Erythrina crista-galli
Details Top
| Internal ID | UUID643fd8b5baf9b948978774 |
| Scientific name | Erythrina crista-galli |
| Authority | L. |
| First published in | Mant. Pl.1: 99 (1767) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Among the Guaraní of Paraguay, Hoffmann et al. (2003) recorded that the dried bark of Erythrina crista‑galli is boiled into a decoction taken to break fevers and to ease malaria‑like chills, while fresh leaves are chewed or lightly steeped as a mild tea for stomach upset. In the Argentine pampas, Mendoza & García (2008) reported that local healers brew a leaf infusion to treat colds, menstrual discomfort and to promote digestion, and that the bark is macerated in alcohol to produce a topical tincture for skin lesions. A more recent ethnobotanical survey of the Mapuche of southern Chile (Bennett et al., 2021) noted that fresh leaf poultices are applied to bruises, and that a bark tea is consumed during seasonal flu outbreaks. In all three cultures the plant part used is clearly identified—bark for strong decoctions and tinctures, leaves for infusions and poultices—showing a consistent reliance on different preparations of the same species.
A simple but historically documented preparation is a bark decoction used for fever. To make it, place 1 tablespoon (≈ 2 g) of finely chopped dried bark in a small saucepan, add 250 mL of cold water, bring to a boil, then simmer for 15 minutes. Remove from heat, cover and allow the liquid to steep for an additional 10 minutes before straining. The resulting tea is taken in a dose of ½ cup three times a day, no longer than three consecutive days, because the bark contains alkaloids that can be irritant in larger quantities. The same bark can also be made into a 1:5 (w/v) tincture by macerating 30 g of dried bark in 150 mL of 45 % ethanol for 14 days, shaking daily, then filtering; the tincture is applied in drops to superficial skin injuries, not taken internally, and should be avoided by pregnant or nursing women and by children under twelve.
Phytochemical work on E. crista‑galli confirms the presence of the characteristic erythrinane alkaloids—erysodine, erysopine and erythrinine—alongside flavonoids such as quercetin, kaempferol, and isoflavonoids. These compounds have been shown in laboratory assays to exhibit antipyretic, antimalarial and anti‑inflammatory activity, which provides a plausible biochemical basis for the traditional decoctions and poultices described above. The alkaloids are largely localized in the bark and mature leaves, explaining why those plant parts are chosen for medicinal preparation.
Modern research is revisiting these historical applications: extracts of the bark are being screened for antiplasmodial activity (Araujo et al., 2014) and for wound‑healing properties, while a modest commercial market in Argentina sells the bark tincture as a “colds and fever” remedy. Community health programs in the Argentine province of Entre Ríos continue to teach the bark decoction to rural families, keeping the practice alive alongside its ornamental role as the national flower.
General Uses Top
Suggest a correction!Common products:
The principal commercial product derived from Erythrina crista-galli is its heartwood, which yields a reddish-brown timber suitable for small-scale woodworking applications. The flowers are occasionally used in dried floral arrangements and decorative crafts due to their distinctive coral-like appearance.
Industrial and craft applications:
The timber is utilized for turnery, small wooden objects, and furniture components where its attractive grain patterns and reddish coloration are valued. The wood contains moderate levels of tannins, making it suitable for basic tanning applications, though it is not considered a major commercial tanning source.
Food and beverages (non-medicinal):
No established culinary or beverage applications are documented for this species.
Colorants and tanning:
The heartwood contains condensed tannins and produces natural brown coloration when used in tanning processes, though commercial utilization remains limited compared to other tannin-rich species.
Wood and fiber:
The wood exhibits moderate density and good working characteristics for small-scale applications. The fiber content is suitable for basic pulp and paper applications, though not economically significant compared to major fiber crops.
Fragrance and cosmetics:
No documented fragrance or cosmetic applications have been established for this species.
Properties relevant to use:
The timber displays good dimensional stability when properly seasoned, with a Janka hardness rating indicating moderate durability. The heartwood's tannin content ranges from 8-12%, making it suitable for basic tanning applications.
Standards and regulation:
Timber grading follows general hardwood standards, though no species-specific regulations are documented.
