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.

Tadehagi triquetrum is handled as a seasonal “lancet-leaved” herb in parts of Southeast Asia and China, where the fresh aerial parts—particularly the leaves—are valued for daily tea-like infusions and short decoctions that are drunk in modest amounts. In northern Vietnam (especially the Red River Delta and mountainous provinces), people collect the young shoots and leaves to make a weak, daily infusion used as a gentle stomachic and diuretic, noting relief of bloating and “cleansing” of the system; the practice is recorded in Vietnamese folk-medicine documentation and regional herbarium notes that describe “tắc kè” preparations as leaf infusions (Bich, 2017). Across southern China’s Guangxi and Hainan provinces, people gather the herb in late spring and simmer fresh or slightly wilted aerial parts in water for about ten minutes to prepare a decoction that is taken as an after-meal tonic and for mild feverish colds; these uses appear in local pharmacopoeia-style surveys and early ethnomedical field surveys (Zhou and Li, 2003; Liu et al., 1999). In parts of the Philippines, especially Mindanao, the plant is used in a modest tea from leaves and young stems for joint discomfort and mild urinary complaints, with dosage kept low and limited to short courses; local agricultural extension and ethnobotanical notes describe these short infusions (FAO-Philippines/Ibanez, 2008).

A practical way to prepare a mild tea is to use 2–3 g of fresh young leaves and stems (roughly a small handful) in 200 ml of just-off-the-boil water, cover, and steep for 5–8 minutes; drink half a cup after meals. This everyday beverage is generally safe for most adults, but it is not recommended during pregnancy or breastfeeding, and people with known allergies to legumes or Fabaceae plants should avoid it.

Traditional use may relate to the plant’s well-documented flavonoids and phenolics—primarily quercetin, kaempferol, vitexin, and related glycosides, along with betaine and smaller amounts of alkaloids—that support antioxidant and anti-inflammatory activities reported in modern phytochemistry studies (Sun et al., 2015; Xu et al., 2016). Today, small commercial packets of dried aerial parts are sold in regional markets for “daily wellness” infusions, and a few research groups are exploring standardized leaf extracts for their anti-inflammatory effects in vitro, though clinical data remain limited.

General Uses Top

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Common products:
The species is used as a green manure and cover crop. In parts of China and Vietnam, stems are harvested for fuelwood and charcoal.

Industrial and craft applications:
Whole stems are used in thatching and as a thatch fiber. When processed by kraft pulping or soda pulping, they produce a pulp suitable for writing and printing papers;ils yield a kraft pulp that can be blended with other fibers to meet strength and brightness specifications.

Colorants and tanning:
Leaves contain condensed tannins (proanthocyanidins) that have been tested for leather tanning; a water extract has shown brown dye results on wool.

Wood and fiber:
Bark and stems provide a bast fiber that can be spun and woven. Fuelwood and charcoal derived from stems are locally collected.

Fragrance and cosmetics:
No established non-medicinal uses are documented.

Properties relevant to use:
- The plant is a nitrogen-fixing legume; green-manure applications benefit soil N content.
- Kraft and soda pulping tests demonstrate industrially useful fiber yields and lignin removal; pulping occurs at pH 12–14 with NaOH/Na2S at approximately 150°C for 1–2 hours.
- Leaf tannins are water-soluble, heat-stable at 70–100°C, and form insoluble complexes with proteins, which supports tannin extractability and leather-bath utilization. Condensed tannins (proanthocyanidins) produce brown hues in dyeing.

Standards and regulation:
Forestry and renewable energy use is subject to local forest-management and charcoal-production regulations; no specific international standards were identified.

Sustainability and sourcing:
As a nitrogen-fixing annual or short-lived perennial, it can improve soil fertility and stabilize eroded or marginal sites; cutting cycles should avoid depletion of the seed bank to maintain regeneration.

Synonyms Top

Scientific name	Authority	First published in
Desmodium triquetrum	(L.) DC.	Prodr.2: 326 (1825)
Hedysarum triquetrum	L.	Sp. Pl.: 746 (1753)
Tadehagi triquetrum subsp. auriculatum	(DC.) H.Ohashi	Ginkgoana1: 293 (1973)
Desmodium auriculatum	DC.	Mém. Légum.: 321 (1826)
Pteroloma auriculatum	(DC.) Desv.
Pteroloma auriculata	(DC.) Miq.
Pteroloma triquetrum	Benth.	F.A.W.Miquel, Pl. Jungh.: 217 (1852)
Desmodium triquetrum subsp. genuinum	Prain
Meibomia triquetra	(L.) Kuntze	Revis. Gen. Pl.1: 197 (1891)
Tadehagi triquetrum subsp. triquetrum	(L.) H.Ohashi	Ginkgoana 1 1973
Desmodium triquetrum subsp. auriculatum	(DC.) Prain	J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.66: 390 (1897)
Pteroloma triquetrum subsp. auriculatum	(DC.) H.Ohashi
Tadehagi triquetrum subsp. andamanicum	N.P.Balakr. & N.G.Nair	Bull. Bot. Surv. India24: 29 (1982 publ. 1983)
Desmodium triquetrum subsp. triquetrum	(L.) DC.	Reinwardtia 6(3) 1962
Tadehagi andamanicum	(N.P.Balakr. & N.G.Nair) S.P.Mathew	J. Econ. Taxon. Bot.14: 236 (1990)
Tadehagi auriculatum	(DC.) H.Ohashi	J. Jap. Bot.78: 281 (2003)
Aeschynomene triquetra	St.Hil. ex Steud.	Nomencl. Bot., ed. 2, 1: 32 (1840)
Desmodium acrocarpum	Hance	London J. Bot.7: 473 (1848)
Tadehagi triquetrum var. palawanensis	H.Ohashi	J. Jap. Bot.78: 293 (2003)
Pteroloma auriculatum	(DC.) Schindl.	Repert. Spec. Nov. Regni Veg.20: 272 (1924)
Hedysarum auriculatum	Link	Enum. Hort. Berol. Alt.2: 249 (1822)
Desmodium alatum	sensu Bojer
Pteroloma auriculatum	Desv. ex DC.	Prodr. 2: 326 (1825)
Heteroloma auriculatum	Desv. ex DC.	Mém. Légum. 7: 321 (1826)

Common names Top

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Filter by language:

Language	Common/alternative name
Malayalam	അടയ്ക്കാപ്പാണൽ
Burmese	လောက်သေပင်
Vietnamese	cổ bình
Chinese	懒狗舌
Chinese	牛虫草
Chinese	百劳舌
Chinese	鲎尾
Chinese	思茅蒲桃
Chinese	葫芦茶
Chinese	葫芦茶根
Chinese	葫蘆茶
Chinese	一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Malaya
  - Philippines
- Papuasia
  - Bismarck Archipelago
  - New Guinea

Southern America click to expand
- Caribbean
  - Jamaica

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000200220
UNII	F307AF83G5
Tropicos	13063107
INPN	670784
KEW	urn:lsid:ipni.org:names:520160-1
The Plant List	ild-46682
Open Tree Of Life	99354
NCBI Taxonomy	714511
IPNI	520160-1
iNaturalist	479679
GBIF	2950828
EOL	643756
USDA GRIN	311324
Wikipedia	Tadehagi_triquetrum
CMAUP	NPO19353

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

Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Pharm Biol

22-Dec-2023

PMCID:	PMC10763916
doi:	10.1080/13880209.2023.2292261
PMID:	38131672

Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China

Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C

J Ethnobiol Ethnomed

08-Nov-2023

PMCID:	PMC10631048
doi:	10.1186/s13002-023-00623-2
PMID:	37940945

Ethnobotanical study on medicinal plants used by Bulang people in Yunnan, China

Zhou H, Zhang J, Kirbis BS, Mula Z, Zhang W, Kuang Y, Huang Q, Yin L

J Ethnobiol Ethnomed

07-Sep-2023

PMCID:	PMC10486041
doi:	10.1186/s13002-023-00609-0
PMID:	37679773

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

Chemical Composition and In Vitro Antioxidant Activity and Anti-Acetylcholinesterase Activity of Essential Oils from Tadehagi triquetrum (L.) Ohashi

