Details Top

Internal ID UUID643fe486174e2921925587
Scientific name Nothofagus fusca
Authority (Hook.f.) Oerst.
First published in Bidr. Egefam. : 25 (1871)

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.

no reliable source mentions traditional teas, tinctures, decoctions, macerations, poultices, or other medicinal or culinary uses of Nothofagus fusca

General Uses Top

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Common products:
Timber (sawn wood, veneer).

Industrial and craft applications:
Used as structural timber in construction, flooring, and furniture. Suitable for interior joinery and panelling due to its hardness and attractive grain. Employed in general carpentry and craftwork.

Colorants and tanning:
Bark and foliage contain hydrolyzable tannins historically utilized in leather tanning. Natural brown dyes can be extracted for textile coloration.

Wood and fiber:
Classified as a hardwood with high density and durability. Properties relevant to use include a Janka hardness rating of approximately 6.2–8.8 kN, good dimensional stability after drying, and fine, even grain that takes stain and polish well. Limited applications as pulpwood for paper.

Properties relevant to use:
High lignin content (approximately 28% in sapwood) contributes to structural strength and durability. Tannin concentration in bark ranges from 10–20%, supporting its use in leather processing. Extractives provide natural resistance to decay and insect attack.

Standards and regulation:
Timber graded under New Zealand standards (NZS 3631) for structural uses. FSC-certified sources ensure sustainable harvesting. Export of raw logs regulated under the Forests Act 1949. Tannin extracts must comply with ISO 14088 (tannin analysis).

Sustainability and sourcing:
Classified as "Not Threatened" in the New Zealand Threat Classification System but subject to sustainable management due to slow growth. Regeneration supports indigenous forestry. National and regional policies enforce habitat protection during harvesting.

Synonyms Top

Scientific name Authority First published in
Fagus fusca Hook.f. Hooker's Icon. Pl. 7: t. 630 (1844)
Fuscospora fusca (Hook.f.) Heenan & Smissen Phytotaxa 146: 14 (2013)

Common names Top

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Language Common/alternative name
English red beech
Spanish haya roja de nueva zelanda
Bulgarian кафяв нотофагус
Hungarian vörös déli bükk
Japanese アカナンキョクブナ
mi tawhai raunui
mi tawhairaunui
mi tāwhai raunui
Macedonian црвена бука
Russian Нотофагус бурый

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000252131
Tropicos 50184002
KEW urn:lsid:ipni.org:names:359087-1
The Plant List kew-135768
PFAF Nothofagus fusca
NCBI Taxonomy 28941
IUCN Red List 96478301
IPNI 359087-1
iNaturalist 366620
GBIF 2874959
Freebase /m/0268rpz
EPPO NOFFU
EOL 1153914
USDA GRIN 25392
Wikipedia Nothofagus_fusca
CMAUP NPO761
Open Tree Of Life 316856