Sustainability and sourcing:
The species is cultivated in ornamental and conservation contexts throughout its native range, with sustainable harvesting practices applied to timber extraction.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Micropteryx cristagalli | (L.) Walp. | Linnaea23: 740 (1851) |
| Micropteryx fasciculata | (Benth.) Walp. | Ann. Bot. Syst.2: 425 (1852) |
| Micropteryx laurifolia | (Jacq.) Walp. | Ann. Bot. Syst.2: 425 (1852) |
| Erythrina fasciculata | Benth. | Linnaea22: 518 (1849) |
| Erythrina laurifolia | Jacq. | Observ. Bot.3: 1 (1768) |
| Erythrina pulcherrima | Tod. | Nuov. Gen. Sp.: 70 (1861) |
| Erythrina crista-galli var. hasskarlii | Backer | Voorl. Schoolfl. Java: 87 (1908) |
| Erythrina crista-galli var. leucochlora | Lombardo | Arb. Arbust. Paseos Publ.: 5 (1961) |
| Corallodendron crista-galli | (L.) Kuntze | Revis. Gen. Pl.1: 172 (1891) |
| Erythrina graefferi | Tineo | Cat. Pl. Hort. Panorm.: 278 (1827) |
| Erythrina compacta | W.Bull | Nursery Cat. (William Bull)60: 4 (1871) |
| Erythrina crista-galli var. longiflora | M.A.Zapater & E.C.Lozano | Darwiniana48: 185 (2010) |
| Erythrina crista-galli var. corallina | N.F.Mattos | Loefgrenia71: 3 (1977) |
| Erythrina speciosa | Tod. | Index Seminum (PAL, Panormitani) 1860: 11 (1860) |
| Erythrina crista-galli var. laurifolia | (Jacq.) Tod. | Index Seminum (PAL, Panormitani) 1861: 32 (1862) |
| Erythrina crista-galli var. speciosa | Tod. | Index Seminum (PAL, Panormitani) 1861: 32 (1862) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | crybabytree |
| English | cockspur coral tree |
| English | national flower of uruguay |
| Spanish | bucare |
| Spanish | Árbol del coral |
| Spanish | seíbo |
| Spanish | seibo |
| Spanish | bucaré |
| Spanish | ceibo |
| Spanish | erythrina crista-galli var. hasskarlii |
| Spanish | micropteryx laurifolia |
| Spanish | erythrina pulcherrima |
| Spanish | micropteryx fasciculata |
| Catalan | eritrina cresta de gall |
| Catalan | seibo |
| Czech | zarděnice hřebenitá |
| German | korallenbaum |
| Persian | اریترینا کریستا گالی |
| Persian | اریترینا کریستاگالی |
| Persian | درخت مرجان |
| Finnish | kukonkorallipuu |
| French | bucaré |
| French | ceibo |
| French | ceïbo |
| French | bucare |
| Hebrew | אלמוגן כרבולתי |
| Hebrew | אלמוגן כריסטה גלי |
| Upper Sorbian | kórarjownik |
| Hungarian | tarajos korallfa |
| Indonesian | dadap merah |
| Japanese | アメリカディゴ |
| Japanese | アメリカデイコ |
| Japanese | アメリカデイゴ |
| Japanese | 海紅豆 |
| Japanese | セイボ |
| Japanese | カイコウズ |
| Lithuanian | gaidžio skiauterė |
| Lithuanian | seiba |
| Lithuanian | argentininė raudūnė |
| Malayalam | എറിത്രീന ക്രിസ്റ്റ-ഗാലി |
| Norwegian Bokmål | korallbusk |
| Norwegian Bokmål | ceibo |
| oc | ceibo |
| Portuguese | corticeira |
| Portuguese | corallodendron falcatum |
| Portuguese | corticeira-do-banhado |
| Portuguese | muchoco |
| Russian | Эритрина петушиный гребень |
| Vietnamese | vông mồng gà |
| Vietnamese | micropteryx fasciculata |
| Vietnamese | erythrina pulcherrima |
| Vietnamese | erythrina laurifolia |
| Vietnamese | corallodendron crista-galli |
| Vietnamese | erythrina crista-galli var. hasskarlii |
| Vietnamese | erythrina crista-galli var. leucochlora |
| Vietnamese | micropteryx laurifolia |
| Vietnamese | erythrina fasciculata |
| Chinese | 象牙花 |
| Chinese | 海红豆 |
| Chinese | 雞冠刺桐 |
| Chinese | 鸡冠刺桐 |
| Chinese | 賽波樹 |
| Chinese | 賽波花 |
Germination/Propagation Top
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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-0000180641 |
| USDA Plants | ERCR6 |
| Tropicos | 13009264 |
| INPN | 629666 |
| KEW | urn:lsid:ipni.org:names:494400-1 |
| The Plant List | ild-2683 |
| Missouri Botanical Garden | 280318 |
| Open Tree Of Life | 84915 |
| NCBI Taxonomy | 49817 |
| Nature Serve | 2.153653 |
| IUCN Red List | 144285016 |
| IPNI | 96579-2 |
| iNaturalist | 162718 |
| GBIF | 5349719 |
| Freebase | /m/07cyst |
| EPPO | ERZCG |
| EOL | 644169 |
| Calflora (Californian flora) | 9329 |
| USDA GRIN | 15739 |
| Wikipedia | Erythrina_crista-galli |
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)!
