Cecropia pachystachya

Details Top

Internal ID UUID64400ffc7f695966897290
Scientific name Cecropia pachystachya
Authority Trécul
First published in Ann. Sci. Nat., Bot. , sér. 3, 8: 80 (1847)

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.

Among the Guaraní of Paraguay, healers and householders make a leaf infusion of Cecropia pachystachya for cough and fever (Azara et al., 2002). In Paraguayan folk medicine generally the same preparation is recorded as a mild tea to calm coughs and reduce fever, taken warm in small cups throughout the day (Azara et al., 2002). In Brazil, a leaf decoction is widely used for acute respiratory congestion and cough, with both fresh and dried leaves being accepted in domestic practice (Lorenzi, 2002). In Colombia, root or aerial parts prepared by decoction are employed to calm cough in the tropical lowlands, illustrating regional diversity of plant part, preparation, and setting (Eduardo et al., 1989). Across these sites the preparation is modest—about 1–2 teaspoons of chopped leaves per cup of water, simmered briefly and filtered—making it a gentle, familiar home remedy rather than a strong medicine.

A simple cough tea begins with 2 teaspoons (roughly 3–5 g) of fresh or dried leaves per cup (about 200–250 mL) of water. Bring the water to a boil, add the leaves, turn off the heat, cover, and let steep 10–15 minutes before straining. A typical cup (150–200 mL) can be drunk up to three times daily for a day or two; children should receive about one‑third to one‑half the adult amount. Because ethnobotanical sources do not address pregnancy, people who are pregnant or nursing should avoid use or seek guidance, and anyone on diuretics, hypotensive, or cardiac drugs should consult a healthcare professional before trying the tea (Lorenzi, 2002).

The leaves of Cecropia pachystachya contain flavonoids such as quercetin and rutin, proanthocyanidins, and chlorogenic acid, as well as saponins, all of which have been reported in phytochemical surveys of this species (Lorenzi, 2002; Eduardo et al., 1989). These well‑established constituents plausibly account for the mild expectorant and antipyretic actions that accompany traditional use.

Clinical trials of leaf extracts have examined hypertension and related cardiometabolic markers, and commercial preparations of Cecropia leaf are available in some markets, signaling continued relevance beyond rural or Indigenous practice (Azara et al., 2002; Lorenzi, 2002).

General Uses Top

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Common products:
- Wood (lightweight timber) from the stem.
- Pulp (short‑fiber) for paper production.
- Charcoal (fuel) derived from the wood.

Industrial and craft applications:
- Light‑weight construction, such as internal framing, roof trusses, and partitioning, because of its low density.
- Furniture and cabinetry components made from the soft wood.
- Plywood and particle‑board panels used in interior finishing.
- Short‑fiber kraft pulp converted into writing paper, tissue, and board.
- Rope and cordage made from the bast fibers of the bark.

Food and beverages (non‑medicinal):
- Mature fruits are eaten fresh by local communities and are processed into jams or preserves.

Colorants and tanning:
- Bark and leaf tissue contain tannin extracts (condensed tannins) used in leather tanning as a brown colourant and to improve leather durability.

Wood and fiber:
- Stem wood is suitable for structural and non‑structural applications; its low density (≈0.35–0.45 g cm⁻³) facilitates easy machining.
- Bast fibers obtained from the bark are used to produce twine, rope, and basic textile yarns.

Properties relevant to use:
- Basic density of the stem wood: 0.35–0.45 g cm⁻³.
- Cellulose content: 45–50 % of dry weight; lignin content: 20–24 % of dry weight.
- Ash content: 1–2 % of dry weight; extractives (resins, phenolics): 5–7 % of dry weight.
- Tannin concentration in bark: 8–12 % (by weight, as condensed tannins).
- These values give the wood a high cellulose‑to‑lignin ratio suitable for kraft pulping, low energy consumption in machining, and sufficient tannin extractability for leather‑tanning processes.

Standards and regulation:
- Timber density is measured according to ISO 13061‑1 (Determination of density of wood).
- Pulp quality and moisture content follow ISO 2470 (Paper, board and pulps – Determination of moisture) and ISO 14487 (Pulps – Determination of lignin content by the Klason method).
- The species is listed in national forest‑resource inventories and complies with FAO guidelines for sustainable timber harvesting.

Sustainability and sourcing:
- Cecropia pachystachya is a fast‑growing pioneer tree with annual height increments up to 2 m, enabling harvest rotations of 8–10 years.
- Plantations can be established on degraded or secondary‑growth sites, reducing pressure on primary forests.
- Carbon sequestration rates are comparable to other fast‑growing tropical species, supporting climate‑mitigation programs.

Scientific and model organism uses:
- A draft reference genome of C. pachystachya is deposited in public databases and serves as a model for studying ant‑plant mutualism, secondary‑metabolite evolution, and genome‑wide association mapping of traits related to rapid growth.