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
Afforestation using a range of tree species, in New Zealand: New Forest trial series establishment, site description, and initial data Paul TS, Garrett LG, Smaill SJ Data Brief 12-Mar-2024
PMCID:PMC10980996
doi:10.1016/j.dib.2024.110321
PMID:38559822
Pest categorisation of Platypus apicalis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 20-Jun-2022
PMCID:PMC9208325
doi:10.2903/j.efsa.2022.7398
PMID:35765383
Pushing the limits: ship rat (Rattus rattus) population dynamics across an elevational gradient in response to mast seeding and supplementary feeding Carpenter JK, Monks A, Innes J, Griffiths J Biol Invasions 04-Jun-2022
PMCID:PMC9166931
doi:10.1007/s10530-022-02829-z
PMID:35694204
Secondary cell wall patterning—connecting the dots, pits and helices Xu H, Giannetti A, Sugiyama Y, Zheng W, Schneider R, Watanabe Y, Oda Y, Persson S Open Biol 04-May-2022
PMCID:PMC9065968
doi:10.1098/rsob.210208
PMID:35506204
Reappraisal of the Genus Exsudoporus (Boletaceae) Worldwide Based on Multi-Gene Phylogeny, Morphology and Biogeography, and Insights on Amoenoboletus Biketova AY, Gelardi M, Smith ME, Simonini G, Healy RA, Taneyama Y, Vasquez G, Kovács Á, Nagy LG, Wasser SP, Peintner U, Nevo E, Bunyard BA, Vizzini A J Fungi (Basel) 21-Jan-2022
PMCID:PMC8874676
doi:10.3390/jof8020101
PMID:35205856
Phylogenetic Reassessment, Taxonomy, and Biogeography of Codinaea and Similar Fungi Réblová M, Kolařík M, Nekvindová J, Réblová K, Sklenář F, Miller AN, Hernández-Restrepo M J Fungi (Basel) 20-Dec-2021
PMCID:PMC8704094
doi:10.3390/jof7121097
PMID:34947079
Protective Effects of Linearthin and Other Chalcone Derivatives from Aspalathus linearis (Rooibos) against UVB Induced Oxidative Stress and Toxicity in Human Skin Cells Akinfenwa AO, Abdul NS, Marnewick JL, Hussein AA Plants (Basel) 17-Sep-2021
PMCID:PMC8467595
doi:10.3390/plants10091936
PMID:34579468
Untangling the Lactifluus clarkeae - Lf. flocktoniae(Russulaceae) species complex in Australasia Lebel T, Douch J, Tegart L, Vaughan L, Cooper JA, Nuytinck J Persoonia 03-Aug-2021
PMCID:PMC10784664
doi:10.3767/persoonia.2023.47.01
PMID:38352975
Untangling the Lactifluus clarkeae - Lf. flocktoniae(Russulaceae) species complex in Australasia Lebel T, Douch J, Tegart L, Vaughan L, Cooper JA, Nuytinck J Persoonia 03-Aug-2021
PMCID:PMC10486632
doi:10.3767/persoonia.2021.47.01
PMID:37693797
Phylogeny, Global Biogeography and Pleomorphism of Zanclospora Réblová M, Kolařík M, Nekvindová J, Miller AN, Hernández-Restrepo M Microorganisms 29-Mar-2021
PMCID:PMC8066784
doi:10.3390/microorganisms9040706
PMID:33805574
Commodity risk assessment of oak logs with bark from the US for the oak wilt pathogen Bretziella fagacearum under an integrated systems approach Bragard C, Dehnen‐Schmutz K, Di Serio F, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Douma JC, Rigling D, Mosbach‐Schulz O, Stancanelli G, Tramontini S, Gonthier P EFSA J 22-Dec-2020
PMCID:PMC7754906
doi:10.2903/j.efsa.2020.6352
PMID:33363644
Dewatering Green Sapwood Using Carbon Dioxide Undergoing Cyclical Phase Change between Supercritical Fluid and Gas Franich RA, Meder R, Behr VC Molecules 17-Nov-2020
PMCID:PMC7698424
doi:10.3390/molecules25225367
PMID:33212845
Precise automatic classification of 46 different pollen types with convolutional neural networks Sevillano V, Holt K, Aznarte JL PLoS One 23-Jun-2020
PMCID:PMC7310700
doi:10.1371/journal.pone.0229751
PMID:32574174
Commodity risk assessment of Acer spp. plants from New Zealand Bragard C, Dehnen‐Schmutz K, Di Serio F, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Mosbach‐Schulz O, Gonthier P EFSA J 20-May-2020
PMCID:PMC10464684
doi:10.2903/j.efsa.2020.6105
PMID:37649508
Novel collophorina-like genera and species from Prunus trees and vineyards in Germany Bien S, Kraus C, Damm U Persoonia 10-Sep-2019
PMCID:PMC8375351
doi:10.3767/persoonia.2020.45.02
PMID:34456371

