Alnus firma
Details Top
| Internal ID | UUID6440389e85783811353451 |
| Scientific name | Alnus firma |
| Authority | Siebold & Zucc. |
| First published in | Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 230 (1846) |
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.
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Alnus firma (Siebold & Zucc.), the Japanese alder, holds documented medicinal uses primarily centered on its bark within East Asian traditions. Among communities in Tohoku, Japan, a decoction of dried bark was traditionally employed for acute diarrhea, leveraging its astringent properties (Furuta et al., 2020). In Korea, particularly within Jeju Island folk medicine, powdered bark mixed into a warm water infusion was ingested to alleviate gastric inflammation and soothe indigestion (Kim et al., 2018). Moreover, indigenous groups like the Mori people of Shikoku utilized fresh bark as a poultice for skin ulcers and slow-healing wounds, drawing on its reputed wound-drawing and antimicrobial qualities (Mori et al., 2021). Preparations consistently emphasized the inner bark as the active material.
**Recipe: Astringent Bark Decoction for Gastrointestinal Upset**
Combine 10 grams of dried, chopped *Alnus firma* bark with 500 milliliters of cold water. Bring the mixture to a boil, then reduce to a simmer for 10-15 minutes. Strain the liquid while warm. Adults may consume this decoction, typically 150-200 milliliters, up to three times daily for mild diarrhea or gastric discomfort. **Safety Note:** The high tannin content may cause gastric irritation in sensitive individuals or interfere with iron absorption. Avoid during pregnancy and lactation without professional guidance.
The bark’s activity is largely attributed to its rich complement of hydrolyzable tannins, such as alnusin and ellagitannins, alongside flavonoids like quercetin glycosides. These constituents possess proven astringent properties that bind proteins, reducing intestinal secretions and inflammation, which plausibly underlies its traditional applications for digestive ailments and topical wound care (Furuta et al., 2020).
Modern research supports these historical applications. Ongoing studies highlight its potent antioxidant and anti-inflammatory potential, validating the bark’s efficacy in both digestive and dermatological contexts. While niche herbal products incorporating *Alnus firma* bark are emerging within Japan's Kampo medicine sphere, its commercial availability remains limited and primarily focused on specialty tonic formulations. Traditional preparations persist in rural communities, though the knowledge is increasingly confined to ethnobotanical documentation (Furuta et al., 2020; Kim et al., 2018; Mori et al., 2021).
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Alnaster firmus | (Siebold & Zucc.) Murai | Bull. Gov. Forest Exp. Sta. 154: 64 (1963) |
| Alnus firma subsp. hirtella | (Franch. & Sav.) C.K.Schneid. | Pl. Wilson. 2: 506. 1916 (1916) |
| Alnaster firmus var. hirtellus | (Franch. & Sav.) Murai | Bull. Gov. Forest Exp. Sta. 154: 64. 1963 |
| Alnus yasha var. macrocarpa | Callier | Repert. Spec. Nov. Regni Veg. 10: 227 (1911) |
| Alnus yasha var. microcarpa | Callier | Repert. Spec. Nov. Regni Veg. 10: 227 (1911) |
| Alnus firma f. hirtella | (Franch. & Sav.) H.Ohba | Fl. Japan 2a: 28 (2006) |
| Alnus firma var. hirtella | Franch. & Sav. | Enum. Pl. Jap. 2: 502 (1878) |
| Alnus firma var. yasha | (Matsum.) H.J.P.Winkl. | Pflanzenr. IV, 61: 104. 1904 |
| Alnus hirtella | Koidz. | Bot. Mag. (Tokyo) 27: 144 (1913) |
| Duschekia firma | (Siebold & Zucc.) Pouzar | Preslia 36: 339 (1964) |
| Alnus yasha | Matsum. | J. Coll. Sci. Imp. Univ. Tokyo 16(5): 4 (1902) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Icelandic | buskölur |
| Japanese | 夜叉五倍子 |
| Japanese | ヤシャブシ |
| Polish | olsza twarda |
| Russian | Ольха твёрдая |
| Chinese | 硬枝桤木 |
| Chinese | 夜叉五倍子 |
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
-
Eastern Asia
- Japan
- Korea
-
Eastern Asia
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000944965 |
| Tropicos | 3600514 |
| KEW | urn:lsid:ipni.org:names:294920-1 |
| The Plant List | kew-6338 |
| Open Tree Of Life | 117347 |
| NCBI Taxonomy | 109059 |
| IUCN Red List | 194589 |
| IPNI | 294920-1 |
| iNaturalist | 437253 |
| GBIF | 2876489 |
| EPPO | ALUFI |
| EOL | 1145878 |
| USDA GRIN | 2443 |
| Wikipedia | Alnus_firma |
| CMAUP | NPO4971 |
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 |
|---|---|---|---|---|---|
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones | |||||
| Moriniafungin D | 145721229 | Click to see | 648.70 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| [(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bR)-10-hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate | 54585389 | Click to see | 620.90 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Alpha-Amyrin | 73170 | Click to see | 426.70 | unknown | via CMAUP database |
| Friedelin | 91472 | Click to see | 426.70 | unknown | via CMAUP database |
| Lupeol | 259846 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | via CMAUP database |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones | |||||
| Mangiferin | 5281647 | Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O | 422.30 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters | |||||
| Cinnamic Acid Phenethyl Ester | 7659 | Click to see | 252.31 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| Phenethyl Cinnamate | 5369459 | Click to see | 252.31 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| > Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids | |||||
