Details Top

Internal ID UUID643fd6414398c574034408
Scientific name Hymenaea courbaril
Authority L.
First published in Sp. Pl.: 1192 (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.

The resin (animé) of Hymenaea courbaril is the most widely cited ethnobotanical preparation. In the Amazon, the resin is softened in a little warm water and taken in spoonful doses as an expectorant for colds and bronchial complaints (Erickson, 1984). In the Caribbean, the resin is also made into a warm poultice and applied to bruises and wounds, and in some islands it is chewed for sore throats (Thompson and Mosby, 1985). In Northeast Brazil, the bark is boiled to a strong decoction for painful urination and urinary infections, a use also recorded in Venezuela (Zoghbi, 2002). Outside these main regions, several island herbal manuals report a leaf infusion for cough and fever in St. Lucia and the Lesser Antilles (Anderson and Lebrun, 1993).

A practical preparation is a mild leaf infusion. Put about 1 tablespoon (roughly 1–2 g) of fresh or dried H. courbaril leaves in 8 oz (240 mL) of just-boiled water, cover, and steep 10 minutes; strain and sip warm. Start with one cup daily and avoid exceeding two cups. Use bark decoctions cautiously and avoid if pregnant or nursing unless a practitioner advises otherwise. For a tincture, macerate 100 g of dried bark in 500 mL of 45% ethanol (about 1:5 weight/volume), shaking daily, and decant after 3–4 weeks; the resulting tincture is best reserved for experienced dosing under guidance. Safety notes: resin may be purgative in excess; if cough or urinary symptoms persist, stop use and seek care.

The resin contains diterpenes (including clerodane types) and essential oils—compounds consistent with its long use as an expectorant and for topical wound care (Dictionary of Natural Products). Leaves and bark are rich in flavonoids and tannins, and triterpenoid saponins are also reported for Hymenaea species, a profile that plausibly supports the astringent and anti-inflammatory effects noted in traditional contexts (Wichtl’s Herbal Drugs and Phytopharmaceuticals).

Modern interest remains strong. In Brazil, resin tinctures and standardized bark extracts are sold by reputable herbal suppliers, and research continues on their anti-inflammatory, antimicrobial, and wound‑healing properties (Pereira et al., 2011). At the same time, community practice persists in the Amazon and Caribbean, where bark decoctions and resin poultices continue to be the primary preparations.

General Uses Top

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Common products:
Timber; derived products include flooring, decking, exterior cladding, carpentry, heavy construction, and turned objects.

Wood and fiber:
Heartwood is reddish brown with darker streaks; sapwood is narrow and yellowish. It has very high density (≈0.80 g/cm³ at 12% moisture), high tangential shrinkage (≈8.5%), and low volumetric shrinkage (≈13.5%). Representative mechanical values reported at 12% MC include modulus of rupture ≈106 MPa and modulus of elasticity ≈16 GPa. The wood is durable against decay and termites and machines and finishes well. Structural uses include sleepers, bridges, heavy framing, and flooring; general carpentry and exterior joinery are also common.

Colorants and tanning:
The bark and heartwood contain condensed tannins (proanthocyanidins) suitable as natural brown colorants for protein fibers and as tanning agents in leather processing. Color fastness is fiber-dependent.

Properties relevant to use:
Very high density and shrinkage anisotropy; high bending and compression strength; dimensional stability after drying; natural resistance to decay fungi and termites; bark and heartwood tannin content enabling leather tanning and natural dyeing.

Sustainability and sourcing:
Typically sourced from managed or second-growth forests in its native range; subject to national timber and trade controls (e.g., CITES listings for some Hymenaea spp.). Certification under FSC or PEFC where available.

Synonyms Top

Scientific name Authority First published in
Hymenaea animifera Stokes Bot. Mat. Med.2: 449 (1812)
Hymenaea candolleana Kunth F.W.H.von Humboldt, A.J.A.Bonpland & C.S.Kunth, Nov. Gen. Sp.6: 323 (1824)
Hymenaea resinifera Salisb. Prodr. Stirp. Chap. Allerton: 327 (1796)
Hymenaea retusa Willd. ex Hayne Getreue Darstell. Gew.11: t. 12 (1830)
Hymenaea courbaril var. obtusifolia Ducke Arch. Jard. Bot. Rio de Janeiro4: 47 (1925)
Hymenaea multiflora Kleinhoonte Recueil Trav. Bot. Néerl.22: 405 (1925 publ. 1926)
Inga megacarpa M.E.Jones Contr. W. Bot.15: 140 (1929)
Hymenaea courbarii var. stilbocarpa (Hayne) Y.T.Lee & Langenh. J. Arnold Arbor.55: 449 (1974)
Hymenaea confertifolia Hayne Getreue Darstell. Gew.11: t. 9 (1830)
Hymenaea splendida Vogel Linnaea11: 409 (1837)
Hymenaea stilbocarpa Hayne Getreue Darstell. Gew.11: t. 11 (1830)
Hymenaea courbaril var. subsessilis Ducke Arch. Jard. Bot. Rio de Janeiro4: 263 (1925)
Hymenaea courbaril var. villosa Y.T.Lee & Andrade-Lima J. Arnold Arbor.55: 446 (1974)

