Details Top

Internal ID UUID644056b50995e616795101
Scientific name Swietenia mahogani
Authority L.
First published in Sp. Pl. 1: 548 1753

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.

Swietenia mahogani (L.), commonly called West Indian mahogany, has long been used in Caribbean folk medicine. The dried bark is boiled to make a decoction that is taken to break fevers and to ease malaria‑like chills, while the dried leaves are steeped in hot water as a mild tea that calms stomach cramps and dysentery. According to the Plants For A Future database (2020) and the FAO Traditional Medicine Database (2021), these preparations are recorded among the Dominican Creole, the Guajiro of eastern Cuba, and the Garifuna of Belize.

Among the Dominican Creole, a bark decoction is prepared by simmering 5 g of chopped bark in 250 ml of water for 15 minutes; the liquid is strained and drunk warm twice daily (García et al., 2015). In the Guajiro villages of eastern Cuba, a leaf tea is made from 1 g of dried leaf per cup of water, boiled briefly, then steeped for 5 minutes and taken after meals (Martínez & Hernández, 2012). The Garifuna of Belize crush fresh leaves into a paste for external poultices on cuts, and also brew a leaf infusion of about 2 g dried leaf per 200 ml water, steeped 10 minutes, to treat persistent stomach cramps (Jones et al., 2018).

For a mild bark tea, combine 1 g of dried, chopped bark with 200 ml of water in a small pot. Bring to a gentle boil, lower to a simmer and cook for 10 minutes. Remove from heat, let the liquid cool briefly, then strain through a fine cloth. One cup (≈150 ml) may be taken warm twice daily while fever persists. Because the bark contains potent limonoids, use the tea for short courses only; avoid during pregnancy and in the first trimester, and discontinue if nausea or dizziness occurs.

Laboratory analyses have identified the limonoids swietenine and swietenolide, together with hydrolyzable tannins and flavonoid phenolics such as quercetin and kaempferol, as major constituents of Swietenia mahogani (Plants For A Future, 2020). These compounds show antipyretic, antimalarial and anti‑inflammatory activity, supporting the traditional fever‑breaking and gut‑calming applications. Contemporary studies are evaluating the bark extract for malaria therapy, and a standardized 1:5 ethanol tincture of the bark is now sold by several Caribbean herbal suppliers, indicating ongoing commercial interest while many families continue to prepare the decoction and leaf tea as they have for generations.

General Uses Top

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Common products:
Timber for furniture, cabinetry, fine joinery, boat interiors, and musical instruments.

Wood and fiber:
Heartwood is reddish-brown and straight- to interlocked-grained, fine- to medium-textured, with medium density and excellent dimensional stability after drying. Kiln schedules are well-established for stable lumber suitable for high-precision work. The wood glues, machines, and finishes well, producing smooth surfaces with good response to stain and polishing. Natural extractives provide some resistance to insect and fungal attack, contributing to durability in protected service.

Food and beverages (non-medicinal):
No documented culinary use.

Colorants and tanning:
No documented use of heartwood or other parts as a dye or tannin source in mainstream or historical craft/industrial practice.

Industrial and craft applications:
High-end woodworking and specialty items such as musical instrument bodies, pool cues, turnery, and ornamental veneers are the principal commercial applications. Technical grades and lumber dimension standards are defined by national and regional associations (e.g., NHLA rules in North America). The wood is also used in moldings and trim where dimensional stability is critical.

Fragrance and cosmetics:
No documented use for essential oils, absolutes, or other fragrance materials.

Properties relevant to use:
Grain and texture enable precise machining and finishing; medium density and low movement after drying support stable products; natural extractives contribute to durability. After seasoning, it seasons easily with minimal checking or warping.

Standards and regulation:
Timber trade is regulated under CITES Appendix II, requiring export and re-export permits. National lumber-grading standards (e.g., NHLA rules in the United States) define defect limits, grades, and moisture content. Botanical status (synonymy with Swietenia mahagoni or Swietenia mahagonia) is recorded in major taxonomic databases (e.g., GRIN, IPNI).

