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]

Common names Top

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Filter by language:

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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No forms added yet.

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 click to expand
- China
  - China Southeast
- Eastern Asia
  - Japan
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

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

Add a new one!

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
> 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 CC1=C(C=C(C=C1O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C=C(C2=O)OC)O)O	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 CC1=C(C=C(C=C1O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C=C(C2=O)OC)O)O	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 CC1=C(C=C(C(=C1O)O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C=C(C2=O)OC)O)O	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 COC1=CC(=O)C(=C(C1=O)CCCCCCCC=CCCCCCCCC2=C(C(=CC(=C2)O)O)O)O	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 CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO	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 COC1=CC(=O)C(=C(C1=O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C(=C(C2=O)OC)OC)O)O	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 CC1CC(=O)C=C(C12CCC(C2)C(=C)CO)CO	250.33	unknown	https://doi.org/10.1016/S0031-9422(01)00317-X
Helicobasidin	166831	Click to see CC1=C(C(=O)C(=C(C1=O)O)C2(CCCC2(C)C)C)O	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 CC1=CC(=O)CC(=C)C(C(C(CC1)C(C)C)O)O	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
Sirodesmin H	442874	Click to see CC1C(C(=O)C2(O1)CC3C(C2OC(=O)C)(CC45N3C(=O)C(S4)(N(C5=O)C)CO)O)(C)C	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 CC1=C(C(=O)C(=C(C1=O)O)CCCCCCCC=CCCCCCCCC2=C(C(=O)C=C(C2=O)OC)O)OC(=O)C	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/10.1016/S0040-4039(01)98959-2 https://doi.org/10.1248/CPB.43.1391 https://doi.org/10.1248/CPB.16.1709
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/10.1016/S0040-4039(01)98959-2 https://doi.org/10.1248/CPB.43.1391 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 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/10.1016/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 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.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 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
> 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 CC(CO)C1CC2=C(O1)C(=CC(=C2)C=CC(=O)O)CC=C(C)C	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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Ardisia sieboldii

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top