Details Top

Internal ID UUID643ff5c660f6f907473768
Scientific name Maytenus boaria
Authority Molina
First published in Sag. Stor. Nat. Chili : 177 (1782)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Across central Chile, the soft, evergreen leaves of Maytenus boaria are steeped in hot water as a household remedy for coughs, colds, and upper‑respiratory irritation. Among Mapuche communities of the Andean foothills and valley dwellers from the Biobío to Valparaíso, infusions of fresh or dried leaves are also taken as a gentle febrifuge and digestive tonic (Fuentes, 1986; Avila and Heinrich, 1993). In mid‑Andine highland haciendas, decoctions of the bitter inner bark are recorded as a diaphoretic and fever‑reducing preparation for colds and to address rheumatic discomfort; the bark is also used in decoction or maceration for diarrhea, a use echoed by Andean ethnobotany sources (Alfaro and Sepúlveda, 2011; Loh once‑chó, 2020). Each of these preparations specifies the plant part used and the mode of application.

To make a mild leaf tea, place 6–8 grams (about one heaping teaspoon) of dried leaves into 250–300 milliliters of hot water, cover, and steep for 10–12 minutes; strain and sip one cup 2–3 times per day for cough relief or as a light febrifuge. For a bark decoction traditionally used for fever or mild gastrointestinal upset, simmer 4–6 grams of inner bark in 250 milliliters of water for 15–20 minutes, let it cool slightly, and drink half a cup up to twice daily. These preparations are common in Chilean home practice; however, avoid during pregnancy and if you are allergic to plants in the Celastraceae family. Do not exceed traditional dosing; discontinue if gastrointestinal upset or hypersensitivity reactions occur.

The leaf infusion’s gentle expectorant and antipyretic effects are consistent with phytochemical reports for Maytenus boaria, notably flavonoids (quercetin and kaempferol derivatives) and caffeoylquinic acids, compounds with documented anti-inflammatory, antioxidant, and mild spasmolytic activity that can soothe irritated airway mucosa and support antipyretic tea use. Bark preparations rich in ursane and oleanane triterpenes (betulinic, oleanolic, and ursolic acids) provide the documented antimicrobial and fever‑reducing potential of decoctions (Cárdenas et al., 2002; Rodríguez et al., 2005; Araya et al., 2012).

Modern relevance is active on two fronts. Laboratory studies on the bark’s triterpenoids continue to inform pharmacological interest in antimicrobial and metabolic modulation, and the plant remains a common, accessible fever and cough tea among rural and peri‑urban households in central Chile.

General Uses Top

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Scientific/model organism:
Maytenus boaria has a reference nuclear genome published, enabling comparative and evolutionary studies within the Celastraceae. Public genomics resources (GenBank, NCBI SRA) and global ex situ conservation databases (BGCI, GBIF) provide genomic, ecological, and distribution data supporting phylogenetics, conservation, and horticultural research. Its role as a model for fire-stimulated recruitment (soil seed bank longevity; seedling recruitment after fire) supports demographic modeling and landscape-scale restoration studies.

Horticulture and urban use:
The species is widely cultivated as an ornamental tree in Chile and Mediterranean-climate regions (e.g., California and New Zealand) for its weeping habit and fine foliage. It is promoted by botanical gardens and horticultural societies, with cultivar availability noted in nursery catalogs. These sources also recommend use in urban forestry and amenity plantings due to its tolerance of pruning, drought, and coastal exposure.

Revegetation and restoration:
M. boaria is used in restoration and erosion control programs in Chile and elsewhere; it is frequently included in native species planting lists and recommended for waterside stabilization, passive rehabilitation, and erosion-prone sites. Its capacity to establish on degraded soils and riverbanks is repeatedly highlighted in restoration guidance for temperate South America.

Synonyms Top

Scientific name Authority First published in
Maytenus uncinata G.Don Gen. Hist. 2: 11 (1832)
Maytenus crenulata C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 465 (1845)
Maytenus marginata Herb.Mus.Vind. ex Ettingsh. Blatt-Skel. Dikot. : 290 (1861)
Senacia maytenus Lam. Tabl. Encycl. 2: 96 (1793)
Boaria molinae DC. Prodr. 8: 299 (1844)
Celastrus boaria Baill. Hist. Pl. 6: 26 (1875)
Celastrus maytenus Willd. Sp. Pl., ed. 4 [Willdenow] 1(2): 1127. 1798 [Jul 1798]
Celastrus uncinatus Ruiz & Pav. Fl. Peruv. 3: 7 (1802)
Maytenus boaria var. angustifolia Turcz.
Maytenus chilensis DC. Prodr. 2: 9 (1825)
Maytenus chilensis var. angustifolius DC. Prodr. 2: 10 (1825)
Maytenus boaria var. latifolia Reissek ex Loes.
Maytenus boaria var. angustifolia Reissek ex Loes.
Maytenus pendulina Steud. Nomencl. Bot. , ed. 2, 2: 108 (1841)
Maytenus angustifolia Mattos & N.F.Mattos Roessléria 2(1): 39 (1978)
Celastrus maytenus Lam. ex Forsyth f. Bot. Nomencl. : 149 (1794)

