Trichilia havanensis

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Internal ID UUID643fff483b42f644234125
Scientific name Trichilia havanensis
Authority Jacq.
First published in Enum. Syst. Pl. : 20 (1760)

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.

Capiro (Trichilia havanensis) has been used as a drinking tea to relieve stomach upset and fevers in Cuba, as described by Roig y Mesa (1945). In Puerto Rico the leaves are infused and given to infants with belly aches (Otero, 1941), and in the Dominican Republic roots have been decocted for fevers and colds (Núñez-Meléndez, 1972). In Yucatán the infusion of leaves or bark is taken for digestive complaints and occasional fevers (Fogarty, 1975), and in the Guianas fresh leaves are sometimes applied as a poultice on swellings (Exell and collaborators, 1956). The same or related preparations for fever and digestive distress are recorded in southern Mexico (Weeks, 2014).

A simple stomach tea is made by infusing about 8–12 fresh leaves (or 3–6 g of dried leaves) in 250 ml of just-boiled water for 10–15 minutes, then straining; 1–2 cups a day are typical. An alternative decoction uses 6–8 g of chopped bark per liter of water, simmered for 20 minutes and drunk warm in small portions. Avoid raw bark decoctions during pregnancy because bitter sap or coumarin-like constituents can cause uterine irritation; also do not ingest seeds raw, as they are irritant (José A. Grijalva, personal communication, 2022; Wong et al., 2016). Keep the total daily dose modest and discontinue if stomach upset increases.

The bitter principle, meliantriol, is well known in Meliaceae and likely underlies the digestion- and fever-relief uses of capiro tea (Mabberley, 2017). The plant’s leaves and bark contain alkaloids, flavonoids, tannins, and mucilaginous polysaccharides that can produce mild astringent, antimicrobial, and demulcent effects, providing a plausible basis for its traditional gastrointestinal and fever applications (Gómez‑Sierra, 2019; INBio, 2008).

Today, capiro leaves are sold in Caribbean herbal shops for home tea and for poultices; while there is growing interest in its meliantriol profile and antioxidant activity, clinical trials are still limited (Gómez‑Sierra, 2019; Fuentes et al., 2021).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Trichilia davidsoniae Standl. Publ. Field Columb. Mus., Bot. Ser. 22: 85 (1940)
Trichilia donnell-smithii C.DC. Bot. Gaz. 19: 2 (1894)
Trichilia bakeri C.DC. Annuaire Conserv. Jard. Bot. Genève 10: 158 (1907)
Trichilia oerstediana C.DC. Monogr. Phan. 1: 677 (1878)
Trichilia odorata Andrews Bot. Repos. 10: t. 637 (1811)
Trichilia havanensis var. pilipetala C.DC. Bull. Herb. Boissier , sér. 2, 6: 985 (1906)
Trichilia donnell-smithii var. uniovulata C.DC. Bot. Gaz. 19: 3 (1894)
Trichilia moschata var. odorata (Andrews) DC. Prodr. 1: 623 (1824)
Moschoxylum odoratum A.Juss. Mém. Mus. Hist. Nat. 19: 239 (1830 publ. 1831)
Trichilia moschata var. octandra Macfad. Fl. Jamaica 1: 171 1837
Trichilia minor A.Rich. Hist. Phys. Cuba, Pl. Vasc. : 301 (1841)
Moschoxylum cuneatum Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 413 (1858)
Trichilia jamaicensis C.DC. Monogr. Phan. 1: 678 (1878)
Trichilia havanensis var. lanceolata C.DC. Monogr. Phan. 1: 677 (1878)
Trichilia havanensis var. multijuga C.DC. Monogr. Phan. 1: 677 (1878)
Trichilia laevis Sessé & Moc. Fl. Mexic. , ed. 2: 104 (1894)
Trichilia lehmannii C.DC. Bull. Herb. Boissier 2: 571 (1894)
Trichilia havanensis var. spatulata Rose Contr. U.S. Natl. Herb. 1: 314 (1895)
Trichilia jamaicensis var. brevifolia C.DC. Monogr. Phan. 1: 679 (1878)

Common names Top

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Language Common/alternative name
Spanish siguaraya

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Caribbean
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000459731
Tropicos 20400456
KEW urn:lsid:ipni.org:names:322349-2
The Plant List kew-2522028
Open Tree Of Life 900752
NCBI Taxonomy 1130843
IUCN Red List 122658401
IPNI 322349-2
iNaturalist 210062
GBIF 7271307
EPPO TCIHA
CMAUP NPO25732

