Details Top

Internal ID UUID643fd9aaad976726218253
Scientific name Pterodon emarginatus
Authority Vogel
First published in Linnaea11: 384 (1837)

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 rural dwellers of the Caatinga–Cerrado transition in Pernambuco and the semi-arid Caatinga of Ceará, decoctions of the dried branches or bark of Pterodon emarginatus have been used to “wash” rheumatic joints and to drink for coughs and bronchitis, according to Di Stasi et al., 2002. In the southern Caatinga of Minas Gerais, healers record infusions or strong teas of the seed coat as a throat gargle and a gentle internal drink for throat pain, as reported by Harter et al., 2012. In the Caatinga of Bahia, traditional practitioners use a maceration of the ground seeds to loosen phlegm, either by sipping the “macerate tea” with honey or by dripping the liquid into the nose for sinusitis, as described by Albuquerque et al., 2007. The same seed maceration is employed topically for arthritic limbs by rural healers in Goiás and Minas Gerais, and internally for asthma and bronchitis, as reviewed by Di Stasi et al., 2002. Leaf infusions or decoctions have also been used locally in the Brazilian Northeast for inflammatory pains, and are documented in ethnobotanical surveys of the Cerrado (see Albuquerque et al., 2007). Across these regions the plant part varies—seeds for respiratory complaints and rheumatism; branches/bark for coughs and joint bathing; leaves for anti-inflammatory teas—reflecting a diversity of preparation methods that fit each therapeutic need.

To prepare a mild seed infusion, grind 3–5 g of well-dried, mature seeds and place the coarse powder in a pot. Add 250 ml of freshly boiled water, cover, and steep for 5–10 minutes. Strain and drink up to one cup daily, optionally sweetened with a little honey. This gentle “seed tea” is used in the Caatinga for coughs and sore throats (Harter et al., 2012). A separate maceration can be made by grinding 10–20 g of seeds, adding 250 ml of water, and macerating 6–12 hours with occasional shaking; the liquid is drunk in small doses (one to two tablespoonfuls) as an expectorant or used topically on inflamed joints, a method noted by Albuquerque et al., 2007. These preparations are generally strong in flavor and should not be used during pregnancy or by children without professional guidance, as ethanol extracts of the seeds show central depressant effects in animal tests (Vieira et al., 2016).

Phytochemically, Pterodon emarginatus seeds contain a mixture of fatty acids (oleic, linoleic, palmitic, stearic), fixed oils, and mucilaginous polysaccharides that together give the infusions and macerations a demulcent, mucilaginous quality (Gbolade et al., 2014; Maciel et al., 2002). The seeds also yield furanodiene-type diterpenoids— vouacapane skeletons such as voucapane and 6α,7β-diacetoxy-vouacapan-17β-yl acetate—that are responsible for strong anti-inflammatory and antinociceptive activity in animal models (Pereira et al., 2004; Gbolade et al., 2014). These diterpenoids plausibly underlie the traditional internal and topical uses for coughs, bronchitis, and rheumatism, while the fatty/mucilaginous matrix may soothe irritated mucous membranes.

Today, research on Pterodon emarginatus remains active, with modern bioassays confirming anti-inflammatory and antitussive effects linked to its furanodiene diterpenoids (Pereira et al., 2004; Gbolade et al., 2014). Seeds and fixed oil are sold in regional markets in Minas Gerais and the Caatinga, and preparations such as the macerated seed “tea” or essential-oil distillates are still used by some local practitioners for respiratory and rheumatic complaints, while clinical data on human efficacy and safety remain limited.

General Uses Top

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Common products:
• Seed essential oil and resinous seed extracts (e.g., flower scent composition, 14,15-dihydroxyvouacapan-17-oic acid; SD–GC-MS profiling).

Industrial and craft applications:
• Seed essential oil is reported as a specialty fragrance material and as a source of diterpenes used in minor flavor-fragrance research and analysis.

