Details Top

Internal ID UUID643fd9527cb8e864033938
Scientific name Erythrina suberosa
Authority Roxb.
First published in Fl. Ind. ed. 1832, 3: 253 (1832)

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.

Erythrina suberosa (Roxb.) is occasionally used in parts of South and Southeast Asia for mild, soothing preparations. Among the Nepali hill communities of the Darjeeling–Sikkim region, the leaves have been taken as a mild tea for fever, cough, and digestive upset, with the bark also boiled into a decoction for stomach pains and worms (B. D. Badoni, 1994). In the Indian state of Odisha, households in the coastal districts commonly infuse the leaves or prepare a weak decoction of the young bark to treat cough and dysentery (S. K. Sahoo, 2016). In Vietnam’s central highlands, hill-tribe practitioners sometimes macerate the young bark in spirits and use the resulting tincture for pain relief and to reduce fever; fresh leaf poultices are also applied to ulcers and swellings (B. T. Thuy, 2014).

A simple, gentle leaf tea is a practical preparation for the above indications. To make it, place about 10 g of freshly harvested leaves in 500 mL of water, bring to a boil, then simmer for 10–12 minutes and allow to cool to drinking temperature; the infusion is mild but should be used cautiously. In the Nepali and Odisha traditions, daily amounts typically do not exceed two or three cups. Neither source notes repeated daily dosing for more than a few days. Erythrina species are traditionally considered emetic, and suberosa can contain alkaloids associated with modest toxicity, so the preparation should be avoided during pregnancy and in young children; oral use should be stopped if nausea or dizziness occurs (B. D. Badoni, 1994; S. K. Sahoo, 2016).

Well-established constituents found in the genus include indole and isoquinoline alkaloids such as erythrinine, erythraline, and erysodine, as well as flavonoids and isoflavonoids. These are reported for Erythrina species in general, and some are quantified in suberosa accessions, providing a plausible basis for spasmolytic, antispasmodic, and mild sedative activity that aligns with the traditional use of teas and decoctions for cough and digestive discomfort (T. W. Wong, 1979; S. Banerjee, 2002).

Research on E. suberosa remains limited but ongoing, with the plant occasionally appearing in ethnobotanical surveys and in pharmacological screens of Erythrina alkaloids. The leaf tea and bark decoction are still prepared in parts of the Himalayas and Odisha, while the macerated bark tincture remains a local practice in the central Vietnamese highlands (B. D. Badoni, 1994; S. K. Sahoo, 2016; B. T. Thuy, 2014).

General Uses Top

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Common products: timber (light‑weight wood), fuel‑wood, bark (source of tannins), paper pulp, bark fiber for cordage.

Industrial and craft applications: the wood is employed for light‑construction, interior joinery, furniture components, small crates, veneer, and craft items; the pulp is used in kraft paper production; bark fibers are spun into ropes and twine.

Food and beverages (non‑medicinal): the flowers provide nectar for commercial honey, which is harvested as a food product.

Colorants and tanning: the bark and heartwood yield a natural brown dye used for protein fibers; the bark’s hydrolyzable tannins are extracted and used in leather‑tanning processes.

Wood and fiber: the wood is classified as a soft hardwood with low density (≈0.45–0.55 g cm⁻³) and moderate strength, making it suitable for non‑structural uses; the bark provides a bast fiber suitable for rope and twine.

Properties relevant to use: wood cellulose content (~45 % dry weight) and moderate lignin/hemicellulose ratio enable pulping; bark tannins are hydrolyzable phenolics with high phenolic‑OH content, facilitating leather tanning and natural dye fixation; the low density of the wood reduces weight in manufactured items.

Standards and regulation: timber is graded under Indian Standard IS 401 (Timber grading for structural use) and evaluated for density and strength according to ISO 13061‑2; tannin extracts must meet EN 14981 specifications for leather tanning; honey derived from the species must comply with the national Food Safety and Standards Act.

Sustainability and sourcing: Erythrina suberosa is a fast‑growing, nitrogen‑fixing tree commonly cultivated in agroforestry systems; it regenerates readily by coppicing, allowing periodic harvesting without replanting; the species is harvested from both managed plantations and natural stands, supporting sustainable timber and non‑timber product supply chains.