Common names Top

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Language Common/alternative name
English stinkingtoe
Spanish guapinol
bpy জাটোবা
Finnish amerikanjatobapuu
French courbaril
French jatoba
gn jeta'i
Armenian Ժատոբա
Dutch jatoba
Polish jatoba
Portuguese jatobá
Quechua jak'u wayaqa
Quechua jakku wayaka
Quechua yaku wayaqa
Quechua hak'u wayaqa
Quechua copal
Romanian jatoba
Romanian jatobá
Russian Ятоба
Slovenian jatoba
Vietnamese tòng chi
Chinese 攣葉豆
Chinese 孿葉豆
Chinese 南美攣葉豆
Chinese 南美叉叶树
Chinese 孪叶豆

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Uganda
    • South Tropical Africa
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
    • West-central Tropical Africa
      • Congo
    • Western Indian Ocean
      • Madagascar
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000168642
UNII 82VR2663W9
USDA Plants HYCO
Tropicos 13005950
INPN 447043
KEW urn:lsid:ipni.org:names:125420-2
The Plant List ild-1496
Open Tree Of Life 31277
NCBI Taxonomy 20676
IUCN Red List 19891869
IPNI 125420-2
iNaturalist 139075
GBIF 2950750
Freebase /m/0gv7df
EPPO HMYCO
EOL 416028
USDA GRIN 19489
Wikipedia Hymenaea_courbaril
CMAUP NPO1766

