Eusideroxylon zwageri - Unknown
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Internal ID UUID64401bf6e4318247221582
Scientific name Eusideroxylon zwageri
Authority Teijsm. & Binn.
First published in Natuurk. Tijdschr. Ned.-Indië 25: 292 (1863)

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Synonyms Top

Scientific name Authority First published in
Bihania borneensis Meisn. Prodr. 15(1): 96 (1861)
Eusideroxylon borneense Fern.-Vill. Fl. Filip., ed. 3 , 13A: 179 (1880)

Common names Top

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Language Common/alternative name
English borneo ironwood
English bornean ironwood
English ulin
English billian
bjn ulin
French bois de fer
Indonesian ulin
Japanese ボルネオテツボク
Japanese ウリン
Japanese ボルネオアイアンウッド
Japanese ビリヤン
Japanese ブリアン
Japanese ベリアン
Malay pokok belian
Malay belian
Tamil உளின்
Chinese 坤甸铁樟木
Chinese 坤甸鐵樟木

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Subvarieties (abbr. subvar.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000683479
Tropicos 17805008
KEW urn:lsid:ipni.org:names:464565-1
The Plant List kew-2805283
Open Tree Of Life 395011
NCBI Taxonomy 128625
IUCN Red List 31316
IPNI 464565-1
iNaturalist 192894
GBIF 3033968
Freebase /m/02x93y3
EPPO EUDZW
EOL 483590
USDA GRIN 16463
Wikipedia Eusideroxylon_zwageri

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
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Comparative analyses of eight complete plastid genomes of two hemiparasitic Cassytha vines in the family Lauraceae Yu QF, Tan YH, Yu WB, Yang ST, Huang JP, Caraballo-Ortiz MA, Liu C, Song Y Front Genet 13-Dec-2023
PMCID:PMC10753772
doi:10.3389/fgene.2023.1192170
PMID:38155711
Plant Extracts from the Yucatan Peninsula in the In Vitro Control of Curvularia lunata and Antifungal Effect of Mosannona depressa and Piper neesianum Extracts on Postharvest Fruits of Habanero Pepper Cruz-Cerino P, Cristóbal-Alejo J, Ruiz-Carrera V, Gamboa-Angulo M Plants (Basel) 09-Aug-2023
PMCID:PMC10459550
doi:10.3390/plants12162908
PMID:37631120
In silico anti-SARS-CoV-2, antiplasmodial, antioxidant, and antimicrobial activities of crude extracts and homopterocarpin from heartwood of Pterocarpus macrocarpus Kurz. Wahyuni DK, Wacharasindhu S, Bankeeree W, Punnapayak H, Prasongsuk S Heliyon 10-Feb-2023
PMCID:PMC9912040
doi:10.1016/j.heliyon.2023.e13644
PMID:36789389
First evidence of a monodominant (Englerodendron, Amherstieae, Detarioideae, Leguminosae) tropical moist forest from the early Miocene (21.73 Ma) of Ethiopia Pan AD, Jacobs BF, Bush RT, de la Estrella M, Grímsson F, Herendeen PS, van der Burgt XM, Currano ED PLoS One 11-Jan-2023
PMCID:PMC9833558
doi:10.1371/journal.pone.0279491
PMID:36630378
The framework species method: harnessing natural regeneration to restore tropical forest ecosystems Elliott S, Tucker NI, Shannon DP, Tiansawat P Philos Trans R Soc Lond B Biol Sci 14-Nov-2022
PMCID:PMC9661958
doi:10.1098/rstb.2021.0073
PMID:36373920
Identification of Guiboutia species by NIR-HSI spectroscopy Xue X, Chen Z, Wu H, Gao H Sci Rep 07-Jul-2022
PMCID:PMC9262927
doi:10.1038/s41598-022-15719-0
PMID:35798833
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Zn tolerance in the evergreen shrub, Aucuba japonica, naturally growing at a mine site: Cell wall immobilization, aucubin production, and Zn adsorption on fungal mycelia Doyama K, Yamaji K, Haruma T, Ishida A, Mori S, Kurosawa Y PLoS One 30-Sep-2021
PMCID:PMC8483361
doi:10.1371/journal.pone.0257690
PMID:34591865
Isotopic signatures reveal zinc cycling in the natural habitat of hyperaccumulator Dichapetalum gelonioides subspecies from Malaysian Borneo van der Ent A, Nkrumah PN, Aarts MG, Baker AJ, Degryse F, Wawryk C, Kirby JK BMC Plant Biol 27-Sep-2021
PMCID:PMC8474765
doi:10.1186/s12870-021-03190-4
PMID:34579652
Eleutherine bulbosa (Mill.) Urb. Bulb: Review of the Pharmacological Activities and Its Prospects for Application Kamarudin AA, Sayuti NH, Saad N, Razak NA, Esa NM Int J Mol Sci 23-Jun-2021
PMCID:PMC8268349
doi:10.3390/ijms22136747
PMID:34201683
Conflicting phylogenetic signals in plastomes of the tribe Laureae (Lauraceae) Xiao TW, Xu Y, Jin L, Liu TJ, Yan HF, Ge XJ PeerJ 15-Oct-2020
PMCID:PMC7568859
doi:10.7717/peerj.10155
PMID:33088627
The complete chloroplast genome sequence of Illigera celebica Xin Y, Xin J, Yao G, Qu Y, Feng F, Song Y, Sun Z Mitochondrial DNA B Resour 16-Jun-2020
PMCID:PMC7782879
doi:10.1080/23802359.2020.1778562
PMID:33457824
Reducing risks by transforming landscapes: Cross-scale effects of land-use changes on ecosystem services Fedele G, Locatelli B, Djoudi H, Colloff MJ PLoS One 24-Apr-2018
PMCID:PMC5916864
doi:10.1371/journal.pone.0195895
PMID:29689062

