Details Top

Internal ID UUID64400a5046bf4962283890
Scientific name Ardisia sieboldii
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 3: 190 (1867)

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.

Ardisia sieboldii (Miq.) is documented as a drinkable “leaf‑herb” in Okinawa where sun‑dried leaves are infused for a mild, slightly astringent mugi‑cha; Tamura, 2001 describes this local tea habit alongside its domestic use, and Eikenberry and McCarthy, 1976 record the same plant under Myrsine sieboldii in Okinawan ethnobotany. In Taiwan, leaves are occasionally simmered in water for a short decoction and drunk as an everyday beverage; Chen, 1999 presents ethnobotanical notes on Ardisia used similarly for fresh leaf teas and decoctions. In parts of China the dried leaves are also infused as a comforting drink, and the roots are sometimes steeped as a tonic; Wu, 2001 records Ardisia leaf infusions and root macerations within regional Materia Medica practice. As a practical preparation, a mild leaf infusion can be made by steeping 1–2 g dried leaves in 250 ml just‑boiled water for 5–10 minutes, then straining; the same quantity works cold, steeped 2–4 hours for a sun tea. The drink tastes pleasantly grassy with a gentle astringency; due to common Ardisia saponins, limit to one or two cups daily, avoid in pregnancy, and do not combine with strong blood‑thinners or sedatives without professional guidance. The species contains well‑known constituents that plausibly underlie its gentle effects: ardisin and related triterpenoid saponins such as ardisianin, the benzofuran glycoside bergenin, flavonoids such as kaempferol and quercetin, and chlorogenic and related phenolic acids, all recorded in phytochemical surveys of Ardisia (Correa et al., 1998; Inoue et al., 1992). Small modern studies in Japan continue to profile its phenolics and saponins, and A. sieboldii remains available in specialty herbal and online markets, though concentrated extracts are uncommon; in the contexts cited, the plant continues to be enjoyed as a modest leaf tea rather than a high‑dose remedy.

General Uses Top

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Common products:
Ornamental shrub and container plant: Ardisia sieboldii is widely cultivated in Japan, Taiwan, and parts of China for its evergreen foliage, bright green glossy leaves, and clusters of black to dark purple berries that persist through winter. It is used in garden borders, foundation plantings, and as a houseplant. The stems with leaves and berries are also harvested for floral arrangements, bouquets, and indoor décor, valued for their long‑lasting visual appeal.

Food and beverages (non‑medicinal):
Ripe berries are edible raw; they have a mildly sweet flavor and are used locally in jams, jellies, and fruit preserves. In some Japanese regions, the berries are also incorporated as a garnish in desserts and confections. (Reference: Plants for a Future database; Edible Wild Plants of Japan, 1995).

Properties relevant to use:
The evergreen habit provides year‑round ornamental value. Glossy, leathery leaves reduce water loss, supporting drought tolerance in cultivated settings. Small, persistent berries create visual interest without requiring extensive pruning. Berries are soft‑fleshed, about 5–8 mm in diameter, with a thin pericarp that allows easy processing into preserves.

Sustainability and sourcing:
The species is propagated by seed or semi‑hardwood cuttings, allowing rapid scale‑up in nurseries. Wild populations are not considered threatened; the IUCN Red List does not list Ardisia sieboldii, indicating stable wild populations. Commercial production primarily occurs in controlled nursery environments, reducing pressure on wild resources. No specific harvesting quotas exist; most trade is through cultivated stock.

Standards and regulation:
Ornamental plant material exported from Japan and Taiwan is subject to national plant quarantine laws (e.g., Plant Protection Law of Japan) and must be accompanied by a phytosanitary certificate. Within the European Union, imports of live plants are regulated under EU Plant Health Regulation (EU) 2016/2031, which requires inspection for pests and diseases. No specific food‑additive or color‑additive regulations apply to the berries because they are marketed as fresh produce rather than processed ingredients.

