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.

In parts of the Cape and KwaZulu‑Natal, traditional practitioners have long recorded the use of silver wattle bark as an astringent for sore throats and inflamed gums; the Decoction is made from shredded bark, applied as a mild gargle, and sometimes used as a wash for cuts and sores. In neighboring Botswana, the Tswana make a similar preparation from bark fragments taken in water, employing it internally as an astringent and externally for wound care, a practice noted in the African Herbal Pharmacopoeia (2010). Along the coastal lowlands of Kenya’s inland districts near the Rift, Maasai and related communities also prepare bark decoctions for oral inflammations and sore throats; the method and plant part are detailed by Maundu and Tengnäs (2005). In all cases, the astringent effect is attributed to the bark’s high tannin content, a profile well‑documented for this species.

An efficient bark decoction for a soothing gargle is straightforward: place 10–15 g of coarsely chopped air‑dried bark in 500 ml of water, bring to a boil, and simmer gently for 20–30 minutes; cool, strain, and use the liquid warm as a gentle gargle 2–3 times daily. A 1:5 ethanol (45–50% v/v) tincture can be made by macerating 20 g of finely powdered bark in 100 ml of ethanol for 3–4 weeks, shaking daily, then pressing and filtering; taken in small doses it serves as a strong astringent in mouth sprays or applied externally to minor abrasions. Safety notes are prudent: condensed tannins can bind and reduce absorption of medicines and nutrients, so avoid prolonged high‑dose internal use and keep topical applications dilute; because evidence is insufficient to rule out uterine activity, the bark is best avoided in pregnancy and while breastfeeding.

Silver wattle bark is rich in condensed proanthocyanidins and hydrolyzable gallotannins, constituents known for protein‑precipitating astringency that underlies its traditional actions, and it also contains flavonoids such as quercetin derivatives that have demonstrated antioxidant activity in contemporary analyses of the species (African Herbal Pharmacopoeia, 2010; Buirski et al., 2006). These phytochemicals plausibly account for its astringent and mild antimicrobial effects in oral and topical contexts.

Modern relevance is growing: Kenyan and South African research continues to examine its antioxidant and antimicrobial properties in wound‑care models, and the bark remains available in local markets as “miganje” (Kenya) and in herbal supply chains for astringent teas and tinctures, while some commercial wound washes incorporate it as an alternative astringent base (Maundu & Tengnäs, 2005; African Herbal Pharmacopoeia, 2010).

General Uses Top

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Common products:
Acacia mearnsii provides concentrated tannin extracts from bark and heartwood, high-density timber and poles, and fuelwood/charcoal. It is also a source of wood chips for pulping and sawdust used for colorants.

Industrial and craft applications:
Tannin extracts are used industrially for leather tanning and in adhesives for wood-based panels, where they function as natural extenders or partial replacements for phenol–formaldehyde resins in selected systems. The species yields poles for fencing and posts, hardwood for flooring, furniture, and specialty items, and small-dimension utility timber. Sawdust and extracts are employed as brown colorants in wood stains and craft dyeing.

Colorants and tanning:
The bark and heartwood contain condensed tannins (proanthocyanidins), enabling production of natural brown dyes for protein fibers and wood, and for leather tanning. Tannins are typically marketed as aqueous extracts or spray-dried powders standardized to active tannin content. Physical–chemical properties relevant to these uses include high tannin concentration, low/non-hydrolyzable behavior consistent with condensed tannin chemistry, and suitability for acid or salt-bath tanning systems depending on formulation.

Wood and fiber:
Timber is characterized by high density, good dimensional stability after drying, and moderate workability. The heartwood contains natural extractives that contribute to durability in ground-contact and exterior applications. Wood chips are used for kraft or neutral sulfite semi-chemical pulping to produce packaging, tissue, and printing grades where brightness targets permit.

Properties relevant to use:
Condensed-tannin chemistry enables crosslinking in tanning and resin systems; extractives and density improve weathering and durability; lignin/cellulose profiles support fiber yield in pulping; color is derived from soluble tannin and extractives in sawdust/extract.

Standards and regulation:
Tannin extracts are traded according to established quality specifications for leather tanning. Timber and poles are typically classified under national grading systems; exports may follow standard shipping practices for hardwood species. Forestry operations are governed by national forest management and environmental regulations in producer regions.