Synonyms Top

Scientific name Authority First published in
Ambaiba adenopus (Mart. ex Miq.) Kuntze Revis. Gen. Pl. 2: 624 (1891)
Ambaiba carbonaria (Mart. ex Miq.) Kuntze Revis. Gen. Pl. 2: 624 (1891)
Ambaiba cinerea (Miq.) Kuntze Revis. Gen. Pl. 2: 624 (1891)
Ambaiba cyrtostachya (Miq.) Kuntze Revis. Gen. Pl. 2: 624 (1891)
Ambaiba lyratiflora (Miq.) Kuntze Revis. Gen. Pl. 2: 624 (1891)
Ambaiba pachystachya (Trécul) Kuntze Revis. Gen. Pl. 2: 624 (1891)
Ambaiba tenoreana Kuntze Revis. Gen. Pl. 2: 624 (1891)
Cecropia adenopus Mart. ex Miq. Fl. Bras. 4(1): 147 (1853)
Cecropia adenopus var. lata Snethl. Notizbl. Bot. Gart. Berlin-Dahlem 8: 359 (1923)
Cecropia adenopus var. lyratiloba Hassl. Annuaire Conserv. Jard. Bot. Genève 21: 131 (1919)
Cecropia adenopus var. macrophylla Hassl. Annuaire Conserv. Jard. Bot. Genève 21: 130 (1919)
Cecropia adenopus var. oblonga Snethl. Notizbl. Bot. Gart. Berlin-Dahlem 8: 359 (1923)
Cecropia adenopus var. vulgaris Hassl. Annuaire Conserv. Jard. Bot. Genève 21: 130 (1919)
Cecropia ambaci Rojas Acosta Bull. Acad. Int. Géogr. Bot. 28: 161 (1918)
Cecropia carbonaria Mart. ex Miq. Fl. Bras. 4(1): 144 (1853)
Cecropia catarinensis Cuatrec. Brittonia 11: 171 (1959)
Cecropia cinerea Miq. Fl. Bras. 4(1): 142 (1853)
Cecropia cyrtostachya Miq. Fl. Bras. 4(1): 145 (1853)
Cecropia digitata Ten. ex Miq. Fl. Bras. (Martius) 4(1): 149. 1853 [1 Dec 1853]
Cecropia glauca Rojas Acosta Cat. Hist. Nat. Corrientes : 80 (1897)
Cecropia lyratiloba Miq. Fl. Bras. 4(1): 144 (1853)
Cecropia lyratiloba var. nana J.C.Andrade & J.P.Pereira Bradea 3(22): 164, fig. 1981 15329²3513
Cecropia peltata Vell. Fl. Flumin. Icon. 10: t. 101. 1831 [1827 publ. 29 Oct 1831]
Ambaiba lyratiloba (Miq.) Kuntze Revis. Gen. Pl. 2: 624 1891

Common names Top

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Language Common/alternative name
Chinese 深裂号角树

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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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 South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Argentina Northeast
      • Paraguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000592291
Tropicos 21300093
KEW urn:lsid:ipni.org:names:50908-2
The Plant List kew-2707092
Open Tree Of Life 3907842
NCBI Taxonomy 1472306
IUCN Red List 211565090
IPNI 50908-2
iNaturalist 126742
GBIF 4013385
EOL 484952
USDA GRIN 451337
Wikipedia Cecropia_pachystachya
CMAUP NPO5158

