Peucedanum palustre - Unknown
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Details Top

Internal ID UUID643ff77960d71835463878
Scientific name Peucedanum palustre
Authority (L.) Moench
First published in Methodus : 82 (1794)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oreoselis pisana (Savi) Raf. Good Book : 57 (1840)
Peucedanum sylvestre DC. Prodr. 4: 179 (1830)
Peucedanum schiwereckii Eichw. Skizze : 155 (1830)
Peucedanum idanense Gand. Fl. Lyon. : 103 (1875)
Thysselinum sylvestre Hoffm. Gen. Pl. Umbell. : 154 (1814)
Thysselinum palustre (L.) Hoffm. Gen. Pl. Umbell. : 154 (1814)
Thysselinum plinii Spreng. Sp. Umbell. : 69 (1818)
Thysselinum schiwerekii Besser Enum. Pl. Volh. : 12 (1821)
Thyselium palustre (L.) Raf. Good Book : 52 (1840)
Thysselinum angustifolium Rchb. Fl. Germ. Excurs. 2: 453 (1832)
Thysselinum crouanorum Boreau Bull. Soc. Bot. France 20: 30 (1873)
Selinum palustre L. Sp. Pl. : 244 (1753)
Selinum intermedium Besser Prim. Fl. Galiciae Austriac. 1: 205 (1809)
Selinum schiwerekii Besser Prim. Fl. Galiciae Austriac. 1: 205 (1809)
Selinum tysselinum Crantz Stirp. Austr. Fasc. 3: 35 (1767)
Selinum sylvestre L. Sp. Pl. : 244 (1753)
Athamanta flexuosa Juss. ex DC. Prodr. 4: 179 (1830)
Athamanta pisana Savi Ann. Bot. (Usteri) 21: 7 (1797)
Calestania palustris Koso-Pol. Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 175 (1915 publ. 1916)
Callisace schiefereckii Hoffm. Gen. Pl. Umbell. ed. 2: 170 1816
Cnidium palustre Rchb. Fl. Germ. Excurs. : 469 (1832)

Common names Top

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Language Common/alternative name
English hogfennel
English milk-parsley
English marsh hog’s fennel
English milk parsley

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Area

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Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000391781
USDA Plants PEPA22
Tropicos 1700186
KEW urn:lsid:ipni.org:names:846318-1
The Plant List kew-2403630
Plantarium 27509
PFAF Peucedanum palustre
Open Tree Of Life 5801609
Observations.org 7163
NCBI Taxonomy 1572681
NBN Atlas NBNSYS0000003707
Nature Serve 2.132564
IPNI 846318-1
iNaturalist 166550
GBIF 3034225
Freebase /m/07t4ty
EPPO PCDPA
EOL 581423
Elurikkus 6167
USDA GRIN 468591
Wikipedia Peucedanum_palustre
CMAUP NPO7718
PaleoBotany 58265

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
Total Soil CO2 Efflux from Drained Terric Histosols Vigricas E, Čiuldienė D, Armolaitis K, Valujeva K, Laiho R, Jauhiainen J, Schindler T, Bārdule A, Lazdiņš A, Butlers A, Kazanavičiūtė V, Belova O, Kamil-Sardar M, Soosaar K Plants (Basel) 04-Jan-2024
PMCID:PMC10780588
doi:10.3390/plants13010139
PMID:38202448
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
Adaptive Relationships in Hemi-Boreal Forests: Tree Species Responses to Competition, Stress, and Disturbance Petrokas R, Manton M Plants (Basel) 13-Sep-2023
PMCID:PMC10535793
doi:10.3390/plants12183256
PMID:37765418
Biochemometry identifies ostruthin as pluripotent antimicrobial and anthelmintic agent from masterwort Zwirchmayr J, Cruz CD, Grienke U, Tammela P, Rollinger JM iScience 03-Aug-2023
PMCID:PMC10457539
doi:10.1016/j.isci.2023.107523
PMID:37636068
The Search for Suitable Habitats for Endangered Species at Their Historical Sites—Conditions for the Success of Salix lapponum and Salix myrtilloides Reintroduction Arciszewski M, Pogorzelec M, Bronowicka-Mielniczuk U, Niedźwiecki M, Parzymies M, Serafin A Int J Environ Res Public Health 09-Jan-2023
PMCID:PMC9859233
doi:10.3390/ijerph20021133
PMID:36673887
“Cow Healers Use It for Both Horses and Cattle”: The Rise and Fall of the Ethnoveterinary Use of Peucedanum ostruthium (L.) Koch (fam. Apiaceae) in Sweden de Vahl E, Mattalia G, Svanberg I Plants (Basel) 26-Dec-2022
PMCID:PMC9823300
doi:10.3390/plants12010116
PMID:36616243
Scrub encroachment promotes biodiversity in temperate European wetlands under eutrophic conditions Brunbjerg AK, Fløjgaard C, Frøslev TG, Andersen DK, Bruun HH, Dalby L, Goldberg I, Lehmann LJ, Moeslund JE, Ejrnæs R Ecol Evol 01-Nov-2022
PMCID:PMC9627074
doi:10.1002/ece3.9445
PMID:36340817
Traditional Uses of Medicinal Plants in South-Western Part of Lithuania Karpavičienė B Plants (Basel) 11-Aug-2022
PMCID:PMC9413674
doi:10.3390/plants11162093
PMID:36015397
Interspecific and intraspecific analysis of Selinum spp. collected from Indian Himalayas using DNA barcoding Srivastava RP, Saxena G, Singh L, Singh A, Verma PC, Kaur G J Genet Eng Biotechnol 22-Apr-2022
PMCID:PMC9033919
doi:10.1186/s43141-022-00345-0
PMID:35451659
Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities Mottaghipisheh J Plants (Basel) 30-Jul-2021
PMCID:PMC8401860
doi:10.3390/plants10081577
PMID:34451622
Chemical and Phytocoenological Characteristics of Two Different Slovak Peatlands Fazekašová D, Barančíková G, Fazekaš J, Štofejová L, Halas J, Litavec T, Liptaj T Plants (Basel) 24-Jun-2021
PMCID:PMC8309078
doi:10.3390/plants10071290
PMID:34202908
Chemical profiles of birch and alder bark by ambient mass spectrometry Räsänen RM, Hieta JP, Immanen J, Nieminen K, Haavikko R, Yli-Kauhaluoma J, Kauppila TJ Anal Bioanal Chem 23-Oct-2019
PMCID:PMC6875546
doi:10.1007/s00216-019-02171-9
PMID:31642944
Karst dolines provide diverse microhabitats for different functional groups in multiple phyla Bátori Z, Vojtkó A, Maák IE, Lőrinczi G, Farkas T, Kántor N, Tanács E, Kiss PJ, Juhász O, Módra G, Tölgyesi C, Erdős L, Aguilon DJ, Keppel G Sci Rep 09-May-2019
PMCID:PMC6509348
doi:10.1038/s41598-019-43603-x
PMID:31073136
Botanical Provenance of Traditional Medicines From Carpathian Mountains at the Ukrainian-Polish Border Kozlowska W, Wagner C, Moore EM, Matkowski A, Komarnytsky S Front Pharmacol 05-Apr-2018
PMCID:PMC5895925
doi:10.3389/fphar.2018.00295
PMID:29674964
Diverse fen plant communities enhance carbon-related multifunctionality, but do not mitigate negative effects of drought Robroek BJ, Jassey VE, Beltman B, Hefting MM R Soc Open Sci 25-Oct-2017
PMCID:PMC5666246
doi:10.1098/rsos.170449
PMID:29134063

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
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines
Benzylamine 7504 Click to see C1=CC=C(C=C1)CN 107.15 unknown https://doi.org/10.1055/S-2006-958068
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL 5318042 Click to see CCCC=CCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown via CMAUP database
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin 5281238 Click to see CC1=CC(CC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C)(C)C)O 584.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[3-acetyloxy-1,2-dihydroxy-17-(6-hydroxy-6-methylhept-4-en-2-yl)-4,8,10,14-tetramethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]methyl acetate 162892564 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1CCC3C2(CCC4C3(C(C(C(C4(C)COC(=O)C)OC(=O)C)O)O)C)C)C 576.80 unknown https://doi.org/10.1055/S-2006-962542
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 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 nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
2-Amino-1-phenylethanol 1000 Click to see C1=CC=C(C=C1)C(CN)O 137.18 unknown https://doi.org/10.1055/S-2006-958068
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
1,4-Diaminobutane 1045 Click to see C(CCN)CN 88.15 unknown https://doi.org/10.1055/S-2006-958068
Amylamine 8060 Click to see CCCCCN 87.16 unknown https://doi.org/10.1055/S-2006-958068
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Spermidine 1102 Click to see C(CCNCCCN)CN 145.25 unknown https://doi.org/10.1055/S-2006-958068
Spermine 1103 Click to see C(CCNCCCN)CNCCCN 202.34 unknown https://doi.org/10.1055/S-2006-958068
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp 70680285 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O 356.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Neoamygdalin 441462 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hexenal 5281168 Click to see CCCC=CC=O 98.14 unknown via CMAUP database
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Tryptamine 1150 Click to see C1=CC=C2C(=C1)C(=CN2)CCN 160.22 unknown https://doi.org/10.1055/S-2006-958068
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one 7057972 Click to see CCCCC1CCC(=O)O1 142.20 unknown via CMAUP database
(R)-gamma-Decalactone 183870 Click to see CCCCCCC1CCC(=O)O1 170.25 unknown via CMAUP database
2(3H)-Furanone, dihydro-5-octyl-, (5R)- 10888889 Click to see CCCCCCCCC1CCC(=O)O1 198.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol 6428573 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-(2-Oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl)propan-2-yl 2-hydroxy-2-methyl-3-(2-methylbut-2-enoyloxy)butanoate 162896988 Click to see CC=C(C)C(=O)OC(C)C(C)(C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 444.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.19-0601
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (2S,3R)-2-hydroxy-2-methyl-3-[(E)-2-methylbut-2-enoyl]oxybutanoate 163194939 Click to see CC=C(C)C(=O)OC(C)C(C)(C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 444.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.19-0601
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (Z)-2-methylbut-2-enoate 53399217 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 328.40 unknown https://doi.org/10.1007/BF02066241
Columbianadin 6436246 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 328.40 unknown https://doi.org/10.1002/CBDV.201500198
https://doi.org/10.1055/S-2006-961919
https://doi.org/10.1007/BF02066241
https://doi.org/10.1055/S-2006-962542
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1055/S-2006-961919
https://doi.org/10.1055/S-2006-962542
4-(2,3-Dihydroxy-3-Methylbutoxy)Furo(3,2-G)Chromen-7-One 483513 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown via CMAUP database
4-[(3,3-Dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one 160544 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown via CMAUP database
5-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 53316971 Click to see CC1(C(O1)COC2=CC(=O)OC3=C2C=C4C=COC4=C3)C 286.28 unknown via CMAUP database
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.18-1379
https://doi.org/10.1055/S-2006-961919
https://doi.org/10.1055/S-2006-962542
Ostruthol 6441273 Click to see CC=C(C)C(=O)OC(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C(C)(C)O 386.40 unknown https://doi.org/10.1055/S-2006-961919
https://doi.org/10.1055/S-2006-962542
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1055/S-2006-961919
> 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/10.1055/S-2006-961919
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
(S,Z)-3-Hydroxy-1-((9-methoxy-7-oxo-7H-furo[3,2-g]chromen-4-yl)oxy)-3-methylbutan-2-yl 2-methylbut-2-enoate 40507908 Click to see CC=C(C)C(=O)OC(COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C(C)(C)O 416.40 unknown https://doi.org/10.1055/S-2006-962542
[3-Hydroxy-1-(9-methoxy-7-oxofuro[3,2-g]chromen-4-yl)oxy-3-methylbutan-2-yl] 2-methylbut-2-enoate 164018 Click to see CC=C(C)C(=O)OC(COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C(C)(C)O 416.40 unknown https://doi.org/10.1007/BF02066241
2-Butenoic acid, 2-methyl-, (1S)-2-hydroxy-1-[[(9-methoxy-7-oxo-7H-furo[3,2-g][1]benzopyran-4-yl)oxy]methyl]-2-methylpropyl ester, (2Z)- 40507909 Click to see CC=C(C)C(=O)OC(COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C(C)(C)O 416.40 unknown https://doi.org/10.1007/BF02066241
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 73353883 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate 10723070 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)OC(=O)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)O 664.60 unknown via CMAUP database
ent-Epiafzelechin-(2alpha-O-7,4alpha-8)-ent-epiafzelechin 5317051 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Geranin A 5317050 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Mahuannin A 5317052 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 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
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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