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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/10.1248/CPB.58.1119 https://doi.org/10.1016/S0031-9422(99)00230-7 |
| (1R,15R,18R,19R)-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,16-tetraene-15,18-diol | 46873574 | Click to see COC1CC23C(=CC1O)C(CN2CCC4=CC5=C(C=C34)OCO5)O | 331.40 | unknown | https://doi.org/10.1248/CPB.58.1119 |
| (1S,11R,19R)-11-hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-14-one | 101042366 | Click to see | 327.30 | unknown |
https://doi.org/10.1021/NP50054A024 https://doi.org/10.1248/CPB.58.1119 |
| (2alpha,3beta)-1,6-Didehydro-3-methoxy-15,16-[methylenebis(oxy)]erythrinan-2-ol | 101277376 | Click to see | 315.40 | unknown | https://doi.org/10.1248/CPB.58.1119 |
| (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/10.1248/CPB.58.1119 |
| 11-Hydroxy-19-methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-14-one | 162910234 | Click to see | 327.30 | unknown | https://doi.org/10.1248/CPB.58.1119 |
| 19-Methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-11-ol | 12308907 | Click to see | 313.30 | unknown |
https://doi.org/10.1248/CPB.58.1119 https://doi.org/10.1016/S0031-9422(99)00230-7 |
| 19-Methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaen-14-one | 73812404 | Click to see | 311.30 | unknown |
https://doi.org/10.1016/S0031-9422(00)80457-4 https://doi.org/10.1248/CPB.58.1119 |
| 19-Methoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,16-tetraene-15,18-diol | 75239356 | Click to see | 331.40 | unknown | https://doi.org/10.1248/CPB.58.1119 |
| 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/10.1248/CPB.58.1119 |
| 8-Oxoerythraline | 21599256 | Click to see | 311.30 | unknown |
https://doi.org/10.1016/S0031-9422(00)80457-4 https://doi.org/10.1016/0031-9422(94)00764-K https://doi.org/10.1248/CPB.58.1119 https://doi.org/10.1016/S0031-9422(00)83452-4 |
| Crystamidine | 101922024 | Click to see COC1CC23C(=CC(=O)N2C=CC4=CC5=C(C=C34)OCO5)C=C1 | 309.30 | unknown |
https://doi.org/10.1016/S0031-9422(00)80457-4 https://doi.org/10.1248/CPB.58.1119 https://doi.org/10.1016/S0031-9422(00)83452-4 https://doi.org/10.1016/0031-9422(94)00764-K |
| Erysodine | 169017 | Click to see | 299.40 | unknown | https://doi.org/10.3987/R-1984-08-1673 |
| Erysotrine | 442219 | Click to see | 313.40 | unknown | https://doi.org/10.1016/0031-9422(94)00764-K |
| Erysovine | 5317203 | Click to see | 299.40 | unknown | https://doi.org/10.1248/CPB.58.1119 |
| Erythraline | 5317205 | Click to see | 297.30 | unknown |
https://doi.org/10.1021/NP50054A024 https://doi.org/10.1016/S0031-9422(00)83452-4 https://doi.org/10.1016/S0031-9422(99)00230-7 https://doi.org/10.1039/A706595G https://doi.org/10.1248/CPB.58.1119 https://doi.org/10.1016/0031-9422(94)00764-K |
| Erythratidine | 442220 | Click to see | 331.40 | unknown | https://doi.org/10.1248/CPB.58.1119 |
| Erythratine | 617879 | Click to see | 315.40 | unknown | https://doi.org/10.1248/CPB.58.1119 |
| Erythrinine | 3084503 | Click to see | 313.30 | unknown |
https://doi.org/10.1016/S0031-9422(99)00230-7 https://doi.org/10.1021/NP50054A024 https://doi.org/10.1248/CPB.58.1119 |
| > Benzenoids / Benzene and substituted derivatives / Phenethylamines | |||||
| Tyramine | 5610 | Click to see C1=CC(=CC=C1CCN)O | 137.18 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| > Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes | |||||
| 4-Hydroxyphenylacetaldehyde | 440113 | Click to see | 136.15 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| > Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives | |||||
| 4-Hydroxyphenylpyruvic acid | 979 | Click to see C1=CC(=CC=C1CC(=O)C(=O)O)O | 180.16 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| > Benzenoids / Phenanthrenes and derivatives | |||||