Sustainability and sourcing:
The species is widely cultivated in managed plantations in eastern and southern Africa, Brazil, China, and other regions. Plantation-grown material helps reduce pressure on native forests, though the species is recognized as invasive in several ecosystems, necessitating containment and monitoring. Chain-of-custody and plantation registry (e.g., FSC) are commonly applied by producers and exporters to support sustainable supply.

Synonyms Top

Scientific name	Authority	First published in
Racosperma mearnsii	(De Wild.) Pedley	Bot. J. Linn. Soc.92: 249 (1986)

Common names Top

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Filter by language:

Language	Common/alternative name
English	tan wattle
English	black wattle
Afrikaans	swartwattel
Arabic	سنط رخو
Azerbaijani	racosperma mearnsii
Azerbaijani	albizia mearnsii
Czech	akácie mearnsova
Persian	اقاقیا مرنسی
Finnish	parkkiakaasia
Japanese	ブラックワトル
Malayalam	കറുത്ത വാറ്റിൽ
Kinyarwanda	barakatsi
Chinese	澳洲金合欢
Chinese	默氏相思
Chinese	黑荊
Chinese	栲皮树
Chinese	黑荆树
Chinese	黑荆

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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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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Macaronesia
  - Cape Verde
  - Madeira
- Middle Atlantic Ocean
  - Saint Helena
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Sudan
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia
- South Tropical Africa
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Cape Provinces
  - Free State
  - Kwazulu-Natal
  - Lesotho
  - Northern Provinces
  - Swaziland
- West-central Tropical Africa
  - Rwanda
  - Zaïre
- Western Indian Ocean
  - Madagascar
  - Réunion

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Tasmania
  - Victoria
  - Western Australia
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Southeastern Europe
  - Italy
- Southwestern Europe
  - Corse
  - Portugal
  - Spain

Northern America click to expand
- Southwestern U.S.A.
  - California

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Brazil
  - Brazil South
- Caribbean
  - Jamaica
- Western South America
  - Ecuador

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000203882
UNII	H5WWP3W9NY
USDA Plants	ACME80
Tropicos	13037485
INPN	79700
Flora of Italy	8376
KEW	urn:lsid:ipni.org:names:470860-1
The Plant List	ild-502
PFAF	Acacia mearnsii
Open Tree Of Life	343265
Observations.org	133789
NCBI Taxonomy	139012
Nature Serve	2.150031
IPNI	470860-1
iNaturalist	75250
GBIF	2979775
Freebase	/m/0gq0kf
EPPO	ACAMR
EOL	686955
Calflora (Californian flora)	35
USDA GRIN	101107
Wikipedia	Acacia_mearnsii
CMAUP	NPO6062

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

Supplementation of Acacia dealbata versus Acacia mearnsii leaf-meal has potential to maintain growth performance of lambs grazing low-quality communal rangelands in South Africa

Mushunje LH, Marandure T, Chikwanha OC, Bennett J, Hawkins HJ, Palmer AR, Wu L, M.C M, Mapiye C

Trop Anim Health Prod

09-May-2024

PMCID:	PMC11082017
doi:	10.1007/s11250-024-04004-z
PMID:	38722369

Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview

Szmechtyk T, Małecka M

Materials (Basel)

30-Apr-2024

PMCID:	PMC11084627
doi:	10.3390/ma17092123
PMID:	38730929

Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia

Masresha G, Melkamu Y, Mulu G

Scientifica (Cairo)

04-Apr-2024

PMCID:	PMC11008979
doi:	10.1155/2024/3961434
PMID:	38605976

Alternative Approaches to Feeding Small Ruminants and Their Potential Benefits

Boudalia S, Smeti S, Dawit M, Senbeta EK, Gueroui Y, Dotas V, Bousbia A, Symeon GK

Animals (Basel)

14-Mar-2024

PMCID:	PMC10967440
doi:	10.3390/ani14060904
PMID:	38540002

Effects of Nutritional Factors on Fat Content, Fatty Acid Composition, and Sensorial Properties of Meat and Milk from Domesticated Ruminants: An Overview

Ponnampalam EN, Priyashantha H, Vidanarachchi JK, Kiani A, Holman BW

Animals (Basel)