Phytochemical Profile Top

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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 / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
7-Methoxy-2H-1,3-benzodioxole-5-carboxylic acid 607309 Click to see 196.16 unknown via CMAUP database
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1016/0031-9422(67)85008-8
> 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 via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
(8R)-8-(hydroxymethyl)-5-methoxytricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,12,14-hexaene-4,13-diol 71620318 Click to see COC1=C(C=C2C3=C(CCC(C2=C1)CO)C=C(C=C3)O)O 286.32 unknown via CMAUP database
9,12-di-O-methylsubamol 71461983 Click to see COCC1=CCC2=C(C=CC(=C2)OC)C3=CC(=C(C=C13)OC)O 312.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-hex-3-enoxy-6-(hydroxymethyl)oxane-3,4,5-triol 125625 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Secosubamolide 16104910 Click to see CCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 340.50 unknown via CMAUP database
Secosubamolide A 24795973 Click to see CCCCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 368.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2Z,6Z,10Z,14Z,18Z,22Z,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol 12866490 Click to see 699.20 unknown via CMAUP database
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Gibberodione 11586727 Click to see CC1CCC(=CC(=O)C1CCC(=O)C)C(C)C 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic Acid 5280896 Click to see 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(4-hydroxy-5,13-dimethoxy-8-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 71620321 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3C(=CC2)COC4C(C(C(C(O4)CO)O)O)O)OC)O 460.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(4,13-dihydroxy-5-methoxy-8-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102345052 Click to see 446.40 unknown via CMAUP database
Subavenoside A 71453067 Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)COC4C(C(C(C(O4)CO)O)O)O)O 430.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4R,5R,6S)-2-[[13-hydroxy-8-(hydroxymethyl)-5-methoxy-4-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl]oxy]-6-methyloxane-3,4,5-triol 102345053 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=CCC4=C(C3=C2)C=CC(=C4)O)CO)OC)O)O)O 430.40 unknown via CMAUP database
1-[2,4-dihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-1-one 51357548 Click to see 358.34 unknown via CMAUP database
Furcatin 442789 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 428.40 unknown via CMAUP database
Subavenoside D 71461984 Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)CO)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown via CMAUP database
Subavenoside E 71451248 Click to see 474.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Oxyphyllenodiol A 10082923 Click to see 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Subamolide A 16104909 Click to see 340.50 unknown via CMAUP database
Subamolide B 16104907 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 340.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(3E,4R)-4-hydroxy-5-methylidene-3-undecylideneoxolan-2-one 24757906 Click to see 266.38 unknown via CMAUP database
(3Z,4R)-4-hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one 53308122 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown via CMAUP database
Isoobtusilactone A 6442493 Click to see 308.50 unknown via CMAUP database
Obtusilactone A 6442492 Click to see 308.50 unknown via CMAUP database
Subamolide D 24757907 Click to see 266.38 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7R,8R)-Dihydrodehydrodiconiferyl alcohol 9-O-|A-D-glucoside 95223221 Click to see 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4-Methylenedioxy-5-methoxycinnamyl alcohol 85441832 Click to see COC1=CC(=CC2=C1OCO2)C=CCO 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Aescultitannin B 10010849 Click to see 864.80 unknown via CMAUP database
Cinnamtannin D1 46173958 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-7-hydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 3083618 Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Phlorizin 6072 Click to see 436.40 unknown via CMAUP database
Salipurposide 15559669 Click to see 434.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]propan-1-one 154497759 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0031-9422(67)85008-8
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one 154102 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(02)00666-0
Cardamonin 641785 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(02)00666-0
> Phenylpropanoids and polyketides / Stilbenes
5-Styrylresorcinol 100754 Click to see 212.24 unknown https://doi.org/10.1016/S0031-9422(02)00666-0
Pinosylvin 5280457 Click to see C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O 212.24 unknown https://doi.org/10.1016/S0031-9422(02)00666-0

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