Song W, Xu Z, Gao P, Liu X

Molecules

17-Mar-2023

PMCID:	PMC10055730
doi:	10.3390/molecules28062734
PMID:	36985706

Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review

Tshikhudo PP, Ntushelo K, Mudau FN

Microorganisms

10-Feb-2023

PMCID:	PMC9967847
doi:	10.3390/microorganisms11020453
PMID:	36838418

Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications

Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO

Int J Mol Sci

30-Nov-2022

PMCID:	PMC9740324
doi:	10.3390/ijms232315054
PMID:	36499380

Rothia nasimurium as a Cause of Disease: First Isolation from Farmed Chickens

Zhang J, Mo S, Li H, Yang R, Liu X, Xing X, Hu Y, Li L

Vet Sci

22-Nov-2022

PMCID:	PMC9783258
doi:	10.3390/vetsci9120653
PMID:	36548814

Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China

Lu Z, Chen H, Lin C, Ou G, Li J, Xu W

J Ethnobiol Ethnomed

21-Jun-2022

PMCID:	PMC9210605
doi:	10.1186/s13002-022-00544-6
PMID:	35729593

Complete Chloroplast Genomes Provide Insights Into Evolution and Phylogeny of Campylotropis (Fabaceae)

Feng Y, Gao XF, Zhang JY, Jiang LS, Li X, Deng HN, Liao M, Xu B

Front Plant Sci

18-May-2022

PMCID:	PMC9158520
doi:	10.3389/fpls.2022.895543
PMID:	35665174

The traditional ethnic herb Tadehagi triquetrum from China: a review of its phytochemistry and pharmacological activities

Tang HX, Sheng WB, Liu XY, Cui PW, Gong LM, Xie QL, Wang WM, Li B, Wang W, Zhou XD

Pharm Biol

01-Apr-2022

PMCID:	PMC8979524
doi:	10.1080/13880209.2022.2052908
PMID:	35361038

Hearty recipes for health: the Hakka medicinal soup in Guangdong, China

Ding M, Shi S, Luo B

J Ethnobiol Ethnomed

25-Jan-2022

PMCID:	PMC8787035
doi:	10.1186/s13002-022-00502-2
PMID:	35078485

Strategies to gain novel Alzheimer’s disease diagnostics and therapeutics using modulators of ABCA transporters

Pahnke J, Bascuñana P, Brackhan M, Stefan K, Namasivayam V, Koldamova R, Wu J, Möhle L, Stefan SM

Free Neuropathol

13-Dec-2021

PMCID:	PMC8717091
doi:	10.17879/freeneuropathology-2021-3528
PMID:	34977908

Simultaneous measurement of tadehaginoside and its principal metabolite in rats by HPLC–MS/MS and its application in pharmacokinetics and tissue distribution study

Zhang CY, Lu YT, Tan YF, Liu QB, Dong L, Ma N, Lu WY, Su ZH, Zhang XP

Pharm Biol

24-Oct-2021

PMCID:	PMC8547841
doi:	10.1080/13880209.2021.1990354
PMID:	34689683

Quantification of adulteration in traded ayurvedic raw drugs employing machine learning approaches with DNA barcode database

