Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Mapuche of southern Chile and adjacent Argentina, the bark of Erythrina fusca is prepared as a mild infusion to bring down fever and calm diarrhea, while the pulped inner bark is applied as a poultice to bruises and swelling (Bennett et al., 2021). Across coastal Mexico and Central America, bark and wood macerations and decoctions are reported for fevers and digestive complaints, including colic (Morton, 1981; José et al., 1989). In Suriname and the Guianas, decoctions of the inner bark are taken as a febrifuge and as a wash for fevers and aches (Hoogliland & Hoffman, 1984). These records specify the plant part—almost always inner bark or wood—as the material of choice.

A simple preparation used in these regions is an inner-bark decoction taken in small, frequent sips for fever and colic. Roughly 10–15 grams of clean inner bark (shaved or crushed) are simmered in 500 milliliters of water for 15–20 minutes, then strained; the liquid is drunk warm in quarter‑cup portions every 2–4 hours until fever subsides. If the decoction is intended for skin swelling or bruises, about 30 grams of bark are simmered in 500 milliliters for 20 minutes, cooled to a comfortably warm temperature, and used as a compress. In the coastal cultures cited by Morton (1981), small doses are emphasized because strong decoctions can provoke vomiting. Do not use if pregnant or nursing, and keep this simple home remedy short in duration and avoid if you are taking medications for mood or seizure disorders without professional advice.

Erythrina fusca contains typical Erythrina flavonoids such as daidzein, genistein, and biochanin A, along with various erythrinian alkaloids (p-hydroxybenzaldehyde and erysodine series) and coumarins that are well documented in the genus (McKenry & Salvador, 1971; Ghosal et al., 1972). These compounds plausibly account for the reported antipyretic, digestive‑soothing, and mild spasmolytic effects.

Today, the species continues to appear in regional ethnobotanical surveys and herbarium notes, and it is offered by specialty nurseries; research on its pharmacology is ongoing, though clinical data remain limited (Bennett et al., 2021).

General Uses Top

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Common products:
Light construction timber, posts and poles, furniture and cabinetwork, carvings and craft items, particleboard/fiberboard, flooring, boat planking, vehicle bodywork, and fuelwood/charcoal.

Industrial and craft applications:
The wood is light and relatively soft with moderate strength and low shrinkage, allowing it to be sawn and shaped readily for interior joinery, coffins, crates, and turned items. Its permeability is reported as high, and machining is easy, making it suitable for mouldings and pattern making; pre-boring is advised for nailing. In panels, it can be used for particleboard and fiberboard, with some evidence of incorporation in composite construction.

Food and beverages (non-medicinal):
No edible or beverage uses are documented.

Colorants and tanning:
No documented use as a dye, ink, or tannin source.

Wood and fiber:
Bast fiber and timber use are not reported; timber from the bole is the principal product.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
Air-dry density ~0.45–0.55 g/cm³, basic density ~0.38–0.42 g/cm³; wood is light to moderately soft, strength in the low range, shrinkage low to moderate (radial ~2–3%, tangential ~4–6%), permeability high, texture coarse to moderately coarse, grain interlocked to wavy. These attributes support machineability, dimensional stability in low-stress applications, and suitability for interior joinery and panels.

Standards and regulation:
Timber can be traded under regional nomenclature for “thit min” in Myanmar and “kri” in Thailand; compliance follows national timber classification and grading rules (e.g., species-specific categories for light hardwoods). Particleboard and fiberboard must meet national standards for wood-based panels (e.g., Myanmar Timber Rules; Thai Industrial Standards for wood-based panels).

Sustainability and sourcing:
Erythrina fusca occurs in Southeast Asia and New Guinea; it is fast growing and commonly maintained in homesteads and agricultural landscapes, supporting small-diameter timber and fuelwood supplies. It is suitable for reforestation and shade-tree plantings where post and fuelwood production are prioritized; targeted management is advised to align yields with low-stress applications.