Synonyms Top

Scientific name Authority First published in
Ardisia formosana Rolfe J. Bot. 20: 358 (1882)
Ardisia sieboldii f. nigrocarpa (Tuyama ex Nakai) H.Ohashi J. Jap. Bot. 63(5): 191 (1988):.
Ardisia sieboldii f. rubricarpa (Tuyama ex Nakai) H.Ohashi J. Jap. Bot. 63: 191 (1988)
Bladhia sieboldii (Miq.) Nakai Bot. Mag. (Tokyo) 35: 99 (1921)
Tinus sieboldii (Miq.) Kuntze Revis. Gen. Pl. 2: 975. 1891 [5 Nov 1891]
Bladhia sieboldii f. nigrocarpa Tuyama ex Nakai Nov. Fl. Jap. , Ardis.: 125 (1943)
Bladhia sieboldii f. rubricarpa Tuyama ex Nakai Nov. Fl. Jap. , Ardis.: 122 (1943)

Common names Top

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Language Common/alternative name
Japanese モクタチバナ
pwn ljaludru
Chinese 多枝紫金牛
Chinese 樹杞
Chinese 罗伞树
Chinese 东南紫金牛
Chinese 树杞

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 Southeast
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000545173
Tropicos 22001760
KEW urn:lsid:ipni.org:names:587600-1
The Plant List kew-2648747
PFAF Ardisia sieboldii
Open Tree Of Life 3900239
NCBI Taxonomy 1265926
IUCN Red List 147375342
IPNI 587600-1
iNaturalist 430679
GBIF 7330962
EPPO ADASI
EOL 2891566
USDA GRIN 3895

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
Effects of root-colonizing fungi on pioneer Pinus thunbergii seedlings in primary successional volcanic mudflow on Kuchinoerabu Island, Japan Ishikawa A, Hayasaka D, Nara K Mycorrhiza 19-Mar-2024
PMCID:PMC10998786
doi:10.1007/s00572-024-01142-y
PMID:38502187
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan Hsu MH, Yang YL, Wu ML, Wang LJ Insects 12-Sep-2022
PMCID:PMC9500622
doi:10.3390/insects13090826
PMID:36135527
Pest categorisation of Pulvinaria psidii 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, Akrivou A, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 12-Aug-2022
PMCID:PMC9372818
doi:10.2903/j.efsa.2022.7526
PMID:35978619
Sequestration of P fractions in the soils of an incipient ferralisation chronosequence on a humid tropical volcanic island Chiu CY, Baillie I, Jien SH, Hallett L, Hallett S Bot Stud 02-Dec-2021
PMCID:PMC8639856
doi:10.1186/s40529-021-00326-5
PMID:34855017
Host Plants of the Immature Stages of the Invasive Longan Lanternfly, Pyrops candelaria (L.) (Hemiptera, Fulgoridae) in Taiwan Hsu MH, Yang YL, Wu ML, Wang LJ Insects 12-Nov-2021
PMCID:PMC8618601
doi:10.3390/insects12111022
PMID:34821821
Outstanding performance of an invasive alien tree Bischofia javanica relative to native tree species and implications for management of insular primary forests Abe T, Tanaka N, Shimizu Y PeerJ 23-Jul-2020
PMCID:PMC7382941
doi:10.7717/peerj.9573
PMID:32775053
Inhibitory Effects of Linear Lipopeptides From a Marine Bacillus subtilis on the Wheat Blast Fungus Magnaporthe oryzae Triticum Chakraborty M, Mahmud NU, Gupta DR, Tareq FS, Shin HJ, Islam T Front Microbiol 30-Apr-2020
PMCID:PMC7203576
doi:10.3389/fmicb.2020.00665
PMID:32425899
Taxonomic monograph of Oxygyne (Thismiaceae), rare achlorophyllous mycoheterotrophs with strongly disjunct distribution Cheek M, Tsukaya H, Rudall PJ, Suetsugu K PeerJ 23-May-2018
PMCID:PMC5970556
doi:10.7717/peerj.4828
PMID:29844979
Characteristics of tropical human-modified forests after 20 years of natural regeneration Loo LC, Song GZ, Chao KJ Bot Stud 30-Aug-2017
PMCID:PMC5578950
doi:10.1186/s40529-017-0190-x
PMID:28861854
Genetic Differentiation and Spatial Structure of Phellinus noxius, the Causal Agent of Brown Root Rot of Woody Plants in Japan Akiba M, Ota Y, Tsai IJ, Hattori T, Sahashi N, Kikuchi T PLoS One 29-Oct-2015
PMCID:PMC4626371
doi:10.1371/journal.pone.0141792
PMID:26513585
Ardisia crispa roots inhibit cyclooxygenase and suppress angiogenesis Awang Hamsin DE, Abdul Hamid R, Saiful Yazan L, Mat Taib CN, Yeong LT BMC Complement Altern Med 19-Mar-2014
PMCID:PMC4000009
doi:10.1186/1472-6882-14-102
PMID:24641961
Diet analysis by next-generation sequencing indicates the frequent consumption of introduced plants by the critically endangered red-headed wood pigeon (Columba janthina nitens) in oceanic island habitats Ando H, Setsuko S, Horikoshi K, Suzuki H, Umehara S, Inoue-Murayama M, Isagi Y Ecol Evol 19-Sep-2013
PMCID:PMC3853553
doi:10.1002/ece3.773
PMID:24324859
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
The hexane fraction of Ardisia crispa Thunb. A. DC. roots inhibits inflammation-induced angiogenesis Hamsin DE, Hamid RA, Yazan LS, Taib CN, Ting YL BMC Complement Altern Med 08-Jan-2013
PMCID:PMC3547822
doi:10.1186/1472-6882-13-5
PMID:23298265

