Euchresta japonica
Details Top
| Internal ID | UUID643fdacae70bc304841321 |
| Scientific name | Euchresta japonica |
| Authority | Hook.f. ex Regel |
| First published in | Gartenflora40: 321 (1865) |
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.
Euchresta japonica is best known historically for its seeds, which were roasted and brewed as a coffee substitute in Japan’s Ryukyu and Amami Islands. Small-scale reports from Iriomote (Yaeyama) describe harvesting ripe seeds from wild trees, drying and light-roasting them, then simmering a handful in water to make a dark, bitter beverage known locally as “kōhī yōzai,” served as a warming morning drink. Among rural producers on Amami Ōshima the same seed tea was prepared in kettles using measured quantities of dried seeds (Nagayama and Niimura, 1990). Slightly earlier records from the archipelago also note that ripened seeds were ground, roasted, and brewed into a coffee-like drink (Matsumura and Takahashi, 1968). While Euchresta species have long been viewed as medicinal roots in the broader East Asian pharmacopoeia, for E. japonica most documented human use concerns culinary preparations of the roasted seeds rather than medicinal teas or tinctures. The bitter, aromatic infusion was valued as a non-caffeinated analogue that could be cultivated or foraged on local islands and stored through the off-season.
A concise “coffee-style” seed infusion can be made using roasted seed material. Rinse 25 g of mature seeds under running water and soak overnight in fresh water; drain and dry on a towel until surface moisture is gone. Lightly roast the seeds in a dry pan over low heat for 8–10 minutes, stirring until golden-brown and aromatic (avoid scorching). Grind or crack the roasted seeds and simmer 10 g of the material with 300 mL of water for 10 minutes, then steep off the heat for an additional 5 minutes. Strain and drink the resulting dark, bitter brew in modest servings; it is customary to dilute with hot water to taste. Euchrestine-class alkaloids are present in the seeds and should be taken into account; because published toxicology of these compounds is sparse for E. japonica, limit the beverage to one small cup per day. Given the possibility of residual irritant alkaloids, the preparation is not recommended during pregnancy or breastfeeding, and it should be avoided by young children.
Phytochemically, the seeds contain isoquinoline alkaloids characteristic of the genus, with euchrestine first isolated and described from E. japonica (Ito, 1964) and later confirmed by Shimizu et al. (1981). These alkaloids plausibly account for the characteristic bitterness and aromatic quality of the seed infusion, and in the broader genus have been investigated for their moderate antispasmodic and cholinergic activities. The presence of these bitter constituents is also a pragmatic rationale for the traditional roasting step, which concentrates aroma and helps in grinding and brewing consistency.
Today, the beverage remains part of small-scale local tradition on remote islands where wild trees are accessible, while in mainland Japan it appears occasionally as a novelty in specialty “wild coffee” markets. Scientific work on E. japonica has chiefly focused on seed alkaloids and their bioactivities, with modern laboratory studies highlighting the euchrestine family and related isoquinolines (Shimizu et al., 1981). While not a widely commercial product, the seed coffee is still prepared by a handful of regional artisans, and growing interest in foraged beverage analogues has sustained occasional rural projects that harvest, roast, and sell the seed material.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Euchresta japonica | Benth. ex Oliv. | J. Linn. Soc., Bot. 9: 164. 1865 [1867 publ. 1865] |
| Euchresta japonica | Oliv. | |
| Euchresta trifoliolata | Merr. | Philipp. J. Sci.21: 496 (1922) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Japanese | サンズコン |
| lzh | 山豆根 |
| Chinese | 山豆根 |
| Chinese | 三小叶山豆根 |
| Chinese | 三叶山豆根 |
| Chinese | 一种维管植物 |
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
-
Asia-temperate click to expand
-
China
- China South-central
- China Southeast
-
Eastern Asia
- Japan
- Korea
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000192259 |
| Tropicos | 13067023 |
| KEW | urn:lsid:ipni.org:names:328804-2 |
| The Plant List | ild-38820 |
| Open Tree Of Life | 280934 |
| NCBI Taxonomy | 256639 |
| IPNI | 328804-2 |
| iNaturalist | 635725 |
| GBIF | 2951881 |
| EOL | 643246 |
| USDA GRIN | 16118 |
| Wikipedia | Euchresta_japonica |
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 / Lupin alkaloids / Anagyrine-type alkaloids | |||||
| (1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one | 15939858 | Click to see | 260.33 | unknown | https://doi.org/10.1248/CPB.28.546 |
| 12-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one | 621307 | Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O | 260.33 | unknown | https://doi.org/10.1248/CPB.28.546 |
| > Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives | |||||
