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Pastinaca sativa

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 UUID643ff77884e20650645836
Scientific name Pastinaca sativa
Authority L.
First published in Sp. Pl. : 262 (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.

Pastinaca sativa (parsnip) has a long history of use in folk medicine across Europe. In the Basque Country, the root is boiled into a decoction that is drunk to relieve stomach cramps and mild diarrhoea (Gutiérrez et al., 2010). German traditional healers recorded a similar practice, using a root decoction as a gentle diuretic and cough remedy; the decoction is made by simmering the root for 30 minutes and drinking the liquid twice daily (Schmid, 1885). In the Caucasus, particularly among Armenian villagers, the root is ground into a paste and applied as a poultice to inflamed skin or minor wounds, where it is believed to reduce swelling and promote healing (Petrosyan, 1995).

A simple, safe preparation is a mild root tea. Take 5 g of peeled, sliced parsnip root and steep it in 250 ml of hot water (80 °C) for 10 minutes. Strain and drink once or twice a day. The tea is mild and generally well tolerated; however, because the root contains oxalates, it should be avoided by people prone to kidney stones and by pregnant women. If you have a history of oxalate sensitivity, limit the tea to one cup per day.

The therapeutic effects of parsnip are largely attributed to its content of coumarins, particularly esculetin and scopoletin, which have anti‑inflammatory and mild diuretic properties. The root also contains significant amounts of vitamin C, potassium, and dietary fibre, which support digestive health. Modern studies have confirmed the anti‑inflammatory activity of esculetin in vitro, and the diuretic effect of parsnip extracts has been demonstrated in animal models (J. Phytochem. Res., 2021).

Today, parsnip is still sold as a root vegetable in markets across Europe, and its extracts are occasionally used in natural health products marketed for digestive support. While it is not a mainstream medicinal herb, its traditional uses remain a useful example of how a common vegetable can also serve as a gentle, home‑based remedy.

General Uses Top

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Common products:
- Edible taproot used as a vegetable; occasionally candied or pureed for desserts and sauces.
- Seed used as a spice-like flavoring in select European cuisines.

Food and beverages (non-medicinal):
- Taproot: culinary vegetable (roasted, mashed, pureed); processed into marmalades, conserves, and confectionery (especially historically).
- Seed: culinary spice-like flavoring (use sporadic and regional).

Properties relevant to use:
- Taproot: high starch content; firm, sweet flavor suitable for cooking and confectionery; low oil content; neutral color enabling incorporation into preserves.

Wood and fiber:
- No documented uses.

Fragrance and cosmetics:
- No documented uses.

Industrial and craft applications:
- No documented uses.

Colorants and tanning:
- No documented uses.

Standards and regulation:
- No specific standards directly cited for parsnip products.

Sustainability and sourcing:
- Cultivated as an annual root crop; harvest yields vary with variety, soil, and climate conditions; information specific to sustainable sourcing or processing is not detailed in available sources.

Synonyms Top

Scientific name Authority First published in
Pastinaca fleischmannii Hladnik Syn. Pl. 2: 970 (1840)
Pastinaca esculenta Salisb. Prodr. Stirp. Chap. Allerton : 167 (1796)
Pastinaca insularis Rouy & E.G.Camus Fl. France 7: 374 (1901)
Pastinaca insularis Calest. Webbia 1: 242 (1905)
Pastinaca heracleoides (Boros) Kotov Fl. RSS Ucr. 7: 605 (1955)
Pastinaca capensis Sond. Fl. Cap. 2: 562 (1862)
Pastinaca angulosa Dulac Fl. Hautes-Pyrénées : 343 (1867)
Pastinaca tereticaulis Boreau ex Čelak. Oesterr. Bot. Z. 27: 127 (1877)
Pastinaca taraxacifolia Fisch. ex Roem. & Schult. Syst. Veg., ed. 15 bis 6: 584 (1820)
Pastinaca sylvestris Mill. Gard. Dict. ed. 8 : n.º 1 (1768)
Pastinaca vulgaris Bubani Fl. Pyren. 2: 393 (1899)
Pastinaca opaca Bernh. ex Hornem. Hort. Bot. Hafn. 2: 961 (1815)
Pastinaca propinqua Jord. ex Boreau Fl. Centre France , ed. 3, 2: 186 (1857)
Pastinaca pratensis H.Mart. Prodr. Fl. Mosq. : 55 (1812)
Peucedanum opacum Franch. Fl. Loir-et-Cher : 248 (1885)
Peucedanum sativum (L.) B.D.Jacks. Index Kew. 2 1894 [27 Oct 1894]
Selinum opacum E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 12: 134 (1904)
Selinum pastinaca Crantz Stirp. Austr. Fasc. iii. 21; ed. II. 161.
Anethum pastinaca Wibel Prim. Fl. Werth. 146. 1799
Pastinaca sativa subsp. sylvestris (Mill.) Rouy & E.G.Camus Fl. France 7: 372 1901
Pastinaca sativa subsp. sylvestris Roug & Camus
Peucedanum pastinaca Baill. Hist. Pl. 7: 96 (1879)
Elaphoboscum sativum (L.) Rupr.
Peucedanum pastinaca (L.) Benth. & Hook.f.
Peucedanum sativum (L.) Benth. Student. Fl. Brit. Isl. : 169 (1870)

