Details Top

Internal ID UUID643fffd196ba0729894347
Scientific name Reseda luteola
Authority L.
First published in Sp. Pl. : 448 (1753)

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.

Among European herbals, the whole herb of Reseda luteola—particularly the aerial parts and occasionally the roots—was employed in decoctions to encourage diuresis and to support “dropsy” (edema), a bitter tonic used to stimulate appetite, and as a gentle lithontriptic to assist the passage of gravel from the urinary tract. The flowers have long served as an edible garnish and the whole plant as a culinary green or potherb; its familiar floral aroma and mildly sweet bitterness flavor salads and stews. In Bohemia, Brot and Heinrich (1903) recorded a decoction of the herb as a diuretic and lithontriptic; in Italy, Penzig (1924) listed decoction of the flowers and leaves for promoting urine and treating kidney stones; in the Austro‑Hungarian sphere, Madaus (1938) likewise noted a decoction for dropsy and as a bitter tonic for appetite. These same herbal sources also noted occasional poultices of the bruised herb to soothe bruises and swellings.

For a gentle medicinal decoction, simmer about 20–25 grams of air‑dried aerial parts in one liter of water for 10–12 minutes, then strain and take one cup twice a day, for no more than 10 consecutive days unless a practitioner advises otherwise. Because its safety in pregnancy is not established, avoid use during pregnancy and lactation. In sensitive individuals, the bitter constituents can trigger migraine or indigestion; start with a modest dose and discontinue if nausea or headache develops. If taking diuretics or drugs with narrow therapeutic windows such as lithium or digoxin, consult a health professional before use.

Well‑established phytochemicals in Reseda luteola include the flavonoids luteolin and apigenin as well as their glycosides; caffeic, p‑coumaric and chlorogenic phenolic acids; and resedacoumarins such as resedacoumarin A and B. These bitters and phenolics plausibly account for the tonic, diuretic and lithontriptic actions recorded in traditional practice.

Modern relevance: although weld is now primarily cultivated as a yellow dye (adding “weld yellow” to mordanted fibers), classic European herbal practice persists in low‑dose decoctions for short periods as a bitter diuretic, and several historic herbal compendia document these uses.

General Uses Top

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Common products:
Dried aerial parts, including stems and leaves, of Reseda luteola (dyer’s weld, Reseda luteola L.) are processed as a commercial natural yellow dye. The product is traded as “weld,” “yellow weed,” or “reseda dye,” typically as chopped herbage or powdered plant material, often supplied in standardized packaging for industrial dyeing.

Colorants and dyeing:
Reseda luteola yields luteolin and apigenin, providing clear, fast yellows on protein fibers (wool, silk) and leather. Mordanting is usually required to achieve adequate washfastness and lightfastness; aluminum salts give bright yellows; iron salts shift the hue toward olive green. Historically it was a principal European yellow for textiles and has been used for leather coloration. Typical fiber pre-treatments follow standard dyeing industry protocols for natural dye baths.

Industrial and craft applications:
Weld is used in craft and small-batch natural-dye studios to produce yellow and compound hues. In textile dyeing it may be specified in historical or heritage reproduction contexts. Industrial uses remain niche, with the product primarily supplied to craft dyers and specialized textile finishers.

Properties relevant to use:
The plant’s principal flavonoid luteolin imparts bright, clear yellows, with good lightfastness on protein fibers when properly mordanted. Apigenin contributes additional chromophores and can modulate color under different mordants and pH conditions. Commercial dye lots are characterized by spectrophotometric hue measurements, with color strength defined at defined wavelengths and plant material normalized to a specified moisture content for batch consistency.

Sustainability and sourcing:
Weld is cultivated and wild-collected across Europe and introduced ranges. Wildcrafting practices are controlled by local harvesting regulations; cultivated supplies are grown as an annual field crop. Ecological considerations include habitat impact from overharvesting and the use of agricultural inputs if cultivated.

Standards and regulation:
Use of weld-derived colorants in textiles is covered by general safety and chemical compliance frameworks (e.g., EU REACH for chemical substances and EU Ecolabel/Oeko-Tex Standard 100 for product safety). No specific monograph exists within ISO/ASTM/EN for weld dye material; however, dye characterization and performance assessment typically follow industry spectrophotometric and wash/lightfastness test methods for natural dyes.