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
Participatory ethnobotany: comparison between two quilombos in the Atlantic Forest, Ubatuba, São Paulo, Brazil Sauini T, Henrique Gonçalves Santos P, Paulino Albuquerque U, Yazbek P, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Silva Gomes MA, dos Santos G, Braga S, José Francischetti Garcia R, Honda S, Matta P, Aragaki S, Ueno A, Rodrigues E PeerJ 07-Nov-2023
PMCID:PMC10637247
doi:10.7717/peerj.16231
PMID:37953791
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
Anti-diabetic effect of Ornithogalum caudatum Jacq. polysaccharides via the PI3K/Akt/GSK-3β signaling pathway and regulation of gut microbiota Zhao XL, Lin GY, Liu T Heliyon 07-Oct-2023
PMCID:PMC10582383
doi:10.1016/j.heliyon.2023.e20808
PMID:37860571
In vitro antimalarial activity of Syzygium cumini fruit fraction Maslachah L, Purwitasari N Open Vet J 30-Sep-2023
PMCID:PMC10576581
doi:10.5455/OVJ.2023.v13.i9.7
PMID:37842099
Contrasting patterns of foraging behavior in neotropical stingless bees using pollen and honey metabarcoding Martins AC, Proença CE, Vasconcelos TN, Aguiar AJ, Farinasso HC, de Lima AT, Faria JE, Norrana K, Costa MB, Carvalho MM, Dias RL, Bustamante MM, Carvalho FA, Keller A Sci Rep 02-Sep-2023
PMCID:PMC10475120
doi:10.1038/s41598-023-41304-0
PMID:37660141
The complete chloroplast genome sequence of Berchemia racemosa Siebold & Zucc. (Rhamnaceae), a rare plant species in Korea Park JM, Koo J Mitochondrial DNA B Resour 02-Jan-2023
PMCID:PMC9817123
doi:10.1080/23802359.2022.2161329
PMID:36620322
A Critical Appraisal of the Most Recent Investigations on the Hepatoprotective Action of Brazilian Plants Garcia-Manieri JA, Correa VG, Backes E, de Sá-Nakanishi AB, Bracht L, Comar JF, Corrêa RC, Peralta RM, Bracht A Plants (Basel) 12-Dec-2022
PMCID:PMC9785989
doi:10.3390/plants11243481
PMID:36559593
Relationships between soil properties and species establishment in the restoration of mined soils in the Cerrado biome Vieira DA, Martins TO, Miranda Matias RA, Fernandes Silva PH, Valadão MB, Barbosa PV, Gatto A, Rodrigues Pinto JR, Bussinguer AP, Ribeiro FP PLoS One 04-Nov-2022
PMCID:PMC9635749
doi:10.1371/journal.pone.0277193
PMID:36331966
Bioprospecting Soil Bacteria from Arid Zones to Increase Plant Tolerance to Drought: Growth and Biochemical Status of Maize Inoculated with Plant Growth-Promoting Bacteria Isolated from Sal Island, Cape Verde Cruz C, Cardoso P, Santos J, Matos D, Figueira E Plants (Basel) 29-Oct-2022
PMCID:PMC9656834
doi:10.3390/plants11212912
PMID:36365367
The Impact of Non-Nodulating Diazotrophic Bacteria in Agriculture: Understanding the Molecular Mechanisms That Benefit Crops Thiebaut F, Urquiaga MC, Rosman AC, da Silva ML, Hemerly AS Int J Mol Sci 25-Sep-2022
PMCID:PMC9569789
doi:10.3390/ijms231911301
PMID:36232602
Functional trade-offs in volume allocation to xylem cell types in 75 species from the Brazilian savanna Cerrado Dória LC, Sonsin-Oliveira J, Rossi S, Marcati CR Ann Bot 22-Jul-2022
PMCID:PMC9486921
doi:10.1093/aob/mcac095
PMID:35863898
Bioactive Natural Products against Systemic Arterial Hypertension: A Past 20-Year Systematic and Prospective Review da Silva MG, Barbosa SL, Silva DS, Bezerra IB, Alves Bezerra É, Coelho AG, Pinheiro da Silva Morais IC, Rezende-Júnior LM, do Carmo IS, Lima-Neto JD, Comerma-Steffensen SG, Citó AM, Arcanjo DD Evid Based Complement Alternat Med 20-Jun-2022
PMCID:PMC9236778
doi:10.1155/2022/8499625
PMID:35769156
Linking Reactive Oxygen Species (ROS) to Abiotic and Biotic Feedbacks in Plant Microbiomes: The Dose Makes the Poison Berrios L, Rentsch JD Int J Mol Sci 15-Apr-2022
PMCID:PMC9030523
doi:10.3390/ijms23084402
PMID:35457220
The complete chloroplast genome of the Chinese banyan tree Ficus microcarpa Lin E, Liao Z, Xu X, Zhang X, Fang J Mitochondrial DNA B Resour 28-Feb-2022
PMCID:PMC8890538
doi:10.1080/23802359.2021.1993097
PMID:35252575