Food and beverages (non-medicinal):
• No documented food or beverage use.

Colorants and tanning:
• No documented dye or tannin use.

Wood and fiber:
• No documented timber or fiber product use.

Fragrance and cosmetics:
• Seed essential oil and resinous extracts are used in fragrance research and as analytical standards in phytochemical studies; no established commercial perfumery entry reported.

Properties relevant to use:
• Key volatile constituents include (E)-β-farnesene, α-humulene, and other sesquiterpenes; non-volatile constituents include vouacapane-type diterpenes such as 14,15-dihydroxyvouacapan-17-oic acid.

Standards and regulation:
• No species-specific standards or regulatory frameworks identified.

Sustainability and sourcing:
• No formal conservation or sustainability assessments reported.

Synonyms Top

Scientific name Authority First published in
Pterodon polygaliflorus (Benth.) Benth. Hooker's J. Bot. Kew Gard. Misc.2: 236 (1850)
Sweetia inornata Mohlenbr. Webbia17: 237 (1963)
Acosmium inornatum (Mohlenbr.) Yakovlev Notes Roy. Bot. Gard. Edinburgh29: 355 (1969)
Pterodon polygalaeflorus (Benth.) Benth.
Commilobium polygalaeflorus Benth. Comm. Legum. Gen.: 47 (1837)
Commilobium pubescens Benth. Comm. Legum. Gen.: 47 (1837)
Dipteryx emarginata Spreng. ex Walp. Repert. Bot. Syst.1: 805 (1843)

Common names Top

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Language Common/alternative name
bpy সুকুপিরা
Persian پتردن امارجیناتوس
French sucupira
Portuguese sucupira
Chinese 微毛翼豆

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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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 Southeast
      • Brazil West-central
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186722
Tropicos 13032432
KEW urn:lsid:ipni.org:names:516615-1
The Plant List ild-33212
Open Tree Of Life 662552
NCBI Taxonomy 1079077
IUCN Red List 144304793
IPNI 516615-1
iNaturalist 552658
GBIF 5342608
Freebase /m/0bc03p
EOL 642801
USDA GRIN 433215
Wikipedia Pterodon_emarginatus
CMAUP NPO7949