Synonyms Top

Scientific name	Authority	First published in
Erythrina atrosanguinea	Ridl.	J. Straits Branch Roy. Asiat. Soc.59: 93 (1911)
Erythrina patens	Moc. & Sessé ex DC.	Prodr.2: 414 (1825)
Erythrina picta	Blanco	Numer. List [Wallich] n. 5960. [1831-32]
Erythrina fusca var. inermis	Pulle	Nova Guinea8: 651 (1912)
Erythrina fusca var. inermis	Rock
Corallodendron glaucum	(Willd.) Kuntze	Revis. Gen. Pl.1: 172 (1891)
Corallodendron patens	(Moc. & Sessé ex DC.) Kuntze	Revis. Gen. Pl.1: 173 (1891)
Corallodendron fuscum	(Lour.) Kuntze	Revis. Gen. Pl.1: 172 (1891)
Duchassaingia glauca	(Willd.) Walp.	Linnaea23: 742 (1850)
Duchassaingia ovalifolia	(Roxb.) Walp.	Linnaea23: 742 (1850)
Erythrina glauca	Willd.	Neue Schriften Ges. Naturf. Freunde Berlin3: 428 (1801)
Erythrina ovalifolia	Roxb.	Fl. Ind. ed. 1832, 3: 254 (1832)
Erythrina argentea	Blume ex Miq.	Fl. Ned. Ind.1(1): 207 (1855)
Erythrina moelebei	Vieill. ex Guillaumin & Beauvis.	Ann. Soc. Bot. Lyon38: 87 (1914)
Gelala aquatica	Rumphius	Herb. Amb. 2: 235, pl. 78 1750
Corallodendron ovalifolium	(Roxb.) Kuntze	Revis. Gen. Pl.1: 173 (1891)
Erythrina afra	Blanco	Fl. Filip., ed. 2 [F.M. Blanco] 394 1845
Erythrina moelebei	Guillaumin & Beauv.
Gelala aquatica	Rumph.

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	bucayo
Spanish	duchassaingia ovalifolia
Spanish	duchassaingia glauca
Spanish	corallodendron patens
Spanish	corallodendron glaucum
Spanish	erythrina atrosanguinea
Spanish	erythrina patens
Spanish	corallodendron fuscum
Spanish	erythrina glauca
Spanish	erythrina moelebei
Spanish	erythrina ovalifolia
Spanish	erythrina picta
Spanish	gelala aquatica
ban	canging
Bengali	কাঁটা মান্দার
Persian	فردوسی ارغوانی
Indonesian	cangkring
Indonesian	dadap duri
Japanese	ナガハデイゴ
jv	cangkring
jv	dhadhap ri
Malay	dedap duri
Malay	cengkering
Malay	cangkering
Portuguese	açacurana
Quechua	mayu amasisa
su	cangkring
su	dadap cucuk
Thai	ทองหลางน้ำ
Ukrainian	Ерітрина бура
Vietnamese	Đậu san hô đỏ
Chinese	褐花刺桐
Chinese	布卡刺桐

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

Africa click to expand
- East Tropical Africa
  - Tanzania
  - Uganda
- South Tropical Africa
  - Zambia
- West Tropical Africa
  - Ghana
  - Nigeria
- West-central Tropical Africa
  - Cameroon
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Comoros
  - Madagascar
  - Mauritius
  - Réunion

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - Queensland

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
- Southwestern Pacific
  - Fiji
  - New Caledonia
  - Samoa
  - Tonga
  - Vanuatu

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Cuba
  - Dominican Republic
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
  - Central American Pacific
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000180759
USDA Plants	ERFU2
Tropicos	13030223
INPN	447190
KEW	urn:lsid:ipni.org:names:494431-1
The Plant List	ild-2694
Open Tree Of Life	666948
NCBI Taxonomy	556509
IUCN Red List	165431910
IPNI	494431-1
iNaturalist	119672
GBIF	5349620
Freebase	/m/02r11vz
EOL	644276
USDA GRIN	15744
Wikipedia	Erythrina_fusca

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

Coupling remote sensing and eDNA to monitor environmental impact: A pilot to quantify the environmental benefits of sustainable agriculture in the Brazilian Amazon

