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Phyllanthus acuminatus

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fe74448688238588985
Scientific name Phyllanthus acuminatus
Authority Vahl
First published in Symb. Bot. 2: 95 (1791)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phyllanthus averrhoifolius Steud. Nomencl. Bot. , ed. 2, 2: 326 (1841)
Phyllanthus cumanensis Willd. ex Steud. Nomencl. Bot. , ed. 2, 2: 327 (1841)
Phyllanthus foetidus Pav. ex Baill. Recueil Observ. Bot. 1: 34 (1860)
Phyllanthus lycioides Kunth Nov. Gen. Sp. 2: 112 (1817)
Phyllanthus mucronatus Kunth Nov. Gen. Sp. 2: 112 (1817)
Phyllanthus ruscoides Kunth Nov. Gen. Sp. 2: 113 (1817)
Phyllanthus sessei Briq. Annuaire Conserv. Jard. Bot. Genève 4: 224 (1900)
Phyllanthus acuminatus var. paraguariensis Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 5: 488 (1905)
Diasperus acuminatus (Vahl) Kuntze Revis. Gen. Pl. 2: 598 (1891)

Common names Top

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Language Common/alternative name
English jamaican gooseberry tree
Spanish grosella de jamaica
Spanish jobillo

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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000270410
USDA Plants PHAC7
Tropicos 12802298
INPN 630393
KEW urn:lsid:ipni.org:names:194611-2
The Plant List kew-153283
Open Tree Of Life 98948
NCBI Taxonomy 319566
IUCN Red List 208170194
IPNI 194611-2
iNaturalist 275307
GBIF 5381441
Freebase /m/05xm9_
EOL 1153256
USDA GRIN 28114
Wikipedia Phyllanthus_acuminatus

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
Evaluation of Salicylic Acid and Methyl Jasmonate as Elicitors in Phyllanthus acuminatus Hairy Roots by Non-Targeted Analysis Using High-Resolution Mass Spectrometry Benavides K, Sánchez-Kopper A, Jiménez-Quesada K, Perez R, Garro-Monge G Molecules 22-Dec-2023
PMCID:PMC10780090
doi:10.3390/molecules29010080
PMID:38202663
Temperate Zone Plant Natural Products—A Novel Resource for Activity against Tropical Parasitic Diseases Hameed H, King EF, Doleckova K, Bartholomew B, Hollinshead J, Mbye H, Ullah I, Walker K, Van Veelen M, Abou-Akkada SS, Nash RJ, Horrocks PD, Price HP Pharmaceuticals (Basel) 07-Mar-2021
PMCID:PMC7998250
doi:10.3390/ph14030227
PMID:33800005
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
Pressurized hot water extraction of hydrosable tannins from Phyllanthus tenellus Roxb. Mohd Jusoh NH, Subki A, Yeap SK, Yap KC, Jaganath IB BMC Chem 21-Dec-2019
PMCID:PMC6925506
doi:10.1186/s13065-019-0653-0
PMID:31891160
Leafflower–leafflower moth mutualism in the Neotropics: Successful transoceanic dispersal from the Old World to the New World by actively-pollinating leafflower moths Kawakita A, Sato AA, Salazar JR, Kato M PLoS One 30-Jan-2019
PMCID:PMC6353133
doi:10.1371/journal.pone.0210727
PMID:30699166
Flavonoid Functions in Plants and Their Interactions with Other Organisms Mathesius U Plants (Basel) 03-Apr-2018
PMCID:PMC6027123
doi:10.3390/plants7020030
PMID:29614017
Flavonoids and Ellagitannins Characterization, Antioxidant and Cytotoxic Activities of Phyllanthus acuminatus Vahl Navarro M, Moreira I, Arnaez E, Quesada S, Azofeifa G, Vargas F, Alvarado D, Chen P Plants (Basel) 15-Dec-2017
PMCID:PMC5750638
doi:10.3390/plants6040062
PMID:29244711
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Justicidin B: A Promising Bioactive Lignan Hemmati S, Seradj H Molecules 23-Jun-2016
PMCID:PMC6272961
doi:10.3390/molecules21070820
PMID:27347906
The structures of phyllanthostatin 1 and phyllanthoside from the Central American tree <i>Phyllanthus</i><i>acuminatus</i> Vahl George R. Pettit, Gordon M. Cragg, Devens Gust, Peter Brown, Jean M. Schmidt Canadian Science Publishing 17-May-2006
doi:10.1139/V82-141
Antineoplastic agents. 104. Isolation and structure of the Phyllanthus acuminatus Vahl (Euphorbiaceae) glycosides George R. Pettit, Gordon M. Cragg, Matthew I. Suffness, Devens Gust, Fred E. Boettner, M. Williams, J. A. Saenz-Renauld, Peter Brown, Jean M. Schmidt, Paul D. Ellis American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00196A029
Eukaryotic protein synthesis inhibitors identified by comparison of cytotoxicity profiles CHAN J, KHAN SN, HARVEY I, MERRICK W, PELLETIER J RNA 01-Mar-2004
PMCID:PMC1370947
doi:10.1261/rna.5200204
PMID:14970397
Antineoplastic agents, 177. Isolation and structure of phyllanthostatin 6. Pettit GR, Schaufelberger DE, Nieman RA, Dufresne C, Saenz-Renauld JA J Nat Prod 01-Nov-1990
doi:10.1021/NP50072A002
PMID:2089115
Isolation and structure of the cytostatic lignan glycoside phyllanthostatin A. Pettit GR, Schaufelberger DE J Nat Prod 01-Nov-1988
doi:10.1021/NP50060A009
PMID:3236006
High-performance liquid chromatographic assay for the antitumor glycoside phyllanthoside and its stability in plasma of several species. Powis G, Moore DJ J Chromatogr 12-Jul-1985
doi:10.1016/S0378-4347(00)84495-3
PMID:4044742

