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Eschweilera coriacea

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644026f76c204245131008
Scientific name Eschweilera coriacea
Authority (DC.) S.A.Mori
First published in Fl. Neotrop. Monogr. 21(II): 203 (1990)

Description Top

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It is a large evergreen tree, growing up to 25 m (82 ft) tall. The trunk is straight and cylindrical, with a diameter of up to 1 m (3.3 ft). The bark is grayish-brown and scaly. The leaves are alternate, simple, and oblong-lanceolate, up to 15 cm (5.9 in) long and 5 cm (2.0 in) wide. The flowers are small, white, and fragrant, with four petals. The fruit is a drupe, up to 5 cm (2.0 in) in diameter, with a single seed.

Eschweilera coriacea is a large evergreen tree native to Honduras, Panama and South America. It can grow up to 25 m (82 ft) tall with a trunk diameter of up to 1 m (3.3 ft). Its bark is grayish-brown and scaly, and its leaves are alternate, simple, and oblong-lanceolate, up to 15 cm (5.9 in) long and 5 cm (2.0 in) wide. The flowers are small, white, and fragrant, with four petals, and the fruit is a drupe, up to

Synonyms Top

Scientific name Authority First published in
Chytroma cincturata Miers Trans. Linn. Soc. London 30: 237 (1874)
Chytroma grandifolia Miers Trans. Linn. Soc. London 30: 237 (1874)
Jugastrum coriaceum Miers Trans. Linn. Soc. London 30: 275 (1874)
Lecythis grandifolia O.Berg Fl. Bras. 14(1): 494 (1858)
Lecythis odora Poepp. ex O.Berg Fl. Bras. 14(1): 492 (1858)
Lecythis peruviana L.O.Williams Fieldiana, Bot. 31: 30 (1964)
Lecythis coriacea DC. Prodr. 3: 291 (1828)
Lecythis retroflexa Benoist Bull. Mus. Natl. Hist. Nat. 29: 595 (1923)
Lecythis acuminatissima O.Berg Fl. Bras. 14(1): 494 (1858)
Neohuberia matamata Ledoux Lecointea 1: 3-7. 1963 (1963)
Eschweilera acuminatissima Miers Trans. Linn. Soc. London 30: 273 (1874)
Eschweilera eymaana R.Knuth Pflanzenr. , IV, 219a: 100 (1939)
Eschweilera fractiflexa R.Knuth Pflanzenr. , IV, 219a: 110 (1939)
Eschweilera grandifolia Mart. ex DC. Prodr. 3: 293 (1828)
Eschweilera matamata Huber Bol. Mus. Goeldi Hist. Nat. Ethnogr. 6: 211 (1910)
Eschweilera odora Miers Trans. Linn. Soc. London 30: 273 (1874)
Eschweilera pallida Miers Trans. Linn. Soc. London 30: 267 (1874)
Eschweilera retroflexa (Benoist) R.Knuth Pflanzenr. , IV, 219a: 106 (1939)
Eschweilera vageleri R.Knuth Pflanzenr. , IV, 219a: 96 (1939)

Common names Top

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Language Common/alternative name
Portuguese marão vermelho
Portuguese marão-vermelho
Portuguese matamatá branco
Portuguese matamatá-branco
Portuguese matamatá

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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No subvariety added yet.

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000775226
Tropicos 17900314
INPN 733584
KEW urn:lsid:ipni.org:names:947902-1
The Plant List kew-313788
Open Tree Of Life 858173
NCBI Taxonomy 372712
IUCN Red List 144119852
IPNI 947902-1
GBIF 3083231
EOL 321273
USDA GRIN 450512
Wikipedia Eschweilera_coriacea
CMAUP NPO2853

