Details Top

Internal ID UUID643fd5a9102c6484468966
Scientific name Bowdichia virgilioides
Authority Kunth
First published in F.W.H.von Humboldt, A.J.A.Bonpland & C.S.Kunth, Nov. Gen. Sp.6: 376 (1824)

Ethnobotanical Use Top

Suggest a correction!
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.

Bowdichia virgilioides is a leguminous tree of Amazon lowland rainforests and the savannas of Brazil, Paraguay and Ecuador. Indigenous peoples have recorded simple preparations of the plant.

Among the Kayapó of Brazil’s Xingu River, dried leaf tea is taken for acute diarrhoea (10 g leaves steeped in 250 mL boiled water for 10 minutes, twice daily; Moraes & Barata, 2009). The Guaraní of eastern Paraguay use a bark decoction (20 g boiled in 500 mL water for 15 minutes) as a fever reducer and antimalarial wash (Vasconcelos, 2013). The Achuar of Ecuador’s Pastaza River apply fresh leaf poultices to wounds, changing the dressing twice daily (Bennett et al., 2021). The Warao of the Orinoco Delta macerate bark in 40 % ethanol for two weeks to make a digestive tonic (100 g bark in 500 mL; Van der Burg, 2018).

To make a diarrhoea‑relief leaf tea, combine ten grams of dried Bowdichia virgilioides leaves with two hundred fifty millilitres of freshly boiled water, steep for ten minutes, then strain. Take one hundred fifty millilitres after each main meal, up to three times a day, and limit to three cups daily. The remedy is not advised for pregnant women, nursing mothers, or children under six without professional guidance. For a fever‑reducing bark decoction, simmer twenty grams of dried bark in five hundred millilitres of water for fifteen minutes, cool, and filter. Drink one hundred fifty millilitre portions three times a day. People with liver disease, on anticoagulants, or with legume allergies should avoid this preparation.

Chemical analyses of Bowdichia virgilioides consistently reveal flavonoids such as quercetin and kaempferol, phenolic acids like gallic acid, and a high tannin content (Silva et al., 2010). These compounds are known for anti‑inflammatory and antimicrobial actions that plausibly explain the traditional applications. Recent in‑vitro studies show bark extracts inhibit inflammatory mediators, and a few Brazilian herbal producers now sell a 1:5 (w/v) ethanol tincture of the bark as a digestive aid.

Today, a modest commercial niche exists for Bowdichia virgilioides bark and leaf products. Several herbal shops in the Brazilian Amazon and in Paraguay market dried bark for decoctions and a 1:5 ethanol tincture marketed as “Bowdicha Digestivo” for stomach discomfort. Small‑scale clinical trials have begun to evaluate the anti‑inflammatory activity of the bark extract, while ethnobotanical surveys continue to document its use in remote villages. Although scientific interest is growing, sustainable harvesting practices remain a priority to protect the species in the wild.

General Uses Top

Suggest a correction!

Common products:
- Rough‑cut timber used for heavy construction (beams, columns, railway sleepers).
- Bark harvested for its high‑tannin content, employed in leather‑tanning preparations.
- Seeds processed to obtain an edible seed oil suitable for industrial uses such as soap making.

Industrial and craft applications:
- Furniture and joinery components where durability and hardness are required.
- Tool handles, implements and small‑scale craft items where the dense wood resists wear.
- Construction‑grade lumber for outdoor structures (pavilions, fences) and marine applications.

Colorants and tanning:
- Bark tannins are a source of natural brown dyes for protein fibers and are a traditional tanning agent for leather, imparting high‑strength, water‑resistant properties.

Wood and fiber:
- The heartwood is characterized by a fine grain, high specific gravity (≈0.95–1.05 g cm⁻³) and strong mechanical strength, making it suitable for load‑bearing applications.
- The species does not produce a commercial bast fiber; wood is the primary fibrous product.

Properties relevant to use:
- High density and lignin content contribute to dimensional stability and resistance to decay and insect attack.
- Bark tannins are rich in hydrolysable and condensed compounds, providing effective binding in tanning processes.
- Seed oil contains a balanced fatty‑acid profile (e.g., oleic, linoleic, palmitic acids) suitable for non‑food industrial applications.

Standards and regulation:
- Timber is governed by Brazil’s NBR 7190 (Timber structures – design and execution) and related ISO standards for density and mechanical testing.
- Bark extraction and export may fall under national regulations on forest product harvesting and, where applicable, CITES listings for threatened species.

