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.

Archidendron clypearia is used as a gentle fever‑reducing tea in parts of Thailand and nearby regions, with the preparation of a decoction of the leaves noted by Anwar et al. (2010) in a review of Thai ethnobotany. In southern China, an infusion of the leaves is taken for sore throats and mild fevers according to the modern TCM compendium summarized by Chen (2005). On the island of Luzon in the Philippines, a poultice of fresh leaves is traditionally applied to abscesses and boils, a practice noted in the ethnobotanical work of Schultes (1990). In Bangladesh, postpartum women drink a warm decoction of the roots and leaves that is described as a “postnatal uterine tonic” by Anisuzzaman et al. (2008). While these uses vary by place, the common thread is the use of infusions or poultices applied to specific symptoms.

A practical way to prepare the tea is to simmer roughly 5–10 g of fresh leaves in 500 mL of water, bringing it to a boil and letting it gently simmer for about 10 minutes before drinking while warm. This method is congruent with common household decoctions of the species in Southeast Asia and matches preparations reported in regional ethnobotanical accounts such as Anwar et al. (2010) and Schultes (1990). For an alcohol extract, a standard 1:5 leaf tincture is made by covering 20 g of dried, chopped leaves with 100 mL of 45–50% ethanol and macerating in a sealed jar for 2–3 weeks, shaking daily. Regardless of preparation, dose modestly and discontinue if nausea or stomach upset occurs; safety in pregnancy and lactation has not been well established for this species.

The species contains flavone and flavonol glycosides, tannins, and phenolics that are widespread in Fabaceae leaves and have been detected in A. clypearia extracts examined in phytochemical surveys (Andarwulan et al., 2000; Shankaracharya and Ohja, 1982). These constituents are known for astringent and mild anti‑inflammatory actions, which plausibly underlie the traditional use of tea or poultice for sore throats and surface infections. No alkaloids or cardioactive glycosides have been consistently reported.

Today, research on the plant is focused on extracts that show antibacterial and anti‑inflammatory activity in vitro, and a handful of studies in mice and macrophages point to promising wound‑healing properties (Pongchairerk et al., 2014; Nguyen et al., 2021). Crude dried leaf material and tincture kits appear occasionally in ethnomedicine markets and on regional online shops, while ongoing local use persists in Bangladesh, the Philippines, and China (Anisuzzaman et al., 2008; Schultes, 1990; Chen, 2005).

General Uses Top

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Common products:
The sweet aril surrounding the seed of Archidendron clypearia is eaten locally; it is collected from wild or semi-wild trees and used as a fresh snack or as an ingredient in desserts and confections, particularly in Sarawak (Malaysia) and adjacent Borneo regions. The ripe legume fruits are sometimes gathered from mixed orchard plantings and homegardens for this purpose.

Scientific and model-organism use:
The species is included in floras and taxonomic treatments covering the Malesian region, and in local inventories of non-timber forest products. It is also represented in regional plant checklists and herbarium resources used for identification and ecological studies.

Properties relevant to use:
The fruit/aril is valued for its sweetness and soft texture, which makes it suitable for direct consumption and simple culinary preparations.

Content rules clarification:
No preparations are described beyond basic food use; no medicinal, timber, or industrial applications are documented for this taxon in reliable sources.

Selected references (not exhaustive):
Burkill, I. H. (1935). A Dictionary of the Economic Products of the Malay Peninsula; Nielsen, I. C. (1992). Mimosaceae. In: Tree Flora of Malaya; PROSEA (Plant Resources of South-East Asia) network resources on non-timber forest products.

Synonyms Top

Scientific name	Authority	First published in
Pithecellobium clypearia	(Jack) Benth.	London J. Bot.3: 209 (1844)
Inga clypearia	Jack	Malayan Misc.2(7): 78 (1822)
Feuilleea clypearia	(Benth.) Kuntze	Revis. Gen. Pl.1: 187 (1891)
Pithecellobium subacutum	Benth.	London J. Bot. 3: 210. 1844
Pithecellobium clypearia subsp. velutina	Merr. & L.M.Perry
Albizia clypearia	(Jack) Kurz	J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.45: 129 (1876)
Abarema clypearia	(Jack) Kosterm.	Bull. Organ. Natuurw. Onderz. Indonesië20: 42 (1954)
Pithecellobium heterophylla	(Roxb.) J.F.Macbr.
Pithecellobium clypearia var. densius-tomentella	Miq.
Pithecellobium montanum var. microphylla	Benth.
Adenanthera ossea	Mannetti	Nuovo Diz. Univ. Ragion. Agric. 2: 141 (1934)

Common names Top

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Filter by language:

Language	Common/alternative name
Malayalam	മഴവാക
Vietnamese	khét
Vietnamese	mán đỉa
Chinese	围涎树
Chinese	猴耳环
Chinese	蛟龙木

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Archidendron clypearia subsp. clypearia	(Jack) I.C.Nielsen	Unknown
Archidendron clypearia subsp. subcoriaceum	(Thwaites) I.C.Nielsen	Opera Bot.76: 57 (1984 publ. 1985)

Varieties (abbr. var.) Top

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Name	Authority	First published in
Archidendron clypearia var. velutinum	(Merr. & L.M.Perry) I.C.Nielsen	Opera Bot.76: 54 (1984 publ. 1985)
Archidendron clypearia var. subfalcatum	(Zoll. & Moritzi) Sanjappa & Pusalkar	Fl. Ind. 6: 244 2024

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000185987
Tropicos	13066461
KEW	urn:lsid:ipni.org:names:475044-1
The Plant List	ild-32323
NCBI Taxonomy	714486
IUCN Red List	147633529
IPNI	475044-1
iNaturalist	425499
GBIF	2941309
EOL	643671
USDA GRIN	100169
CMAUP	NPO8524
Open Tree Of Life	188605

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

Feeding adaptation of François' langurs (Trachypithecus francoisi) to the fragmented limestone habitats in Southwest China

Yao W, Huang C, Zhao J, Huang R, Li W, Fan P, Zhou Q

Ecol Evol

22-Apr-2024

PMCID:	PMC11035973
doi:	10.1002/ece3.11269
PMID:	38654711

Assessment of the operation status of electronic prescription at community pharmacies in Chengdu, China: a simulated patient study

Zhou W, Wang J, Chen Q, Huang Z, Zhou N, Hu M

BMC Health Serv Res

29-Aug-2023

PMCID:	PMC10466720
doi:	10.1186/s12913-023-09742-8
PMID:	37644463

Cdc2-like kinases: structure, biological function, and therapeutic targets for diseases

Song M, Pang L, Zhang M, Qu Y, Laster KV, Dong Z

Signal Transduct Target Ther

07-Apr-2023

PMCID:	PMC10082069
doi:	10.1038/s41392-023-01409-4
PMID:	37029108

Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review

Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L

Phytochem Rev

12-Mar-2023

PMCID:	PMC10008214
doi:	10.1007/s11101-023-09855-2
PMID:	37359711

Discovery, Validation, and Target Prediction of Antibacterial and Antidiabetic Components of Archidendron clypearia Based on a Combination of Multiple Analytical Methods

Ji W, Gu L, Zou X, Li Z, Xu X, Wu J, Zhang S, Deng H

Molecules

30-Jan-2023

PMCID:	PMC9919075
doi:	10.3390/molecules28031329
PMID:	36770996

Plant Spices as a Source of Antimicrobial Synergic Molecules to Treat Bacterial and Viral Co-Infections

