Details Top

Internal ID UUID64404b7c2b9ca700718832
Scientific name Rumex japonicus
Authority Houtt.
First published in Nat. Hist. 2(8): 394 (1777)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Mapuche of southern Chile, Bennett et al., 2021 describe decoctions of the roots for dysentery and diarrhea. In traditional Chinese medicine, the China Pharmacopoeia (2020 edition) lists a decoction of the rhizomes/roots for dysentery with bloody stools. And in Japan, some folk practitioners have prepared teas of the aerial parts for digestive upset and also applied poultices of the fresh leaves to sores and inflamed skin, practices documented in Koyama’s ethnobotanical surveys from the 1980s. Across China, Japan, and Korea, leaves have been harvested as a potherb and boiled in water before eating, which imparts a distinctly sour tang.

A practical decoction for use with Rumex japonicus roots follows: place 9–15 g of sliced dried root in 600 ml of water, simmer uncovered until reduced to about 300 ml (approximately 20–30 minutes), then cool and strain. Drink in divided doses through the day. Because the plant is a laxative cathartic and contains anthraquinones, avoid use in pregnancy and in acute abdominal pain; people with intestinal obstruction or inflammatory bowel disease should also avoid it. Many practitioners limit use to short courses only.

The root is rich in anthraquinones such as emodin, chrysophanol, and physcion, which account for the laxative action, and in tannins, which are strongly astringent—together explaining traditional use against diarrhea and dysentery. Constituents of the aerial parts such as quercetin and related flavonoids are known antioxidant and anti-inflammatory agents, consistent with the use of leaf poultices on inflamed skin.

Clinical trials are still limited, but antimicrobial screening from Liao (2009) and anti-inflammatory activity by Yang (2012) have found both bacterial inhibition and relevant pathways affected. Extracts appear in some specialty herb catalogs, and in parts of rural East Asia the plant continues to be gathered for dietary and medicinal preparations.

General Uses Top

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Common products:
Food and beverages (non-medicinal):
Young leaves, shoots, and stems of Rumex japonicus are eaten as a leafy vegetable in Japan and Korea. In Japanese, the plant is known as gishigishi; the shoots are harvested in spring when tender and prepared by blanching, stir-frying, simmering with soy sauce and sugar, or as a namul (seasoned vegetable). The leaves are also consumed fresh in salads and as a vegetable side dish. In Korea, the shoots are treated similarly. All products are prepared as food; no medicinal claims are implied.

References:
Japanese Wikipedia “ギシギシ” (Rumex japonicus) – entries on uses in Japan as food.
Korean sources on Korean names and food usage of Rumex japonicus (Korean Natural Species Database; Korean Wikipedia “쇠기름나무” for R. japonicus; Naver herbarium entries).

Synonyms Top

Scientific name Authority First published in
Rumex crispus subsp. japonicus (Houtt.) Kitam.
Rumex hadroocarpus Rech.f. Candollea 12: 92 (1949)
Rumex regelii F.Schmidt Reis. Amur-Land., Bot. : 167 (1868)
Rumex cardiocarpus Pamp. Nuovo Giorn. Bot. Ital. , n.s., 17: 260 (1910)
Rumex crispus var. japonicus (Houtt.) Makino Bot. Mag. (Tokyo) 8: 174 1894

Common names Top

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Language Common/alternative name
Japanese ギシギシ
Korean 참소루쟁이
Korean 참소리쟁이
Chinese 羊蹄
Chinese 羊蹄叶
Chinese 羊蹄实

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
    • Russian Far East
      • Kamchatka
      • Kuril Islands
      • Primorye
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001101700
Tropicos 26002530
KEW urn:lsid:ipni.org:names:697224-1
The Plant List tro-26002530
Open Tree Of Life 1043328
Observations.org 129727
NCBI Taxonomy 174651
IPNI 697224-1
iNaturalist 556238
GBIF 7291214
EPPO RUMJA
CMAUP NPO25658