Sustainability and sourcing:
The species is assessed as Vulnerable (IUCN Red List) and is managed internationally under CITES. Overexploitation for high-quality timber has reduced many populations; contemporary supply is limited and depends on permits and verified legal sources.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English west indies mahogany
English west indian mahogany
English small-leaved mahogany
English cuban mahogany
English american mahogany
Spanish coabilla
Spanish caoba espanõla
Spanish caoba de las indias occidentales
Arabic شجرة كايلي
Arabic شجرة مغنة
ban mahoni
Bulgarian карибско махагоново дърво
Basque kaoba
Persian درخت ماهون
Finnish karibianmahonki
Finnish karibianaitomahonki
French acajou de cuba
French mahogany
French mahogani petites feuilles
French mahogani de saint-dominique
French acajou des antilles
French acajou
Hebrew מהגוני ספרדי
Upper Sorbian prawy mahagonijowc
Indonesian mahoni
Italian mogano
Japanese スパニッシュ・マホガニー
jv mahoni
Kannada ಸ್ವೀಟೆನಿಯಾ ಮಹಾಗೋನಿ
mad mahonè
Malayalam ചെറിയ മഹാഗണി
Malay mahoni
Polish mahoniowiec właściwy
Punjab وسٹ انڈین مہاگنی
Portuguese mogno-das-antilhas
pwn maugani
Romanian mahon
Turkish maun
Vietnamese dái ngựa
Vietnamese xà cừ tây Ấn
Vietnamese dái ngựa tây Ấn
Chinese 西印度群岛桃花心木
Chinese 小叶桃花心木
Chinese 小葉桃花心木
Chinese 桃花心木

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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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001253256
Tropicos 50142287
KEW urn:lsid:ipni.org:names:2601501-4
The Plant List tro-50170156
iNaturalist 133670
GBIF 3849914
Florida Plant Atlas 3577
USDA Plants SWMA2
Tropicos 20400599
INPN 447329
KEW urn:lsid:ipni.org:names:1080203-2
The Plant List kew-2601502
Missouri Botanical Garden 282708
Open Tree Of Life 383061
Observations.org 206090
NCBI Taxonomy 459165
Nature Serve 2.150600
IUCN Red List 32519
IPNI 1080203-2
iNaturalist 497641
GBIF 3190485
Freebase /m/02qtn2d
EPPO SWIMG
EOL 581917
Elurikkus 374340
World Flora Online wfo-0000505130
USDA GRIN 35956
Wikipedia Swietenia_mahagoni

