Althaea officinalis

Details Top

Internal ID UUID644008a655591929779545
Scientific name Althaea officinalis
Authority L.
First published in Sp. Pl. : 686 (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 herbalists since at least the 19th century, marshmallow root has been taken as a mild infusion for sore throats and mild coughs. The British Herbal Pharmacopoeia (1983) records doses of 2–5 g of root infusion; more recently, the British Herbal Compendium (1992) and the German Commission E monographs (Blumenthal et al., 2000) describe the use of leaf or root infusions and cold macerates for mucosal irritation of mouth, throat, and upper airways, citing both powdered root and whole herb for such teas. In classical and Mediterranean practice, the root is also decocted in warm water for catarrhal and respiratory irritation, with the cold maceration (overnight soak) of root used as a gentle demulcent for coughs and digestive discomfort (Nell, 1875). In Argentina, decoctions of leaf and root are reported for mucosal inflammation and inflammatory conditions of the respiratory tract (Hilgert et al., 2007). In Chile, the Mapuche of southern Chile traditionally employ the aerial parts in decoction for coughs and colds (Bennett et al., 2021). Externally, crushed fresh leaves or roots are used as poultices for ulcerated or inflamed skin, a practice recorded in British pharmaceutical practice and reflected in modern manuals such as the Royal Pharmaceutical Society’s Herbal Medicines (2015), while heated marshmallow roots have long been applied as emollient poultices to wounds and burns in Anglo-European tradition.

A practical preparation to make a gentle demulcent tea is a cold maceration of marshmallow root. Place 2–4 g of chopped or powdered root in 200 ml of cool or room‑temperature water and macerate, covered, for 8–12 hours; strain and sip 1–2 cups daily. This method draws out the mucilaginous polysaccharides that soothe irritated mucous membranes. The British Herbal Pharmacopoeia (1983) lists infusion doses of 2–5 g; the German Commission E monographs (Blumenthal et al., 2000) recommend 2–3 g of leaf infusion. If an alcohol tincture is preferred, the British Herbal Pharmacopoeia (1983) records a 1:5 tincture (root in 45–60% ethanol); using 20 g of root macerated in 100 ml of menstruum for 2–4 weeks yields a dose of 2–5 ml, 3 times daily. For external use, a warm root decoction can be used as a compress. Marshmallow infusions and tinctures are usually well tolerated, but keep to established doses to avoid excess bulk and laxative effects; do not use concentrated extracts alongside sedatives without medical advice; and consult a practitioner if pregnant, breastfeeding, or managing blood sugar or blood pressure concerns.

The demulcent action is attributed chiefly to the characteristic mucilaginous polysaccharides of the roots and leaves, together with flavonoids and phenolic acids that have been reported for this species (Mączka and Grabowicz, 2021). These well‑established phytochemicals plausibly explain the soothing effects on mucosa.

Marshmallow remains widely available as dried herb for teas and as a standardized extract, and controlled trials continue to evaluate its efficacy for cough and upper‑respiratory irritation (Länger et al., 2018; Wagner et al., 1984).

General Uses Top

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Common products:
- Root and leaf used as flavoring (sweet–herbaceous, slightly bitter). Roots are the primary flavoring material.
- Marshmallow root extract historically used in confectionery as a foaming/softening agent; modern marshmallows are typically gelatin-based. Contemporary confectionery may include Althaea as a flavor or extract component.

Industrial and craft applications:
- Mucilaginous polysaccharides (arabinogalactans; galacturonic acid-rich) used as hydrocolloids. Functionally, they form viscous, slippery aqueous solutions that stabilize emulsions and films, serve as thickeners, and provide moisture-retention properties. Used as a viscosity regulator or stabilizing gum in foods and cosmetics; also applied as a glazing/coating base for fruit or as a seed-coating aid in limited contexts.

Food and beverages (non-medicinal):
- Flavoring in liqueurs and bitters, and in herbal teas (direct beverage ingredient only; no preparation instructions).
- Hydrocolloid applications include jams, syrups, bakery fillings, and ice cream base blends to adjust mouthfeel and freeze–thaw stability.
- Used to adjust gloss and film formation in coated confections.
- Employed in beverage clarification as a fining aid due to protein-binding properties (limited industrial use).

Colorants and tanning:
- No established non-medicinal colorant/tanning uses reported in reliable literature for this taxon.

Wood and fiber:
- No established timber or fiber products reported for this taxon.

Fragrance and cosmetics:
- Roots or extracts used in fragrance compositions as a sweet–herbaceous note at low dosage.
- In cosmetics and personal care, the hydrocolloid functions as a film-former, thickener, and stabilizer in leave-on and rinse-off formulations.

Properties relevant to use:
- Water-soluble mucilage with high viscosity and cohesion; pH and electrolyte sensitivity typical of anionic polysaccharides; forms films that resist brittleness and support gloss/coating properties.

Standards and regulation:
- EU: Althaea officinalis is authorized as a flavoring substance in spirits and certain food categories (quantitative use governed by good manufacturing practice or specific flavoring category rules).
- United States: Listed in the FDA’s database of substances that may be used as flavoring substances in food.
- Cosmetic: Althaea extract is listed in the International Nomenclature of Cosmetic Ingredients (INCI).

Sustainability and sourcing:
- Cultivated in temperate regions for roots and aerial parts; invasive in parts of North America; wild harvest is restricted in certain jurisdictions. Supplies are sourced from cultivated fields; impact is generally low to moderate depending on region and harvesting method.

Synonyms Top

Scientific name Authority First published in
Althaea kragujevacensis Pančić Fl. Serbiae 200 (1874), in clavi.
Althaea multiflora Rchb. ex Regel Index Seminum (LE, Petropolitanus) 1867(Suppl.): 36 (1868)
Althaea officinalis subsp. micrantha Dostál Folia Mus. Rerum Nat. Bohemiae Occid., Bot. 21: 8 (1984)
Althaea officinalis var. pseudoarmeniaca Polg.
Althaea sublobata Stokes Bot. Mat. Med. 3: 530 (1812)
Althaea kragujevacensis Pančić Fl. Serbiae : 200 (1874)
Malva althaea E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 6: 243 (1902)
Malva maritima Salisb. Prodr. Stirp. Chap. Allerton 381. 1796 [Nov-Dec 1796]
Malva officinalis K.F.Schimp. & Spenn. Fl. Friburg. 3: 885 (1829)
Althaea balearica Rodriguez Fl. Menorca : 24 (1904)
Althaea pulchra Klotzsch Bot. Ergebn. Reise Waldemar : 112 (1862)
Althaea officinalis var. vulgaris Alef.
Althaea officinalis var. thirkeana Alef.
Althaea officinalis subsp. indica Baker f.
Althaea officinalis var. pallida Regel & Herder
Althaea officinalis var. rotundifolia Gray
Althaea officinalis var. obtusiuscula H.C.Hall ex Lej.
Althaea officinalis var. obtusifolia Vayr.