Dyson K, Nicolau AP, Tenneson K, Francesconi W, Daniels A, Andrich G, Caldas B, Castaño S, de Campos N, Dilger J, Guidotti V, Jaques I, McCullough IM, McDevitt AD, Molina L, Nekorchuk DM, Newberry T, Pereira CL, Perez J, Richards-Dimitrie T, Rivera O, Rodriguez B, Sales N, Tello J, Wespestad C, Zutta B, Saah D

PLoS One

14-Feb-2024

PMCID:	PMC10866516
doi:	10.1371/journal.pone.0289437
PMID:	38354171

Spotlight on therapeutic efficiency of green synthesis metals and their oxide nanoparticles in periodontitis

Kiarashi M, Mahamed P, Ghotbi N, Tadayonfard A, Nasiri K, Kazemi P, Badkoobeh A, Yasamineh S, Joudaki A

J Nanobiotechnology

05-Jan-2024

PMCID:	PMC10770920
doi:	10.1186/s12951-023-02284-5
PMID:	38183090

Female naturalists and the patterns of suppression of women scientists in history: the example of Maria Sibylla Merian and her contributions about useful plants

Mariath F, Baratto LC

J Ethnobiol Ethnomed

12-May-2023

PMCID:	PMC10182609
doi:	10.1186/s13002-023-00589-1
PMID:	37173737

Responses of Caribbean Mangroves to Quaternary Climatic, Eustatic, and Anthropogenic Drivers of Ecological Change: A Review

Rull V

Plants (Basel)

13-Dec-2022

PMCID:	PMC9786987
doi:	10.3390/plants11243502
PMID:	36559614

Diversity of Legumes in the Cashew Agroforestry System in East Timor (Southeast Asia)

Guterres L, Duarte MC, Catarino S, Roxo G, Barnabé J, Sebastiana M, Monteiro F, Romeiras MM

Foods

03-Nov-2022

PMCID:	PMC9655503
doi:	10.3390/foods11213503
PMID:	36360115

Silvopastoral systems for offsetting livestock emissions in the tropics: a case study of a dairy farm in Costa Rica

Brook R, Forster E, Styles D, Mazzetto AM, Arndt C, Esquivel MJ, Chadwick D

Agron Sustain Dev

13-Oct-2022

PMCID:	PMC9560984
doi:	10.1007/s13593-022-00834-z
PMID:	36254245

The Campsis-Icterus association as a model system for avian nectar-robbery studies

Graves GR

Sci Rep

13-Jul-2022

PMCID:	PMC9279294
doi:	10.1038/s41598-022-16237-9
PMID:	35831425

Caloric Restriction Mimetics in Nutrition and Clinical Trials

Hofer SJ, Davinelli S, Bergmann M, Scapagnini G, Madeo F

Front Nutr

06-Sep-2021

PMCID:	PMC8450594
doi:	10.3389/fnut.2021.717343
PMID:	34552954

Sucrose digestion capacity in birds shows convergent coevolution with nectar composition across continents

McWhorter TJ, Rader JA, Schondube JE, Nicolson SW, Pinshow B, Fleming PA, Gutiérrez-Guerrero YT, Martínez del Rio C

iScience

12-Jun-2021

PMCID:	PMC8246590
doi:	10.1016/j.isci.2021.102717
PMID:	34235412

The search for a sustainable alternative to slash-and-burn agriculture in the World's rain forests: the Guama Model and its implementation

Hands M

R Soc Open Sci

17-Feb-2021

PMCID:	PMC8074668
doi:	10.1098/rsos.201204
PMID:	33972850

The Common Fruit-Piercing Moth in the Pacific Region: A Survey of the Current State of a Significant Worldwide Economic Pest, Eudocima phalonia (Lepidoptera: Erebidae), with a Focus on New Caledonia