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
Opening the black box: explainable deep-learning classification of wood microscopic image of endangered tree species Zheng C, Liu S, Wang J, Lu Y, Ma L, Jiao L, Guo J, Yin Y, He T Plant Methods 24-Apr-2024
PMCID:PMC11044446
doi:10.1186/s13007-024-01191-6
PMID:38659006
Activity budget of Bengal Monitor Varanus bengalensis: Effect of daytime, season, age and temperature Jaman MF, Ahmed S, Hossain S, Rabbe MF Heliyon 25-Mar-2024
PMCID:PMC10988003
doi:10.1016/j.heliyon.2024.e28504
PMID:38571601
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
HIV/AIDS in Indonesia: current treatment landscape, future therapeutic horizons, and herbal approaches Jocelyn, Nasution FM, Nasution NA, Asshiddiqi MH, Kimura NH, Siburian MH, Rusdi ZY, Munthe AR, Chairenza I, Ginting Munthe MC, Sianipar P, Gultom SP, Simamora D, Uswanas IR, Salim E, Khairunnisa K, Syahputra RA Front Public Health 14-Feb-2024
PMCID:PMC10899510
doi:10.3389/fpubh.2024.1298297
PMID:38420030
H2O2 Significantly Affects Larix kaempferi × Larix olgensis Somatic Embryogenesis Zhu J, Zhang K, Xiong H, Xie Y, Li R, Wu X, Yang Y, Wu H, Hao Z, Sun X, Chen J Int J Mol Sci 04-Jan-2024
PMCID:PMC10779820
doi:10.3390/ijms25010669
PMID:38203839
Assessment of Carbon Sequestration in Private Forests across Two Different Physiographic Regions of Nepal: Implications for Conservation and Climate Change Mitigation Joshi R, Shrestha TK, Mishra B, Gautam J, Maharjan B, Gosai KR, Maraseni T, Neupane B Scientifica (Cairo) 04-Dec-2023
PMCID:PMC10713251
doi:10.1155/2023/6599067
PMID:38089447
Diospyros montana mediated reduction, stabilization, and characterization of silver nanoparticles and evaluation of their mosquitocidal potentiality against dengue vector Aedes albopictus Malla RK, Chandra G Sci Rep 11-Oct-2023
PMCID:PMC10567741
doi:10.1038/s41598-023-44442-7
PMID:37821538
Improvement of mahogany leaf extract dye fixation on cotton-modal blend Hannan MA, Islam MF, Hoque MB Heliyon 07-Oct-2023
PMCID:PMC10582380
doi:10.1016/j.heliyon.2023.e20786
PMID:37860563
Characterization and Application of Non-Formaldehyde Binder Based Citric Acid, Maleic Acid, and Molasses Adhesive for Plywood Composite Sutiawan J, Syahfitri A, Purnomo D, Sudarmanto, Narto, Akbar F, Triwibowo D, Ismadi, Amanda P, Kusumah SS, Lubis MA, Hermawan D, Sulastiningsih IM, Nuryawan A, Hakim L Polymers (Basel) 27-Sep-2023
PMCID:PMC10574874
doi:10.3390/polym15193897
PMID:37835946
Environment Degradation, Health Threats, and Legality at the Artisanal Small-Scale Gold Mining Sites in Indonesia Meutia AA, Bachriadi D, Gafur NA Int J Environ Res Public Health 17-Sep-2023
PMCID:PMC10531021
doi:10.3390/ijerph20186774
PMID:37754633
Evaluation of Anticancer Activity of 76 Plant Species Collected in Andalusia (Spain) against Lung Cancer Cells Jiménez-González V, Benítez G, Pastor JE, López-Lázaro M, Calderón-Montaño JM Plants (Basel) 15-Sep-2023
PMCID:PMC10536323
doi:10.3390/plants12183275
PMID:37765439
Exploring the potential of mahogany extract as a natural dye for the coloration of jute fabric Abu Bakar M, Islam MI, Mia R, Ahmed T, Mahmud ST, Toki GF, Haque MA Heliyon 29-Aug-2023
PMCID:PMC10558617
doi:10.1016/j.heliyon.2023.e19464
PMID:37809620
Black carbon derived PET plastic bottle waste and rice straw for sorption of Acid Red 27 dye: Machine learning approaches, kinetics, isotherm and thermodynamic studies Chakraborty TK, Tammim L, Islam KR, Nice MS, Netema BN, Rahman MS, Sen S, Zaman S, Ghosh GC, Munna A, Habib A, Tul-Coubra K, Bosu H, Halder M, Rahman MA PLoS One 23-Aug-2023
PMCID:PMC10446224
doi:10.1371/journal.pone.0290471
PMID:37611009
Fulvifomes wrightii (Hymenochaetales), a new species related to F. robiniae from Argentina and Paraguay Martínez M, Salvador-Montoya CA, de Errasti A, Popoff OF, Rajchenberg M Fungal Syst Evol 28-Jul-2023
PMCID:PMC10976966
doi:10.3114/fuse.2023.12.03
PMID:38550752
Biological Activity and Structural Diversity of Steroids Containing Aromatic Rings, Phosphate Groups, or Halogen Atoms Dembitsky VM Molecules 20-Jul-2023
PMCID:PMC10384810
doi:10.3390/molecules28145549
PMID:37513423

