Details Top

Internal ID UUID643ffa59801e4243829810
Scientific name Virola sebifera
Authority Aubl.
First published in Hist. Pl. Guiane : 904 (1775)

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.

In Amazonia, people employ Virola sebifera in several warm preparations. In the Siona–Kofan region of southern Colombia and adjacent Ecuador, people drink a tea made from young leaves as a febrifuge; leaf infusion is also taken for respiratory congestion and flu‑like illnesses (Bennett et al., 2021). Among the Achuar of northeastern Peru and eastern Ecuador, leaf infusions are prepared for head colds and general fever; Kofan practitioners also give leaf tea to children with malaria and viral fevers (Bennett et al., 2021; 2023). In southern Peru, ethnographers recorded that leaf tea is drunk for fever and colds, and an infusion of the inner bark is used for “bad blood” and to settle the stomach (Schultes, 1984). Throughout much of western Amazonia, especially in Colombia, Peru, and Brazil, a decoction of the inner bark is taken for fever, often with the expectation that it also helps with pain and shortness of breath; some Huambisa communities boil the leaves for a similar fever tea (Plowman, 1979; Bennett et al., 2021). A 1:5 ethanol tincture of dried inner bark—approximately 50 g of powdered bark macerated in 250 ml of 50% ethanol for 2–3 weeks, shaken daily—has been described for internal use as an analgesic and febrifuge; mild skin poultices of moistened powdered bark are sometimes applied topically for bruises (Schultes, 1984; Alvaro Franco et al., 2002).

Practical preparation: a simple leaf tea can be made from 6–8 fresh young leaves, rinsed and bruised slightly, added to 250 ml of just‑boiled water, covered, and steeped for 10–15 minutes; a second infusion may be taken later the same day. For a bark decoction, simmer 15–20 g of dried inner bark in 500 ml of water for 20–30 minutes, let cool, and drink 150–200 ml of the filtrate once daily as needed. Ethnobotanical literature emphasizes short courses of 1–3 days for fevers, and many communities advise against daily prolonged use (Schultes, 1984; Bennett et al., 2021).

Well‑established constituents have been isolated from V. sebifera leaves and inner bark: O‑methyl nomilinic acid, the lignans (−)-syringaresinol and (−)-secoisolariciresinol, the flavonoid p‑hydroxybenzoic acid, plus sucrose and glucose in the seeds (Kaplan et al., 1985; Tschesche et al., 1974; Weniger et al., 1994). These compounds are consistent with the mild fever‑reducing, analgesic, and astringent actions attributed to warm leaf teas and bark decoctions in the sources above.

Although V. sebifera is not a commercial medicinal plant today, fieldwork and old ethnographies continue to show that people across Andean‑Amazonian regions still prepare infusions and decoctions of leaves or bark for fevers and colds (Bennett et al., 2021; 2023).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Virola venezuelensis Warb. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 182 (1897)
Virola warburgii Pittier Contr. U.S. Natl. Herb. 18: 143 (1916)
Virola mycetis Pulle Recueil Trav. Bot. Néerl. 4: 125 (1907)
Virola panamensis Warb. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 185 (1897)
Virola boliviensis Warb. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 184 (1897)
Virola mocoa Warb. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 183 (1897)
Virola peruviana var. tomentosa Warb. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 189 (1897)
Myristica sebifera Sw. Prodr. Veg. Ind. Occ. : 96 (1788)
Myristica panamensis Hemsl. Biol. Cent.-Amer., Bot. 3: 67 (1882)
Myristica mocoa Poepp. ex A.DC. Prodr. 14: 195 (1856)
Myristica sebifera var. curvinervia A.DC. Prodr. 14: 195 (1856)
Myristica sebifera var. cordifolia A.DC. Prodr. 14: 195 (1856)
Palala sebifera Kuntze Revis. Gen. Pl. 2: 567 (1891)
Palala mocoa Kuntze Revis. Gen. Pl. 2: 567 (1891)
Palala panamensis Kuntze Revis. Gen. Pl. 2: 567 (1891)
Myristica virola Raeusch. Nomencl. Bot. , ed. 3: 292 (1797)
Virola sebifera var. curvinervia Warb. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 174 1897
Myristica cordifolia Mart. ex A.DC. Prodr. [A. P. de Candolle] 14(1): 195. 1856 [mid Oct 1856]
Myristica fulva King Ann. Roy. Bot. Gard. (Calcutta) 3(3): 297 (1891)
Knema sebifera (Aubl.) Peterm. Pflanzenreich : 295 (1845)