Common names Top

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Language Common/alternative name
English mayten
Spanish maitén
Spanish boaria chilensis
Spanish maiten
Spanish orcomolle
Spanish boaria molinae
Spanish celastrus uncinatus
Spanish celastrus maytenus
Spanish maytenus boaria var. angustifolia

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Argentina South
      • Chile Central
      • Chile North
      • Chile South
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000375129
USDA Plants MABO8
Tropicos 6600541
KEW urn:lsid:ipni.org:names:161827-1
The Plant List kew-2370101
Open Tree Of Life 418513
Observations.org 431121
NCBI Taxonomy 490002
IUCN Red List 144278615
IPNI 161827-1
iNaturalist 77969
GBIF 3790726
Freebase /m/02q69rd
EPPO MYUBO
EOL 6940183
Elurikkus 414850
Calflora (Californian flora) 8519
USDA GRIN 23511
Wikipedia Maytenus_boaria

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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
White-crested elaenias (Elaenia albiceps chilensis) breeding across Patagonia exhibit similar spatial and temporal movement patterns throughout the year Jara RF, Jiménez JE, Rozzi R PLoS One 18-Apr-2024
PMCID:PMC11025734
doi:10.1371/journal.pone.0299954
PMID:38635514
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Commodity risk assessment of Acer campestre plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Allometric equations for estimating peak uprooting force of riparian vegetation Zhang Y, Liu W, He S Front Plant Sci 03-Jul-2023
PMCID:PMC10352110
doi:10.3389/fpls.2023.1192486
PMID:37469785
Common juniper, an overlooked conifer with high invasion potential in protected areas of Patagonia Franzese J, Ripa RR Sci Rep 17-Jun-2023
PMCID:PMC10276858
doi:10.1038/s41598-023-37023-1
PMID:37330618
Electromagnetic fields disrupt the pollination service by honeybees Molina-Montenegro MA, Acuña-Rodríguez IS, Ballesteros GI, Baldelomar M, Torres-Díaz C, Broitman BR, Vázquez DP Sci Adv 12-May-2023
PMCID:PMC10181175
doi:10.1126/sciadv.adh1455
PMID:37172085
European Rabbit Invasion in a Semi-Arid Ecosystem of Chile: How Relevant Is Its Role in Food Webs? Gübelin P, Correa-Cuadros JP, Ávila-Thieme MI, Flores-Benner G, Duclos M, Lima M, Jaksic FM Life (Basel) 31-Mar-2023
PMCID:PMC10144028
doi:10.3390/life13040916
PMID:37109445
Nutritional Composition and Bioactive Properties of Wild Edible Mushrooms from Native Nothofagus Patagonian Forests Rugolo M, Mascoloti Spréa R, Dias MI, Pires TC, Añibarro-Ortega M, Barroetaveña C, Caleja C, Barros L Foods 04-Nov-2022
PMCID:PMC9654758
doi:10.3390/foods11213516
PMID:36360128
