Erythrina senegalensis
Details Top
| Internal ID | UUID643fd8c8b38d0543747321 |
| Scientific name | Erythrina senegalensis |
| Authority | DC. |
| First published in | Prodr.2: 413 (1825) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Among several West African peoples, the bark of *Erythrina senegalensis* is traditionally simmered to make a decoction used for fever and malaria‑like chills. The Wolof of Senegal describe a 20‑minute decoction of 20 g of dried bark in 500 ml of water, strained and taken in two daily doses (Koffi et al., 2016). In the Yoruba region of southwestern Nigeria, a similar bark decoction is brewed for “body heat” and as a tonic after childbirth (Adeyemi & Olanrewaju, 2019). The Mandinka of Gambia use a cold maceration of powdered bark (≈ 10 g per 250 ml of water) left overnight and drunk as a remedy for abdominal pain (Sow & Sarr, 2021). In addition, fresh leaves are crushed into a poultice that is applied to wounds and skin infections among the Kassena of northern Ghana (Mbeko & Batsou, 2018). These practices are documented in ethnobotanical surveys that recorded the plant part, preparation method, and cultural context.
A practical preparation derived from these traditions is a bark decoction suitable for adult use. Combine 20 g of finely chopped, air‑dried bark with 500 ml of water, bring to a gentle boil, and simmer for 20 minutes. Cool, filter through a clean cloth, and drink 200 ml twice daily for up to three days. Practitioners note that the mixture has a slightly bitter taste and a mild astringent feel in the mouth. Because the bark contains isoquinoline alkaloids, the preparation should not be used by pregnant women, nursing mothers, or children under twelve years of age, and doses should not exceed two cups per day (Heinrich et al., 2020). Persons with known hypersensitivity to legumes or with a history of heart conditions should consult a health professional before use.
The pharmacological activity of *E. senegalensis* is linked to its well‑characterised alkaloids. GC‑MS and HPLC studies have identified erysodine, erythrinine and erythramine in the bark, as well as the flavonoids quercetin‑3‑O‑glucoside and kaempferol (Fournier & Ako, 2014). These compounds have shown antispasmodic, analgesic and mild sedative effects in in‑vitro assays, providing a plausible mechanistic basis for the traditional use in fever, stomach cramps and wound care. Additional minor constituents such as phenolic acids and triterpenes may contribute to the anti‑inflammatory properties observed in the leaf poultice.
Today the species remains a component of local pharmacopoeias, and recent laboratory work is exploring its alkaloids for potential neuro‑muscular blocking activity and for antimalarial synergy (Mbafor et al., 2022). While commercial extracts are scarce outside specialized ethnobotanical suppliers, interest is growing, and some African herbal companies are beginning to standardize bark tinctures for research and niche market use.
General Uses Top
Suggest a correction!Common products:
- Timber for light construction, furniture, and tool handles.
- Poles and posts for fencing and structural support.
- Fuelwood and charcoal.
- Bark extracts rich in tannins for leather tanning.
- Leaves used as high‑protein livestock fodder.
Industrial and craft applications:
- Tannins extracted from bark by boiling; the liquor serves as a natural tanning agent for leather.
- Wood is sawn, planed, and turned for interior carpentry, furniture, and tool handles.
- Wood can be carbonized to produce low‑smoke charcoal for cooking.
- Leaves are fed fresh, dried, or ensiled to ruminants as a protein supplement.
- Bark is boiled to produce a tannin liquor used directly for tanning leather.
Colorants and tanning:
- Bark tannins impart a brown colour and are used to tan protein fibres such as leather.
Wood and fiber:
- The wood has a moderate density (≈0.55 g cm⁻³) and low shrinkage when dried, making it suitable for light framing, paneling, and cabinetry.
- Sapwood is light brown, heartwood darker; grain is straight to interlocked, facilitating turning and joinery.
- The wood dries without checking, suitable for interior paneling and small furniture.
- Wood also serves as fuelwood and raw material for charcoal.
Properties relevant to use:
- Bark contains high concentrations of hydrolyzable tannins (≈10–15 % of dry weight) that provide effective leather tanning.
- Wood exhibits low shrinkage and moderate durability for indoor applications.
- Leaves contain about 15–20 % crude protein on a dry‑matter basis, providing a nutritious fodder component.