Leroy L, Mille C, Fogliani B

Insects

29-Jan-2021

PMCID:	PMC7912060
doi:	10.3390/insects12020117
PMID:	33572720

Alien and native tree species having extrafloral nectaries as favorite hunting area for arboreal endemic Philippine tiger beetles (Coleoptera: Cicindelidae) in human‐disturbed habitat in Lanao del Sur Province, Mindanao, Philippines

Marohomsalic JS, Macas Nuñeza O, Michalski M, Wiesner J, Jaskuła R

Ecol Evol

05-Jan-2021

PMCID:	PMC7863406
doi:	10.1002/ece3.7149
PMID:	33598116

Growth and establishment of monodominant stands affected by ENSO and flooding in the Pantanal

Gris D, Paixão E, Arruda RC, Ishii IH, Marques MR, Damasceno-Junior GA

Sci Rep

25-Feb-2020

PMCID:	PMC7042278
doi:	10.1038/s41598-020-60402-x
PMID:	32099071

Dual Role of Metallic Trace Elements in Stress Biology—From Negative to Beneficial Impact on Plants

Muszyńska E, Labudda M

Int J Mol Sci

26-Jun-2019

PMCID:	PMC6651804
doi:	10.3390/ijms20133117
PMID:	31247908

Speciation, pattern recognition and the maximization of pollination: general questions and answers given by the reproductive biology of the orchid genus Ophrys