08-Mar-2024

PMCID:	PMC10967350
doi:	10.3390/ani14060840
PMID:	38539939

Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity

Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M

Stud Mycol

27-Feb-2024

PMCID:	PMC11003442
doi:	10.3114/sim.2024.107.04
PMID:	38600961

Bio-mordants: a review

Benli H

Environ Sci Pollut Res Int

23-Feb-2024

PMCID:	PMC10948525
doi:	10.1007/s11356-024-32174-8
PMID:	38396176

Dormancy break, sprouting and later tuber reproduction in response to different tuber sizes of tiger nut (Cyperus esculentus L.)

Liu B, Li H, Chen W, Wang Y, Chen Y, Wei X

R Soc Open Sci

14-Feb-2024

PMCID:	PMC10864778
doi:	10.1098/rsos.231616
PMID:	38356873

Bioactive Fiber Foam Films from Cellulose and Willow Bark Extract with Improved Water Tolerance

Lohtander T, Koso T, Huynh N, Hjelt T, Gestranius M, King AW, Österberg M, Arola S

ACS Omega

09-Feb-2024

PMCID:	PMC10883019
doi:	10.1021/acsomega.3c08906
PMID:	38405518

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

Black (Acacia mearnsii) and silver wattle (Acacia dealbata) invasive tree species impact on soil physicochemical properties in South Africa: A systematic literature review

Lusizi Z, Motsi H, Nyambo P, Elephant DE

Heliyon

09-Jan-2024

PMCID:	PMC10825353
doi:	10.1016/j.heliyon.2024.e24102
PMID:	38293477

Enhancing Pectin Particles with Polymer Additives: Mitigating Rumen Degradation and Minimizing Yellowish Milk Color in Grazed Cows

Vera-Vázquez F, Ramírez-Bribiesca JE, Cruz-Monterrosa RG, Crosby-Galvan MM, Barcena-Gama JR, Ramírez DT, Mejía-Méndez JL, Vallejo-Hernández LH, López-Mena ER

Polymers (Basel)

29-Dec-2023

PMCID:	PMC10780586
doi:	10.3390/polym16010106
PMID:	38201771

Anti-methanogenic potential of seaweeds and seaweed-derived compounds in ruminant feed: current perspectives, risks and future prospects

McGurrin A, Maguire J, Tiwari BK, Garcia-Vaquero M

J Anim Sci Biotechnol

02-Dec-2023

PMCID:	PMC10693045
doi:	10.1186/s40104-023-00946-w
PMID:	38041152

Expanding the Scope of an Amphoteric Condensed Tannin, Tanfloc, for Antibacterial Coatings

Baghersad S, Madruga LY, Martins AF, Popat KC, Kipper MJ

J Funct Biomater

18-Nov-2023

PMCID:	PMC10672460
doi:	10.3390/jfb14110554
PMID:	37998123

Induction of tetraploids in Paper Mulberry (Broussonetia papyrifera (L.) L’Hér. ex Vent.) by colchicine

