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.
  • 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.

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).

General Uses Top

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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

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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

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
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Links to other databases Top

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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

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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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Title Authors Publication Released IDs
Plant-Associated Bacillus thuringiensis and Bacillus cereus: Inside Agents for Biocontrol and Genetic Recombination in Phytomicrobiome Sorokan A, Gabdrakhmanova V, Kuramshina Z, Khairullin R, Maksimov I Plants (Basel) 30-Nov-2023
PMCID:PMC10707757
doi:10.3390/plants12234037
PMID:38068672
Metal-Catalyzed Enantioconvergent Transformations Yus M, Nájera C, Foubelo F, Sansano JM Chem Rev 04-Oct-2023
PMCID:PMC10603790
doi:10.1021/acs.chemrev.3c00059
PMID:37793021
Microbe-Plant Interactions Targeting Metal Stress: New Dimensions for Bioremediation Applications Saharan BS, Chaudhary T, Mandal BS, Kumar D, Kumar R, Sadh PK, Duhan JS J Xenobiot 01-Jun-2023
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doi:10.3390/jox13020019
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A review of the effects of environmental hazards on humans, their remediation for sustainable development, and risk assessment Gunjyal N, Rani S, Asgari Lajayer B, Senapathi V, Astatkie T Environ Monit Assess 01-Jun-2023
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doi:10.1007/s10661-023-11353-z
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Radical oxygen species: an important breakthrough point for botanical drugs to regulate oxidative stress and treat the disorder of glycolipid metabolism Luo M, Zheng Y, Tang S, Gu L, Zhu Y, Ying R, Liu Y, Ma J, Guo R, Gao P, Zhang C Front Pharmacol 12-May-2023
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Phytoremediation as an Effective Remedy for Removing Trace Elements from Ecosystems Mocek-Płóciniak A, Mencel J, Zakrzewski W, Roszkowski S Plants (Basel) 14-Apr-2023
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doi:10.3390/plants12081653
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doi:10.1186/s12906-023-03916-x
PMID:36934258
Current Scenario and Future Prospects of Endophytic Microbes: Promising Candidates for Abiotic and Biotic Stress Management for Agricultural and Environmental Sustainability Anand U, Pal T, Yadav N, Singh VK, Tripathi V, Choudhary KK, Shukla AK, Sunita K, Kumar A, Bontempi E, Ma Y, Kolton M, Singh AK Microb Ecol 14-Mar-2023
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doi:10.1007/s00248-023-02190-1
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Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review Tshikhudo PP, Ntushelo K, Mudau FN Microorganisms 10-Feb-2023
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Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
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doi:10.3389/fpls.2022.999866
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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

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