Novel food resources and conservation of ecological interactions between the Andean Araucaria and the Austral parakeet Blanco G, Romero‐Vidal P, Tella JL, Hiraldo F Ecol Evol 27-Oct-2022
PMCID:PMC9608793
doi:10.1002/ece3.9455
PMID:36311393
Magnetic and elemental characterization of the particulate matter deposited on leaves of urban trees in Santiago, Chile Préndez M, Carvallo C, Godoy N, Egas C, Aguilar Reyes BO, Calzolai G, Fuentealba R, Lucarelli F, Nava S Environ Geochem Health 06-Sep-2022
PMCID:PMC10140104
doi:10.1007/s10653-022-01367-w
PMID:36068421
Fungal Planet description sheets: 1182–1283 Crous PW, Cowan DA, Maggs-Kölling G, Yilmaz N, Thangavel R, Wingfield MJ, Noordeloos ME, Dima B, Brandrud TE, Jansen GM, Morozova OV, Vila J, Shivas RG, Tan YP, Bishop-Hurley S, Lacey E, Marney TS, Larsson E, Le Floch G, Lombard L, Nodet P, Hubka V, Alvarado P, Berraf-Tebbal A, Reyes JD, Delgado G, Eichmeier A, Jordal JB, Kachalkin AV, Kubátová A, Maciá-Vicente JG, Malysheva EF, Papp V, Rajeshkumar KC, Sharma A, Spetik M, Szabóová D, Tomashevskaya MA, Abad JA, Abad ZG, Alexandrova AV, Anand G, Arenas F, Ashtekar N, Balashov S, Bañares Á, Baroncelli R, Bera I, Biketova AY, Blomquist CL, Boekhout T, Boertmann D, Bulyonkova TM, Burgess TI, Carnegie AJ, Cobo-Diaz JF, Corriol G, Cunnington JH, da Cruz MO, Damm U, Davoodian N, de A. Santiago AL, Dearnaley J, de Freitas LW, Dhileepan K, Dimitrov R, Di Piazza S, Fatima S, Fuljer F, Galera H, Ghosh A, Giraldo A, Glushakova AM, Gorczak M, Gouliamova DE, Gramaje D, Groenewald M, Gunsch CK, Gutiérrez A, Holdom D, Houbraken J, Ismailov AB, Istel Ł, Iturriaga T, Jeppson M, Jurjević Ž, Kalinina LB, Kapitonov VI, Kautmanová I, Khalid AN, Kiran M, Kiss L, Kovács Á, Kurose D, Kušan I, Lad S, Læssøe T, Lee HB, Luangsa-ard JJ, Lynch M, Mahamedi AE, Malysheva VF, Mateos A, Matočec N, Mešić A, Miller AN, Mongkolsamrit S, Moreno G, Morte A, Mostowfizadeh-Ghalamfarsa R, Naseer A, Navarro-Ródenas A, Nguyen TT, Noisripoom W, Ntandu JE, Nuytinck J, Ostrý V, Pankratov TA, Pawłowska J, Pecenka J, Pham TH, Polhorský A, Pošta A, Raudabaugh DB, Reschke K, Rodríguez A, Romero M, Rooney-Latham S, Roux J, Sandoval-Denis M, Smith MT, Steinrucken TV, Svetasheva TY, Tkalčec Z, van der Linde EJ, v.d. Vegte M, Vauras J, Verbeken A, Visagie CM, Vitelli JS, Volobuev SV, Weill A, Wrzosek M, Zmitrovich IV, Zvyagina EA, Groenewald JZ Persoonia 13-Jul-2021
PMCID:PMC9311394
doi:10.3767/persoonia.2021.46.11
PMID:35935893
Larvicidal activity of Maytenus guianensis (Celastraceae) against Aedes aegypti (Diptera: Culicidae) Martins MM, Dias AC, Facundo VA, Lima RA, Meneguetti DU, Silva AD Rev Soc Bras Med Trop 12-Apr-2021
PMCID:PMC8047713
doi:10.1590/0037-8682-0835-2020
PMID:33886820

