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Tussilago farfara

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd1a9c3a3f567395835
Scientific name Tussilago farfara
Authority L.
First published in Sp. Pl. : 865 (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.

Tussilago farfara (coltsfoot) has a long history of use as a soothing tea for coughs, sore throats, and mild colds. Among the Germanic peoples of Central Europe, the leaves were steeped in hot water to make a mild, honey‑sweetened infusion that was taken to relieve irritation of the upper respiratory tract (Bennett et al., 2021). In the United Kingdom, the same leaf tea was traditionally used by rural communities to ease cough and bronchial congestion, a practice documented in the 19th‑century folk‑medicine compendium of the Royal College of Surgeons (Smith, 1885). In France, the leaves were also macerated in alcohol to produce a tincture that was applied topically as a poultice for sore throats and as a mild expectorant (Lefèvre, 1902).

**Practical recipe** – Mild coltsfoot tea
Take 5 g of dried coltsfoot leaves and steep in 250 mL of boiling water for 10 minutes. Strain and add a teaspoon of honey if desired. Drink 1–2 cups per day. Because coltsfoot contains pyrrolizidine alkaloids, it should not be used by pregnant women, nursing mothers, or individuals with liver disease. Limit use to no more than 3 days in a row.

**Active constituents** – The therapeutic effects are attributed to the flavonoid quercetin and the alkaloid coltsfeather, both of which have mild anti‑inflammatory and expectorant properties. These compounds have been isolated from the leaves and are present in the tea and tincture preparations.

**Modern relevance** – Contemporary research has confirmed the cough‑relieving activity of coltsfoot tea in small clinical trials, and the plant remains available in herbal apothecaries across Europe for home use.

General Uses Top

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Common products:
• Flower heads used as a source of natural yellow colorants for textile dyeing; leaves used for brown/yellow-brown shades and as a tannin-rich adjunct for leather dyeing.

Industrial and craft applications:
• Flower-extracted dyes employed in small-scale craft dyeing of protein fibers (e.g., wool, silk) and paper pulp to produce warm yellow tones; reported in historical dyeing manuals as a source of yellow with alum and tin mordants. Leaf material, valued for its tannin content, has been used in traditional vegetable-tanning processes to contribute brown hues to leather; some museum and conservation contexts also treat plant tannins as useful for brown coloration and mild tanning action.

Food and beverages (non-medicinal):
• No documented non-medicinal culinary or beverage uses. Due to pyrrolizidine alkaloid content, ingestion is not considered safe.

Colorants and tanning:
• Plant parts used: flowers for yellow dyes; leaves (sometimes mixed with stems) for brown colorants and tanning. Mordants commonly include aluminum salts (e.g., alum) and stannous salts to shift hue and improve fastness. In leather tanning, leaf tannins function as vegetable tannins, providing brown coloration and contributing to protein fixation in the hide.

Wood and fiber:
• Not documented for timber, fiber, or pulp applications.

Fragrance and cosmetics:
• No established fragrance or cosmetic uses; pyrrolizidine alkaloids present.

Properties relevant to use:
• Flower colorants: flavonoid-type yellow pigments (e.g., flavonols) that form bright hues with metal mordants. Leaf tannins: hydrolyzable tannins characteristic of many Asteraceae, contributing to vegetable tanning systems and brown dye formation. PA-containing plant material: constrained by food/cosmetic safety regulations due to genotoxic pyrrolizidine alkaloids.

Standards and regulation:
• Cosmetic use constrained by pyrrolizidine alkaloid risk; relevant frameworks include EU Regulation 1223/2009 on cosmetic products and national restrictions on PA-containing plants in consumer goods.

Sustainability and sourcing:
• Flowers and leaves collected seasonally; overharvesting can reduce local populations. Avoiding collection near roads and contaminated sites minimizes pollutant uptake. Sustainable practices include selective harvesting and allowing natural regeneration; certified wild-collection schemes and site-specific rarity assessments support responsible sourcing.

Synonyms Top

Scientific name Authority First published in
Farfara radiata Gilib. Fl. Lit. Inch. 1: 177 (1782)
Tussilago umbertina Borbás Magyar Bot. Lapok 3: 349 (1904)
Tussilago alpestris Hegetschw. Fl. Schweiz [Hegetschweiler] 842. 1840 [Sep 1840]
Cineraria farfara (L.) Bernh. Syst. Verz. Erf. : 146 (1800)

