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Manjishtha

Rubia cordifolia

Manjishtha (Rubia cordifolia) is a plant drug, also called Manjistha and Mamjitha. Rubiadin is moderately lipophilic with reasonable absorption. Purpurin shows enhanced absorption with fatty meals. First-pass hepatic metabolism is moderate. Topical absorption of anthraquinones is good through intact skin.

Key facts
Botanical nameRubia cordifolia
FamilyRubiaceae · other entries in this family
OrderGentianales
Pharmacopoeia statusMonographed in the Ayurvedic Pharmacopoeia of India (API). Classified in Charaka Samhita as varnya (complexion enhancer), jvarahara (antipyretic), visaghna (detoxifier), and rasayana (rejuvenator). European Medicines Agency (EMA) issued a Community Herbal Monograph on Rubia cordifolia L., radix (2022). No standalone WHO monograph identified. Listed in multiple traditional pharmacopeias across Ayurveda, TCM, and Unani systems.
Taxon identifiersGBIF 2892192 · Wikidata Q3237818 · NCBI Taxonomy 339321
Names in other languages
Sanskritमञ्जिष्ठा (mañjiṣṭhā)
Hindiमंजीठ (maṃjīṭha)
Tamilமஞ்சிட்டி

Sources: Ayurvedic Pharmacopoeia of India, MANJISTHA (Stem) monograph, Hindi "Manjitha, Manjit" (Urdu "Majeeth"); MMPND Rubia page, Hindi "Majith, Manjit".; MMPND Rubia page, Sanskrit line "Gandari, Manjishta, Manjishtha, Manjistha, Manjit, Munjistha"; Ayurvedic Pharmacopoeia of India monograph title MANJISTHA for Rubia cordifolia.; efloraofindia, Rubia cordifolia page, Tamil "மஞ்சிட்டி (mancitti)"; Ayurvedic Pharmacopoeia of India, MANJISTHA monograph, Tamil "Manjitte".. How we source.

The evidence at a glance

12papers on this site for this drug, published 2011 to 2026, every one with a DOI.

  • 1Randomised controlled trials
  • 9Other clinical studies and reviews
  • 2Laboratory and animal studies

A count is not a conclusion and a tier is a study design, not a verdict. Each paper is listed with what it measured on the page below. See the research index for how papers are tiered.

Names and identification

LanguageName
EnglishManjishtha

What is it made of?

The marker compounds are listed under Dosage forms and preparation, below.

How does it work?

  • Anticancer (hexapeptides): Cyclic hexapeptides RA-V and RA-VII inhibit multiple cancer signaling pathways. Mollugin inhibits cell proliferation via suppression of HER2/Akt/SREBP-1c/FAS pathway in breast and ovarian cancer cells.
  • Anticancer (NF-kB): Mollugin suppresses NF-kB activation, thereby inhibiting HER2 expression in cancer cells.
  • Anti-inflammatory: Mollugin suppresses pro-inflammatory mediators including iNOS, COX-2, TNF-alpha, and IL-1beta in LPS-stimulated BV2 cells in a concentration-dependent manner.
  • Antioxidant: Anthraquinones with hydroxyl substitutions modulate antioxidant activity through radical stabilization and metal chelation.
  • Neuroprotective: Purpurin exhibits neuroprotection through antioxidant mechanisms and DNA intercalation properties.
  • Antimicrobial: Structure-activity relationships of anthraquinones reveal antibacterial properties linked to hydroxyl group positioning.
  • Gut microbiota modulation: Prebiotic-like effects suggested in a small human pilot RCT (16S rRNA profiling).
  • Key active constituents: Alizarin, munjistin, rubiadin, purpurin, mollugin, cyclic hexapeptides (RA-V, RA-VII), and xanthopurpurin.

What do recent studies show?

Only studies that could be traced to a published paper are listed here. An absence here means we could not identify the source, not that no work exists.

Recent safety updates

  • Limited clinical safety data; few pharmacokinetic and toxicity studies in humans available.
  • Ethanol extract toxicity study: harmful effects on liver observed at doses of 100-1000 mg/kg body weight in rats. LD50 higher than 1000 mg/kg.
  • Contraindicated in pregnancy and lactation unless prescribed by healthcare professional.
  • May interact with anticoagulant medications, increasing bleeding risk.
  • May discolor urine, perspiration, tears, and breast milk (harmless but notable).
  • Use with caution in individuals with kidney disorders.
  • Common side effects: mild gastrointestinal upset, allergic reactions (rash/itching), nausea in some cases.
  • Hypersensitivity to Rubia cordifolia or its components is a contraindication.
  • Human toxic dose not yet established from animal studies; clinical trials needed.