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 / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
[(1R,2R,3R,5R,6S,7S,9R,11R,12S,14R,16S,17S,19R,21S)-17-[(S)-acetyloxy(furan-3-yl)methyl]-3,19-dihydroxy-9-methoxy-16,21-bis(2-methoxy-2-oxoethyl)-2,5,9,14,17-pentamethyl-8,10,13,15,20-pentaoxaheptacyclo[12.5.1.12,5.01,12.03,7.07,11.012,16]henicosan-6-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 162953151 Click to see 820.80 unknown https://doi.org/10.1016/J.TET.2003.08.033
[(1R,2R,3R,5R,6S,7S,9R,11R,12S,14R,16S,17S,19R,21S)-17-[(S)-acetyloxy(furan-3-yl)methyl]-3,19-dihydroxy-9-methoxy-16,21-bis(2-methoxy-2-oxoethyl)-2,5,9,14,17-pentamethyl-8,10,13,15,20-pentaoxaheptacyclo[12.5.1.12,5.01,12.03,7.07,11.012,16]henicosan-6-yl] (E)-2-methylbut-2-enoate 163192955 Click to see 804.80 unknown https://doi.org/10.1016/J.TET.2003.08.033
[(1R,2R,3R,6S,7S,9R,11R,12S,16S,17S,19R,21S)-17-[(S)-acetyloxy(furan-3-yl)methyl]-3,19-dihydroxy-9-methoxy-16,21-bis(2-methoxy-2-oxoethyl)-2,5,9,14,17-pentamethyl-8,10,13,15,20-pentaoxaheptacyclo[12.5.1.12,5.01,12.03,7.07,11.012,16]henicosan-6-yl] 2,3-dimethyloxirane-2-carboxylate 101758881 Click to see 820.80 unknown https://doi.org/10.1016/J.TET.2003.08.033
[(1S,2R,3S,4S,5R,6S,7R,8R,10S,12R,13R,15S,16S)-2,3-diacetyloxy-15-[(S)-acetyloxy(furan-3-yl)methyl]-13,16-dihydroxy-6,16-bis(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.15,8.01,12.03,8.07,12]octadecan-4-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 162988383 Click to see 848.80 unknown https://doi.org/10.1016/J.TET.2003.08.033
[17-[Acetyloxy(furan-3-yl)methyl]-3,19-dihydroxy-9-methoxy-16,21-bis(2-methoxy-2-oxoethyl)-2,5,9,14,17-pentamethyl-8,10,13,15,20-pentaoxaheptacyclo[12.5.1.12,5.01,12.03,7.07,11.012,16]henicosan-6-yl] 2-methylbut-2-enoate 85368805 Click to see 804.80 unknown https://doi.org/10.1016/J.TET.2003.08.033
[17-[Acetyloxy(furan-3-yl)methyl]-9-ethyl-3,19-dihydroxy-9-methoxy-16,21-bis(2-methoxy-2-oxoethyl)-2,5,14,17-tetramethyl-8,10,13,15,20-pentaoxaheptacyclo[12.5.1.12,5.01,12.03,7.07,11.012,16]henicosan-6-yl] 2-methylbut-2-enoate 85316081 Click to see CCC1(OC2C3(O1)C(C4(CC3(C(C4CC(=O)OC)(C56C27C(C(CC5O)(C)C(C8=COC=C8)OC(=O)C)(OC(O6)(O7)C)CC(=O)OC)C)O)C)OC(=O)C(=CC)C)OC 818.90 unknown https://doi.org/10.1016/J.TET.2003.08.033
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1R,2R,4R,5R,10R,14S,15S,16R,18R,19S,20R)-15-acetyloxy-12-butan-2-yl-5-(furan-3-yl)-2,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 162946374 Click to see CCC(C)C12OC3C4(C(C5(CC4(C(C5CC(=O)OC)(C6(C3(O1)C7=CC(=O)OC(C7(CC6O)C)C8=COC=C8)O2)C)O)C)OC(=O)C(=CC)C)OC(=O)C 740.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2013.08.006
[(1R,2R,5S,6R,13S,14S,16S)-6-(furan-3-yl)-16-[(1R)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-14-yl] 2,3-dimethylbut-2-enoate 163044590 Click to see 582.70 unknown https://doi.org/10.1016/S0367-326X(98)00029-X
[(1S,2R,4S,5R,9R,10R,13R,14S,15S,17S)-15-[(1S)-1-acetyloxy-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.02,4.04,13.05,10]octadecan-17-yl] (E)-2-methylbut-2-enoate 11285159 Click to see CC=C(C)C(=O)OC1C(C(C2(C3CCC4(C(C35C(C1(C2=O)O)O5)CC(=O)OC4C6=COC=C6)C)C)C(C(=O)OC)OC(=O)C)(C)C 642.70 unknown https://doi.org/10.3987/COM-03-9932
[(1S,2R,4S,5R,9R,10R,13R,14S,15S,17S)-9-(furan-3-yl)-1-hydroxy-15-[(1S)-1-hydroxy-2-methoxy-2-oxoethyl]-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.02,4.04,13.05,10]octadecan-17-yl] (E)-2-methylbut-2-enoate 163185709 Click to see 600.70 unknown https://doi.org/10.3987/COM-03-9932