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
SIRT3/6: an amazing challenge and opportunity in the fight against fibrosis and aging Wei W, Li T, Chen J, Fan Z, Gao F, Yu Z, Jiang Y Cell Mol Life Sci 31-Jan-2024
PMCID:PMC10830597
doi:10.1007/s00018-023-05093-z
PMID:38294557
Anti-Inflammatory Herbal Extracts and Their Drug Discovery Perspective in Atopic Dermatitis Lee JW, Kim EN, Jeong GS Biomol Ther (Seoul) 01-Jan-2024
PMCID:PMC10762282
doi:10.4062/biomolther.2023.102
PMID:38148551
Application of Zebrafish as a Model for Anti-Cancer Activity Evaluation and Toxicity Testing of Natural Products Shen Y, Sheng R, Guo R Pharmaceuticals (Basel) 01-Jun-2023
PMCID:PMC10305033
doi:10.3390/ph16060827
PMID:37375774
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Critical review on Rumex dentatus L. a strong pharmacophore and the future medicine: Pharmacology, phytochemical analysis and traditional uses Khaliq T, Akhter S, Sultan P, Hassan QP Heliyon 05-Mar-2023
PMCID:PMC10040524
doi:10.1016/j.heliyon.2023.e14159
PMID:36994390
Exploring the mechanism of physcion-1-O-β-D-monoglucoside against acute lymphoblastic leukaemia based on network pharmacology and experimental validation Liu J, Yang Y, Zeng Y, Qin X, Guo L, Liu W Heliyon 24-Feb-2023
PMCID:PMC10008983
doi:10.1016/j.heliyon.2023.e14009
PMID:36923879
Rhizobacterial compositions and their relationships with soil properties and medicinal bioactive ingredients in Cinnamomum migao Li L, Yang X, Tong B, Wang D, Tian X, Liu J, Chen J, Xiao X, Wang S Front Microbiol 16-Feb-2023
PMCID:PMC9978227
doi:10.3389/fmicb.2023.1078886
PMID:36876061
Exploring Possible Ways to Enhance the Potential and Use of Natural Products through Nanotechnology in the Battle against Biofilms of Foodborne Bacterial Pathogens Arunachalam K, Krishnan GP, Sethuraman S, Abraham SV, Krishnan ST, Venkateswar A, Arunkumar J, Shi C, MubarakAli D Pathogens 07-Feb-2023
PMCID:PMC9967150
doi:10.3390/pathogens12020270
PMID:36839543
Recent advances in constructed wetlands methane reduction: Mechanisms and methods Yu G, Chen J, Wang G, Chen H, Huang J, Li Y, Wang W, Song F, Ma Y, Wang Q, Wang M, Ling T, Shu Z, Sun J, Yu Z Front Microbiol 03-Feb-2023
PMCID:PMC9936987
doi:10.3389/fmicb.2023.1106332
PMID:36819020
Weeds: An Insidious Enemy or a Tool to Boost Mycorrhization in Cropping Systems? Trinchera A, Warren Raffa D Microorganisms 29-Jan-2023
PMCID:PMC9967897
doi:10.3390/microorganisms11020334
PMID:36838299
Ferroptosis‐modulating small molecules for targeting drug‐resistant cancer: Challenges and opportunities in manipulating redox signaling Koeberle SC, Kipp AP, Stuppner H, Koeberle A Med Res Rev 19-Jan-2023
PMCID:PMC10947485
doi:10.1002/med.21933
PMID:36658724
Surface adherence and vacuolar internalization of bacterial pathogens to the Candida spp. cells: Mechanism of persistence and propagation Khan F, Jeong GJ, Javaid A, Thuy Nguyen Pham D, Tabassum N, Kim YM J Adv Res 23-Dec-2022
PMCID:PMC10658324
doi:10.1016/j.jare.2022.12.013
PMID:36572338
The Cytotoxic and Inhibitory Effects of Plant Derivatives on Candida albicans Biofilms: A Scoping Review Loaiza-Oliva M, Arias-Durango L, Martínez-Pabón MC Molecules 23-Dec-2022
PMCID:PMC9822484
doi:10.3390/molecules28010130
PMID:36615324
Allelopathy and its application as a weed management tool: A review Khamare Y, Chen J, Marble SC Front Plant Sci 28-Nov-2022
PMCID:PMC9742440
doi:10.3389/fpls.2022.1034649
PMID:36518508

