Maytenus magellanica

Details Top

Internal ID UUID64405b2f1bb60609003278
Scientific name Maytenus magellanica
Authority Hook.f.
First published in Fl. Antarct. : 254 (1845)

Ethnobotanical Use Top

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Synonyms Top

Scientific name Authority First published in
Cassine magellanica Lam. Tabl. Encycl. 2: 92 (1797)
Celastrus magellanicus DC. Prodr. 2: 8 (1825)
Euthalis lucida Banks & Sol. ex Hook.f. Fl. Antarct. : 254 (1845)
Maytenus andina Phil. Linnaea 28: 617 (1857)

Common names Top

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Language Common/alternative name
Russian Майтенус магелланов
Russian Майтенус магелланский
Ukrainian Майтенус магелланський

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina South
      • Chile Central
      • Chile South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001292519
Tropicos 6600178
KEW urn:lsid:ipni.org:names:161977-1
The Plant List tro-6600178
Open Tree Of Life 433237
NCBI Taxonomy 1081521
IPNI 161977-1
iNaturalist 181910
GBIF 3792012
Freebase /m/02q5sqz
EPPO MYUMA
Calflora (Californian flora) 11208
USDA GRIN 23513
Wikipedia Maytenus_magellanica
EOL 6940371

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
Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis Smyrska-Wieleba N, Mroczek T Int J Mol Sci 01-Feb-2023
PMCID:PMC9916849
doi:10.3390/ijms24032722
PMID:36769043
Dyhidro-β-agarofurans natural and synthetic as acetylcholinesterase and COX inhibitors: interaction with the peripheral anionic site (AChE-PAS), and anti-inflammatory potentials Alarcón-Enos J, Muñoz-Núñez E, Gutiérrez M, Quiroz-Carreño S, Pastene-Navarrete E, Céspedes Acuña C J Enzyme Inhib Med Chem 10-Jul-2022
PMCID:PMC9278454
doi:10.1080/14756366.2022.2091554
PMID:35815566
The extreme rainfall gradient of the Cape Horn Biosphere Reserve and its impact on forest bird richness Quilodrán CS, Sandvig EM, Aguirre F, de Aguilar JR, Barroso O, Vásquez RA, Rozzi R Biodivers Conserv 20-Jan-2022
PMCID:PMC9035007
doi:10.1007/s10531-022-02353-5
PMID:35529023
Maytenus disticha Extract and an Isolated β-Dihydroagarofuran Induce Mitochondrial Depolarization and Apoptosis in Human Cancer Cells by Increasing Mitochondrial Reactive Oxygen Species González-Chavarría I, Duprat F, Roa FJ, Jara N, Toledo JR, Miranda F, Becerra J, Inostroza A, Kelling A, Schilde U, Heydenreich M, Paz C Biomolecules 29-Feb-2020
PMCID:PMC7175306
doi:10.3390/biom10030377
PMID:32121436
Using forest historical information to target landscape ecological restoration in Southwestern Patagonia Zegers G, Arellano E, Östlund L Ambio 30-Jul-2019
PMCID:PMC7028889
doi:10.1007/s13280-019-01232-8
PMID:31364006
Temperate rain forest species partition fine-scale gradients in light availability based on their leaf mass per area (LMA) Fajardo A, Siefert A Ann Bot 06-Sep-2016
PMCID:PMC5155601
doi:10.1093/aob/mcw184
PMID:27604280
A monograph of Allantonectria, Nectria, and Pleonectria (Nectriaceae, Hypocreales, Ascomycota) and their pycnidial, sporodochial, and synnematous anamorphs Hirooka Y, Rossman AY, Samuels GJ, Lechat C, Chaverri P Stud Mycol 29-Feb-2012
PMCID:PMC3310236
doi:10.3114/sim0001
PMID:22685364
Terpenoids from Maytenus species and assessment of their reversal activity against a multidrug-resistant Leishmania tropica line. Kennedy ML, Llanos GG, Castanys S, Gamarro F, Bazzocchi IL, Jiménez IA Chem Biodivers 01-Dec-2011
doi:10.1002/CBDV.201000356
PMID:22162167
Magellanin, a New Triterpene Dimer from<i>Maytenus magellanica</i>(Celastraceae) Antonio G. Gonzalez, I. Ana Crespo, Angel G. Ravelo, Orlando M. Muñoz Informa UK Limited 07-Jul-2007
doi:10.1080/10575639408043900
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Absolute configuration of triterpene dimers from Maytenus species (Celastraceae) Antonio G González, Marı́a L Kennedy, Félix M Rodrı́guez, Isabel L Bazzocchi, Ignacio A Jiménez, Angel G Ravelo, Laila Moujir Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(00)01119-4
New sesquiterpenes fromMaytenus species (Celastraceae). Taxonomic and chemotaxonomic considerations concerning chileanMaytenus. González AG, Jiménez IA, Núñez MP, Ravelo AG, Bazzocchi IL, Muñoz OM, Aguilar MA J Chem Ecol 01-Apr-1994
doi:10.1007/BF02059580
PMID:24242198

