Eucryphia cordifolia - Unknown
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Internal ID UUID64401bbaa231f182309032
Scientific name Eucryphia cordifolia
Authority Cav.
First published in Icon. 4: 49 (1798)

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Synonyms Top

Scientific name Authority First published in
Eucryphia patagonica Speg. Anales Mus. Nac. Buenos Aires 7: 281 (1902)
Fagus glutinosa Poepp. & Endl. Nov. Gen. Sp. Pl. 2: 68 (1838)

Common names Top

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Language Common/alternative name
English ulmo
Spanish ulmo
German chilenische scheinulme
Estonian tšiili kuisma
Russian Эвкрифия сердцелистная
Chinese 尼曼香花木
Chinese 心叶银香茶
Chinese 银香茶

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
  • Southern America
    • Southern South America
      • Argentina South
      • Chile Central
      • Chile South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000681179
USDA Plants EUCO40
Tropicos 12700001
KEW urn:lsid:ipni.org:names:724849-1
The Plant List kew-2802761
PFAF Eucryphia cordifolia
Open Tree Of Life 650184
NCBI Taxonomy 92928
IUCN Red List 33901
IPNI 724849-1
iNaturalist 178226
GBIF 3920287
Freebase /m/02x8yy8
EPPO EUACO
EOL 5553307
USDA GRIN 16128
Wikipedia Eucryphia_cordifolia
CMAUP NPO24021

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)!
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Title Authors Publication Released IDs
In Situ Accumulation of CaOx Crystals in C. quitensis Leaves and Its Relationship with Anatomy and Gas Exchange Gómez-Espinoza O, Fuentes FI, Ramírez CF, Bravo LA, Sáez PL Plants (Basel) 08-Mar-2024
PMCID:PMC10975422
doi:10.3390/plants13060769
PMID:38592779
Jelleine, a Family of Peptides Isolated from the Royal Jelly of the Honey Bees (Apis mellifera), as a Promising Prototype for New Medicines: A Narrative Review Lima WG, Brito JC, Verly RM, de Lima ME Toxins (Basel) 02-Jan-2024
PMCID:PMC10819630
doi:10.3390/toxins16010024
PMID:38251241
Antimicrobial, Antioxidant, and Anti-Inflammatory Properties of Monofloral Honeys from Chile Poulsen-Silva E, Gordillo-Fuenzalida F, Velásquez P, Llancalahuen FM, Carvajal R, Cabaña-Brunod M, Otero MC Antioxidants (Basel) 21-Sep-2023
PMCID:PMC10526086
doi:10.3390/antiox12091785
PMID:37760088
The functional mechanism behind the latitudinal pattern of liana diversity: Freeze–thaw embolism reduces the ecological performance of liana species Lobos‐Catalán P, Jiménez‐Castillo M Ecol Evol 19-Sep-2023
PMCID:PMC10509155
doi:10.1002/ece3.10486
PMID:37736281
Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH Front Plant Sci 10-Jul-2023
PMCID:PMC10364642
doi:10.3389/fpls.2023.1193573
PMID:37492778
Antibacterial and wound-healing action of Ulmo honey (Eucryphia cordifolia) of differing degrees of purity Muñoz M, del Sol M, Vásquez B Front Vet Sci 12-May-2023
PMCID:PMC10213365
doi:10.3389/fvets.2023.1172025
PMID:37252390
Decrypting the multi-functional biological activators and inducers of defense responses against biotic stresses in plants Khoshru B, Mitra D, Joshi K, Adhikari P, Rion MS, Fadiji AE, Alizadeh M, Priyadarshini A, Senapati A, Sarikhani MR, Panneerselvam P, Mohapatra PK, Sushkova S, Minkina T, Keswani C Heliyon 18-Feb-2023
PMCID:PMC9981932
doi:10.1016/j.heliyon.2023.e13825
PMID:36873502
Activity patterns and interactions of rodents in an assemblage composed by native species and the introduced black rat: implications for pathogen transmission Salgado R, Barja I, Hernández MD, Lucero B, Castro-Arellano I, Bonacic C, Rubio AV BMC Zool 26-Aug-2022
PMCID:PMC9412813
doi:10.1186/s40850-022-00152-7
PMID:36042784
Endophytes in Lignin Valorization: A Novel Approach Mattoo AJ, Nonzom S Front Bioeng Biotechnol 19-Jul-2022
PMCID:PMC9343868
doi:10.3389/fbioe.2022.895414
PMID:35928943
Antibacterial and Biofilm Degradation Effects of Hungarian Honeys Linked With Botanical Origin, Antioxidant Capacity and Mineral Content Farkas Á, Balázs VL, Kõszegi T, Csepregi R, Kerekes E, Horváth G, Szabó P, Gaál K, Kocsis M Front Nutr 13-Jul-2022
PMCID:PMC9326441
doi:10.3389/fnut.2022.953470
PMID:35911104
A Comprehensive Survey of Phenolic Constituents Reported in Monofloral Honeys around the Globe Lawag IL, Lim LY, Joshi R, Hammer KA, Locher C Foods 15-Apr-2022
PMCID:PMC9025093
doi:10.3390/foods11081152
PMID:35454742
Honeybee Pollen From Southern Chile: Phenolic Profile, Antioxidant Capacity, Bioaccessibility, and Inhibition of DNA Damage Bridi R, Echeverría J, Larena A, Nuñez Pizarro P, Atala E, De Camargo AC, Oh WY, Shahidi F, Garcia O, Ah-Hen KS, Montenegro G Front Pharmacol 07-Mar-2022
PMCID:PMC8937017
doi:10.3389/fphar.2022.775219
PMID:35321331
Mineral and Botanical Composition of Honey Produced in Chile’s Central-Southern Region Lobos I, Silva M, Ulloa P, Pavez P Foods 18-Jan-2022
PMCID:PMC8834323
doi:10.3390/foods11030251
PMID:35159403
Suitable Areas for Apiculture Expansion Determined by Antioxidant Power, Chemical Profiles, and Pesticide Residues in Caldcluvia paniculata Honey and Beeswax Samples Mejías E, Gómez C, Garrido T Insects 28-Dec-2021
PMCID:PMC8777965
doi:10.3390/insects13010031
PMID:35055874
Naturally Occurring Chromone Glycosides: Sources, Bioactivities, and Spectroscopic Features Amen Y, Elsbaey M, Othman A, Sallam M, Shimizu K Molecules 16-Dec-2021
PMCID:PMC8704703
doi:10.3390/molecules26247646
PMID:34946728