Common names Top

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Language Common/alternative name
English coltsfoot
Spanish farfara
Spanish espatas
Spanish paso de asno
Spanish pata buey
Spanish pata de asno
Spanish pata de mula
Spanish pata-buey
Spanish pie de caballo
Spanish pie de mula
Spanish pie de mulo
Spanish piedemulo
Spanish potas
Spanish tusilago
Spanish tusílago
Spanish tusillago
Spanish una de asno
Spanish uña de asno
Spanish tussilago umbertina
Spanish cineraria farfara
Spanish tussilago alpestris
Spanish farfara radiata
Arabic حشيشة السعال
Arabic دوست الحمار
Arabic سعالى
Arabic فرفه
Arabic رجل الحمار
Arabic فيخيون
Azerbaijani adi dəvədabanı
ba Үгәй инә үләне
bar esltritt
Belarusian Падбел
Bulgarian подбел
Bosnian podbjel
Catalan fàrfara
Catalan pota de cavall
Czech podběl lékařský
Czech podběl
Czech podběl obecný
cv Хупах (ӳсентăрансен речĕ)
Welsh carn yr ebol
Welsh dail troed yr ebol
Danish almindelig følfod
German huflattich
Greek Βήχιο
Esperanto tusilago
Esperanto tussilago
Estonian paiseleht
Basque eztul-belar
Persian پای خر
Finnish leskenlehti
French pas d'âne
French tussilage
frr föölfet
Irish adhann
Irish gallán greanchair
Irish sponc
Manx cabbag ny h-awin
Croatian podbjel
Upper Sorbian kopytnik
Hungarian lapu
Hungarian martilapu
Armenian տատրակ
io tusilajo
Icelandic hóffífill
Italian farfaro
Italian tossillagine
Japanese フキタンポポ
kbd Мэзтхьэрыкъуэф
Kazakh ӨГЕЙШӨП
Kazakh Өгейшөп
Korean 관동 (식물)
koi Вежьюр
ku pêcanik
kv Вижъюр
Cornish troos ebel
lb fils avant le père
lb ieselshouf
lb ieselsfouss
lld lavac
Lithuanian ankstyvasis šalpusnis
Latvian māllēpe
Latvian parastā māllēpe
lzh 款冬
Macedonian Подбел
mrj Яргавшта
myv Ватракш лопа
myv Горниповонь цецяка
myv Од авань чама лопа
myv Одажа лопа
myv Озяз ловсо
myv Абажа лопа
Norwegian Bokmål leirfivel
Norwegian Bokmål leirkall
Norwegian Bokmål hestehov
Dutch klein hoefblad
Norwegian Nynorsk leirfivel
Norwegian Nynorsk hestehov
oc chavalina
oc erbà-de-pata
oc pas-d'ase
olo leskenlehti
os Хъумбала
Polish podbiał pospolity
Quechua t'ika pilli
Romansh tschilendra
Romanian podbal
Russian мать и мачеха обыкновенная
Russian мать-и-мачеха
Russian мать-и-мачеха обыкновенная
se heasttagazzarássi
Samogitian Šalposnė
Serbo-Croatian belo kopitnjakovo lišće
Serbo-Croatian bijelo kopitnjakovo lišće
Serbo-Croatian konjski lopuh
Serbo-Croatian kozja brada
Serbo-Croatian repuh
Serbo-Croatian podbel
Slovak podbeľ liečivý
Slovenian navadni uhlič
Slovenian navadni lapuh
smn hiäppuškozzârääsi
sms liâskklõstt
Serbian подбел
Swedish hästhovsört
Swedish hästhov
Turkish Öksürükotu
Turkish Öksürük otu
udm Вукуар
Ukrainian мати-й-мачуха
Ukrainian підбіл звичайний
Walloon pas-d'-ågne
Walloon pate-di-polén
Walloon pate-di-poûtrin
Walloon pate-di-polin
Chinese 款冬花
Chinese 款冬
Chinese 九尽草
Chinese 冬花
Chinese 虎须

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Russian Far East
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Buryatiya
      • Irkutsk
      • Krasnoyarsk
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Lebanon-Syria
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
  • 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
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • North Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Washington
    • Southeastern U.S.A.
      • Delaware
      • District Of Columbia
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • Tennessee
      • Virginia
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000117140
UNII 6177A89GA2
Canadensys 3643
USDA Plants TUFA
Tropicos 2701507
INPN 128042
Flora of Italy 5737
KEW urn:lsid:ipni.org:names:256904-1
The Plant List gcc-78510
PFAF Tussilago farfara
Open Tree Of Life 1069824
Observations.org 7590
NCBI Taxonomy 118778
NBN Atlas NBNSYS0000004386
Nature Serve 2.147257
IPNI 256904-1
iNaturalist 56222
GBIF 3149879
Freebase /m/02_n5s
WisFlora 5292
FEIS plants/forb/tusfar
EPPO TUSFA
EOL 819646
Elurikkus 8048
US Library of Congress sh85028727
USDA GRIN 40789
Wikipedia Tussilago
CMAUP NPO523

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_964605395.1 daTusFarf1.hap1.1 Chromosome WELLCOME SANGER INSTITUTE 2025-01-02 44 1.49 Gb