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
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Knowledge and perception of milk producers about thermal stress in Brazilian dairy farms Brettas PK, Nascimento FG, Guimarães EC, Faria PN, Ferreira AV, Nascimento MR Heliyon 17-Feb-2024
PMCID:PMC10884848
doi:10.1016/j.heliyon.2024.e26115
PMID:38404894
Progress of nanopreparation technology applied to volatile oil drug delivery systems Ye ZW, Yang QY, Lin QH, Liu XX, Li FQ, Xuan HD, Bai YY, Huang YP, Wang L, Wang F Heliyon 08-Jan-2024
PMCID:PMC10825498
doi:10.1016/j.heliyon.2024.e24302
PMID:38293491
Complete Chloroplast Genomes of Pterodon emarginatus Vogel and Pterodon pubescens Benth: Comparative and Phylogenetic Analyses Brito JB, Antunes AM, Ferreira RD, de Campos Telles MP, Targueta CP, Soares TN Curr Genomics 12-Dec-2023
PMCID:PMC10758126
doi:10.2174/0113892029244147231016050434
PMID:38169762
Beneficial Effects of Plant Oils Supplementation on Multiple Sclerosis: A Comprehensive Review of Clinical and Experimental Studies Al-Naqeb G, Kalmpourtzidou A, De Giuseppe R, Cena H Nutrients 18-Nov-2023
PMCID:PMC10674509
doi:10.3390/nu15224827
PMID:38004221
Pterodon emarginatus Seed Preparations: Antiradical Activity, Chemical Characterization, and In Silico ADMET Parameters of β-caryophyllene and Farnesol Froldi G, Benetti F, Mondin A, Roverso M, Pangrazzi E, Djeujo FM, Pastore P Molecules 09-Nov-2023
PMCID:PMC10673522
doi:10.3390/molecules28227494
PMID:38005216
Microwave‐assisted extraction optimization of sesquiterpene lactones from Inula helenium roots: A sustainable approach to reduce energy consumption and carbon footprint Özcan FŞ, Dikmen H, Özcan N, Çetin Ö, Çelik M, Trendafilova A Food Sci Nutr 13-Oct-2023
PMCID:PMC10804079
doi:10.1002/fsn3.3775
PMID:38268885
Iron-Dependent Cell Death: A New Treatment Approach against Pancreatic Ductal Adenocarcinoma Lopez-Blazquez C, Lacalle-Gonzalez C, Sanz-Criado L, Ochieng’ Otieno M, Garcia-Foncillas J, Martinez-Useros J Int J Mol Sci 07-Oct-2023
PMCID:PMC10573128
doi:10.3390/ijms241914979
PMID:37834426
Cryo-attenuated properties of Tilia miqueliana pericarps and seeds Wu Y, Sun XR, Peng CY, Shen YB, Visscher AM, Pritchard HW, Wang MZ, Deng ZY Front Plant Sci 15-Aug-2023
PMCID:PMC10486270
doi:10.3389/fpls.2023.1228069
PMID:37692432
Mesosphaerum suaveolens Essential Oil Attenuates Inflammatory Response and Oxidative Stress in LPS-Stimulated RAW 264.7 Macrophages by Regulating NF-κB Signaling Pathway Mohanta O, Ray A, Jena S, Sahoo A, Panda SS, Das PK, Nayak S, Panda PC Molecules 02-Aug-2023
PMCID:PMC10420984
doi:10.3390/molecules28155817
PMID:37570786
Topical Microemulsions: Skin Irritation Potential and Anti-Inflammatory Effects of Herbal Substances Leanpolchareanchai J, Teeranachaideekul V Pharmaceuticals (Basel) 13-Jul-2023
PMCID:PMC10384732
doi:10.3390/ph16070999
PMID:37513911
Pharmacological Potential of Betulin as a Multitarget Compound Adepoju FO, Duru KC, Li E, Kovaleva EG, Tsurkan MV Biomolecules 12-Jul-2023
PMCID:PMC10377123
doi:10.3390/biom13071105
PMID:37509141
Nanoliposomes containing three essential oils from the Artemisia genus as effective larvicides against Aedes aegypti and Anopheles stephensi Sanei-Dehkordi A, Ghasemian A, Zarenezhad E, Qasemi H, Nasiri M, Osanloo M Sci Rep 07-Jul-2023
PMCID:PMC10328918
doi:10.1038/s41598-023-38284-6
PMID:37420038
Dietary phytochemical and metabolic disease prevention: Focus on plant proteins Yang SH, Tao G, Yang L, Wu X, Liu JW, Dagher F, Ou SY, Song Y, Huang JQ Front Nutr 25-Jan-2023
PMCID:PMC9905127
doi:10.3389/fnut.2023.1089487
PMID:36761228
Plants causing poisoning outbreaks of livestock in South America: A review Riet-Correa F, Machado M, Micheloud JF Toxicon X 21-Jan-2023
PMCID:PMC9898795
doi:10.1016/j.toxcx.2023.100150
PMID:36747993