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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Tetralins
(4S)-10-Nor-calamenen-10-one 73350586 Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C 202.29 unknown via CMAUP database
Oxyphyllenotriol A 51041015 Click to see CC(C)C1=C2C(C(CCC2=C(C=C1)O)(C)O)O 236.31 unknown via CMAUP database
Oxyphyllone G 51041016 Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O 218.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-diene-15,16-dial 11077520 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see CC(C)C1=CC(C(CC1)(C)O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one 76285513 Click to see CC1CCC2C1C3(C(=CC(=O)C2(O3)C)C(C)C)O 250.33 unknown via CMAUP database
Oxyphyllanene D 57396910 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
Oxyphyllol E 51041018 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol 15601439 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(CO)O)C 252.35 unknown via CMAUP database
(1S)-1,2,3,4,4a,5,6,7-Octahydro-4beta,4abeta-dimethyl-6alpha-(1-methylethenyl)naphthalene-1beta-ol 44576208 Click to see CC1CCC(C2=CCC(CC12C)C(=C)C)O 220.35 unknown via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione 72715093 Click to see CC1CC(=O)C=C2C1(CC(CC2=O)C(=C)C)C 232.32 unknown via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one 117654813 Click to see CC1CC(=O)C=C2C1(C=C(CC2)C(=O)C)C 218.29 unknown via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 89960876 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(C)O)C 236.35 unknown via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 53249021 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)CO)C 234.33 unknown via CMAUP database
(4R)-4beta,4abeta-Dimethyl-6alpha-isopropenyl-8alpha-hydroxy-2,3,4,4a,5,6,7,8-octahydronaphthalene-2-one 11651584 Click to see CC1CC(=O)C=C2C1(CC(CC2O)C(=C)C)C 234.33 unknown via CMAUP database
Nootkatene 25200342 Click to see CC1CC=CC2=CCC(CC12C)C(=C)C 202.33 unknown via CMAUP database
Nootkatol 182645 Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O 220.35 unknown via CMAUP database
Nootkatone 1268142 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
oxyphyllol C 10857540 Click to see CC1CCC(C2(C1(CC(CC2)C(=C)C)C)O)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 15560338 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown via CMAUP database
(4aS,7S,8R)-8-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 57393410 Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=C)C)O 234.33 unknown via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one 57335617 Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O 234.33 unknown via CMAUP database
7-Epi-Teucrenone B 57393409 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
Ligucyperonol 14681770 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C 234.33 unknown via CMAUP database
Oxyphyllol A 637451 Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C 220.35 unknown via CMAUP database
Rel-Oxyphyllanene E 57400339 Click to see CC(=C)C1(CCC2(CCC(C(=C)C2C1)O)C)O 236.35 unknown via CMAUP database
Teucrenone 10105443 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione 71681246 Click to see CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3C2)C)C 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone 102054514 Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O 222.32 unknown via CMAUP database
Spiro[4.4]nonan-2-one 549163 Click to see C1CCC2(C1)CCC(=O)C2 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 71681103 Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(=O)C)O)C 236.31 unknown via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one 71681245 Click to see CC1=C2C=C(CCC2(CCC1=O)C)C(=O)C 218.29 unknown via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one 15153217 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
OxyphyllaneneA 122402647 Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C 192.25 unknown via CMAUP database
Oxyphyllenodiol A 10082923 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenone A 10262534 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllenone B 44310512 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllone C 44255203 Click to see CC(C)C1CCC(=O)C2=C1C3C(O3)(CC2)C 220.31 unknown via CMAUP database
Teuhetenone A 15153216 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene 12014673 Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C 57335616 Click to see CC1=C2C3C(O3)(CCC2(CCC1=O)C)C(=O)C 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one 6440365 Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O 310.40 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one 72708396 Click to see COC1=CC=C(C=C1)CCCCC(=O)CCC2=C(C(=C(C=C2)O)OC)O 358.40 unknown via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one 72708395 Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O 328.40 unknown via CMAUP database
Yakuchinone-A 133145 Click to see COC1=C(C=CC(=C1)CCC(=O)CCCCC2=CC=CC=C2)O 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 5378823 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database

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