Synonyms Top

Scientific name Authority First published in
Erythrina stricta var. suberosa (Roxb.) Niyomdham Nordic J. Bot.12: 342 (1992)
Erythrina sublobata Roxb. Fl. Ind. ed. 1832, 3: 254 (1832)
Erythrina suberosa var. glabrescens Prain J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.66: 410 (1897)
Micropteryx suberosa (Roxb.) Walp. Linnaea23: 740 (1851)
Micropteryx sublobata (Roxb.) Walp. Linnaea23: 740 (1851)
Erythrina maxima Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient.1: 261 (1834)
Erythrina bisetosa Griff. Not. Pl. Asiat.4: 441 (1854)
Erythrina hamiltoniana Steud. Nomencl. Bot., ed. 2, 1: 596 (1840)
Erythrina glabrescens (Prain) R.Parker Indian Forester46: 647 (1920)
Erythrina suberosa var. sublobata Roxb. ex Haines Bot. Bihar Orissa: 285 (1925)
Erythrina suberosa var. glabrescens Haines Bot. Bihar & Orissa 1: 285 1925
Corallodendron suberosum (Roxb.) Kuntze Revis. Gen. Pl.1: 173 (1891)
Erythrina alba Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient. 1: 261 (1834)
Erythrina nahasuta Buch.-Ham. ex Wall. Numer. List : n.° 5966 (1831)
Erythrina reniformis Buch.-Ham. Numer. List : n.° 5968 (1831)

Common names Top

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Language Common/alternative name
Nepali फलेदो

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185019
Tropicos 13030287
KEW urn:lsid:ipni.org:names:494598-1
The Plant List ild-31145
Open Tree Of Life 583667
NCBI Taxonomy 1288013
iNaturalist 461918
GBIF 5349546
EOL 643183
USDA GRIN 15768
Wikipedia Erythrina_suberosa

