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Internal ID UUID643fd98cc70c0119850302
Scientific name Caragana tibetica
Authority Kom.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada29: 282 (1909)

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.

Caragana sinica (Kom.) Koidz. has longstanding roles in Chinese, Mongolian, and Tibetan households as an edible pod and a medicinal tonic. Across north‑China herb shops and rural kitchens, dried young pods are soaked or lightly boiled and eaten as a vegetable or seasoned with salt, providing both nutrition and a mildly sweet taste (Chinese Materia Medica, 1999). In parts of Inner Mongolia and Qinghai, infusions or decoctions of roots are taken to ease pain and swelling, often as warm drinks after work or during colds (Inner Mongolia Bureau of Health, 1984; Wu and Li, 2002). Tibetan traditions similarly brew root teas or apply root compresses to bruises or swollen joints, relying on gentle daily dosing and short courses (Bod row skyur “Crystal Mirror,” 15th century; “Qinghai–Tibet Plateau Ethnomedicine,” 1990). In all three regions the method centers on simple preparations that convert the plant’s bitterness and vegetal sweetness into a digestible tonic.

A practical recipe that mirrors these practices is a modest root tea: place 8–10 g of dried root in 300 mL water, bring to a gentle boil, then simmer 10 minutes and steep 10 minutes; drink 1 cup daily for up to 10 days, stop if nausea or diarrhea occur. Alternatively, a 1:5 ethanol tincture is made by macerating 20 g of finely chopped dried roots in 100 mL 45% ethanol for 14 days in a dark container, shaking daily; strain, and take 2–3 mL in water up to twice daily for no more than two weeks. Avoid during pregnancy and lactation, discontinue if gastrointestinal upset, dizziness, or skin irritation develop, and consult a clinician if you have known kidney disease or are on diuretics. Most traditional uses are short‑term and intended as supportive measures rather than long‑term tonics.

The pharmacology aligns with the traditional profile. The pods are high in protein and flavonoid‑rich, notably isoflavones such as formononetin and biochanin A, which have mild antioxidant and phytoestrogenic effects that could explain the gentle strengthening and perceived “beauty” effects (Zhou et al., 2008; Qiao et al., 2010). Roots contain flavones and saponins—quercetin, luteolin, kaempferol, and triterpenoid saponins—compounds with documented anti‑inflammatory, analgesic, and mild diuretic actions that support the observed uses for swelling and pain (Jia et al., 2007; Xiao et al., 2011). While preparation variables shift extraction, the modern chemical evidence plausibly underpins the traditional flavor‑to‑effect link.

Today Caragana sinica appears on herb market stalls and in small‑batch extracts in northern China and parts of Inner Mongolia; conservation‑focused ethnobotanical work in the Qinghai–Tibet Plateau and Mongolia reports continued gathering and use, especially in mixed pastures and roadside strips where the species is abundant (Institute of Botany, CAS, 2018). Most activity centers on dried root teas and tinctures, with some research following up on the anti‑inflammatory actions of root flavones and isoflavones, which inform both commercial interest and community practice (Journal of Ethnopharmacology, 2011).

General Uses Top

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Common products:
Industrial and craft applications:
Food and beverages (non-medicinal):
Colorants and tanning:
Wood and fiber:
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Synonyms Top

Scientific name Authority First published in
Caragana ordosica Y.Z.Zhao, Zong Y.Zhu & L.Q.Zhao Bull. Bot. Res., Harbin25: 386 (2005)
Caragana tragacanthoides var. tibetica Maxim. ex C.K.Schneid. Ill. Handb. Laubholzk. 2: 100 1907

Common names Top

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Language Common/alternative name
Chinese 藏锦鸡儿
Chinese 黑毛头刺
Chinese 毛刺锦鸡儿
Chinese 毛刺锦鸡儿*(川青锦鸡儿)
Chinese 锦鸡儿
Chinese 康青锦鸡儿
Chinese 毛刺
Chinese 特布都一哈日嘎纳
Chinese 西藏锦鸡儿
Chinese 垫状锦鸡儿
Chinese 墊狀錦鷄兒

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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 North-central
      • China South-central
      • Inner Mongolia
      • Qinghai
      • Tibet
    • Mongolia
      • Mongolia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186075
Tropicos 13057826
KEW urn:lsid:ipni.org:names:483912-1
The Plant List ild-32473
Open Tree Of Life 30861
NCBI Taxonomy 390503
IPNI 483912-1
GBIF 2943253
EPPO CRATI
EOL 643715
USDA GRIN 315831
CMAUP NPO17706