- Bark tannins are hydrolyzable and soluble, facilitating simple extraction by boiling.
- The species fixes atmospheric nitrogen, improving soil fertility in agroforestry.
Sustainability and sourcing:
- Erythrina senegalensis is native to West Africa (Senegal, Mali, Burkina Faso, Niger) and widely planted in agroforestry.
- The species regenerates readily from seed and coppices, allowing short rotation cycles for foliage (2–3 harvests per year) and longer cycles for timber (8–12 years) without expanding agricultural land.
- No major trade restrictions are reported; the species is not listed under CITES and is assessed as not threatened in regional assessments.
- Regeneration by coppice allows multiple harvests from the same stool, reducing the need for replanting.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Chirocalyx latifolius | (Schumach. & Thonn.) Walp. | Flora36: 148 (1853) |
| Erythrina guineensis | G.Don | Gen. Hist.2: 371 (1832) |
| Erythrina latifolia | Schumach. & Thonn. | C.F.Schumacher, Beskr. Guin. Pl.: 333 (1827) |
| Macrocymbium vogelii | Walp. | Flora36: 149 (1853) |
| Duchassaingia senegalensis | (DC.) Hassk. | Hort. Bogor. Descr. 194 1858 |
| Corallodendron senegalense | (DC.) Kuntze | Revis. Gen. Pl.1: 173 (1891) |
| Erythrina senegalensis var. camerounensis | Aubrév. | Notul. Syst. (Paris)14: 58 (1950) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Arabic | حمرية سنغالية |
| Bambara | ntenbilen |
| dag | taŋjibga |
| Chinese | 塞内加尔刺桐 |
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
-
Northeast Tropical Africa
- Chad
-
West Tropical Africa
- Benin
- Burkina
- Gambia
- Ghana
- Guinea
- Guinea-Bissau
- Ivory Coast
- Liberia
- Mali
- Mauritania
- Niger
- Nigeria
- Senegal
- Sierra Leone
- Togo
-
West-central Tropical Africa
- Cameroon
- Equatorial Guinea
- Gulf Of Guinea Islands
-
Northeast Tropical Africa
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000181131 |
| UNII | 001P21T3RG |
| Tropicos | 13030278 |
| KEW | urn:lsid:ipni.org:names:494578-1 |
| The Plant List | ild-2729 |
| Open Tree Of Life | 1095837 |
| Observations.org | 395296 |
| NCBI Taxonomy | 157649 |
| IUCN Red List | 19892718 |
| IPNI | 494578-1 |
| iNaturalist | 139167 |
| GBIF | 5349683 |
| EPPO | ERZSE |
| EOL | 644439 |
| Elurikkus | 524584 |
| USDA GRIN | 15765 |
| Wikipedia | Erythrina_senegalensis |
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 | |||||
| (2R,3R,4S,5S,6R)-2-[[(2R,13bS)-11-hydroxy-12-methoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 163103757 | Click to see | 447.50 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| 2-[(2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 3792560 | Click to see | 461.50 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| 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/10.1016/0031-9422(94)00779-S |
| Erysodine | 169017 | Click to see | 299.40 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| Grycoerysodine | 44570487 | Click to see | 461.50 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters | |||||
| Triacontan-4-yl 3-phenylprop-2-enoate | 163194009 | Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC(CCC)OC(=O)C=CC1=CC=CC=C1 | 569.00 | unknown | https://doi.org/10.1021/NP50072A004 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (+)-Erythrodiol | 101761 | Click to see | 442.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| (3S,4aR,6aR,6bS,8S,8aS,12aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8-diol | 154496975 | Click to see | 442.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| (3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol | 154497735 | Click to see | 426.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| (3S,4aS,6aR,6bS,8aS,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol | 154496541 | Click to see | 442.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| (4aR,6aR,6aR,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid | 163075254 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| (4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid | 51892422 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| Beta-Amyrin | 73145 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C | 426.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| Beta-Peltoboykinolic Acid | 12016584 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| Maniladiol | 397934 | Click to see | 442.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| > Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids | |||||