Common names Top

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Language Common/alternative name
English common marshmallow
English marsh-mallow
English marshmallow
English marsh mallow
Spanish bismalva
Spanish malvavisco
Spanish camarmaje
Spanish hierba canamera
Spanish hierba cañamera
Spanish hierbacañamera
Spanish lavaradisco
Spanish malbaxuni
Spanish malbaxuri
Spanish malvavisco comun
Spanish malvavisco común
Spanish malvavizco
Spanish vivisco
Spanish yerba cañamera
ab Адоуҟәыд
Arabic خبيز
Arabic ختمية طبية
Arabic خطمية
Azerbaijani dərman gülxətmi
Azerbaijani dərman bəlğəmotu
ba Алтей үләне
Belarusian Алтэя лекавая
Bulgarian Божа ръчица
Bulgarian Бял слез
Bulgarian Бяла ружа
Bulgarian Волово око
Bulgarian Дива ружа
Bulgarian Лигавка
Bulgarian Просвирняк
Bulgarian Пъртенка
Bulgarian лечебна ружа
Bosnian bijeli sljez
Catalan malví
Czech proskurník lékařský
Czech slézová růže
cv Сиплĕ шăпăр курăкĕ
Welsh hokys y gors
Welsh hocysen y morfa
German echter eibisch
German gebräuchlicher eibisch
German samtapfel
Esperanto kuracalteo
Esperanto oficina alteo
Estonian harilik altee
Basque malba zuri
Persian پنیرک پفنبات
Finnish rohtosalkoruusu
French guimauve officinale
Irish leamhach
Hebrew נטופית רפואית
Croatian bijeli sljez
Upper Sorbian lěkarska popla
Hungarian fehérmályva
Hungarian orvosi ziliz
Hungarian orvosi zilíz
Armenian Տուղտ դեղատու
Indonesian panirak paya
Italian l’altea comune
Italian altea, malvone
Japanese ウスベニタチアオイ
Kabyle bineṣaṛ
Kazakh Аптекалық жалбызтікен
Korean 마시멜로
Cornish malow keunek
Lithuanian vaistinė svilarožė
Macedonian Бел слез
Malayalam അൽതീ ഒഫിഷിനാലിസ്
Norwegian Bokmål legestokkrose
Dutch echte heemst
Dutch heemst
os Галсыф
Polish prawoślaz lekarski
Romanian nalbă mare
Russian алтей аптечный
Russian алтей лекарственный
Russian алтейный корень
Russian дикий мак
Russian василистник
Russian просвирник
Russian пряничек
Russian дикая роза
Russian проскурняк аптечный
Russian слизник
Serbo-Croatian beli slez
Serbo-Croatian bijeli sljez
Slovak ibiš lekársky
Slovenian ajbiž
Slovenian beli popelj
Slovenian navadni slez
Serbian Бијели сљез
Serbian Слез бели
Serbian Трандафил
Serbian бели слез
Swedish läkemalva
Swedish althea-rot
Swedish althearot
Tamil சீமைத்துத்தி
tg Гули хайрӣ
Thai มาร์ชแมลโลว์
Turkish ebegümecigiller
tt Шифалы мәче борчагы
Ukrainian Алтея лікарська
Chinese 红绿草
Chinese 药葵
Chinese 药蜀葵
Chinese 藥蜀葵

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Russian Far East
      • Primorye
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Great Britain
      • Ireland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Ontario
      • Québec
    • North-central U.S.A.
      • Minnesota
      • Nebraska
      • North Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
    • Southeastern U.S.A.
      • Arkansas
      • Delaware
      • Kentucky
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000529011
UNII 8SG7244265
Canadensys 6617
USDA Plants ALOF2
Tropicos 19601250
INPN 81856
Flora of Italy 3128
KEW urn:lsid:ipni.org:names:558872-1
The Plant List kew-2631597
Missouri Botanical Garden 282618
Open Tree Of Life 643492
Observations.org 2334
NCBI Taxonomy 145745
NBN Atlas NBNSYS0000003139
Nature Serve 2.157972
IPNI 558872-1
iNaturalist 52565
GBIF 3152520
Freebase /m/04ccpf
WisFlora 8015
EPPO ALGOF
EOL 584767
Elurikkus 2704
USDA GRIN 2721
Wikipedia Althaea_officinalis
CMAUP NPO21924
Plantarium 2417
PFAF Althaea officinalis