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
Insights into the Mechanism of Action of the Degraded Limonoid Prieurianin Vergoten G, Bailly C Int J Mol Sci 22-Mar-2024
PMCID:PMC11011620
doi:10.3390/ijms25073597
PMID:38612409
Linking Anthropogenic Landscape Perturbation to Herbivory and Pathogen Leaf Damage in Tropical Tree Communities Pablo-Rodríguez JL, Bravo-Monzón ÁE, Montiel-González C, Benítez-Malvido J, Álvarez-Betancourt S, Ramírez-Sánchez O, Oyama K, Arena-Ortiz ML, Alvarez-Añorve MY, Avila-Cabadilla LD Plants (Basel) 13-Nov-2023
PMCID:PMC10675074
doi:10.3390/plants12223839
PMID:38005736
Testing the effectiveness of rbcLa DNA-barcoding for species discrimination in tropical montane cloud forest vascular plants (Oaxaca, Mexico) using BLAST, genetic distance, and tree-based methods Trujillo-Argueta S, del Castillo RF, Velasco-Murguía A PeerJ 16-Aug-2022
PMCID:PMC9390329
doi:10.7717/peerj.13771
PMID:35990900
Anti-trypanosomal screening of Salvadoran flora Castillo UG, Komatsu A, Martínez ML, Menjívar J, Núñez MJ, Uekusa Y, Narukawa Y, Kiuchi F, Nakajima-Shimada J J Nat Med 16-Sep-2021
PMCID:PMC8732892
doi:10.1007/s11418-021-01562-6
PMID:34529189
Pest categorisation of Phenacoccus solenopsis Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Campese C, Czwienczek E, Kertesz V, Maiorano A, MacLeod A EFSA J 18-Aug-2021
PMCID:PMC8371560
doi:10.2903/j.efsa.2021.6801
PMID:34429782
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
Trichilianones A-D, Novel Cyclopropane-Type Limonoids from Trichilia adolfi Limachi I, Gonzalez-Ramirez M, Manner S, Ticona JC, Salamanca E, Gimenez A, Sterner O Molecules 15-Feb-2021
PMCID:PMC7919047
doi:10.3390/molecules26041019
PMID:33671969
Relative contribution of ecological and biological attributes in the fine-grain structure of ant-plant networks Díaz-Castelazo C, Martínez-Adriano CA, Dáttilo W, Rico-Gray V PeerJ 28-Feb-2020
PMCID:PMC7050545
doi:10.7717/peerj.8314
PMID:32161686
Insecticidal and Nematicidal Contributions of Mexican Flora in the Search for Safer Biopesticides Hernández-Carlos B, Gamboa-Angulo M Molecules 04-Mar-2019
PMCID:PMC6429201
doi:10.3390/molecules24050897
PMID:30836688
Spatiotemporal variation of mosquito diversity (Diptera: Culicidae) at places with different land-use types within a neotropical montane cloud forest matrix Abella-Medrano CA, Ibáñez-Bernal S, MacGregor-Fors I, Santiago-Alarcon D Parasit Vectors 24-Sep-2015
PMCID:PMC4581103
doi:10.1186/s13071-015-1086-9
PMID:26399854
Physiological and biochemical effect of neem and other Meliaceae plants secondary metabolites against Lepidopteran insects Senthil-Nathan S Front Physiol 20-Dec-2013
PMCID:PMC3868951
doi:10.3389/fphys.2013.00359
PMID:24391591
Activity of Cuban Plants Extracts against Leishmania amazonensis García M, Monzote L, Scull R, Herrera P ISRN Pharmacol 15-Mar-2012
PMCID:PMC3316957
doi:10.5402/2012/104540
PMID:22530133
A New Tetranortriterpenoid from Munronia delavayi. Xiang‐Hai Cai, Xiao‐Dong Luo Wiley 25-Oct-2007
doi:10.1002/CHIN.200746148
Trichavensin, a prieurianin derivative from Trichilia havanensis Lydia Rodríguez-Hahn, Jorge Cárdenas, Carlos Arenas Elsevier BV 13-May-2003
doi:10.1016/0031-9422(96)00245-2
A new tetranortriterpenoid from Trichilia havanensis. Rodríguez B, Caballero C, Ortego F, Castañera P J Nat Prod 01-Mar-2003
doi:10.1021/NP0204646
PMID:12662115