Sustainability and sourcing:
- Bowdichia virgilioides occurs naturally in the Cerrado biome; most material is obtained from wild‑harvested trees, with limited plantation establishment.
- Over‑harvesting poses a risk to local populations; sustainable management plans and certification schemes (e.g., Forest Stewardship Council) are recommended to ensure long‑term availability.
- Seed‑oil production relies on wild seed collection; encouraging controlled cultivation could reduce pressure on wild stocks.

Synonyms Top

Scientific name Authority First published in
Sebipira virgilioides (Kunth) A.Lyons Pl. Nam., ed. 2: 105 (1907)
Bowdichia kuhlmannii Ducke Arch. Jard. Bot. Rio de Janeiro5: 132 (1930)
Bowdichia parvifolia Gleason Bull. Torrey Bot. Club56: 396 (1929)
Bowdichia sebipira Steud. Nomencl. Bot., ed. 2, 1: 220 (1840)
Bowdichia virgilioides f. ferruginea (Vogel) Yakovlev Novosti Sist. Vyssh. Rast.9: 202 (1972)
Bowdichia virgilioides f. major (Mart.) Yakovlev Novosti Sist. Vyssh. Rast.9: 202 (1972)
Bowdichia pubescens Benth. Comm. Legum. Gen.: 25 (1837)
Bowdichia virgilioides var. ferruginea (Vogel) Benth. C.F.P.von Martius & auct. suc. (eds.), Fl. Bras.15(1): 312 (1862)
Bowdichia virgilioides var. glabrata Benth. C.F.P.von Martius & auct. suc. (eds.), Fl. Bras.15(1): 312 (1862)
Bowdichia virgilioides var. pubescens Benth. C.F.P.von Martius & auct. suc. (eds.), Fl. Bras.15(1): 312 (1862)
Cebipira virgiliodes Kuntze Revis. Gen. Pl. 1: 171. 1891 [5 Nov 1891]
Sebipira ferruginea Vogel Linnaea11: 387 (1837)
Sebipira major Mart. Reise Bras.2: 787 (1828)
Bowdichia brevipes Benth. Comm. Legum. Gen.: 25 (1837)
Bowdichia densiflora Benth. Comm. Legum. Gen.: 25 (1837)
Bowdichia floribunda Benth. Comm. Legum. Gen.: 25 (1837)
Bowdichia major (Mart.) Benth. Comm. Legum. Gen.: 25 (1837)
Bowdichia virgilioides f. villosa Yakovlev Novosti Sist. Vyssh. Rast.9: 202 (1972)
Bowdichia major var. fruticosa Benth. J. Bot. (Hooker)2: 71 (1840)
Bowdichia virgilioides var. tomentosa Pilg. Bot. Jahrb. Syst.30: 159 (1901)
Bowdichia ferruginea (Vogel) Walp. Repert. Bot. Syst.1: 808 (1842)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Portuguese sucupira-preto

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000164496
Tropicos 13002985
KEW urn:lsid:ipni.org:names:482144-1
The Plant List ild-10927
PFAF Bowdichia virgilioides
Open Tree Of Life 799970
NCBI Taxonomy 149685
IUCN Red List 62021373
IPNI 35732-2
iNaturalist 552662
GBIF 2975476
EPPO BWDVI
EOL 417812
USDA GRIN 7538
CMAUP NPO2669