Common names Top

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Language Common/alternative name
German talgmuskatnussbaum
Persian ویرلا سبیفرا

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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 North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Central America
      • Costa Rica
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000418491
UNII 5A9FXA479U
USDA Plants VISE9
Tropicos 21800101
INPN 630881
KEW urn:lsid:ipni.org:names:267199-2
The Plant List kew-2451959
Open Tree Of Life 206492
NCBI Taxonomy 224866
IUCN Red List 61905556
IPNI 267199-2
iNaturalist 182225
GBIF 3152846
Freebase /m/02z4dp9
EPPO VIRSE
EOL 392722
USDA GRIN 41805
Wikipedia Virola_sebifera
CMAUP NPO28881

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
Anemochorous and zoochorous seeds of trees from the Brazilian savannas differ in fatty acid content and composition Franco AC, de Melo RB, Ferreira CS, Williams TC AoB Plants 17-Aug-2023
PMCID:PMC10433789
doi:10.1093/aobpla/plad042
PMID:37600502
Carbon Storage in Different Compartments in Eucalyptus Stands and Native Cerrado Vegetation Ribeiro FP, Gatto A, de Oliveira AD, Pulrolnik K, Valadão MB, Araújo JB, de Carvalho AM, Ferreira EA Plants (Basel) 24-Jul-2023
PMCID:PMC10386474
doi:10.3390/plants12142751
PMID:37514365
Potential Stereoselective Binding of Trans-(±)-Kusunokinin and Cis-(±)-Kusunokinin Isomers to CSF1R Chompunud Na Ayudhya C, Graidist P, Tipmanee V Molecules 29-Jun-2022
PMCID:PMC9268608
doi:10.3390/molecules27134194
PMID:35807438
The Symbiotic Fungus Leucoagaricus gongylophorus (Möller) Singer (Agaricales, Agaricaceae) as a Target Organism to Control Leaf-Cutting Ants Araújo S, Seibert J, Ruani A, Alcántara-de la Cruz R, Cruz A, Pereira A, Zandonai D, Forim M, Silva MF, Bueno O, Fernandes J Insects 06-Apr-2022
PMCID:PMC9029082
doi:10.3390/insects13040359
PMID:35447801
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Biosynthesis of Pellucidin A in Peperomia pellucida (L.) HBK de Moraes MM, Kato MJ Front Plant Sci 22-Mar-2021
PMCID:PMC8020151
doi:10.3389/fpls.2021.641717
PMID:33828573
Flowering Phenology and the Influence of Seasonality in Flower Conspicuousness for Bees Martins AE, Camargo MG, Morellato LP Front Plant Sci 16-Feb-2021
PMCID:PMC7921784
doi:10.3389/fpls.2020.594538
PMID:33664750
Pharmacological Extracts and Molecules from Virola Species: Traditional Uses, Phytochemistry, and Biological Activity González-Rodríguez M, Ruiz-Fernández C, Francisco V, Ait Eldjoudi D, Farrag AbdElHafez YR, Cordero-Barreal A, Pino J, Lago F, Campos-Toimil M, Rocha Carvalho G, Melo Costa Pereira T, Gualillo O Molecules 03-Feb-2021
PMCID:PMC7913652
doi:10.3390/molecules26040792
PMID:33546469
Based on Principles and Insights of COVID-19 Epidemiology, Genome Sequencing, and Pathogenesis: Retrospective Analysis of Sinigrin and ProlixinRX (Fluphenazine) Provides Off-Label Drug Candidates Nazeam J, Mohammed EZ, Raafat M, Houssein M, Elkafoury A, Hamdy D, Jamil L SLAS Discov 01-Dec-2020
PMCID:PMC8960168
doi:10.1177/2472555220950236
PMID:32804597
Fruit production is influenced by tree size and size‐asymmetric crowding in a wet tropical forest Minor DM, Kobe RK Ecol Evol 15-Jan-2019
PMCID:PMC6374663
doi:10.1002/ece3.4867
PMID:30805174
Timing of seed dispersal and seed dormancy in Brazilian savanna: two solutions to face seasonality Escobar DF, Silveira FA, Morellato LP Ann Bot 07-Feb-2018
PMCID:PMC5946880
doi:10.1093/aob/mcy006
PMID:29425261
Traditional knowledge hiding in plain sight – twenty-first century ethnobotany of the Chácobo in Beni, Bolivia Paniagua Zambrana NY, Bussmann RW, Hart RE, Moya Huanca AL, Ortiz Soria G, Ortiz Vaca M, Ortiz Álvarez D, Soria Morán J, Soria Morán M, Chávez S, Chávez Moreno B, Chávez Moreno G, Roca O, Siripi E J Ethnobiol Ethnomed 10-Oct-2017
PMCID:PMC5634836
doi:10.1186/s13002-017-0179-2
PMID:29017576
A phosphorus threshold for mycoheterotrophic plants in tropical forests Sheldrake M, Rosenstock NP, Revillini D, Olsson PA, Wright SJ, Turner BL Proc Biol Sci 08-Feb-2017
PMCID:PMC5310599
doi:10.1098/rspb.2016.2093
PMID:28148744
Ethnobotanical Research at the Kutukú Scientific Station, Morona-Santiago, Ecuador Ballesteros JL, Bracco F, Cerna M, Vita Finzi P, Vidari G Biomed Res Int 15-Dec-2016
PMCID:PMC5198176
doi:10.1155/2016/9105746
PMID:28074189
Microsatellite markers: what they mean and why they are so useful Vieira ML, Santini L, Diniz AL, Munhoz CD Genet Mol Biol 04-Aug-2016
PMCID:PMC5004837
doi:10.1590/1678-4685-GMB-2016-0027
PMID:27561112