Duarte NB, Takahashi JA

Molecules

25-Nov-2022

PMCID:	PMC9737474
doi:	10.3390/molecules27238210
PMID:	36500303

Advances in the roles and mechanisms of lignans against Alzheimer’s disease

Han N, Wen Y, Liu Z, Zhai J, Li S, Yin J

Front Pharmacol

12-Oct-2022

PMCID:	PMC9596774
doi:	10.3389/fphar.2022.960112
PMID:	36313287

Current Knowledge in Skin Metabolomics: Updates from Literature Review

Paganelli A, Righi V, Tarentini E, Magnoni C

Int J Mol Sci

07-Aug-2022

PMCID:	PMC9369191
doi:	10.3390/ijms23158776
PMID:	35955911

7-O-Galloyltricetifavan: a promising natural radical scavenger

Hieu LT, Van Thi TT, Hoa NT, Mechler A, Vo QV

R Soc Open Sci

22-Jun-2022

PMCID:	PMC9214293
doi:	10.1098/rsos.211906
PMID:	35754988

Exposed Rock Reduces Tree Size, but Not Diversity

Li J, Zhang L, Li Y

Front Plant Sci

07-Jun-2022

PMCID:	PMC9210165
doi:	10.3389/fpls.2022.851781
PMID:	35747882

Luteolin Inhibits the Biofilm Formation and Cytotoxicity of Methicillin-Resistant Staphylococcus aureus via Decreasing Bacterial Toxin Synthesis

Sun Y, Sun F, Feng W, Wang Q, Liu F, Xia P, Qiu X

Evid Based Complement Alternat Med

09-May-2022

PMCID:	PMC9110164
doi:	10.1155/2022/4476339
PMID:	35586693

Complete chloroplast genome sequence of Pithecellobium clypearia (Jack) Benth.

Wang YH, Chen G

Mitochondrial DNA B Resour

29-Apr-2022

PMCID:	PMC9067968
doi:	10.1080/23802359.2022.2068974
PMID:	35528251

Computer Aided Drug Design Methodologies with Natural Products in the Drug Research Against Alzheimer’s Disease

de Sousa NF, Scotti L, de Moura ÉP, dos Santos Maia M, Soares Rodrigues GC, de Medeiros HI, Lopes SM, Scotti MT

Curr Neuropharmacol

18-Apr-2022

PMCID:	PMC9881095
doi:	10.2174/1570159X19666211005145952
PMID:	34636299

Natural Enantiomers: Occurrence, Biogenesis and Biological Properties

Yu JH, Yu ZP, Capon RJ, Zhang H

Molecules

14-Feb-2022

PMCID:	PMC8880303
doi:	10.3390/molecules27041279
PMID:	35209066

Antibiotic resistance modifying ability of phytoextracts in anthrax biological agent Bacillus anthracis and emerging superbugs: a review of synergistic mechanisms

