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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Name	Authority	First published in
Nothofagus fusca var. colensoi	(Hook.f.) Cheeseman	Man. New Zealand Fl. 641 1906

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

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

Links to other databases Top

Suggest others/fix!

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

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 / 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 COC1=CC(=CC2=C1OCO2)C(=O)O	196.16	unknown	via CMAUP database
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	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 C1=C(C=C(C(=C1O)O)O)C(=O)O	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 COC1=C(C=CC(=C1)CC=C)O	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 CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	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 CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C	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 CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	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 CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasterol glucoside	6602508	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	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
3-Methoxy-5-(beta-D-glucopyranosyloxymethyl)-7H-dibenzo[a,c]cycloheptene-2,9-diol	102345052	Click to see COC1=C(C=C2C3=C(CC=C(C2=C1)COC4C(C(C(C(O4)CO)O)O)O)C=C(C=C3)O)O	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 CCCC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O	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 COCC1=CCC2=C(C=CC(=C2)OC)C3=CC(=C(C=C13)OC)OC4C(C(C(C(O4)CO)O)O)O	474.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Oxyphyllenodiol A	10082923	Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O	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 CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O	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 COC1=CC(=CC2=C1OCO2)CC=C	192.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(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
(4R)-3-[(E)-Undecylidene]-4beta-hydroxy-5-methylenetetrahydrofuran-2-one	24757906	Click to see CCCCCCCCCCC=C1C(C(=C)OC1=O)O	266.38	unknown	via CMAUP database
Isooblusilactonc A	6442493	Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O	308.50	unknown	via CMAUP database
Obtusilactone A	6442492	Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O	308.50	unknown	via CMAUP database
Subamolide D	24757907	Click to see CCCCCCCCCCC=C1C(C(=C)OC1=O)O	266.38	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[[(2R,3R)-2,3-Dihydro-2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxypropyl)-7-methoxybenzofuran-3-yl]methyl]beta-D-glucopyranoside	95223221	Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)CCCO	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 COC1=C(C=CC(=C1)C=CC(=O)O)O	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 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
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
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	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
Helichrysin A	15559669	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 C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O	436.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	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 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
> Phenylpropanoids and polyketides / Stilbenes
5-Styrylresorcinol	100754	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
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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Nothofagus fusca

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