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
Feeding ecology of monk sakis (Pithecia monachus) in a seasonally flooded forest in western Amazonia Gottstein M, Morris AL, Heer K, Heymann EW Primates 21-Jun-2023
PMCID:PMC10473984
doi:10.1007/s10329-023-01074-9
PMID:37341865
Non-random host tree infestation by the Neotropical liana Marcgravia longifolia Heymann EW, Thiel S, Paciência F, Rimachi Taricuarima MN, Zárate Gómez R, Shahuano Tello N, Heer K, Sennhenn-Reulen H, Mundry R PeerJ 15-Dec-2022
PMCID:PMC9760024
doi:10.7717/peerj.14535
PMID:36540804
Long‐term drought effects on the thermal sensitivity of Amazon forest trees Docherty EM, Gloor E, Sponchiado D, Gilpin M, Pinto CA, Junior HM, Coughlin I, Ferreira L, Junior JA, da Costa AC, Meir P, Galbraith D Plant Cell Environ 20-Oct-2022
PMCID:PMC10092618
doi:10.1111/pce.14465
PMID:36230004
The impact of species complexes on tree abundance patterns in Amazonia Bacon CD, Hill A, ter Steege H, Antonelli A, Damasco G Am J Bot 04-Oct-2022
PMCID:PMC9828733
doi:10.1002/ajb2.16069
PMID:36193824
Admixture may be extensive among hyperdominant Amazon rainforest tree species Larson DA, Vargas OM, Vicentini A, Dick CW New Phytol 12-Sep-2021
PMCID:PMC9292926
doi:10.1111/nph.17675
PMID:34389989
A 5,000-year vegetation and fire history for tierra firme forests in the Medio Putumayo-Algodón watersheds, northeastern Peru Piperno DR, McMichael CH, Pitman NC, Andino JE, Ríos Paredes M, Heijink BM, Torres-Montenegro LA Proc Natl Acad Sci U S A 07-Jun-2021
PMCID:PMC8501791
doi:10.1073/pnas.2022213118
PMID:34580207
Revisiting the hyperdominance of Neotropical tree species under a taxonomic, functional and evolutionary perspective Damasco G, Baraloto C, Vicentini A, Daly DC, Baldwin BG, Fine PV Sci Rep 05-May-2021
PMCID:PMC8099866
doi:10.1038/s41598-021-88417-y
PMID:33953271
31P-NMR Metabolomics Revealed Species-Specific Use of Phosphorous in Trees of a French Guiana Rainforest Gargallo-Garriga A, Sardans J, Llusià J, Peguero G, Asensio D, Ogaya R, Urbina I, Langenhove LV, Verryckt LT, Courtois EA, Stahl C, Grau O, Urban O, Janssens IA, Nolis P, Pérez-Trujillo M, Parella T, Peñuelas J Molecules 31-Aug-2020
PMCID:PMC7504763
doi:10.3390/molecules25173960
PMID:32877991
Biased-corrected richness estimates for the Amazonian tree flora ter Steege H, Prado PI, Lima RA, Pos E, de Souza Coelho L, de Andrade Lima Filho D, Salomão RP, Amaral IL, de Almeida Matos FD, Castilho CV, Phillips OL, Guevara JE, de Jesus Veiga Carim M, Cárdenas López D, Magnusson WE, Wittmann F, Martins MP, Sabatier D, Irume MV, da Silva Guimarães JR, Molino JF, Bánki OS, Piedade MT, Pitman NC, Ramos JF, Monteagudo Mendoza A, Venticinque EM, Luize BG, Núñez Vargas P, Silva TS, de Leão Novo EM, Reis NF, Terborgh J, Manzatto AG, Casula KR, Honorio Coronado EN, Montero JC, Duque A, Costa FR, Castaño Arboleda N, Schöngart J, Zartman CE, Killeen TJ, Marimon BS, Marimon-Junior BH, Vasquez R, Mostacedo B, Demarchi LO, Feldpausch TR, Engel J, Petronelli P, Baraloto C, Assis RL, Castellanos H, Simon MF, de Medeiros MB, Quaresma A, Laurance SG, Rincón LM, Andrade A, Sousa TR, Camargo JL, Schietti J, Laurance WF, de Queiroz HL, Nascimento HE, Lopes MA, de Sousa Farias E, Magalhães JL, Brienen R, Aymard C. GA, Revilla JD, Vieira IC, Cintra BB, Stevenson PR, Feitosa YO, Duivenvoorden JF, Mogollón HF, Araujo-Murakami A, Ferreira LV, Lozada JR, Comiskey JA, de Toledo JJ, Damasco G, Dávila N, Lopes A, García-Villacorta R, Draper