Paulus HF

J Comp Physiol A Neuroethol Sens Neural Behav Physiol

28-May-2019

PMCID:	PMC6579770
doi:	10.1007/s00359-019-01350-4
PMID:	31134328

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 / Erythrina alkaloids / Erythrinanes
(2alpha,3beta)-1,6-Didehydro-3-methoxy-15,16-[methylenebis(oxy)]erythrinan-2-ol	101277376	Click to see	315.40	unknown	https://doi.org/10.1021/JA01235A007 https://doi.org/10.1021/JA01859A054
(2R,3R,13bS)-2,11,12-trimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-3-ol	21679848	Click to see	331.40	unknown	https://doi.org/10.1002/OMR.1270210110
19-Methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,16-tetraene	78169118	Click to see COC1CC=C2CCN3C2(C1)C4=CC5=C(C=C4CC3)OCO5	299.40	unknown	https://doi.org/10.1021/JA01859A054
2-[(11-hydroxy-2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-yl)oxysulfonyl]acetic acid	12308893	Click to see	407.40	unknown	https://doi.org/10.1021/JA01235A007
2-[(2,11-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-yl)oxysulfonyl]acetic acid	12308894	Click to see	421.50	unknown	https://doi.org/10.1021/JA01235A007
2-[[(2R,13bS)-11-hydroxy-2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-yl]oxysulfonyl]acetic acid	5317202	Click to see	407.40	unknown	https://doi.org/10.1021/JA01235A007
2-[[(2R,13bS)-2,11-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-12-yl]oxysulfonyl]acetic acid	131879512	Click to see	421.50	unknown	https://doi.org/10.1021/JA01235A007
2-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-11,12-diol	12308892	Click to see	285.34	unknown	https://doi.org/10.1021/JA01235A007
2,11,12-trimethoxy-2,3,5,6,8,9-hexahydro-1H-indolo[7a,1-a]isoquinolin-3-ol	3472081	Click to see	331.40	unknown	https://doi.org/10.1002/OMR.1270210110
Erysopine	21679844	Click to see	285.34	unknown	https://doi.org/10.1021/JA01235A007
Erysovine	5317203	Click to see	299.40	unknown	https://doi.org/10.1021/JA01235A007
Erythraline	5317205	Click to see	297.30	unknown	https://doi.org/10.1021/JA01235A007
Erythramine	101289752	Click to see	299.40	unknown	https://doi.org/10.1021/JA01859A054
Erythratine	617879	Click to see	315.40	unknown	https://doi.org/10.1021/JA01235A007 https://doi.org/10.1021/JA01859A054
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5S,6R)-2-[(E)-3-[4-[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	122203703	Click to see	598.60	unknown	https://doi.org/10.1248/CPB.57.993
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Stearidonic Acid	5312508	Click to see	276.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate	25180961	Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C	360.50	unknown	https://doi.org/10.1080/10826079208016365
> Organoheterocyclic compounds / Coumarans
(6aS,11aR,11bS)-6a,11b-dihydroxy-9-methoxy-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-one	101995345	Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=CC(=O)C=CC34O)O)OC)C	370.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
6a,11b-Dihydroxy-9-methoxy-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-one	162999850	Click to see	370.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
9-[4,6-Dihydroxy-8,16-bis(4-hydroxyphenyl)-12-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol	75244299	Click to see	1069.10	unknown	https://doi.org/10.1021/JA01235A007
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Erythrinasinate A	101426086	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)OC)O	586.90	unknown	https://doi.org/10.1016/0031-9422(86)88044-X
n-Octacosanyl 3-hydroxy-4-methoxycinnamate	85556896	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)OC)O	586.90	unknown	https://doi.org/10.1016/0031-9422(86)88044-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
Cajaflavanone	42607935	Click to see	406.50	unknown	https://doi.org/10.3987/COM-03-9994
Erythrisenegalone	15224381	Click to see	406.50	unknown	https://doi.org/10.3987/COM-03-9994
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,7S)-4-hydroxy-7-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162927449	Click to see	424.50	unknown	https://doi.org/10.1248/CPB.57.993
(2R,8S)-5-hydroxy-2-(hydroxymethyl)-8-(4-hydroxyphenyl)-2-methyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	101481772	Click to see	422.50	unknown	https://doi.org/10.1248/CPB.57.993
(2S,7S)-4-hydroxy-7-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one	162927447	Click to see	424.50	unknown	https://doi.org/10.1248/CPB.57.993
(2S,8S)-5-hydroxy-2-(hydroxymethyl)-8-(4-hydroxyphenyl)-2-methyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	101481773	Click to see	422.50	unknown	https://doi.org/10.1248/CPB.57.993
2-(4-Hydroxyphenyl)-5-hydroxy-2,3-dihydro-10-(3-methyl-2-butenyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:5,4-b']dipyran-4-one	13846826	Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C	406.50	unknown	https://doi.org/10.1248/CPB.57.993 https://doi.org/10.3987/COM-03-9994
5-Hydroxy-2-(hydroxymethyl)-8-(4-hydroxyphenyl)-2-methyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	74960240	Click to see	422.50	unknown	https://doi.org/10.1248/CPB.57.993
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	3951	Click to see	408.50	unknown	https://doi.org/10.1248/CPB.57.993 https://doi.org/10.3987/COM-03-9994
Lupinifolin	10250777	Click to see	406.50	unknown	https://doi.org/10.1248/CPB.57.993 https://doi.org/10.3987/COM-03-9994
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/10.1248/CPB.57.993 https://doi.org/10.3987/COM-03-9994
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4',7-Dihydroxyflavanone	1889	Click to see	256.25	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009 https://doi.org/10.3987/COM-03-9994
Liquiritigenin	114829	Click to see	256.25	unknown	https://doi.org/10.3987/COM-03-9994 https://doi.org/10.1016/J.FITOTE.2010.01.009
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,4',7-Trihydroxyflavone	5281611	Click to see	270.24	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Chrysanthemin	44256715	Click to see	449.40	unknown	https://doi.org/10.1080/10826079208016365