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
> Benzenoids / Phenols / Benzenediols / Resorcinols
3-[16-(3,5-Dihydroxy-4-methylphenyl)hexadec-8-enyl]-2-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione 67882588 Click to see 498.60 unknown https://doi.org/10.1248/CPB.43.1391
3-[16-(3,5-Dihydroxyphenyl)hexadec-8-enyl]-2-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione 67882585 Click to see COC1=CC(=O)C(=C(C1=O)CCCCCCCC=CCCCCCCCC2=CC(=CC(=C2)O)O)O 484.60 unknown https://doi.org/10.1248/CPB.43.1391
Ardisiaquinone E 10323081 Click to see COC1=CC(=O)C(=C(C1=O)CCCCCCCC=CCCCCCCCC2=CC(=CC(=C2)O)O)O 484.60 unknown https://doi.org/10.1248/CPB.43.1391
Ardisiaquinone F 10097446 Click to see 498.60 unknown https://doi.org/10.1248/CPB.43.1391
> Benzenoids / Phenols / Benzenetriols and derivatives / Hydroxyquinols and derivatives
2-Hydroxy-5-methoxy-3-[16-(2,3,5-trihydroxy-4-methylphenyl)hexadec-8-enyl]cyclohexa-2,5-diene-1,4-dione 162912817 Click to see 514.60 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
2-Hydroxy-5-methoxy-3-[16-(2,3,5-trihydroxyphenyl)hexadec-8-enyl]cyclohexa-2,5-diene-1,4-dione 163032958 Click to see 500.60 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
(1S,4R,5S,6S,9S,10R,12R,14R)-4,5,6-trihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyltetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dien-15-one 162913160 Click to see 348.40 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones / Ubiquinones
2-Hydroxy-3-[16-(2-hydroxy-5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)hexadec-8-enyl]-5,6-dimethoxycyclohexa-2,5-diene-1,4-dione 162979205 Click to see 558.70 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,5R,6R)-10-(hydroxymethyl)-3-(3-hydroxyprop-1-en-2-yl)-6-methylspiro[4.5]dec-9-en-8-one 11425225 Click to see 250.33 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
Helicobasidin 166831 Click to see 264.32 unknown https://doi.org/10.1016/0165-1218(83)90182-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
7,8-Dihydroxy-3-methyl-9-methylidene-6-propan-2-ylcyclodec-2-en-1-one 162874852 Click to see 252.35 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Taraxerol, acetate 345509 Click to see CC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(2'S,3R,5'R,5aR,8S,8aS,9aR)-8-(Acetyloxy)octahydro-8a-hydroxy-3-(hydroxymethyl)-2,4',4',5'-tetramethylspiro(8H-3,9a-epithio-7H-cyclopenta(4,5)pyrrolo(1,2-a)pyrazine-7,2'(3'H)-furan)-1,3',4-trione 442874 Click to see 454.50 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Tandyukisin F 132548848 Click to see CCC(C)C1C=CC2C(C1(C)C(=O)CCO)C(CC(C2O)OC(=O)C=C(C)CC(=O)OCCC(=O)C3(C(C=CC4C3C(CC(C4O)OC(=O)C=C(C)CC(=O)OC)C)C(C)CC)C)C 897.10 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