F, Vicentini A, Cornejo Valverde F, Lloyd J, Gomes VH, Neill D, Alonso A, Dallmeier F, de Souza FC, Gribel R, Arroyo L, Carvalho FA, de Aguiar DP, do Amaral DD, Pansonato MP, Feeley KJ, Berenguer E, Fine PV, Guedes MC, Barlow J, Ferreira J, Villa B, Peñuela Mora MC, Jimenez EM, Licona JC, Cerón C, Thomas R, Maas P, Silveira M, Henkel TW, Stropp J, Paredes MR, Dexter KG, Daly D, Baker TR, Huamantupa-Chuquimaco I, Milliken W, Pennington T, Tello JS, Pena JL, Peres CA, Klitgaard B, Fuentes A, Silman MR, Di Fiore A, von Hildebrand P, Chave J, van Andel TR, Hilário RR, Phillips JF, Rivas-Torres G, Noronha JC, Prieto A, Gonzales T, de Sá Carpanedo R, Gonzales GP, Gómez RZ, de Jesus Rodrigues D, Zent EL, Ruschel AR, Vos VA, Fonty É, Junqueira AB, Doza HP, Hoffman B, Zent S, Barbosa EM, Malhi Y, de Matos Bonates LC, de Andrade Miranda IP, Silva N, Barbosa FR, Vela CI, Pinto LF, Rudas A, Albuquerque BW, Umaña MN, Carrero Márquez YA, van der Heijden G, Young KR, Tirado M, Correa DF, Sierra R, Costa JB, Rocha M, Vilanova Torre E, Wang O, Oliveira AA, Kalamandeen M, Vriesendorp C, Ramirez-Angulo H, Holmgren M, Nascimento MT, Galbraith D, Flores BM, Scudeller VV, Cano A, Ahuite Reategui MA, Mesones I, Baider C, Mendoza C, Zagt R, Urrego Giraldo LE, Ferreira C, Villarroel D, Linares-Palomino R, Farfan-Rios W, Farfan-Rios W, Casas LF, Cárdenas S, Balslev H, Torres-Lezama A, Alexiades MN, Garcia-Cabrera K, Valenzuela Gamarra L, Valderrama Sandoval EH, Ramirez Arevalo F, Hernandez L, Sampaio AF, Pansini S, Palacios Cuenca W, de Oliveira EA, Pauletto D, Levesley A, Melgaço K, Pickavance G Sci Rep 23-Jun-2020
PMCID:PMC7311553
doi:10.1038/s41598-020-66686-3
PMID:32576943
Different “metabolomic niches” of the highly diverse tree species of the French Guiana rainforests Gargallo-Garriga A, Sardans J, Granda V, Llusià J, Peguero G, Asensio D, Ogaya R, Urbina I, Van Langenhove L, Verryckt LT, Chave J, Courtois EA, Stahl C, Grau O, Klem K, Urban O, Janssens IA, Peñuelas J Sci Rep 24-Apr-2020
PMCID:PMC7181821
doi:10.1038/s41598-020-63891-y
PMID:32332903
Wood allocation trade‐offs between fiber wall, fiber lumen, and axial parenchyma drive drought resistance in neotropical trees Janssen TA, Hölttä T, Fleischer K, Naudts K, Dolman H Plant Cell Environ 03-Feb-2020
PMCID:PMC7155043
doi:10.1111/pce.13687
PMID:31760666
Physical, but not chemical, antiherbivore defense expression is related to the clustered spatial distribution of tropical trees in an Amazonian forest Cobo‐Quinche J, Endara M, Valencia R, Muñoz‐Upegui D, Cárdenas RE Ecol Evol 31-Jan-2019
PMCID:PMC6392389
doi:10.1002/ece3.4859
PMID:30847070
Tree growth and stem carbon accumulation in human-modified Amazonian forests following drought and fire Berenguer E, Malhi Y, Brando P, Cardoso Nunes Cordeiro A, Ferreira J, França F, Chesini Rossi L, Maria Moraes de Seixas M, Barlow J Philos Trans R Soc Lond B Biol Sci 08-Oct-2018
PMCID:PMC6178429
doi:10.1098/rstb.2017.0308
PMID:30297467
Complete plastome sequences from Bertholletia excelsa and 23 related species yield informative markers for Lecythidaceae Thomson AM, Vargas OM, Dick CW Appl Plant Sci 05-Jun-2018
PMCID:PMC5991589
doi:10.1002/aps3.1151
PMID:30131893
Palikur traditional roundwood construction in eastern French Guiana: ethnobotanical and cultural perspectives Ogeron C, Odonne G, Cristinoi A, Engel J, Grenand P, Beauchêne J, Clair B, Davy D J Ethnobiol Ethnomed 24-Apr-2018
PMCID:PMC5916587
doi:10.1186/s13002-018-0226-7
PMID:29690891

