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Linaria vulgaris

Linaria vulgaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Linaria vulgaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Linaria vulgaris - Unknown
Part: Unknown
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 UUID643ffdbae4bb6992845265
Scientific name Linaria vulgaris
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 1 (1768)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Linaria ciliata Lange ex Rchb. Iconogr. Bot. Pl. Crit. 5: 13 (1827)
Linaria vulgariformis Nikitina Fl. Kirgizsk. SSR 10: 379 (1962)
Linaria linaria (L.) H.Karst. Deut. Fl. (Karsten) 947. 1882 [Nov 1882]
Linaria linarioides Steud. Nomencl. Bot. 1: 482 (1821)
Linaria linifolia F.Dietr. Nachtr. Vollst. Lex. Gärtn. 4: 415 (1818)
Linaria elongata Dumort. Fl. Belg. : 34 (1827)
Linaria gebleri Besser ex Chav. Monogr. Antirrh. : 132 (1833)
Linaria speciosa Ten. Fl. Napol. 5: 40 (1836)
Linaria versicolor (L.) Moench Methodus : 523 (1794)
Linaria perrieri (Rouy) Beauverd Bull. Soc. Bot. Genève , sér. 2, 24: 234 (1931-1932 publ. 1933)
Linaria pensylvanica Scheele Flora 26: 586 (1843)
Linaria racemosa F.Dietr. Nachtr. Vollst. Lex. Gärtn. 4: 405 (1818)
Peloria linaria (L.) Raf. Autik. Bot. : 156 (1840)
Antirrhinum commune Lam. Fl. Franç. 2: 340 (1779)
Antirrhinum genistifolium Lapeyr. Hist. Pl. Pyrenées 354. 1813
Antirrhinum glandulosum Lej. Fl. Spa 2: 320 (1813)
Antirrhinum linaria L. Sp. Pl. : 616 (1753)
Antirrhinum linaria var. peloria With. Bot. Arr. Brit. Pl. 1: 379 (1776)
Antirrhinum linarioides L. Sp. Pl. ed. 2 : 853 (1763)
Antirrhinum linifolium L. Sp. Pl. ed. 2 : 858 (1763)
Antirrhinum ochroleucum Salisb. Prodr. Stirp. Chap. Allerton : 98 (1796)
Antirrhinum versicolor L. Sp. Pl. 866 1753
Linaria vulgaris var. communis Krylov Fl. Zap. Sibiri 10: 2417 1939
Linaria vulgaris f. peloria (With.) Rouleau Naturaliste Canad. 71: 268. 1944

Common names Top

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Language Common/alternative name
English yellow toadflax
English common toadflax
Spanish lino montesino
Arabic لسان عصفور
Arabic محاجم
Arabic فحم ذئب
Arabic حباحب
Arabic أبو قالس
Arabic مكنسة
Arabic سيسم
Arabic مخلصة
Arabic قرشيه
Azerbaijani adi mahmızca
azb عادی ماهمیزجا
Belarusian Зарніца звычайная
Bulgarian обикновена луличка
Catalan palometa
Catalan linaire commune
Czech lnice květel
Czech lnice obecná
Welsh llin y llyffant
Danish almindelig torskemund
German echtes leinkraut
German frauenflachs
German gemeines leinkraut
German gewöhnliches leinkraut
German kleines löwenmaul
German linaire commune
Estonian harilik käokannus
Basque igitai-belar arrunt
Persian گل کتانی
Finnish kannusruoho
Finnish keltakannusruoho
French linaire commune
French chasse-venin
French linaire sauvage
frr bridjen
Croatian obični lanilist
Upper Sorbian swjateje marijny len
Upper Sorbian Žonjace zelo
Upper Sorbian dobry lenčk
Hungarian közönséges gyújtoványfű
Armenian Կտավախոտ սովորական
Japanese 細葉海蘭 (hosobaunran)
Kabyle tifukatin
ku newroz
Cornish lin gwyls
Lithuanian linaire commune
Lithuanian paprastoji linažolė
Latvian parastā vīrcele
Macedonian Обичен ленолист
Macedonian обичен ленолист
Macedonian ленолист
Norwegian Bokmål lintorskemunn
Dutch vlasbekje
Norwegian Nynorsk torskemunn
Norwegian Nynorsk lintorskemunn
Polish lnica pospolita
Russian Льнянка обыкновенная
Yakutian Көбүөр от
Slovak pyštek obyčajný
Slovenian navadna madronščica
Serbian Ланилист
Swedish gulsporre
Swedish gulsporreblomma
Swedish sporreblomma
Swedish linaire commune
Ukrainian Яблучне дерево
Ukrainian Льонок звичайний
Ukrainian Яблуні
Ukrainian malus
Chinese 欧洲柳穿鱼
Chinese 柳穿鱼
Chinese 柳穿魚
Chinese 新疆柳穿鱼