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
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Justicidin B 442882 Click to see COC1=CC2=CC3=C(C(=C2C=C1OC)C4=CC5=C(C=C4)OCO5)C(=O)OC3 364.30 unknown https://doi.org/10.1021/JO00196A029
Phyllanthostatin A 128959 Click to see CC(=O)OCC1=C(C(=C2C=C(C(=CC2=C1)OC)OC)C3=CC4=C(C=C3)OCO4)C(=O)OC5C(C(C(C(O5)CO)O)O)O 586.50 unknown https://doi.org/10.1021/NP50060A009
Retrochinensin 122805 Click to see COC1=C(C=C(C=C1)C2=C3C=C4C(=CC3=CC5=C2COC5=O)OCO4)OC 364.30 unknown https://doi.org/10.1021/JO00196A029
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
[4-Acetyloxy-3-(4-acetyloxy-3,5-dihydroxy-6-methyloxan-2-yl)oxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl] 3-hydroxy-3-(hydroxymethyl)-5'-methyl-4'-(3-phenylprop-2-enoyloxy)spiro[3a,4,5,6,7,7a-hexahydro-1-benzofuran-2,2'-oxane]-6-carboxylate 162916357 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C(C4CCC(CC4O2)C(=O)OC5C(C(C(C(O5)CO)O)OC(=O)C)OC6C(C(C(C(O6)C)O)OC(=O)C)O)(CO)O 838.80 unknown https://doi.org/10.1139/V82-141
CID 163194156 163194156 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)CO)O)OC(=O)C)OC7C(C(C(C(O7)C)O)OC(=O)C)O 820.80 unknown https://doi.org/10.1139/V82-141
CID 433406 433406 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)CO)O)OC(=O)C)OC7C(C(C(C(O7)C)O)OC(=O)C)O 820.80 unknown https://doi.org/10.1139/V82-141
CID 44567111 44567111 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O 736.80 unknown https://doi.org/10.1021/NP50072A002
Phyllanthastatin 2 5477548 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)CO)O)OC(=O)C)OC7C(C(C(C(O7)C)O)OC(=O)C)O 820.80 unknown https://doi.org/10.1021/JO00196A029
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
[8-formyl-4-[2-(furan-3-yl)ethyl]-4a,8-dimethyl-3-methylidene-2,4,5,6,7,8a-hexahydro-1H-naphthalen-2-yl] acetate 163039964 Click to see CC(=O)OC1CC2C(CCCC2(C(C1=C)CCC3=COC=C3)C)(C)C=O 358.50 unknown https://doi.org/10.1021/NP50072A002
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
3-O-Acetyl-2-O-(3-O-acetyl-6-deoxyhexopyranosyl)-6-deoxy-1-O-{5-methyl-4-[(3-phenylprop-2-enoyl)oxy]hexahydrodispiro[oxane-2,2'-[1]benzofuran-3',2''-oxirane]-6'-carbonyl}hexopyranose 332244 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)C)O)OC(=O)C)OC7C(C(C(C(O7)C)O)OC(=O)C)O 804.80 unknown https://doi.org/10.1139/V82-141
5LV0N6K0CA 100992284 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)C)O)OC(=O)C)OC7C(C(C(C(O7)C)O)OC(=O)C)O 804.80 unknown https://doi.org/10.1021/NP50072A002
https://doi.org/10.1021/JO00196A029
https://doi.org/10.1016/S0378-4347(00)84495-3
CID 163185749 163185749 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)C)O)OC(=O)C)OC7C(C(C(C(O7)C)O)OC(=O)C)O 804.80 unknown https://doi.org/10.1139/V82-141
CID 163188353 163188353 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)C)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC(=O)C)O 804.80 unknown https://doi.org/10.1139/V82-141
CID 433532 433532 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)C)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC(=O)C)O 804.80 unknown https://doi.org/10.1139/V82-141
Phyllanthostatin 1 5358585 Click to see CC1COC2(CC1OC(=O)C=CC3=CC=CC=C3)C4(CO4)C5CCC(CC5O2)C(=O)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)C)O)OC(=O)C)O)OC(=O)C)O 804.80 unknown https://doi.org/10.1021/JO00196A029
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2R,3S,4S,5R,6S)-3,4-dihydroxy-5,6-bis(1H-pyrrole-2-carbonyloxy)oxan-2-yl]methyl 1H-pyrrole-2-carboxylate 101414001 Click to see C1=CNC(=C1)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC=CN3)OC(=O)C4=CC=CN4)O)O 459.40 unknown https://doi.org/10.1139/V82-141

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