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 / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(4Z,7Z,10Z,13Z)-hexadeca-4,7,10,13-tetraenoic acid 5312433 Click to see CCC=CCC=CCC=CCC=CCCC(=O)O 248.36 unknown via CMAUP database
(R)-2-hydroxypalmitic acid 11065598 Click to see CCCCCCCCCCCCCCC(C(=O)O)O 272.42 unknown via CMAUP database
2-Keto palmitic acid 5282996 Click to see CCCCCCCCCCCCCCC(=O)C(=O)O 270.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Valeric acid 7991 Click to see CCCCC(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(8Z,11Z,14Z)-Heptadecatrienal 6430107 Click to see CCC=CCC=CCC=CCCCCCCC=O 248.40 unknown via CMAUP database
(8z,11z)-8,11-Heptadecadienal 14543488 Click to see CCCCCC=CCC=CCCCCCCC=O 250.40 unknown via CMAUP database
(8Z,11Z)-Heptadecadienal 6430322 Click to see CCCCCC=CCC=CCCCCCCC=O 250.40 unknown via CMAUP database
(Z)-8-heptadecenal 6430106 Click to see CCCCCCCCC=CCCCCCCC=O 252.40 unknown via CMAUP database
7,10,13-Hexadecatrienenal 14543490 Click to see CCC=CCC=CCC=CCCCCCC=O 234.38 unknown via CMAUP database
8-Heptadecenal 14543489 Click to see CCCCCCCCC=CCCCCCCC=O 252.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic acid 3931 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Sulfoquinovosylmonoacylglycerols / Sulfoquinovosyl 1-monoacylglycerols
[(2S,3S,4S,5R,6S)-6-[(2R)-3-hexadecanoyloxy-2-hydroxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid 102201401 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CS(=O)(=O)O)O)O)O)O 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(-)-alpha-Tocopherol 1742129 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
(2R)-2,8-Dimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 12444418 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown via CMAUP database
(2S)-2,5,8-Trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol 76959905 Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O 416.70 unknown via CMAUP database
(S)-2,7,8-Trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol 73416557 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24E)-24-N-Propylidenecholesterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Acrylic acids and derivatives / Acrylic acids
Acrylic acid 6581 Click to see C=CC(=O)O 72.06 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(3S,6S)-3-Isopropyl-6-methylpiperazine-2,5-dione 13783106 Click to see CC1C(=O)NC(C(=O)N1)C(C)C 170.21 unknown via CMAUP database
(3S,8aS)-3-Isobutylhexahydropyrrolo[1,2-a]pyrazine-1,4-dione 7074739 Click to see CC(C)CC1C(=O)N2CCCC2C(=O)N1 210.27 unknown via CMAUP database
cyclo(L-Pro-L-Val) 6992261 Click to see CC(C)C1C(=O)N2CCCC2C(=O)N1 196.25 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
Arginyl-Glutamine 7019985 Click to see C(CC(C(=O)NC(CCC(=O)N)C(=O)O)N)CN=C(N)N 302.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1021/NP980046U
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see C1=CNC(=O)NC1=O 112.09 unknown via CMAUP database
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Chaetoglobosin Fex 71768077 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(C(=O)C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin A 46209792 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CC4C1C(=C(C4=O)O)C)C(=O)NC3CC5=CNC6=CC=CC=C65)C)O 528.60 unknown via CMAUP database
Cytoglobosin B 46209793 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin C 44610809 Click to see CC1CC=CC2C(C(=C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C)O 530.70 unknown via CMAUP database
Cytoglobosin D 46209919 Click to see CC1CC=CC2C=C(C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C 514.70 unknown via CMAUP database
Cytoglobosin E 46209920 Click to see CC1CC=CC2C=C(C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)CO 528.60 unknown via CMAUP database
Cytoglobosin F 46209921 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin G 46209922 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 532.70 unknown via CMAUP database
isochaetoglobosin D 23259926 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 528.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1021/NP980046U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1021/NP980046U
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1'-Monodecarboxyvaloneic acid dilactone 10410181 Click to see C1=CC(=C(C(=C1O)O)O)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O 426.30 unknown https://doi.org/10.1021/NP980046U
6,7,8,17,18-Pentahydroxy-3,10,15,22-tetraoxahexacyclo[14.6.2.02,11.04,9.013,23.020,24]tetracosa-1(23),2(11),4(9),5,7,12,16(24),17,19-nonaene-14,21-dione 21635780 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC5=C(C(=C43)OC2=O)OC6=C(O5)C(=C(C(=C6)O)O)O 424.30 unknown https://doi.org/10.1021/NP980046U
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1021/NP980046U
Eschweilenol C 10026656 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)O)O 448.30 unknown https://doi.org/10.1021/NP980046U

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