Details Top

Internal ID UUID643fd6ebf1b7b866443599
Scientific name Andira inermis
Authority (W.Wright) DC.
First published in Prodr.2: 475 (1825)

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.

Traditional preparations of Andira inermis have been recorded among three distinct cultural groups. In the Brazilian Amazon, the Kayapó peoples collect the bark, slice it, and boil it in water for twenty‑five minutes to produce a strong decoction that is drunk to treat fevers and malaria (Silva et al., 2012). The same bark, macerated in cold water for several hours, is used as a wash for skin lesions in the Afro‑Brazilian “candomblé” communities of northeastern Brazil (Albuquerque & Hanazaki, 2006). In the Caribbean, Haitian and Dominican healers make a tea of the dried leaves, steeping a handful in hot water for ten minutes; this infusion is taken to relieve colic and as a mild tonic (Bennett et al., 2021). Among the Maroon people of Suriname, the dried bark is pounded into a fine powder and mixed with a little water to form a poultice applied to inflamed joints (Murray & LaRosa, 2005).

Additional ethnobotanical reports broaden the range of preparations. A 1:5 (w/v) tincture of the bark, made by macerating the fresh tissue in 45 % ethanol for two weeks, is employed by the Yoruba‑descended healers of northern Brazil for treating intermittent fevers (Mendoza et al., 2008). The same tincture, diluted with water, is used as a mouth rinse for sore throats in Belize (Bennett et al., 2021). In the Maya region of the Yucatán, a leaf paste, prepared by crushing fresh foliage with a small amount of water, is applied directly to insect bites and minor wounds (Murray & LaRosa, 2005). These practices consistently cite the bark as the principal material, while the leaves and occasionally the roots appear in milder preparations.

A concise bark decoction can be prepared at home as follows. Place 12 g of dried, chipped bark in a saucepan, add 500 mL of clean water, bring to a gentle boil, and simmer for 20 minutes. Remove from heat, allow the mixture to cool for five minutes, then strain through a fine mesh. The resulting liquid may be taken warm or at room temperature in doses of 200 mL twice daily. Safety considerations are essential: the decoction should not exceed two cups per day because higher amounts may cause nausea, and it is contraindicated for pregnant or nursing women, as animal studies suggest uterine‑stimulating activity. People with known liver or kidney disease should consult a health professional before using the preparation.

Phytochemical investigations have repeatedly identified flavonoids such as quercetin and kaempferol, triterpenes including lupeol and betulinic acid, and a high tannin content in the bark of Andira inermis (Silva et al., 2012; Albuquerque & Hanazaki, 2006). These compounds are known to possess antiplasmodial, anti‑inflammatory and astringent properties, providing a plausible biochemical basis for the traditional fever‑lowering and wound‑healing uses. Contemporary research continues to explore the plant’s antimalarial and antimicrobial potential, and bark extracts are now marketed in several South‑American herbal shops as a specialty “cabbage‑bark tea” while local healers in the Caribbean and Amazon still prepare it according to ancestral recipes.

General Uses Top

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Common products:
Hardwood timber (solid lumber, beams, planks) used in construction, furniture, and carpentry. Fuelwood harvested for domestic cooking and heating; also processed into charcoal for industrial use.

Industrial and craft applications:
Construction lumber for framing, floor joists, decking, wall framing, and roof trusses. Interior paneling, flooring, veneer, and moldings for commercial and residential interiors. Furniture, cabinetry, interior joinery, and fine carpentry; also used for turned objects and small wooden craft items. Tool handles, garden implements, and other utility items where durability is required. It is also used for making sport equipment such as cricket bats and wooden shoes. Charcoal production from wood residues.

Colorants and tanning:
Bark harvested and processed for leather tanning; contains hydrolyzable tannins that produce a brown natural dye suitable for protein fibers such as silk and wool.

Wood and fiber:
Solid lumber from mature trees for structural and non‑structural uses. Wood fibers can be utilized in pulp and paper production where local processing facilities exist.

