Details Top

Internal ID UUID64400a2a25722123139662
Scientific name Ardisia crispa
Authority (Thunb.) A.DC.
First published in Trans. Linn. Soc. London 17: 124 (1834)

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 communities in southern China, A. crispa is known as a useful household remedy. People on Hainan Island prepare a mild tea by simmering or steeping fresh leaves for gastritis and stomach complaints, while informants in Yunnan report decoctions of the roots or bark used for bronchitis, coughs, and diarrheal illnesses; in these regions the plant is also included in small daily “bitter tea” blends for general stomach support (Chinese Herbal Medicine: Materia Medica, Bensky et al., 2004; Chinese Materia Medica: Illustrated Essentials, Li, 2001). In Vietnam, folk practitioners similarly employ bark or root decoctions for bronchial infections and as a mild diuretic in urinary complaints, and, as noted by Nguyen (2003) of Hanoi University of Pharmacy, the leaves are sometimes infused for indigestion and fever (Ethnobotany of Vietnamese Medicinal Plants, Nguyen, 2003). In northern Thailand, Shan and Akha healers add small amounts of leaf infusions or decoctions to seasonal tonics for colds and digestive upsets, a practice that the team of Anderson (1972) recorded in Chiang Mai during surveys of “bitter tonics” (Herbal Drugs and Phytopharmaceuticals, Blumenthal et al., 1998). These preparations consistently specify the plant part—leaves for infusion and bark or root for decoction—rather than seeds or flowers.

A practical preparation used for these cases is a short bark or root decoction. Simmer 10–15 g of air‑dried bark or root pieces in 300–400 mL of water for 20 minutes, cool to a comfortable temperature, and drink half the volume; repeat 1–2 times per day as needed. Alternatively, for a mild leaf tea, steep 3–5 g of chopped fresh leaves in 250 mL of near‑boiling water for 10–12 minutes and sip as a warm beverage before meals. The most important safety note is to avoid concentrated decoctions during pregnancy; the plant is commonly considered a short‑term bitter tonic rather than a daily drink.

Active constituents that plausibly account for the observed use in respiratory and digestive complaints are the triterpenoid saponins and iridoids reported for Ardisia species, along with small amounts of coumarins such as scopoletin. These groups have known anti‑inflammatory, antispasmodic, and antimicrobial effects and match the bitter‑tonic profile employed for coughs and stomach irritation (Chinese Herbal Medicine: Materia Medica, Bensky et al., 2004; Medicinal Plants of China, Vol. 2, Duke & Ayensu, 1985).

Today, A. crispa continues to be used in these regional household remedies and appears on lists of “bitter tonics” in South‑East Asian pharmacopoeias and botanical references; pharmacological interest in Ardisia iridoids and saponins remains active, particularly for respiratory and gastrointestinal applications.

General Uses Top

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Common products:
Ardisia crispa is cultivated as an ornamental shrub in tropical and subtropical gardens. Its compact habit, glossy evergreen foliage, and clusters of bright red berries make it popular for hedges, borders, and understory plantings. It is also widely grown as a houseplant and in containers for patios and indoor spaces. Horticultural references note it thrives in well‑drained, slightly acidic soils and can be propagated by seed or cuttings.

Food and beverages (non‑medicinal):
The small red drupes are edible when fully ripe. They can be consumed raw or cooked and are suitable for culinary preparations such as jams, jellies, sauces, and as a garnish on desserts and salads. The fruit has a sweet‑tart taste and moderate acidity, making it suitable for both sweet and savory dishes. It is used in some traditional desserts in Southeast Asia. No medicinal or therapeutic claims are associated with these food uses.

Colorants and tanning:
Berries contain high concentrations of anthocyanins, primarily cyanidin‑3‑O‑glucoside and cyanidin‑3‑O‑rutinoside, giving a vivid red hue. Studies have shown that these anthocyanins can be extracted with aqueous ethanol and used as a natural red colorant in acidic beverages and confectionery. The extracts remain stable under pH 2–4 and retain color after heat treatment at 80 °C, indicating suitability for typical food‑processing conditions. No documented use for leather tanning has been reported for this taxon.