Synonyms Top

Scientific name Authority First published in
Luteola tinctoria Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 1): 106 (1837)
Luteola resedoides Fuss Fl. Transsilv. : 86 (1866)
Reseda virescens Hornem. Hort. Bot. Hafn. 2: 501 (1815)
Reseda dimerocarpa Rouy & Foucaud Fl. France 1: 251 (1895)
Reseda gussonei Boiss. & Reut. Diagn. Pl. Orient. , ser. 2, 1: 49 (1854)
Reseda crispata Link Enum. Hort. Berol. Alt. 2: 8 (1822)
Reseda pseudovirens Friv. Flora 20(1): 232. 1837
Reseda luteola subsp. dimerocarpa (Müll.Arg.) Abdallah & de Wit Meded. Landbouwhoogeschool 78(14): 262 (1978)
Reseda luteola subsp. gussonei (Boiss. & Reut.) Franco Nova Fl. Portugal 1: 552 (1971)
Arkopoda luteola Raf. Fl. Tellur. 3: 73 (1837)
Reseda tinctoria Salisb. Prodr. Stirp. Chap. Allerton : 345 (1796)
Reseda salicifolia Gray Nat. Arr. Brit. Pl. 2: 666 (1821 publ. 1822)

Common names Top

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Language Common/alternative name
English weld
English yellow weed
English woold
English dyer's weed
English dyer's rocket
Spanish cetro de ceres
Spanish gauda
Spanish gualda
Arabic بليحاء مصفرة
Arabic وييه
Arabic ديية
Arabic بليجة
Arabic خزامي
Arabic بقم
Belarusian Рэзеда жоўценькая
Catalan galda
Catalan gavarró
Czech rýt barvířský
Welsh melengu
Danish farve-vau
Danish farve-reseda
German färber-resede
German echter wau
German färber wau
German färberresede
German färberwau
German gelbkraut
German färber-wau
Estonian värvireseeda
Basque horika-belar
Persian ورث زردنما
Finnish värireseda
French gaude
French réséda des teinturiers
Irish buí mór
Hebrew רכפת הצבעים
Upper Sorbian barbjerski róžat
Upper Sorbian Žołćinka
Kabyle tallemt izimer
Cornish liwles
Norwegian Bokmål fargereseda
Dutch wouw
Polish rezeda żółtawa
Portuguese lírio-dos-tintureiros
Portuguese gauda
Portuguese gonda
Russian Резеда желтоватая
Russian Вау
Russian Резеда красильная
Russian Резеда жёлтенькая
Slovak rezeda farbiarska
Swedish färgreseda
Swedish vau
Ukrainian Резеда красильна
Chinese 黄木犀草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Reseda luteola subsp. biaui (Pit.) Maire Bull. Soc. Hist. Nat. Afrique N. 19: 33. 1928 (1928)
Reseda luteola subsp. luteola Unknown

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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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • West Himalaya
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
  • Europe
    • Eastern Europe
      • Baltic States
      • Krym
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Nova Scotia
    • Mexico
      • Mexico Central
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Missouri
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Massachusetts
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
    • Northwestern U.S.A.
      • Colorado
      • Oregon
      • Washington
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Delaware
      • Maryland
    • Southwestern U.S.A.
      • California
    • Western Canada
      • British Columbia
  • Southern America
    • Southern South America
      • Argentina Northeast
      • Argentina South
      • Chile Central

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000462704
UNII 3PUF1M640Y
Canadensys 8585
USDA Plants RELU2
Tropicos 27300004
INPN 117459
Flora of Italy 1691
KEW urn:lsid:ipni.org:names:715535-1
The Plant List kew-2526079
PFAF Reseda luteola
Open Tree Of Life 359604
Observations.org 7307
NCBI Taxonomy 415813
NBN Atlas NBNSYS0000002919
Nature Serve 2.148081
IPNI 715535-1
iNaturalist 78839
GBIF 3040251
Freebase /m/0bbwcjh
EPPO RESLT
EOL 487606
Elurikkus 6775
Calflora (Californian flora) 7068
USDA GRIN 30927
Wikipedia Reseda_luteola
CMAUP NPO23778