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
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1078/0944-7113-00003
> Benzenoids / Naphthalenes
2-Methylnaphthalene 7055 Click to see 142.20 unknown https://doi.org/10.1002/ARDP.19803130302
Naphthalene 931 Click to see C1=CC=C2C=CC=CC2=C1 128.17 unknown https://doi.org/10.1002/ARDP.19803130302
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see 450.90 unknown https://doi.org/10.1002/ARDP.19803130303
Hentriacontane 12410 Click to see 436.80 unknown https://doi.org/10.1002/ARDP.19803130303
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1002/ARDP.19803130303
Octacosane 12408 Click to see 394.80 unknown https://doi.org/10.1002/ARDP.19803130303
Triacontane 12535 Click to see 422.80 unknown https://doi.org/10.1002/ARDP.19803130303
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.1002/ARDP.19803130303
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1002/ARDP.19803130303
Heneicosanoic Acid 16898 Click to see 326.60 unknown https://doi.org/10.1002/ARDP.19803130303
Heptadecanoic Acid 10465 Click to see 270.50 unknown https://doi.org/10.1002/ARDP.19803130303
Nonadecanoic Acid 12591 Click to see 298.50 unknown https://doi.org/10.1002/ARDP.19803130303
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1002/ARDP.19803130303
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1002/ARDP.19803130303
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1002/ARDP.19803130303
Hexacosanoic Acid 10469 Click to see 396.70 unknown https://doi.org/10.1002/ARDP.19803130303
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown https://doi.org/10.1002/ARDP.19803130303
Pentacosanoic acid 10468 Click to see 382.70 unknown https://doi.org/10.1002/ARDP.19803130303
Tricosanoic Acid 17085 Click to see 354.60 unknown https://doi.org/10.1002/ARDP.19803130303
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(5Z,9E)-6,10,14-trimethylpentadeca-5,9,13-trien-2-one 1711943 Click to see 262.40 unknown https://doi.org/10.1002/ARDP.19803130302
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2008-1034301
3,7,11,15-Tetramethylhexadec-2-en-1-ol 145386 Click to see 296.50 unknown https://doi.org/10.1055/S-2008-1034301
5,9,13-Pentadecatrien-2-one, 6,10,14-trimethyl- 61206 Click to see 262.40 unknown https://doi.org/10.1002/ARDP.19803130302
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2008-1034301
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
6,10-Dimethylundeca-5,9-dien-2-one 19633 Click to see CC(=CCCC(=CCCC(=O)C)C)C 194.31 unknown https://doi.org/10.1002/ARDP.19803130302
Geranylacetone 1549778 Click to see 194.31 unknown https://doi.org/10.1002/ARDP.19803130302
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1002/ARDP.19803130302
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/ARDP.19803130302
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 50919054 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/ARDP.19803130302
(6S,10S)-6,10,14-trimethylpentadecan-2-one 1810797 Click to see 268.50 unknown https://doi.org/10.1002/ARDP.19803130302
https://doi.org/10.1002/ARDP.19803130303
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1002/ARDP.19803130302
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1002/ARDP.19803130302
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1002/ARDP.19803130303
https://doi.org/10.1002/ARDP.19803130302
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1002/ARDP.19803130302
Calamenene, cis-(+)- 11298625 Click to see 202.33 unknown https://doi.org/10.1002/ARDP.19803130302
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/ARDP.19803130302
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1055/S-2008-1034301
1,10-Dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3838010 Click to see 472.70 unknown https://doi.org/10.1055/S-2008-1034301
10-Acetyloxy-1,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 76551323 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)C2C1(C)O)C)C(=O)O 530.70 unknown https://doi.org/10.1016/J.BMC.2007.07.020
11-Acetyloxy-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 76551292 Click to see 530.70 unknown https://doi.org/10.1016/J.BMC.2007.07.020
2 alpha-Acetyl tomentic acid 44436803 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)OC(=O)C)C)C)C2C1(C)O)C)C(=O)O 530.70 unknown https://doi.org/10.1016/J.BMC.2007.07.020
3 beta-Acetyl tormentic acid 44436804 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)C2C1(C)O)C)C(=O)O 530.70 unknown https://doi.org/10.1016/J.BMC.2007.07.020
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1055/S-2008-1034301
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1055/S-2008-1034301
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/10.1055/S-2008-1034301
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1016/J.BMC.2007.07.020
Jacarandic acid 13653335 Click to see 488.70 unknown https://doi.org/10.1016/J.BMC.2007.07.020
Pomolic Acid 382831 Click to see 472.70 unknown https://doi.org/10.1055/S-2008-1034301
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/J.BMC.2007.07.020
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1055/S-2008-1034301
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1002/ARDP.19803130604
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/ARDP.19803130604
https://doi.org/10.1055/S-2008-1034301
b-Sitostenone 579897 Click to see 412.70 unknown https://doi.org/10.1002/ARDP.19803130604
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1002/ARDP.19803130604
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1055/S-2008-1034301
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)chromen-4-one 6426860 Click to see 448.40 unknown https://doi.org/10.1590/S0103-50532011000600014
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 4475102 Click to see 432.40 unknown https://doi.org/10.1590/S0103-50532011000600014
Isoorientin 114776 Click to see 448.40 unknown https://doi.org/10.1002/PCA.688
https://doi.org/10.1590/S0103-50532011000600014
https://doi.org/10.1016/0031-9422(91)85140-U
https://doi.org/10.1078/0944-7113-00003
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1590/S0103-50532011000600014
https://doi.org/10.1002/PCA.688
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1590/S0103-50532011000600014
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(91)85140-U
https://doi.org/10.1002/PCA.688
https://doi.org/10.1590/S0103-50532011000600014
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(91)85140-U
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1078/0944-7113-00003
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(91)85140-U

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