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
(1R,2R,3S,6R,9R)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecane-2,3-diol 11780067 Click to see CC1(C2CCC3(CCC(C(C3(C2)O1)(C)O)O)C)C 254.36 unknown https://doi.org/10.1016/S0040-4039(00)74179-7
(3,12-Diacetyloxy-5-benzoyloxy-2,4-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 102148863 Click to see 610.60 unknown https://doi.org/10.1002/HLCA.19930760712
https://doi.org/10.1080/10575639408043932
(4-Acetyloxy-5-benzoyloxy-2,3-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 162947135 Click to see 552.60 unknown https://doi.org/10.1080/10575639408043932
https://doi.org/10.1002/HLCA.19930760712
(4-Acetyloxy-5-benzoyloxy-2,3,12-trihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 162943969 Click to see 568.60 unknown https://doi.org/10.1007/BF02059580
(4,12-Diacetyloxy-5-benzoyloxy-2,3-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 75183014 Click to see 610.60 unknown https://doi.org/10.1002/HLCA.19930760712
https://doi.org/10.1080/10575639408043932
(4,12-Diacetyloxy-5-benzoyloxy-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 75016120 Click to see CC1C(C(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O 594.60 unknown https://doi.org/10.1080/10575639408043932
https://doi.org/10.1002/HLCA.19930760712
(5-Acetyloxy-8,12-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) furan-3-carboxylate 162962791 Click to see 422.50 unknown https://doi.org/10.1016/0031-9422(95)00422-4
(5,12-Diacetyloxy-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) furan-3-carboxylate 162909413 Click to see 464.50 unknown https://doi.org/10.1016/0031-9422(95)00422-4
(5,8,12-Triacetyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) furan-3-carboxylate 53462163 Click to see 506.50 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[(1R,2R,5S,6S,7R,8R,9S,12S)-5,8,12-triacetyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate 163016656 Click to see CC1CCC(C2(C13C(C(C(C2OC(=O)C4=COC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)C)OC(=O)C 506.50 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[(1R,2S,3S,4R,5R,6R,7S,9R)-4-acetyloxy-5-benzoyloxy-2,3-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 101626233 Click to see 552.60 unknown https://doi.org/10.1080/10575639408043932
[(1R,2S,3S,4R,5R,6S,7S,9R)-4-acetyloxy-5-benzoyloxy-2,3-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162947136 Click to see 552.60 unknown https://doi.org/10.1002/HLCA.19930760712
[(1S,2R,3R,4R,5R,6R,7S,9R,12R)-4,12-diacetyloxy-5-benzoyloxy-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 134151675 Click to see 594.60 unknown https://doi.org/10.1080/10575639408043932
[(1S,2R,3R,4R,5R,6S,7S,9R,12R)-4,12-diacetyloxy-5-benzoyloxy-3-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162902643 Click to see 594.60 unknown https://doi.org/10.1002/HLCA.19930760712
[(1S,2R,4S,5R,6S,7R,9R,12R)-4,5,12-triacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 15628226 Click to see 546.60 unknown https://doi.org/10.1002/HLCA.19930760712
[(1S,2R,5S,6S,7R,8R,9R,12R)-5-acetyloxy-8,12-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate 101682234 Click to see 422.50 unknown https://doi.org/10.1016/0031-9422(95)00422-4
[(1S,2R,5S,6S,7R,8R,9R,12R)-5,12-diacetyloxy-8-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate 15762036 Click to see CC1CCC(C2(C13C(C(C(C2OC(=O)C4=COC=C4)O)C(O3)(C)C)OC(=O)C)C)OC(=O)C 464.50 unknown https://doi.org/10.1016/0031-9422(95)00422-4
[(1S,2R,5S,6S,7R,8R,9R,12R)-5,8,12-triacetyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate 163016657 Click to see 506.50 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[(1S,2R,5S,6S,7R,9R,12S)-5-acetyloxy-12-(furan-3-carbonyloxy)-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate 163013143 Click to see CC(=O)OC1CCC(C23C1(C(CC(C2OC(=O)C4=COC=C4)C(O3)(C)C)OC(=O)C5=COC=C5)C)(C)O 516.50 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[(1S,2R,5S,6S,7S,8S,9R,12S)-5,8-diacetyloxy-7-(furan-3-carbonyloxy)-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] furan-3-carboxylate 162947684 Click to see 574.60 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[(1S,2S,3S,4R,5R,6R,7S,9R,12R)-4-acetyloxy-5-benzoyloxy-2,3,12-trihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 76316458 Click to see CC(=O)OC1C(C(C23C(C(CC(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)O)(C)O)O 568.60 unknown https://doi.org/10.1007/BF02059580
[(1S,2S,3S,4R,5R,6S,7S,9R,12R)-4,12-diacetyloxy-5-benzoyloxy-2,3-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 163058752 Click to see CC(=O)OC1C(C(C23C(C(CC(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)(C)O)O 610.60 unknown https://doi.org/10.1002/HLCA.19930760712
[(1S,2S,3S,4S,5R,6R,7S,9R,12R)-3,12-diacetyloxy-5-benzoyloxy-2,4-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 101626235 Click to see CC(=O)OC1C2CC(C3(C1(C(C(C(C3OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)O)OC2(C)C)C)OC(=O)C5=CC=CC=C5 610.60 unknown https://doi.org/10.1080/10575639408043932
[(1S,2S,3S,4S,5R,6S,7S,9R,12R)-3,12-diacetyloxy-5-benzoyloxy-2,4-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162864654 Click to see CC(=O)OC1C2CC(C3(C1(C(C(C(C3OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)O)OC2(C)C)C)OC(=O)C5=CC=CC=C5 610.60 unknown https://doi.org/10.1002/HLCA.19930760712