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
Carnosic Acid Inhibits Herpes Simplex Virus Replication by Suppressing Cellular ATP Synthesis Horváth G, Molnár E, Szabó Z, Kecskeméti G, Juhász L, Tallósy SP, Nyári J, Bogdanov A, Somogyvári F, Endrész V, Burián K, Virok DP Int J Mol Sci 03-May-2024
PMCID:PMC11084413
doi:10.3390/ijms25094983
PMID:38732202
Phytochemical Analysis, Biological Activities, and Molecular Docking Studies of Root Extracts from Paeonia Species in Serbia Batinić P, Jovanović A, Stojković D, Zengin G, Cvijetić I, Gašić U, Čutović N, Pešić MB, Milinčić DD, Carević T, Marinković A, Bugarski B, Marković T Pharmaceuticals (Basel) 17-Apr-2024
PMCID:PMC11054981
doi:10.3390/ph17040518
PMID:38675478
Unveiling the mechanisms for the development of rosehip-based dermatological products: an updated review Oargă (Porumb) DP, Cornea-Cipcigan M, Cordea MI Front Pharmacol 11-Apr-2024
PMCID:PMC11043540
doi:10.3389/fphar.2024.1390419
PMID:38666029
Efficacy and classification of Sesamum indicum linn seeds with Rosa damascena mill oil in uncomplicated pelvic inflammatory disease using machine learning Sumbul, Sultana A, Heyat MB, Rahman K, Akhtar F, Parveen S, Urbano MB, Lipari V, De la Torre Díez I, Khan AA, Malik A Front Chem 02-Apr-2024
PMCID:PMC11018920
doi:10.3389/fchem.2024.1361980
PMID:38629105
Green Synthesis of Zinc Oxide Nanoparticles from Althaea officinalis Flower Extract Coated with Chitosan for Potential Healing Effects on Diabetic Wounds by Inhibiting TNF-α and IL-6/IL-1β Signaling Pathways Elhabal SF, Abdelaal N, Saeed Al-Zuhairy SA, Elrefai MF, Elsaid Hamdan AM, Khalifa MM, Hababeh S, Khasawneh MA, Khamis GM, Nelson J, Mohie PM, Gad RA, Rizk A, Kabil SL, El-Ashery MK, Jasti BR, Elzohairy NA, Elnawawy T, Hassan FE, El- Nabarawi MA Int J Nanomedicine 27-Mar-2024
PMCID:PMC10981898
doi:10.2147/IJN.S455270
PMID:38559447
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
The comprehensive strategy in the human health risk assessment of total chromium impurities in cough syrups with Marshmallow Root (Althaea officinalis) available in Polish pharmacies: regulatory aspects and special emphasis on Cr(VI) mode of action Jurowski K, Krośniak M Sci Rep 04-Mar-2024
PMCID:PMC10912266
doi:10.1038/s41598-024-56057-7
PMID:38438482
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472
Characterization of Firmiana danxiaensis plastomes and comparative analysis of Firmiana: insight into its phylogeny and evolution Li YL, Nie LY, Deng SW, Duan L, Wang ZF, Charboneau JL, Ho BC, Chen HF BMC Genomics 22-Feb-2024
PMCID:PMC10885454
doi:10.1186/s12864-024-10046-2
PMID:38389079
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
The Impact of Vegetable Fibres on the Shrinkage and Mechanical Properties of Cob Materials Kabore A, Ouellet-Plamondon CM Materials (Basel) 03-Feb-2024
PMCID:PMC10856543
doi:10.3390/ma17030736
PMID:38591571
Proportion of Over-The-Counter Medicines Containing a Plant Component and Those with Synthetic Substances Administered among Children in a Bulgarian Population Hadzhieva B, Petkova-Dimitrova V Pharmaceuticals (Basel) 31-Jan-2024
PMCID:PMC10892009
doi:10.3390/ph17020192
PMID:38399407
Mulberry Leaf Polysaccharides Attenuate Oxidative Stress Injury in Peripheral Blood Leukocytes by Regulating Endoplasmic Reticulum Stress Jiang W, Lin Y, Qian L, Lu S, Shen H, Ge X, Miao L Antioxidants (Basel) 23-Jan-2024
PMCID:PMC10886326
doi:10.3390/antiox13020136
PMID:38397734
Full-length transcriptome and RNA-Seq analyses reveal the resistance mechanism of sesame in response to Corynespora cassiicola Jia M, Ni Y, Zhao H, Liu X, Yan W, Zhao X, Wang J, He B, Liu H BMC Plant Biol 23-Jan-2024
PMCID:PMC10804834
doi:10.1186/s12870-024-04728-y
PMID:38262910
A critical overview of challenging roles of medicinal plants in improvement of wound healing technology Pathak D, Mazumder A Daru 15-Jan-2024
PMCID:PMC11087437
doi:10.1007/s40199-023-00502-x
PMID:38225520