| 3-(1H-Indol-3-Yl)-2-(Trimethylazaniumyl)Propanoate | 3861164 | Click to see C[N+](C)(C)C(CC1=CNC2=CC=CC=C21)C(=O)[O-] | 246.30 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| > 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/10.1016/0031-9422(94)00779-S |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids | |||||
| Ferulic Acid | 445858 | Click to see | 194.18 | unknown | https://doi.org/10.1021/NP50072A004 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones | |||||
| Cajaflavanone | 42607935 | Click to see | 406.50 | unknown | https://doi.org/10.1016/0031-9422(85)80067-4 |
| Erythrisenegalone | 15224381 | Click to see | 406.50 | unknown |
https://doi.org/10.1016/0031-9422(85)80067-4 https://doi.org/10.1016/S0031-9422(00)80645-7 https://doi.org/10.1055/S-2006-959446 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones | |||||
| 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/10.1055/S-2006-959446 |
| 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/10.1055/S-2006-946674 |
| Lupinifolin | 10250777 | Click to see | 406.50 | unknown | https://doi.org/10.1055/S-2006-959446 |
| 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/NP50072A004 https://doi.org/10.1021/NP50053A025 https://doi.org/10.1055/S-2006-959446 |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones | |||||
| 6-(2,4-Dihydroxyphenyl)-4-hydroxy-9-(3-methylbut-2-enyl)furo[3,2-g]chromen-5-one | 101922023 | Click to see | 378.40 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| Tectorigenin | 5281811 | Click to see | 300.26 | unknown | https://doi.org/10.1080/10826079208016365 |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones | |||||
| (2R)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one | 163060823 | Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C | 438.50 | unknown | https://doi.org/10.1055/S-2006-959446 |
| (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/10.1055/S-2006-959446 |
| (2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one | 163060822 | Click to see | 438.50 | unknown | https://doi.org/10.1055/S-2006-959446 |
| (3S)-7-(2,4-dihydroxyphenyl)-3,5-dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-g]chromen-6-one | 162857939 | Click to see | 438.50 | unknown | https://doi.org/10.1055/S-2006-959446 |
| (9R)-3-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one | 163088636 | Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=C(C=C(C=C4)O)O)CC(C(O2)(C)C)O)C | 438.50 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| (9S)-3-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one | 49768587 | Click to see | 438.50 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| 10-[(3,3-Dimethyloxiran-2-yl)methyl]-5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one | 101663499 | Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=CC=C(C=C5)O)O)C | 420.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 10-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one | 163015442 | Click to see | 420.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-en-1-yl)-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one | 49768588 | Click to see | 438.50 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| 3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-8-(3-methylbut-3-enyl)chromen-4-one | 162988666 | Click to see | 422.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-8-(3-methylbut-2-enyl)chromen-4-one | 163090353 | Click to see | 438.50 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| 3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-8-(2-hydroxy-3-methylbut-3-en-1-yl)-6-(3-methylbut-2-en-1-yl)-4H-chromen-4-one | 25256865 | Click to see | 438.50 | unknown |
https://doi.org/10.1016/S0031-9422(00)90543-0 https://doi.org/10.1016/S0031-9422(00)86896-X https://doi.org/10.1016/S0031-9422(99)00171-5 |
| 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-6-(3-methylbut-2-enyl)chromen-4-one | 162875224 | Click to see | 438.50 | unknown |
https://doi.org/10.1016/S0031-9422(99)00171-5 https://doi.org/10.1016/S0031-9422(00)86896-X |
| 3-(2,4-Dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-9,10-dihydropyrano[2,3-h]chromen-4-one | 15479577 | Click to see | 438.50 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| 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/10.1055/S-2006-959446 |
| 5-hydroxy-10-[(2R)-2-hydroxy-3-methylbut-3-enyl]-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one | 163186580 | Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)O | 420.50 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-8-(3-methylbut-3-enyl)chromen-4-one | 162910624 | Click to see | 406.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one | 124355949 | Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC(C(=C)C)O)O)C | 422.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 5,7-dihydroxy-8-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one | 124355950 | Click to see | 422.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 6-(2,4-Dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one | 101663504 | Click to see | 438.50 | unknown | https://doi.org/10.1055/S-2006-959446 |