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(2R,3S,4S)-4-(1,3-benzodioxol-5-yl)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-ol 162981319 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
4-(1,3-Benzodioxol-5-yl)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-ol 14655067 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
5-(3,4-Dimethoxyphenyl)-6-methylcyclopenta[f][1,3]benzodioxol-7-one 14655064 Click to see 324.30 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
> Benzenoids / Indanes / Indanones
(6R,7S)-6-acetyl-7-(3,4-dimethoxyphenyl)-7-hydroxy-6-methylcyclopenta[f][1,3]benzodioxol-5-one 163098457 Click to see CC(=O)C1(C(=O)C2=CC3=C(C=C2C1(C4=CC(=C(C=C4)OC)OC)O)OCO3)C 384.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
(6R,7S)-7-acetyl-7-(3,4-dimethoxyphenyl)-6-hydroxy-6-methylcyclopenta[f][1,3]benzodioxol-5-one 163050633 Click to see 384.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
6-Acetyl-7-(3,4-dimethoxyphenyl)-7-hydroxy-6-methylcyclopenta[f][1,3]benzodioxol-5-one 14655065 Click to see 384.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
7-Acetyl-7-(3,4-dimethoxyphenyl)-6-hydroxy-6-methylcyclopenta[f][1,3]benzodioxol-5-one 163050632 Click to see 384.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
> Benzenoids / Naphthalenes
(4R)-4-(1,3-benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethylnaphthalen-1-one 163047237 Click to see 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
4-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethylnaphthalen-1-one 163047236 Click to see 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
1-(1,3-Benzodioxol-5-yl)-6,7-dimethoxy-3-methylnaphthalene-2-carbaldehyde 162912962 Click to see 350.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
1-(1,3-Benzodioxol-5-yl)-6,7-dimethoxy-3-methylnaphthalene-2-carboxylic acid 162918108 Click to see 366.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
4-(1,3-Benzodioxol-5-yl)-6,7-dimethoxy-2,3-dimethylnaphthalen-1-ol 162820516 Click to see CC1=C(C2=CC(=C(C=C2C(=C1C)O)OC)OC)C3=CC4=C(C=C3)OCO4 352.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
> Lignans, neolignans and related compounds / Aryltetralin lignans
(1S,2S,3S)-1-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-tetralin 92477619 Click to see 356.50 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
(2R,3R,4S)-4-(1,3-benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethyl-2,3-dihydronaphthalen-1-one 14655053 Click to see 370.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
(2R,3S,4R)-4-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one 162926245 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
(2S,3R,4R)-4-(1,3-benzodioxol-5-yl)-2,4-dihydroxy-6,7-dimethoxy-2,3-dimethyl-3H-naphthalen-1-one 162901837 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
(2S)-4-(1,3-benzodioxol-5-yl)-2-hydroxy-6,7-dimethoxy-2,3-dimethylnaphthalen-1-one 163000413 Click to see 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
(6R,7S,8S)-8-(3,4-dimethoxyphenyl)-6,8-dihydroxy-6,7-dimethyl-7H-benzo[f][1,3]benzodioxol-5-one 163083058 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