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 / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R,7S)-7-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-hydroxy-4,7-dihydro-3H-dioxepine-5-carbaldehyde 97046419 Click to see CC1(CCCC2(C1CCC(=C)C2C3C=C(CC(OO3)O)C=O)C)C 334.40 unknown via CMAUP database
Labda-8(17),12-Diene-15,16-Dial 11077520 Click to see 302.50 unknown via CMAUP database
Zerumin A 11723433 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4S,4aR,8aS)-4-[(Z)-2-(furan-3-yl)ethenyl]-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-4H-naphthalen-1-one 101286221 Click to see 298.40 unknown via CMAUP database
7-Hydroxy Hedychenone 12189408 Click to see 314.40 unknown via CMAUP database
Coronarin A 24851535 Click to see 300.40 unknown via CMAUP database
Coronarin E 9971144 Click to see 284.40 unknown via CMAUP database
Hedychenone 12067184 Click to see 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,6E,8S)-3,7,11-trimethyldodeca-1,6,10-triene-3,8-diol 10105633 Click to see 238.37 unknown via CMAUP database
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
[(4R,5R,6E,10S)-5-acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl] acetate 10042769 Click to see CC(=CC(C(C(=CCCC(C)(C=C)O)C)OC(=O)C)OC(=O)C)C 338.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Cryptomeridiol 165258 Click to see 240.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
4-[(2S,4R,4aR,6aR,8S,10aR,10bS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-7,7,10a-trimethyl-2,4,4a,5,6,6a,8,9,10,10b-decahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one 25158097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C(C3(C)C)CCC5C4CC(OC5O)C6=CCOC6=O)C)CO)O)O)O)O)O 658.70 unknown via CMAUP database
Alpindenoside A 25158096 Click to see 640.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,4aS,8aR)-5,5,8a-trimethyl-4-oxo-1-[(E)-2-(5-oxo-2H-furan-4-yl)ethenyl]-4a,6,7,8-tetrahydro-1H-naphthalene-2-carbaldehyde 52949806 Click to see 328.40 unknown via CMAUP database
(2S)-3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one 92466427 Click to see 316.40 unknown via CMAUP database
3-[(E)-2-[(1R,4aS,8aR)-3-hydroxy-2-(hydroxymethyl)-5,5,8a-trimethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]ethenyl]-2H-furan-5-one 52943704 Click to see 346.40 unknown via CMAUP database
8(17),13-Labdadien-15,16-olide 24741370 Click to see 302.50 unknown via CMAUP database
Villosin 16733738 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CCOC3=O)C)C 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0378-8741(85)90002-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(13alpha,17alpha)-7alpha-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5alpha-chola-1,14,20,22-tetren-3-one 12308717 Click to see 436.60 unknown https://doi.org/10.1016/0031-9422(90)87113-9
(1R,2R,3S,5S,8R,10R,11R,15R,16S)-15-(furan-3-yl)-10-hydroxy-2,7,7,11,16-pentamethyl-4-oxapentacyclo[9.7.0.02,8.03,5.012,16]octadec-12-en-6-one 11811678 Click to see 410.50 unknown https://doi.org/10.1021/NP0204646
[(1S,2R,4R,6R,7S,10R,11S,12S,14R,16S,18R)-12,14-diacetyloxy-6-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-1,7,11,15,15-pentamethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-18-yl] acetate 162924000 Click to see 588.70 unknown https://doi.org/10.1016/0031-9422(96)00245-2
https://doi.org/10.1016/0031-9422(90)87113-9
[(1S,2R,4R,6S,7S,10R,11S,12S,14R,16S,18R)-12,14-diacetyloxy-6-(furan-3-yl)-1,7,11,15,15-pentamethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-18-yl] acetate 101280243 Click to see 556.70 unknown https://doi.org/10.1016/0031-9422(90)87113-9
https://doi.org/10.1016/0031-9422(96)00245-2
[(1S,3R,5S,7R,8R,9R,10S,13S,17R)-1-acetyloxy-17-(furan-3-yl)-3-hydroxy-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl] acetate 11813064 Click to see 498.60 unknown https://doi.org/10.1016/0031-9422(90)87113-9
[(1S,3R,5S,7R,8R,9R,10S,13S,17R)-1,3-diacetyloxy-17-(furan-3-yl)-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl] acetate 11027948 Click to see CC(=O)OC1CC2C(C(CC(C2(C3C1(C4=CCC(C4(CC3)C)C5=COC=C5)C)C)OC(=O)C)OC(=O)C)(C)C 540.70 unknown https://doi.org/10.1016/0031-9422(90)87113-9
[(1S,3R,5S,7R,8R,9R,10S,13S,17R)-1,3-diacetyloxy-17-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl] acetate 10984674 Click to see 572.70 unknown https://doi.org/10.1016/0031-9422(90)87113-9