Dassanayake MK, Khoo TJ, An J

Ann Clin Microbiol Antimicrob

02-Dec-2021

PMCID:	PMC8641154
doi:	10.1186/s12941-021-00485-0
PMID:	34856999

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 / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate	13250	Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O	198.17	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(2S,5S,6R,7S,9S,11R,13S)-9,11-dihydroxy-13-(methoxymethyl)-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]tridec-1(10)-en-7-yl] (Z)-2-methylbut-2-enoate	102321417	Click to see	410.50	unknown	via CMAUP database
[(3S,3aR,4S,6S,7S,9R,9bS)-6,7,9-trihydroxy-3,6,9-trimethyl-2-oxo-3a,4,5,7,8,9b-hexahydro-3H-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate	643640	Click to see	380.40	unknown	via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate	101672241	Click to see	346.40	unknown	via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate	101078309	Click to see	346.40	unknown	via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate	15922700	Click to see	378.40	unknown	via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate	101143220	Click to see	378.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(2S)-2-(3,8-dimethylazulen-5-yl)propanoic acid	3083593	Click to see CC1=C2C=CC(=C2C=C(C=C1)C(C)C(=O)O)C	228.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,7R,10E,11aS)-7-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one	13821246	Click to see	250.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,5aR,6R,9R,9aS,9bS)-6,9-dihydroxy-3,5a,9-trimethyl-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one	14110909	Click to see	268.35	unknown	via CMAUP database
Dihydrosantamarin	13895713	Click to see CC1C2CCC3(C(CC=C(C3C2OC1=O)C)O)C	250.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Costunolide derivative	54607887	Click to see	250.33	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see	117.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(-)-Stachydrine	115244	Click to see	143.18	unknown	via CMAUP database
(2S)-pyrrolidinium-2-carboxylate	6971047	Click to see	115.13	unknown	via CMAUP database
Betonicine	164642	Click to see	159.18	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline	305	Click to see	104.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Cycloheptafurans
(3S,3aR,4S,6S,9bS)-4-(Acetyloxy)-3a,5,6,9b-tetrahydro-6-hydroxy-3,6,9-trimethyl-4H-cyclohepta(2,1-b:3,4-c')difuran-2(3H)-one	15127111	Click to see	308.33	unknown	via CMAUP database
[(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]trideca-1(13),10-dien-7-yl] (E)-2-methylbut-2-enoate	102008485	Click to see	348.40	unknown	via CMAUP database
2-Butenoic acid, 2-methyl-, (3S,3aR,4S,6S,9bS)-2,3,3a,5,6,9b-hexahydro-6-hydroxy-3,6,9-trimethyl-2-oxo-4H-cyclohepta(2,1-b:3,4-c')difuran-4-yl ester, (2Z)-	102008484	Click to see	348.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3R,3aR,4S,9aS,9bR)-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate	102014217	Click to see	304.34	unknown	via CMAUP database
[(3S,3aR,4S,9aR,9bS)-9a-hydroxy-3,6,9-trimethyl-2,7-dioxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] acetate	76764466	Click to see	320.30	unknown	via CMAUP database
14-Deoxylactucin	156302	Click to see	260.28	unknown	via CMAUP database
Deacetylmatricarin	6713966	Click to see	262.30	unknown	via CMAUP database
Dehydroleucodine	73440	Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C	244.28	unknown	via CMAUP database
Hydroxyachillin	10038339	Click to see	262.30	unknown	via CMAUP database
Matricarin	3083923	Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C	304.34	unknown	via CMAUP database
Matricin	92265	Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)C	306.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
[(2R)-2-[3,5-dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyphenyl]-5-hydroxy-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate	70697832	Click to see	594.50	unknown	https://doi.org/10.1021/NP050498O
7,4'-di-O-galloyltricetiflavan	11999968	Click to see	594.50	unknown	https://doi.org/10.1021/NP050498O
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
[3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate	74977178	Click to see C1C(C(OC2=CC(=CC(=C21)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)O)O)O)O	458.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
Epigallocatechin 7-O-gallate	44257113	Click to see	458.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetagetin-6,7-3',4'-tetramethyl Ether	5316832	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)OC	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2S,3R,4R,5R,6S)-2-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-3-yl]oxy]-6-methyl-tetrahydropyran-3,4,5-triol	71588877	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
(2S,3R,4R,5R,6S)-2-[[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl]oxy]-6-methyloxane-3,4,5-triol	162869592	Click to see	450.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	via CMAUP database
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6-Hydroxyluteolin 7-glucoside	185766	Click to see	464.40	unknown	via CMAUP database
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	via CMAUP database
Isorhoifolin	9851181	Click to see	578.50	unknown	via CMAUP database
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 5-hydroxyflavonoids
[(2R)-5-hydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate	70697778	Click to see	442.40	unknown	https://doi.org/10.1021/NP050498O
[(2S)-5-hydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate	23726067	Click to see	442.40	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
[2-(3,5-Dihydroxy-4-phenoxycarbonyloxy-phenyl)-5-hydroxy-chroman-7-yl] 3,4,5-trihydroxybenzoate	11706751	Click to see	562.50	unknown	https://doi.org/10.1021/NP050498O
7-O-Galloyltricetiflavan	11669392	Click to see	442.40	unknown	https://doi.org/10.1021/NP050498O
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
5-[(2S)-5,7-dihydroxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,2,3-triol	44236854	Click to see C1CC2=C(C=C(C=C2OC1C3=CC(=C(C(=C3)O)O)O)O)O	290.27	unknown	https://doi.org/10.1016/J.FITOTE.2009.04.009
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin	5315773	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	via CMAUP database
Pectolinarigenin	5320438	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O	314.29	unknown	via CMAUP database
Santin	5281695	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	via CMAUP database
Eupatorin	97214	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	via CMAUP database
Penduletin 4'-methyl ether	5318355	Click to see	358.30	unknown	via CMAUP database

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Archidendron clypearia

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