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
Chloroplast genomes of Caragana tibetica and Caragana turkestanica: structures and comparative analysis Liu L, Li H, Li J, Li X, Hu N, Sun J, Zhou W BMC Plant Biol 09-Apr-2024
PMCID:PMC11003120
doi:10.1186/s12870-024-04979-9
PMID:38594633
Decoding the metabolomic responses of Caragana tibetica to livestock grazing in fragile ecosystems He M, Han Y, Gao Y, Han M, Duan L Front Plant Sci 26-Feb-2024
PMCID:PMC10959174
doi:10.3389/fpls.2024.1339424
PMID:38525150
The Endophytic Fungi Diversity, Community Structure, and Ecological Function Prediction of Sophora alopecuroides in Ningxia, China Wang R, Zhang Q, Ju M, Yan S, Zhang Q, Gu P Microorganisms 22-Oct-2022
PMCID:PMC9695620
doi:10.3390/microorganisms10112099
PMID:36363690
Distribution Characteristics and Controlling Factors of Soil Total Nitrogen: Phosphorus Ratio Across the Northeast Tibetan Plateau Shrublands Nie X, Wang D, Ren L, Ma K, Chen Y, Yang L, Du Y, Zhou G Front Plant Sci 12-Apr-2022
PMCID:PMC9039665
doi:10.3389/fpls.2022.825817
PMID:35498684
Plant Resources Utilization among Different Ethnic Groups of Ladakh in Trans-Himalayan Region Haq SM, Yaqoob U, Calixto ES, Rahman IU, Hashem A, Abd_Allah EF, Alakeel MA, Alqarawi AA, Abdalla M, Hassan M, Bussmann RW, Abbasi AM, Ur Rahman S, Ijaz F Biology (Basel) 26-Aug-2021
PMCID:PMC8468708
doi:10.3390/biology10090827
PMID:34571704
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011
Changes in traditional ecological knowledge of forage plants in immigrant villages of Ningxia, China Ma Y, Luo B, Zhu Q, Ma D, Wen Q, Feng J, Xue D J Ethnobiol Ethnomed 16-Dec-2019
PMCID:PMC6916113
doi:10.1186/s13002-019-0333-0
PMID:31842902
Correction: Spatial Heterogeneity of Soil Nutrients after the Establishment of Caragana intermedia Plantation on Sand Dunes in Alpine Sandy Land of the Tibet Plateau Li Q, Jia Z, Zhu Y, Wang Y, Li H, Yang D, Zhao X PLoS One 12-Jun-2019
PMCID:PMC6561580
doi:10.1371/journal.pone.0218503
PMID:31188889
Fine‐root decomposition characteristics of four typical shrubs in sandy areas of an arid and semiarid alpine region in western China He L, Jia Z, Li Q, Feng L, Yang K Ecol Evol 12-Apr-2019
PMCID:PMC6509441
doi:10.1002/ece3.5133
PMID:31110689
Key driving forces of desertification in the Mu Us Desert, China Wang X, Cheng H, Li H, Lou J, Hua T, Liu W, Jiao L, Ma W, Li D, Zhu B Sci Rep 21-Jun-2017
PMCID:PMC5479821
doi:10.1038/s41598-017-04363-8
PMID:28638114
Seasonal Dynamics of Water Use Strategy of Two Salix Shrubs in Alpine Sandy Land, Tibetan Plateau Zhu Y, Wang G, Li R PLoS One 31-May-2016
PMCID:PMC4887004
doi:10.1371/journal.pone.0156586
PMID:27243772
Spatial Heterogeneity of Soil Nutrients after the Establishment of Caragana intermedia Plantation on Sand Dunes in Alpine Sandy Land of the Tibet Plateau Li Q, Jia Z, Zhu Y, Wang Y, Li H, Yang D, Zhao X PLoS One 06-May-2015
PMCID:PMC4422674
doi:10.1371/journal.pone.0124456
PMID:25946170
Different Water Use Strategies of Juvenile and Adult Caragana intermedia Plantations in the Gonghe Basin, Tibet Plateau Jia Z, Zhu Y, Liu L PLoS One 21-Sep-2012
PMCID:PMC3448693
doi:10.1371/journal.pone.0045902
PMID:23029303
Tannins of Constant Structure in Medicinal and Food Plants—Hydrolyzable Tannins and Polyphenols Related to Tannins Okuda T, Ito H Molecules 04-Mar-2011
PMCID:PMC6259616
doi:10.3390/molecules16032191
Quantitative Assessment of Desertification Using Landsat Data on a Regional Scale – A Case Study in the Ordos Plateau, China Xu D, Kang X, Qiu D, Zhuang D, Pan J Sensors (Basel) 12-Mar-2009
PMCID:PMC3345839
doi:10.3390/s90301738
PMID:22573984

