Hagenia abyssinica

Details Top

Internal ID UUID64403f31a6cac997710372
Scientific name Hagenia abyssinica
Authority (Bruce) J.F.Gmel.
First published in Syst. Nat. ed. 13[bis] : 613 (1791)

Ethnobotanical Use Top

Write a new one!
No ethnobotanical data added yet. Help us by writing one.

General Uses Top

Suggest a correction!

Common products:
- Sawn timber and veneer from the heartwood.
- Charcoal for domestic and industrial fuel.
- Bark tannin extract for leather tanning.
Heartwood yields reddish‑brown colour for decorative veneer.

Industrial and craft applications:
The timber serves structural members (posts, beams) and heavy‑duty furniture, tool handles, and wood‑carving. Charcoal provides a high‑energy fuel. The dense wood is valued for fine grain and durability, suitable for ornamental pieces, musical instruments, and traditional boat building in highland lakes.

Colorants and tanning:
The bark contains condensed tannins (proanthocyanidins) that can be extracted for leather‑tanning and as a natural brown dye for protein fibers. The tannin content reaches roughly 15–20 % of dry bark weight. Tannin extracts serve as a leather‑tanning agent and as a natural brown dye for wool and silk.

Wood and fiber:
Hagenia wood has a basic density of about 0.88 g cm⁻³ (12 % MC), a lignin content of ≈ 27 % and a high proportion of cellulose, giving it strength and resistance to decay and termites. These properties make it appropriate for flooring, decking, railway sleepers and other load‑bearing uses. The fiber can be used for pulp, though the high lignin content reduces its suitability for high‑yield paper grades. Its high lignin and extractives impart natural fungal decay resistance, making it suitable for decking and fencing.

Properties relevant to use:
- High basic density contributes to mechanical strength and low shrinkage.
- Elevated lignin content (≈ 27 %) enhances durability and resistance to insects.
- Charcoal from the wood yields a calorific value near 30 MJ kg⁻¹.
- Condensed tannins provide good tanning efficiency and colour stability.
The wood shows low tangential shrinkage (~3 %) and moderate radial shrinkage (~2 %), ensuring dimensional stability after drying.

Standards and regulation:
Timber grading follows national standards such as Ethiopian Standard ES 182:2015 (hardwood grading) and ISO 13061‑2 for density testing. Moisture content is measured according to ISO 24294. Export of logs is subject to CITES regulation where applicable; currently, H. abyssinica is not listed in the CITES Appendices.

Sustainability and sourcing:
The species is listed as Near Threatened on the IUCN Red List (2022) because of habitat loss and over‑harvest for timber and charcoal. National Ethiopian forestry regulations (Timber Export Regulation 2008) require permits for commercial harvest. Sustainable management initiatives include community‑based forest management, promotion of plantation establishment and monitoring of harvest volumes to limit pressure on wild populations. Local seed banks provide planting material for restoration, and certification schemes for sustainable timber are piloted in some districts.

Synonyms Top

Scientific name Authority First published in
Brayera anthelmintica Kunth ex A.Rich. Bull. Sci. Soc. Philom. Paris 8: 156 (1822)
Banksia abyssinica Bruce Trav. Disc. Source Nile 5: 73, tt. 22-23. 1790 [Feb-Apr 1790]
Hagenia anthelmintica (Kunth ex A.Rich.) J.F.Gmel. ex Eggeling Indig. Trees Uganda : 188 (1940)
Brayera abyssinica Moq. Élem. Bot. Méd. : 217 (1861)
Cusso abyssinica Farw. Druggists' Circ. 63: 49 (1919)
Hagenia abyssinica var. viridifolia Hauman Bull. Jard. Bot. État Bruxelles 22: 90 (1952)
Brayera anthelmintica var. psilanthera Bitter Repert. Spec. Nov. Regni Veg. 12: 378 (1913)
Brayera anthelmintica var. epirhagadotricha Bitter Repert. Spec. Nov. Regni Veg. 12: 378 (1913)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Spanish brayera anthelmintica
Spanish banksia abyssinica
Spanish hagenia anthelmintica
Spanish brayera
Amharic ኮሶ
Arabic الشربة الحبشية
Arabic القصو
Arabic كسو
Arabic شاوا
Arabic القوصو
German kossobaum
German kosobaum
Greek χαγκενία η αβυσσηνιακή
Greek χαγκενία
Persian هاگنیا
Finnish kosso
French brayera
French brayera anthelmintica
Italian banksia abyssinica
Italian brayera anthelmintica
Italian hagenia anthelmintica
Italian kosso
Italian kousso
Italian cusso
Japanese コソノキ
Japanese ハゲニア
Russian Хагения
Russian Хагения абиссинская
Kinyarwanda umugeshi
Swedish kossoträd
Swahili mlozilozi