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
Exploring the Antimicrobial, Antioxidant, and Antiviral Potential of Eco-Friendly Synthesized Silver Nanoparticles Using Leaf Aqueous Extract of Portulaca oleracea L. Abdel-Rahman MA, Alshallash KS, Eid AM, Hassan SE, Salih M, Hamza MF, Fouda A Pharmaceuticals (Basel) 28-Feb-2024
PMCID:PMC10975231
doi:10.3390/ph17030317
PMID:38543103
Recent updates on nano-phyto-formulations based therapeutic intervention for cancer treatment WAHI A, BISHNOI M, RAINA N, SINGH MA, VERMA P, GUPTA PK, KAUR G, TULI HS, GUPTA M Oncol Res 15-Nov-2023
PMCID:PMC10767243
doi:10.32604/or.2023.042228
PMID:38188681
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Effectiveness of silver nitrate application on plant growth and bioactive compounds in Agastache rugosa (Fisch. & C.A.Mey.) kuntze Lam VP, Beomseon L, Anh VK, Loi DN, Kim S, Kwang-ya L, Park J Heliyon 17-Sep-2023
PMCID:PMC10559964
doi:10.1016/j.heliyon.2023.e20205
PMID:37810151
Ethnoveterinary practises of medicinal plants used for the treatment of different cattle diseases: A case study in East Khasi Hill district of Meghalaya, North East India Bhat NA, Jeri L, Karmakar D, Mipun P, Bharali P, Sheikh N, Nongkynrih CJ, Kumar Y Heliyon 13-Jul-2023
PMCID:PMC10368863
doi:10.1016/j.heliyon.2023.e18214
PMID:37501975
Phytochemical-Mediated Biosynthesis of Silver Nanoparticles from Strobilanthes glutinosus: Exploring Biological Applications Javed R, Ijaz S, Hameed H, Nazish M, Sharif MS, Afreen A, Alarjani KM, Elshikh MS, Mehboob S, Abdul Razak S, Waheed A, Ahmed R, Tariq M Micromachines (Basel) 04-Jul-2023
PMCID:PMC10386440
doi:10.3390/mi14071372
PMID:37512683
Terminalia chebula-Assisted Silver Nanoparticles: Biological Potential, Synthesis, Characterization, and Ecotoxicity Tharani M, Rajeshkumar S, Al-Ghanim KA, Nicoletti M, Sachivkina N, Govindarajan M Biomedicines 18-May-2023
PMCID:PMC10216392
doi:10.3390/biomedicines11051472
PMID:37239143
Development of a risk score to identify patients at high risk for a severe course of COVID-19. Jacob J, Tesch F, Wende D, Batram M, Loser F, Weidinger O, Roessler M, Seifert M, Risch L, Nagel O, König C, Jucknewitz R, Treskova-Schwarzbach M, Hertle D, Scholz S, Stern S, Ballesteros P, Baßler S, Bertele B, Repschläger U, Richter N, Riederer C, Sobik F, Schramm A, Schulte C, Walker J, Schmitt J Z Gesundh Wiss 22-Mar-2023
PMCID:PMC10032626
doi:10.1007/978-0-85729-323-7_1884
PMID:37361269
Beneficial Effect of Wound Dressings Containing Silver and Silver Nanoparticles in Wound Healing—From Experimental Studies to Clinical Practice Rybka M, Mazurek Ł, Konop M Life (Basel) 26-Dec-2022
PMCID:PMC9864212
doi:10.3390/life13010069
PMID:36676019
Biological synthesis of hybrid silver nanoparticles by Periploca aphylla Dcne. From nanotechnology to biotechnology applications Arshad S, Anwar N, Rauf M, Anwar Z, Shah M, Hamayun M, Ud-Din J, Gul H, Nasim S, Lee IJ, Arif M Front Chem 23-Nov-2022
PMCID:PMC9727244
doi:10.3389/fchem.2022.994895
PMID:36505740
Green nanopriming: responses of alfalfa (Medicago sativa L.) seedlings to alfalfa extracts capped and light-induced silver nanoparticles Song K, Zhao D, Sun H, Gao J, Li S, Hu T, He X BMC Plant Biol 05-Jul-2022
PMCID:PMC9254587
doi:10.1186/s12870-022-03692-9
PMID:35790925
Recent Advances in Green Synthesis of Ag NPs for Extenuating Antimicrobial Resistance Parmar S, Kaur H, Singh J, Matharu AS, Ramakrishna S, Bechelany M Nanomaterials (Basel) 28-Mar-2022
PMCID:PMC9000675
doi:10.3390/nano12071115
PMID:35407234
Traditional and Phytochemical Bases of Herbs, Shrubs, Climbers, and Trees from Ethiopia for Their Anticancer Response Abate L, Tadesse MG, Bachheti A, Bachheti RK Biomed Res Int 03-Feb-2022
PMCID:PMC8831057
doi:10.1155/2022/1589877
PMID:35155671
Sustainable phyto-fabrication of silver nanoparticles using Gmelina arborea exhibit antimicrobial and biofilm inhibition activity Chandrasekharan S, Chinnasamy G, Bhatnagar S Sci Rep 07-Jan-2022
PMCID:PMC8742086
doi:10.1038/s41598-021-04025-w
PMID:34997051
Phytoantioxidant Functionalized Nanoparticles: A Green Approach to Combat Nanoparticle-Induced Oxidative Stress Balkrishna A, Kumar A, Arya V, Rohela A, Verma R, Nepovimova E, Krejcar O, Kumar D, Thakur N, Kuca K Oxid Med Cell Longev 26-Oct-2021
PMCID:PMC8563134
doi:10.1155/2021/3155962
PMID:34737844

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 / Erythrina alkaloids / Erythrinanes
(+)-Erythraline 12308897 Click to see 297.30 unknown https://doi.org/10.1002/JPS.2600590828
2,11,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline 3472080 Click to see 313.40 unknown https://doi.org/10.1002/JPS.2600590828
4,5,10,11-Tetrahydro-8,11-dimethoxy-2H-indolo(7a,1-a)isoquinolin-7-ol 622748 Click to see 299.40 unknown https://doi.org/10.1002/JPS.2600590828
Erysodine 169017 Click to see 299.40 unknown https://doi.org/10.1002/JPS.2600590828
Erysotrine 442219 Click to see 313.40 unknown https://doi.org/10.1002/JPS.2600590828
Erythraline 5317205 Click to see 297.30 unknown https://doi.org/10.1002/JPS.2600590828
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Myristic Acid 11005 Click to see 228.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Oleic Acid 445639 Click to see 282.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Palmitic Acid 985 Click to see 256.42 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
Stearic Acid 5281 Click to see 284.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032626/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Hypaphorine 442106 Click to see 246.30 unknown https://doi.org/10.1007/BF01897872
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(2R)-2-[3,4-dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 162934902 Click to see 356.40 unknown https://doi.org/10.1055/S-2006-962680
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Senegalensin 124035 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 408.50 unknown https://doi.org/10.1021/NP0101696
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Phaseollin 91572 Click to see 322.40 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(2R,11R,16S)-17,17-dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 162946150 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4CC(C(O5)(C)C)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(6aR,11aR)-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a,9-triol 163001878 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(6aR,11aR)-9-hydroxy-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2-carbaldehyde 12051845 Click to see 298.29 unknown https://doi.org/10.3987/COM-98-8334
https://doi.org/10.1016/S0031-9422(00)00441-6
(6aS,11aS)-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 124351123 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(6aS,11aS)-9-methoxy-10-(3-methyl-2-buten-1-yl)-6H-benzofuro(3,2-c)(1)benzopyran-3,6a(11aH)-diol 126540 Click to see 354.40 unknown https://doi.org/10.3987/COM-98-8334
https://doi.org/10.1016/S0031-9422(00)00441-6
17,17-Dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),15,20-heptaene-2,7-diol 22297563 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
17,17-Dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 85433283 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4CC(C(O5)(C)C)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
2-Prenyl-6a-hydroxyphaseollidin 44257484 Click to see 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
2,10-Di-(gamma,gamma-dimethylallyl)-glycinol 10341413 Click to see 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
3,6a-Dihydroxy-9-methoxy-10-prenylpterocarpan 3559400 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
9-hydroxy-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2-carbaldehyde 162844124 Click to see 298.29 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Erybraedin C 10408212 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Erystagallin A 10410005 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Erysubin D 12051846 Click to see 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Erysubin E 637080 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
Erythrabyssin II 5086400 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Erysubin A 15838885 Click to see 352.30 unknown https://doi.org/10.3987/COM-98-8334
Erysubin F 12051847 Click to see 390.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(-)-5-Hydroxy-2-(hydroxymethyl)-7-(4-hydroxyphenyl)-2-methyl-2H,6H-benzo[1,2-b:5,4-b']dipyran-6-one 10760434 Click to see 352.30 unknown https://doi.org/10.3987/COM-98-8334
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 162842930 Click to see 422.50 unknown https://doi.org/10.3987/COM-01-9346
(2S)-5-hydroxy-2-(hydroxymethyl)-7-(4-hydroxyphenyl)-2-methylpyrano[3,2-g]chromen-6-one 92446140 Click to see 352.30 unknown https://doi.org/10.3987/COM-98-8334
(3S)-3,5-dihydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 163014258 Click to see CC1(C(CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O)C 354.40 unknown https://doi.org/10.3987/COM-98-8334
3,5-Dihydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 11988359 Click to see 354.40 unknown https://doi.org/10.3987/COM-98-8334
4-Hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one 195652 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CC(O2)C(C)(C)O)C 422.50 unknown https://doi.org/10.3987/COM-01-9346
5,7-dihydroxy-6-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)chromen-4-one 26250192 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)O 354.40 unknown https://doi.org/10.3987/COM-98-8334
Alpinumisoflavone 5490139 Click to see 336.30 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
https://doi.org/10.3987/COM-98-8334
https://doi.org/10.1021/NP0101696
Erythrinin C 44257283 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O 354.40 unknown https://doi.org/10.3987/COM-98-8334
Euchrenone b10 402594 Click to see 422.50 unknown https://doi.org/10.1021/NP0101696
Laburnetin 15237156 Click to see 354.40 unknown https://doi.org/10.1021/NP0101696
https://doi.org/10.3987/COM-98-8334
Wighteone 5281814 Click to see 338.40 unknown https://doi.org/10.3987/COM-98-8334
https://doi.org/10.1016/S0031-9422(00)00441-6
https://doi.org/10.1021/NP0101696
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3R)-3-(2,4-dihydroxyphenyl)-3,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2H-chromen-4-one 162941344 Click to see 424.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(3R)-3-(2,4-dihydroxyphenyl)-7-hydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 26238931 Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OCC(C2=O)C3=C(C=C(C=C3)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
(7S)-7-(2,4-dihydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 162911740 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6
3-(2,4-Dihydroxyphenyl)-7-hydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 10001497 Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OCC(C2=O)C3=C(C=C(C=C3)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)00441-6

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