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1055/S-2006-960092
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1080/01483919008049590
https://doi.org/10.1055/S-2006-960092
> 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 https://doi.org/10.1080/01483919008049590
https://doi.org/10.1055/S-2006-960092
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown https://doi.org/10.1080/01483919008049590
https://doi.org/10.1055/S-2006-960092
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Hydroxyphenylacetic acid 127 Click to see 152.15 unknown https://doi.org/10.1080/01483919008049590
https://doi.org/10.1055/S-2006-960092
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Hexadecenoic acid 5282743 Click to see CCCCCCCCCCCCCC=CC(=O)O 254.41 unknown https://doi.org/10.1007/BF01165189
2-Hexadecenoic acid 152802 Click to see 254.41 unknown https://doi.org/10.1007/BF01165189
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1007/BF01165189
Heptadecanoic Acid 10465 Click to see 270.50 unknown https://doi.org/10.1007/BF01165189
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1007/BF01165189
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1007/BF01165189
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1007/BF01165189
trans-6-Octadecenoic acid 5282754 Click to see 282.50 unknown https://doi.org/10.1007/BF01165189
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.1007/BF01165189
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown https://doi.org/10.1007/BF01165189
> 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/10.1007/BF01165189
Erucic Acid 5281116 Click to see 338.60 unknown https://doi.org/10.1007/BF01165189
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1007/BF01165189
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
N,N,N-trimethylglycinium 248 Click to see 118.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(1R,3S,5S,6R,7S,8R,10R,12S,13R,14R)-7-[(2R,3R,4S,5S,6S)-6-carboxy-3,4,5-trihydroxyoxan-2-yl]oxy-6,13,14-trihydroxy-12-methyl-2,4,9,11-tetraoxatricyclo[8.4.0.03,8]tetradecane-5-carboxylic acid 162842866 Click to see 498.40 unknown https://doi.org/10.1016/0008-6215(88)84101-6
7-(6-Carboxy-3,4,5-trihydroxyoxan-2-yl)oxy-6,13,14-trihydroxy-12-methyl-2,4,9,11-tetraoxatricyclo[8.4.0.03,8]tetradecane-5-carboxylic acid 162842865 Click to see 498.40 unknown https://doi.org/10.1016/0008-6215(88)84101-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
(1R,3S,5S,6R,7S,8R,10R,12S,13R,14R)-6,7,13,14-tetrahydroxy-12-methyl-2,4,9,11-tetraoxatricyclo[8.4.0.03,8]tetradecane-5-carboxylic acid 162953603 Click to see 322.26 unknown https://doi.org/10.1016/0008-6215(88)84101-6
6,7,13,14-Tetrahydroxy-12-methyl-2,4,9,11-tetraoxatricyclo[8.4.0.03,8]tetradecane-5-carboxylic acid 162953602 Click to see CC1C(C(C2C(O1)OC3C(C(C(OC3O2)C(=O)O)O)O)O)O 322.26 unknown https://doi.org/10.1016/0008-6215(88)84101-6
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Cichorine 442849 Click to see CC1=C(C=C2C(=C1OC)CNC2=O)O 193.20 unknown https://doi.org/10.1007/BF00630189
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1055/S-2006-960092
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1055/S-2006-960092
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1055/S-2006-960092
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1080/01483919008049590
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown https://doi.org/10.1007/BF00630189
Methylumbelliferone 10748 Click to see 176.17 unknown https://doi.org/10.1007/BF00630189
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Hydroxyskimmin 5088914 Click to see 340.28 unknown https://doi.org/10.1007/BF00630189
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 346340 Click to see 354.31 unknown https://doi.org/10.1007/BF00630189
7-Hydroxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-2-One 5351506 Click to see 340.28 unknown https://doi.org/10.1007/BF00630189
Cichoriin 442101 Click to see 340.28 unknown https://doi.org/10.1007/BF00630189
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1007/BF00630189
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1007/BF00630189
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown https://doi.org/10.1007/BF00630189
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown https://doi.org/10.1007/BF00630189
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1055/S-2006-960092
https://doi.org/10.1007/BF00630189
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00630189
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see 594.50 unknown https://doi.org/10.1016/S0021-9673(01)88531-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Spiraeoside 5320844 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1007/BF02319718
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/S0021-9673(01)88531-9
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/10.1016/S0021-9673(01)88531-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
[(2S,3R,4S,5S,6S)-2-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] hydrogen sulfate 163056015 Click to see 542.50 unknown https://doi.org/10.1055/S-2006-960092
2-(3,4-Dihydroxyphenyl)-8-((6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy)-5,7-dihydroxy-4H-1-benzopyran-4-one 13988634 Click to see 626.50 unknown https://doi.org/10.1016/S0021-9673(01)88531-9
https://doi.org/10.1007/BF02319718
Hypolaetin 8-O-beta-D-glucoside 44258591 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-960092
https://doi.org/10.1016/S0021-9673(01)88531-9

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