Dosage forms and preparation

Dosage Forms: Churna (powder), Kwatha (decoction), Capsules, Tablets, Asava/Arishta, Taila (medicated oil), Topical cream/gel, Ghrita (medicated ghee)

Standard Dosage: 3-6 g root powder per day in divided doses; 50-100 mL decoction twice daily; 500-1000 mg standardized extract daily; 15-30 mL Arishta after meals

Optimal Timing: Between meals for blood purification; morning for skin health; Arishta after meals; topical application morning and evening

Storage: Store in airtight, light-resistant (amber) containers below 25 deg C. Anthraquinones degrade with light exposure. Root powder protected from moisture. Arishta at room temperature in glass containers. Topical products at 15-25 deg C.

Marker Compounds: Alizarin, Purpurin, Munjistin, Rubiadin, Rubiadinmethylether, Mollugin, Furanoquinones, Beta-sitosterol

Synergistic Combinations

Published research

Literature indexed in PubMed that concerns this subject, grouped by study type. A paper appearing here is a record of what has been published, not evidence that the subject works, and laboratory or animal results do not transfer to people. Study titles link to PubMed so you can read the source rather than take our word.

Randomised controlled trials1

  1. Peterson CT, Pourang A, Dhaliwal S and others. 2020. Modulatory Effects of Triphala and Manjistha Dietary Supplementation on Human Gut Microbiota: A Double-Blind, Randomized, Placebo-Controlled Pilot StudyJournal of alternative and complementary medicine (New York, N.Y.). PMID 32955913 · doi:10.1089/acm.2020.0148

Other clinical studies and reviews9

  1. Sharma D, Jain D, Bhatia D. 2026. Unveiling the Modern Therapeutic Properties and Folk Medicinal Riches of Rubia cordifoliaRecent patents on biotechnology. PMID 41992461 · doi:10.2174/0118722083359338250611055647
  2. Xu G, Liu M, Wang Z and others. 2024. Cytotoxic and Antitumor Agents from Genus RubiaChemistry & biodiversity. PMID 39183172 · doi:10.1002/cbdv.202401498
  3. Wen M, Chen Q, Chen W and others. 2022. A comprehensive review of Rubia cordifolia L.: Traditional uses, phytochemistry, pharmacological activities, and clinical applicationsFrontiers in pharmacology. PMID 36160419 · doi:10.3389/fphar.2022.965390
  4. Murthy HN, Joseph KS, Paek KY and others. 2022. Anthraquinone Production from Cell and Organ Cultures of Rubia Species: An OverviewMetabolites. PMID 36676964 · doi:10.3390/metabo13010039
  5. Watroly MN, Sekar M, Fuloria S and others. 2021. Chemistry, Biosynthesis, Physicochemical and Biological Properties of Rubiadin: A Promising Natural Anthraquinone for New Drug Discovery and DevelopmentDrug design, development and therapy. PMID 34764636 · doi:10.2147/DDDT.S338548
  6. Shen CH, Liu CT, Song XJ and others. 2018. Evaluation of analgesic and anti-inflammatory activities of Rubia cordifolia L. by spectrum-effect relationshipsJournal of chromatography. B, Analytical technologies in the biomedical and life sciences. PMID 29793098 · doi:10.1016/j.jchromb.2018.05.021
  7. Nirumand MC, Hajialyani M, Rahimi R and others. 2018. Dietary Plants for the Prevention and Management of Kidney Stones: Preclinical and Clinical Evidence and Molecular MechanismsInternational journal of molecular sciences. PMID 29518971 · doi:10.3390/ijms19030765
  8. Shan M, Yu S, Yan H and others. 2016. A Review of the Botany, Phytochemistry, Pharmacology and Toxicology of Rubiae Radix et RhizomaMolecules (Basel, Switzerland). PMID 27999402 · doi:10.3390/molecules21121747
  9. Casetti F, Wölfle U, Gehring W and others. 2011. Dermocosmetics for dry skin: a new role for botanical extractsSkin pharmacology and physiology. PMID 21709432 · doi:10.1159/000329214

Laboratory and animal studies2

  1. Zhang D, Tang Q, He X and others. 2026. Rubimaillin ameliorates liver fibrosis by triggering the ferroptosis of activated hepatic stellate cells through targeting CPT1AInternational journal of biological sciences. PMID 41694586 · doi:10.7150/ijbs.120415
  2. Xia M, Li Z, Yang C and others. 2025. Rubia cordifolia L. extract ameliorates vitiligo by inhibiting the CXCL10/CXCL9/STAT1 signaling pathwayJournal of ethnopharmacology. PMID 40412781 · doi:10.1016/j.jep.2025.120027

Reviewed by Dr. Awadesh Pratap Singh, BAMS, on 11 October 2026. What that review covered.

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