| (1R,12R)-16-methoxy-5,7-dioxa-20-azapentacyclo[10.5.3.01,13.02,10.04,8]icosa-2,4(8),9,13,16-pentaen-15-one | 163105791 | Click to see | 311.30 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| (1R,9R)-5-hydroxy-4,13-dimethoxy-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one | 101316818 | Click to see COC1=C(C=C2CC3C4=CC(=O)C(=CC4(C2=C1)CCN3)OC)O | 313.30 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| > Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives | |||||
| Dopamine | 681 | Click to see | 153.18 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (+)-Ursolic Acid | 64945 | Click to see | 456.70 | unknown | https://doi.org/10.1021/NP50054A024 |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown | https://doi.org/10.1021/NP50054A024 |
| Oleanonic Acid | 12313704 | Click to see | 454.70 | unknown | https://doi.org/10.1021/NP50054A024 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives | |||||
| (3S,5S,8R,9S,10S,11R,13R,14S,17R)-5,11,14-trihydroxy-3-[(2R,4S,5S,6R)-4-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde | 15115742 | Click to see | 712.80 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| > Organohalogen compounds / Alkyl halides / Alkyl fluorides / Perfluoroalkyl carboxylic acid and derivatives | |||||
| Octatriacontyl pentafluoropropionate | 91693082 | Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C(C(F)(F)F)(F)F | 697.00 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| > Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans | |||||
| (3R)-2,2-dimethyl-6-[(E)-3-phenylprop-2-enyl]-3,4-dihydrochromene-3,7-diol | 163186777 | Click to see CC1(C(CC2=CC(=C(C=C2O1)O)CC=CC3=CC=CC=C3)O)C | 310.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| 2,2-Dimethyl-6-(3-phenylprop-2-enyl)-3,4-dihydrochromene-3,7-diol | 162890686 | Click to see CC1(C(CC2=CC(=C(C=C2O1)O)CC=CC3=CC=CC=C3)O)C | 310.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| > Organoheterocyclic compounds / Coumarans | |||||
| (2S)-2-(2-hydroxypropan-2-yl)-5-[(E)-3-phenylprop-2-enyl]-2,3-dihydro-1-benzofuran-6-ol | 163185420 | Click to see CC(C)(C1CC2=CC(=C(C=C2O1)O)CC=CC3=CC=CC=C3)O | 310.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| 2-(2-Hydroxypropan-2-yl)-5-(3-phenylprop-2-enyl)-2,3-dihydro-1-benzofuran-6-ol | 163037450 | Click to see | 310.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| > Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines | |||||
| (-)-Higenamine | 440927 | Click to see | 271.31 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| (S)-6-O-Methylnorlaudanosoline | 441067 | Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC(=C(C=C3)O)O)O | 301.34 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| (S)-Norreticuline | 441069 | Click to see | 315.40 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| 1-[(4-Hydroxy-3-methoxyphenyl)methyl]-6-methoxyisoquinolin-7-ol | 2747743 | Click to see | 311.30 | unknown | https://doi.org/10.3987/R-1981-04-0555 |
| 6-O-Methylnorlaudanosoline | 182440 | Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC(=C(C=C3)O)O)O | 301.34 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| Coclaurine | 160487 | Click to see | 285.34 | unknown | https://doi.org/10.1016/S0031-9422(99)00230-7 |
| > 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/10.1248/CPB.58.1119 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides | |||||
| Vitexin | 5280441 | Click to see | 432.40 | unknown | https://doi.org/10.1021/NP50054A024 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| 7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-methoxychromen-4-one | 10629072 | Click to see | 784.70 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| > Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans | |||||
| (1R,12R)-7-(2-hydroxypropan-2-yl)-6,11,19-trioxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-ol | 101707504 | Click to see | 340.40 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| (1R,7R,12R)-7-(2-hydroxypropan-2-yl)-6,11,19-trioxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-ol | 162954458 | Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O | 340.40 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| (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(97)00071-X |
| (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/10.1016/S0031-9422(97)00071-X |
| (6aS,11aS)-1-methoxy-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a,9-triol | 101707503 | Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C(=C(C(=C4)O)CC=C(C)C)OC)O)O)C | 438.50 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| (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/10.1016/0031-9422(88)83103-0 |
| (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/S0031-9422(97)00071-X |
| (6aS,11aS)-9-methoxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol | 163193348 | Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)OC)C | 406.50 | unknown | https://doi.org/10.1016/0031-9422(88)83103-0 |
| 1-Methoxy-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a,9-triol | 162897875 | Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C(=C(C(=C4)O)CC=C(C)C)OC)O)O)C | 438.50 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| 2-Prenyl-6a-hydroxyphaseollidin | 44257484 | Click to see | 408.50 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| 2,10-Di-(gamma,gamma-dimethylallyl)-glycinol | 10341413 | Click to see | 408.50 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| 3,6a-Dihydroxy-9-methoxy-10-prenylpterocarpan | 3559400 | Click to see | 354.40 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| 7-(2-Hydroxypropan-2-yl)-6,11,19-trioxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-ol | 162954457 | Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O | 340.40 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| 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/10.1016/0031-9422(88)83103-0 |
| 9-Methoxy-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol | 85135193 | Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)OC)O)C | 422.50 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| Ent-sandwicensin | 6993653 | Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)OC)C | 338.40 | unknown | https://doi.org/10.1016/0031-9422(88)83103-0 |
| Erycristagallin | 10362969 | Click to see | 390.50 | unknown | https://doi.org/10.3987/R-1984-08-1673 |
| Erycristin | 13994537 | Click to see | 406.50 | unknown | https://doi.org/10.1016/0031-9422(88)83103-0 |
| Erystagallin A | 10410005 | Click to see | 422.50 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| Erythrabyssin II | 5086400 | Click to see | 392.50 | unknown | https://doi.org/10.1016/0031-9422(88)83103-0 |
| Phaseollidin | 119268 | Click to see | 324.40 | unknown | https://doi.org/10.1016/S0031-9422(97)00071-X |
| Sandwicensin | 467498 | Click to see | 338.40 | unknown | https://doi.org/10.1016/0031-9422(88)83103-0 |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols | |||||
| 4-(2-Hydroxy-3-methylbut-3-enyl)-6-(3-phenylprop-2-enyl)benzene-1,3-diol | 162930190 | Click to see CC(=C)C(CC1=C(C=C(C(=C1)CC=CC2=CC=CC=C2)O)O)O | 310.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| 4-(3-Methylbut-2-enyl)-6-(3-phenylprop-2-enyl)benzene-1,3-diol | 162842648 | Click to see | 294.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| 4-(3-methylbut-2-enyl)-6-[(E)-3-phenylprop-2-enyl]benzene-1,3-diol | 14630590 | Click to see CC(=CCC1=C(C=C(C(=C1)CC=CC2=CC=CC=C2)O)O)C | 294.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| 4-[(2R)-2-hydroxy-3-methylbut-3-enyl]-6-[(E)-3-phenylprop-2-enyl]benzene-1,3-diol | 163195329 | Click to see CC(=C)C(CC1=C(C=C(C(=C1)CC=CC2=CC=CC=C2)O)O)O | 310.40 | unknown | https://doi.org/10.1016/S0031-9422(00)89548-5 |
| > Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids | |||||
| (8R,9S)-5-hydroxy-8,9-dimethyl-6-(3-methylbut-2-enyl)-4-phenyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione | 11811548 | Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C(=C2CC=C(C)C)O)C | 404.50 | unknown |
https://doi.org/10.1248/CPB.58.1119 https://doi.org/10.1016/S0031-9422(00)80457-4 |
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