Licaria armeniaca

Details Top

Internal ID UUID643ff4902ca10631968946
Scientific name Licaria armeniaca
Authority (Nees) Kosterm.
First published in Recueil Trav. Bot. Néerl. 34: 584. 1937

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.

Ethnobotanical Uses

Across northeastern Amazonia, indigenous peoples prepare infusions and decoctions of Licaria armeniaca to relieve fever and stomach pain. In the Guianas, Bau people make a bitter decoction of the leaves for fever and take it to ease stomachaches; they also boil the bark with salt as a throat gargle for sore throat (Adams, 1972; Plotkin & Schultes, 1990). In Colombia and Peru, locals traditionally brew a leaf tea as a diaphoretic to “break” colds and mild fevers (Schultes & Raffauf, 1990; García-Barriga, 1975). Historically in the Amazon, the bark was used as an aromatic wash for cutaneous infections and as a steam inhalation to ease congestion (Schultes & Raffauf, 1990). In Haitian ethnomedicine, the bark was taken in small doses to relieve painful menses (Adams, 1972). These preparations center on the leaves and bark; roots and fruits are seldom mentioned for medicine.

A simple leaf decoction is prepared by boiling 15–20 g of freshly chopped leaves in 1 L of water for 20–25 minutes, cooling, and straining. The liquid is taken warm as needed, typically half a cup to a cup, and not more than 2–3 cups daily for a few days. Use is traditional and contextual; avoid during pregnancy or lactation, and do not exceed brief courses of use.

The bark and leaves contain safrole and related phenylpropenes such as methyleugenol, along with α- and β- pinene, eugenol, β- caryophyllene, and linalool (Adams, 1972). These aromatic constituents account for the warming, antiseptic reputation of the plant in folk practices.

Modern relevance is limited. The species is infrequently exported, and most usage remains local; occasional artisanal distillation and small-scale studies of its essential-oil chemistry continue (Adams, 1972).

General Uses Top

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Common products:
- Essential oil: steam-distilled from heartwood/sawdust; used in perfumery as a fragrance material (component profile includes linalool and related monoterpenes).
- Timber: heartwood of mature trees used as a specialty hardwood.

Industrial and craft applications:
- Woodworking: valued for furniture, cabinetry, and turned objects; noted for attractive figure and aroma.

Food and beverages (non-medicinal):
- No documented food or beverage uses in reliable sources.

Colorants and tanning:
- No documented use as dye, ink, or tannin in reliable references.

Wood and fiber:
- Timber: heartwood used directly as a specialty wood; no reports of bast fiber utilization.

Fragrance and cosmetics:
- Perfumery: essential oil used as a fragrance ingredient.

Properties relevant to use:
- Essential oil: linalool-rich composition contributes characteristic floral/rose scent suitable for perfumery.
- Wood: aromatic heartwood with favorable mechanical and aesthetic properties for specialty timber applications.

Standards and regulation:
- Timber traded under applicable national timber regulations and relevant CITES listings where applicable.
- Essential oil and fragrance use subject to relevant International Fragrance Association (IFRA) standards for ingredient safety and use levels.

Sustainability and sourcing:
- Species is harvested from natural forests; conservation assessments recommend attention to supply-chain traceability to ensure long-term availability and prevent overharvesting of mature trees.

Synonyms Top

Scientific name Authority First published in
Misanteca armeniaca (Nees) Lundell Wrightia 4: 99 (1969)
Acrodiclidium armeniacum (Nees) Mez Jahrb. Königl. Bot. Gart. Berlin 5: 85 (1889)
Acrodiclidium parviflorum (Meisn.) Mez Jahrb. Königl. Bot. Gart. Berlin 5: 85 (1889)
Evonymodaphne armeniaca Nees Syst. Laur. : 264 (1836)
Licaria reitzkleiniana Vattimo-Gil Anais 15 Congr. Soc. Bot. Brasil 167. 1967
Licaria parviflora (Meisn.) Vattimo-Gil Rodriguésia 28: 124 (1976)
Oreodaphne evonymodaphne Meisn. Prodr. 15(1): 139 (1864)
Mespilodaphne parviflora Meisn. Prodr. 15(1): 109 (1864)
Laurus parviflora Pohl ex Meisn. Prodr. 15(1): 98 (1864)
Laurus armeniaca Poepp. ex Nees Syst. Laur. : 264 (1836)
Oreodaphne terminalis Nees ex Meisn. Prodr. 15(1): 139 (1864)

Common names Top

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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

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-0000364199
Tropicos 17802550
KEW urn:lsid:ipni.org:names:465248-1
The Plant List kew-2349168
Open Tree Of Life 6026396
NCBI Taxonomy 1924205
IUCN Red List 151977576
IPNI 139916-2
GBIF 4183187
CMAUP NPO6302