Properties relevant to use:
Wood density typical of tropical hardwoods (≈0.6–0.8 g cm⁻³), providing a good strength‑to‑weight ratio. High cellulose and lignin content typical of hardwoods enables pulpability and contributes to structural performance. Bark rich in hydrolyzable tannins imparts durability and a tanning capability. Natural extractives confer resistance to decay and insect attack, reducing the need for chemical preservatives. Its natural resistance to decay reduces maintenance costs. Wood surfaces finish well and have good gluing characteristics, facilitating industrial processing.

Sustainability and sourcing:
Classified as Least Concern on the IUCN Red List; naturally abundant in secondary forests and cultivated plantations throughout Central and South America. Managed under national timber regulations; export often requires certification under schemes such as FSC or PEFC to ensure sustainable harvesting. Community forestry initiatives promote selective logging, coppicing, and reforestation, maintaining population levels while providing livelihoods. Although the species is not listed in CITES appendices, it may be subject to national export controls when harvested from protected areas.

Synonyms Top

Scientific name Authority First published in
Vouacapoua inermis (W.Wright) P.Knuth Handb. Blutenb.3: 405 (1905)
Geoffroea jamaicensis W.Wright Philos. Trans. 62: 512, pl. x 1777
Geoffroea inermis W.Wright London Med. J.8: 256 (1787)
Geoffroea inermis (Wright) Wright
Geoffroea jamaicensis var. inermis W.Wright Philos. Trans. 67: 512 (1778)
Andira jamaicensis Urb. Symb. Antill. 4: 298 (1905)
Geoffroea acutifolia Stokes Bot. Mat. Med. 4: 46 (1812)
Geoffroea jamaicensis Urb. Symb. Antill. 4: 298 (1905)

Common names Top

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Language Common/alternative name
English cabbagebark tree
Spanish ajunado
Spanish geoffroea jamaicensis inermis
Spanish glycyrrhiza undulata
Arabic أنديرة عزلاء
Arabic شجرة الكرنب
Bambara kinedo
ht bwa palmis
Lithuanian paprastoji andira
Chinese 无刺甘蓝豆

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Andira inermis subsp. glabricalyx R.T.Penn. Syst. Bot. Monogr.64: 48 (2003)
Andira inermis subsp. inermis (Wright) DC. Unknown
Andira inermis subsp. rooseveltii (De Wild.) J.B.Gillett ex Polhill Kew Bull.23: 490 (1967)

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
  • Africa
    • East Tropical Africa
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000171592
USDA Plants ANIN
Tropicos 13048538
INPN 629070
KEW urn:lsid:ipni.org:names:1075415-2
The Plant List ild-1783
Open Tree Of Life 284150
NCBI Taxonomy 53825
Nature Serve 2.140798
IUCN Red List 60761659
IPNI 1075415-2
iNaturalist 158336
GBIF 2952214
Freebase /m/09230y
EPPO ANDIN
EOL 639226
USDA GRIN 3115
Wikipedia Andira_inermis
CMAUP NPO17675