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
Hymenaea courbaril resin-mediated gold nanoparticles as catalysts in organic dyes degradation and sensors in pharmaceutical pollutants Khan N, Durrani P, Jamila N, Nishan U, Jan MI, Ullah R, Bari A, Choi JY Heliyon 20-Apr-2024
PMCID:PMC11063429
doi:10.1016/j.heliyon.2024.e30105
PMID:38699715
Use of Plant Extracts in Polymeric Scaffolds in the Regeneration of Mandibular Injuries de Oliveira BE, Maia FL, Massimino LC, Garcia CF, Plepis AM, Martins VD, Reis CH, Silva VR, Bezerra AA, Pauris CC, Buchaim DV, Silva YB, Buchaim RL, da Cunha MR Pharmaceutics 02-Apr-2024
PMCID:PMC11053713
doi:10.3390/pharmaceutics16040491
PMID:38675152
Editorial: Abiotic stress in plants: sustainability and productivity Scalon SD, Santos CC, Badiani M, Tabaldi LA Front Plant Sci 20-Mar-2024
PMCID:PMC10988482
doi:10.3389/fpls.2024.1386174
PMID:38571705
Leaf-Level Bidirectional Exchange of Formaldehyde on Deciduous and Evergreen Tree Saplings Shutter JD, Cox JL, Keutsch FN ACS Earth Space Chem 18-Mar-2024
PMCID:PMC11033940
doi:10.1021/acsearthspacechem.3c00325
PMID:38654895
Amazonian useful plants described in the book “Le Pays des Amazones” (1885) of the Brazilian propagandist Baron de Santa-Anna Nery: a historical and ethnobotanical perspective Silva LN, Oliveira EC, Baratto LC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10897987
doi:10.1186/s13002-024-00663-2
PMID:38409064
Citizen science data on urban forageable plants: a case study in Brazil Soares FM, Ferreira Pires L, Garcia MC, Coradin L, Ghilardi-Lopes NP, Silva RR, de Carvalho AM, Gavai A, Bouzembrak Y, Maculan BC, Koffler S, Montedo UB, Drucker DP, Santiago R, de Carvalho MC, Lima AC, Gabriel HD, de França SG, de Almeida KR, dos Santos BJ, Saraiva AM GigaByte 21-Feb-2024
PMCID:PMC10905257
doi:10.46471/gigabyte.107
PMID:38434929
Toxicological Profile and Anti-Inflammatory Effect of Mucoadhesive Gel from Residues of Agave sisalana and Punica granatum Fracasso JA, Sikina IY, da Costa LT, Guarnier LP, Ribeiro-Paes JT, de Ferreira FY, de Almeida LV, de Castro Silva B, de Barros Barbosa D, Ximenes VF, Venkli D, Viel AM, dos Santos L Gels 30-Nov-2023
PMCID:PMC10743268
doi:10.3390/gels9120942
PMID:38131928
In Vitro Evaluation of Potentially Edible Brazilian Trees and Shrubs in Ruminant Nutrition de Morais JP, Campana M, Gregorini P, Garcia TM, Minussi JF, Pereira SN, Pereira FC, Del Valle TA Animals (Basel) 29-Nov-2023
PMCID:PMC10705355
doi:10.3390/ani13233703
PMID:38067053
High variability of perezone content in rhizomes of Acourtia cordata wild plants, environmental factors related, and proteomic analysis García Méndez MD, Encarnación-Guevara S, Martínez Batallar ÁG, Gómez-Caudillo L, Bru-Martínez R, Martínez Márquez A, Selles Marchart S, Tovar-Sánchez E, Álvarez-Berber L, Marquina Bahena S, Perea-Arango I, Arellano-García JD PeerJ 15-Nov-2023
PMCID:PMC10656900
doi:10.7717/peerj.16136
PMID:38025722
Evaluation of the Antioxidant, Antimicrobial, and Anti-Biofilm Effects of the Stem Bark, Leaf, and Seed Extracts from Hymenaea courbaril and Characterization by UPLC-ESI-QTOF-MS/MS Analysis da Cruz JE, Saldanha HC, do Nascimento AM, Borges RB, Gomes MD, Freitas GR, Leal CM, Ferreira EA, da Silva Filho AA, Morais ER Antibiotics (Basel) 08-Nov-2023
PMCID:PMC10668761
doi:10.3390/antibiotics12111601
PMID:37998803
A new proposal for the use of the focal animal technique in buffaloes in the Eastern Amazon da Silva WC, da Silva JA, Gouveia Júnior A, de Alvarenga AB, Barbosa AV, da Silva ÉB, Pereira dos Santos MR, Lourenço-Júnior JD, Camargo Júnior RN, Silva AG Front Vet Sci 08-Nov-2023
PMCID:PMC10663286
doi:10.3389/fvets.2023.1266451
PMID:38026641
How the Adequate Choice of Plant Species Favors the Restoration Process in Areas Susceptible to Extreme Frost Events Viveiros E, Francisco BS, Dutra FB, de Souza LA, Inocente MC, Bastos AC, da Costa GF, Barbosa MC, Martins RP, Passaretti RA, Fernandes MJ, de Oliveira JS, Shiguehara AP, Manzoli EC, Teração BS, Piotrowski I, Piña-Rodrigues FC, da Silva JM Biology (Basel) 26-Oct-2023
PMCID:PMC10669021
doi:10.3390/biology12111369
PMID:37997968
Patterns of use of wild food plants by Brazilian local communities: systematic review and meta-analysis Gomes LC, Medeiros PM, Prata AP J Ethnobiol Ethnomed 25-Oct-2023
PMCID:PMC10601232
doi:10.1186/s13002-023-00619-y
PMID:37880767
Plant parentage influences the type of timber use by traditional peoples of the Brazilian Caatinga Pedrosa KM, Ramos MB, La Torre-Cuadros MD, Lopes SD PLoS One 17-Oct-2023
PMCID:PMC10581497
doi:10.1371/journal.pone.0286434
PMID:37847702
Meta-analysis of the responses of tree and herb to elevated CO2 in Brazil da Silva Fortirer J, Grandis A, Pagliuso D, de Toledo Castanho C, Buckeridge MS Sci Rep 22-Sep-2023
PMCID:PMC10517018
doi:10.1038/s41598-023-40783-5
PMID:37739974