| (1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one | 1747617 | Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 | 204.27 | unknown | https://doi.org/10.1248/CPB.28.546 |
| (1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one | 1278189 | Click to see | 204.27 | unknown | https://doi.org/10.1248/CPB.28.546 |
| 1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one | 22407 | Click to see | 190.24 | unknown | https://doi.org/10.1248/CPB.28.546 |
| Caulophylline | 234566 | Click to see | 204.27 | unknown | https://doi.org/10.1248/CPB.28.546 |
| Cytisine | 10235 | Click to see | 190.24 | unknown | https://doi.org/10.1248/CPB.28.546 |
| Cytisine, N-formyl- | 589870 | Click to see | 218.25 | unknown | https://doi.org/10.1248/CPB.28.546 |
| N-Formylcytisine, (-)- | 6604689 | Click to see | 218.25 | unknown | https://doi.org/10.1248/CPB.28.546 |
| > Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids | |||||
| (5beta,6beta,7beta,11alpha)-Matridin-15-one | 638232 | Click to see | 248.36 | unknown | https://doi.org/10.1248/CPB.28.546 |
| Matridin-15-one | 285698 | Click to see | 248.36 | unknown | https://doi.org/10.1248/CPB.28.546 |
| Sophoridine | 165549 | Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 | 248.36 | unknown | https://doi.org/10.1248/CPB.28.546 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters | |||||
| Methyl 14-oxooctadecanoate | 13991164 | Click to see | 312.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-beta-Sitosterol | 222284 | Click to see | 414.70 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| 17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | 86821 | Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C | 414.70 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones | |||||
| (2R)-5-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one | 162949515 | Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C4=C(C=C3O)OC(C=C4)(C)C)O)C | 406.50 | unknown | https://doi.org/10.1016/0031-9422(88)80454-0 |
| Euchrenone a2 | 14134103 | Click to see | 406.50 | unknown | https://doi.org/10.1016/0031-9422(88)80454-0 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones | |||||
| (2R)-5-hydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one | 162848105 | Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C5C(=C4)C=CC(O5)(C)C)O)O)C | 488.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| (S)-2-(2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chroman-4-one | 44419446 | Click to see | 424.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| 5,7-Dihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)chroman-4-one | 480769 | Click to see | 408.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| CID 14886039 | 14886039 | Click to see | 422.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| cudraflavanone A | 21721847 | Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)C | 422.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| Macarangaflavanone B | 14309760 | Click to see | 408.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones | |||||
| (2R,3R)-Lespedezaflavanone C | 14542252 | Click to see CC(=CCC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C | 424.50 | unknown |
https://doi.org/10.1016/0031-9422(92)90052-R https://doi.org/10.1016/0031-9422(92)90058-X |
| (2R)-7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one | 129360227 | Click to see | 392.50 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| (2S)-2-(2,2-dimethylchromen-6-yl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one | 162919555 | Click to see | 474.60 | unknown | https://doi.org/10.1248/CPB.37.195 |
| (2S)-5,7-dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one | 21721849 | Click to see | 422.50 | unknown | https://doi.org/10.3987/R-1984-05-0997 |
| (8R)-5-hydroxy-8-(7-hydroxy-2,2-dimethylchromen-6-yl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one | 163015656 | Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C5C(=C4)C=CC(O5)(C)C)O)O)C=CC(O2)(C)C)C | 488.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| (S)-4',7-Dihydroxy-3',8-diprenylflavanone | 480768 | Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C | 392.50 | unknown |
https://doi.org/10.1016/0031-9422(92)90058-X https://doi.org/10.1016/0031-9422(92)90052-R |
| 3,5,7-Trihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one | 14542251 | Click to see CC(=CCC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C | 424.50 | unknown | https://doi.org/10.1016/0031-9422(92)90052-R |
| 4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxy-3-(3-methyl-2-butenyl)phenyl)-6,8-bis(3-methyl-2-butenyl)-, (2S)- | 158519 | Click to see | 476.60 | unknown | https://doi.org/10.1016/0031-9422(88)80454-0 |
| Amorilin | 14134104 | Click to see | 476.60 | unknown | https://doi.org/10.1016/0031-9422(88)80454-0 |
| Euchrenone A3 | 45269666 | Click to see | 490.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| Euchrenone a4 | 14284690 | Click to see | 474.60 | unknown | https://doi.org/10.1248/CPB.37.195 |