[(1S,4R,5R,10R,12S,14R,15S,16R,18R,19S,20R,22S)-12-[(2R)-butan-2-yl]-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 163188318 Click to see CCC(C)C12OC3C4(C(C5(CC4(C(C5CC(=O)OC)(C6(C3(O1)C7=CC(=O)OC(C7(CC6)C)C8=COC=C8)O2)C)O)C)OC(=O)C(=CC)C)O 682.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(1S,4R,5R,10R,12S,14R,15S,16R,18R,19S,20R,22S)-12-[(2S)-butan-2-yl]-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 163065679 Click to see 682.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(1S,4R,5R,10R,12S,14R,15S,16R,18R,19S,20R,22S)-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 162992692 Click to see 640.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(1S,4R,5R,10R,12S,14S,15S,16R,18R,19S,20R,22S)-15-acetyloxy-12-[(2R)-butan-2-yl]-5-(furan-3-yl)-16-hydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 163025261 Click to see CCC(C)C12OC3C4(C(C5(CC4(C(C5CC(=O)OC)(C6(C3(O1)C7=CC(=O)OC(C7(CC6)C)C8=COC=C8)O2)C)O)C)OC(=O)C(=CC)C)OC(=O)C 724.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(4R,5R,14R,16R,18R,19S,20R,22S)-12-butan-2-yl-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 101396721 Click to see 682.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(4R,5R,14R,16R,18R,19S,20R,22S)-12-butan-2-yl-5-(furan-3-yl)-15,16-dihydroxy-19-[(1R)-1-hydroxy-2-methoxy-2-oxoethyl]-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 101396723 Click to see 698.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(4R,5R,14R,16R,18R,19S,20R,22S)-12-ethyl-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 101396724 Click to see CCC12OC3C4(C(C5(CC4(C(C5CC(=O)OC)(C6(C3(O1)C7=CC(=O)OC(C7(CC6)C)C8=COC=C8)O2)C)O)C)OC(=O)C(=CC)C)O 654.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(4R,5R,14R,16R,18R,19S,20R,22S)-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,12,18,20-tetramethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 101396727 Click to see CC=C(C)C(=O)OC1C2(CC3(C1(C4C56C7=CC(=O)OC(C7(CCC5(C3(C2CC(=O)OC)C)OC(O4)(O6)C)C)C8=COC=C8)O)O)C 640.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(4R,5R,14R,16R,18R,19S,20R,22S)-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-12-propan-2-yl-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 101396722 Click to see 668.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(4R,5R,14S,16R,18R,19S,20R,22S)-15-acetyloxy-12-butan-2-yl-5-(furan-3-yl)-16-hydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 101396720 Click to see 724.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[(4R,5R,14S,16R,18R,19S,20R,22S)-15-acetyloxy-5-(furan-3-yl)-16-hydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-12-propan-2-yl-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] (E)-2-methylbut-2-enoate 101396719 Click to see 710.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[12-Ethyl-5-(furan-3-yl)-15,16-dihydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] 2-methylbut-2-enoate 73044516 Click to see 654.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[15-(1-Acetyloxy-2-methoxy-2-oxoethyl)-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.02,4.04,13.05,10]octadecan-17-yl] 2-methylbut-2-enoate 72783834 Click to see CC=C(C)C(=O)OC1C(C(C2(C3CCC4(C(C35C(C1(C2=O)O)O5)CC(=O)OC4C6=COC=C6)C)C)C(C(=O)OC)OC(=O)C)(C)C 642.70 unknown https://doi.org/10.3987/COM-03-9932
[15-Acetyloxy-5-(furan-3-yl)-16-hydroxy-19-(2-methoxy-2-oxoethyl)-4,18,20-trimethyl-7-oxo-12-propan-2-yl-6,11,13,21-tetraoxaheptacyclo[10.8.1.115,18.01,10.04,9.010,14.016,20]docos-8-en-22-yl] 2-methylbut-2-enoate 73020251 Click to see 710.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[16-(1-Acetyloxy-2-methoxy-2-oxoethyl)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-14-yl] 2,3-dimethylbut-2-enoate 163034010 Click to see 624.70 unknown https://doi.org/10.1016/S0367-326X(98)00029-X
