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

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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)

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

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Varieties (abbr. var.) Top

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Name Authority First published in
Hagenia abyssinica var. viridifolia Hauman

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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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
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
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
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
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
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
Djaffa Mountains guereza (Colobus guereza gallarum) abundance in forests of the Ahmar Mountains, Ethiopia Kufa CA, Bekele A, Atickem A, Zinner D Primate Biol 20-Oct-2023
PMCID:PMC10654609
doi:10.5194/pb-10-13-2023
PMID:38039330
Anti-Diabetic Effects of the 80% Methanolic Extract of Datura Stramonium Linn (Solanaceae) Leaves in Streptozotocin- Induced Diabetic Mice Baylie T, Kebad A, Ayelgn T, Tiruneh M, Hunie Tesfa K J Exp Pharmacol 18-Oct-2023
PMCID:PMC10590592
doi:10.2147/JEP.S426925
PMID:37873553
Antioxidant Potential of Ethiopian Medicinal Plants and Their Phytochemicals: A Review of Pharmacological Evaluation Nigussie G, Siyadatpanah A, Norouzi R, Debebe E, Alemayehu M, Dekebo A Evid Based Complement Alternat Med 12-Oct-2023
PMCID:PMC10586904
doi:10.1155/2023/1901529
PMID:37868204
Biosynthesis and Optimization of ZnO Nanoparticles Using Ocimum lamifolium Leaf Extract for Electrochemical Sensor and Antibacterial Activity Tilahun E, Adimasu Y, Dessie Y ACS Omega 24-Jul-2023
PMCID:PMC10399153
doi:10.1021/acsomega.3c02709
PMID:37546677
Biosorption of Escherichia coli Using ZnO-Trimethyl Chitosan Nanocomposite Hydrogel Formed by the Green Synthesis Route Bwatanglang IB, Mohammad F, Janet JN, Dahan WM, Al-Lohedan HA, Soleiman AA Gels 17-Jul-2023
PMCID:PMC10378975
doi:10.3390/gels9070581
PMID:37504460
Modeling impacts of climate change on the geographic distribution and abundances of Tamarindus indica in Tigray region, Ethiopia Gufi Y, Manaye A, Tesfamariam B, Abrha H, Tesfaye M, Hintsa S Heliyon 27-Jun-2023
PMCID:PMC10336433
doi:10.1016/j.heliyon.2023.e17471
PMID:37449191

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
> 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 CC1CC2(C(C1OC(=O)C)C(C3(CCC4C(C3(C2=O)C)C(C4(C)C)O)C)O)OC(=O)C5=CC=CC=C5 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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/0731-7085(90)80133-A
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
> 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 CC1=C(C(=C(C(=C1OC)C(=O)CC(C)C)O)CC2=C(C(=C(C(=C2O)C)OC)C(=O)C(C)C)O)O 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 CC1=C(C(=C(C(=C1OC)C(=O)CC(C)C)O)CC2=C(C(=C(C(=C2O)C)OC)C(=O)CC(C)C)O)O 488.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
alpha-Kosin 160529 Click to see CC1=C(C(=C(C(=C1OC)C(=O)C(C)C)O)CC2=C(C(=C(C(=C2O)C)OC)C(=O)C(C)C)O)O 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 CC1=CCC2C(CC(CC2(C1CCC(=O)C)C)O)(C)C 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 CC1C2CCC3=C(C2(CCC1O)C)C(=O)CC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C 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 CC1=C(C(=C(C(=C1OC)C(=O)C(C)C)O)CC2(C(=C(C(=C(C2=O)C(=O)C(C)C)O)C)O)C)O 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 CC1=C(C(=C(C(=C1OC)C(=O)C(C)C)O)CC2(C(=C(C(=O)C(C2=O)(C)CC3=C(C(=C(C(=C3O)C)OC)C(=O)C(C)C)O)C(=O)C(C)C)O)C)O 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 CCC(C)C(=O)C1=C(C(=C(C(=C1O)CC2(C(=C(C(=O)C(C2=O)(C)CC3=C(C(=C(C(=C3O)C)OC)C(=O)CC(C)C)O)C(=O)CC(C)C)O)C)O)C)OC 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 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
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 CC1=C(C(=C(C(=C1OC)C(=O)CC(C)C)O)CC2=C(C(=C(C(=C2O)C(=O)CC(C)C)O)CC3=C(C(=C(C(=C3O)C)OC)C(=O)CC(C)C)O)O)O 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 CC1=C(C(=C(C(=C1OC)C(=O)C(C)C)O)CC2(C(=C(C(=O)C(C2=O)(C)CC3=C(C(=C(C(=C3O)C)OC)C(=O)C(C)C)O)C(=O)C(C)C)O)C)O 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 CCC(C)C(=O)C1=C(C(=C(C(=C1O)CC2(C(=C(C(=O)C(C2=O)(C)CC3=C(C(=C(C(=C3O)C)OC)C(=O)CC(C)C)O)C(=O)CC(C)C)O)C)O)C)OC 738.90 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.28B-1200
Agrimol G 5316836 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)O)O)O 668.70 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

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