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Linaria vulgaris subsp. arenosa Tzvelev Novosti Sist. Vyssh. Rast. 22: 272 (1985)
Linaria vulgaris subsp. sinensis (Bebeaux) D.Y.Hong Fl. Reipubl. Popularis Sin. 67(2): 400 (1979)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000446438
UNII 6Z84RO772C
Flora of Alabama 3469
Canadensys 7252
USDA Plants LIVU2
Tropicos 29207754
INPN 106234
KEW urn:lsid:ipni.org:names:325777-2
The Plant List kew-2498895
Open Tree Of Life 989669
Observations.org 6993
NCBI Taxonomy 43171
NBN Atlas NHMSYS0000460394
Nature Serve 2.143356
IPNI 805039-1
iNaturalist 50790
GBIF 5415020
Freebase /m/09rm9k
WisFlora 4078
EPPO LINVU
EOL 467241
Elurikkus 5500
Calflora (Californian flora) 4901
USDA GRIN 102290
Wikipedia Linaria_vulgaris

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_948329865.1 daLinVulg1.1 Chromosome WELLCOME SANGER INSTITUTE 2023-01-28 28.0x 724.63 Mb

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
Exploring the complex pre-adaptations of invasive plants to anthropogenic disturbance: a call for integration of archaeobotanical approaches Bellini G, Schrieber K, Kirleis W, Erfmeier A Front Plant Sci 15-Mar-2024
PMCID:PMC10978757
doi:10.3389/fpls.2024.1307364
PMID:38559769
New Gall-Forming Insect Model, Smicronyx madaranus: Critical Stages for Gall Formation, Phylogeny, and Effectiveness of Gene Functional Analysis Ushima R, Sugimoto R, Sano Y, Ogi H, Ino R, Hayakawa H, Shimada K, Tsuchida T Insects 16-Jan-2024
PMCID:PMC10816246
doi:10.3390/insects15010063
PMID:38249069
Heritable responses to stress in plants Kovalchuk I Quant Plant Biol 07-Dec-2023
PMCID:PMC10753343
doi:10.1017/qpb.2023.14
PMID:38156078
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
Genetic structure of Trifolium pratense populations in a cityscape Mollashahi H, Urbaniak J, Szymura TH, Szymura M PeerJ 05-Sep-2023
PMCID:PMC10487591
doi:10.7717/peerj.15927
PMID:37692122
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
Oil-Contaminated Soil Remediation with Biodegradation by Autochthonous Microorganisms and Phytoremediation by Maize (Zea mays) Wojtowicz K, Steliga T, Kapusta P, Brzeszcz J Molecules 17-Aug-2023
PMCID:PMC10459520
doi:10.3390/molecules28166104
PMID:37630356
Warmer temperature during asexual reproduction induce methylome, transcriptomic, and lasting phenotypic changes in Fragaria vesca ecotypes Zhang(张宇鹏) Y, Fan G, Toivainen T, Tengs T, Yakovlev I, Krokene P, Hytönen T, Fossdal CG, Grini PE Hortic Res 31-Jul-2023
PMCID:PMC10500154
doi:10.1093/hr/uhad156
PMID:37719273
Prevalence, motivation, and associated factors of medicinal herbs consumption in pregnant women from Eastern Mediterranean Regional Office: a systematic review Bouqoufi A, Lahlou L, Ait El Hadj F, Abdessadek M, Obtel M, Khabbal Y Pharm Biol 14-Jul-2023
PMCID:PMC10351469
doi:10.1080/13880209.2023.2229388
PMID:37452524
Pectolinarigenin inhibits bladder urothelial carcinoma cell proliferation by regulating DNA damage/autophagy pathways Deng Z, Shen D, Yu M, Zhou F, Shan D, Fang Y, Jin W, Qian K, Li S, Wang G, Zhang Y, Ju L, Xiao Y, Wang X Cell Death Discov 01-Jul-2023
PMCID:PMC10314945
doi:10.1038/s41420-023-01508-9
PMID:37393350