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,5R,6R,6aR,7S,11aS,11bR)-1,2,3,4,4a,5,6,6a,7,11,11a,11b-Dodecahydro-5,6-dihydroxy-4,4,11b-trimethylphenanthro(3,2-b)furan-7-carboxylic acid 162431 Click to see 348.40 unknown https://doi.org/10.1016/0024-3205(92)90208-7
https://doi.org/10.1016/S0031-9422(00)97084-5
https://doi.org/10.1016/S0031-9422(00)89084-6
(4aS,5R,6R,6aS,7S,11aS,11bR)-4,4,7,11b-tetramethyl-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5,6,7-triol 15786122 Click to see 334.40 unknown https://doi.org/10.1021/NP960140F
https://doi.org/10.1016/S0031-9422(00)89084-6
(4S,4aR,5R,6R,6aS,7S,11aS,11bR)-4-(hydroxymethyl)-4,7,11b-trimethyl-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5,6,7-triol 10736600 Click to see 350.40 unknown https://doi.org/10.1021/NP960140F
(5-Acetyloxy-4,4,7,11b-tetramethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-6-yl) acetate 315935 Click to see 402.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
(5-Acetyloxy-7-formyl-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-6-yl) acetate 162934747 Click to see 416.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
(5-hydroxy-4,4,11b-trimethyl-7-methylidene-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl) acetate 162953698 Click to see CC(=O)OC1C2C(CC3=C(C2=C)C=CO3)C4(CCCC(C4C1O)(C)C)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
[(4aR,5S,6S,6aS,7R,11aR,11bS)-5-acetyloxy-7-formyl-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-6-yl] acetate 162934749 Click to see 416.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
[(4aS,5R,6R,6aR,11aS,11bR)-5-hydroxy-4,4,11b-trimethyl-7-methylidene-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate 101663355 Click to see CC(=O)OC1C2C(CC3=C(C2=C)C=CO3)C4(CCCC(C4C1O)(C)C)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
[(4aS,6S,6aS,7R,11aS,11bR)-4,4,7,11b-tetramethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-6-yl] acetate 10914915 Click to see 344.50 unknown https://doi.org/10.1016/S0031-9422(97)00140-4
4-(hydroxymethyl)-4,7,11b-trimethyl-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5,6,7-triol 85250186 Click to see CC1(CCCC2(C1C(C(C3C2CC4=C(C3(C)O)C=CO4)O)O)C)CO 350.40 unknown https://doi.org/10.1021/NP960140F
4,4,7,11b-tetramethyl-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5,6,7-triol 85447559 Click to see CC1(CCCC2(C1C(C(C3C2CC4=C(C3(C)O)C=CO4)O)O)C)C 334.40 unknown https://doi.org/10.1021/NP960140F
https://doi.org/10.1016/S0031-9422(00)89084-6
5,6-Dihydroxy-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-7-carboxylic acid 315936 Click to see CC1(CCCC2(C1C(C(C3C2CC4=C(C3C(=O)O)C=CO4)O)O)C)C 348.40 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
https://doi.org/10.1016/S0031-9422(00)89084-6
6Alpha,7Beta-Diacetoxyvouacapane 24863610 Click to see 402.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
methyl (4aS,5R,6R,6aR,7S,11aS,11bR)-5-acetyloxy-6-hydroxy-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-7-carboxylate 145971496 Click to see 404.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
https://doi.org/10.1016/S0031-9422(00)97084-5
methyl (4aS,5R,6R,6aR,7S,11aS,11bR)-5,6-diacetyloxy-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-7-carboxylate 162847444 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
methyl (4aS,5R,6R,6aR,7S,11aS,11bR)-5,6-dihydroxy-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-7-carboxylate 101640159 Click to see CC1(CCCC2(C1C(C(C3C2CC4=C(C3C(=O)OC)C=CO4)O)O)C)C 362.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
methyl (4aS,5R,6R,6aR,7S,11aS,11bR)-6-acetyloxy-5-hydroxy-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-7-carboxylate 145953917 Click to see 404.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
Methyl 5,6-diacetyloxy-4,4,11b-trimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-7-carboxylate 162847442 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
methyl 5,6-diacetyloxy-7-hydroxy-4,7,11b-trimethyl-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylate 162922815 Click to see CC(=O)OC1C2C(CC3=C(C2(C)O)C=CO3)C4(CCCC(C4C1OC(=O)C)(C)C(=O)OC)C 462.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
Methyl 6alpha-acetoxy-7beta-hydroxyvouacapan-17beta-oate 628479 Click to see CC(=O)OC1C(C2C(CC3=C(C2C(=O)OC)C=CO3)C4(C1C(CCC4)(C)C)C)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)97084-5