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
> Lignans, neolignans and related compounds
methyl 7,8,11-trihydroxy-10-[(3-hydroxy-11-methoxycarbonyl-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,10,12,12a,13,14-octahydro-6aH-picen-2-yl)oxy]-2,4a,6a,6a,9,14a-hexamethyl-3,4,5,6,6b,7,8,13,14,14b-decahydro-1H-picene-2-carboxylate 14734029 Click to see 949.30 unknown https://doi.org/10.1016/S0040-4020(00)01119-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
((1R,4aR,7S,8aS,10aS)-1,4a,7-trimethyl-7-vinyl-1,2,3,4,4a,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl)methanol 14239481 Click to see 288.50 unknown https://doi.org/10.1002/CBDV.201000356
(7-ethenyl-1,4a,7-trimethyl-3,4,6,8,8a,9,10,10a-octahydro-2H-phenanthren-1-yl)methanol 14239480 Click to see CC1(CCCC2(C1CCC3C2=CCC(C3)(C)C=C)C)CO 288.50 unknown https://doi.org/10.1002/CBDV.201000356
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4R,9R,10R,13R,14S)-9-methyl-5-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-14-carboxylic acid 162971493 Click to see CC12CCCC(=C)C1CCC34C2CCC(C3)C(C4)C(=O)O 288.40 unknown https://doi.org/10.1002/CBDV.201000356
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1080/10575639408043900
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
24-Nor-D:A-friedooleana-1(10),5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, methyl ester 264268 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1002/CBDV.201000356
Beta-Amyrin 73145 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/10.1080/10575639408043900
dimethyl (3S,8S,11S,14R,16R,17S,20R,24S,29R,32S,33R,35R,38S,41R,42R,44S)-24-hydroxy-44-methoxy-3,8,11,14,17,20,29,32,35,38,41,46-dodecamethyl-23-oxo-2,25-dioxaundecacyclo[24.20.0.03,24.04,21.07,20.08,17.011,16.028,45.029,42.032,41.033,38]hexatetraconta-1(26),4,6,21,27,45-hexaene-14,35-dicarboxylate 21673607 Click to see CC1=C2C(CC3C(C2=CC4=C1OC5(C6=CC=C7C(C6=CC(=O)C5(O4)O)(CCC8(C7(CCC9(C8CC(CC9)(C)C(=O)OC)C)C)C)C)C)(CCC1(C3(CCC2(C1CC(CC2)(C)C(=O)OC)C)C)C)C)OC 961.30 unknown https://doi.org/10.1016/S0040-4020(00)01119-4
dimethyl (3S,8S,11S,14R,16R,17S,20R,24S,29R,32S,33R,35R,38S,41R,42R)-24-hydroxy-3,8,11,14,17,20,29,32,35,38,41,46-dodecamethyl-23-oxo-2,25-dioxaundecacyclo[24.20.0.03,24.04,21.07,20.08,17.011,16.028,45.029,42.032,41.033,38]hexatetraconta-1(26),4,6,21,27,45-hexaene-14,35-dicarboxylate 21673606 Click to see 931.30 unknown https://doi.org/10.1016/S0040-4020(00)01119-4
Dimethyl 24-hydroxy-3,8,11,14,17,20,29,32,35,38,41,46-dodecamethyl-23-oxo-2,25-dioxaundecacyclo[24.20.0.03,24.04,21.07,20.08,17.011,16.028,45.029,42.032,41.033,38]hexatetraconta-1(26),4,6,21,27,43,45-heptaene-14,35-dicarboxylate 73821575 Click to see 929.30 unknown https://doi.org/10.1016/S0040-4020(00)01119-4