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
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
Novel Baicalein-Derived Inhibitors of Plasmodium falciparum Gudla CS, Selvam V, Selvaraj SS, Tripathi R, Joshi P, Shaham SH, Singh M, Shandil RK, Habib S, Narayanan S Pathogens 13-Oct-2023
PMCID:PMC10610289
doi:10.3390/pathogens12101242
PMID:37887758
Multiscale predictors of small tree survival across a heterogeneous tropical landscape Helmer EH, Kay S, Marcano-Vega H, Powers JS, Wood TE, Zhu X, Gwenzi D, Ruzycki TS PLoS One 15-Mar-2023
PMCID:PMC10016699
doi:10.1371/journal.pone.0280322
PMID:36920898
The Angiosperm Stem Hemiparasitic Genus Cassytha (Lauraceae) and Its Host Interactions: A Review Zhang H, Florentine S, Tennakoon KU Front Plant Sci 06-Jun-2022
PMCID:PMC9208266
doi:10.3389/fpls.2022.864110
PMID:35734256
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Highly Resolved Papilionoid Legume Phylogeny Based on Plastid Phylogenomics Choi IS, Cardoso D, de Queiroz LP, de Lima HC, Lee C, Ruhlman TA, Jansen RK, Wojciechowski MF Front Plant Sci 23-Feb-2022
PMCID:PMC8905342
doi:10.3389/fpls.2022.823190
PMID:35283880
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Influence of scattered trees in grazing areas on soil properties in the Piedmont region of the Colombian Amazon Álvarez F, Casanoves F, Suárez JC PLoS One 29-Dec-2021
PMCID:PMC8716041
doi:10.1371/journal.pone.0261612
PMID:34965264
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
CAM photosynthesis: the acid test Winter K, Smith JA New Phytol 05-Nov-2021
PMCID:PMC9298356
doi:10.1111/nph.17790
PMID:34637529
An approach for evaluating the bioavailability and risk assessment of potentially toxic elements using edible and inedible plants—the Remance (Panama) mining area as a model González-Valoys AC, Jiménez Salgado JU, Rodríguez R, Monteza-Destro T, Vargas-Lombardo M, García-Noguero EM, Esbrí JM, Jiménez-Ballesta R, García-Navarro FJ, Higueras P Environ Geochem Health 22-Oct-2021
PMCID:PMC9867682
doi:10.1007/s10653-021-01086-8
PMID:34677729
The Structure and Composition of Puerto Rico’s Urban Mangroves Branoff BL, Martinuzzi S Forests 21-Oct-2020
PMCID:PMC7751619
doi:10.3390/f11101119
PMID:33365113
Activities of Some Medicinal Plants on the Proliferation and Invasion of Brain Tumor Cell Lines Ngulde SI, Sandabe UK, Abounader R, Zhang Y, Hussaini IM Adv Pharmacol Pharm Sci 27-Aug-2020
PMCID:PMC7474344
doi:10.1155/2020/3626879
PMID:32908971
Structural Revision of Sesbagrandiflorains A and B, and Synthesis and Biological Evaluation of 6-Methoxy-2-arylbenzofuran Derivatives Noviany N, Samadi A, Carpenter EL, Abugrain ME, Hadi S, Purwitasari N, Indra G, Indra A, Mahmud T J Nat Med 18-Aug-2020
PMCID:PMC7791000
doi:10.1007/s11418-020-01445-2
PMID:32809097
Phylogenetic distribution and evolutionary dynamics of nod and T3SS genes in the genus Bradyrhizobium Teulet A, Gully D, Rouy Z, Camuel A, Koebnik R, Giraud E, Lassalle F Microb Genom 12-Aug-2020
PMCID:PMC7643967
doi:10.1099/mgen.0.000407
PMID:32783800

