support[4]Traditional · 1/10

inferred from choleretic action

Evidence: 1
Label: Liver support
Menstrual cramps[4]Traditional · 1/10

inferred from antispasmodic action

Evidence: 1
Label: Menstrual cramps
Muscle spasm[4]Traditional · 1/10

inferred from antispasmodic action

Evidence: 1
Label: Muscle spasm
Pain (general)[4]Traditional · 1/10

inferred from analgesic action

Evidence: 1
Label: Pain (general)
Skin irritation[4]Traditional · 1/10

inferred from anti-inflammatory action

Evidence: 1
Label: Skin irritation
Warts[4]Traditional · 1/10

Fresh orange latex traditionally dabbed on warts

Evidence: 1
Label: Warts
Wounds[4]Traditional · 1/10

inferred from antimicrobial action

Evidence: 1
Label: Wounds
Arthritis / joint pain[12, 13]Good · 8/10

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain; General joint pain and arthritis support

Evidence: 8
Label: Arthritis / joint pain
Back pain[12, 13, 14, 15]Strong · 9/10

Effective at standardised doses (~50-60 mg harpagoside/day); an aqueous extract was non-inferior to rofecoxib for short-term chronic low back pain; Relief of chronic non-specific low back pain

Evidence: 9
Label: Back pain
Headache[12, 13]Good · 8/10

inferred from analgesic action

Evidence: 8
Label: Headache
Inflammation (general)[12, 13]Good · 8/10

inferred from anti-inflammatory action

Evidence: 8
Label: Inflammation (general)
Pain (general)[12, 13, 14, 15]Strong · 9/10

Anti-inflammatory and analgesic for osteoarthritis (hip and knee) pain; Effective at standardised doses (~50-60 mg harpagoside/day); an aqueous extract was non-inferior to rofecoxib for short-term chronic low back pain; General joint pain and arthritis support; Relief of chronic non-specific low back pain

Evidence: 9
Label: Pain (general)
Skin irritation[12, 13]Good · 8/10

inferred from anti-inflammatory action

Evidence: 8
Label: Skin irritation

Safety, Cautions & Contraindications

Safety note[13, 14]Serious

SERIOUS: oral greater celandine can cause acute idiosyncratic liver injury (hepatocellular hepatotoxicity with jaundice). Multiple reported cases - dozens of herb-induced liver injury reports in the literature, with continuing recent case reports - led regulators to restrict or suspend oral products. Do not take internally if you have any liver disease, and stop immediately and seek care at any sign of liver problems (jaundice, dark urine, upper-abdominal pain).

Safety note[4, 13]Caution

Avoid in pregnancy and breastfeeding. The fresh orange latex is irritant and caustic - keep it away from the eyes and broken skin.

Safety note[13]Caution

Because it is a bitter that increases stomach-acid and bile secretion, it is contraindicated in active peptic ulcer, gastritis and (without medical supervision) gallstones.

Safety note[13]Caution

May add to the effect of anticoagulants (e.g. warfarin) and may influence blood sugar, blood pressure and heart rhythm; use caution with these medicines.

Safety note[13]Caution

Avoid during pregnancy (oxytocic/uterine effect) and while breastfeeding.

External Ids

Gbif: 5334186
Wikidata: Q156807
Gbif: 3585335
Powo: urn:lsid:ipni.org:names:675824-1
Wikidata: Q386675

Botanical Description

Branching perennial herb with soft, brittle, hairy stems that exude a distinctive bright orange-yellow latex (sap) when cut or broken. The leaves are deeply lobed, pale bluish-green beneath, giving a delicate, almost fern-like appearance. Small, four-petalled, bright yellow flowers are borne in loose umbel-like clusters.[4]

Height: 30-90 cm
Habit: Branching, brittle-stemmed perennial herb
Leaves: Deeply lobed, pale bluish-green beneath
Flowers: Small, four-petalled, bright yellow, in loose umbel-like clusters
Stem: Soft, brittle, hairy, exuding bright orange-yellow latex when broken
Root: Branching taproot, also exuding orange latex
Fruit: Slender, curved capsule
Flowering Period: April-September