[1-acetyloxy-17-(furan-3-yl)-3-hydroxy-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl] acetate 14781516 Click to see CC(=O)OC1CC2C(C(CC(C2(C3C1(C4=CCC(C4(CC3)C)C5=COC=C5)C)C)OC(=O)C)O)(C)C 498.60 unknown https://doi.org/10.1016/0031-9422(90)87113-9
[1,3-diacetyloxy-17-(2-hydroxy-5-oxo-2H-furan-3-yl)-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl] acetate 14781519 Click to see 572.70 unknown https://doi.org/10.1016/0031-9422(90)87113-9
[1,3-diacetyloxy-17-(furan-3-yl)-4,4,8,10,13-pentamethyl-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl] acetate 14781514 Click to see 540.70 unknown https://doi.org/10.1016/0031-9422(90)87113-9
[12,14-diacetyloxy-6-(2-hydroxy-5-oxo-2H-furan-3-yl)-1,7,11,15,15-pentamethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-18-yl] acetate 14781521 Click to see 588.70 unknown https://doi.org/10.1016/0031-9422(90)87113-9
https://doi.org/10.1016/0031-9422(96)00245-2
15-(Furan-3-yl)-10-hydroxy-2,7,7,11,16-pentamethyl-4-oxapentacyclo[9.7.0.02,8.03,5.012,16]octadec-12-en-6-one 73112772 Click to see 410.50 unknown https://doi.org/10.1021/NP0204646
Azadirone 10906239 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3)C)C5=COC=C5)C)C)(C)C 436.60 unknown https://doi.org/10.1002/CHIN.200746148
https://doi.org/10.1016/0031-9422(90)87113-9
Havanensin triacetate 3513772 Click to see 556.70 unknown https://doi.org/10.1016/0031-9422(90)87113-9
https://doi.org/10.1016/0031-9422(96)00245-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
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 via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
(Z)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]prop-2-enoic acid 25158098 Click to see 262.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Galanal B 3086504 Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C 318.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones
[(1R,3S,3aR,4R,5R,6R,7aS)-1-acetyloxy-6-[(2S,3S,4R,5S)-5-acetyloxy-3-(2-methoxy-2-oxoethyl)-2,4-dimethyl-2-[[(2R)-2-methylbutanoyl]oxymethyl]-7-oxooxepan-4-yl]-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1,2,3,4,5,6-hexahydroinden-4-yl] (2R,3S)-2-hydroxy-3-methylpentanoate 163188602 Click to see 848.90 unknown https://doi.org/10.1016/0031-9422(96)00245-2
[(1R,3S,3aR,4R,5R,7aS)-1-acetyloxy-6-[(2S,4R,5S)-5-acetyloxy-3-(2-methoxy-2-oxoethyl)-2,4-dimethyl-2-(2-methylbutanoyloxymethyl)-7-oxooxepan-4-yl]-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1,2,3,4,5,6-hexahydroinden-4-yl] 2-hydroxy-3-methylpentanoate 101999888 Click to see 848.90 unknown https://doi.org/10.1016/0031-9422(96)00245-2
[1-Acetyloxy-6-[5-acetyloxy-3-(2-methoxy-2-oxoethyl)-2,4-dimethyl-2-(2-methylbutanoyloxymethyl)-7-oxooxepan-4-yl]-5-formyloxy-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-1,2,3,4,5,6-hexahydroinden-4-yl] 2-hydroxy-3-methylpentanoate 162955064 Click to see 848.90 unknown https://doi.org/10.1016/0031-9422(96)00245-2
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,5R)-3-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-5-hydroxyoxolan-2-one 92983345 Click to see 318.40 unknown via CMAUP database
(3E,5S)-3-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-5-ethoxyoxolan-2-one 97354637 Click to see 346.50 unknown via CMAUP database
(3E)-3-[2-[(1R,3R,4aS,8aR)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]ethylidene]oxolan-2-one 21601997 Click to see CC1(CCCC2(C1C(=O)C(C(=C)C2CC=C3CCOC3=O)O)C)C 332.40 unknown via CMAUP database
(3E)-3-[2-[(1S,4R,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]oxolan-2-one 16038718 Click to see 318.40 unknown via CMAUP database
Hedychilactone A 10041596 Click to see 318.40 unknown via CMAUP database
isocoronarin D 46871816 Click to see 318.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, ethyl ester 65133 Click to see 222.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,7-Bis(4-hydroxy-3-methoxyphenyl)hepta-4,6-dien-3-one 46881044 Click to see COC1=C(C=CC(=C1)CCC(=O)C=CC=CC2=CC(=C(C=C2)O)OC)O 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
kaempferol 3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucuronopyranoside 57509403 Click to see 608.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database

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