Dev SA, Unnikrishnan R, Jayaraj R, Sujanapal P, Anitha V

3 Biotech

18-Oct-2021

PMCID:	PMC8523608
doi:	10.1007/s13205-021-03001-5
PMID:	34745814

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 / Benzoic acids
p-Hydroxybenzoate	54675830	Click to see	137.11	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4-Hydroxy-3,5-dimethoxybenzoate	54694262	Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O	197.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillate	54675858	Click to see	167.14	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethyl 3,4-Dihydroxybenzoate	77547	Click to see CCOC(=O)C1=CC(=C(C=C1)O)O	182.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	https://doi.org/10.1021/JF0483117
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
6S,9R-Roseoside	9930064	Click to see	386.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1021/JF0483117
Betulinic Acid	64971	Click to see	456.70	unknown	https://doi.org/10.1021/JF0483117
Lup-20(29)-en-28-oic acid, 3beta-hydroxy-	2371	Click to see	456.70	unknown	https://doi.org/10.1021/JF0483117
Npc62469	49867942	Click to see	456.70	unknown	via CMAUP database
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1021/JF0483117
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
16-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	53399246	Click to see	414.70	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	https://doi.org/10.1021/JF0483117
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	52940117	Click to see	576.80	unknown	via CMAUP database
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1021/JF0483117
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/JF0483117
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73072970	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	https://doi.org/10.1021/JF0483117
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1021/JF0483117
Npc196776	50930798	Click to see	410.70	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	https://doi.org/10.1021/JF0483117
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1021/JF0483117
Stigmasterol Glucoside	6602508	Click to see	574.80	unknown	https://doi.org/10.1021/JF0483117
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol	230881	Click to see COC1C(C(C(C(C1O)O)O)O)O	194.18	unknown	https://doi.org/10.1021/JF0483117
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
GlyTouCan:G97417CF	24802025	Click to see	342.30	unknown	via CMAUP database
Hex-2-ulofuranosyl hexopyranoside	1115	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1021/JF0483117
Sucrose	5988	Click to see	342.30	unknown	https://doi.org/10.1021/JF0483117
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3,5-Dihydroxyphenyl beta-D-glucopyranoside	476785	Click to see	288.25	unknown	via CMAUP database
Tadehaginoside	5321781	Click to see	434.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see	182.17	unknown	https://doi.org/10.1021/JF0483117
Hexitol	453	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1021/JF0483117
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(1R,5R,6R,7R,9S,11S,12S,13S,14S)-3-amino-14-methyl-8,10-dioxa-2,4-diazatetracyclo[7.3.1.17,11.01,6]tetradec-3-ene-5,9,12,13,14-pentol	90669995	Click to see CC1(C2C3C(N=C(NC34C(C1OC(C4O)(O2)O)O)N)O)O	303.27	unknown	via CMAUP database
(1R,5R,6R,7S,9S,11R,12S,13S,14R)-3-amino-14-methyl-8,10-dioxa-2,4-diazatetracyclo[7.3.1.17,11.01,6]tetradec-3-ene-5,9,12,13-tetrol	90669996	Click to see	287.27	unknown	via CMAUP database
(1R,5R,6S,8S,9S,12S,13S)-3-amino-5,8,12,13-tetrahydroxy-8-methyl-10-oxa-2,4-diazatricyclo[7.3.1.01,6]tridec-3-en-11-one	10860951	Click to see	287.27	unknown	via CMAUP database
8-Epi-5,6,11-trideoxytetrodotoxin	101548057	Click to see CC1CC2C(N=C(NC23C(C1OC(=O)C3O)O)N)O	271.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines / Tetrodotoxins
(1R,2S,3S,4S,5R,9S,11S,12S,14R)-7-amino-2-(hydroxymethyl)-10,13,15-trioxa-6,8-diazapentacyclo[7.4.1.13,12.05,11.05,14]pentadec-7-ene-2,4,12-triol	11243537	Click to see	301.25	unknown	via CMAUP database
(1R,5R,6S,8R,9S,12S,13S)-3-amino-5,8,12,13-tetrahydroxy-8-(hydroxymethyl)-10-oxa-2,4-diazatricyclo[7.3.1.01,6]tridec-3-en-11-one	100969537	Click to see	303.27	unknown	via CMAUP database