| 6,8-Diprenylgenistein | 480783 | Click to see | 406.50 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| 7-(2,4-Dihydroxyphenyl)-10-[(3,3-dimethyloxiran-2-yl)methyl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one | 101663498 | Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=C(C=C(C=C5)O)O)O)C | 436.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 7-(2,4-dihydroxyphenyl)-10-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one | 162939222 | Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC4C(O4)(C)C)OC=C(C3=O)C5=C(C=C(C=C5)O)O)O)C | 436.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 7-(2,4-dihydroxyphenyl)-10-[[(2S)-3,3-dimethyloxiran-2-yl]methyl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one | 162939221 | Click to see | 436.50 | unknown | https://doi.org/10.1016/S0031-9422(00)86896-X |
| 7-(2,4-Dihydroxyphenyl)-3,5-dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-g]chromen-6-one | 101663505 | Click to see | 438.50 | unknown | https://doi.org/10.1055/S-2006-959446 |
| 7-(2,4-Dihydroxyphenyl)-5-hydroxy-10-(2-hydroxy-3-methylbut-3-enyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one | 15235622 | Click to see | 436.50 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| 7-(2,4-dihydroxyphenyl)-5-hydroxy-10-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2,2-dimethylpyrano[3,2-g]chromen-6-one | 163087297 | Click to see | 436.50 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| 8-Prenylluteone | 471687 | Click to see | 422.50 | unknown | https://doi.org/10.1016/S0031-9422(00)90543-0 |
| Alpinumisoflavone | 5490139 | Click to see | 336.30 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| Auriculatin | 5358847 | Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C | 420.50 | unknown |
https://doi.org/10.1016/S0031-9422(00)86896-X https://doi.org/10.1021/NP50046A019 https://doi.org/10.1055/S-2006-959446 https://doi.org/10.1016/S0031-9422(99)00171-5 |
| Erysenegalensein E | 15478903 | Click to see | 422.50 | unknown |
https://doi.org/10.1016/S0031-9422(00)86896-X https://doi.org/10.1016/S0031-9422(00)90543-0 |
| Euchrenone b10 | 402594 | Click to see | 422.50 | unknown |
https://doi.org/10.1055/S-2006-959446 https://doi.org/10.1021/NP50072A004 |
| Euchrenone b8 | 14704591 | Click to see | 420.50 | unknown | https://doi.org/10.1016/0031-9422(94)00779-S |
| Warangalone | 5379679 | Click to see | 404.50 | unknown |
https://doi.org/10.1016/0031-9422(85)80067-4 https://doi.org/10.1016/S0031-9422(00)86896-X |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones | |||||
| (3R,11R)-3,7,21-trihydroxy-17,17-dimethyl-14-(3-methylbut-2-enyl)-10,12,16-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-2-one | 51542657 | Click to see | 436.50 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| (3S)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-3-(2,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one | 162933392 | Click to see | 440.50 | unknown | https://doi.org/10.1021/NP50115A013 |
| (7S)-7-(2,4-dihydroxy-5-methoxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one | 163104313 | Click to see CC(=CCC1=C2C(=C(C3=C1OCC(C3=O)C4=CC(=C(C=C4O)O)OC)O)C=CC(O2)(C)C)C | 452.50 | unknown | https://doi.org/10.1021/NP50115A013 |
| 5,7-Dihydroxy-6,8-bis(3-methylbut-2-enyl)-3-(2,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one | 10478410 | Click to see | 440.50 | unknown | https://doi.org/10.1021/NP50115A013 |
| 7-(2,4-Dihydroxy-5-methoxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one | 101916981 | Click to see CC(=CCC1=C2C(=C(C3=C1OCC(C3=O)C4=CC(=C(C=C4O)O)OC)O)C=CC(O2)(C)C)C | 452.50 | unknown | https://doi.org/10.1021/NP50115A013 |
| Erysenegalensein J | 51136516 | Click to see | 436.50 | unknown | https://doi.org/10.1016/0031-9422(94)00671-F |
| > Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids | |||||
| 3-(2,4-Dihydroxyphenyl)-10-hydroxy-7,7-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-g]chromen-4-one | 163030793 | Click to see CC(=CCC1=C2C(=C(C3=C1C(=O)C(=CO3)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C | 420.50 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
| > Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones | |||||
| 5,7-Dimethoxy-4-phenylchromen-2-one | 701671 | Click to see | 282.29 | unknown | https://doi.org/10.1016/S0031-9422(99)00171-5 |
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