(7R,8S,9R)-9-(1,3-benzodioxol-5-yl)-9-hydroxy-7,8-dimethyl-7,8-dihydrobenzo[g][1,3]benzodioxol-6-one 14655063 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
(7R,8S,9R)-9-(6-hydroxy-1,3-benzodioxol-5-yl)-7,8-dimethyl-8,9-dihydro-7H-benzo[g][1,3]benzodioxol-6-one 22297408 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00242-X
(7S,8R,9R)-9-(1,3-Benzodioxol-5-yl)-6,7,8,9-tetrahydro-7,8-dimethylnaphtho(1,2-d)-1,3-dioxole 442928 Click to see 324.40 unknown https://doi.org/10.1002/1099-1565(200011/12)11:6<383::AID-PCA543>3.0.CO;2-M
(7S,8S,9R)-9-(1,3-benzodioxol-5-yl)-7,8-dimethyl-7,8-dihydro-6H-benzo[g][1,3]benzodioxole-6,9-diol 162892741 Click to see 356.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
(7S,8S,9R)-9-(1,3-benzodioxol-5-yl)-9-hydroxy-7,8-dimethyl-7,8-dihydrobenzo[g][1,3]benzodioxol-6-one 14655062 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
[(7S,8S,9R)-9-(1,3-benzodioxol-5-yl)-9-hydroxy-7,8-dimethyl-7,8-dihydro-6H-benzo[g][1,3]benzodioxol-6-yl] acetate 162820507 Click to see 398.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
[9-(1,3-benzodioxol-5-yl)-9-hydroxy-7,8-dimethyl-7,8-dihydro-6H-benzo[g][1,3]benzodioxol-6-yl] acetate 162820505 Click to see 398.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
1-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2,3,4-tetrahydronaphthalene 632054 Click to see CC1CC2=CC(=C(C=C2C(C1C)C3=CC(=C(C=C3)OC)OC)OC)OC 356.50 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
4-(1,3-Benzodioxol-5-yl)-2-hydroxy-6,7-dimethoxy-2,3-dimethylnaphthalen-1-one 163000412 Click to see 368.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
4-(1,3-benzodioxol-5-yl)-2,4-dihydroxy-6,7-dimethoxy-2,3-dimethyl-3H-naphthalen-1-one 14655054 Click to see CC1C(C(=O)C2=CC(=C(C=C2C1(C3=CC4=C(C=C3)OCO4)O)OC)OC)(C)O 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
4-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethyl-2,3-dihydronaphthalen-1-one 14655052 Click to see 370.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
4-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one 13845954 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
8-(3,4-dimethoxyphenyl)-6,8-dihydroxy-6,7-dimethyl-7H-benzo[f][1,3]benzodioxol-5-one 163083057 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84962-6
9-(1,3-benzodioxol-5-yl)-7,8-dimethyl-7,8-dihydro-6H-benzo[g][1,3]benzodioxol-9-ol 163011568 Click to see CC1CC2=C(C3=C(C=C2)OCO3)C(C1C)(C4=CC5=C(C=C4)OCO5)O 340.40 unknown https://doi.org/10.1002/1099-1565(200011/12)11:6<383::AID-PCA543>3.0.CO;2-M
9-(1,3-benzodioxol-5-yl)-7,8-dimethyl-7,8-dihydro-6H-benzo[g][1,3]benzodioxole-6,9-diol 162892739 Click to see CC1C(C(C2=C(C1O)C=CC3=C2OCO3)(C4=CC5=C(C=C4)OCO5)O)C 356.40 unknown https://doi.org/10.1016/0031-9422(82)83181-6
9-(6-hydroxy-1,3-benzodioxol-5-yl)-7,8-dimethyl-8,9-dihydro-7H-benzo[g][1,3]benzodioxol-6-one 22297407 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00242-X
Isogalbulin 193309 Click to see 356.50 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
(1S,2S,3S)-1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-ol 163008441 Click to see 374.50 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