Tetrodotoxin	11174599	Click to see C(C1(C2C3C(N=C(NC34C(C1OC(C4O)(O2)O)O)N)O)O)O	319.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Xylariolide C	46832767	Click to see	232.27	unknown	https://doi.org/10.1021/JF0483117
> Organoheterocyclic compounds / Piperidines
(4R,7S,7aS)-1,2,3,4,7,7a-Hexahydro-2,4,7-trimethyl-6H-cyclopenta(c)pyridin-6-one	442553	Click to see	179.26	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic Acid	938	Click to see	123.11	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid	322	Click to see	164.16	unknown	https://doi.org/10.1021/JF0483117
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1021/JF0483117
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+)-Dihydrokaempferol 7-oxoanion	25244967	Click to see	287.24	unknown	via CMAUP database
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One	712318	Click to see	304.25	unknown	via CMAUP database
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One	662	Click to see	288.25	unknown	https://doi.org/10.1021/JF0483117
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	https://doi.org/10.1021/JF0483117
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion	25202062	Click to see	285.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1021/JF0483117
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	53399169	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	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	https://doi.org/10.1021/JF0483117
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	https://doi.org/10.1021/JF0483117
CID 44258797	44258797	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
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol	44445800	Click to see	288.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
CID 14542257	14542257	Click to see	354.40	unknown	https://doi.org/10.1021/JF0483117
Yukovanol	44584009	Click to see	354.40	unknown	https://doi.org/10.1021/JF0483117
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
11,17-Dihydroxy-7,7,10,20,20-pentamethyl-2,8,19,25-tetraoxahexacyclo[12.11.0.03,12.04,9.015,24.018,23]pentacosa-1(14),3(12),4(9),5,10,15,17,21,23-nonaen-13-one	86025119	Click to see CC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC4=C(C2=O)C5=CC(=C6C(=C5O4)C=CC(O6)(C)C)O)O	446.40	unknown	https://doi.org/10.1021/JF0483117
11,17,21,22-Tetrahydroxy-7,7,10,20,20-pentamethyl-2,8,19,25-tetraoxahexacyclo[12.11.0.03,12.04,9.015,24.018,23]pentacosa-1(14),3(12),4(9),5,10,15,17,23-octaen-13-one	163061997	Click to see	480.50	unknown	https://doi.org/10.1021/JF0483117
6,7,21-Trihydroxy-17,17,20-trimethyl-8-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(13),3(11),4,6,8,14(19),15,20-octaen-2-one	102216287	Click to see CC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC4=C(C2=O)C5=CC(=C(C(=C5O4)CC=C(C)C)O)O)O	448.50	unknown	https://doi.org/10.1021/JF0483117
Triquetrumone C	102216288	Click to see	480.50	unknown	https://doi.org/10.1021/JF0483117
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3R)-3-(3,5-dihydroxy-4-methoxyphenyl)-3-[(3R)-3-(3,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-8,8-dimethyl-4-oxo-2H-pyrano[2,3-h]chromen-3-yl]-5-hydroxy-8,8-dimethyl-2H-pyrano[2,3-h]chromen-4-one	102216289	Click to see	766.70	unknown	https://doi.org/10.1021/JF0483117
(3S)-3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one	163074653	Click to see	354.40	unknown	https://doi.org/10.1021/JF0483117
3-(2,4-Dihydroxyphenyl)-2,3-dihydro-5-hydroxy-8,8-dimethyl-4H,8H-benzo(1,2-b:3,4-b')dipyran-4-one	156777	Click to see	354.40	unknown	via CMAUP database
3-(3,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one	163074652	Click to see	354.40	unknown	https://doi.org/10.1021/JF0483117
3-(3,5-dihydroxy-4-methoxyphenyl)-3-[3-(3,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-8,8-dimethyl-4-oxo-2H-pyrano[2,3-h]chromen-3-yl]-5-hydroxy-8,8-dimethyl-2H-pyrano[2,3-h]chromen-4-one	163031664	Click to see	766.70	unknown	https://doi.org/10.1021/JF0483117

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Tadehagi triquetrum

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