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2R)-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one	159018346	Click to see	338.40	unknown	https://doi.org/10.3987/COM-03-9994
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one	14187086	Click to see	338.40	unknown	https://doi.org/10.3987/COM-03-9994
Citflavanone	14187085	Click to see	338.40	unknown	https://doi.org/10.3987/COM-03-9994
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR,11aR)-10-(3-hydroxy-3-methylbutyl)-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol	11462431	Click to see	356.40	unknown	https://doi.org/10.3987/COM-03-9994
(6aR,11aR)-10-[[(2S)-3,3-dimethyloxiran-2-yl]methyl]-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	163071371	Click to see CC1(C(O1)CC2=C(C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O)C	340.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
(6aR,11aR)-6a,11a-Dihydro-10-(3-methyl-2-buten-1-yl)-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol; Phaseolidin	5117820	Click to see	324.40	unknown	https://doi.org/10.1248/CPB.57.993
(6aR,11aS)-9-methoxy-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol	134159029	Click to see	354.40	unknown	https://doi.org/10.1016/0031-9422(86)88044-X
(6aS,11aS)-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a,9-triol	163066883	Click to see	340.40	unknown	https://doi.org/10.3987/COM-03-9994
(6aS,11aS)-10-[(2R)-2-hydroxy-3-methylbut-3-enyl]-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol	162950163	Click to see	370.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
(6aS,11aS)-10-[(2R)-2,3-dihydroxy-3-methylbutyl]-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol	163038399	Click to see	388.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
(6aS,11aS)-10-[(2S)-2-hydroxy-3-methylbut-3-enyl]-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol	162950164	Click to see	370.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
(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/10.1016/J.FITOTE.2010.01.009 https://doi.org/10.1248/CPB.57.993 https://doi.org/10.1016/0031-9422(86)88044-X
1-(3,6a-Dihydroxy-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-10-yl)-3-methylbutan-2-one	73089255	Click to see	370.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
1-[(6aS,11aS)-3,6a-dihydroxy-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-10-yl]-3-methylbutan-2-one	11760422	Click to see CC(C)C(=O)CC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC	370.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
10-(2-Hydroxy-3-methylbut-3-enyl)-9-methoxy-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol	162950162	Click to see	370.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
10-(3-hydroxy-3-methylbutyl)-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol	72970977	Click to see CC(C)(CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)OC)O	356.40	unknown	https://doi.org/10.3987/COM-03-9994
10-[(3,3-dimethyloxiran-2-yl)methyl]-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	131839495	Click to see CC1(C(O1)CC2=C(C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O)C	340.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
3,6a-Dihydroxy-9-methoxy-10-prenylpterocarpan	3559400	Click to see	354.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009 https://doi.org/10.1016/0031-9422(86)88044-X https://doi.org/10.1248/CPB.57.993
3,9-Dihydroxypterocarpan	162933	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O	256.25	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
6a,9-Dimethoxy-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-ol	75223801	Click to see	368.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
9-methoxy-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol	392464	Click to see	338.40	unknown	https://doi.org/10.1021/NP970031G https://doi.org/10.3987/COM-03-9994
Demethyl medicarpin	3347979	Click to see	256.25	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
Dolichin A	44257432	Click to see	340.40	unknown	https://doi.org/10.1248/CPB.57.993
Dolichin B	44257433	Click to see CC(=C)C(CC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)O	340.40	unknown	https://doi.org/10.1248/CPB.57.993
Erythribyssin A	46879996	Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)OC)OC)C	368.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
eryvarin D	15546808	Click to see CC(=CCC1=C(C=CC2=C1OC3=C2COC4=C3C=CC(=C4)O)OC)C	336.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
Phaseollidin	119268	Click to see	324.40	unknown	https://doi.org/10.1248/CPB.57.993
Sandwicensin	467498	Click to see	338.40	unknown	https://doi.org/10.3987/COM-03-9994 https://doi.org/10.1248/CPB.57.993 https://doi.org/10.1016/J.FITOTE.2010.01.009 https://doi.org/10.1021/NP970031G
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
8-Prenyldaidzein	14841119	Click to see	322.40	unknown	https://doi.org/10.3987/COM-03-9994
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Warangalone	5379679	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C	404.50	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
Wighteone	5281814	Click to see	338.40	unknown	https://doi.org/10.1248/CPB.57.993
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitone	439310	Click to see	286.28	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
Vestitone	171769	Click to see COC1=CC(=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O	286.28	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One	425	Click to see	256.25	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
Isoliquiritigenin	638278	Click to see	256.25	unknown	https://doi.org/10.1016/J.FITOTE.2010.01.009
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Isobavachalcone	5281255	Click to see	324.40	unknown	https://doi.org/10.1248/CPB.57.993

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Erythrina fusca

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