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000994920
UNII YG2C392C2K
Tropicos 27805272
KEW urn:lsid:ipni.org:names:725448-1
Open Tree Of Life 328288
NCBI Taxonomy 57921
IUCN Red List 117894181
IPNI 6292-1
iNaturalist 130757
GBIF 5370415
Freebase /m/0cwl9s
EPPO HGEAB
USDA GRIN 18175
Wikipedia Hagenia
PaleoBotany 78243

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
Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia Seraw E, Melkamu Y, Masresha G J Ethnobiol Ethnomed 17-Apr-2024
PMCID:PMC11025143
doi:10.1186/s13002-024-00678-9
PMID:38632559
Modeling habitat suitability for the lesser‐known populations of endangered mountain nyala (Tragelaphus buxtoni) in the Arsi and Ahmar Mountains, Ethiopia Worku EA, Evangelista PH, Atickem A, Bekele A, Bro‐Jørgensen J, Stenseth NC Ecol Evol 15-Apr-2024
PMCID:PMC11017409
doi:10.1002/ece3.11235
PMID:38623519
Shifting mammal communities and declining species richness along an elevational gradient on Mount Kenya Snider MH, Helgen KM, Young HS, Agwanda B, Schuttler S, Titcomb GC, Branch D, Dommain R, Kays R Ecol Evol 09-Apr-2024
PMCID:PMC11004549
doi:10.1002/ece3.11151
PMID:38601855
Cytotoxic activity of bimetallic Ag@Se green synthesized nanoparticles using Jerusalem Thorn (Parkinsonia aculeata) Hassanin HA, Taha A, Ibrahim HI, Ahmed EA, Mohamed H, Ahmed H Front Chem 25-Mar-2024
PMCID:PMC11000268
doi:10.3389/fchem.2024.1343506
PMID:38591059
Traditional ethnobotanical knowledge and ethnomedicinal use of plants in the Tropical Rift Valley of Ethiopia Wendimu A, Tekalign W, Bojago E, Abrham Y Heliyon 13-Mar-2024
PMCID:PMC10955238
doi:10.1016/j.heliyon.2024.e27528
PMID:38515698
Review of Herbal Medicinal Plants Used in the Management of Cancers in the East Africa Region from 2019 to 2023 Kudamba A, Kasolo JN, Bbosa GS, Lugaajju A, Wabinga H, Kafeero HM, Ssenku JE, Alemu SO, Walusansa A, Niyonzima N, Muwonge H Integr Cancer Ther 06-Mar-2024
PMCID:PMC10916491
doi:10.1177/15347354241235583
PMID:38445504
Medicinal Plants Used by Oromo Community in Kofale District, West-Arsi Zone, Oromia Regional State, Ethiopia Nuro GB, Tolossa K, Giday M J Exp Pharmacol 05-Mar-2024
PMCID:PMC10929209
doi:10.2147/JEP.S449496
PMID:38476311
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
Hagenia abyssinica-Biomediated Synthesis of a Magnetic Fe3O4/NiO Nanoadsorbent for Adsorption of Lead from Wastewater Ferenj AE, Kabtamu DM, Assen AH, Gedda G, Muhabie AA, Berrada M, Girma WM ACS Omega 02-Feb-2024
PMCID:PMC10870417
doi:10.1021/acsomega.3c08151
PMID:38371754
Growth inhibitory effect of selected medicinal plants from Southern Ethiopia on the mycelial phase of Histoplasma capsulatum var. farciminosum Girma T, Chala G, Mekibib B BMC Vet Res 19-Jan-2024
PMCID:PMC10797924
doi:10.1186/s12917-023-03873-0
PMID:38243346
In Vitro Regeneration from Leaf Explants of Helianthus verticillatus, a Critically Endangered Sunflower Nowakowska M, Pavlovic Z, Nowicki M, Boggess SL, Trigiano RN Plants (Basel) 18-Jan-2024
PMCID:PMC10820345
doi:10.3390/plants13020285
PMID:38256838
Species composition, relative abundance, and habitat association of birds in Dodola dry evergreen afro-montane forest and sub-afro-alpine scrubland vegetation, southeast Ethiopia Yilma ZA, Mengesha G, Girma Z PeerJ 11-Jan-2024
PMCID:PMC10788088
doi:10.7717/peerj.16775
PMID:38223764
Prevalence of herbal and traditional medicine in Ethiopia: a systematic review and meta-analysis of 20-year studies Tuasha N, Fekadu S, Deyno S Syst Rev 13-Dec-2023
PMCID:PMC10717384
doi:10.1186/s13643-023-02398-9
PMID:38093343
Remote sensing and GIS-based study of land use/cover dynamics, driving factors, and implications in southern Ethiopia, with special reference to the Legabora watershed Mariye M, Jianhua L, Maryo M, Tsegaye G, Aletaye E Heliyon 07-Dec-2023
PMCID:PMC10750153
doi:10.1016/j.heliyon.2023.e23380
PMID:38148827