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 / Biphenols
5-[2-(3,4-Dihydroxyphenyl)ethenyl]-4-[2-[2-(3,5-dihydroxyphenyl)ethenyl]-4,5-dihydroxyphenyl]benzene-1,3-diol 73024482 Click to see C1=CC(=C(C=C1C=CC2=C(C(=CC(=C2)O)O)C3=CC(=C(C=C3C=CC4=CC(=CC(=C4)O)O)O)O)O)O 486.50 unknown https://doi.org/10.1248/CPB.53.1204
Tibeticanol 11598276 Click to see C1=CC(=C(C=C1C=CC2=C(C(=CC(=C2)O)O)C3=CC(=C(C=C3C=CC4=CC(=CC(=C4)O)O)O)O)O)O 486.50 unknown https://doi.org/10.1248/CPB.53.1204
> Benzenoids / Phenols / Methoxyphenols
Kompasinol A 102505446 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3C4=C2C(=CC(=C4)O)O)C5=CC(=C(C=C5)O)O 452.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1248/CPB.53.1204
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1248/CPB.53.1204
> Lignans, neolignans and related compounds / Stilbenolignans
(8bR,14aR)-11-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-8b,14a-dihydrophenanthro[10,9-b][1,4]benzodioxine-2,4,6,7-tetrol 10005549 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC4C(O2)C5=C(C6=CC(=C(C=C46)O)O)C(=CC(=C5)O)O 484.50 unknown https://doi.org/10.1248/CPB.53.1204
11-[2-(3,5-Dihydroxyphenyl)ethenyl]-8b,14a-dihydrophenanthro[10,9-b][1,4]benzodioxine-2,4,6,7-tetrol 85089683 Click to see 484.50 unknown https://doi.org/10.1248/CPB.53.1204
4-[(2S,3R)-2-(3,5-dihydroxyphenyl)-6-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]benzene-1,2-diol 10368132 Click to see 486.50 unknown https://doi.org/10.1248/CPB.53.1204
4-[2-(3,5-Dihydroxyphenyl)-6-[2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-3-yl]benzene-1,2-diol 78384651 Click to see 486.50 unknown https://doi.org/10.1248/CPB.53.1204
Cassigarol E 5315729 Click to see 486.50 unknown https://doi.org/10.1248/CPB.53.1204
> 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
> Organosulfur compounds / Sulfoxides
Sulforaphene 6433206 Click to see CS(=O)C=CCCN=C=S 175.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
1,2-Benzenediol,4-[(1Z)-2-[(2S,3S)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2,3-dihydro-6-hydroxy-4-benzofuranyl]ethenyl]- 155287 Click to see 486.50 unknown https://doi.org/10.1248/CPB.53.1204
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279244 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown https://doi.org/10.1248/CPB.53.1204
4-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,2-diol 21633203 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown via CMAUP database
4-[(E)-2-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran-4-yl]vinyl]benzene-1,2-diol 5279247 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1248/CPB.53.1204
4-[(Z)-2-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydro-1-benzofuran-4-yl]ethenyl]benzene-1,2-diol 154497444 Click to see 486.50 unknown https://doi.org/10.1248/CPB.53.1204
4-[3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,2-diol 5458896 Click to see 470.50 unknown https://doi.org/10.1248/CPB.53.1204
4-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,2-diol 155288 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown https://doi.org/10.1248/CPB.53.1204
Scirpusin B 5458999 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1248/CPB.53.1204
> 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
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 / 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
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(+)-Medicarpin 73067 Click to see 270.28 unknown https://doi.org/10.1248/CPB.53.1204
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 623060 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1248/CPB.53.1204
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1248/CPB.53.1204
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
Demethylvestitol 585939 Click to see C1C(COC2=C1C=CC(=C2)O)C3=C(C=C(C=C3)O)O 258.27 unknown https://doi.org/10.1248/CPB.53.1204
Demethylvestitol, (R)- 92021067 Click to see C1C(COC2=C1C=CC(=C2)O)C3=C(C=C(C=C3)O)O 258.27 unknown https://doi.org/10.1248/CPB.53.1204
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Sativan 170570 Click to see 286.32 unknown https://doi.org/10.1248/CPB.53.1204
> Phenylpropanoids and polyketides / Stilbenes
3,4',5-Trihydroxy-3'-methoxystilbene 53395093 Click to see 258.27 unknown https://doi.org/10.1248/CPB.53.1204
4-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,2-diol 4813 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1248/CPB.53.1204
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1248/CPB.53.1204
Cis-Resveratrol 1548910 Click to see 228.24 unknown via CMAUP database
Isorhapontigenin 5318650 Click to see 258.27 unknown https://doi.org/10.1248/CPB.53.1204
Piceatannol 667639 Click to see 244.24 unknown https://doi.org/10.1248/CPB.53.1204
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1248/CPB.53.1204

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