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

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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

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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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Structures of new Erythrinan alkaloids and nitric oxide production inhibitors from Erythrina crista-galli. Ozawa M, Kawamata S, Etoh T, Hayashi M, Komiyama K, Kishida A, Kuroda C, Ohsaki A Chem Pharm Bull (Tokyo) 01-Aug-2010
doi:10.1248/CPB.58.1119
PMID:20686273
Erythlaurine and Erythramide, Two New Erythrinan Alkaloids Possessing a Directrly Attached C1-Unit to the Aromatic Ring Motoharu Ju-ichi, Yukari Fujitani, Tetsuro Shingu, Hiroshi Furukawa The Japan Institute of Heterocyclic Chemistry 10-Mar-2009
doi:10.3987/R-1981-04-0555
Antimicrobial Agents from Higher Plants. Erycristagallin, a New Pterocarpene from the Roots of the Bolivian Coral Tree, Erythrina crista-galli Lester A. Mitscher, Jeffrey A. Ward, Steven Drake, Gollapudi S. Rao The Japan Institute of Heterocyclic Chemistry 19-Feb-2009
doi:10.3987/R-1984-08-1673
Alkaloidal Constituents of Erythrina crista-galli Flowers Amrik Singh Chawla, M. P. Gupta, Anthony H. Jackson American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50054A024
Direct analysis of aromatic diene Erythrina alkaloids by capillary GC-MS P Mantle Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00764-K
Three pterocarpans from Erythrina crista-galli Hitoshi Tanaka, Toshihiro Tanaka, Hideo Etoh Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00071-X
(S)-Norreticuline is the precursor for the biosynthesis of Erythrina alkaloids Ulrich H. Maier, Meinhart H. Zenk Royal Society of Chemistry (RSC) 26-Jul-2002
doi:10.1039/A706595G
Erycristin, a new antimicrobial petrocarpan from Erythrina crista-galli Lester A. Mitscher, Sitaraghav R. Gollapudi, David C. Gerlach, Steven D. Drake, Eduardo A. Ve´liz, Jeffrey A. Ward Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83103-0
8-Oxo-erythraline, a naturally-occurring principal alkaloid from Erythrina crista-galli Peter G. Mantle, Ian Laws, David A. Widdowson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80457-4
Biosynthesis of radiolabelled alkaloids from 14C-tyrosine in Erythrina crista-galli Peter G. Mantle, Mark J. Coleman Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83452-4
Three new cinnamylphenols in heartwood of Erythrina crista-galli Munekazu Iinuma, Yasutoshi Okawa, Toshiyuki Tanaka Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89548-5
Biosynthesis of Erythrina alkaloids in Erythrina crista-galli. Maier UH, Rödl W, Deus-Neumann B, Zenk MH Phytochemistry 01-Oct-1999
doi:10.1016/S0031-9422(99)00230-7
PMID:10501023

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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