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Cassia tora L.

Edagaja/Chakramarda
Section/Chapter Herb database/Edagaja
Botanical name(s) Cassia tora L.
Family Fabaceae
Availability Available
Contributors Team Dravyaguna
Year of publication 2026
Publisher Charak Samhita Research, Training and Skill Development Centre
DOI Awaited

Cassia tora L. (commonly known as Edagaja, Chakramarda, or the ring-worm plant) is an annual herbaceous plant widely distributed throughout tropical regions. In Ayurveda it is used for skin disorders (Kushtha), ringworm (Dadru), itching and constipation.

English name

Ring-worm plant

Therapeutic uses

Kaphavata janya vikara, kustha (skin disease), vrana (wound), dadru (tinea), pakshaghata (paralysis), vibandha (constipation), gulma (abdominal lump), krumi (worm), pama (scabies), kandu (itching), swasa (breathlessness), kasa (cough)[1]

Synonyms in Charak Samhita

Edagaja, Chakramarda

Synonyms in bhavprakasa nighantu

Prapunnata, dadrudhna, meshalochana, punnata[2]

Ayurvedic pharmacological properties

Properties
Sr.no. Pharmacological criteria Properties
1 Taste (rasa) Pungent (katu)
2 Potency (veerya) Hot (ushna)
3 Post digestion effect (vipaka) Pungent (katu)
4 Qualities (guna) Light (laghu), Rough (ruksha)
5 Actions (karma) Reduces kapha and vata

Reference in Charak Samhita and its actions

Herbs and their activities
Sr.no. Reference in Charak Samhita Activity
1 Cha.Sa.Sutra Sthana 3/3 Siddhatama churna pradeha (external application)

Dose

  • 1-3 gm of powder[1]

Important formulation

As per A.P.I.[1]

  • Nimbadi churna
  • Kasisadi ghruta
  • Maha vishagarbha taila
  • Bruhata marichyadi taila

Current availability

Available

  • India – throughout India in waste places and roadsides.

Current researches

Phytoconstituents

Only constituents supported by a checked reference are listed (one reference per class).

Phytoconstituents of Cassia tora
Class Reported constituents Plant part Reference
Anthraquinones and related compounds Chrysophanol (marker constituent), physcion, emodin, toralactone, rubrofusarin; seeds mainly anthraquinone glycosides; leaves rich in emodin, tricontan-1-ol and stigmasterol Seeds, leaves [3]

Pharmacological Activities & Therapeutic Efficacy

All findings below come from animal or in vitro experiments; no human clinical trial was identified during reference checking. The classical uses not listed below (for example vibandha and kandu) have no checked modern reference here.

Antifungal Activity (Dadru)

An 80% ethanolic extract of the seeds was fractionated and analysed by HPLC; four anthraquinones (aloe-emodin, emodin, chrysophanol and physcion) were identified. The extract and its subfractions were tested against Trichophyton mentagrophytes (a dermatophyte) by broth microdilution; the anthraquinone-rich subfractions inhibited the fungus about 4 to 8 times more strongly than the crude extract, but less potently than ketoconazole (MIC 125 versus 20 as printed in the abstract).[4]

Hepatoprotective Activity

A methanolic leaf extract (400 mg/kg, orally) protected rats against carbon-tetrachloride-induced liver injury, lowering serum SGOT, SGPT, bilirubin and alkaline phosphatase; the effect was comparable to a standard hepatoprotective agent.[5]

Anti-inflammatory and Analgesic Activity

In a master's thesis (not a journal article), a methanolic leaf extract given intraperitoneally (100–200 mg/kg) reduced egg-albumin-induced paw oedema in rats, comparable to aspirin (150 mg/kg). At 200–400 mg/kg it reduced acetic-acid-induced writhing in mice comparably to aspirin, and at 50–100 mg/kg it increased tolerance of mechanical pain in a dose-dependent manner. This is thesis-level evidence and should be confirmed by peer-reviewed studies.[6]

Safety, Toxicity, and Dosage

  • Toxicity: Limited toxicity data were found in the sources checked, so no safety margin is stated here.
  • Precautions: Use under clinical guidance, particularly in pregnancy and lactation; human safety data were not found in the sources checked.
  • Classical dose: 1–3 g of powder (see Dose above).

Summary of Therapeutic Profile

Experimental evidence for Cassia tora (see sections above for references)
Indication Part and extract Principal finding
Dermatophytosis (Dadru) Seed, 80% ethanol extract and subfractions Inhibited T. mentagrophytes in vitro; anthraquinone-rich fractions more active than crude extract
Chemical liver injury (rat) Leaf, methanolic, 400 mg/kg orally Lower SGOT, SGPT, bilirubin and ALP
Inflammation and pain (rat, mouse) Leaf, methanolic, i.p. (thesis) Reduced oedema and writhing; raised mechanical pain tolerance

References

  1. ↑ 1.0 1.1 1.2 Anonymous. The Ayurvedic Pharmacopoeia of India. Department of Ayush, Ministry of Health and Family Welfare, Govt. of India, New Delhi, Part I. 1986; Volume 3 :69
  2. ↑ Pro. Krushnachandra Chunekar, Bhavaprakash Nighantu. Reprint Edition 2020, Chaukhambha Bharati Academy, haritakyadi varga, verse no.-210
  3. ↑ Jain S, Patil UK. Phytochemical and pharmacological profile of Cassia tora Linn.: an overview. Indian J Nat Prod Resour. 2010;1(4):430–437.
  4. ↑ Charoenchai L, Chankana N. Identification of anthraquinones from Cassia tora L. seeds and antifungal activity. Interprof J Health Sci. 2018;16(1).
  5. ↑ Maity TK, Mandal SC, Mukherjee PK, Saha K, Das J, Saha BP, Pal M. Evaluation of hepatoprotective potential of Cassia tora leaf extract. Nat Prod Sci. 1997;3(2):122–126.
  6. ↑ Chidume FC. Immunogenic and some pharmacological activities of crude extracts of Cassia tora Linn (Family: Caesalpiniaceae). MSc thesis, Department of Pharmacology and Clinical Pharmacy, Ahmadu Bello University, Zaria, Nigeria; 2000.