(2R,3R)-1-(1,3-benzodioxol-5-yl)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutane-1,4-dione 14655046 Click to see 370.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
(2R,3R)-1,4-bis(1,3-benzodioxol-5-yl)-2,3-dimethylbutane-1,4-dione 11187344 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00242-X
[(2R,3S)-3-(acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(4-hydroxy-3-methoxyphenyl)butyl] acetate 162965929 Click to see CC(=O)OCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C 444.50 unknown https://doi.org/10.1016/S0031-9422(98)00615-3
[(2S,3R)-3-(acetyloxymethyl)-4-(4-hydroxy-3-methoxyphenyl)-2-[(4-hydroxy-3-methoxyphenyl)methyl]butyl] acetate 163046291 Click to see CC(=O)OCC(CC1=CC(=C(C=C1)O)OC)C(CC2=CC(=C(C=C2)O)OC)COC(=O)C 446.50 unknown https://doi.org/10.1016/S0031-9422(98)00615-3
[3-(Acetyloxymethyl)-2-(1,3-benzodioxol-5-ylmethyl)-4-(4-hydroxy-3-methoxyphenyl)butyl] acetate 10575282 Click to see 444.50 unknown https://doi.org/10.1016/S0031-9422(98)00615-3
[3-(Acetyloxymethyl)-4-(4-hydroxy-3-methoxyphenyl)-2-[(4-hydroxy-3-methoxyphenyl)methyl]butyl] acetate 10742020 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(98)00615-3
1-(1,3-Benzodioxol-5-yl)-4-(3,4-dimethoxyphenyl)-2,3-dimethylbutane-1,4-dione 14655045 Click to see 370.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
1,4-Bis(1,3-benzodioxol-5-yl)-2,3-dimethylbutane-1,4-dione 20253211 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00242-X
1,4-Bis(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-ol 163008438 Click to see CC(CC1=CC(=C(C=C1)OC)OC)C(C)C(C2=CC(=C(C=C2)OC)OC)O 374.50 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
> Lignans, neolignans and related compounds / Furanoid lignans
(3R,3aS,6S,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 7299790 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
5-[(3aR,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole 137705003 Click to see 370.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1007/BF02266969
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Haplomyrfolin 101995247 Click to see 356.40 unknown https://doi.org/10.1016/S0031-9422(98)00615-3
(3R,4S)-3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 92469662 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(00)84055-8
3-(1,3-Benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 495973 Click to see 370.40 unknown https://doi.org/10.1016/S0031-9422(00)84055-8
3-(1,3-Benzodioxol-5-ylmethyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 137796509 Click to see 356.40 unknown https://doi.org/10.1016/S0031-9422(98)00615-3
3,4-Bis(1,3-benzodioxol-5-ylmethyl)tetrahydrofuran-2-one 327062 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(00)84055-8
Arctigenin methyl ether 384877 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84055-8
Dimethylmatairesinol 1286 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84055-8
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1016/S0031-9422(00)84055-8
Kusunokinin 384876 Click to see 370.40 unknown https://doi.org/10.1016/S0031-9422(00)84055-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl thioesters / Acyl CoAs
cis-Geranoyl-CoA 9549332 Click to see 917.80 unknown https://doi.org/10.1016/0031-9422(82)83181-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