Low-growing, sprawling perennial herb with trailing stems and deeply lobed, greyish-green leaves arising from a large, fleshy primary taproot bearing smaller secondary storage tubers (the part used medicinally). Striking funnel-shaped, purplish-pink to violet flowers give way to a distinctive woody fruit covered in long, hooked spines - the origin of the common name.[13]

Height: Trailing stems to 1.5 m, low-growing
Habit: Low-growing, sprawling perennial herb
Leaves: Deeply lobed, greyish-green
Flowers: Funnel-shaped, purplish-pink to violet
Stem: Trailing, sprawling stems
Root: Large primary taproot with smaller secondary storage tubers (the medicinal part)
Fruit: Woody capsule covered in long, hooked spines ('devil's claw')
Flowering Period: Summer (during the rainy season)

Habitat

Grows in shaded, nutrient-rich ground - hedgerows, walls, waste ground and woodland edges, often near old buildings; native to Europe and Western Asia and naturalised in North America.[4]

Native to the dry savannas and semi-desert regions of southern Africa, particularly the Kalahari Desert region of Namibia, Botswana and South Africa.[13]

Harvesting

The flowering aerial parts are cut in spring to summer; the fresh orange latex is collected by breaking a stem or leaf as needed for topical (wart) use. Given the documented hepatotoxicity of oral preparations, harvesting for internal use is not recommended.[4]

Parts: Aerial parts (and fresh orange latex)
Season: Spring to summer, while flowering

The secondary root tubers are dug by hand, sliced and dried in the sun, traditionally by local harvesters in southern Africa; sustainable wild-harvesting practices are important given the plant's slow growth and habitat sensitivity.

Parts: Secondary root tuber

Traditional Uses

Greater celandine has a long European folk history, reflected in its name 'tetterwort', as a topical remedy for warts and skin blemishes (the fresh orange latex dabbed directly on), and internally as a bitter choleretic digestive remedy for biliary and upper-abdominal dyspepsia - though oral use is now medically restricted because of documented liver injury.[4]

Devil's claw has a long southern African traditional-medicine history as a remedy for fever, pain and digestive complaints, and is now one of the most clinically studied herbal analgesics for osteoarthritis and chronic low back pain, with standardised extracts showing efficacy comparable to some conventional analgesics in trials.[13]

Preparations

Fresh latex (topical, warts only)[4]

Fresh orange latex from a broken stem dabbed directly onto warts, the classic external folk use; kept well away from eyes, mucous membranes and broken skin.

Infusion/tincture (historical, oral - restricted)[13]

Historically taken as an infusion or tincture for biliary dyspepsia, but oral use is now restricted in several jurisdictions due to hepatotoxicity risk and should only be considered under professional supervision, if at all.

Standardised extract[13, 14]

Root tuber extract standardised to harpagoside content, taken as capsules or tablets; the best-studied clinical form for osteoarthritis and back pain.

Dosage

All internal preparations[13, 14]

Because of a documented risk of acute liver injury, no internal dose is given here; oral use should be avoided, especially by anyone with liver disease, and any sign of jaundice, dark urine or upper-abdominal pain warrants immediate medical attention. Educational reference only, not a prescription.

Standardised extract[14]

Clinical trials for osteoarthritis and back pain commonly use extracts providing around 50-60 mg harpagoside daily. Educational reference only, not a prescription.

References

REF-0770, REF-0771, REF-0772, REF-0460, REF-2264, REF-2265, REF-2266, REF-2267, REF-2268, REF-2269, REF-2270, REF-2271
REF-1829, REF-1830, REF-1831, REF-1832, REF-1833, REF-1834, REF-1835, REF-1836, REF-1837, REF-1838, REF-1839

Lookalikes Review

Outcome: none-known
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-07
Outcome: none-known
Reviewed By: Omnia Sana (owner-authorized)
Reviewed Date: 2026-07-07