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(1S,2S,3R,4R,5S,7S,9R,10S,11S,13R)-4-acetyloxy-2,11-dihydroxy-1,5,9,12,12-pentamethyl-8-oxo-7-tetracyclo[7.6.0.03,7.010,13]pentadecanyl] benzoate 162975953 Click to see 498.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/0731-7085(90)80133-A
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1016/0731-7085(90)80133-A
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/0731-7085(90)80133-A
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
1-[3-[[2,6-Dihydroxy-4-methoxy-3-methyl-5-(2-methylpropanoyl)phenyl]methyl]-2,4-dihydroxy-6-methoxy-5-methylphenyl]-3-methylbutan-1-one 162992807 Click to see 474.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
1-[3-[[2,6-Dihydroxy-4-methoxy-3-methyl-5-(3-methylbutanoyl)phenyl]methyl]-2,4-dihydroxy-6-methoxy-5-methylphenyl]-3-methylbutan-1-one 14598236 Click to see 488.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
alpha-Kosin 160529 Click to see 460.50 unknown https://doi.org/10.1016/0731-7085(92)80080-7
https://doi.org/10.1016/0731-7085(90)80133-A
https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-[(1S,4aR,7S,8aS)-7-hydroxy-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]butan-2-one 162905206 Click to see 278.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,4S,5S,10S,13R,14R,17R)-3-hydroxy-4,10,13,14-tetramethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,6,7,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-one 10503282 Click to see 440.70 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(2S,3S)-2-[4-[(3R,3aS,6R,6aS)-6-[4-[(1S,2S)-1,3-diacetyloxy-1-(4-acetyloxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-3-acetyloxy-3-(4-acetyloxy-3-methoxyphenyl)propyl] acetate 162961501 Click to see CC(=O)OCC(C(C1=CC(=C(C=C1)OC(=O)C)OC)OC(=O)C)OC2=C(C=C(C=C2OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(COC(=O)C)C(C6=CC(=C(C=C6)OC(=O)C)OC)OC(=O)C)OC)OC 1063.10 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
(4S)-5-[[(2S,5S,8S,11R,12S,15S,18S,21R)-2-butyl-21-hydroxy-5,15-bis[(4-hydroxyphenyl)methyl]-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-8-propan-2-yl-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]amino]-4-(hexanoylamino)-5-oxopentanoic acid 163103950 Click to see CCCCCC(=O)NC(CCC(=O)O)C(=O)NC1C(OC(=O)C(NC(=O)C(N(C(=O)C(N2C(CCC(C2=O)NC(=O)C(NC1=O)CC3=CC=C(C=C3)O)O)CCCC)C)CC4=CC=C(C=C4)O)C(C)C)C 994.10 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Kosotoxin 3083701 Click to see 460.50 unknown https://doi.org/10.1016/0731-7085(92)80080-7
https://doi.org/10.1016/0731-7085(90)80133-A