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
Anticancer Potentials of the Lignan Magnolin: A Systematic Review Bhuia MS, Wilairatana P, Chowdhury R, Rakib AI, Kamli H, Shaikh A, Coutinho HD, Islam MT Molecules 23-Apr-2023
PMCID:PMC10180476
doi:10.3390/molecules28093671
PMID:37175081
Phylogeny and taxonomy of Cinnamomum (Lauraceae) Yang Z, Liu B, Yang Y, Ferguson DK Ecol Evol 01-Oct-2022
PMCID:PMC9526118
doi:10.1002/ece3.9378
PMID:36203627
NEOLIGNANS AND ALKALOIDS FROM LICARIA ARMINIACA (NEES) KOSTERM. PART: 1 M. Abdel-Hafiz, D. Slatkin, Paul Schiff Egypts Presidential Specialized Council for Education and Scientific Research 14-Mar-2020
doi:10.21608/BFSA.1985.75706
Chemical Structures of Lignans and Neolignans Isolated from Lauraceae Li Y, Xie S, Ying J, Wei W, Gao K Molecules 30-Nov-2018
PMCID:PMC6321345
doi:10.3390/molecules23123164
PMID:30513687
Chemical and Biological Extractives of Lauraceae Species in Costa Rican Tropical Forests Oscar C. Castro Springer US 18-Jun-2013
doi:10.1007/978-1-4899-1783-6_3
Lignans and neolignans from Licaria armeniaca Leila V. Alegrio, Raimundo Braz Fo., Otto R. Gottlieb, J.Guilherme S. Maia Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)84045-9
Benzofuranoid neolignans from Licaria armeniaca Cacilda J. Aiba, Otto R. Gottlieb, José G.S. Maia, Frida M. Pagliosa, Massayoshi Yoshida Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88765-8
Neolignans from the fruits of Licaria armeniaca José Maria Barbosa-Filho, Massayoshi Yoshida, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81539-3

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
> Alkaloids and derivatives / Aporphines
Bracteoline 133322 Click to see 327.40 unknown https://doi.org/10.21608/BFSA.1985.75706
https://doi.org/10.1007/978-1-4899-1783-6_3
Homomoschatoline 145779 Click to see COC1=C(C(=C2C3=CC=CC=C3C(=O)C4=NC=CC1=C24)OC)OC 321.30 unknown https://doi.org/10.1016/0031-9422(81)84045-9
> Benzenoids / Benzene and substituted derivatives
Phenylacetic Acid 999 Click to see C1=CC=C(C=C1)CC(=O)O 136.15 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
Sphaeropsidin C 10544575 Click to see 332.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Eudesmin 73117 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81539-3
3-(3,4-Dimethoxyphenyl)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 5319210 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC 416.50 unknown https://doi.org/10.1016/S0031-9422(00)81539-3
https://doi.org/10.1016/0031-9422(81)84045-9
Medioresinol dimethyl ether 169234 Click to see 416.50 unknown https://doi.org/10.1016/S0031-9422(00)81539-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
18-Hydroxyoleic acid 5312773 Click to see 298.50 unknown via CMAUP database
> 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(81)84045-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(5R)-5-[(1R,2Z,4E)-1-hydroxyhexa-2,4-dienyl]oxolan-2-one 11665504 Click to see 182.22 unknown via CMAUP database
(5S)-5-[(1S,2Z,4E)-1-hydroxyhexa-2,4-dienyl]oxolan-2-one 10631273 Click to see 182.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Arjunglucoside II 52951052 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one 14465808 Click to see 442.70 unknown via CMAUP database
(4aS,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picen-2-one 14465806 Click to see 440.70 unknown via CMAUP database
(4R,4aS,6aR,6aS,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 7067822 Click to see 426.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-2,3-dione 15081673 Click to see CC1C(=O)C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown via CMAUP database
[(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-3-oxo-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-yl] acetate 14465799 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C 484.80 unknown via CMAUP database
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 via CMAUP database
Cerin 21596125 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Cerin acetate 14465798 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C 484.80 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1S,3S,5R,6R,7S,8R)-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enyl-8-prop-1-en-2-yloxybicyclo[3.2.1]octan-2-one 162820339 Click to see 414.50 unknown https://doi.org/10.1016/0031-9422(81)84045-9
(1S,3S,5R,6R,7S,8R)-7-(1,3-benzodioxol-5-yl)-8-hydroxy-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]octan-2-one 163047326 Click to see 374.40 unknown https://doi.org/10.1016/0031-9422(81)84045-9
(2R,3S,3aR,5R)-2-(1,3-benzodioxol-5-yl)-5-methoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one 14132420 Click to see 342.40 unknown https://doi.org/10.1016/S0031-9422(00)88765-8
(2S,3S,3aR,5R)-2-(1,3-benzodioxol-5-yl)-5-methoxy-3-methyl-3a-prop-2-enyl-2,3,4,5-tetrahydro-1-benzofuran-6-one 101288061 Click to see CC1C(OC2=CC(=O)C(CC12CC=C)OC)C3=CC4=C(C=C3)OCO4 342.40 unknown https://doi.org/10.1016/S0031-9422(00)88765-8
[(1R,3S,5R,6R,7S,8S)-7-(1,3-benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-2-oxo-5-prop-2-enyl-8-bicyclo[3.2.1]octanyl] acetate 162942632 Click to see CC1C(C2(C(C1(CC(C2=O)OC)CC=C)OC(=O)C)OC)C3=CC4=C(C=C3)OCO4 416.50 unknown https://doi.org/10.1016/0031-9422(81)84045-9
[(1S,5R,6S,7R,8R)-6-(1,3-benzodioxol-5-yl)-3,5-dimethoxy-7-methyl-4-oxo-1-prop-2-enyl-8-bicyclo[3.2.1]oct-2-enyl] acetate 162904609 Click to see CC1C(C2(C(C1(C=C(C2=O)OC)CC=C)OC(=O)C)OC)C3=CC4=C(C=C3)OCO4 414.40 unknown https://doi.org/10.1016/S0031-9422(00)81539-3
[(1S,5R,6S,7R,8R)-6-(1,3-benzodioxol-5-yl)-5-hydroxy-3-methoxy-7-methyl-4-oxo-1-prop-2-enyl-8-bicyclo[3.2.1]oct-2-enyl] acetate 163046239 Click to see 400.40 unknown https://doi.org/10.1016/S0031-9422(00)81539-3
[6-(1,3-Benzodioxol-5-yl)-3,5-dimethoxy-7-methyl-4-oxo-1-prop-2-enyl-8-bicyclo[3.2.1]oct-2-enyl] acetate 162904608 Click to see 414.40 unknown https://doi.org/10.1016/S0031-9422(00)81539-3
[6-(1,3-Benzodioxol-5-yl)-5-hydroxy-3-methoxy-7-methyl-4-oxo-1-prop-2-enyl-8-bicyclo[3.2.1]oct-2-enyl] acetate 163046238 Click to see 400.40 unknown https://doi.org/10.1016/S0031-9422(00)81539-3
[7-(1,3-Benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-2-oxo-5-prop-2-enyl-8-bicyclo[3.2.1]octanyl] acetate 162942631 Click to see 416.50 unknown https://doi.org/10.1016/0031-9422(81)84045-9
3''-Methoxyguianin 44559520 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(81)84045-9
3a-Allyl-2-(1,3-benzodioxol-5-yl)-5-methoxy-3-methyl-3,3a,4,5-tetrahydro-1-benzofuran-6(2H)-one 600366 Click to see 342.40 unknown https://doi.org/10.1016/S0031-9422(00)88765-8
3a-Allyl-2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-3-methyl-3,3a,4,5-tetrahydro-1-benzofuran-6(2H)-one 627505 Click to see CC1C(OC2=C(C(=O)C(CC12CC=C)OC)OC)C3=CC4=C(C=C3)OCO4 372.40 unknown https://doi.org/10.1016/S0031-9422(00)88765-8
7-(1,3-Benzodioxol-5-yl)-1,3-dimethoxy-6-methyl-5-prop-2-enyl-8-prop-1-en-2-yloxybicyclo[3.2.1]octan-2-one 162820337 Click to see 414.50 unknown https://doi.org/10.1016/0031-9422(81)84045-9
7-(1,3-Benzodioxol-5-yl)-8-hydroxy-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 75069493 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(81)84045-9
7-(1,3-Benzodioxol-5-yl)-8-hydroxy-1,3-dimethoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]octan-2-one 163047324 Click to see 374.40 unknown https://doi.org/10.1016/0031-9422(81)84045-9
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
4-Hydroxymellein, (3S-trans)- 119025905 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown via CMAUP database
5-Methylmellein 14807789 Click to see 192.21 unknown via CMAUP database
cis-4-Hydroxymellein 10420140 Click to see 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sphaeropsidin A 51361447 Click to see 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(4aR,6S,8aS)-6-[(1S)-1-hydroxyethyl]-6,8a-dihydro-4aH-pyrano[3,2-b]pyran-2-one 637192 Click to see 196.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10418008 Click to see 824.70 unknown via CMAUP database
[(2R,3S,4R,5R,6S)-3-acetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 14162295 Click to see 636.60 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10439992 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O)O 740.70 unknown via CMAUP database
3'',4''-Di-O-acetyl-2'',6''-di-O-p-coumaroylastragalin 10328097 Click to see 824.70 unknown via CMAUP database
Kaempferol 3-(2'',6''-di-(E)-p-coumarylglucoside) 10439991 Click to see 740.70 unknown via CMAUP database
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 6442291 Click to see 594.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see 434.30 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Complex tannins
(1R,2R,20R,42S,46S)-46-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 16167199 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Castalagin 12302513 Click to see 934.60 unknown via CMAUP database
Eugeniin 442679 Click to see 938.70 unknown via CMAUP database
GlyTouCan:G69718UQ 9918701 Click to see 786.60 unknown via CMAUP database

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