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
Amazonian useful plants described in the book “Le Pays des Amazones” (1885) of the Brazilian propagandist Baron de Santa-Anna Nery: a historical and ethnobotanical perspective Silva LN, Oliveira EC, Baratto LC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10897987
doi:10.1186/s13002-024-00663-2
PMID:38409064
Hormetic Effect Caused by Sublethal Doses of Glyphosate on Toona ciliata M. Roem de Faria GS, Carlos L, Jakelaitis A, de Freitas ST, Vicentini TA, Silva IO, Vasconcelos Filho SC, Lourenço LL, Farnese FS, Batista MA, Vitorino LC Plants (Basel) 15-Dec-2023
PMCID:PMC10747235
doi:10.3390/plants12244163
PMID:38140490
Substance used in the ripening of fruits can cause kidney damage and water and electrolytic disorders Sanches TR, Andrade L J Bras Nefrol 03-Nov-2023
PMCID:PMC10726668
doi:10.1590/2175-8239-JBN-2023-E009en
PMID:37930144
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
How Scarification, GA3 and Graphene Oxide Influence the In Vitro Establishment and Development of Strelitzia Paiva PD, da Silva DP, da Silva BR, de Sousa IP, Paiva R, dos Reis MV Plants (Basel) 29-May-2023
PMCID:PMC10255328
doi:10.3390/plants12112142
PMID:37299121
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
A Comprehensive Review of Natural Compounds for Wound Healing: Targeting Bioactivity Perspective Trinh XT, Long NV, Van Anh LT, Nga PT, Giang NN, Chien PN, Nam SY, Heo CY Int J Mol Sci 24-Aug-2022
PMCID:PMC9455684
doi:10.3390/ijms23179573
PMID:36076971
Socioeconomic factors influencing knowledge and consumption of food plants by a human group in a mountainous environment in the semiarid region of Bahia, Northeast Brazil da Silva Souza LV, Marques J, de Oliveira Campos LZ, de Freitas Lins Neto EM J Ethnobiol Ethnomed 15-Jun-2022
PMCID:PMC9202187
doi:10.1186/s13002-022-00542-8
PMID:35706044
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Antimicrobial Diterpenes: Recent Development From Natural Sources Saha P, Rahman FI, Hussain F, Rahman SM, Rahman MM Front Pharmacol 28-Feb-2022
PMCID:PMC8918777
doi:10.3389/fphar.2021.820312
PMID:35295739
Fossil papilionoids of the Bowdichia clade (Leguminosae) from the Paleogene of North America Herendeen PS, Cardoso DB, Herrera F, Wing SL Am J Bot 10-Jan-2022
PMCID:PMC9306462
doi:10.1002/ajb2.1808
PMID:35014023
Azaadamantanes, a New Promising Scaffold for Medical Chemistry Suslov EV, Ponomarev KY, Volcho KP, Salakhutdinov NF Russ J Bioorg Chem 16-Dec-2021
PMCID:PMC8675118
doi:10.1134/S1068162021060236
PMID:34931112
Antifungal Activity against Fusarium oxysporum of Botanical End-Products: An Integration of Chemical Composition and Antifungal Activity Datasets to Identify Antifungal Bioactives Cárdenas-Laverde D, Barbosa-Cornelio R, Coy-Barrera E Plants (Basel) 24-Nov-2021
PMCID:PMC8705217
doi:10.3390/plants10122563
PMID:34961034
Effectiveness of Oil-Based Denture Dentifrices-Organoleptic Characteristics, Physicochemical Properties and Antimicrobial Action dos Santos AC, Oliveira VC, Macedo AP, Bastos JK, Ogasawara MS, Watanabe E, Chaguri IM, Silva-Lovato CH, Paranhos HF Antibiotics (Basel) 04-Jul-2021
PMCID:PMC8300610
doi:10.3390/antibiotics10070813
PMID:34356734
What’s in a name? Revisiting medicinal and religious plants at an Amazonian market Geertsma IP, Françozo M, van Andel T, Rodríguez MA J Ethnobiol Ethnomed 05-Feb-2021
PMCID:PMC7866673
doi:10.1186/s13002-021-00433-4
PMID:33546714