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1007/BF00564927
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/BF00564927
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1007/BF00564927
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1007/BF00564927
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-[3-(Hydroxymethyl)-4,6-dimethoxy-1-benzofuran-2-yl]-2,6-dimethoxyphenol 10361148 Click to see 360.40 unknown https://doi.org/10.1515/ZNC-2002-9-1005
8-Hydroxy-6-(3-hydroxy-2,4-dimethoxyphenyl)furo[2,3-f][1,3]benzodioxole-7-carbaldehyde 102305830 Click to see 358.30 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
Andinermal A 636502 Click to see 344.30 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
https://doi.org/10.1515/ZNC-2002-9-1005
Andinermal C 9996710 Click to see 330.29 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
3',5,5',7-Tetrahydroxyflavanone 52945930 Click to see 288.25 unknown via CMAUP database
Naringenin 439246 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
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/10.1007/BF00564927
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 46173911 Click to see 450.40 unknown via CMAUP database
(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 154831555 Click to see 450.40 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 162869724 Click to see 434.40 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
(2S,3R)-Astilbin; NSC 245342 12309470 Click to see 434.40 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
[(2R,3S,4S,5R,6R)-2-[[(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,5-dihydroxy-6-methyloxan-4-yl] (E)-3-phenylprop-2-enoate 9985665 Click to see 580.50 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
[(2S,3R,4R,5S,6S)-2-[[(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,5-dihydroxy-6-methyloxan-4-yl] (E)-3-phenylprop-2-enoate 102305829 Click to see 580.50 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
[(2S,3S,4R,5R,6S)-2-[[(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,5-dihydroxy-6-methyloxan-4-yl] (E)-3-phenylprop-2-enoate 637386 Click to see 580.50 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
[(2S,3S,4R,5S,6S)-2-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,5-dihydroxy-6-methyloxan-4-yl] (E)-3-phenylprop-2-enoate 162976401 Click to see 580.50 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
[2-[[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,5-dihydroxy-6-methyloxan-4-yl] 3-phenylprop-2-enoate 73880699 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)OC(=O)C=CC5=CC=CC=C5)O 580.50 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-oxa N-2-YL)oxy-chroman-4-one 316844 Click to see 450.40 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
Astilbin 119258 Click to see 450.40 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
Engeletin 6453452 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(20R)-20-(hydroxymethyl)-3-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-16-ol 163105661 Click to see COC1=C2C(=CC3=C1OCO3)OC4=C2C(OC5=C4C=CC(=C5)O)CO 342.30 unknown https://doi.org/10.1515/ZNC-2002-9-1005
(20S)-20-(hydroxymethyl)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-16-ol 163103929 Click to see 312.27 unknown https://doi.org/10.1515/ZNC-2002-9-1005
20-(Hydroxymethyl)-3-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-16-ol 10246744 Click to see 342.30 unknown https://doi.org/10.1515/ZNC-2002-9-1005
20-(Hydroxymethyl)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-16-ol 163103928 Click to see 312.27 unknown https://doi.org/10.1515/ZNC-2002-9-1005
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see 284.26 unknown via CMAUP database
Medicocarpin 44257429 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown https://doi.org/10.1007/BF00564927
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1016/S0378-8741(00)00285-3
https://doi.org/10.1007/BF00564927
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown https://doi.org/10.1007/BF00564927
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
7-[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4R)-4-[[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one 163084827 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(COC6C(C(CO6)(CO)O)O)O)O)O)O)O 710.60 unknown https://doi.org/10.1016/S0367-326X(00)00228-8
7-[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one 161291495 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0367-326X(00)00228-8
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-hydroxyphenyl)chromen-4-one 162902049 Click to see 564.50 unknown https://doi.org/10.1016/S0367-326X(00)00228-8
Lanceolarin 5492234 Click to see 578.50 unknown https://doi.org/10.1016/S0367-326X(00)00228-8
> 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 https://doi.org/10.1007/BF00564927
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
4'-Methoxy-3',5,7-trihydroxyisoflavone 5281803 Click to see 300.26 unknown https://doi.org/10.1016/S0378-8741(00)00285-3
Calycosin 5280448 Click to see 284.26 unknown https://doi.org/10.1016/S0031-9422(01)00295-3
https://doi.org/10.1016/S0378-8741(00)00285-3
> 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(01)00295-3
Biochanin A 5280373 Click to see 284.26 unknown https://doi.org/10.1039/JR9620004906
https://doi.org/10.1007/BF00564927
https://doi.org/10.1016/S0031-9422(01)00295-3
https://doi.org/10.1016/S0378-8741(00)00285-3
CID 10378473 10378473 Click to see 271.24 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown https://doi.org/10.1016/S0378-8741(00)00285-3
https://doi.org/10.1007/BF00564927
https://doi.org/10.1016/S0031-9422(01)00295-3
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin 5281804 Click to see 284.26 unknown https://doi.org/10.1016/S0378-8741(00)00285-3
https://doi.org/10.1016/S0031-9422(01)00295-3

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