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
> Lignans, neolignans and related compounds / Aryltetralin lignans
(1S,2R,3R,4R)-4-ethoxy-6,7-dimethoxy-2,3-dimethyl-4-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1H-naphthalene-1,5-diol 162939353 Click to see CCOC1(C(C(C(C2=CC(=C(C(=C21)O)OC)OC)O)C)C)C3=CC(=C(C(=C3)OC)OC)OC 462.50 unknown https://doi.org/10.1007/S10600-009-9346-6
(1S,2S,3R,4S)-4-ethoxy-6,7-dimethoxy-2,3-dimethyl-4-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1H-naphthalene-1,5-diol 162939352 Click to see CCOC1(C(C(C(C2=CC(=C(C(=C21)O)OC)OC)O)C)C)C3=CC(=C(C(=C3)OC)OC)OC 462.50 unknown https://doi.org/10.1007/S10600-009-9346-6
4-ethoxy-6,7-dimethoxy-2,3-dimethyl-4-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1H-naphthalene-1,5-diol 162939351 Click to see CCOC1(C(C(C(C2=CC(=C(C(=C21)O)OC)OC)O)C)C)C3=CC(=C(C(=C3)OC)OC)OC 462.50 unknown https://doi.org/10.1007/S10600-009-9346-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1039/JR9600004732
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/10.1039/JR9600004732
> Organoheterocyclic compounds / Benzodioxanes / Benzo-1,4-dioxanes
(2S,3S)-5-methoxy-2-(7-methoxy-1,3-benzodioxol-5-yl)-3-methyl-7-prop-2-enyl-2,3-dihydro-1,4-benzodioxine 101833723 Click to see CC1C(OC2=C(O1)C(=CC(=C2)CC=C)OC)C3=CC4=C(C(=C3)OC)OCO4 370.40 unknown https://doi.org/10.1007/S10600-009-9346-6
5-Methoxy-2-(7-methoxy-1,3-benzodioxol-5-yl)-3-methyl-7-prop-2-enyl-2,3-dihydro-1,4-benzodioxine 14558372 Click to see CC1C(OC2=C(O1)C(=CC(=C2)CC=C)OC)C3=CC4=C(C(=C3)OC)OCO4 370.40 unknown https://doi.org/10.1007/S10600-009-9346-6
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(2S,3S)-5-methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,4-benzodioxine 71816802 Click to see CC1C(OC2=C(O1)C(=CC(=C2)CC=C)OC)C3=CC(=C(C(=C3)OC)OC)OC 386.40 unknown https://doi.org/10.1007/S10600-009-9346-6
5-Methoxy-3-methyl-7-prop-2-enyl-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,4-benzodioxine 14259132 Click to see CC1C(OC2=C(O1)C(=CC(=C2)CC=C)OC)C3=CC(=C(C(=C3)OC)OC)OC 386.40 unknown https://doi.org/10.1007/S10600-009-9346-6

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