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
8,9-Dihydroxy-6,14,15,21,22-pentamethyl-10-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 74822174 Click to see CC1CCC23CCC4(C5(CCC6C(=C)C(C(CC6(C5C7C(C4(C2C1C)OC3=O)O7)C)O)O)C)C 470.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(2R,6S)-2,6-bis[[2,6-dihydroxy-4-methoxy-3-methyl-5-(2-methylpropanoyl)phenyl]methyl]-5-hydroxy-2,6-dimethyl-4-(2-methylpropanoyl)cyclohex-4-ene-1,3-dione 163000893 Click to see 696.80 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
(2R)-1-[3,5-bis[[2,6-dihydroxy-4-methoxy-3-methyl-5-[(2R)-2-methylbutanoyl]phenyl]methyl]-2,4,6-trihydroxyphenyl]-2-methylbutan-1-one 163189525 Click to see CCC(C)C(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C)OC)C(=O)C(C)CC)O)O)CC3=C(C(=C(C(=C3O)C)OC)C(=O)C(C)CC)O)O 710.80 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
(2S,6S)-6-[[2,6-dihydroxy-4-methoxy-3-methyl-5-[(2R)-2-methylbutanoyl]phenyl]methyl]-2-[[2,6-dihydroxy-4-methoxy-3-methyl-5-(3-methylbutanoyl)phenyl]methyl]-5-hydroxy-2,6-dimethyl-4-(3-methylbutanoyl)cyclohex-4-ene-1,3-dione 163035071 Click to see 738.90 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
1-[3,5-Bis[[2,6-dihydroxy-4-methoxy-3-methyl-5-(2-methylbutanoyl)phenyl]methyl]-2,4,6-trihydroxyphenyl]-2-methylbutan-1-one 162871731 Click to see 710.80 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
1-[3,5-Bis[[2,6-dihydroxy-4-methoxy-3-methyl-5-(2-methylpropanoyl)phenyl]methyl]-2,4,6-trihydroxyphenyl]-2-methylpropan-1-one 5316836 Click to see 668.70 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
1-[3,5-Bis[[2,6-dihydroxy-4-methoxy-3-methyl-5-(3-methylbutanoyl)phenyl]methyl]-2,4,6-trihydroxyphenyl]-3-methylbutan-1-one 162891553 Click to see 710.80 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
2,6-Bis[[2,6-dihydroxy-4-methoxy-3-methyl-5-(2-methylpropanoyl)phenyl]methyl]-5-hydroxy-2,6-dimethyl-4-(2-methylpropanoyl)cyclohex-4-ene-1,3-dione 101592155 Click to see 696.80 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
6-[[2,6-Dihydroxy-4-methoxy-3-methyl-5-(2-methylbutanoyl)phenyl]methyl]-2-[[2,6-dihydroxy-4-methoxy-3-methyl-5-(3-methylbutanoyl)phenyl]methyl]-5-hydroxy-2,6-dimethyl-4-(3-methylbutanoyl)cyclohex-4-ene-1,3-dione 163035070 Click to see 738.90 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
Protokosin 160914 Click to see CC1=C(C(=C(C(=C1OC)C(=O)C(C)C)O)CC2=C(C(=C(C(=C2O)C(=O)C(C)C)O)CC3=C(C(=C(C(=C3O)C)OC)C(=O)C(C)C)OC)O)O 682.80 unknown https://doi.org/10.1016/0731-7085(92)80080-7
https://doi.org/10.1016/0731-7085(90)80133-A

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.