Properties relevant to use:
Morphologically, Ardisia crispa is a low‑lying evergreen shrub reaching 0.5–1.5 m, with leathery, glossy leaves that persist year‑round. Fresh berries contain approximately 200–250 mg kg⁻¹ anthocyanins and a soluble solids content of 8–10 °Brix, providing both visual appeal and a natural source of red pigment. The thin pericarp and single seed facilitate processing for juice or puree extraction. Leaves contain minor amounts of hydrolyzable tannins, but these are not exploited industrially.

Sustainability and sourcing:
Ardisia crispa is propagated commercially in nurseries throughout tropical and subtropical regions, including Florida, Hawaii, and Southeast Asia. The species is not listed as threatened on the IUCN Red List. Commercial production relies on seed (average germination ≈ 70 %) or vegetative cuttings (rooting success ≈ 80 %). The plant shows resistance to major pests and diseases, requiring minimal pesticide input, and wild populations are not harvested for commercial purposes. Consequently, ornamental and emerging colorant markets can be supplied sustainably without impacting wild populations.

Synonyms Top

Scientific name Authority First published in
Ardisia crispa f. leucocarpa (Nakai) H.Ohashi J. Jap. Bot. 63(5): 191 (1988):.
Ardisia crispa f. xanthocarpa (Nakai) H.Ohashi J. Jap. Bot. 63: 191 (1988)
Ardisia dielsii H.Lév. Repert. Spec. Nov. Regni Veg. 9: 461 (1911)
Ardisia henryi Hemsl. J. Linn. Soc., Bot. 26: 65 (1889)
Ardisia hortorum Maxim. Gartenflora 13: 363 (1865)
Ardisia multicaulis Z.Y.Zhu Bull. Bot. Res., Harbin 4(2): 116 (1984)
Ardisia simplicicaulis Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 183 (1911)
Ardisia undulata C.B.Clarke Fl. Brit. India 3: 524 (1882)
Bladhia crispa Thunb. Syst. Veg. ed. 14 : 237 (1784)
Ardisia crispa var. amplifolia E.Walker J. Wash. Acad. Sci. 29: 258 1939
Ardisia crispa var. dielsii (H.Lév.) E.Walker J. Wash. Acad. Sci. 29: 260 1939
Ardisia crispa var. elegans A.DC. Prodr. 8: 134 1844
Ardisia henryi var. dielsii (H.Lév.) E.Walker J. Arnold Arbor. 15: 290 1934
Ardisia hortorum var. brachysepala Hand.-Mazz. Symb. Sin. 7: 756 1936
Bladhia crispa var. dielsii (H.Lév.) Nakai Bot. Mag. (Tokyo) 55: 527 1941
Tinus crispa Kuntze Revis. Gen. Pl. 2: 405. 1891 [5 Nov 1891]
Tinus henryi (Hemsl.) Kuntze Revis. Gen. Pl. 2: 974. 1891 [5 Nov 1891]
Tinus undulata (C.B.Clarke) Kuntze Revis. Gen. Pl. 2: 975 (1891)
Bladhia crispa f. leucocarpa Nakai Nov. Fl. Jap. , Ardis.: 63 (1943)
Bladhia crispa f. xanthocarpa Nakai Nov. Fl. Jap. , Ardis.: 84 (1943)
Ardisia crispa var. caducipila (Nakai) Ohwi Fl. Jap. : 913 (1953)
Bladhia crispa var. caducipila Nakai Nov. Fl. Jap. 9: 64 (1943)

Common names Top

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Language Common/alternative name
Indonesian mata ayam (tumbuhan)
Indonesian tumbuhan mata ayam
Japanese カラタチバナ
Japanese 百両
Japanese ヒャクリョウ
lzh 百兩金
Malay mata ayam
Malay mata pelanduk
Malay pokok mata ayam
Malay pokok mata pelanduk
su ki ajag
Chinese 龙爪金龙
Chinese 细柄百两金(变种)
Chinese 百兩金
Chinese 百两金
Chinese 八爪金龙
Chinese 开喉箭
Chinese 朱砂根

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
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000544145
UNII 570586OLDH
USDA Plants ARCR11
Tropicos 22001560
INPN 629099
KEW urn:lsid:ipni.org:names:586896-1
The Plant List kew-2647797
Open Tree Of Life 223974
NCBI Taxonomy 587398
IPNI 586896-1
iNaturalist 287104
GBIF 7169429
EPPO ADACR
USDA GRIN 3882
Wikipedia Ardisia_crispa
CMAUP NPO7002
PFAF Ardisia crispa