Dimethyl 24-hydroxy-3,8,11,14,17,20,29,32,35,38,41,46-dodecamethyl-23-oxo-2,25-dioxaundecacyclo[24.20.0.03,24.04,21.07,20.08,17.011,16.028,45.029,42.032,41.033,38]hexatetraconta-1(26),4,6,21,27,45-hexaene-14,35-dicarboxylate 73821576 Click to see CC1=C2CCC3C(C2=CC4=C1OC5(C6=CC=C7C(C6=CC(=O)C5(O4)O)(CCC8(C7(CCC9(C8CC(CC9)(C)C(=O)OC)C)C)C)C)C)(CCC1(C3(CCC2(C1CC(CC2)(C)C(=O)OC)C)C)C)C 931.30 unknown https://doi.org/10.1016/S0040-4020(00)01119-4
Dimethyl 24-hydroxy-44-methoxy-3,8,11,14,17,20,29,32,35,38,41,46-dodecamethyl-23-oxo-2,25-dioxaundecacyclo[24.20.0.03,24.04,21.07,20.08,17.011,16.028,45.029,42.032,41.033,38]hexatetraconta-1(26),4,6,21,27,45-hexaene-14,35-dicarboxylate 73109666 Click to see CC1=C2C(CC3C(C2=CC4=C1OC5(C6=CC=C7C(C6=CC(=O)C5(O4)O)(CCC8(C7(CCC9(C8CC(CC9)(C)C(=O)OC)C)C)C)C)C)(CCC1(C3(CCC2(C1CC(CC2)(C)C(=O)OC)C)C)C)C)OC 961.30 unknown https://doi.org/10.1016/S0040-4020(00)01119-4
Pristimerin 159516 Click to see 464.60 unknown https://doi.org/10.1002/CBDV.201000356
https://doi.org/10.1080/10575639408043900
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
(4,8-Diacetyloxy-7,12-dibenzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl) benzoate 162869417 Click to see 714.80 unknown https://doi.org/10.1007/BF02059580
(4,8,12-Triacetyloxy-7-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl) benzoate 162954342 Click to see CC(=O)OC1CC(C23C(C(C(C(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)OC(=O)C)C(O3)(C)C)OC(=O)C)(C)O 652.70 unknown https://doi.org/10.1007/BF02059580
[(1S,2S,4R,5R,6S,7R,8S,9R,12R)-4,8-diacetyloxy-7,12-dibenzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 162869418 Click to see 714.80 unknown https://doi.org/10.1007/BF02059580
[(1S,2S,4R,5R,6S,7R,8S,9R,12R)-4,8,12-triacetyloxy-7-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 162954343 Click to see CC(=O)OC1CC(C23C(C(C(C(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)OC(=O)C)C(O3)(C)C)OC(=O)C)(C)O 652.70 unknown https://doi.org/10.1007/BF02059580
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aR,6bR,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 441687 Click to see 420.60 unknown https://doi.org/10.1080/10575639408043900
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Magellanine 442489 Click to see 275.40 unknown https://doi.org/10.1080/10575639408043900
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
4-(4-Methoxy-2-methyl-6-oxopyran-3-yl)but-2-enoic acid 86084831 Click to see 224.21 unknown https://doi.org/10.1016/S0040-4020(00)01119-4

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