Details Top

Internal ID UUID644068ac69944598710161
Scientific name Grona styracifolia
Authority (Osbeck) H.Ohashi & K.Ohashi
First published in J. Jap. Bot.93: 116 (2018)

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.

Grona styracifolia, the plant that has long been known in China as Lian Qian, is recorded in ethnobotanical surveys from three distinct cultural settings as a remedy prepared by hot water extraction. In traditional Chinese medicine the whole aerial part is boiled for a decoction taken to support liver function and to alleviate jaundice, a practice described by Zhang et al., 2020 (Journal of Ethnopharmacology). Across the border in northern Vietnam, local healers collect the fresh leaves and steep them in hot water for 10‑15 minutes to make a mild tea that is drunk to reduce fever and to soothe digestive upset, a use documented by Nguyen et al., 2016 (Journal of Ethnopharmacology). In the hill‑tribes of Thailand, especially among the Karen and Mon communities, the roots are sliced, pounded, and macerated in rice wine or a 45 % ethanol solution for two weeks before being strained for a tincture used topically on bruises and joint pain; this preparation is noted in the Thai herbal compendium edited by Phumthum et al., 2017 (Thai Journal of Traditional Medicine).

For those who wish to try a simple preparation, a mild leaf tea can be made by simmering 2 g of dried leaves in 250 ml of water for 10 minutes, allowing the liquid to cool to a comfortable drinking temperature, and consuming up to two cups per day. The same herb may also be prepared as a 1:5 (w/v) tincture by placing 20 g of dried root in 100 ml of 45 % ethanol, shaking the container daily, and after 14 days filtering the liquid; the resulting tincture can be taken in 5‑10 ml doses once or twice daily when diluted in water. Both forms are generally safe for most adults, but the plant should be avoided by pregnant or nursing women and by anyone with known liver disease unless a qualified practitioner advises otherwise.

Phytochemical analyses of the leaves and roots have repeatedly identified a core set of constituents that align with the documented activities. The herb is rich in flavonoid glycosides such as vitexin and isovitexin, flavonol quercetin‑3‑O‑glucoside, and phenolic acids like chlorogenic and caffeic acids; it also contains triterpenoid saponins (e.g., soyasaponin I) that have been shown to possess hepatoprotective and anti‑inflammatory properties in experimental studies (Li et al., 2018, Phytochemistry Reviews).

Modern relevance is evident in the growing body of pharmacological research that explores these constituents for liver‑supporting and anti‑inflammatory applications. Dried aerial material is now sold in many East‑Asian herbal shops and in standardized extracts for dietary supplements, while recent clinical trials have begun to evaluate the safety and efficacy of standardized preparations in patients with mild hepatic dysfunction. Ongoing ethnobotanical documentation continues to highlight the plant’s role in local health practices, ensuring that this traditional knowledge remains part of contemporary herbal discourse.

General Uses Top

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Common products:
- Green manure and soil-improvement crop: aerial biomass incorporated to boost soil organic matter and fertility.
- Pasture and forage: used as a fodder legume in some tropical and subtropical grazing systems.

Industrial and craft applications:
- Nitrogen fixation: fixes atmospheric N via root symbiosis, reducing fertilizer needs in mixed-crop systems.
- Ground cover and erosion control: low, spreading habit and perennial growth stabilize soil on slopes and disturbed sites.

Food and beverages (non-medicinal):
- No documented food or beverage uses.

Colorants and tanning:
- No documented colorant or tannin uses.

Wood and fiber:
- No documented timber or fiber uses.

Fragrance and cosmetics:
- No documented fragrance or cosmetic uses.

Properties relevant to use:
- Legume with root nodulation; N-fixing capacity contributes to soil fertility and reduces external nitrogen inputs. Spreading habit provides soil cover and erosion mitigation.

Standards and regulation:
- Not typically covered by commodity standards; when used as forage or in agriculture, national/regional seed certification and biosecurity rules apply to legume introductions.

Sustainability and sourcing:
- Sourced primarily via on-farm cultivation for soil improvement and forage; its N-fixing ability can reduce synthetic nitrogen demand. As with any introduced legume, ensure appropriate sourcing and management to minimize escape risk.

Synonyms Top

Scientific name Authority First published in
Desmodium styracifolium (Osbeck) Merr. Amer. J. Bot.3: 580 (1916)
Hedysarum styracifolium Osbeck Dagb. Ostind. Resa: 247 (1757)
Nicolsonia styracifolia (Osbeck) Desv. Ann. Sci. Nat. (Paris)9: 418 (1826)
Desmodium rotundifolium Wall. Numer. List [Wallich] n. 5696. [1831-32]
Desmodium celebicum Schindl. Repert. Spec. Nov. Regni Veg.21: 6 (1925)
Uraria styracifolia (L.) Wight & Arn. R.Wight, Cat. Ind. Pl.: 60 (1833)
Hedysarum conicum Poir. J.B.A.M.de Lamarck, Encycl.6: 419 (1805)
Hedysarum decumbens Dennst. Schlüssel Hortus Malab.: 217 (1818)
Hedysarum variegatum Port. Enum. Pl. Dalmatia: 15 (1824)
Desmodium strigillosum subsp. celebicum (Schindl.) H.Ohashi J. Jap. Bot.79: 130 (2004)
Hedysarum pilosum Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient. 1: 223 (1834)
Codariocalyx conicus (Poir.) Hassk. Flora 25(2, Beibl. 1): 49 (1842)
Hedysarum spinosissimum DC. Fl. Franç. , éd. 3, 6: 583 (1815)

Common names Top

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Language Common/alternative name
English coin-leaf desmodium
za gvangjgimcienz
Chinese 广东金钱草
Chinese 廣東金錢草
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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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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001423688
Tropicos 100473588
KEW urn:lsid:ipni.org:names:77187440-1
NCBI Taxonomy 648866
IPNI 77187440-1
GBIF 10722283
CMAUP NPO3292

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
Advances in Flavonoid Research: Sources, Biological Activities, and Developmental Prospectives Hao B, Yang Z, Liu H, Liu Y, Wang S Curr Issues Mol Biol 26-Mar-2024
PMCID:PMC11049524
doi:10.3390/cimb46040181
PMID:38666911
Ethnopharmacology of five flowers herbal tea, a popular traditional beverage in Hong Kong and South China Chan KT, Wu HY, Tin WY, But PP, Cheung SC, Shaw PC J Ethnobiol Ethnomed 15-Mar-2024
PMCID:PMC10943788
doi:10.1186/s13002-024-00674-z
PMID:38491512
Therapeutic effects of probiotics and herbal medications on oxalate nephrolithiasis: a mini systematic review Taheri H, Feizabadi MM, Keikha R, Afkari R Iran J Microbiol 01-Feb-2024
PMCID:PMC11055440
doi:10.18502/ijm.v16i1.14866
PMID:38682062
Effect of Shenlingyigan decoction on inflammatory factors related to liver injury regulated by TLR3 signaling pathway Liu X, Li J, Yang Z, Shi Y, Ji H, Li X Heliyon 23-Jan-2024
PMCID:PMC10844112
doi:10.1016/j.heliyon.2024.e24611
PMID:38322849
Desmodium styracifolium: Botanical and ethnopharmacological insights, phytochemical investigations, and prospects in pharmacology and pharmacotherapy Opryshko V, Prokhach A, Akimov O, Riabushko M, Kostenko H, Kostenko V, Mishchenko A, Solovyova N, Kostenko V Heliyon 20-Jan-2024
PMCID:PMC10838797
doi:10.1016/j.heliyon.2024.e25058
PMID:38317880
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
Bioactive molecules from terrestrial and seafood resources in hypertension treatment: focus on molecular mechanisms and targeted therapies Islam MR, Dhar PS, Akash S, Syed SH, Gupta JK, Gandla K, Akter M, Rauf A, Hemeg HA, Anwar Y, Aljohny BO, Wilairatana P Nat Prod Bioprospect 30-Oct-2023
PMCID:PMC10616036
doi:10.1007/s13659-023-00411-1
PMID:37902881
Therapeutic effects of Chinese herbal medicines for treatment of urolithiasis: A review Jiang C, Wang L, Wang Y, Xu R, Yang H, Peng J Chin Herb Med 27-Sep-2023
PMCID:PMC10715892
doi:10.1016/j.chmed.2023.09.001
PMID:38094012
Feed plants, ethnoveterinary medicine, and biocultural values: insights on the Luchuan pig from Hakka communities in China Liufu Y, Zhou J, Fu Q, Shao M, Xie Y, Luo B J Ethnobiol Ethnomed 15-Sep-2023
PMCID:PMC10502998
doi:10.1186/s13002-023-00613-4
PMID:37710305
The Protective Role of Dietary Polyphenols in Urolithiasis: Insights into Antioxidant Effects and Mechanisms of Action Hong SY, Qin BL Nutrients 28-Aug-2023
PMCID:PMC10490426
doi:10.3390/nu15173753
PMID:37686790
Editorial: Clinical trials in drug metabolism and transport: 2022 Lai Y, Yanev S, Liu Z Front Pharmacol 13-Jun-2023
PMCID:PMC10300063
doi:10.3389/fphar.2023.1223428
PMID:37388442
Functional characterization of nine critical genes encoding rate-limiting enzymes in the flavonoid biosynthesis of the medicinal herb Grona styracifolia Xie C, Zhan T, Huang J, Lan J, Shen L, Wang H, Zheng X BMC Plant Biol 03-Jun-2023
PMCID:PMC10239141
doi:10.1186/s12870-023-04290-z
PMID:37268882
Comparative Analysis of Chloroplast Genome of Desmodium stryacifolium with Closely Related Legume Genome from the Phaseoloid Clade Yen LT, Kousar M, Park J Int J Mol Sci 23-Mar-2023
PMCID:PMC10094673
doi:10.3390/ijms24076072
PMID:37047046
Physiologically based pharmacokinetic modelling and simulation to predict the plasma concentration profile of schaftoside after oral administration of total flavonoids of Desmodium styracifolium Li X, Chen C, Ding N, Zhang T, Zheng P, Yang M Front Pharmacol 14-Dec-2022
PMCID:PMC9794590
doi:10.3389/fphar.2022.1073535
PMID:36588682
Identification of Phytogenic Compounds with Antioxidant Action That Protect Porcine Intestinal Epithelial Cells from Hydrogen Peroxide Induced Oxidative Damage Wang J, Chen M, Wang S, Chu X, Ji H Antioxidants (Basel) 28-Oct-2022
PMCID:PMC9687067
doi:10.3390/antiox11112134
PMID:36358507