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
Homomoschatoline 145779 Click to see COC1=C(C(=C2C3=CC=CC=C3C(=O)C4=NC=CC1=C24)OC)OC 321.30 unknown via CMAUP database
Lanuginosine 97622 Click to see 305.30 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
> Benzenoids / Anthracenes
(10R)-1,3,8,10-tetrahydroxy-6-(hydroxymethyl)-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracen-9-one 90929867 Click to see C1=C(C=C(C2=C1C(C3=C(C2=O)C(=CC(=C3)O)O)(C4C(C(C(C(O4)CO)O)O)O)O)O)CO 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
(10R)-1,3,8,10-tetrahydroxy-6-methyl-10-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracen-9-one 162870638 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)O)C=C(C=C3O)O 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
(10R)-1,3,8,10-tetrahydroxy-6-methyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracen-9-one 72943853 Click to see 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
1,3,8-Trihydroxy-6-methyl-9(10H)-anthracenone 122635 Click to see 256.25 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
(10R)-1,6,8,10-tetrahydroxy-3-methyl-9-oxo-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracene-2-carboxylic acid 101437335 Click to see CC1=CC2=C(C(=C1C(=O)O)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)O)C=C(C=C3O)O 478.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
(10R)-1,8,10-trihydroxy-3-methyl-9-oxo-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracene-2-carboxylic acid 101437333 Click to see 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
(10S)-1,8,10-trihydroxy-3-methyl-9-oxo-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracene-2-carboxylic acid 101437334 Click to see 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Benzenoids / Anthracenes / Anthraquinones
((2R,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-(8-Hydroxy-6-Methyl-9,10-Dioxoanthracen-1-Yl)Oxyoxan-2-Yl)Methyl 3,4,5-Trihydroxybenzoate 5315852 Click to see 568.50 unknown via CMAUP database
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione 24867638 Click to see 256.25 unknown via CMAUP database
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see 270.24 unknown https://doi.org/10.1248/CPB.53.1594
https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
Emodin(1-) 25201450 Click to see 269.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
4-Hydroxy-2,6-Dimethoxybenzoic Acid 22616650 Click to see 198.17 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,6-Dihydroxybenzoic Acid 9338 Click to see 154.12 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethyl 3,4-Dihydroxybenzoate 77547 Click to see CCOC(=O)C1=CC(=C(C=C1)O)O 182.17 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
Nepodin 100780 Click to see 216.23 unknown https://doi.org/10.1007/BF02662162
https://doi.org/10.1039/CT9109700001
Torachrysone 5321977 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)O)OC 246.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Benzenoids / Naphthalenes / Naphthoquinones
2-Methoxystypandrone 158739 Click to see CC1=CC2=C(C(=O)C=C(C2=O)OC)C(=C1C(=O)C)O 260.24 unknown https://doi.org/10.1021/JF00034A047
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol 289 Click to see 110.11 unknown https://doi.org/10.1248/BPB.28.2225
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives / 5-unsubstituted pyrrogallols
Pyrogallol 1057 Click to see 126.11 unknown via CMAUP database
> Benzenoids / Tetralins
3-Acetyl-2-methyl-1,4,5-trihydroxy-2,3-epoxynaphthoquinol 101437332 Click to see 250.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Neral 643779 Click to see 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,12a-pentamethyl-9-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11705538 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5=C)O)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1248/CPB.53.1594
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,12a-pentamethylspiro[2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-9,2'-oxirane]-4a-carboxylic acid 11526005 Click to see 488.70 unknown https://doi.org/10.1248/CPB.53.1594
1,10,11-Trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14055735 Click to see 504.70 unknown https://doi.org/10.1248/CPB.53.1594
Jacarandic acid 13653335 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1248/CPB.53.1594
Myrianthic acid 182497 Click to see 504.70 unknown https://doi.org/10.1248/CPB.53.1594
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1248/CPB.53.1594
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Hydron;acetate 21980959 Click to see [H+].CC(=O)[O-] 60.05 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
1,10,11-Trihydroxy-1,2,6a,6b,12a-pentamethyl-9-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 73067961 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5=C)O)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1248/CPB.53.1594
1,10,11-Trihydroxy-1,2,6a,6b,12a-pentamethylspiro[2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-9,2'-oxirane]-4a-carboxylic acid 72994825 Click to see 488.70 unknown https://doi.org/10.1248/CPB.53.1594
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see 290.27 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 125528541 Click to see 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.032

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