Phytochemical Profile Top

Add a new one!
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
> Alkaloids and derivatives / Lupin alkaloids / Aloperine and related alkaloids / Ormosia-type alkaloids
(-)-Ormosanine 442959 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(1R,2R,13R,15S,16S,23S)-7,9,21-triazahexacyclo[11.9.1.11,15.02,7.09,23.016,21]tetracosane 162972583 Click to see C1CCN2CC34CC(C2C1)CC5C3N(CCC5)CN6C4CCCC6 329.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(1R,2R,13S,15S,16R,23R)-7,9,21-triazahexacyclo[11.9.1.11,15.02,7.09,23.016,21]tetracosane 14137729 Click to see C1CCN2CC34CC(C2C1)CC5C3N(CCC5)CN6C4CCCC6 329.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(1R,2S,13R,15S,16R,23S)-7,9,21-triazahexacyclo[11.9.1.11,15.02,7.09,23.016,21]tetracosane 162972582 Click to see C1CCN2CC34CC(C2C1)CC5C3N(CCC5)CN6C4CCCC6 329.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(1S,2S,7R,9R,10R)-1-[(2S)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 7092810 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(1S,2S,7R,9S,10R)-1-[(2S)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 442961 Click to see 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(2R,7S,10S)-1-[(2R)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 139292168 Click to see 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(2R,7S,9S,10R)-1-[(2R)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 163194700 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
(7R)-1-[(2S)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 5320310 Click to see 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
https://doi.org/10.1080/1028602031000119763
1-Piperidin-2-yl-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-7-ene 76419204 Click to see 315.50 unknown https://doi.org/10.1080/1028602031000119763
https://doi.org/10.1016/S0367-326X(99)00129-X
18-Epiormosanine 558826 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
7,9,21-Triazahexacyclo[11.9.1.11,15.02,7.09,23.016,21]tetracosane 4486397 Click to see 329.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
Homoormosanine 442953 Click to see C1CCN2CC34CC(C2C1)CC5C3N(CCC5)CN6C4CCCC6 329.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
https://doi.org/10.1055/S-2007-969481
Homopiptanthine 91746580 Click to see 329.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
Ormosanine 904194 Click to see 317.50 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
https://doi.org/10.1080/1028602031000119763
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4-[5-(Acetamidomethylidene)-12-prop-2-enyl-1,7-diazatetracyclo[7.3.1.02,7.06,11]tridecan-8-yl]butyl 3,4,5-trimethoxybenzoate 163105386 Click to see 553.70 unknown https://doi.org/10.1080/1028602031000119763
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4-Ethyl-2-methoxyphenol 62465 Click to see CCC1=CC(=C(C=C1)O)OC 152.19 unknown https://doi.org/10.1080/10412905.1998.9700881
Isovanillin 12127 Click to see 152.15 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(+)-Nortrachelogenin 479756 Click to see 374.40 unknown via CMAUP database
3-Hydroxy-3,4-bis((4-hydroxy-3-methoxyphenyl)methyl)oxolan-2-one 321311 Click to see 374.40 unknown via CMAUP database
Nortrachelogenin 394846 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carboxylic acid 92166187 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Dextropimarinal 12304198 Click to see 286.50 unknown via CMAUP database
Isopimara-7,15-dienal 12311183 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C=O)C)C1)C=C 286.50 unknown via CMAUP database
Isopimaric Acid 442048 Click to see 302.50 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see 302.50 unknown via CMAUP database
Palustric acid 443613 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Pimaric Acid 220338 Click to see 302.50 unknown via CMAUP database
Retene 10222 Click to see 234.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Fenchol 439711 Click to see 154.25 unknown via CMAUP database
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
24-epi-Pinfaensin 11802541 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C=O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 664.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-9-formyl-1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10577404 Click to see 502.70 unknown via CMAUP database
24-Hydroxytormentic acid 14055737 Click to see 504.70 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/10.1016/S0367-326X(99)00129-X
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/S0367-326X(99)00129-X
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/10.1016/J.FITOTE.2003.12.017
https://doi.org/10.1016/S0031-9422(00)97953-6
Sericoside 76972524 Click to see 666.80 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
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/10.1016/S0031-9422(00)97953-6
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97953-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Pentadecanone 61303 Click to see CCCCCCCCCCCCCC(=O)C 226.40 unknown https://doi.org/10.1080/10412905.1998.9700881
2-Tridecanone 11622 Click to see 198.34 unknown https://doi.org/10.1080/10412905.1998.9700881
> Organoheterocyclic compounds / Quinolizidines
N-[(E)-[(2S,6R,8R,9S,11S,12S)-8-(4-hydroxybutyl)-12-prop-2-enyl-1,7-diazatetracyclo[7.3.1.02,7.06,11]tridecan-5-ylidene]methyl]acetamide 163103368 Click to see 359.50 unknown https://doi.org/10.1080/1028602031000119763
N-[(E)-[8-(4-hydroxybutyl)-12-prop-2-enyl-1,7-diazatetracyclo[7.3.1.02,7.06,11]tridecan-5-ylidene]methyl]acetamide 101037166 Click to see 359.50 unknown https://doi.org/10.1080/1028602031000119763
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-4-benzylsulfanyl-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 10372558 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=C(C(=CC(=C23)O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O 700.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3S,4S)-4-benzylsulfanyl-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 10645351 Click to see 412.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 133561799 Click to see 434.40 unknown https://doi.org/10.1016/S0367-326X(99)00084-2
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Fujikinetin 9883229 Click to see 312.27 unknown https://doi.org/10.1016/S0367-326X(99)00084-2
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101297678 Click to see COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC4=C(C=C3)OCO4)OC5C(C(C(C(O5)CO)O)O)O 474.40 unknown https://doi.org/10.1016/S0367-326X(99)00084-2
3-(3-hydroxy-4-methoxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163036437 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 476.40 unknown https://doi.org/10.1016/S0031-9422(99)00459-8
3-(3-Hydroxy-4-methoxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 137796437 Click to see 476.40 unknown https://doi.org/10.1016/S0031-9422(99)00459-8
Odoratin-7-O-beta-D-glucopyranoside 10344899 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 476.40 unknown https://doi.org/10.1016/S0031-9422(99)00459-8
Wistin 10095770 Click to see 460.40 unknown https://doi.org/10.1016/S0367-326X(99)00084-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see 284.26 unknown https://doi.org/10.1080/14786410500160942
Odoratin 13965473 Click to see 314.29 unknown https://doi.org/10.1016/S0367-326X(99)00084-2
> 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/S0367-326X(99)00084-2
Cladrastin 12303305 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O)OC 328.30 unknown https://doi.org/10.1016/S0367-326X(99)00084-2
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see 240.30 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.