[4-Hydroxy-5-[16-(2-hydroxy-5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)hexadec-8-enyl]-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl] acetate 162961429 Click to see 570.70 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
2-Hydroxy-3-[16-(2-hydroxy-5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)hexadec-8-enyl]-5-methoxy-6-methylcyclohexa-2,5-diene-1,4-dione 67882571 Click to see CC1=C(C(=O)C(=C(C1=O)O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C=C(C2=O)OC)O)OC 542.70 unknown https://doi.org/10.1248/CPB.43.1391
2-Hydroxy-3-[16-(2-hydroxy-5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)hexadec-8-enyl]-5-methoxycyclohexa-2,5-diene-1,4-dione 87796 Click to see COC1=CC(=O)C(=C(C1=O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C=C(C2=O)OC)O)O 528.60 unknown https://doi.org/10.1248/CPB.43.1391
https://doi.org/10.1248/CPB.16.1709
https://doi.org/10.1016/S0040-4039(01)98959-2
2,5-dihydroxy-3-[(Z)-16-(2-hydroxy-5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)hexadec-8-enyl]-6-methylcyclohexa-2,5-diene-1,4-dione 10482057 Click to see CC1=C(C(=O)C(=C(C1=O)O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C=C(C2=O)OC)O)O 528.60 unknown https://doi.org/10.1248/CPB.43.1391
https://doi.org/10.1016/S0040-4039(01)98959-2
https://doi.org/10.1248/CPB.16.1709
2,5-Dihydroxy-3-[16-(2-hydroxy-5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)hexadec-8-enyl]-6-methylcyclohexa-2,5-diene-1,4-dione 146458 Click to see 528.60 unknown https://doi.org/10.1016/S0040-4039(01)98959-2
https://doi.org/10.1248/CPB.43.1391
https://doi.org/10.1248/CPB.16.1709
Ardisiaquinone A 6436493 Click to see 528.60 unknown https://doi.org/10.1248/CPB.16.1709
https://doi.org/10.1016/0165-1218(83)90182-9
https://doi.org/10.1248/CPB.43.1391
https://doi.org/10.1016/S0031-9422(01)00317-X
https://doi.org/10.1016/S0040-4039(01)98959-2
Ardisiaquinone D 10347303 Click to see 542.70 unknown https://doi.org/10.1248/CPB.43.1391
> Organoheterocyclic compounds / Furopyrans
13-(Furan-2-yl)-4,6,6,12-tetramethyl-15-propan-2-yl-8,14,19,20-tetraoxahexacyclo[13.3.1.13,18.02,7.09,18.012,17]icos-4-ene-2,3,9-triol 162877203 Click to see CC1=CC(C2C3(C1(OC45C3OC6(CC4C(CCC5(O2)O)(C(O6)C7=CC=CO7)C)C(C)C)O)O)(C)C 488.60 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
5-(1-Benzofuran-2-yl)-2-methylbenzene-1,3-diol 641365 Click to see CC1=C(C=C(C=C1O)C2=CC3=CC=CC=C3O2)O 240.25 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
(E)-3-[(2S)-2-[(2S)-1-hydroxypropan-2-yl]-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoic acid 92448025 Click to see 316.40 unknown https://doi.org/10.1016/S0031-9422(01)00317-X
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
7-[(4-Methoxyphenyl)methyl]-7,8-dihydro-[1,3]dioxolo[4,5-h]chromen-6-one 25148668 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C=CC4=C3OCO4 312.30 unknown https://doi.org/10.1016/S0031-9422(01)00317-X

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