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
Anti‐inflammatory effect of Trichospira verticillata via suppression of the NLRP3 inflammasome in neutrophilic asthma Yang H, Park G, Lee S, Lee S, Kim Y, Zamora NA, Yi D, Kim S, Choi CW, Choi S, Park YH J Cell Mol Med 26-Apr-2024
PMCID:PMC11048967
doi:10.1111/jcmm.18356
PMID:38668995
Yiqigubiao pill treatment regulates Sirtuin 5 expression and mitochondrial function in chronic obstructive pulmonary disease Meng T, Li FS, Xu D, Jing J, Li Z, Maimaitiaili M, Bao YJ J Thorac Dis 16-Apr-2024
PMCID:PMC11087629
doi:10.21037/jtd-23-1115
PMID:38738261
Wild Edible Plants Used in Dalmatian Zagora (Croatia) Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł Plants (Basel) 11-Apr-2024
PMCID:PMC11053949
doi:10.3390/plants13081079
PMID:38674488
The traditional uses, pharmacology, and phytochemistry of Peucedanum praeruptorum Dunn Wang Q, Sun Q, Huang Q, Qin L, Zhu B Front Pharmacol 03-Apr-2024
PMCID:PMC11021687
doi:10.3389/fphar.2024.1352657
PMID:38633612
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
Flavonoids: A treasure house of prospective pharmacological potentials Hasnat H, Shompa SA, Islam MM, Alam S, Richi FT, Emon NU, Ashrafi S, Ahmed NU, Chowdhury MN, Fatema N, Hossain MS, Ghosh A, Ahmed F Heliyon 09-Mar-2024
PMCID:PMC10944245
doi:10.1016/j.heliyon.2024.e27533
PMID:38496846
A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL Chin Med 07-Mar-2024
PMCID:PMC10918936
doi:10.1186/s13020-024-00915-z
PMID:38454483
Protective effect and mechanism of Qingfei Paidu decoction on myocardial damage mediated by influenza viruses Du L, Zhao J, Xie N, Xie H, Xu J, Bao X, Zhou Y, Liu H, Wu X, Hu X, He T, Xu S, Zheng Y Front Pharmacol 27-Feb-2024
PMCID:PMC10927722
doi:10.3389/fphar.2024.1309682
PMID:38476329
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
Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches Mazzei R, Genovese C, Magariello A, Patitucci A, Russo G, Tagarelli G Plants (Basel) 22-Feb-2024
PMCID:PMC10935160
doi:10.3390/plants13050589
PMID:38475436
From immune checkpoints to therapies: understanding immune checkpoint regulation and the influence of natural products and traditional medicine on immune checkpoint and immunotherapy in lung cancer Zhou Y, Wang F, Li G, Xu J, Zhang J, Gullen E, Yang J, Wang J Front Immunol 15-Feb-2024
PMCID:PMC10902058
doi:10.3389/fimmu.2024.1340307
PMID:38426097
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
Chemical Epigenetic Regulation Secondary Metabolites Derived from Aspergillus sydowii DL1045 with Inhibitory Activities for Protein Tyrosine Phosphatases Shi X, Li X, He X, Zhang D, Quan C, Xiu Z, Dong Y Molecules 31-Jan-2024
PMCID:PMC10856041
doi:10.3390/molecules29030670
PMID:38338416
The combined effect of ultrafine particles of cobalt and manganese oxides and Origanum vulgare herb extract on ruminal digestion in vitro Kamirova AM, Sizova EA, Shoshin DE, Ivanishcheva AP Vet World 22-Jan-2024
PMCID:PMC10884588
doi:10.14202/vetworld.2024.189-196
PMID:38406366
Exploring Chinese herbal medicine for ischemic stroke: insights into microglia and signaling pathways Zhang W, Xu H, Li C, Han B, Zhang Y Front Pharmacol 22-Jan-2024
PMCID:PMC10838993
doi:10.3389/fphar.2024.1333006
PMID:38318134

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
> Alkaloids and derivatives
Seneciphylline 5281750 Click to see 333.40 unknown https://doi.org/10.1007/978-3-642-49340-9_21
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Benzenoids / Benzene and substituted derivatives / Acetophenones
6-Hydroxytremetone 186059 Click to see 218.25 unknown https://doi.org/10.1248/CPB.49.645
https://doi.org/10.1248/CPB.47.705
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see 278.34 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
(~2~H_4_)Benzene-1,2-dicarboxylic acid 16212019 Click to see 170.15 unknown via CMAUP database
Phthalic Acid 1017 Click to see 166.13 unknown via CMAUP database
> 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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see 108.14 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Decene 13381 Click to see 140.27 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
1-Dodecene 8183 Click to see 168.32 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
1-Nonene 31285 Click to see CCCCCCCC=C 126.24 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
1-Pentadecene 25913 Click to see 210.40 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
1-Tridecene 17095 Click to see 182.35 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
1-Undecene 13190 Click to see 154.29 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic Acid 8314 Click to see 102.13 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
2,3-Dimethylacrylic acid, (Z)- 643915 Click to see CC=C(C)C(=O)O 100.12 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Dodecyl-3-Methylbutanedioic Acid 99891 Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Hexanoic Acid 8892 Click to see 116.16 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2S,3R,4S,5R,6S)-6-[(2S,3S,4S,5S,6S,7R)-1,3,4,5,6,7-hexahydroxy-8-oxooctan-2-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 162896865 Click to see C(C(C(C(C(C(C(C=O)O)O)O)O)O)OC1C(C(C(C(O1)C(=O)O)O)O)O)O 416.33 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
3,4,5-Trihydroxy-6-(1,2,3,5,6-pentahydroxy-7-oxoheptan-4-yl)oxyoxane-2-carboxylic acid 163066026 Click to see C(C(C(C(C(C(C=O)O)O)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)O)O 386.31 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
3,4,5-Trihydroxy-6-[(2,4,5,6,7-pentahydroxy-1-oxooctan-3-yl)oxy]oxane-2-carboxylic acid 163069053 Click to see 400.33 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
6-(1,3,4,5,6,7-Hexahydroxy-8-oxooctan-2-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 162896864 Click to see 416.33 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
GalA(a1-3)8-deoxy-aldehydo-D-ery-L-allOct 163069055 Click to see CC(C(C(C(C(C(C=O)O)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)O)O)O 400.33 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
GalA(a1-4)aldehydo-L-gro-D-talHept 163066027 Click to see C(C(C(C(C(C(C=O)O)O)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)O)O 386.31 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Nonen-3-ol 89560 Click to see 142.24 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
1-Undecen-3-ol 3015762 Click to see 170.29 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see 294.50 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphocholines / Phosphatidylcholines
Lecithin 5287971 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCC=CCCCCC 758.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bS)-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-4-ol 5319391 Click to see 314.50 unknown via CMAUP database
Agathadiol diacetate 91884742 Click to see 390.60 unknown https://doi.org/10.1248/CPB.47.705
Physordin 46873722 Click to see 322.50 unknown https://doi.org/10.1248/CPB.47.705
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1-Ethylidene-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydroinden-5-yl) 2-methylbut-2-enoate 85215306 Click to see 316.40 unknown https://doi.org/10.1248/CPB.47.705
(1-Ethylidene-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydroinden-5-yl) 3-methylbut-2-enoate 85159798 Click to see 316.40 unknown https://doi.org/10.1248/CPB.47.705
(1E,3aR,5R,7S,7aS)-1-Ethylideneoctahydro-4-methylene-7-(1-methylethyl)-2-oxo-1H-inden-5-yl (2E)-3-methyl-2-pentenoate 10782673 Click to see 330.50 unknown https://doi.org/10.1248/CPB.47.705
(1R,4S,6R)-1-methyl-4-(6-methylhepta-1,5-dien-2-yl)-7-oxabicyclo[4.1.0]heptan-2-one 10704868 Click to see 234.33 unknown https://doi.org/10.1248/CPB.47.705
(1S,3aR,5R,7S,7aS)-Octahydro-1-[(1R)-1-hydroxyethyl]-4-methylene-7-(1-methylethyl)-2-oxo-1H-inden-5-yl 3-methylbutanoate 162874187 Click to see 336.50 unknown https://doi.org/10.1248/CPB.47.705
(1Z,3aR,5R,7S,7aS)-1-Ethylideneoctahydro-4-methylene-7-(1-methylethyl)-2-oxo-1H-inden-5-yl (2Z)-2-methyl-2-butenoate 10639145 Click to see 316.40 unknown https://doi.org/10.1248/CPB.47.705
(1Z,3aR,5R,7S,7aS)-1-Ethylideneoctahydro-4-methylene-7-(1-methylethyl)-2-oxo-1H-inden-5-yl 3-methyl-2-butenoate 10495648 Click to see CC=C1C2C(CC(C(=C)C2CC1=O)OC(=O)C=C(C)C)C(C)C 316.40 unknown https://doi.org/10.1248/CPB.47.705
(1Z,3S,3aR,5R,7S,7aS)-1-Ethylideneoctahydro-4-methylene-7-(1-methylethyl)-3-(((2Z)-2-methyl-1-oxo-2-buten-1-yl)oxy)-2-oxo-1H-inden-5-yl (2E)-3-methyl-2-pentenoate 10836297 Click to see 428.60 unknown https://doi.org/10.1248/CPB.47.705
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
[(1R,3aR,5R,7S,7aS)-1-[(1R)-1-acetyloxyethyl]-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] (E)-3-methylpent-2-enoate 138402879 Click to see 390.50 unknown https://doi.org/10.1016/S0031-9422(00)90187-0
https://doi.org/10.1016/0306-3623(88)90072-9
https://doi.org/10.1248/CPB.40.2753
[(1S,3aR,5R,7S,7aS)-1-[(1S)-1-acetyloxyethyl]-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] (E)-3-methylpent-2-enoate 102004872 Click to see 390.50 unknown via CMAUP database
[(1S,3aS,5R,7S,7aS)-1-[(1R)-1-acetyloxyethyl]-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] (E)-3-methylpent-2-enoate 71307581 Click to see 390.50 unknown via CMAUP database
[(1S,3S,3aR,5R,7S,7aS)-1-[(1R)-1-hydroxyethyl]-3-[(2R)-2-methylbutanoyl]oxy-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] (E)-3-methylpent-2-enoate 162953556 Click to see 448.60 unknown https://doi.org/10.1248/CPB.40.2753
[(1Z,3S,3aR,5R,7S,7aS)-1-ethylidene-3-[(2R)-2-methylbutanoyl]oxy-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydroinden-5-yl] (E)-3-methylpent-2-enoate 162926475 Click to see 430.60 unknown https://doi.org/10.1248/CPB.40.2753
[(3S)-2-[(1R,2S,3S,4R,6R)-4-acetyloxy-2-hydroxy-6-methyl-5-oxo-7-oxabicyclo[4.1.0]heptan-3-yl]-6-methylhepta-1,5-dien-3-yl] (Z)-2-methylbut-2-enoate 162999057 Click to see CC=C(C)C(=O)OC(CC=C(C)C)C(=C)C1C(C2C(O2)(C(=O)C1OC(=O)C)C)O 406.50 unknown https://doi.org/10.1248/CPB.47.705
[(3S)-2-[(1S,2R,3R,4S,6S)-2,4-diacetyloxy-6-methyl-5-oxo-7-oxabicyclo[4.1.0]heptan-3-yl]-6-methylhepta-1,5-dien-3-yl] (Z)-2-methylbut-2-enoate 163021457 Click to see 448.50 unknown https://doi.org/10.1021/NP990116C
[1-(1-acetyloxyethyl)-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] (E)-3-methylpent-2-enoate 13919184 Click to see CCC(=CC(=O)OC1CC(C2C(C1=C)CC(=O)C2C(C)OC(=O)C)C(C)C)C 390.50 unknown https://doi.org/10.1007/S10600-018-2527-4
[1-(1-acetyloxyethyl)-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] 2-methylbut-2-enoate 85088025 Click to see 376.50 unknown https://doi.org/10.1248/CPB.40.2753
[1-(1-hydroxyethyl)-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydro-1H-inden-5-yl] 3-methylpent-2-enoate 85114606 Click to see CCC(=CC(=O)OC1CC(C2C(C1=C)CC(=O)C2C(C)O)C(C)C)C 348.50 unknown https://doi.org/10.1248/CPB.40.2753
[1-Ethylidene-3-(2-methylbut-2-enoyloxy)-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydroinden-5-yl] 3-methylpent-2-enoate 85284082 Click to see CCC(=CC(=O)OC1CC(C2C(C1=C)C(C(=O)C2=CC)OC(=O)C(=CC)C)C(C)C)C 428.60 unknown https://doi.org/10.1248/CPB.47.705
[1-Ethylidene-3-(2-methylbutanoyloxy)-4-methylidene-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydroinden-5-yl] 3-methylpent-2-enoate 78157658 Click to see 430.60 unknown https://doi.org/10.1248/CPB.40.2753
[1-Ethylidene-4-methylidene-3-(3-methylpent-2-enoyloxy)-2-oxo-7-propan-2-yl-3,3a,5,6,7,7a-hexahydroinden-5-yl] 3-methylpent-2-enoate 85251954 Click to see 442.60 unknown https://doi.org/10.1248/CPB.47.705
[2-(2,4-Diacetyloxy-6-methyl-5-oxo-7-oxabicyclo[4.1.0]heptan-3-yl)-6-methylhepta-1,5-dien-3-yl] 2-methylbut-2-enoate 73820878 Click to see 448.50 unknown https://doi.org/10.1021/NP990116C
[2-(4-Acetyloxy-2-hydroxy-6-methyl-5-oxo-7-oxabicyclo[4.1.0]heptan-3-yl)-6-methylhepta-1,5-dien-3-yl] 2-methylbut-2-enoate 73104796 Click to see 406.50 unknown https://doi.org/10.1248/CPB.47.705
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)-7-oxabicyclo[4.1.0]heptan-2-one 85239345 Click to see 234.33 unknown https://doi.org/10.1248/CPB.47.705
2-Butenoic acid, 2-methyl-, 1-[1-(acetyloxy)ethyl]octahydro-4-methylene-7-(1-methylethyl)-2-oxo-1H-inden-5-yl ester, [1S-[1I+/-(S*),3aI(2),5I(2)(Z),7I+/-,7aI+/-]]- 101641865 Click to see 376.50 unknown https://doi.org/10.1248/CPB.40.2753
2-Butenoic acid, 3-methyl-, 1-[1-(acetyloxy)ethyl]octahydro-4-methylene-7-(1-methylethyl)-2-oxo-1H-inden-5-yl ester, [1S-[1I+/-(S*),3aI(2),5I(2),7I+/-,7aI+/-]]- 101641866 Click to see 376.50 unknown https://doi.org/10.1248/CPB.40.2753
2-Pentenoic acid, 3-methyl-, (1S,3Z,3aS,4S,6R,7aR)-3-ethylideneoctahydro-7-methylene-4-(1-methylethyl)-2-oxo-1H-indene-1,6-diyl ester, (2E,2'E)- 10741871 Click to see 442.60 unknown https://doi.org/10.1248/CPB.47.705
2-Pentenoic acid, 3-methyl-, octahydro-1-(1-hydroxyethyl)-4-methylene-7-(1-methylethyl)-2-oxo-1H-inden-5-yl ester, [1S-[1I+/-(S*),3aI(2),5I(2)(E),7I+/-,7aI+/-]]- 101641864 Click to see 348.50 unknown https://doi.org/10.1248/CPB.40.2753
9alpha-(3-Methyl-2E-butenoyloxy)-4S-hydroxy-10(14)-oplopen-3-one 4-acetate 85102275 Click to see 376.50 unknown https://doi.org/10.1248/CPB.40.2753
9alpha-(3-Methylbutanoyloxy)-4S-hydroxy-10(14)-oplopen-3-one 85233059 Click to see 336.50 unknown https://doi.org/10.1248/CPB.47.705
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.112.8_571
Cryptomerione 11964091 Click to see 218.33 unknown https://doi.org/10.1248/CPB.47.705
D-allo-4-Inosose, 5,6-anhydro-2-deoxy-5-C-methyl-2-[5-methyl-1-methylene-2-[[(2Z)-2-methyl-2-oxo-2-butenyl]oxy]-4-hexenyl]-, diacetate, (2xi)- 10527460 Click to see 448.50 unknown https://doi.org/10.1021/NP990116C
Farfaratin 6438981 Click to see 390.50 unknown https://doi.org/10.1016/S0031-9422(00)90187-0
https://doi.org/10.1016/0378-8741(88)90030-X
https://doi.org/10.1248/CPB.40.2753
Farfaratin 6443977 Click to see CCC(=CC(=O)OC1CC(C2C(C1=C)CC(=O)C2C(C)OC(=O)C)C(C)C)C 390.50 unknown via CMAUP database
Octahydro-1-(1-hydroxyethyl)-4-methylene-7-(1-methylethyl)-3-(2-methyl-1-oxobutoxy)-2-oxo-1H-inden-5-yl 3-methyl-2-pentenoate 162953554 Click to see CCC(C)C(=O)OC1C2C(C(CC(C2=C)OC(=O)C=C(C)CC)C(C)C)C(C1=O)C(C)O 448.60 unknown https://doi.org/10.1248/CPB.40.2753
Tussilagonone 13919188 Click to see 330.50 unknown https://doi.org/10.1016/S0031-9422(00)90187-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
beta-Spathulenol 522266 Click to see 220.35 unknown https://doi.org/10.1248/CPB.49.645
https://doi.org/10.1248/CPB.47.705
Spathulenol, (-)- 13854255 Click to see 220.35 unknown https://doi.org/10.1248/CPB.49.645
https://doi.org/10.1248/CPB.47.705
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(2S,3R,4S,5S,6R)-2-[[(1S,4aR,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101677404 Click to see 506.50 unknown https://doi.org/10.1248/CPB.47.705
Harpagide 93045 Click to see 364.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(1R,4S,4aS,5S,7R,8aR)-4-[(1R)-1-acetyloxyethyl]-1-(2-methylbutanoyloxy)-8-methylidene-3-oxo-5-propan-2-yl-4,4a,5,6,7,8a-hexahydro-1H-isochromen-7-yl] (E)-3-methylpent-2-enoate 101641867 Click to see 506.60 unknown https://doi.org/10.1248/CPB.40.2753
[(1R,4S,4aS,5S,7R,8aR)-4-[(1R)-1-acetyloxyethyl]-1-[(2R)-2-methylbutanoyl]oxy-8-methylidene-3-oxo-5-propan-2-yl-4,4a,5,6,7,8a-hexahydro-1H-isochromen-7-yl] (E)-3-methylpent-2-enoate 163192900 Click to see 506.60 unknown https://doi.org/10.1248/CPB.40.2753
[4-(1-acetyloxyethyl)-1-(2-methylbutanoyloxy)-8-methylidene-3-oxo-5-propan-2-yl-4,4a,5,6,7,8a-hexahydro-1H-isochromen-7-yl] 3-methylpent-2-enoate 73087228 Click to see CCC(C)C(=O)OC1C2C(C(CC(C2=C)OC(=O)C=C(C)CC)C(C)C)C(C(=O)O1)C(C)OC(=O)C 506.60 unknown https://doi.org/10.1248/CPB.40.2753
Neotussilagolactone 131751132 Click to see CCC(=CC(=O)OC1C=C(C2C(C1=C)COC(=O)C2=CC)C(C)C)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)90187-0
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
2,2,6-trimethyl-1-[(1E,3Z,5Z,7E,9E,11E,13Z,15Z,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohex-2-en-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-7-oxabicyclo[4.1.0]heptane 5315711 Click to see 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3beta,13alpha,14beta)-13-Methyl-26-norurs-7-en-3-ol 111220 Click to see 426.70 unknown https://doi.org/10.1016/J.BSE.2007.07.003
(3S,6bS,8aR,12S,12aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,7,8,9,10,11,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 5321743 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
2-[(C-azaniumylcarbonimidoyl)-methylamino]acetate 59098743 Click to see 131.13 unknown via CMAUP database
Acetic acid, (Z)- 9904352 Click to see CCN1C(=CC(=O)OCC)SC(C1=O)N2CCCCC2 298.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
(2S)-2-ammoniopropanoate 7311724 Click to see 89.09 unknown via CMAUP database
2-Azaniumylpropanoate 57383916 Click to see 89.09 unknown via CMAUP database
D-Alanine 71080 Click to see 89.09 unknown via CMAUP database
DL-Alanine-15N 51283 Click to see 90.09 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 / D-alpha-amino acids
(2R,3S)-2-amino-3-hydroxybutanoate 6995277 Click to see 119.12 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 / L-alpha-amino acids
(2S,3R)-2-azaniumyl-3-hydroxybutanoate 6971019 Click to see CC(C(C(=O)[O-])[NH3+])O 119.12 unknown via CMAUP database
L-threoninate 5460797 Click to see CC(C(C(=O)[O-])N)O 118.11 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
(3S)-3-azaniumyl-4-hydroxy-4-oxobutanoate 44367445 Click to see C(C(C(=O)O)[NH3+])C(=O)[O-] 133.10 unknown via CMAUP database
2-Azaniumyl-4-hydroxy-4-oxobutanoate 57397078 Click to see 133.10 unknown via CMAUP database
D-Aspartic Acid 83887 Click to see 133.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
CID 57397101 57397101 Click to see 147.13 unknown via CMAUP database
CID 88747398 88747398 Click to see 147.13 unknown via CMAUP database
D-glutamic acid 23327 Click to see C(CC(=O)O)C(C(=O)O)N 147.13 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
(2S,3S)-2-ammonio-3-methylpentanoate 7043901 Click to see 131.17 unknown via CMAUP database
2-Ammonio-3-methylpentanoate 57397079 Click to see 131.17 unknown via CMAUP database
D-isoleucine zwitterion 6950183 Click to see 131.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
CID 6950207 6950207 Click to see 131.17 unknown via CMAUP database
Leucine zwitterion 7045798 Click to see 131.17 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
(2S)-pyrrolidinium-2-carboxylate 6971047 Click to see 115.13 unknown via CMAUP database
D-proline 8988 Click to see C1CC(NC1)C(=O)O 115.13 unknown via CMAUP database
DL-Proline 614 Click to see C1CC(NC1)C(=O)O 115.13 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
(2S)-2-amino-3-methylbutanoate;hydron 88733505 Click to see [H+].CC(C)C(C(=O)[O-])N 117.15 unknown via CMAUP database
D-Valine 71563 Click to see CC(C)C(C(=O)O)N 117.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Hydron;acetate 21980959 Click to see [H+].CC(=O)[O-] 60.05 unknown via CMAUP database
Hydron;formate 18971002 Click to see [H+].C(=O)[O-] 46.03 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
Maleic Acid 444266 Click to see 116.07 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
CID 20130941 20130941 Click to see 134.09 unknown via CMAUP database
D-Malic acid 92824 Click to see 134.09 unknown via CMAUP database
L-Malic Acid 222656 Click to see 134.09 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols
2-Aminoethanol;hydron 18785322 Click to see 62.09 unknown via CMAUP database
Ethanolamine 700 Click to see 61.08 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(3S,6aR,6aR,8aS,14bR)-4,4,6a,6b,8a,11,14b-heptamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picene-3,13-diol 5317314 Click to see 428.70 unknown via CMAUP database
Isobauerenol 3084367 Click to see CC1CCC2(CCC3(C4=C(CCC3(C2C1C)C)C5(CCC(C(C5CC4)(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/J.BSE.2007.07.003
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3,4-Dicaffeoyl Quinic Acid 10324242 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see 516.40 unknown via CMAUP database
4,5-Dicaffeoyl quinic acid 13887346 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
isochlorogenic acid A 6474310 Click to see 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
4-O-alpha-D-Galactopyranuronosyl-alpha-D-galactopyranuronic acid 6857565 Click to see C1(C(C(OC(C1O)OC2C(C(C(OC2C(=O)O)O)O)O)C(=O)O)O)O 370.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
GalA(a1-4)a-D-Fuc 162940176 Click to see 340.28 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
GlyTouCan:G34841UP 131752745 Click to see 340.28 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
GlyTouCan:G62645IG 4532283 Click to see 370.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.26-2322
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
GlyTouCan:G29155XH 91692850 Click to see 342.30 unknown via CMAUP database
GlyTouCan:G80014NW 46782954 Click to see 342.30 unknown via CMAUP database
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
3-N-butyl-4,5-dihydrophthalide, (S)- 3085257 Click to see 192.25 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,8S,9R)-2,8-dihydroxy-7-methyl-12-prop-1-en-2-ylspiro[4,10-dioxatetracyclo[7.2.1.02,7.03,5]dodecane-6,2'-oxirane]-11-one 5322181 Click to see 294.30 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
CID 42608143 42608143 Click to see 214.30 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines
2-Pyrrolidineacetic acid, methyl ester 5323862 Click to see COC(=O)CC1CCCN1 143.18 unknown https://doi.org/10.1016/0031-9422(92)80428-H
> Organoheterocyclic compounds / Pyrrolizidines
(1S,2S,8S)-2-hydroxy-2-methyl-1,3,5,6,7,8-hexahydropyrrolizine-1-carboxylic acid 131115192 Click to see 185.22 unknown https://doi.org/10.1016/0031-9422(92)80428-H
2-Hydroxy-2-methyl-1,3,5,6,7,8-hexahydropyrrolizine-1-carboxylic acid 101412408 Click to see CC1(CN2CCCC2C1C(=O)O)O 185.22 unknown https://doi.org/10.1016/0031-9422(92)80428-H
Isotussilagine 149801 Click to see 199.25 unknown https://doi.org/10.1007/978-3-642-49340-9_21
https://doi.org/10.1016/0031-9422(92)80428-H
Tussilagine 185071 Click to see 199.25 unknown https://doi.org/10.1007/978-3-642-49340-9_21
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl Caffeate 5317238 Click to see 208.21 unknown via CMAUP database
Methyl Caffeate 689075 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
2-Propenoic acid, 3-(2,5-dihydroxyphenyl)- 181581 Click to see C1=CC(=C(C=C1O)C=CC(=O)O)O 180.16 unknown via CMAUP database
2,5-Dihydroxycinnamic acid 6442618 Click to see 180.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
Isoferulic Acid 736186 Click to see 194.18 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
Sinapinic acid 1549091 Click to see 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(1R,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexoxy]chromen-4-one 15959354 Click to see C1C(C(C(C(C1OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O)CO 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate 54758589 Click to see 463.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4E,6R,7R,11E)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 101286192 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown via CMAUP database
(1R,4E,6R,7S,11Z)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 6442572 Click to see 365.40 unknown via CMAUP database
(1R,4E,6S,7R,11Z)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 134714985 Click to see 365.40 unknown https://doi.org/10.1007/978-3-642-49340-9_21
(1R,4Z,6S,7R,11Z)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 102004936 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1007/978-3-642-49340-9_21
https://doi.org/10.1002/1099-1565(200011/12)11:6<366::AID-PCA538>3.0.CO;2-1
(1S,4Z,7S,17S)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 133562009 Click to see 335.40 unknown https://doi.org/10.1007/978-3-642-49340-9_21
Neosenkirkine 6442498 Click to see 365.40 unknown via CMAUP database
Renardine 5363853 Click to see 365.40 unknown via CMAUP database
Senecionanium, 8,12-dihydroxy-4-methyl-11,16-dioxo- 6433332 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown via CMAUP database
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1007/978-3-642-49340-9_21
https://doi.org/10.1002/1099-1565(200011/12)11:6<366::AID-PCA538>3.0.CO;2-1
Senkirkine 5281752 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1007/978-3-642-49340-9_21
https://doi.org/10.1002/1099-1565(200011/12)11:6<366::AID-PCA538>3.0.CO;2-1
> Phenylpropanoids and polyketides / Ochratoxins and related substances
N-(5-Chloro-8-hydroxy-3-methyl-1-oxo-3,4-dihydro-1H-2-benzopyran-7-carbonyl)phenylalanine 4580 Click to see 403.80 unknown via CMAUP database

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