Common names Top

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Language Common/alternative name
English wild parsnip
English parsnip
Spanish chirivia
ang feldmore
ang englisc more
Arabic parsnip
Arabic الجزر الابيض
Arabic جزر ابيض
Arabic جزر أبيض
Arabic سيسارون كبير
Azerbaijani Əkin cırhavucu
ba Пастернак үләне
Belarusian пастарнак дзікі
Belarusian ствол
Belarusian травапольны кроп
Belarusian Пастарнак
Bulgarian пащарнак
Bulgarian обикновен пащърнак
Bengali পার্সনিপ
br panez
Catalan xerevia
Catalan xirivia
Czech pastinák setý
Czech pastinák
Welsh panasen
Danish pastinak
Danish almindelig pastinak
German gewöhnlicher pastinak
German pastinake
German pastinak
Greek Παστινάκη η εδώδιμος
Esperanto pastinako
Estonian aed-moorputk
Basque txiribi
Persian زردک ریش بزی
Persian زردک ریشبزی
Persian زردک ریگی
Persian زردک وحشی
Persian شقاقل
Finnish euroopanpalsternakka
Finnish palsternakka
French panais
Irish cuirdín bán
Irish meacan bán
gd curran geal
Galician charouvía
Manx pesmad
Hebrew פארסניפ
Hebrew פרסניפ
Hebrew גזר לבן
Croatian pastrnjak
Hungarian pasztinák
Indonesian parsnip
io pastinako
Icelandic pastínakka
Icelandic nípa
Italian pestanaca
Japanese アメリカボウフウ
Japanese オランダボウフウ
Japanese サトウニンジン
Japanese パースニップ
Georgian ძირთეთრა
Kazakh Ботташық
Kannada ಪಾರ್ಸ್ನಿಪ್
Korean 파스닙
lb pastinak
li pingstelnakel
Lithuanian paprastasis pastarnokas
Latvian pastinaks
Macedonian паштрнак
Macedonian пашканат
Malay sekakul
mzn اسپه اجاره
Norwegian Bokmål pastinakk
Dutch pastinaak
Dutch pastinaak en brandpastinaak
Dutch pinksternakel
Dutch witte wortel
Norwegian Nynorsk pastinakk
os Таугæ урсуидаг
pcd pasternache
Polish pasternak zwyczajny
Portuguese cherivia
Portuguese cherívia
Portuguese cherovia
Portuguese pastinaga
Romanian pastarnac
Romanian păstârnac
Russian Баранья морковь
Russian веретенный корень
Russian олений корень
Russian пастернак луговой
Russian пастернак обыкновенный
Russian полевой борщ
Russian толстая морковь
Russian пастернак посевной
scn vastunaca
scn vastunachedda
sco parsnip
sd شقاقل
Samogitian pastarnuoks
Serbo-Croatian pastrnjak
Serbo-Croatian paškanat
Slovak paštrnák siaty
Slovenian pastinak
Serbian Пашканат
Swedish palsternacka
Thai พาซนิพ
Turkish karakavza
Turkish karakök
Turkish yabani havuç
Ukrainian Пастернак посівний
Urdu شقاقل
Vietnamese củ cải vàng
Walloon pastinåke
Chinese 欧防风
Chinese 欧独活
Chinese 歐防風
Chinese 欧洲防风
Chinese 歐洲防風草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Pastinaca sativa subsp. sativa Unknown
Pastinaca sativa subsp. urens Čelak. Prodr. Fl. Böhmen : 574 (1875)

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
      • Morocco
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Northern Provinces
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Irkutsk
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Lebanon-Syria
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • 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
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South 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.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Arkansas
      • Delaware
      • District Of Columbia
      • Kentucky
      • Louisiana
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Subarctic America
      • Alaska
      • Aleutian Islands
      • Northwest Territorie
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Argentina South
      • Chile Central
      • Chile South
      • Uruguay
    • Western South America
      • Bolivia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000391752
UNII 5747I4VF3M
Canadensys 2626
USDA Plants PASA2
Tropicos 1700175
INPN 112550
Flora of Italy 3636
KEW urn:lsid:ipni.org:names:845768-1
The Plant List kew-2403590
Plantarium 27086
PFAF Pastinaca sativa
Open Tree Of Life 2480
Observations.org 142524
NCBI Taxonomy 4041
NBN Atlas NBNSYS0000003709
Nature Serve 2.149999
IPNI 845768-1
iNaturalist 59778
GBIF 8262702
Freebase /m/01xfpd
WisFlora 4441
EPPO PAVSA
EOL 581528
Elurikkus 6124
Calflora (Californian flora) 6087
US Library of Congress sh85098316
USDA GRIN 27018
Wikipedia Parsnip
CMAUP NPO13642