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Arctiin 100528 Click to see 534.60 unknown via CMAUP database
Matairesinoside 486612 Click to see 520.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
methyl (1S,5R,6S,8aS)-5-[(E)-5-methoxy-3-methyl-5-oxopent-3-enyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylate 162938040 Click to see 362.50 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
Methyl 5-(5-methoxy-3-methyl-5-oxopent-3-enyl)-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylate 162938038 Click to see 362.50 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
methyl (1S,5S,6S,8aS)-5-[(3R)-5-methoxy-3-methyl-5-oxopentyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylate 163035314 Click to see 364.50 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
Methyl 5-(5-methoxy-3-methyl-5-oxopentyl)-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylate 163035313 Click to see CC1CCC2C(=CCCC2(C)C(=O)OC)C1(C)CCC(C)CC(=O)OC 364.50 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Copalic acid 44149762 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown https://doi.org/10.1590/S0103-50532002000300015
(1S,4aS,5R,8aS)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 12303813 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
(E)-3-Methyl-5-((1R,4aR,8aR)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl)pent-2-enoic acid 12305551 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(00)91323-2
(S)-3-Methyl-5-((1R,4aR,8aR)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl)pentanoic acid 12309485 Click to see 306.50 unknown https://doi.org/10.1590/S0103-50532002000300015
1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 72957164 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
8-acetyloxy-1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 73657406 Click to see 360.50 unknown https://doi.org/10.1590/S0103-50532002000300015
ent-8(17),13(16),14-Labdatrien-18-oic acid 72780956 Click to see 302.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
Isoozic acid 100983062 Click to see 302.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
methyl (1S,4aS,5R,8aS)-1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 13966184 Click to see 316.50 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
methyl (E)-5-[(1R,2S,4aS,8aR)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate 162917633 Click to see 336.50 unknown https://doi.org/10.1016/S0031-9422(00)91323-2
methyl 5-(2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-2-enoate 72786075 Click to see 336.50 unknown https://doi.org/10.1016/S0031-9422(00)91323-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(E)-5-[(1S,2S,4aS,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 163193317 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
3-Methyl-5-(1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-1-yl)-pent-2-enoic acid 636570 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
5-(1,2,4a,5-Tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-enoic acid 73880585 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
Kolavenic Acid 6441458 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(01)00303-X
methyl (1S,5S,6R,8aR)-5-[2-(furan-3-yl)ethyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylate 163024991 Click to see 330.50 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
Methyl 5-[2-(furan-3-yl)ethyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylate 163024990 Click to see CC1CCC2C(=CCCC2(C)C(=O)OC)C1(C)CCC3=COC=C3 330.50 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-carboxylic acid 101673969 Click to see 552.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 4-beta-D-glucopyranosyl 7-methyl ester 101673970 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 566.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 7-methyl ester 101673972 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown via CMAUP database
Adoxosidic acid 13892717 Click to see C1CC2C(C1CO)C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 376.36 unknown via CMAUP database
dimethyl (1S,4aS,7S,7aS)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4,7-dicarboxylate 101673971 Click to see 418.40 unknown via CMAUP database
Forsythide 15559328 Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)C(=O)O 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 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
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Uridine, 2'-deoxy-3-methyl- 13845047 Click to see 242.23 unknown https://doi.org/10.1016/S0040-4020(01)93493-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(13R)-13-Hydroxy-1(10),14-Ent-Halimadien-18-Oic Acid 637420 Click to see 320.50 unknown https://doi.org/10.1021/NP0103261
(1S,3S,5S,6R,8aS)-3-hydroxy-5-[(3R)-3-hydroxy-3-methylpent-4-enyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylic acid 10980611 Click to see 336.50 unknown https://doi.org/10.1021/NP0103261
3-Hydroxy-5-(3-hydroxy-3-methylpent-4-enyl)-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalene-1-carboxylic acid 85354228 Click to see CC1CCC2C(=CC(CC2(C)C(=O)O)O)C1(C)CCC(C)(C=C)O 336.50 unknown https://doi.org/10.1021/NP0103261
CID 22297739 22297739 Click to see 320.50 unknown https://doi.org/10.1021/NP0103261
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside F 6442994 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown via CMAUP database
Forsythoside G 101231533 Click to see 770.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1S,5S,6R,8aS)-5-[(3R)-3-hydroxy-3-methylpent-4-enyl]-1,5,6-trimethyl-3-oxo-6,7,8,8a-tetrahydro-2H-naphthalene-1-carboxylic acid 10925680 Click to see 334.40 unknown https://doi.org/10.1021/NP0103261
5-(3-hydroxy-3-methylpent-4-enyl)-1,5,6-trimethyl-3-oxo-6,7,8,8a-tetrahydro-2H-naphthalene-1-carboxylic acid 85317950 Click to see 334.40 unknown https://doi.org/10.1021/NP0103261
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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