https://doi.org/10.1016/S0031-9422(00)89084-6
Methyl 6alpha,7beta-dihydroxyvouacapan-17beta-oate 315937 Click to see CC1(CCCC2(C1C(C(C3C2CC4=C(C3C(=O)OC)C=CO4)O)O)C)C 362.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
Methyl 7alpha-acetoxy-6beta-hydroxyvouacapan-17beta-oate 628477 Click to see 404.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Dehydrosoyasaponin I 656760 Click to see 941.10 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 21119301 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1590/S0103-50531998000300014
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1590/S0103-50531998000300014
Sophoradiol 9846221 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
cycloart-23Z-ene-3beta,25-diol 101690746 Click to see 442.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
9,10-Dihydroxy-6-methoxy-3,3-dimethylpyrano[2,3-c]xanthen-7-one 162953656 Click to see 340.30 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
> Organoheterocyclic compounds / Naphthofurans
methyl 5,6-diacetyloxy-7,10a-dihydroxy-4,7,11b-trimethyl-9-oxo-2,3,4a,5,6,6a,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylate 162989641 Click to see 494.50 unknown https://doi.org/10.1016/S0031-9422(00)89084-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 98049813 Click to see 304.25 unknown via CMAUP database
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1590/S0103-50532000000200015
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isoscoparin 442611 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
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 via CMAUP database
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 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
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=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
2-(4,5-Dihydroxy-2-methoxyphenyl)-6,7-dimethoxychromen-4-one 162971139 Click to see COC1=CC(=C(C=C1C2=CC(=O)C3=CC(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/S0031-9422(00)97301-1
6,7-Dimethoxy-2-(2,3,4-trimethoxyphenyl)chromen-4-one 162990536 Click to see 372.40 unknown https://doi.org/10.1016/S0031-9422(00)97301-1
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,9-Dihydroxypterocarpan 162933 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
1,3,8-Trihydroxy-9-methoxy-[1]benzofuro[2,3-b]chromen-11-one 15126297 Click to see 314.25 unknown via CMAUP database
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown via CMAUP database
Genistein 5280961 Click to see 270.24 unknown via CMAUP database
Lupinalbin A 5324349 Click to see 284.22 unknown via CMAUP database
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Ambocin 5491738 Click to see 564.50 unknown via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside 20055730 Click to see 548.50 unknown via CMAUP database
Genistin 5281377 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-3-(2,4-dimethoxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 92143157 Click to see 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Odoratin 13965473 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(00)86942-3
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin 5281704 Click to see 298.29 unknown https://doi.org/10.1016/S0031-9422(00)86942-3
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
Panchovillin 21676203 Click to see 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
6,7-Dimethoxy-3-(2,3,4-trimethoxyphenyl)-2,3-dihydrochromen-4-one 162921485 Click to see 374.40 unknown https://doi.org/10.1016/S0031-9422(00)97301-1
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
4',7-Dimethoxyisoflavone 136419 Click to see 282.29 unknown https://doi.org/10.1016/0031-9422(75)85263-0
6,7,2',3',4'-Pentamethoxyisoflavone 44257251 Click to see 372.40 unknown https://doi.org/10.1016/S0031-9422(00)97301-1
6,7,3',4'-Tetramethoxyisoflavone 631176 Click to see 342.30 unknown https://doi.org/10.1016/S0031-9422(00)97301-1
6,7,3',4',5'-Pentamethoxyisoflavone 44257254 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(75)85263-0
Milldurone 6728947 Click to see 356.30 unknown https://doi.org/10.1016/S0031-9422(00)97301-1

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