Lin J, Zhang B, Zou J, Luo Z, Yang H, Zhou P, Chen X, Zhou W

BMC Plant Biol

17-Nov-2023

PMCID:	PMC10655367
doi:	10.1186/s12870-023-04487-2
PMID:	37978431

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 / Gallic acid and derivatives
Syringic Acid	10742	Click to see	198.17	unknown	https://doi.org/10.1021/NP100372T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1002/JSFA.2740390303
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1002/JSFA.2740390303
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Coronaric acid	5316080	Click to see	296.40	unknown	https://doi.org/10.1002/JSFA.2740390303
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see	280.40	unknown	https://doi.org/10.1002/JSFA.2740390303
Octadecadienoic acid, (Z,Z)-	154212	Click to see CCCCCCCCCCCCCC=CC=CC(=O)O	280.40	unknown	https://doi.org/10.1007/BF02901545
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
(3S,5S,8R,9S,10R,11S,13R,14S,17R)-11,14-dihydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,5,6,7,8,9,11,15,16,17-dodecahydrocyclopenta[a]phenanthrene-4,12-dione	21579652	Click to see	562.60	unknown	via CMAUP database
[(2R,3R,4R,5R,8R,9S,10R,12S,13S,14S,17R)-3,4,12,14-tetrahydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-2-yl] acetate	21579662	Click to see CC(=O)OC1CC2(C(CCC3C2CC(C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)C(C1O)O)C	476.60	unknown	via CMAUP database
[(2R,3S,4R,5R,8R,9S,10S,11S,13R,14S,17R)-2,3,11,14-tetrahydroxy-10,13-dimethyl-12-oxo-17-(6-oxopyran-3-yl)-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate	21579654	Click to see	490.50	unknown	via CMAUP database
[(2R,3S,4R,5R,8R,9S,10S,11S,13R,14S,17R)-2,4,11,14-tetrahydroxy-10,13-dimethyl-12-oxo-17-(6-oxopyran-3-yl)-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	21579655	Click to see	490.50	unknown	via CMAUP database
[(2R,3S,4R,5R,8R,9S,10S,11S,13R,14S,17R)-4-acetyloxy-3,11,14-trihydroxy-10,13-dimethyl-12-oxo-17-(6-oxopyran-3-yl)-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-2-yl] acetate	21579659	Click to see CC(=O)OC1CC2(C(CCC3C2C(C(=O)C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)C(C1O)OC(=O)C)C	532.60	unknown	via CMAUP database
2alpha-Acetoxy-3beta,4beta,11alpha,14beta-tetrahydroxy-12-oxo-20,21,22,23-tetradehydro-5alpha-bufanolide	21579658	Click to see CC(=O)OC1CC2(C(CCC3C2C(C(=O)C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)C(C1O)O)C	490.50	unknown	via CMAUP database
5-[(2R,3S,4R,5R,8R,9S,10R,12S,13S,14S,17R)-2,3,4,12,14-pentahydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one	21579661	Click to see	434.50	unknown	via CMAUP database
5-[(2R,3S,4R,5R,8R,9S,10S,11S,13R,14S,17R)-2,3,4,11,14-pentahydroxy-10,13-dimethyl-12-oxo-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one	21579653	Click to see	448.50	unknown	via CMAUP database
5-[(3S,4R,5R,8R,9S,10S,11S,13R,14S,17R)-3,4,11,14-tetrahydroxy-10,13-dimethyl-12-oxo-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one	21579657	Click to see	432.50	unknown	via CMAUP database
5-[(3S,4R,5R,8R,9S,10S,11S,13R,14S,17R)-4,11,14-trihydroxy-10,13-dimethyl-12-oxo-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one	21579656	Click to see	564.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(3R,5S,8R,10S,13R,14S,17R)-11,14-dihydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,5,6,7,8,15,16,17-decahydrocyclopenta[a]phenanthrene-4,12-dione	21579663	Click to see	560.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose	5988	Click to see	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-methylbutan-1-one	5323592	Click to see	372.40	unknown	https://doi.org/10.1021/NP100372T
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	13965334	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CO	346.33	unknown	https://doi.org/10.1021/NP100372T
Di-O-Methylcrenatin	10736338	Click to see	346.33	unknown	https://doi.org/10.1021/NP100372T
Glucopyranoside, 4-hydroxy-2-methoxyphenyl, beta-D-(8CI); 4-Hydroxy-2-methoxyphenyl beta-D-glucopyranoside	72744980	Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O	302.28	unknown	https://doi.org/10.1021/NP100372T
Isotachioside	15098566	Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O	302.28	unknown	https://doi.org/10.1021/NP100372T
Multifidol glucoside	14412552	Click to see	372.40	unknown	https://doi.org/10.1021/NP100372T
> Phenylpropanoids and polyketides / Coumarins and derivatives
Urolithin C	60198001	Click to see	244.20	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol	102115501	Click to see	562.50	unknown	via CMAUP database
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol	101297694	Click to see	562.50	unknown	via CMAUP database
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol	102115500	Click to see	562.50	unknown	via CMAUP database
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	102400061	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
(2R,3S)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	102400062	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	594.50	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-8-[3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	75605032	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP100372T
6-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	75604966	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	578.50	unknown	https://doi.org/10.1021/NP100372T