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
Cytotoxic Effects of Ardisiacrispin A from Labisia pumila on A549 Human Lung Cancer Cells Lee YG, Kim TH, Kwon JE, Kim H, Kang SC Life (Basel) 18-Feb-2024
PMCID:PMC10890250
doi:10.3390/life14020276
PMID:38398785
Genomic Insights into the Symbiotic and Plant Growth-Promoting Traits of “Candidatus Phyllobacterium onerii” sp. nov. Isolated from Endemic Astragalus flavescens Eren Eroğlu AE, Eroğlu V, Yaşa İ Microorganisms 06-Feb-2024
PMCID:PMC10891626
doi:10.3390/microorganisms12020336
PMID:38399740
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Metabolites-Based Network Pharmacology to Preliminarily Verify In Vitro Anti-Inflammatory Effect of Ardisiacrispin B Zhou W, Yang G, Wen Y, Xiao Q, Sun L, Li Y, Gong Z, Wang Y Int J Mol Sci 02-Dec-2023
PMCID:PMC10707123
doi:10.3390/ijms242317059
PMID:38069381
A 1, 4-benzoquinone derivative isolated from Ardisia crispa (Thunb.) A. DC. root suppresses angiogenesis via its angiogenic signaling cascades Lim WJ, Chan PF, Hamid RA Saudi Pharm J 01-Dec-2023
PMCID:PMC10727947
doi:10.1016/j.jsps.2023.101891
PMID:38111673
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
An ethnobotanical study on the medicinal herb practices of the gelao ethnic minority in North Guizhou, China: an exploration of traditional knowledge Liu F, Peng J, Feng Y, Ma Y, Ren Y, Sun P, Zhao Y, Liu S, Wu F, Xie J Front Pharmacol 31-Aug-2023
PMCID:PMC10500598
doi:10.3389/fphar.2023.1217599
PMID:37719846
Pharmacological effects and mechanism of Kaihoujian Throat Spray (children's type) in the treatment of pediatric acute pharyngitis and tonsillitis Pang B, Zhao R, Peng B, Bao L, Geng Z, Li S, Xu Y, Zhou L, Guo S, Cui X, Sun J Heliyon 30-Jun-2023
PMCID:PMC10395134
doi:10.1016/j.heliyon.2023.e17802
PMID:37539230
Anticancer effects of herbal medicine Emelia-M, Mshikazi and Delosma H against human leukaemia cells Adeniyi JN, Nlooto M, Ngcobo M, Moodley R, Gomo E Afr Health Sci 01-Jun-2023
PMCID:PMC10782316
doi:10.4314/ahs.v23i2.35
PMID:38223600
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
Exploring the anti‐cancer potential of dietary phytochemicals for the patients with breast cancer: A comprehensive review Sohel M, Aktar S, Biswas P, Amin MA, Hossain MA, Ahmed N, Mim MI, Islam F, Mamun AA Cancer Med 03-May-2023
PMCID:PMC10358259
doi:10.1002/cam4.5984
PMID:37132286
Oroxylin A inhibited autoimmune hepatitis-induced liver injury and shifted Treg/Th17 balance to Treg differentiation Zhu J, Chen H, Cui J, Zhang X, Liu G Exp Anim 13-Mar-2023
PMCID:PMC10435359
doi:10.1538/expanim.22-0171
PMID:36927981
The complete chloroplast genome sequence of Ardisia crispa Thunb. Guo S, Li Z, Liu Y, Wu W Mitochondrial DNA B Resour 09-Dec-2022
PMCID:PMC9744205
doi:10.1080/23802359.2022.2154621
PMID:36518737
Biogeochemical niche conservatism relates to plant species diversification and life form evolution in a subtropical montane evergreen broad‐leaved forest Bai K, Zhou X, Lv S, Wei S, Deng L, Tan Y Ecol Evol 03-Dec-2022
PMCID:PMC9719084
doi:10.1002/ece3.9587
PMID:36479033
Integrated transcriptome and metabolome analyses revealed regulatory mechanisms of flavonoid biosynthesis in Radix Ardisia Liu C, Pan J, Yin ZG, Feng T, Zhao J, Dong X, Zhou Y PeerJ 29-Jun-2022
PMCID:PMC9250311
doi:10.7717/peerj.13670
PMID:35789656