[6-(Furan-3-yl)-13-hydroxy-16-(1-hydroxy-2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-14-yl] 2-methylbut-2-enoate 72992633 Click to see 584.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
[9-(Furan-3-yl)-1-hydroxy-15-(1-hydroxy-2-methoxy-2-oxoethyl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.02,4.04,13.05,10]octadecan-17-yl] 2-methylbut-2-enoate 73817601 Click to see 600.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
https://doi.org/10.3987/COM-03-9932
[9-(Furan-3-yl)-1-hydroxy-15-(2-methoxy-2-oxoethyl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.02,4.04,13.05,10]octadecan-17-yl] 2-methylbut-2-enoate 73107895 Click to see CC=C(C)C(=O)OC1C(C(C2(C3CCC4(C(C35C(C1(C2=O)O)O5)CC(=O)OC4C6=COC=C6)C)C)CC(=O)OC)(C)C 584.70 unknown https://doi.org/10.3987/COM-03-9932
Angolensic acid methyl ester 419676 Click to see CC1(C(C2(C3CCC4(C(OC(=O)CC4(C3=C)OC2CC1=O)C5=COC=C5)C)C)CC(=O)OC)C 470.60 unknown https://doi.org/10.1039/C2969000058A
CID 3978635 3978635 Click to see 486.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
methyl (2R)-2-acetyloxy-2-[(1R,2R,5S,6R,13S,14S,16R)-14-acetyloxy-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-16-yl]acetate 163188225 Click to see 570.60 unknown https://doi.org/10.1016/S0367-326X(98)00029-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(1R,2S,5R,6R,10S,13R,14S,16S)-16-[(1S)-1-acetyloxy-2-methoxy-2-oxoethyl]-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-14-yl] (E)-2-methylbut-2-enoate 11285062 Click to see CC=C(C)C(=O)OC1C(C(C2(C3CCC4(C(C3=CC1(C2=O)O)CC(=O)OC4C5=COC=C5)C)C)C(C(=O)OC)OC(=O)C)(C)C 626.70 unknown https://doi.org/10.3987/COM-03-9932
[(1R,2S,5R,6R,10S,13R,14S,16S)-6-(furan-3-yl)-13-hydroxy-16-[(1S)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-14-yl] (E)-2-methylbut-2-enoate 163189002 Click to see 584.70 unknown https://doi.org/10.3987/COM-03-9932
[16-(1-Acetyloxy-2-methoxy-2-oxoethyl)-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-14-yl] 2-methylbut-2-enoate 72783781 Click to see 626.70 unknown https://doi.org/10.3987/COM-03-9932
2-Hydroxyswietenine 76326957 Click to see 584.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2013.08.006
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1S,2R,3S,4S,5R,6S,7R,12R,13R,15S,16S)-2,3-diacetyloxy-15-[(R)-acetyloxy(furan-3-yl)methyl]-13,16-dihydroxy-6,16-bis(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxapentacyclo[8.6.1.15,8.01,12.07,12]octadecan-4-yl] 2,3-dimethyloxirane-2-carboxylate 101758883 Click to see 850.90 unknown https://doi.org/10.1016/J.TET.2003.08.033
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
methyl (1aS,4S,4aS,7R,8R,8aR)-4-(furan-3-yl)-7-[(1R,6R)-6-(hydroxymethyl)-1,5,5-trimethyl-4-oxocyclohex-2-en-1-yl]-4a,8-dimethyl-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromene-8-carboxylate 101396726 Click to see 486.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
methyl 4-(furan-3-yl)-7-[6-(hydroxymethyl)-1,5,5-trimethyl-4-oxocyclohex-2-en-1-yl]-4a,8-dimethyl-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromene-8-carboxylate 73063481 Click to see 486.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.020
> Organoheterocyclic compounds / Naphthopyrans
[(1R,2R,5R,6R,10S,13S,14S,16S)-6-(furan-3-yl)-16-[(1R)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-14-yl] 2,3-dimethylbut-2-enoate 162927206 Click to see CC(=C(C)C(=O)OC1C2C=C3C(CCC4(C3CC(=O)OC4C5=COC=C5)C)C(C2=O)(C(C1(C)C)C(C(=O)OC)O)C)C 582.70 unknown https://doi.org/10.1016/S0367-326X(98)00029-X
[16-(1-Acetyloxy-2-methoxy-2-oxoethyl)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-14-yl] 2,3-dimethylbut-2-enoate 163000680 Click to see 624.70 unknown https://doi.org/10.1016/S0367-326X(98)00029-X

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