8-[3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	77916041	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP100372T
Epifisetinidol-(4beta->8)-catechin	14332863	Click to see	562.50	unknown	https://doi.org/10.1021/NP100372T
Epirobinetinidol-(4beta,8)-catechin	51042196	Click to see	578.50	unknown	https://doi.org/10.1021/NP100372T
Fisetinidol-(4A8)-catechin	14332862	Click to see	562.50	unknown	via CMAUP database
Fisetinidol-(4alpha,6)-gallocatechin	51041987	Click to see	578.50	unknown	https://doi.org/10.1021/NP100372T
Fisetinidol-(4alpha,8)-catechin	11731408	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	562.50	unknown	https://doi.org/10.1021/NP100372T
Robinetinidol-(4alpha->8)-catechin-(6->4alpha)-robinetinidol	442689	Click to see	866.80	unknown	via CMAUP database
Robinetinidol-(4alpha,8)-catechin	70697937	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP100372T
Robinetinidol-(4alpha,8)-gallocatechin	70697956	Click to see	594.50	unknown	https://doi.org/10.1021/NP100372T
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	https://doi.org/10.1021/NP100372T
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1039/P19930002467 https://doi.org/10.1021/NP100372T
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1039/P19930002467
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin	65084	Click to see	306.27	unknown	https://doi.org/10.1016/S0031-9422(00)85974-9 https://doi.org/10.1021/NP100372T https://doi.org/10.1039/P19930002467
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(-)-Fisetinidol	442397	Click to see	274.27	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137845/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096474/ https://doi.org/10.1080/10286020.2011.597384
3,3',4',7-Tetrahydroxyflavan	3984814	Click to see	274.27	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096474/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137845/ https://doi.org/10.1080/10286020.2011.597384
5-[(2R,3R)-3,7-dihydroxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,2,3-triol	101846310	Click to see	290.27	unknown	via CMAUP database
Robinetinidol	12314983	Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC(=C(C(=C3)O)O)O)O	290.27	unknown	https://doi.org/10.1021/NP100372T
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
3',4',7-Trihydroxyflavaonone	3496769	Click to see	272.25	unknown	https://doi.org/10.1021/NP100372T
Butin	92775	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O	272.25	unknown	https://doi.org/10.1021/NP100372T
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin	471	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1021/NP100372T
Garbanzol	442410	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O	272.25	unknown	via CMAUP database
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1021/NP100372T
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
(2R,3S,4S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7-triol	442398	Click to see	290.27	unknown	https://doi.org/10.1016/S0031-9422(00)86352-9
ent-Epifisetinidol-4beta-ol	44257142	Click to see	290.27	unknown	via CMAUP database
Fisetinidol-4alpha-ol	164762	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O	290.27	unknown	https://doi.org/10.1039/J39700001800 https://doi.org/10.1016/S0031-9422(00)85959-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin	5281614	Click to see	286.24	unknown	via CMAUP database
Isorhamnetin	5281654	Click to see	316.26	unknown	https://doi.org/10.1016/S0031-9422(00)85974-9
Mearnsetin	10359384	Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	332.26	unknown	https://doi.org/10.1016/S0031-9422(00)85974-9
Robinetin	5281692	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[5-(3,7-dihydroxy-3,4-dihydro-2H-chromen-2-yl)-3-hydroxy-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	75604965	Click to see	466.40	unknown	https://doi.org/10.1021/NP100372T
4'-O-methylrobinetinidol 3'-O-beta-D-glucopyranoside	51041986	Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C3C(CC4=C(O3)C=C(C=C4)O)O)O	466.40	unknown	https://doi.org/10.1021/NP100372T
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	154496989	Click to see	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)85974-9
myricetin 3-O-beta-D-glucopyranoside	5318606	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1016/S0031-9422(00)85974-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one	44558988	Click to see	742.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Fisetin 3-methyl ether	9839293	Click to see	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Fisetin Tetramethyl Ether	631171	Click to see	342.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1016/S0031-9422(00)85974-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Butein	5281222	Click to see	272.25	unknown	https://doi.org/10.1016/S0031-9422(00)85959-2
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose	440221	Click to see	484.40	unknown	https://doi.org/10.1021/NP100372T
1,6-Digalloyl-beta-D-glucopyranose	3332212	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	484.40	unknown	https://doi.org/10.1021/NP100372T

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Acacia mearnsii

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