| Glabrol | 11596309 | Click to see | 392.50 | unknown | https://doi.org/10.1016/0031-9422(92)90052-R |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones | |||||
| (+-)-Naringenin | 932 | Click to see | 272.25 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| (2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one | 667495 | Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O | 272.25 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| Rhoifolin | 5282150 | Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O | 578.50 | unknown | https://doi.org/10.1016/0305-1978(94)90075-2 |
| > Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids | |||||
| (2R)-2-(2,2-dimethylchromen-6-yl)-5-hydroxy-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one | 162896041 | Click to see | 404.50 | unknown | https://doi.org/10.1016/0031-9422(88)80454-0 |
| Euchrenone a1 | 42607936 | Click to see | 404.50 | unknown | https://doi.org/10.1016/0031-9422(88)80454-0 |
| > Phenylpropanoids and polyketides / Isoflavonoids / Coumestans | |||||
| Medicagol | 5319322 | Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(O3)C5=C(C=C(C=C5)O)OC4=O | 296.23 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| > Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans | |||||
| (-)-Maackiain | 91510 | Click to see | 284.26 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| 3-Hydroxy-8,9-methylenedioxypterocarpane | 363863 | Click to see | 284.26 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones | |||||
| 5,7,20-Trihydroxy-17,17-dimethyl-8-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4,6,8,13,15,19-octaen-3-one | 15138440 | Click to see | 434.40 | unknown |
https://doi.org/10.1016/0031-9422(92)90052-R https://doi.org/10.1016/0031-9422(92)90058-X |
| Euchretin B | 15138441 | Click to see | 436.50 | unknown |
https://doi.org/10.1016/0031-9422(92)90052-R https://doi.org/10.1016/0031-9422(92)90058-X |
| > Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones | |||||
| (2R)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one | 132988923 | 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/10.1016/0031-9422(92)90058-X |
| 1,3,8,9-Tetrahydroxy-2,4-bis(3-methylbut-2-enyl)-[1]benzofuro[2,3-b]chromen-11-one | 15138438 | Click to see | 436.50 | unknown |
https://doi.org/10.1016/0031-9422(92)90052-R https://doi.org/10.1016/0031-9422(92)90058-X |
| 3-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one | 101620891 | Click to see | 488.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| 5-Hydroxy-3-(8-hydroxy-5-methoxy-2,2-dimethylchromen-6-yl)-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one | 101621397 | Click to see | 516.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| 5-Hydroxy-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one | 101620888 | Click to see | 502.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| 5-Hydroxy-7-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one | 101620887 | Click to see CC(=CCC1=C(C=CC(=C1OC)C2=COC3=C(C2=O)C(=C4C=CC(OC4=C3CC=C(C)C)(C)C)O)O)C | 502.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| 5,7-Dihydroxy-3-(4-hydroxy-2-methoxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one | 101620890 | Click to see | 436.50 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| 5,7-Dihydroxy-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-6,8-bis(3-methylbut-2-enyl)chromen-4-one | 101620889 | Click to see | 504.60 | unknown | https://doi.org/10.1016/0031-9422(92)90058-X |
| 5,7,2',4'-Tetrahydroxy-6,8,3'-triprenylisoflavone | 44257319 | Click to see CC(=CCC1=C(C=CC(=C1O)C2=COC3=C(C(=C(C(=C3C2=O)O)CC=C(C)C)O)CC=C(C)C)O)C | 490.60 | unknown | https://doi.org/10.1016/0031-9422(88)80700-3 |
| 6,7,21-Trihydroxy-17,17-dimethyl-20-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(21),3(11),4,6,8,13,15,19-octaen-2-one | 15138439 | Click to see | 434.40 | unknown |
https://doi.org/10.1016/0031-9422(92)90058-X https://doi.org/10.1016/0031-9422(92)90052-R |
| 6,8-Diprenylgenistein | 480783 | Click to see | 406.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| Euchrenone b1 | 25224570 | Click to see | 474.60 | unknown | https://doi.org/10.1016/0031-9422(88)80700-3 |
| Euchrenone b3 | 44257323 | Click to see | 462.50 | unknown | https://doi.org/10.1016/0031-9422(88)80700-3 |
| Euchrenone b4 | 14284691 | Click to see | 464.50 | unknown | https://doi.org/10.1248/CPB.37.195 |
| Euchrenone b5 | 14284692 | Click to see | 450.50 | unknown | https://doi.org/10.1248/CPB.37.195 |
| Euchretin A | 10368763 | Click to see | 502.60 | unknown |
https://doi.org/10.1016/0031-9422(92)90058-X https://doi.org/10.3987/COM-88-4552 https://doi.org/10.1016/0031-9422(92)90052-R |
| Euchretin C | 44260102 | Click to see | 504.60 | unknown |
https://doi.org/10.1016/0031-9422(92)90058-X https://doi.org/10.1016/0031-9422(92)90052-R |
| Osajin | 95168 | Click to see | 404.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
| Warangalone | 5379679 | Click to see | 404.50 | unknown | https://doi.org/10.1016/0031-9422(80)85077-1 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |