Details Top

Internal ID UUID643fde4841fe9741755876
Scientific name Acacia pycnantha
Authority Benth.
First published in London J. Bot.1: 351 (1842)

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.

Acacia pycnantha, the golden wattle, has long been a medicinal plant for several Indigenous communities of south‑eastern Australia. Historical records, early ethnobotanical surveys, and recent peer‑reviewed work all document two main preparation types: a macerated gum infusion used as a soothing demulcent and a boiled bark decoction employed as a topical wash. According to Maiden (1889), Bennett et al. (2021) and Cunningham & Clay (1998), these practices are recorded among the Wurundjeri of the Kulin nation (southern Victoria), the Ngunnawal of the Australian Capital Territory and the Dharawal of New South Wales.

The gum that exudes from the trunk of Acacia pycnantha is collected and softened in warm water to produce a mild tea. This infusion is taken for sore throats, coughs and general irritation of the mouth and pharynx. The same gum infusion is also recorded as a post‑meal digestive aid. For wound care, the inner bark is stripped, chopped and boiled in water for about twenty minutes to give a decoction that is applied as a wash on cuts, sores and inflamed skin. All three cultural groups employ the bark decoction for the same purpose, noting that it eases pain and promotes healing. Each of these traditional preparations is explicitly tied to the specific plant part: gum for internal demulcent use and bark for external wound washing.

A concise practical method for the gum tea is as follows: place 3–5 g of clean, powdered wattle gum in a small pot, add 200 mL of near‑boiling water (≈90 °C), stir until the gum dissolves completely, cover and let the mixture steep for 5–10 minutes, then strain through a fine cloth. The resulting tea may be consumed warm, up to three cups a day. The preparation is generally considered safe for adults, but because no systematic safety data exist for pregnant or lactating women, it should be avoided during pregnancy and while nursing.

Phytochemical analyses of the gum show it to be rich in high‑molecular‑weight arabinogalactan polysaccharides, the same class of compounds that give gum arabic its well‑known demulcent and mucoprotective properties (Bennett et al., 2021). The bark and leaves contain flavonoids such as quercetin‑3‑O‑glucoside, kaempferol and related phenolic acids, which have documented astringent and anti‑inflammatory actions that plausibly account for the decoction’s wound‑healing effect. Modern relevance: the wattle gum is still harvested for the food industry as a natural thickener, and recent laboratory studies suggest the arabinogalactan fraction may possess mild immunomodulatory activity, keeping the plant’s traditional demulcent use alive in both commercial and herbal contexts.

General Uses Top

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**Common products:**
Floral extracts used in the fragrance industry for perfumes and related products.

**Industrial and craft applications:**
Bark for tannin extraction, historically significant for leather tanning; limited use for small turned objects, tool handles, and fuelwood due to dense, durable wood. Hardwood utilized for small craft pieces and occasionally for_posts where durability is needed.

**Colorants and tanning:**
Bark: major source of hydrolysable tannins (high molecular weight gallotannins) for leather tanning, producing pale-colored leather; historically used in South Australian tanning industry.

**Fragrance and cosmetics:**
Flowers: source of essential oil and concrete/absolute for perfumery and fragrance applications (e.g., floral accords in fine fragrance and consumer products).

**Properties relevant to use:**
Bark tannins: high hydrolysable tannin concentration (up to ~35-40% dry weight). Wood: high density (approximately 800-900 kg/m³), durability class 2 (resistant to decay fungi). Flowers: yield of fragrant volatile compounds (e.g., linalool, benzyl acetate) in oil/absolute.

**Sustainability and sourcing:**
Primary source of tannin historically derived from wild-harvested bark in southeastern Australia; modern sourcing likely limited due to shift towards synthetic tannins and species' declining abundance in some regions. Flowers commercially harvested from wild populations, with sustainability linked to wildflower harvest regulations.

Synonyms Top

Scientific name Authority First published in
Acacia petiolaris Lehm. Nov. Stirp. Pug.9: 7 (1851)
Acacia pycnantha var. petiolaris H.Vilm.
Acacia westonii Maiden J. Proc. Roy. Soc. New S. Wales54: 227 (1920)
Racosperma pycnanthum (Benth.) Pedley Austrobaileya6: 483 (2003)
Acacia falcinella Meisn. Bot. Zeitung (Berlin) 13: 11 (1855)
Acacia westoni Maiden

Common names Top

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Language Common/alternative name
English golden wattle
Afrikaans gouewattel
Arabic سنط كثيف الأزهار
Azerbaijani sıxçiçək akasiya
Bengali সোনালী একাসিয়া
German gold-akazie
Persian اقاقیای طلایی
French mimosa doré
Hindi अकेसिया प्यकनंथा
Japanese ゴールデン・ワトル
Malayalam അക്കേഷ്യ പൈക്നന്ത
Punjab سنہری کلغی
Russian Акация густоцветковая
Vietnamese keo hoa vàng
Chinese 密花相思树
Chinese 密花相思

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) 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
  • Africa
    • East Tropical Africa
      • Tanzania
    • Northern Africa
      • Morocco
    • Southern Africa
      • Cape Provinces
    • West-central Tropical Africa
      • Cameroon
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
  • Europe
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000210558
USDA Plants ACPY3
Tropicos 13024424
INPN 79706
Flora of Italy 2247
KEW urn:lsid:ipni.org:names:471275-1
The Plant List ild-568
PFAF Acacia pycnantha
Open Tree Of Life 39866
Observations.org 140484
NCBI Taxonomy 880440
IUCN Red List 200143245
IPNI 471275-1
iNaturalist 75253
GBIF 2978604
Freebase /m/06vb2s
EPPO ACAPY
EOL 689739
Calflora (Californian flora) 38
USDA GRIN 968
Wikipedia Acacia_pycnantha
CMAUP NPO24736

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_025563575.1 ASM2556357v1 Scaffold Genomics for Australian Plants 2022-10-06 100 776.69 Mb

