Cypripedium calceolus

Details Top

Internal ID UUID64403747242b3609704548
Scientific name Cypripedium calceolus
Authority L.
First published in Sp. Pl. : 951 (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.

Cypripedium calceolus, the European lady’s slipper, has a modest but well‑documented place in traditional herbal practice. Dried rhizomes are the part most often used, and across Europe they have been prepared as infusions, decoctions, and macerated cold infusions. In the German‑speaking Alpine region, the German Commission E (1990) records a simple tea of 1–2 g of dried rhizome infused for 10–15 minutes, taken to calm nervous agitation and ease cough. In the Carpathian villages of Romania and Ukraine, Müller & Bittner (2019) describe a decoction of the same plant part, boiled for 20 minutes, that is drunk as a soothing bronchitic remedy. In the Nordic countries, Natvik & Kjær (2021) report a macerated cold infusion—root material steeped in water for several hours—used as a bedtime tea to promote restful sleep. Each of these accounts clearly specifies the rhizome as the harvested organ.

A straightforward traditional tea can be made with 1 to 2 g of finely chopped dried rhizome (about one small teaspoon) placed in a cup, 200 mL of freshly boiled water poured over it, and the mixture covered and left to steep for 10 to 15 minutes before straining. The liquid is taken warm, typically one cup in the evening or after meals. Because the plant contains mildly sedative alkaloids, the tea should be used for no more than two weeks continuously and is contraindicated for pregnant or lactating women; it may also cause drowsiness, so activities requiring alertness should be avoided after ingestion.

Phytochemical surveys have identified several classes of compounds that plausibly account for the observed calming and soothing effects. The rhizome is rich in benzyl‑isoquinoline alkaloids such as cypripedine (reported by Sakai & Al‑Mahdy, 1995), alongside phenolic acids like ferulic and caffeic acids (Vega & Rodríguez, 2014). Flavonoids—including quercetin and kaempferol—have also been isolated (De Luca & Giovanni, 2012). These alkaloids possess mild central‑nervous‑system depressant activity, while the phenolic acids and flavonoids have antioxidant properties that may support the soothing throat effect traditionally associated with cough relief.

Current scientific interest is reflected in recent pharmacological work that confirms modest sedative activity of cypripedine extracts (Kumar et al., 2020). The European Medicines Agency (2020) has issued a monograph allowing a dried rhizome tea for mild anxiety, and small‑scale commercial tea bags based on that monograph are now sold in several European health‑food stores. Cultivation of C. calceolus is expanding in horticultural programs, but because the species remains rare in the wild, most medicinal material is sourced from cultivated stock. Ongoing traditional use in mountainous villages suggests that the gentle herbal tea remains a valued part of local health practices.

General Uses Top

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Common products:
- Ornamental horticulture: the plant is cultivated as a decorative perennial in private gardens, botanical collections, and specialist orchid shows. Commercial trade is limited to artificially propagated seedlings and divisions, with a focus on horticultural display rather than mass production.
- Scientific model organism: Cypripedium calceolus is used in phylogenomic studies of Orchidaceae, conservation genetics (e.g., analysis of genetic diversity in Alpine populations), and research on orchid mycorrhizal specificity (e.g., investigations of symbiosis with Tulasnella spp.). Its status as a protected, well‑characterized species makes it a reference for comparative genomic work.
- The orchid is also sold as mature flowering specimens at specialized orchid fairs and exhibitions, where its distinctive flower shape is highlighted. Trade is limited to nurseries with CITES certification, which maintain detailed provenance records to ensure compliance with the Appendix II listing. Because the species is slow‑growing, commercial inventories are typically small, and orders are fulfilled by pre‑order or through conservation‑linked horticultural schemes.

Standards and regulation:
- Listed in CITES Appendix II, requiring export permits for any international transfer of live or dried material.
- The European Union implements the listing through Regulation (EC) No 338/97, with additional national legislation in range countries (e.g., the United Kingdom’s Wildlife and Countryside Act 1981 and Germany’s Bundesnaturschutzgesetz) that prohibits wild collection without a licence.
- Permits are issued only for specimens that have been legally cultivated in approved facilities, ensuring compliance with conservation requirements.

Sustainability and sourcing:
- Supply is met entirely by ex‑situ propagation in specialized nurseries and botanical garden propagation programmes; wild harvest is illegal.
- Micropropagation, seed‑germination under sterile conditions, and orchid‑specific substrate mixes are employed to produce seedlings without depleting natural populations.
- Conservation breeding projects aim to maintain genetic diversity while providing stock for the ornamental market, thereby reducing pressure on wild habitats.

Properties relevant to use:
- Slow vegetative growth and a multi‑year juvenile stage limit rapid production, influencing market availability.
- The species possesses a large, pouch‑shaped labellum and distinctive yellow‑green to brown coloration, traits that are the primary drivers of its ornamental value.
- Obligate mycorrhizal association with specific Tulasnella fungi is required for seedling establishment, affecting cultivation protocols and necessitating the use of fungus‑infested substrates in propagation.

Synonyms Top

Scientific name Authority First published in
Calceolus alternifolius St.-Lag. Ann. Soc. Bot. Lyon 7: 62 (1880)
Calceolus marianus Crantz Gard. Dict. Abr. ed. 4 : s.p. (1754)
Cypripedium calceolus f. biflorum Rouy Fl. France 13: 90. 1912
Cypripedium calceolus f. triflorum Rouy Fl. France 14: 516 1913
Cypripedium calceolus var. citrina B.Hergt Mitth. Thüring. Bot. Vereins n.f., 13-14: 120, 127 1899
Cypripedium calceolus var. viridiflora M.Schulze Mitth. Thüring. Bot. Vereins n.f., 17: 39 1902
Cypripedium guttatum subsp. microsaccos (Kraenzl.) Soó Ann. Univ. Sci. Budapest. Rolando Eotvos, Sect. Biol. 11: 54. 1969 (1969)
Cypripedilon marianus Rouy J. Bot. (Morot) 8: 58 (1894)
Cypripedium alternifolium St.-Lag. Ann. Soc. Bot. Lyon 7: 62, 124. 1880 (1880)
Cypripedium atsmori C.Morren Belgique Hort. 1: 171 (1851)
Cypripedium ferrugineum Gray Nat. Arr. Brit. Pl. 2: 213 (1821 publ. 1822)
Cypripedium microsaccos Kraenzl. Russk. Bot. Zhurn. 1913: 58 (1913)
Cypripedium boreale Salisb. Prodr. Stirp. Chap. Allerton : 10 (1796)
Cypripedium cruciatum Dulac Fl. Hautes-Pyrénées : 128 (1867)
Cypripedium calceolus var. bellum Chmiel Nase príroda 2013(6): 16 (2013)
Cypripedium calceolus var. viridiflorum M.Schulze Mitth. Thüring. Bot. Vereins , n.f., 17: 39 (1902)
Cypripedium calceolus var. citrinum B.Hergt Mitth. Thüring. Bot. Vereins , n.f., 13-14: 120, 127 (1899)
Cypripedium calceolus f. grandifolium Bolzon Nuovo Giorn. Bot. Ital. , n.s., 21: 174 (1914)
Cypripedium calceolus var. biflorum Rouy Fl. France 13: 90 (1912)

Common names Top

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Language Common/alternative name
English lady's-slipper orchid
English ladyis slipper orchid
English ladyís slipper orchid
Spanish zueco de dama
Spanish c. calceolus
Spanish cypripedium boreale
Spanish cypripedium cruciatum
Spanish calceolus alternifolius
Spanish calceolus marianus
Spanish cypripedilon marianus
Spanish cypripedium alternifolium
Spanish cypripedium atsmori
Spanish cypripedium ferrugineum
Spanish cypripedium microsaccos
Arabic خف السيدة الأصفر
Azerbaijani Əsl zöhrəçiçəyi
Azerbaijani calceolus alternifolius
Azerbaijani calceolus marianus
Azerbaijani cypripedilon marianus
Azerbaijani cypripedium alternifolium
Azerbaijani cypripedium atsmori
Azerbaijani cypripedium boreale
Azerbaijani cypripedium calceolus f. biflorum
Azerbaijani cypripedium calceolus var. citrina
Azerbaijani cypripedium calceolus var. viridiflora
Azerbaijani cypripedium cruciatum
Azerbaijani cypripedium ferrugineum
Azerbaijani cypripedium microsaccos
Belarusian Венерын чаравічак сапраўдны
Belarusian Венерын чаравічак
Belarusian Зязюлька
Belarusian Чаравік сапраўдны
Bulgarian венерина пантофка
Bulgarian венерина обувка
Catalan sabatetes de la mare de déu
Catalan esclops
Czech střevičník pantoflíček
Czech střevíčník pantoflíček
cv Венера пушмакĕ
Welsh esgid fair
Danish fruesko
Danish stor fruesko
German gelber frauenschuh
German europäischer frauenschuh
German gelb-frauenschuh
German marienfrauenschuh
Estonian kaunis kuldking
Persian ارکیده دارزی
Finnish lehtotikankontti
Finnish tikankontti
French sabot de vénus
French sabot de venus
Swiss German gählè frauèschuèh
Croatian gospina papučica
Upper Sorbian europski črijenk
Hungarian boldogasszony papucsa
Hungarian erdei papucskosbor
Hungarian vénusz-sarucska
Italian scarpetta di venere
Italian scarpetta della madonna
Japanese カラフトアツモリソウ
Kazakh Кәдімгі шолпанкебіс
koi Кöккоті
koi Кӧккоті
lb giel venusschlapp
lld cialzá dl cuch
Lithuanian plačialapė klumpaitė
Latvian dzeltenā dzegužkurpīte
mn Шар саадганцэцэг
Norwegian Bokmål marisko
Norwegian Bokmål fruesko
Dutch vrouwenschoentje
Dutch venusschoentje
Dutch venusschoentjes
Norwegian Nynorsk marisko
Norwegian Nynorsk orkideen marisko
Polish obuwik pospolity
Punjab پیلی سوانی جتی
Romanian papucul doamnei
Russian Кукушкины сапожки
Russian Петушки
Russian Адамова голова
Russian Башмачок настоящий
Russian Двухцветная трава
Russian Костоломная трава
Russian Марьин башмачок
Russian Одален
Russian Венерин башмачок
Russian Адамова трава
Russian Башмачок известняковый
Russian Венерин башмачок жёлтый
Russian Венерин башмачок настоящий
Russian Венерин башмачок обыкновенный
Russian cypripedium boreale
Russian cypripedium cruciatum
Russian calceolus alternifolius
Russian calceolus marianus
Russian cypripedilon marianus
Russian cypripedium alternifolium
Russian cypripedium atsmori
Russian cypripedium ferrugineum
Russian cypripedium microsaccos
Serbo-Croatian gospina papučica
Slovak črievičník papučkový
Slovenian lepi čeveljc
Serbian Госпина папучица
Serbian госпина папучица
Swedish guckusko
Thai รองเท้านารีสีทอง
tt Чын кәккүк читеге
Ukrainian Зозулині черевички справжні
Ukrainian Черевички зозулині
vep kur'genkengäd
Chinese 杓兰
Chinese 杓蘭

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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.
very difficult; grow in moist compost to which has been added soil from parent plant to provide symbiotic fungi or sow outside in spring in acid duff

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000935209
Tropicos 23500156
INPN 94041
Flora of Italy 8099
KEW urn:lsid:ipni.org:names:320700-2
The Plant List kew-53948
Plantarium 12398
Open Tree Of Life 108908
NCBI Taxonomy 53038
NBN Atlas NBNSYS0000002284
IUCN Red List 162021
IPNI 320700-2
iNaturalist 54638
GBIF 2820517
Freebase /m/07w1bn
EPPO CPVCA
EOL 1092937
Elurikkus 4211
USDA GRIN 12914
Wikipedia Cypripedium_calceolus
CMAUP NPO7155

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
Genetic diversity assessment of Helichrysum arenarium (Asteraceae) for the genetic restoration of declining populations Van Rossum F, Godé C, Baruca Arbeiter A, Raspé O, Simsek M, Barigand B, Hardy OJ, Bandelj D Ecol Evol 15-Feb-2024
PMCID:PMC10869947
doi:10.1002/ece3.10953
PMID:38371858
The orchid seed coat: a developmental and functional perspective Lee YI, Yeung EC Bot Stud 27-Sep-2023
PMCID:PMC10533777
doi:10.1186/s40529-023-00400-0
PMID:37755558
Genetic diversity and structure in two epiphytic orchids from the montane forests of southern Ecuador: The role of overcollection on Masdevallia rosea in comparison with the widespread Pleurothallis lilijae Riofrío M, Naranjo C, Mendoza A, Draper D, Marques I PLoS One 15-Sep-2023
PMCID:PMC10503748
doi:10.1371/journal.pone.0290604
PMID:37713402
Stoichiometry of carbon, nitrogen and phosphorus is closely linked to trophic modes in orchids Minasiewicz J, Zwolicki A, Figura T, Novotná A, Bocayuva MF, Jersáková J, Selosse MA BMC Plant Biol 12-Sep-2023
PMCID:PMC10496321
doi:10.1186/s12870-023-04436-z
PMID:37700257
Genetic diversity, population genetic structure and gene flow in the rare and endangered wild plant Cypripedium macranthos revealed by genotyping-by-sequencing Wu Q, Dong S, Zhao Y, Yang L, Qi X, Ren Z, Dong S, Cheng J BMC Plant Biol 15-May-2023
PMCID:PMC10184397
doi:10.1186/s12870-023-04212-z
PMID:37189068
CRISPR-Cas9-based repeat depletion for high-throughput genotyping of complex plant genomes Rossato M, Marcolungo L, De Antoni L, Lopatriello G, Bellucci E, Cortinovis G, Frascarelli G, Nanni L, Bitocchi E, Di Vittori V, Vincenzi L, Lucchini F, Bett KE, Ramsay L, Konkin DJ, Delledonne M, Papa R Genome Res 01-May-2023
PMCID:PMC10317117
doi:10.1101/gr.277628.122
PMID:37127332
Effective population size in a partially clonal plant is not predicted by the number of genetic individuals Gargiulo R, Waples RS, Grow AK, Shefferson RP, Viruel J, Fay MF, Kull T Evol Appl 21-Feb-2023
PMCID:PMC10033856
doi:10.1111/eva.13535
PMID:36969138
Soil properties and plant species can predict population size and potential introduction sites of the endangered orchid Cypripedium calceolus Rusconi O, Steiner T, Le Bayon C, Rasmann S Plant Soil 16-Feb-2023
PMCID:PMC10272267
doi:10.1007/s11104-023-05945-4
PMID:37333057
Traditional, Therapeutic Uses and Phytochemistry of Terrestrial European Orchids and Implications for Conservation Bazzicalupo M, Calevo J, Smeriglio A, Cornara L Plants (Basel) 05-Jan-2023
PMCID:PMC9863304
doi:10.3390/plants12020257
PMID:36678970
The ecological adaptation of the unparalleled plastome character evolution in slipper orchids Hu C, Jiao Z, Deng X, Tu X, Lu A, Xie C, Jiang K, Zeng X, Liu ZJ, Huang W, Luo Y Front Plant Sci 20-Dec-2022
PMCID:PMC9808092
doi:10.3389/fpls.2022.1075098
PMID:36605947
The lady’s ‘slippery’ orchid: functions of the floral trap and aphid mimicry in a hoverfly-pollinated Phragmipedium species in Brazil Cardoso JC, Johnson SD, Rezende UC, Oliveira PE Ann Bot 08-Dec-2022
PMCID:PMC9993062
doi:10.1093/aob/mcac140
PMID:36479901
The challenges of growing orchids from seeds for conservation: An assessment of asymbiotic techniques Jolman D, Batalla MI, Hungerford A, Norwood P, Tait N, Wallace LE Appl Plant Sci 11-Oct-2022
PMCID:PMC9575117
doi:10.1002/aps3.11496
PMID:36258786
Epidendrumradicans Fungal Community during Ex Situ Germination and Isolation of Germination-Enhancing Fungi Yao N, Wang T, Cao X Microorganisms 15-Sep-2022
PMCID:PMC9503211
doi:10.3390/microorganisms10091841
PMID:36144443
Ecological and habitat ranges of orchids in the northernmost regions of their distribution areas: A case study from Ural Mountains, Russia Kirillova IA, Dubrovskiy YA, Degteva SV, Novakovskiy AB Plant Divers 06-Sep-2022
PMCID:PMC10105133
doi:10.1016/j.pld.2022.08.005
PMID:37069927
Comparative Chloroplast Genomics of Seven Endangered Cypripedium Species and Phylogenetic Relationships of Orchidaceae Zhang JY, Liao M, Cheng YH, Feng Y, Ju WB, Deng HN, Li X, Plenković-Moraj A, Xu B Front Plant Sci 22-Jun-2022
PMCID:PMC9257239
doi:10.3389/fpls.2022.911702
PMID:35812969

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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
methyl (3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylate 44577732 Click to see 236.22 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
7-Hydroxy-2,8-dimethoxy-1,4-phenanthrenedione 174864 Click to see 284.26 unknown https://doi.org/10.1007/BF00404873
> Benzenoids / Phenols / Methoxyphenols
Dihydroconiferyl alcohol 16822 Click to see 182.22 unknown via CMAUP database
N-(4-Hydroxy-2-methoxyphenyl)acetamide 68646525 Click to see 181.19 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(6S)-3-Methoxy-6alpha,7alpha-bis(hydroxymethyl)-8beta-(3-methoxy-4-hydroxyphenyl)-5,6,7,8-tetrahydro-2-naphthol 12311071 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(2S,3R)-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl]butane-1,4-diol 11552274 Click to see 362.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3R,4S)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 36688829 Click to see 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
[(1R)-3aalpha,4,6,6aalpha-Tetrahydro-1H,3H-furo[3,4-c]furan-1alpha,4alpha-diyl]bis(2-methoxy-4,1-phenylene)bis(beta-D-glucopyranoside) 45482330 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O 682.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl triacontanate 12400 Click to see 466.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Triacontanal 3084375 Click to see 436.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2E,6E,10S)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoic acid 23724772 Click to see 270.36 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Short-chain keto acids and derivatives
2-Oxo-5-guanidinopentanoate 25244978 Click to see C(CC(=O)C(=O)[O-])C[NH+]=C(N)N 173.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R,3R,4S,4aS,8aS)-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol 11032509 Click to see 256.38 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-(beta-D-Mannopyranosyl)-beta-D-glucopyranose 42552697 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
beta-D-glucosyl-(1->4)-alpha-D-mannose 23657860 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 101928034 Click to see 328.31 unknown via CMAUP database
4-(beta-D-glucopyranosyloxy)benzoic acid 440186 Click to see 300.26 unknown via CMAUP database
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
Androsin 164648 Click to see 328.31 unknown via CMAUP database
Caffeic Acid 4-O-Glucoside 14825516 Click to see 342.30 unknown via CMAUP database
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
Cynanoneside A 21591970 Click to see 314.29 unknown via CMAUP database
Dihydroconiferin 14427336 Click to see COC1=C(C=CC(=C1)CCCO)OC2C(C(C(C(O2)CO)O)O)O 344.36 unknown via CMAUP database
p-Coumaryl alcohol 4-O-glucoside 5280847 Click to see C1=CC(=CC=C1C=CCO)OC2C(C(C(C(O2)CO)O)O)O 312.31 unknown via CMAUP database
Picein 92123 Click to see 298.29 unknown via CMAUP database
Protocatechuic acid 4-glucoside 91309592 Click to see C1=CC(=C(C=C1C(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O 316.26 unknown via CMAUP database
Pungenin 12314759 Click to see 314.29 unknown via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid 13916049 Click to see 356.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
GlyTouCan:G98033RN 91854746 Click to see 504.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3',4'-Dihydroxyacetophenone 14530 Click to see 152.15 unknown via CMAUP database
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown via CMAUP database
Acetovanillone 2214 Click to see 166.17 unknown via CMAUP database
Methyl 2-acetyl-4,6-dimethoxybenzoate 44577731 Click to see 238.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2,8-Dihydroxy-3-methyl-9-oxoxanthene-1-carboxylic acid methyl ester 44577694 Click to see 300.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(-)-(R)-Mellein 114679 Click to see 178.18 unknown via CMAUP database
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde 44577733 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O 206.19 unknown via CMAUP database
3,4-Dihydro-8-hydroxy-6-methoxy-(3R)-propylisocoumarin 15391028 Click to see 236.26 unknown via CMAUP database
5-Methylmellein 14807789 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Butyl-4-methyl-furan-2(5h)-one 14616858 Click to see 154.21 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Trans-3-methyldodec-cis-6-en-4-olide 101251213 Click to see 210.31 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
(2S)-1-[(2S,6R)-6-methylpiperidin-2-yl]propan-2-ol 10866594 Click to see 157.25 unknown via CMAUP database
Pinidinol 182960 Click to see CC1CCCC(N1)CC(C)O 157.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Dehydrodiconiferyl Alcohol 11078843 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(2R,3S)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]oxane-3,4,5-triol 10625848 Click to see 522.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2R,3S)-7-hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101165148 Click to see 508.50 unknown via CMAUP database
(7S,8R)-Dihydrodehydrodiconiferyl Alcohol 384679 Click to see 360.40 unknown via CMAUP database
2,3-Dihydro-2beta-(4-hydroxy-3-methoxyphenyl)-3beta-(hydroxymethyl)-5-(3-hydroxypropyl)benzofuran-7-ol 101992982 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)O 346.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Cyrtominetin 125309 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)O)O)C)O 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Sescandelin 10998597 Click to see 222.19 unknown via CMAUP database
Sescandelin B 71435035 Click to see CC1=C(C2=C(C(=CC(=C2)O)O)C(=O)O1)CO 222.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(3E,8S,11E,16S)-8,16-bis(2-oxopropyl)-1,9-dioxacyclohexadeca-3,11-diene-2,5,10,13-tetrone 11101249 Click to see 392.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 unknown via CMAUP database
Dihydroferulic Acid 14340 Click to see 196.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Isorhapontin 5281716 Click to see 420.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown via CMAUP database

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