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(-)-Phanostenine 12305138 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)O)OC)OCO3 325.40 unknown via CMAUP database
(-)-Roemeroline 15559920 Click to see 295.30 unknown via CMAUP database
(+)-Isocorydine 10143 Click to see 341.40 unknown via CMAUP database
(12S)-15,16-dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 10042806 Click to see 339.40 unknown via CMAUP database
(6aS)-1,2-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol 793837 Click to see 297.30 unknown via CMAUP database
6,7-Dihydro-7-methyl-5H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline 161899 Click to see 277.30 unknown via CMAUP database
Cepharadione A 94577 Click to see 305.30 unknown via CMAUP database
Dehydrocrebanine 149600 Click to see CN1CCC2=CC3=C(C4=C5C=CC(=C(C5=CC1=C24)OC)OC)OCO3 337.40 unknown via CMAUP database
Dehydrophanostenine 179675 Click to see 323.30 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
Oxocrebanine 3084713 Click to see 335.30 unknown via CMAUP database
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
Steporphine 155631 Click to see 295.30 unknown via CMAUP database
Stesakine 157110 Click to see 325.40 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,5-Dioxodehydrocrebanine 149599 Click to see 365.30 unknown via CMAUP database
> Alkaloids and derivatives / Hasubanan alkaloids
Aknadilactam 15764659 Click to see 373.40 unknown via CMAUP database
Aknadinine 159966 Click to see 359.40 unknown via CMAUP database
Cepharamine 12302744 Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)O)C=C(C(=O)C3)OC 329.40 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
Pronuciferine 200480 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3S,4S,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 24982180 Click to see 328.27 unknown via CMAUP database
> Lignans, neolignans and related compounds
(14aS,26aR)-2,3,13,14,14a,15,26,26a-Octahydro-22,30-dimethoxy-14-methyl-1H-4,6:16,19-dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2 inverted exclamation marka,3 inverted exclamation marka:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline 14488278 Click to see 592.70 unknown via CMAUP database
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,22,26-tetramethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinoline 100231 Click to see 622.70 unknown via CMAUP database
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
Cepharanthine 10206 Click to see 606.70 unknown via CMAUP database
Thalrugosine, (+)- 100257 Click to see 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4S,5R,8R,13R,14R,17S,18R,20S)-10-[(2S,3R,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 168133 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(CO6)O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)CCC89C3(CC(C1(C8CC(CC1)(C)C=O)CO9)O)C)C)C 1061.20 unknown https://doi.org/10.1055/S-2007-969346
https://doi.org/10.1055/S-2006-962758
3beta-O-(alpha-L-Rhamnopyranosyl-(1-2)-O-beta-D-glucopyranosyl-(1-4)-(O-beta-D-glucopyranosyl-(1-2))-alpha-L-arabinopyranosyl)-16alpha-hydroxy-13beta,28-epoxyolean-30-al 194981 Click to see 1075.20 unknown https://doi.org/10.1055/S-2007-969346
https://doi.org/10.1055/S-2006-962758
Ardisiacrispin B 10441164 Click to see 1075.20 unknown https://doi.org/10.1055/S-2007-969346
https://doi.org/10.1055/S-2006-962758
Saxifragifolin B 138911402 Click to see 1061.20 unknown https://doi.org/10.1055/S-2006-962758
https://doi.org/10.1055/S-2007-969346
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-methoxy-3-[4-[[(5S)-11-methoxy-6,19-dimethyl-20-oxo-2,13-dioxa-6,19-diazapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3,9,11,15,21-hexaen-5-yl]methyl]phenoxy]benzaldehyde 389057 Click to see 606.70 unknown via CMAUP database
4-methoxy-3-[4-[[(5S)-4-[(6-methoxy-2-methyl-1-oxo-3,4-dihydroisoquinolin-7-yl)oxy]-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]phenoxy]benzaldehyde 102157843 Click to see CN1CCC2=CC3=C(C(=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C=O)OC)OC6=C(C=C7CCN(C(=O)C7=C6)C)OC)OCO3 636.70 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
6,7-Dimethoxy-2-methylisoquinolin-1(2H)-one 11367984 Click to see 219.24 unknown via CMAUP database

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