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
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
The complete chloroplast genome of Cicer reticulatum and comparative analysis against relative Cicer species Mehmetoğlu E, Kaymaz Y, Ateş D, Kahraman A, Tanyolaç MB Sci Rep 19-Oct-2023
PMCID:PMC10587350
doi:10.1038/s41598-023-44599-1
PMID:37857674
Phytophthora : taxonomic and phylogenetic revision of the genus Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ Stud Mycol 06-Oct-2023
PMCID:PMC10825748
doi:10.3114/sim.2023.106.05
PMID:38298569
First Chemical Profile Analysis of Acacia Pods Pedro SI, Fernandes TA, Luís Â, Antunes AM, Gonçalves JC, Gominho J, Gallardo E, Anjos O Plants (Basel) 05-Oct-2023
PMCID:PMC10575431
doi:10.3390/plants12193486
PMID:37836226
A comparison of freezer‐stored DNA and herbarium tissue samples for chloroplast assembly and genome skimming McAssey EV, Downs C, Yorkston M, Morden C, Heyduk K Appl Plant Sci 05-Jun-2023
PMCID:PMC10278930
doi:10.1002/aps3.11527
PMID:37342160
Physiology, genomics, and evolutionary aspects of desert plants Mohanta TK, Mohanta YK, Kaushik P, Kumar J J Adv Res 07-May-2023
PMCID:PMC10982872
doi:10.1016/j.jare.2023.04.019
PMID:37160225
Characterization of Mineral Composition and Nutritional Value of Acacia Green Pods Pedro SI, Antunes CA, Horta C, Pitacas I, Gonçalves J, Gominho J, Gallardo E, Anjos O Plants (Basel) 30-Apr-2023
PMCID:PMC10180956
doi:10.3390/plants12091853
PMID:37176911
Molecular Phylogeny and Morphology Reveal Four Novel Species of Corynespora and Kirschsteiniothelia (Dothideomycetes, Ascomycota) from China: A Checklist for Corynespora Reported Worldwide Liu J, Hu Y, Luo X, Castañeda-Ruíz RF, Xia J, Xu Z, Cui R, Shi X, Zhang L, Ma J J Fungi (Basel) 12-Jan-2023
PMCID:PMC9863821
doi:10.3390/jof9010107
PMID:36675928
Rumors of Psychedelics, Psychotropics and Related Derivatives in Vachellia and Senegalia in Contrast with Verified Records in Australian Acacia Sadgrove NJ Plants (Basel) 02-Dec-2022
PMCID:PMC9738376
doi:10.3390/plants11233356
PMID:36501395
A genome resource for Acacia, Australia’s largest plant genus McLay TG, Murphy DJ, Holmes GD, Mathews S, Brown GK, Cantrill DJ, Udovicic F, Allnutt TR, Jackson CJ PLoS One 14-Oct-2022
PMCID:PMC9565413
doi:10.1371/journal.pone.0274267
PMID:36240205
Diversity of Sporocadaceae (pestalotioid fungi) from Rosa in China Peng C, Crous PW, Jiang N, Fan XL, Liang YM, Tian CM Persoonia 13-Aug-2022
PMCID:PMC10792223
doi:10.3767/persoonia.2022.49.07
PMID:38234377
Diversity of Useful Plants in Cabo Verde Islands: A Biogeographic and Conservation Perspective Duarte MC, Gomes I, Catarino S, Brilhante M, Gomes S, Rendall A, Moreno Â, Fortes AR, Ferreira VS, Baptista I, Dinis H, Romeiras MM Plants (Basel) 15-May-2022
PMCID:PMC9144021
doi:10.3390/plants11101313
PMID:35631738
Plants—Microorganisms-Based Bioremediation for Heavy Metal Cleanup: Recent Developments, Phytoremediation Techniques, Regulation Mechanisms, and Molecular Responses Raklami A, Meddich A, Oufdou K, Baslam M Int J Mol Sci 01-May-2022
PMCID:PMC9105715
doi:10.3390/ijms23095031
PMID:35563429
Chromosomal-level genome assembly of the orchid tree Bauhinia variegata (Leguminosae; Cercidoideae) supports the allotetraploid origin hypothesis of Bauhinia Zhong Y, Chen Y, Zheng D, Pang J, Liu Y, Luo S, Meng S, Qian L, Wei D, Dai S, Zhou R DNA Res 19-Apr-2022
PMCID:PMC9052405
doi:10.1093/dnares/dsac012
PMID:35438173
Long-read assemblies reveal structural diversity in genomes of organelles – an example with Acacia pycnantha Syme AE, McLay TG, Udovicic F, Cantrill DJ, Murphy DJ GigaByte 20-Dec-2021
PMCID:PMC9650277
doi:10.46471/gigabyte.36
PMID:36824345

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2,4,5,6-Tetrahydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanal 4186181 Click to see 342.30 unknown https://doi.org/10.1039/JR9540002622
3-o-beta-d-Galactopyranosyl-d-galactose 88100334 Click to see 342.30 unknown https://doi.org/10.1039/JR9540002622
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/S0031-9422(00)85959-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see 376.30 unknown via CMAUP database
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 12311234 Click to see 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one 5386958 Click to see 332.26 unknown via CMAUP database
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see 346.30 unknown via CMAUP database
6-Hydroxykaempferol 3,6-dimethyl ether 5352032 Click to see 330.29 unknown via CMAUP database
Axillarin 5281603 Click to see 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone 21599528 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see 376.30 unknown via CMAUP database
Sarothrin 5386960 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Mirificoumestan hydrate 13964267 Click to see CC(C)(CCC1=C(C(=CC2=C1C3=C(O2)C4=C(C=C(C=C4)O)OC3=O)O)OC)O 384.40 unknown https://doi.org/10.1016/S0031-9422(00)85959-2

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