Ardisia elliptica - Unknown
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Details Top

Internal ID UUID64400a2e44610822379154
Scientific name Ardisia elliptica
Authority Thunb.
First published in Nov. Gen. Pl. : 119 (1789)

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Synonyms Top

Scientific name Authority First published in
Ardisia kotoensis Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 180 (1911)
Ardisia littoralis Andrews Bot. Repos. 10: t. 630 (1811)
Ardisia sorsogonensis Elmer ex Merr. Enum. Philipp. Fl. Pl. 3: 264 (1923)
Ardisia squamulosa C.Presl Reliq. Haenk. 2: 65 (1835)
Ardisia umbellata Roxb. Fl. Ind. 2: 273 (1824)
Bladhia elliptica (Thunb.) Nakai Nov. Fl. Jap. 9: 120 (1943)
Bladhia kotoensis (Hayata) Nakai Bot. Mag. (Tokyo) 35: 99 (1921)
Bladhia squamulosa (C.Presl) Nakai Nov. Fl. Jap. 9: 120 (1943)
Climacandra littoralis (Andrews) Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 40: 68 (1871)
Icacorea humilis Britton Fl. Bermuda : 284 (1918)
Icacorea zeylanica Lam. ex Schult. Syst. Veg., ed. 15 bis 4: 516 (1819)
Tinus squamulosa (C.Presl) Kuntze Revis. Gen. Pl. 2: 975. 1891 [5 Nov 1891]
Icacorea solanacea Britton Fl. Bermuda : 284 (1918)

Common names Top

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Language Common/alternative name
English shoebutton
Bulgarian елипсовидна ардизия
Indonesian lempeni
Japanese コウトウタチバナ
Japanese セイロンマンリョウ
jv lempeni
mad lampennè
Malayalam കുഴിമുണ്ടൻ
Malay pokok mempenai
su lampeni
Thai รามใหญ่
Chinese 东方紫金牛
Chinese 蘭嶼紫金牛
Chinese 兰屿紫金牛
Chinese 蘭嶼樹杞
Chinese 兰屿树杞

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-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Maldives
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Pacific
    • North-central Pacific
      • Hawaii
    • South-central Pacific
      • Cook Islands
      • Society Islands
  • Southern America
    • Caribbean
      • Bermuda
      • Jamaica
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • El Salvador
    • Northern South America
      • Guyana
      • Venezuela

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000544255
Florida Plant Atlas 1653
USDA Plants AREL4
Tropicos 22001134
INPN 447372
KEW urn:lsid:ipni.org:names:586971-1
The Plant List kew-2647897
Missouri Botanical Garden 367876
Open Tree Of Life 763105
NCBI Taxonomy 693367
Nature Serve 2.134014
IPNI 586971-1
iNaturalist 158587
GBIF 5414375
Freebase /m/0fr3d4
EPPO ADAEL
EOL 596487
USDA GRIN 403463
Wikipedia Ardisia_elliptica