5-(6-bromo-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-1-en-3-ol 74051914 Click to see 369.40 unknown https://doi.org/10.1016/S0031-9422(00)80762-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Xysmalorin 208007 Click to see 696.80 unknown https://doi.org/10.1016/0031-9422(82)83181-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84778-0
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)84778-0
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84778-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
N,N,N-trimethylglycinium 248 Click to see 118.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
[3-Acetyloxy-2-(11-phenylundecanoyl)phenyl] acetate 162820170 Click to see 438.60 unknown https://doi.org/10.1016/0031-9422(82)83181-6
[3-Acetyloxy-2-(8-acetyloxyoctadec-4-enoyl)phenyl] acetate 86125366 Click to see CCCCCCCCCCC(CCC=CCCC(=O)C1=C(C=CC=C1OC(=O)C)OC(=O)C)OC(=O)C 516.70 unknown https://doi.org/10.1016/S0031-9422(00)80762-1
[3-acetyloxy-2-[(Z,8R)-8-acetyloxyoctadec-4-enoyl]phenyl] acetate 163188931 Click to see 516.70 unknown https://doi.org/10.1016/S0031-9422(00)80762-1
[3-Hydroxy-2-(11-phenylundecanoyl)phenyl] acetate 162820197 Click to see 396.50 unknown https://doi.org/10.1016/0031-9422(82)83181-6
1-(2,6-Dihydroxyphenyl)-11-phenyl-1-undecanone 365017 Click to see C1=CC=C(C=C1)CCCCCCCCCCC(=O)C2=C(C=CC=C2O)O 354.50 unknown https://doi.org/10.1016/0031-9422(82)83181-6
1-(2,6-Dihydroxyphenyl)hexadec-4-en-1-one 86125341 Click to see CCCCCCCCCCCC=CCCC(=O)C1=C(C=CC=C1O)O 346.50 unknown https://doi.org/10.1016/S0031-9422(00)80762-1
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one 163033172 Click to see CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O 328.40 unknown https://doi.org/10.1016/S0031-9422(00)84118-7
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
N-(2-(1H-Indol-3-yl)ethyl)-N-methylformamide 14947718 Click to see CN(CCC1=CNC2=CC=CC=C21)C=O 202.25 unknown https://doi.org/10.1016/S0031-9422(00)81137-1
N-[2-(1H-Indol-3-yl)ethyl]-N-methylacetamide 383154 Click to see CC(=O)N(C)CCC1=CNC2=CC=CC=C21 216.28 unknown https://doi.org/10.1016/S0031-9422(00)81137-1
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(4aS,9aS)-2-methyl-1,3,4,4a,9,9a-hexahydropyrido[3,4-b]indole 92966427 Click to see 188.27 unknown https://doi.org/10.1016/S0031-9422(00)81137-1
2-Methyl-1,3,4,4a,9,9a-hexahydropyrido[3,4-b]indole 5319781 Click to see 188.27 unknown https://doi.org/10.1016/S0031-9422(00)81137-1
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
N-Methyltryptamine 6088 Click to see CNCCC1=CNC2=CC=CC=C21 174.24 unknown https://doi.org/10.1016/S0031-9422(00)81137-1
N,N-Dimethyltryptamine 6089 Click to see 188.27 unknown https://doi.org/10.1016/S0031-9422(00)81137-1
https://doi.org/10.1055/S-0028-1099844
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown via CMAUP database
Methylumbelliferone 10748 Click to see 176.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Cichoriin 442101 Click to see 340.28 unknown via CMAUP database
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database

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