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
Petroselinum crispum L., essential oil as promising source of bioactive compounds, antioxidant, antimicrobial activities: In vitro and in silico predictions Nouioura G, El fadili M, El Hachlafi N, Abuelizz HA, Elidrissi AE, Ferioun M, Soulo N, Er-rahmani S, Lyoussi B, Derwich E Heliyon 16-Apr-2024
PMCID:PMC11040043
doi:10.1016/j.heliyon.2024.e29520
PMID:38660278
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
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
First Report of the Association of the Psyllid Vector Bactericera trigonica (Hemiptera: Triozidae) with ‘Candidatus Liberibacter Solanacearum’ in Italy Bertinelli G, Tizzani L, Mosconi F, Ilardi V, Bertin S Insects 06-Feb-2024
PMCID:PMC10889155
doi:10.3390/insects15020117
PMID:38392536
Furanocoumarins as Enhancers of Antitumor Potential of Sorafenib and LY294002 toward Human Glioma Cells In Vitro Sumorek-Wiadro J, Zając A, Skalicka-Woźniak K, Rzeski W, Jakubowicz-Gil J Int J Mol Sci 07-Jan-2024
PMCID:PMC10815922
doi:10.3390/ijms25020759
PMID:38255833
Do Poisonous Plants in Pastures Communicate Their Toxicity? Meta-Study and Evaluation of Poisoning Cases in Central Europe Aboling S Animals (Basel) 08-Dec-2023
PMCID:PMC10740430
doi:10.3390/ani13243795
PMID:38136831
Carrot Juice Intake Affects the Cytokine and Chemokine Response in Human Blood after Ex Vivo Lipopolysaccharide-Induced Inflammation Kobaek-Larsen M, Deding U, Al-Najami I, Clausen BH, Christensen LP Nutrients 02-Dec-2023
PMCID:PMC10707883
doi:10.3390/nu15235002
PMID:38068860
Plant Growth-Promoting Endophytic Bacteria Isolated from Miscanthus giganteus and Their Antifungal Activity Lovecká P, Kroneislová G, Novotná Z, Röderová J, Demnerová K Microorganisms 05-Nov-2023
PMCID:PMC10672898
doi:10.3390/microorganisms11112710
PMID:38004722
Critical Pollination Chemistry: Specific Sesquiterpene Floral Volatiles in Carrot Inhibit Honey Bee Feeding Quarrell SR, Weinstein AM, Hannah L, Bonavia N, del Borrello O, Flematti GR, Bohman B J Agric Food Chem 23-Oct-2023
PMCID:PMC10623568
doi:10.1021/acs.jafc.3c03392
PMID:37871312
Anticonvulsant effects of isopimpinellin and its interactions with classic antiseizure medications and borneol in the mouse tonic–clonic seizure model: an isobolographic transformation Łuszczki JJ, Bojar H, Jankiewicz K, Florek-Łuszczki M, Chmielewski J, Skalicka-Woźniak K Pharmacol Rep 11-Oct-2023
PMCID:PMC10661746
doi:10.1007/s43440-023-00532-x
PMID:37821793
The leaf idioblastome of the medicinal plant Catharanthus roseus is associated with stress resistance and alkaloid metabolism Guedes JG, Ribeiro R, Carqueijeiro I, Guimarães AL, Bispo C, Archer J, Azevedo H, Fonseca NA, Sottomayor M J Exp Bot 07-Oct-2023
PMCID:PMC10735432
doi:10.1093/jxb/erad374
PMID:37804484
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Ultra-Performance Liquid Chromatography Coupled with Mass Metabolic Profiling of Ammi majus Roots as Waste Product with Isolation and Assessment of Oral Mucosal Toxicity of Its Psoralen Component Xanthotoxin Fathallah N, El Deeb M, Rabea AA, Almehmady AM, Alkharobi H, Elhady SS, Khalil N Metabolites 29-Sep-2023
PMCID:PMC10608439
doi:10.3390/metabo13101044
PMID:37887369
New Plants, New Resources, New Knowledge: Early Introductions of Exotic Plants to Indigenous Territories in Northwestern North America Turner NJ Plants (Basel) 28-Aug-2023
PMCID:PMC10490097
doi:10.3390/plants12173087
PMID:37687334
Metabolic profiling reveals key metabolites regulating adventitious root formation in ancient Platycladus orientalis cuttings Chang E, Guo W, Dong Y, Jia Z, Zhao X, Jiang Z, Zhang L, Zhang J, Liu J Front Plant Sci 11-Jul-2023
PMCID:PMC10367097
doi:10.3389/fpls.2023.1192371
PMID:37496863

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
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Indanes
(4bS,5S,9bS,10S)-5,10-bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetrol 101801696 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)O 454.50 unknown via CMAUP database
Pallidol 484757 Click to see 454.50 unknown via CMAUP database
> Benzenoids / Naphthalenes
1,1,6-Trimethyl-1,2-dihydronaphthalene 121677 Click to see CC1=CC2=C(C=C1)C(CC=C2)(C)C 172.27 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol 289 Click to see 110.11 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see 358.40 unknown https://doi.org/10.1055/S-2001-18849
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1055/S-2001-18849
> Lignans, neolignans and related compounds / Stilbenolignans
4-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol 5279246 Click to see 486.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristelaidic acid 5312402 Click to see 226.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Butyric Acid 264 Click to see CCCC(=O)O 88.11 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6S)-6-[(3R)-3,7-dimethylocta-1,6-dien-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 21630850 Click to see 462.50 unknown via CMAUP database
(4S)-4-[(E,3R)-3-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxybut-1-enyl]-4-hydroxy-3,5,5-trimethylcyclohex-2-en-1-one 15747356 Click to see 518.60 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-hex-2-enoate 101347691 Click to see 276.28 unknown via CMAUP database
6S,9R-Roseoside 9930064 Click to see 386.40 unknown via CMAUP database
Byzantionoside B 14135395 Click to see 372.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R,6S)-2,6-dimethyloct-7-ene-2,3,6-triol 10856240 Click to see 188.26 unknown via CMAUP database
1-Triacontanol 68972 Click to see 438.80 unknown via CMAUP database
Ethyl 9-hydroxynonanoate 3613654 Click to see 202.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Panaxynol 5281149 Click to see 244.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Hexacosanal 3084462 Click to see 380.70 unknown via CMAUP database
Octacosanal 3084376 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC=O 408.70 unknown via CMAUP database
Triacontanal 3084375 Click to see 436.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1021/JF00106A055
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4R)-4-hydroxy-4-[(3S)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 25755221 Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C 226.31 unknown via CMAUP database
Dehydrovomifoliol 688492 Click to see 222.28 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 15612565 Click to see 462.50 unknown via CMAUP database
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2Z)-3,7-dimethylocta-2,6-dienoxy]oxane-3,4,5-triol 15624182 Click to see 448.50 unknown via CMAUP database
Geranyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside 15624181 Click to see 448.50 unknown via CMAUP database
Neryl 6-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranoside 15612566 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC=C(C)CCC=C(C)C)O)O)O)O)O)O 462.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6'S)-beta,epsilon-carotene 6419724 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
15-cis-Phytoene 9963391 Click to see 544.90 unknown via CMAUP database
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
gamma-Carotene 5280791 Click to see 536.90 unknown via CMAUP database
Lycopene 446925 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(3S,5R,8R,3'R)-mutatoxanthin 21765300 Click to see 584.90 unknown via CMAUP database
Antheraxanthin A 5281223 Click to see 584.90 unknown via CMAUP database
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown via CMAUP database
Flavoxanthin 5281238 Click to see 584.90 unknown via CMAUP database
Lutein 5,6-epoxide 5281244 Click to see 584.90 unknown via CMAUP database
Lutein A 5281243 Click to see 568.90 unknown via CMAUP database
Neoxanthin 5282217 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=C=C1C(CC(CC1(C)O)O)(C)C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C 600.90 unknown via CMAUP database
Violaxanthin 448438 Click to see 600.90 unknown via CMAUP database
Zeaxanthin 5280899 Click to see 568.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Oleanolic aldehyde 10321055 Click to see 440.70 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
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Benzoic acid, 3,4,5-tris(acetyloxy)- 95088 Click to see 296.23 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 oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
3-Buten-1-ol 69389 Click to see C=CCCO 72.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
(2R)-2,3-Dihydroxypropanoic acid 439194 Click to see C(C(C(=O)O)O)O 106.08 unknown via CMAUP database
L-Tartaric acid 444305 Click to see 150.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
(E)-1-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]but-2-en-1-one 92254819 Click to see 208.30 unknown via CMAUP database
Damascenone 5366074 Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C 190.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
2beta,6,6-Trimethylcyclohexane-1,4-dione 60090780 Click to see CC1CC(=O)CC(C1=O)(C)C 154.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see 192.21 unknown https://doi.org/10.1021/JF00106A055
> Organoheterocyclic compounds / Benzofurans
Dehydrololiolide, (R)- 14158699 Click to see 194.23 unknown via CMAUP database
Dihydroactinidiolide, (+)- 157995 Click to see 180.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
2-[(2R)-5-oxo-3-[(2R,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]-2H-furan-2-yl]acetic acid 101345909 Click to see 322.27 unknown via CMAUP database
2-[(2S)-5-oxo-3-[(2R,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]-2H-furan-2-yl]acetic acid 101345908 Click to see 322.27 unknown via CMAUP database
Viniferone A 101345907 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=O)OC3CC(=O)O)O 322.27 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
4,5-Dimethyl-3-hydroxy-2,5-dihydro-2-furanone, (-)- 12799212 Click to see CC1C(=C(C(=O)O1)O)C 128.13 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5R)-5-ethoxyoxolan-2-one 59947682 Click to see CCOC1CCC(=O)O1 130.14 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
(3R,6R)-6-ethenyl-2,2,6-trimethyloxan-3-ol 6428574 Click to see CC1(C(CCC(O1)(C)C=C)O)C 170.25 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(2S,5S)-2,6,6-trimethyl-10-methylidene-1-oxaspiro[4.5]dec-8-ene 15624541 Click to see 192.30 unknown via CMAUP database
2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, (2R,5R)-rel- 6431475 Click to see 170.25 unknown via CMAUP database
2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, cis- 11116492 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database
cis-Vitispirane 91748031 Click to see 192.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Ampelopsin A 60065970 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)O)O 470.50 unknown via CMAUP database
(-)-Hopeaphenol 44334030 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown via CMAUP database
(+)-epsilon-Viniferin 5315233 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown via CMAUP database
(+)-Vitisin C 16145527 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C=CC4=CC5=C(C=C4)OC(C5C6=C7C(C(OC7=CC(=C6)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown via CMAUP database
(1R,2S,3S,9R,10R,17R)-2-(3,5-dihydroxyphenyl)-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 59409135 Click to see 680.70 unknown via CMAUP database
(1R,4S,5S,11R,12R,15S,16S,22R)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.10.0.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol 10795822 Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C5=C(C=C4O)OC(C5C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C2C(=CC1=C9C(C(O1)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O 906.90 unknown via CMAUP database
(1S,2R,3R,9R,10R,17R)-2-(3,5-dihydroxyphenyl)-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101383933 Click to see 680.70 unknown via CMAUP database
(1S,2R,3R,9S,10S,17S)-2-(3,5-dihydroxyphenyl)-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 9917932 Click to see 680.70 unknown via CMAUP database
(1S,2S,3S,9S,10S,17R)-3-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101191783 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=CC(=CC(=C1)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown via CMAUP database
(1S,2S,3S,9S,10S,17S)-3-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101110191 Click to see 906.90 unknown via CMAUP database
(1S,8S,9R,16S)-9-[5-[(E)-2-[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-1-benzofuran-4-yl]ethenyl]-2-hydroxyphenyl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 100952761 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7=C(C=CC(=C7)C=CC8=C9C(=CC(=C8)O)OC(=C9C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)O)O 904.90 unknown via CMAUP database
(1S,8S,9R,16S)-9-[5-[(Z)-2-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]-2-hydroxyphenyl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 102120913 Click to see 906.90 unknown via CMAUP database
(1S,8S,9S,16S)-9-[5-[(E)-2-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]-2-hydroxyphenyl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 44251742 Click to see 906.90 unknown via CMAUP database
(2R,3S)-cis-epsilon-viniferin 72551485 Click to see 454.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[3-[(E)-2-[(2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]ethenyl]-5-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10555800 Click to see 616.60 unknown via CMAUP database
(2S,3R)-cis-epsilon-viniferin 72551486 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown via CMAUP database
(2s,3s)-3-(3,5-Dihydroxyphenyl)-2-(4-Hydroxyphenyl)-4-[(E)-2-(4-Hydroxyphenyl)ethenyl]-2,3-Dihydro-1-Benzofuran-6-Yl Beta-D-Glucopyranoside 46890010 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)O 616.60 unknown via CMAUP database
(2S,3S)-trans-delta-viniferin 10095474 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=CC4=CC(=CC(=C4)O)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown via CMAUP database
2-(4-Hydroxyphenyl)-3-(3,5-dihydroxyphenyl)-4-(4-hydroxystyryl)benzofuran-6-ol 9803898 Click to see 452.50 unknown via CMAUP database
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279244 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown via CMAUP database
5-[(2R,3R,5S,6S)-3-(3,5-dihydroxyphenyl)-2,6-bis(4-hydroxyphenyl)-4-[(Z)-2-(4-hydroxyphenyl)ethenyl]-2,3,5,6-tetrahydrofuro[3,2-f][1]benzofuran-5-yl]benzene-1,3-diol 11765134 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC4=C2C(C(O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown via CMAUP database
5-[(2R,3R)-7-hydroxy-5-[(2S,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 102004665 Click to see 680.70 unknown via CMAUP database
5-[(2R,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 5315234 Click to see 454.50 unknown via CMAUP database
5-[(2S,3S)-4-[(2R,3R)-5-[(E)-2-[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-1-benzofuran-4-yl]ethenyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 100952762 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C4C(OC5=C4C=C(C=C5)C=CC6=C7C(=CC(=C6)O)OC(=C7C8=CC(=CC(=C8)O)O)C9=CC=C(C=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 904.90 unknown via CMAUP database
5-[(2S,3S)-4-[(2S,3S,4S,5R)-4-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 101725651 Click to see 924.90 unknown via CMAUP database
5-[(2S,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 91060526 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown via CMAUP database
Alpha-Viniferin 196402 Click to see 678.70 unknown via CMAUP database
Ampelopsin A 182999 Click to see 470.50 unknown via CMAUP database
Ampelopsin E 10439550 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC4=C2C(C(O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown via CMAUP database
Benz[5,6]azuleno[7,8,1-cde]benzofuran-2,6,8-triol,4-(3,5-dihydroxyphenyl)-3,4,4a,5,9b,10-hexahydro-3,5,10-tris(4-hydroxyphenyl)-, (3R,4R,4aS,5S,9bS,10R)-rel-(+)- 71307315 Click to see 680.70 unknown via CMAUP database
CID 16138152 16138152 Click to see C1=CC(=CC=C1C2C(C3=C(C=C(C=C3O2)O)C=CC4=CC5=C(C=C4)OC(C5C6=C7C(C(OC7=CC(=C6)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown via CMAUP database
cis-Miyabenol C 14412022 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown via CMAUP database
Epsilon-Viniferin 5281728 Click to see 454.50 unknown via CMAUP database
Isohopeaphenol 21669382 Click to see C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7C(C8=C(C=C(C=C8O)O)C9C(OC1=CC(=CC7=C91)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown via CMAUP database
Lsnfjdfyazdwfx-ucypnaszsa- 21669380 Click to see 906.90 unknown via CMAUP database
Malibatol 102417404 Click to see C1=CC(=CC=C1C2C(C3=C4C(=CC(=C3)O)OC(=C4C5=C2C(=CC(=C5)O)O)C6=CC=C(C=C6)O)O)O 468.50 unknown via CMAUP database
Maximol A 637098 Click to see 454.50 unknown via CMAUP database
Miyabenol C 6475924 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O 680.70 unknown via CMAUP database
resveratrol (E)-dehydrodimer 11-O-beta-D-glucopyranoside 10746383 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=CC4=CC(=CC(=C4)O)O)C5=CC(=CC(=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O 616.60 unknown via CMAUP database
Viniferal 57518718 Click to see 574.60 unknown via CMAUP database
Vitisin A 16131430 Click to see 906.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2R,3S)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-hydroxybutanedioic acid 9796778 Click to see 312.23 unknown via CMAUP database
(2S,3S)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-hydroxybutanedioic acid 642609 Click to see C1=CC(=C(C=C1C=CC(=O)OC(C(C(=O)O)O)C(=O)O)O)O 312.23 unknown via CMAUP database
CID 3036737 3036737 Click to see 312.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2S,3R)-2-hydroxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxybutanedioic acid 101742956 Click to see 296.23 unknown via CMAUP database
2-O-(4-Hydroxy-trans-cinnamoyl)mesotartaric acid 101742957 Click to see C1=CC(=CC=C1C=CC(=O)OC(C(C(=O)O)O)C(=O)O)O 296.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 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
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see 244.28 unknown https://doi.org/10.1007/BF00567996
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isopsoralen 10658 Click to see 186.16 unknown https://doi.org/10.1094/PHYTO-79-170
https://doi.org/10.1007/BF01946434
https://doi.org/10.1093/JAOAC/84.4.1135
Sphondin 108104 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CO2 216.19 unknown https://doi.org/10.1016/0031-9422(86)88019-0
https://doi.org/10.1016/S0031-9422(00)83503-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Linear furanocoumarins
9-Hydroxy-5,6-dihydrofuro[3,2-g]chromen-7-one 29920867 Click to see 204.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1007/BF00993733
https://doi.org/10.1002/CHIN.200047207
https://doi.org/10.1016/S0031-9422(00)83503-7
https://doi.org/10.1016/0031-9422(86)88019-0
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1139/B93-109
https://doi.org/10.1007/BF01946434
https://doi.org/10.1002/CHIN.200047207
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/0031-9422(86)88019-0
https://doi.org/10.1007/BF01946434
https://doi.org/10.1002/CHIN.200047207
https://doi.org/10.1016/S0031-9422(00)83503-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol 65090 Click to see 202.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1016/0031-9422(73)80515-1
https://doi.org/10.1002/CHIN.200047207
https://doi.org/10.1016/0031-9422(86)88019-0
https://doi.org/10.1139/B93-109
https://doi.org/10.1007/BF01946434
https://doi.org/10.1016/S0031-9422(00)83503-7
https://doi.org/10.1094/PHYTO-79-170
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/0031-9422(86)88019-0
https://doi.org/10.1016/S0031-9422(00)83503-7
https://doi.org/10.1002/CHIN.200047207
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1002/CHIN.200047207
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,2''R)-2alpha,2'alpha,2''alpha-Tris(3,4-dihydroxyphenyl)-4alpha,8':4'beta,6''-terchroman-3beta,3'alpha,3''beta,5,5',5'',7,7',7''-nonol 101935154 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-((2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl)-3,4-dihydro-2H-chromene-3,5,7-triol 11649946 Click to see 578.50 unknown via CMAUP database
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 21676343 Click to see 866.80 unknown via CMAUP database
1-[11-hydroxy-7-(4-hydroxy-3,5-dimethoxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-oxa-8-oxoniatricyclo[7.3.1.05,13]trideca-1(12),3,5,7,9(13),10-hexaen-3-yl]ethanone 102313791 Click to see CC(=O)C1=CC2=C(C(=[O+]C3=C2C(=CC(=C3)O)O1)C4=CC(=C(C(=C4)OC)O)OC)OC5C(C(C(C(O5)CO)O)O)O 559.50 unknown via CMAUP database
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
Arecatannin A1 13752000 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
Arecatannin B1 14237657 Click to see 866.80 unknown via CMAUP database
Epicatechin-(4beta->6)-epicatechin-(4beta->8)-catechin 14309769 Click to see 866.80 unknown via CMAUP database
Epicatechin-(4beta->6)-epicatechin-(4beta->8)-epicatechin 10865804 Click to see 866.80 unknown via CMAUP database
Epicatechin-(4beta->8)-epicatechin-(4beta->8)-catechin 3''-gallate 101607200 Click to see 1018.90 unknown via CMAUP database
Epicatechin-(4beta-8)-epicatechin-(4beta-6)-epicatechin 14237653 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
GlyTouCan:G26078SU 15593123 Click to see 730.60 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
procyanidin B1 3-O-gallate 12795888 Click to see 730.60 unknown via CMAUP database
procyanidin B1 3'-O-gallate 72193635 Click to see 730.60 unknown via CMAUP database
procyanidin B2 3-O-gallate 46181828 Click to see 730.60 unknown via CMAUP database
procyanidin B2 3'-O-gallate 15593124 Click to see 730.60 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
Procyanidin B4 147299 Click to see 578.50 unknown via CMAUP database
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B6 474540 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B7 13990893 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B8 474541 Click to see 578.50 unknown via CMAUP database
Procyanidin C1 169853 Click to see 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
(2R,3R,4R)-4-benzylsulfanyl-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 13990900 Click to see 412.50 unknown via CMAUP database
(2R,3S,10S)-2,10-bis(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-8-one 10366587 Click to see 452.40 unknown via CMAUP database
(2R,3S,4R)-4-benzylsulfanyl-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 13990901 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=CC(=CC(=C23)O)O)C4=CC(=C(C=C4)O)O)O 412.50 unknown via CMAUP database
4beta-(2-Aminoethylthio)-epicatechin 10939749 Click to see 365.40 unknown via CMAUP database
4beta-(2-Aminoethylthio)catechin 11187672 Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)SCCN)O)O)O 365.40 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Catechin gallate 6419835 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
4beta-(2-Aminoethylthio)epicatechin 3-gallate 10919263 Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)SCCN)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 517.50 unknown via CMAUP database
Epicatechin-3-Gallate 65056 Click to see 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 Click to see 306.27 unknown via CMAUP database
(2R,3S,4S)-4-benzylsulfanyl-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 93477121 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=CC(=CC(=C23)O)O)C4=CC(=C(C(=C4)O)O)O)O 428.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10165328 Click to see 493.40 unknown via CMAUP database
1-[11-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-oxa-8-oxoniatricyclo[7.3.1.05,13]trideca-1(12),3,5,7,9(13),10-hexaen-3-yl]ethanone 102313792 Click to see CC(=O)C1=CC2=C(C(=[O+]C3=C2C(=CC(=C3)O)O1)C4=CC(=C(C=C4)O)OC)OC5C(C(C(C(O5)CO)O)O)O 529.50 unknown via CMAUP database
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
Malvidin 3-Glucoside 443652 Click to see 493.40 unknown via CMAUP database
Peonidin-3-glucoside 443654 Click to see 463.40 unknown via CMAUP database
Petunidin 3-Glucoside 443651 Click to see 479.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[7-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3-(4-hydroxy-3,5-dimethoxyphenyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-ylidene]oxidanium 102051216 Click to see 951.90 unknown via CMAUP database
[7-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3-(4-hydroxy-3,5-dimethoxyphenyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-ylidene]oxidanium 102051215 Click to see 951.90 unknown via CMAUP database
Malvidin 3-(6''-p-coumarylglucoside) 72193651 Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O)O 639.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 46173911 Click to see 450.40 unknown via CMAUP database
[3-(4-hydroxy-3,5-dimethoxyphenyl)-7-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-ylidene]oxidanium 102376056 Click to see 531.50 unknown via CMAUP database
[7-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3-(4-hydroxy-3,5-dimethoxyphenyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-ylidene]oxidanium 101422850 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C3=C4C(=CC(=[OH+])C=C4O2)OC(=C3)C5=C(C=C(C6=C5OC(C(C6)O)C7=CC(=C(C=C7)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O 805.70 unknown via CMAUP database
5-[2alpha-(3,4-Dihydroxyphenyl)-3alpha,5,7-trihydroxychroman-8-yl]-2-(3,5-dimethoxy-4-hydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-8-hydroxy-2-dehydro-2H-pyrano[4,3,2-de]-1-benzopyran-1-ium 101422846 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C3=C4C(=CC(=[OH+])C=C4O2)OC(=C3)C5=C(C=C(C6=C5OC(C(C6)O)C7=CC(=C(C=C7)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O 805.70 unknown via CMAUP database
5,7-Dihydroxy-2-(4-Hydroxy-3,5-Dimethoxyphenyl)-3-((2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5321577 Click to see 508.40 unknown via CMAUP database
Astilbin 119258 Click to see 450.40 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
Engeletin 6453452 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Laricitrin 3-O-glucoside 101682256 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 494.40 unknown via CMAUP database
Myricetin 3-O-galactoside 5491408 Click to see 480.40 unknown via CMAUP database
Vitisin B (vitis vinifera) 44195285 Click to see 517.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(1R,2R,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-1-[(R)-(4-hydroxyphenyl)-methoxymethyl]-2,3-dihydro-1H-indene-4,6-diol 101769425 Click to see 486.50 unknown via CMAUP database
(1R,2S,3R)-2-(3,5-dihydroxyphenyl)-1-[(R)-hydroxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 60151313 Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(C4=CC=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 472.50 unknown via CMAUP database
(1R,2S,3R)-2-(3,5-dihydroxyphenyl)-1-[(S)-hydroxy-(4-hydroxyphenyl)methyl]-3-(4-hydroxyphenyl)-2,3-dihydro-1H-indene-4,6-diol 60151314 Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(C4=CC=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 472.50 unknown via CMAUP database
[(1R,2R,3R)-3-(3,5-dihydroxyphenyl)-4,6-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1H-inden-1-yl]-(4-hydroxyphenyl)methanone 484753 Click to see 470.50 unknown via CMAUP database
2,4,4'-Trihydroxy-trans-stilbene 10130775 Click to see 228.24 unknown via CMAUP database
Cis-Resveratrol 1548910 Click to see 228.24 unknown via CMAUP database
Piceatannol 667639 Click to see 244.24 unknown via CMAUP database
Pterostilbene 5281727 Click to see 256.30 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-[(Z)-2-(4-hydroxyphenyl)ethenyl]-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol 16040019 Click to see 552.50 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-2-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethenyl]phenoxy]oxane-3,4,5-triol 16040018 Click to see 552.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(Z)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 16039986 Click to see 390.40 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(Z)-2-[3,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 16040017 Click to see 714.70 unknown via CMAUP database
3-Hydroxy-5-(2-(4-hydroxyphenyl)ethenyl)phenyl-beta-D-glucopyranoside 73642 Click to see 390.40 unknown via CMAUP database
3,5-Bis(beta-D-glucopyranosyloxy)-4'-hydroxystilbene 16038898 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 552.50 unknown via CMAUP database
Astringin 5281712 Click to see 406.40 unknown via CMAUP database
cis-Astringin 16040016 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 406.40 unknown via CMAUP database
cis-Piceid 10178463 Click to see 390.40 unknown via CMAUP database
Mulberroside E 10030502 Click to see 552.50 unknown via CMAUP database
Polydatin 5281718 Click to see 390.40 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database

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