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
Efficacy of artesunate combined with Atractylodes lancea or Prabchompoothaweep remedy extracts as adjunctive therapy for the treatment of cerebral malaria Plirat W, Chaniad P, Phuwajaroanpong A, Konyanee A, Viriyavejakul P, Septama AW, Punsawad C BMC Complement Med Ther 20-Sep-2023
PMCID:PMC10510250
doi:10.1186/s12906-023-04150-1
PMID:37730604
Chemistry and Pharmacology of Bergenin or Its Derivatives: A Promising Molecule Salimo ZM, Yakubu MN, da Silva EL, de Almeida AC, Chaves YO, Costa EV, da Silva FM, Tavares JF, Monteiro WM, de Melo GC, Koolen HH Biomolecules 21-Feb-2023
PMCID:PMC10046151
doi:10.3390/biom13030403
PMID:36979338
Antimalarial efficacy and toxicological assessment of medicinal plant ingredients of Prabchompoothaweep remedy as a candidate for antimalarial drug development Chaniad P, Techarang T, Phuwajaroanpong A, Plirat W, Viriyavejakul P, Septama AW, Punsawad C BMC Complement Med Ther 18-Jan-2023
PMCID:PMC9847039
doi:10.1186/s12906-023-03835-x
PMID:36653791
In Vitro, In Vivo, and In Silico Analyses of Molecular Anti-Pigmentation Mechanisms of Selected Thai Rejuvenating Remedy and Bioactive Metabolites Dej-adisai S, Koyphokaisawan N, Wattanapiromsakul C, Nuankaew W, Kang TH, Pitakbut T Molecules 18-Jan-2023
PMCID:PMC9920523
doi:10.3390/molecules28030958
PMID:36770624
A critical look at challenges and future scopes of bioactive compounds and their incorporations in the food, energy, and pharmaceutical sector Pai S, Hebbar A, Selvaraj S Environ Sci Pollut Res Int 02-Mar-2022
PMCID:PMC9079019
doi:10.1007/s11356-022-19423-4
PMID:35233673
Phenolic Acids and Prevention of Cognitive Decline: Polyphenols with a Neuroprotective Role in Cognitive Disorders and Alzheimer’s Disease Caruso G, Godos J, Privitera A, Lanza G, Castellano S, Chillemi A, Bruni O, Ferri R, Caraci F, Grosso G Nutrients 15-Feb-2022
PMCID:PMC8875888
doi:10.3390/nu14040819
PMID:35215469
Phenolic-Rich Plant Extracts With Antimicrobial Activity: An Alternative to Food Preservatives and Biocides? Oulahal N, Degraeve P Front Microbiol 04-Jan-2022
PMCID:PMC8764166
doi:10.3389/fmicb.2021.753518
PMID:35058892
Emerging nanoformulation strategies for phytocompounds and applications from drug delivery to phototherapy to imaging Han HS, Koo SY, Choi KY Bioact Mater 20-Dec-2021
PMCID:PMC8892098
doi:10.1016/j.bioactmat.2021.11.027
PMID:35310344
Antioxidant and α-glucosidase inhibitory activities of eight neglected fruit extracts and UHPLC-MS/MS profile of the active extracts Mohamed Yunus SN, Abas F, Jaafar AH, Azizan A, Zolkeflee NK, Abd Ghafar SZ Food Sci Biotechnol 06-Jan-2021
PMCID:PMC7914318
doi:10.1007/s10068-020-00856-x
PMID:33732510
The Structure and Composition of Puerto Rico’s Urban Mangroves Branoff BL, Martinuzzi S Forests 21-Oct-2020
PMCID:PMC7751619
doi:10.3390/f11101119
PMID:33365113
Biological Activities of Selected Plants and Detection of Bioactive Compounds from Ardisia elliptica Using UHPLC-Q-Exactive Orbitrap Mass Spectrometry Wong PL, Fauzi NA, Mohamed Yunus SN, Abdul Hamid NA, Abd Ghafar SZ, Azizan A, Zolkeflee NK, Abas F Molecules 06-Jul-2020
PMCID:PMC7412327
doi:10.3390/molecules25133067
PMID:32640504
Chemical Standardization and Anti-Proliferative Activity of Ardisia elliptica Fruit against the HCT116 Human Colon Cancer Cell Line Ondee S, Sithisarn P, Mangmool S, Rojsanga P Molecules 25-Feb-2020
PMCID:PMC7179138
doi:10.3390/molecules25051023
PMID:32106546
Invasive alien plant species: Their impact on environment, ecosystem services and human health Kumar Rai P, Singh JS Ecol Indic 09-Jan-2020
PMCID:PMC7194640
doi:10.1016/j.ecolind.2019.106020
PMID:32372880
Consequences of intraspecific variation in seed dispersal for plant demography, communities, evolution and global change Snell RS, Beckman NG, Fricke E, Loiselle BA, Carvalho CS, Jones LR, Lichti NI, Lustenhouwer N, Schreiber SJ, Strickland C, Sullivan LL, Cavazos BR, Giladi I, Hastings A, Holbrook KM, Jongejans E, Kogan O, Montaño-Centellas F, Rudolph J, Rogers HS, Zwolak R, Schupp EW AoB Plants 21-Mar-2019
PMCID:PMC6644487
doi:10.1093/aobpla/plz016
PMID:31346404
A comprehensive review on tyrosinase inhibitors Zolghadri S, Bahrami A, Hassan Khan MT, Munoz-Munoz J, Garcia-Molina F, Garcia-Canovas F, Saboury AA J Enzyme Inhib Med Chem 03-Jan-2019
PMCID:PMC6327992
doi:10.1080/14756366.2018.1545767
PMID:30734608

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
5-Pentadecylresorcinol 76617 Click to see CCCCCCCCCCCCCCCC1=CC(=CC(=C1)O)O 320.50 unknown https://doi.org/10.1080/13880200490886157
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol 68972 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 438.80 unknown https://doi.org/10.1021/NP040041Z
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 163069302 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097577
(3R,4aS,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 163022459 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097577
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1021/NP040041Z
Bauerenol 111220 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097577
Bauerenol 287684 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097577
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097577
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097577
https://doi.org/10.1021/NP040041Z
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP040041Z
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP040041Z
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP040041Z
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP040041Z
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 118.09 unknown https://doi.org/10.1021/NP040041Z
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
[2-[11-(2,6-dihydroxy-4-methoxy-phenyl)-11-oxo-undecyl]-3-hydroxy-phenyl] Acetate 11476642 Click to see CC(=O)OC1=CC=CC(=C1CCCCCCCCCCC(=O)C2=C(C=C(C=C2O)OC)O)O 458.50 unknown https://doi.org/10.1021/NP040041Z
[3-hydroxy-2-[11-oxo-11-(2,4,6-trihydroxyphenyl)undecyl]phenyl] Acetate 11328243 Click to see CC(=O)OC1=CC=CC(=C1CCCCCCCCCCC(=O)C2=C(C=C(C=C2O)O)O)O 444.50 unknown https://doi.org/10.1021/NP040041Z
1-(2,6-Dihydroxy-4-methoxy-phenyl)-11-(2,6-dihydroxyphenyl)undecan-1-one 11395926 Click to see COC1=CC(=C(C(=C1)O)C(=O)CCCCCCCCCCC2=C(C=CC=C2O)O)O 416.50 unknown https://doi.org/10.1021/NP040041Z
11-(2,6-Dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one 11418215 Click to see C1=CC(=C(C(=C1)O)CCCCCCCCCCC(=O)C2=C(C=C(C=C2O)O)O)O 402.50 unknown https://doi.org/10.1021/NP040041Z
Ardisinone E 11234557 Click to see C1=CC=C(C(=C1)CCCCCCCCCCC(=O)C2=C(C=C(C=C2O)O)O)O 386.50 unknown https://doi.org/10.1021/NP040041Z

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