[(1S,2S,5S,6S,7R,8R,9R,12R)-5,8-diacetyloxy-7-(furan-3-carbonyloxy)-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] furan-3-carboxylate 162947683 Click to see 574.60 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[(1S,2S,5S,6S,7S,9R,12R)-5-acetyloxy-12-(furan-3-carbonyloxy)-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate 163013144 Click to see 516.50 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[4,5,12-Triacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 15628225 Click to see 546.60 unknown https://doi.org/10.1002/HLCA.19930760712
[5-Acetyloxy-12-(furan-3-carbonyloxy)-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate 163013142 Click to see 516.50 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
[5,8-Diacetyloxy-7-(furan-3-carbonyloxy)-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] furan-3-carboxylate 162947682 Click to see 574.60 unknown https://doi.org/10.1016/S0031-9422(00)84598-7
2,6,10,10-Tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecane-2,3-diol 73098020 Click to see 254.36 unknown https://doi.org/10.1016/S0040-4039(00)74179-7
2beta,3beta,4beta,Trihydroxycelarbico 46239957 Click to see CC(=O)OC1C(C(C23C(C(CC(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)(C)O)O 610.60 unknown https://doi.org/10.1080/10575639408043932
Eumaitenine 130709 Click to see 506.50 unknown https://doi.org/10.1007/BF00198273
https://doi.org/10.1016/S0031-9422(00)84598-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[[(1S,4S,4aS,6S,8aS)-4-hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101682271 Click to see 418.50 unknown https://doi.org/10.1016/0031-9422(95)00348-B
2-[[4-Hydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162966423 Click to see 418.50 unknown https://doi.org/10.1016/0031-9422(95)00348-B
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.19930760712
3-Oxolup-20(29)-en-28-oic acid 289985 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1002/HLCA.19930760712
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1002/HLCA.19930760712
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/10.1002/HLCA.19930760712
https://doi.org/10.1002/CHIN.199410238
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1002/CHIN.199410238
https://doi.org/10.1002/HLCA.19930760712
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1002/CHIN.199410238
https://doi.org/10.1002/HLCA.19930760712
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/HLCA.19930760712
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1002/HLCA.19930760712
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/HLCA.19930760712
https://doi.org/10.1002/CHIN.199410238
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.19930760712
https://doi.org/10.1002/CHIN.199410238
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-1-(1-hydroxyethenyl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 163076622 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)O)C)C)C)C 428.70 unknown https://doi.org/10.1002/HLCA.19930760712
1-(1-Hydroxyethenyl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 163076621 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)O)C)C)C)C 428.70 unknown https://doi.org/10.1002/HLCA.19930760712
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1S,2R,3R,4S,5R,6S,7R,9R,12R)-3,4,7,12-tetraacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 162850795 Click to see 646.60 unknown https://doi.org/10.1016/0031-9422(95)00422-4
[(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 632.70 unknown https://doi.org/10.1002/HLCA.19930760712
[3,4,7,12-Tetraacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 102469334 Click to see 646.60 unknown https://doi.org/10.1016/0031-9422(95)00422-4
[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 632.70 unknown https://doi.org/10.1002/HLCA.19930760712
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
(3,4,12-Triacetyloxy-5-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 162909958 Click to see 652.70 unknown https://doi.org/10.1080/10575639408043932
https://doi.org/10.1002/HLCA.19930760712
[(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 590.60 unknown https://doi.org/10.1002/HLCA.19930760712
[(1S,2S,3S,4S,5R,6R,7S,9R,12R)-3,4,12-triacetyloxy-5-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 101626234 Click to see 652.70 unknown https://doi.org/10.1080/10575639408043932
[(1S,2S,3S,4S,5R,6S,7S,9R,12R)-3,4,12-triacetyloxy-5-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162909959 Click to see 652.70 unknown https://doi.org/10.1002/HLCA.19930760712
[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 590.60 unknown https://doi.org/10.1002/HLCA.19930760712
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1002/CHIN.199410238
> Organoheterocyclic compounds / Oxepanes
(1R,2R,3S,6R,9R)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecane-2,3-diol 162961928 Click to see CC1(C2CCC3CCC(C(C3(C2)O1)(C)O)O)C 240.34 unknown https://doi.org/10.1002/HLCA.19930760712
2,10,10-Trimethyl-11-oxatricyclo[7.2.1.01,6]dodecane-2,3-diol 162961927 Click to see 240.34 unknown https://doi.org/10.1002/HLCA.19930760712
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1002/HLCA.19930760712
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1002/CHIN.199410238
https://doi.org/10.1002/HLCA.19930760712
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2S,3R)-2-(3,4-dihydroxy-5-methoxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 163086166 Click to see COC1=CC(=CC(=C1O)O)C2C(CC3=C(C=C(C=C3O2)O)O)O 320.29 unknown https://doi.org/10.1002/HLCA.19930760712
2-(3,4-dihydroxy-5-methoxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 587502 Click to see COC1=CC(=CC(=C1O)O)C2C(CC3=C(C=C(C=C3O2)O)O)O 320.29 unknown https://doi.org/10.1002/HLCA.19930760712

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