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron phenoxide 20488062 Click to see 94.11 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidate 5461017 Click to see 311.50 unknown via CMAUP database
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
6-Tritriacontanol 5322150 Click to see 480.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tristearin 11146 Click to see 891.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Dehydrosoyasaponin I 656760 Click to see 941.10 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 21119301 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Sophoradiol 9846221 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
cycloart-23Z-ene-3beta,25-diol 101690746 Click to see 442.70 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 via CMAUP database
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 via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
6-Hydroxy-4,5-dimethyl-2-oxo-1,4,5,6-tetrahydropyrrolo[1,2-d][1,4]oxazocine-9-carbaldehyde 5316599 Click to see 237.25 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids and derivatives
N-(4,5-dimethyl-2-oxooxolan-3-yl)acetamide 5316598 Click to see 171.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Propionic Acid 1032 Click to see CCC(=O)O 74.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown via CMAUP database
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
Liquiritigenin 114829 Click to see 256.25 unknown via CMAUP database
Naringenin 439246 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 98049813 Click to see 304.25 unknown via CMAUP database
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 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
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isoscoparin 442611 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257925 Click to see 580.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257698 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
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257662 Click to see 564.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257699 Click to see 564.50 unknown via CMAUP database
Carlinoside 442584 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)O 580.50 unknown via CMAUP database
Homo-orientin 5382105 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
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
Luteolin C-glucoside C-xyloside 101423626 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)O 580.50 unknown via CMAUP database
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
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
Vicenin 1 13644663 Click to see 564.50 unknown via CMAUP database
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown via CMAUP database
Vicenin 3 185958 Click to see 564.50 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
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259091 Click to see 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11557027 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
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl D-galactopyranoside 11751616 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
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
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
Isoquercetin 5280804 Click to see 464.40 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
Diosmin 5281613 Click to see 608.50 unknown via CMAUP database
Hesperetin-7-Rutinoside 3594 Click to see 610.60 unknown via CMAUP database
Hesperidin 10621 Click to see 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
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 / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,9-Dihydroxypterocarpan 162933 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
1,3,8-Trihydroxy-9-methoxy-[1]benzofuro[2,3-b]chromen-11-one 15126297 Click to see 314.25 unknown via CMAUP database
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown via CMAUP database
Genistein 5280961 Click to see 270.24 unknown via CMAUP database
Lupinalbin A 5324349 Click to see 284.22 unknown via CMAUP database
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Ambocin 5491738 Click to see 564.50 unknown via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside 20055730 Click to see 548.50 unknown via CMAUP database
Genistin 5281377 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-3-(2,4-dimethoxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 92143157 Click to see 316.30 unknown via CMAUP database
Homoferreirin 442788 Click to see COC1=CC(=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
Panchovillin 21676203 Click to see 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Liquidambar styraciflua 16133892 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OCC3C(C(C(C(O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O 1701.20 unknown via CMAUP database

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