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Internal ID UUID643ff5c59b910853016610
Scientific name Maytenus disticha
Authority Urb.
First published in Festschr. Aschers. : 58 (1904)

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Synonyms Top

Scientific name Authority First published in
Myginda disticha Hook.f. Fl. Antarct. : 254 (1845)
Crossopetalum distichum Kuntze Revis. Gen. Pl. 1: 116 (1891)
Rhacoma disticha (Hook.f.) Loes.

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Varieties (abbr. var.) 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-0000375085
Tropicos 6600134
KEW urn:lsid:ipni.org:names:155495-2
The Plant List kew-2370037
Open Tree Of Life 418523
Observations.org 431137
NCBI Taxonomy 490005
IPNI 155495-2
iNaturalist 490879
GBIF 3793780
EOL 11912612
Elurikkus 415431

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
Rock cavity nesting as the norm: Breeding songbirds of the temperate High Andes Altamirano TA, de Zwaan DR, Scridel D, Wilson S, Martin K Ecology 03-Jan-2023
PMCID:PMC10078528
doi:10.1002/ecy.3931
PMID:36451258
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
Plant Terpenoids as the Promising Source of Cholinesterase Inhibitors for Anti-AD Therapy Lai Shi Min S, Liew SY, Chear NJ, Goh BH, Tan WN, Khaw KY Biology (Basel) 14-Feb-2022
PMCID:PMC8869317
doi:10.3390/biology11020307
PMID:35205173
Non-Alkaloid Cholinesterase Inhibitory Compounds from Natural Sources Tamfu AN, Kucukaydin S, Yeskaliyeva B, Ozturk M, Dinica RM Molecules 14-Sep-2021
PMCID:PMC8472022
doi:10.3390/molecules26185582
PMID:34577053
Acetylcholinesterase Inhibitory Potential of Various Sesquiterpene Analogues for Alzheimer’s Disease Therapy Arya A, Chahal R, Rao R, Rahman MH, Kaushik D, Akhtar MF, Saleem A, Khalifa SM, El-Seedi HR, Kamel M, Albadrani GM, Abdel-Daim MM, Mittal V Biomolecules 25-Feb-2021
PMCID:PMC7996600
doi:10.3390/biom11030350
PMID:33669097
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
Opportunities and Scope for Botanical Extracts and Products for the Management of Fall Armyworm (Spodoptera frugiperda) for Smallholders in Africa Rioba NB, Stevenson PC Plants (Basel) 06-Feb-2020
PMCID:PMC7076698
doi:10.3390/plants9020207
PMID:32041322
Triterpenoid and Phenolic Compounds from Two Chilean Celastraceae Orlando Muñoz, Antonio González, Angel Ravelo, Ana Estevez Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1999-1-223
Sesquiterpene esters fromMaytenus disticha Orlando M. Mun˜oz, Antonio G. Gonzalez, Angel G. Ravelo, Javier G. Luis, Jesus T. Vazquez, Mercedes P. Nun˜ez, Ignacio A. Jimenez Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)80189-N

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(8,12-Diacetyloxy-7-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl) benzoate 14705529 Click to see CC(=O)OC1C2C(C3(C(CCC(C3(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)(C)O)OC2(C)C)OC(=O)C 594.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[(1S,2R,5S,6S,7R,8R,9R,12R)-5,12-diacetyloxy-6-(acetyloxymethyl)-8-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14431369 Click to see CC1CCC(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)O)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C 532.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[(1S,2R,5S,6S,7S,9R,12R)-5,12-diacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14705528 Click to see CC1CCC(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)CO)OC(=O)C 474.50 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[(1S,2S,5S,6S,7R,8S,9R,12R)-8,12-diacetyloxy-7-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 14705530 Click to see CC(=O)OC1C2C(C3(C(CCC(C3(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)(C)O)OC2(C)C)OC(=O)C 594.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[5,12-Diacetyloxy-6-(acetyloxymethyl)-8-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14431367 Click to see CC1CCC(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)O)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C 532.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[5,12-Diacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14705527 Click to see CC1CCC(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)CO)OC(=O)C 474.50 unknown https://doi.org/10.1016/0031-9422(90)80189-N
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1S,2R,4S,5R,6S,7R,8R,9R,12R)-4,5,8,12-tetraacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14431374 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 632.70 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[4,5,8,12-Tetraacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14431372 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 632.70 unknown https://doi.org/10.1016/0031-9422(90)80189-N
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,2R,4S,5R,6S,7R,8R,9R,12R)-4,5,8,12-tetraacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 15628215 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)CO)OC(=O)C)OC(=O)C 590.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[(1S,2R,5S,6S,7R,8R,9R,12R)-5,8,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14431362 Click to see CC1CCC(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C 574.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[4,5,8,12-Tetraacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 15628214 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)CO)OC(=O)C)OC(=O)C 590.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
[5,8,12-Triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14431360 Click to see CC1CCC(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C 574.60 unknown https://doi.org/10.1016/0031-9422(90)80189-N
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1515/ZNC-1999-1-223
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1515/ZNC-1999-1-223

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