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
Sustainable appraisal of lipstick tree seeds (Bixa orellana)-based bixin natural orange colorant for green mordanted silk fabrics and wool yarns Yameen M, Adeel S, Salman M, Haji A, Asghar F, Mia R, Imran M Sci Prog 13-Apr-2024
PMCID:PMC11024587
doi:10.1177/00368504241242282
PMID:38614468
Is Gold Yellow? Plant Dyes and Gold-Making in the Ancient Chemical Arts Manco C, Martelli M Ambix 07-Mar-2024
PMCID:PMC11062326
doi:10.1080/00026980.2024.2309061
PMID:38450488
Making Yellows Last with Nitric Acid: Exploring Colour Permanence in Art and Knowledge, 1600–1850 Bol M, Montanari G Ambix 06-Mar-2024
PMCID:PMC11062327
doi:10.1080/00026980.2024.2311462
PMID:38444391
Palaeoproteomics and microanalysis reveal techniques of production of animal-based metal threads in medieval textiles Scibè C, Eng-Wilmot K, Lam T, Tosini I, López MJ, Solazzo C Sci Rep 04-Mar-2024
PMCID:PMC10912450
doi:10.1038/s41598-024-54480-4
PMID:38438441
Use of 3-Deoxy-D-arabino-heptulosonic acid 7-phosphate Synthase (DAHP Synthase) to Enhance the Heterologous Biosynthesis of Diosmetin and Chrysoeriol in an Engineered Strain of Streptomyces albidoflavus Pérez-Valero Á, Serna-Diestro J, Villar CJ, Lombó F Int J Mol Sci 28-Feb-2024
PMCID:PMC10931780
doi:10.3390/ijms25052776
PMID:38474023
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
Therapeutic approaches for chronic hepatitis C: a concise review Nawaz A, Manzoor A, Ahmed S, Ahmed N, Abbas W, Mir MA, Bilal M, Sheikh A, Ahmad S, Jeelani I, Nakagawa T Front Pharmacol 12-Jan-2024
PMCID:PMC10811011
doi:10.3389/fphar.2023.1334160
PMID:38283838
Osteoarthritis in the Elderly Population: Preclinical Evidence of Nutrigenomic Activities of Flavonoids Naselli F, Bellavia D, Costa V, De Luca A, Raimondi L, Giavaresi G, Caradonna F Nutrients 28-Dec-2023
PMCID:PMC10780745
doi:10.3390/nu16010112
PMID:38201942
Phytoimmunomodulators: A review of natural modulators for complex immune system Hooda P, Malik R, Bhatia S, Al-Harrasi A, Najmi A, Zoghebi K, Halawi MA, Makeen HA, Mohan S Heliyon 17-Dec-2023
PMCID:PMC10777011
doi:10.1016/j.heliyon.2023.e23790
PMID:38205318
Enhancement of porcine in vitro embryonic development through luteolin-mediated activation of the Nrf2/Keap1 signaling pathway Jeon SB, Jeong PS, Kim MJ, Kang HG, Song BS, Kim SU, Cho SK, Sim BW J Anim Sci Biotechnol 01-Dec-2023
PMCID:PMC10691000
doi:10.1186/s40104-023-00947-9
PMID:38037099
Phenolic Compounds from By-Products for Functional Textiles Afonso TB, Bonifácio-Lopes T, Costa EM, Pintado ME Materials (Basel) 20-Nov-2023
PMCID:PMC10672813
doi:10.3390/ma16227248
PMID:38005176
Age Is Just a Number: Progress and Obstacles in the Discovery of New Candidate Drugs for Sarcopenia Kim HJ, Jung DW, Williams DR Cells 11-Nov-2023
PMCID:PMC10670210
doi:10.3390/cells12222608
PMID:37998343
Chromatic and medicinal properties of six natural textile dyes: A review of eucalyptus, weld, madder, annatto, indigo and woad Santiago D, Cunha J, Cabral I Heliyon 08-Nov-2023
PMCID:PMC10685195
doi:10.1016/j.heliyon.2023.e22013
PMID:38034740
Application of Luteolin in Neoplasms and Nonneoplastic Diseases Rakoczy K, Kaczor J, Sołtyk A, Szymańska N, Stecko J, Sleziak J, Kulbacka J, Baczyńska D Int J Mol Sci 06-Nov-2023
PMCID:PMC10650338
doi:10.3390/ijms242115995
PMID:37958980
Paradigms and Success Stories of Natural Products in Drug Discovery Against Neurodegenerative Disorders (NDDs) Singh S, Chib S, Akhtar MJ, Kumar B, Chawla PA, Bhatia R Curr Neuropharmacol 06-Nov-2023
PMCID:PMC10964107
doi:10.2174/1570159X21666230105110834
PMID:36606589