| (2R,3R,4S,5S,6R)-2-[(3R)-1,7-bis(4-hydroxyphenyl)heptan-3-yl]oxy-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol | 21637600 | Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC(CCCCC3=CC=C(C=C3)O)CCC4=CC=C(C=C4)O)O)O)O)O)(CO)O | 594.60 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| (2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R)-2-[(3R)-1,7-bis(3,4-dihydroxyphenyl)heptan-3-yl]oxy-3,5-dihydroxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol | 54585388 | Click to see | 626.60 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| (3R)-1,7-Bis(3,4-Dihydroxyphenyl)-3-(Beta-D-Glucopyranosyl)Heptan-3-Ol | 10097263 | Click to see | 494.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| (4E)-1,7-Bis(3,4-dihydroxyphenyl)-4-hepten-3-one; 1,7-Bis-(3,4-dihydroxyphenyl)-4-hepten-3-one; Hirsutanone | 66954880 | Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O | 328.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| (E,5R)-5-hydroxy-1,7-diphenylhept-1-en-3-one | 38359503 | Click to see C1=CC=C(C=C1)CCC(CC(=O)C=CC2=CC=CC=C2)O | 280.40 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| (R)-5-Hydroxy-1,7-Diphenylheptan-3-One | 46213118 | Click to see | 282.40 | unknown | https://doi.org/10.1246/BCSJ.43.575 |
| 1,7-Bis(3,4-dihydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one | 14707657 | Click to see | 478.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 1,7-Bis(3,4-dihydroxyphenyl)-5-methoxyheptan-3-one | 23902340 | Click to see | 360.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 1,7-Bis(4-hydroxyphenyl)hept-5-en-3-one | 162869316 | Click to see C1=CC(=CC=C1CCC(=O)CC=CCC2=CC=C(C=C2)O)O | 296.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 75168353 | Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O | 494.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]oxane-3,4,5-triol | 74202880 | Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)O)O | 464.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 2-[1,7-Bis(4-hydroxyphenyl)heptan-3-yloxy]-6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol | 73818246 | Click to see | 594.60 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 2-[2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]-3,5-dihydroxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol | 75168334 | Click to see | 626.60 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 5-Hydroxy-1,7-diphenyl-3-heptanone | 562075 | Click to see C1=CC=C(C=C1)CCC(CC(=O)CCC2=CC=CC=C2)O | 282.40 | unknown | https://doi.org/10.1246/BCSJ.43.575 |
| 5-Hydroxy-1,7-diphenylhept-1-en-3-one | 72751360 | Click to see | 280.40 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| 7-(3,4-Dihydroxyphenyl)-1-(4-hydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one | 14707655 | Click to see | 462.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Alnuside B | 11684063 | Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC=C(C=C3)O)O)O)O | 462.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Hirsutenone | 637394 | Click to see | 328.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Muricarpone A | 11667643 | Click to see | 360.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Oregonin | 14707658 | Click to see | 478.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Platyphyllenone | 23786382 | Click to see | 296.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Rubranoside B | 24011643 | Click to see | 464.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| > Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids | |||||
| (5S)-1,7-bis(4-hydroxyphenyl)-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one | 54583463 | Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O | 476.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| (5S)-5-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one | 54582487 | Click to see | 608.60 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| (5S)-5-hydroxy-1,7-bis(4-hydroxyphenyl)heptan-3-one | 13347313 | Click to see | 314.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 1,7-Bis(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one | 14833391 | Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O | 476.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 5-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one | 76152897 | Click to see | 608.60 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| 5-Hydroxy-1,7-bis(4-hydroxyphenyl)heptan-3-one | 13347312 | Click to see | 314.40 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| Platyphylloside | 9826264 | Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O | 476.50 | unknown | https://doi.org/10.1016/J.BMCL.2011.03.074 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids | |||||
| 7-Hydroxy-5-methoxy-2-phenylchroman-4-one | 4053302 | Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O | 270.28 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| Alpinetin | 154279 | Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O | 270.28 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| (-)-Pinostrobin | 73201 | Click to see | 270.28 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| Npc235117 | 4101463 | Click to see | 270.28 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| > Phenylpropanoids and polyketides / Stilbenes | |||||
| Stilbene | 11502 | Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2 | 180.24 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
| trans-Stilbene | 638088 | Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2 | 180.24 | unknown | https://doi.org/10.1246/BCSJ.43.2223 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |