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Selinum carvifolium

Selinum carvifolium - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ffc7d79b80099837749
Scientific name Selinum carvifolium
Authority (L.) L.
First published in Sp. Pl. ed. 2 : 350 (1762)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Laserpitium selinoides Scop. Fl. Carniol. , ed. 2, 1: 198 (1771)
Ligusticum carvifolia Caruel Fl. Ital. 8: 339 (1889)
Mylinum carvifolia (L.) Gaudin Fl. Helv. 2: 344 (1828)
Oreoselinum pseudocarvifolium Hoffm. Gen. Pl. Umbell. : 155 (1814)
Peucedanum cuneifolium Vill. ex Steud. Nomencl. Bot. [Steudel] 607. 1821
Selinum pseudocarvifolia All. Fl. Pedem. 2: 9 (1785)
Selinum membranaceum Vill. Cat. Jard. Pl. Strasbourg : t. 6 (1807)
Selinum seguirei Baumg. Enum. Stirp. Transsilv. 1: 224 (1816)
Selinum angulatum Lam. Fl. Franç. 3: 419 (1779)
Selinum acutangulum Gilib. Fl. Lituan. li. 22.
Selinon carvifolium (L.) St.-Lag. Ann. Soc. Bot. Lyon 7: 113 (1880)
Seseli carvifolia L. Sp. Pl. : 260 (1753)
Angelica carvifolia (L.) Vill. Prosp. Hist. Pl. Dauphiné : 25 (1779)
Carum sulcatum Steud. Nomencl. Bot. 1: 164 (1821)
Carvi sulcatum Bernh. Syst. Verz. Erf. : 169 (1800)
Cnidium carvifolium M.Bieb. Fl. Taur.-Caucas. 3: 212 (1819)
Selinum tenuifolium Salisb. Prodr. Stirp. Chap. Allerton : 162 (1796)

Common names Top

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Language Common/alternative name
English little-leaf angelica
Arabic بقدونس جبلي
Belarusian Гірча кменалістая
Czech olešník kmínolistý
Welsh llaethberllys caergrawnt
Danish seline
German kümmelblättrige silge
German kümmelsilge
German kümmel-silge
Estonian harilik aruputk
Finnish harjasärmäputki
French sélin
Norwegian Bokmål krusfrø
Dutch karwijselie
Dutch lichtblauwe peterselie
Norwegian Nynorsk krusfrø
Polish olszewnik kminkolistny
Russian Гирча тминолистная
Swedish krusfrö

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Selinum carvifolium subsp. broteroi (Hoffmanns. & Link) M.Laínz Aport. Conoc. Fl. Gallega 6: 18. 1968 [26 Oct 1968]

Varieties (abbr. var.) Top

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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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Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.
Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.

Distribution (via POWO/KEW) Top

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
      • Portugal
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000434414
USDA Plants SECA20
Tropicos 1702290
INPN 122329
Flora of Italy 3599
KEW urn:lsid:ipni.org:names:848204-1
The Plant List kew-2479118
PaleoBotany 36740
Open Tree Of Life 604908
Observations.org 2745
NCBI Taxonomy 223577
NBN Atlas NBNSYS0000003701
IPNI 848204-1
iNaturalist 204409
GBIF 5371781
Freebase /m/043s47j
EPPO SLNCA
EOL 483080
Elurikkus 7222
USDA GRIN 102142
Wikipedia Selinum_carvifolia
CMAUP NPO13355

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
Are rare plant species less resistant than common ones to herbivores? A multi‐plant species study using above‐ and below‐ground generalist herbivores Bürli S, Ensslin A, Kempel A, Fischer M Ecol Evol 05-Sep-2023
PMCID:PMC10480044
doi:10.1002/ece3.10482
PMID:37674652
Major phenolic compounds, antioxidant, antimicrobial, and cytotoxic activities of Selinum carvifolia (L.) collected from different altitudes in India Srivastava RP, Kumar S, Singh L, Madhukar M, Singh N, Saxena G, Pandey S, Singh A, Devkota HP, Verma PC, Shiva S, Malik S, Rustagi S Front Nutr 13-Jul-2023
PMCID:PMC10382142
doi:10.3389/fnut.2023.1180225
PMID:37521418
The utility of airborne hyperspectral and satellite multispectral images in identifying Natura 2000 non-forest habitats for conservation purposes Jarocińska A, Kopeć D, Niedzielko J, Wylazłowska J, Halladin-Dąbrowska A, Charyton J, Piernik A, Kamiński D Sci Rep 20-Mar-2023
PMCID:PMC10027895
doi:10.1038/s41598-023-31705-6
PMID:36941443
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
Looking for Hidden Enemies of Metabarcoding: Species Composition, Habitat and Management Can Strongly Influence DNA Extraction while Examining Grassland Communities Rucińska A, Olszak M, Świerszcz S, Nobis M, Zubek S, Kusza G, Boczkowska M, Nowak A Biomolecules 19-Feb-2021
PMCID:PMC7921978
doi:10.3390/biom11020318
PMID:33669773
Carbohydrate storage in herbs: the forgotten functional dimension of the plant economic spectrum Lubbe FC, Klimeš A, Doležal J, Jandová V, Mudrák O, Janeček Š, Bartušková A, Klimešová J Ann Bot 17-Feb-2021
PMCID:PMC8103809
doi:10.1093/aob/mcab014
PMID:33595601
Can we learn from the ecology of the Bohemian gentian and save another closely related species of Gentianella? Křenová Z, Brabec J, Rössler S, Kindlmann P PLoS One 19-Dec-2019
PMCID:PMC6922359
doi:10.1371/journal.pone.0226487
PMID:31856191
Ecology, threats and conservation status of Carex buekii (Cyperaceae) in Central Europe Więcław H, Šumberová K, Bosiacka B, Hrivnák R, Dajdok Z, Mesterházy A, Minuzzo C, Martinetto E, Koopman J Sci Rep 01-Aug-2019
PMCID:PMC6671956
doi:10.1038/s41598-019-47563-0
PMID:31371740
Computer-Assisted Recovery of Threatened Plants: Keys for Breaking Seed Dormancy of Eryngium viviparum Ayuso M, Ramil-Rego P, Landin M, Gallego PP, Barreal ME Front Plant Sci 12-Dec-2017
PMCID:PMC5732921
doi:10.3389/fpls.2017.02092
PMID:29312370
Is the scaling relationship between carbohydrate storage and leaf biomass in meadow plants affected by the disturbance regime? Klimešová J, Janeček Š, Bartušková A, Bartoš M, Altman J, Doležal J, Lanta V, Latzel V Ann Bot 07-Oct-2017
PMCID:PMC5710675
doi:10.1093/aob/mcx111
PMID:29190353
Effects of disturbance regime on carbohydrate reserves in meadow plants Janeček Š, Bartušková A, Bartoš M, Altman J, de Bello F, Doležal J, Latzel V, Lanta V, Lepš J, Klimešová J AoB Plants 27-Oct-2015
PMCID:PMC4670489
doi:10.1093/aobpla/plv123
PMID:26507569
Effects of reduced winter duration on seed dormancy and germination in six populations of the alpine herb Aciphyllya glacialis (Apiaceae) Hoyle GL, Cordiner H, Good RB, Nicotra AB Conserv Physiol 30-May-2014
PMCID:PMC4806741
doi:10.1093/conphys/cou015
PMID:27293636
Conspecific and Heterospecific Plant Densities at Small-Scale Can Drive Plant-Pollinator Interactions Janovský Z, Mikát M, Hadrava J, Horčičková E, Kmecová K, Požárová D, Smyčka J, Herben T PLoS One 21-Oct-2013
PMCID:PMC3804547
doi:10.1371/journal.pone.0077361
PMID:24204818
Plant identification credibility in ethnobotany: a closer look at Polish ethnographic studies Łuczaj ŁJ J Ethnobiol Ethnomed 17-Dec-2010
PMCID:PMC3022638
doi:10.1186/1746-4269-6-36
PMID:21167056
Environmental regulation of dormancy loss in seeds of Lomatium dissectum (Apiaceae) Scholten M, Donahue J, Shaw NL, Serpe MD Ann Bot 20-Feb-2009
PMCID:PMC2707919
doi:10.1093/aob/mcp038
PMID:19233890

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 / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
6-O-(3,4,5-Trihydroxybenzoyl)-alpha-D-glucopyranose 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
N-(2,5-Dihydroxyphenyl)pyridinium(1+) 411955 Click to see C1=CC=[N+](C=C1)C2=C(C=CC(=C2)O)O 188.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Sesamin 382073 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Coniferyl 9-O-(6-O-beta-D-apiofuranosyl-beta-D-glucopyranoside) 11408873 Click to see COC1=C(C=CC(=C1)C=CCOC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O)O 474.50 unknown via CMAUP database
Sinapyl 9-O-(6-O-beta-D-apiofuranosyl-beta-D-glucopyranoside) 11386564 Click to see COC1=CC(=CC(=C1O)OC)C=CCOC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 504.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Punicic Acid 5281126 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7048528 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
24-Hydroxyursolic acid 44568920 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
beta-Sitosterol acetate 5354503 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
CID 3003153 3003153 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C2C1)C)C(=O)O)C 470.70 unknown via CMAUP database
Epifriedelin 15559350 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Punicanolic acid 25132490 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C(=O)O)C)C)(C)C)O)C 474.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 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
Estrone 5870 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 / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-Phenylethyl D-rutinoside 11166301 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O 430.40 unknown via CMAUP database
Icariside D1 13893575 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)(CO)O 416.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown via CMAUP database
Mannitol 6251 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
1-[(2R)-piperidin-2-yl]propan-2-one 3034881 Click to see CC(=O)CC1CCCCN1 141.21 unknown via CMAUP database
1-[(2S)-1-methylpiperidin-2-yl]propan-2-one 820378 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
N-Methylpelletierine 1548928 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones
Granatonine 6602484 Click to see CN1C2CCCC1CC(=O)C2 153.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
2-(1-Propenyl)-3,4,5,6-tetrahydropyridine 15937508 Click to see CC=CC1=NCCCC1 123.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Tricetin 5281701 Click to see C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 302.23 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 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 / Anthocyanins / Anthocyanidin-5-O-glycosides
Delphinidin 3,5-diglucoside 10100906 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 627.50 unknown via CMAUP database
Pelargonin 441772 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Apigenin-4'-glucoside 5491384 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
Luteolin 3'-glucoside 12309350 Click to see C1=CC(=C(C=C1C2=CC(=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
Luteolin 3'-xylopyranoside 101675298 Click to see C1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O 418.30 unknown via CMAUP database
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
3,3',4',5,5',7-Hexahydroxyflavylium 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown via CMAUP database
Cyanidin 128861 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
Brevifolin[Geranium] 10131135 Click to see C1CC(=O)C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O 248.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3-Tri-O-galloyl-beta-D-glucose 5322038 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO)O 636.50 unknown via CMAUP database
1,2,4-tri-O-galloyl-beta-glucopyranose 88204715 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO 636.50 unknown via CMAUP database
1,2,4,6-Tetragalloylglucose 11297287 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown via CMAUP database
1,2,6-Trigalloylglucose 440308 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown via CMAUP database
1,3,4-tri-O-galloyl-beta-glucopyranose 16066749 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO 636.50 unknown via CMAUP database
1,4,6-tri-O-galloyl-beta-D-glucose 10077822 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 636.50 unknown via CMAUP database
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R)-10-[(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,11,17,18,19,22,23,34,35-undecahydroxy-9,13,25,32-tetraoxaheptacyclo[25.8.0.02,7.015,20.021,30.024,29.028,33]pentatriaconta-1(35),2,4,6,15,17,19,21,23,27,29,33-dodecaene-8,14,26,31-tetrone 44567110 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C4C5=C3C(=O)OC6=C(C(=C(C7=C(C(=C(C=C7C(=O)O1)O)O)O)C(=C56)C(=O)O4)O)O)O)O)O)O)O)C8C9C(C1=C(C(=C(C(=C1C(=O)O9)C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)O)O 1084.70 unknown via CMAUP database
(1R,35R,37R,38R,55S)-6,7,8,11,12,23,24,27,28,29,37,43,44,45,48,49,50-heptadecahydroxy-2,14,21,33,36,39,54-heptaoxaundecacyclo[33.20.0.04,9.010,19.013,18.016,25.017,22.026,31.038,55.041,46.047,52]pentapentaconta-4,6,8,10,12,16,18,22,24,26,28,30,41,43,45,47,49,51-octadecaene-3,15,20,32,40,53-hexone 16148440 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C8C9=C7C(=O)OC2=C(C(=C(C3=C(C(=C(C=C3C(=O)O1)O)O)O)C(=C92)C(=O)O8)O)O)O)O)O)O)O 1084.70 unknown via CMAUP database
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 17999934 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown via CMAUP database
[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 3,4,5-trihydroxybenzoate 14411426 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 786.60 unknown via CMAUP database
1-Desgalloyleugeniin 9918701 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown via CMAUP database
2-Hydroxy-3-methoxy-7,8-methylenedioxy-4,9-dioxapyrene-5,10-dione 10336592 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC5=C(C(=C43)OC2=O)OCO5)O 328.23 unknown via CMAUP database
2-O,3-O-[4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diylbis(carbonyl)]-beta-D-glucopyranose 11754973 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O 482.30 unknown via CMAUP database
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown via CMAUP database
3-O-methylellagic acid 13915428 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O 316.22 unknown via CMAUP database
3-O-Methylellagic acid 4-O-rhamnoside 16720461 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O 462.40 unknown via CMAUP database
3,3'-Di-O-methylellagic acid 5488919 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O 330.24 unknown via CMAUP database
3,4,4'-Tri-O-methylellagic acid 11674590 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O 344.30 unknown via CMAUP database
3,4,8,9,10-Pentahydroxybenzo[c]chromen-6-one 18504424 Click to see C1=CC(=C(C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O 276.20 unknown via CMAUP database
4,4'-Di-O-methylellagic acid 11580745 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4O)OC)C(=O)O2)O 330.24 unknown via CMAUP database
5-Desgalloylstachyurin 10417809 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown via CMAUP database
8-O-[(1R,19R,21R,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 1-O-methyl (1R,3aR,8bR)-5,6-dihydroxy-3a-(2-methoxy-2-oxoethyl)-3-oxo-1,8b-dihydrofuro[3,4-b][1]benzofuran-1,8-dicarboxylate 71475292 Click to see COC(=O)CC12C(C(OC1=O)C(=O)OC)C3=C(O2)C(=C(C=C3C(=O)OC4C5COC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)OC4C(C(O5)OC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)O)O)O)O)O)O)O 998.70 unknown via CMAUP database
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database
CID 5464368 5464368 Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C(C(=C(C8=C(C(=C(C=C8C(=O)O1)O)O)O)C(=C67)C(=O)O5)O)O)O)O)O)O)O 782.50 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Diellagic acid 4-rhamnosylglucopyranoside 11968423 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)O)OC6C(C(C(C(O6)COC7=C(C8=C9C(=C7)C(=O)OC1=C9C(=CC(=C1O)O)C(=O)O8)O)O)O)O 894.60 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Eschweilenol C 10026656 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)O)O 448.30 unknown via CMAUP database
Flavogallonic acid 14503023 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C=C5C(=O)O)O)O)O)O)O)OC2=O 470.30 unknown via CMAUP database
Gallagic acid 14754405 Click to see C1=C(C(=C(C(=C1O)O)O)C2=C(C(=C3C4=C2C(=O)OC5=C(C(=C(C(=C45)C(=O)O3)C6=C(C(=C(C=C6C(=O)O)O)O)O)O)O)O)O)C(=O)O 638.40 unknown via CMAUP database
Punicafolin 5320800 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 938.70 unknown via CMAUP database
Punigluconin 21637585 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C(=O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 802.60 unknown via CMAUP database
Strictinin 73330 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown via CMAUP database
Terminalin 5281711 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C5=C(C(=C3OC2=O)O)OC(=O)C6=C7C8=C(C(=C(C=C8C(=O)OC7=C(C(=C65)OC4=O)O)O)O)O 602.40 unknown via CMAUP database

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