References & Sources

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  2. Koriem, K.M.M., Arbid, M.S. and Asaad, G.F (2012) 'Chelidonium majus leaves methanol extract and its chelidonine alkaloid ingredient reduce cadmium-induced nephrotoxicity in rats', Journal of Natural Medicines, 67(1), pp. 159-167. doi:10.1007/s11418-012-0667-6 Preclinical
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  5. Popovic, A., Deljanin, M., Popovic, S., Todorovic, D., Djurdjevic, P., Matic, S., Stankovic, M., Avramovic, D. and Baskic, D (2021) 'Chelidonium majus crude extract induces activation of peripheral blood mononuclear cells and enhances their cytotoxic effect toward HeLa cells', International Journal of Environmental Health Research, 32(7), pp. 1554-1566. doi:10.1080/09603123.2021.1897534 Preclinical
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  6. Shen, L., Lee, S.A., Joo, J.C., Hong, E., Cui, Z.Y., Jo, E., Park, S.J. and Jang, H.J (2022) 'Chelidonium majus induces apoptosis of human ovarian cancer cells via ATF3-mediated regulation of Foxo3a by Tip60', Journal of Microbiology and Biotechnology, 32(4), pp. 493-503. doi:10.4014/jmb.2109.09030 Preclinical
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  8. Warowicka, A., Qasem, B., Dera-Szymanowska, A., Wolun-Cholewa, M., Florczak, P., Horst, N., Napierala, M., Szymanowski, K., Popenda, L., Bartkowiak, G., Florek, E., Gozdzicka-Jozefiak, A. and Mlynarz, P (2021) 'Effect of protoberberine-rich fraction of Chelidonium majus L. on endometriosis regression', Pharmaceutics, 13(7), pp. 931. doi:10.3390/pharmaceutics13070931 Preclinical
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  9. Kadan, G., Gozler, T. and Hesse, M (1992) '(+)-Norchelidonine from Chelidonium majus', Planta Medica, 58(5), pp. 477. doi:10.1055/s-2006-961523 Preclinical
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  10. Musidlak, O., Warowicka, A., Broniarczyk, J., Adamczyk, D., Gozdzicka-Jozefiak, A. and Nawrot, R (2022) 'The activity of Chelidonium majus L. latex and its components on HPV reveal insights into the antiviral molecular mechanism', International Journal of Molecular Sciences, 23(16), pp. 9241. doi:10.3390/ijms23169241 Preclinical
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  13. Teschke, R., Frenzel, C., Glass, X., Schulze, J. and Eickhoff, A (2012) 'Greater Celandine hepatotoxicity: a clinical review', Annals of Hepatology. doi:10.1016/s1665-2681(19)31408-5 Clinical study
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  14. Ciornolutchii, V., Ismaiel, A., Sabo, C.M., Al Hajjar, N., Seicean, A. and Dumitrascu, D.L (2024) 'A Hidden Cause of Hypertransaminasemia: Liver Toxicity Caused by Chelidonium Majus L. Report of Two Cases of Herb-Induced Liver Injury and Literature Review', American Journal of Therapeutics, 31(4), pp. e382--e387. doi:10.1097/MJT.0000000000001708 Clinical study
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  1. Mncwangi, N., Chen, W., Vermaak, I., Viljoen, A.M. and Gericke, N (2012) 'Devil's Claw - a review of the ethnobotany, phytochemistry and biological activity of Harpagophytum procumbens', Journal of Ethnopharmacology, 143(3), pp. 755-771. doi:10.1016/j.jep.2012.08.013 Meta-analysis / review
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  3. Mariano, A., Bigioni, I., Mattioli, R., Di Sotto, A., Leopizzi, M., Garzoli, S., Mariani, P.F., Dalla Vedova, P., Ammendola, S. and Scotto d'Abusco, A (2022) 'Harpagophytum procumbens Root Extract Mediates Anti-Inflammatory Effects in Osteoarthritis Synoviocytes through CB2 Activation', Pharmaceuticals, 15(4), pp. 457. doi:10.3390/ph15040457 Preclinical
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Generated automatically from the Omnia Sana plant database and its cited sources. For educational purposes only — not medical advice. Always consult a qualified practitioner before using medicinal plants.