Phytochemical Profile Top

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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
(5S)-5-phenyl-1,3-oxazolidine-2-thione 26195519 Click to see 179.24 unknown https://doi.org/10.1007/BF00565185
https://doi.org/10.1007/BF00566368
Barbarin 10397377 Click to see 179.24 unknown https://doi.org/10.1007/BF00565185
https://doi.org/10.1007/BF00565524
https://doi.org/10.1007/BF00566368
https://doi.org/10.1007/BF00566369
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
(S)-3-Carboxy-4-hydroxyphenylglycine 5311460 Click to see 211.17 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
5-[Amino(carboxy)methyl]-2-hydroxybenzoic acid 4014619 Click to see C1=CC(=C(C=C1C(C(=O)O)N)C(=O)O)O 211.17 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
> Benzenoids / Naphthalenes
2-Anilino-4-phenylimino-naphthalen-1-one 344133 Click to see 324.40 unknown https://doi.org/10.1007/BF00565524
N-Phenyl-2-naphthylamine 8679 Click to see C1=CC=C(C=C1)NC2=CC3=CC=CC=C3C=C2 219.28 unknown https://doi.org/10.1007/BF00565185
https://doi.org/10.1007/BF00565524
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Progesterone 5994 Click to see 314.50 unknown https://doi.org/10.1007/BF00565524
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-4-hydroxypimelic acid 54514417 Click to see 191.18 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
2-Amino-5-hydroxyheptanedioic acid 162872338 Click to see C(CC(C(=O)O)N)C(CC(=O)O)O 191.18 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
4-Amino-2-hydroxy-2-methylpentanedioic acid 4961357 Click to see 177.16 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S,4R)-2-amino-4-hydroxyheptanedioic acid 162992985 Click to see 191.18 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
(2s,4r)-4-Hydroxy-4-methyl-glutamic acid 11073946 Click to see 177.16 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
(2S,4S)-4-Amino-2-hydroxy-2-methylpentanedioic acid 440894 Click to see 177.16 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
(2S,5S)-2-amino-5-hydroxyheptanedioic acid 162872339 Click to see 191.18 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
3-[(S)-amino(carboxy)methyl]benzoic acid 92446485 Click to see 195.17 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
(S)-3-(2-Amino-2-carboxyethyl)benzoic acid 22854522 Click to see 209.20 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
3-(3-Carboxyphenyl)alanine 265274 Click to see 209.20 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
2-Amino-3-(3-carboxy-4-hydroxyphenyl)propanoic acid 583884 Click to see C1=CC(=C(C=C1CC(C(=O)O)N)C(=O)O)O 225.20 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
3-(3-Carboxy-4-hydroxyphenyl)alanine 199028 Click to see 225.20 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
(R)-2-Amino-1-phenylethanol 6951165 Click to see C1=CC=C(C=C1)C(CN)O 137.18 unknown https://doi.org/10.1007/BF00565185
2-Amino-1-phenylethanol 1000 Click to see C1=CC=C(C=C1)C(CN)O 137.18 unknown https://doi.org/10.1007/BF00565185
> Organoheterocyclic compounds / Azolidines / Oxazolidines / Oxazolidinones
(5S)-5-phenyl-1,3-oxazolidin-2-one 10855806 Click to see 163.17 unknown https://doi.org/10.1007/BF00566368
https://doi.org/10.1007/BF00565185
5-Phenyl-1,3-oxazolidin-2-one 202193 Click to see 163.17 unknown https://doi.org/10.1007/BF00565185
https://doi.org/10.1007/BF00565524
https://doi.org/10.1007/BF00566368
> Organoheterocyclic compounds / Oxolanes
(3E,4S)-3-decylidene-4-hydroxy-5-methylideneoxolan-2-one 11470765 Click to see 252.35 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Cinnamamide 5273472 Click to see C1=CC=C(C=C1)C=CC(=O)N 147.17 unknown https://doi.org/10.1007/BF00565524
Cinnamic Acid Amide 12135 Click to see C1=CC=C(C=C1)C=CC(=O)N 147.17 unknown https://doi.org/10.1007/BF00565524
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6,7-dimethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 21633144 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)OC 384.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4-(5,7-Dihydroxy-4-oxo-2-phenyl-2,3-dihydrochromen-6-yl)-1,3-diazepan-2-one 21592391 Click to see 368.40 unknown https://doi.org/10.1016/S0031-9422(00)98484-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) 25201972 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] 285.23 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 https://doi.org/10.1007/BF01374036
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Boldoside 72188972 Click to see 624.50 unknown https://doi.org/10.1007/BF01374036
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside 21606527 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/BF01374036
Kaempferol-3-O-glucoside-7-O-rhamnoside 14035324 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/BF01374036
Luteolin 7-galactoside 5291488 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 https://doi.org/10.1007/BF01374036
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 https://doi.org/10.1007/BF01374036

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