How do you build a nectar spur? A transcriptomic comparison of nectar spur development in Linaria vulgaris and gibba development in Antirrhinum majus Cullen E, Wang Q, Glover BJ Front Plant Sci 23-Jun-2023
PMCID:PMC10328749
doi:10.3389/fpls.2023.1190373
PMID:37426957
Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z Plants (Basel) 31-May-2023
PMCID:PMC10255522
doi:10.3390/plants12112184
PMID:37299162
Winner and losers: examining biotic interactions in forbs and grasses in response to changes in water and temperature in a semi-arid grassland Akin-Fajiye M, Ploughe LW, Greenall A, Fraser LH AoB Plants 24-Apr-2023
PMCID:PMC10184435
doi:10.1093/aobpla/plad017
PMID:37197710
Halophytic Clonal Plant Species: Important Functional Aspects for Existence in Heterogeneous Saline Habitats Ievinsh G Plants (Basel) 21-Apr-2023
PMCID:PMC10144567
doi:10.3390/plants12081728
PMID:37111952
Exogenous Auxin and Gibberellin on Fluoride Phytoremediation by Eichhornia crassipes Vaz LR, Borges AC, Ribeiro DM Plants (Basel) 12-Apr-2023
PMCID:PMC10144029
doi:10.3390/plants12081624
PMID:37111848

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1248/CPB.50.1393
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3S,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496911 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1248/CPB.50.1393
2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107782 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1248/CPB.50.1393
Liriodendrin 226371 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1248/CPB.50.1393
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol 162851137 Click to see CCCCCC(C(CC1C2=C(C=CC(=C2CO1)O)CC=C(C)C)O)O 348.50 unknown https://doi.org/10.1248/CPB.50.1393
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5S,6R,7R,7aS)-6-chloro-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 12311244 Click to see CC1(C2C(OC=CC2(C(C1Cl)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 398.79 unknown https://doi.org/10.1016/0031-9422(93)85258-S
6-Chloro-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 12311243 Click to see CC1(C2C(OC=CC2(C(C1Cl)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 398.79 unknown https://doi.org/10.1016/0031-9422(93)85258-S
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)86487-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1086/326342
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 https://doi.org/10.1086/326342
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
(2S,4R)-2-amino-4-hydroxypentanedioic acid 440854 Click to see C(C(C(=O)O)N)C(C(=O)O)O 163.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-0513
2-Amino-4-hydroxypentanedioic acid 839 Click to see C(C(C(=O)O)N)C(C(=O)O)O 163.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-0513
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[[(1S,2R,4S,5S,6S,10S)-5,6-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162932834 Click to see CC12C3C(OC=CC3(C(C1O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1016/0031-9422(92)80068-P
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1R,2R,4S,5R,6S,10S)-5-hydroxy-2-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]oxane-3,4,5-triol 101928762 Click to see CC12C3C(OC=CC3(C(C1O2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 524.50 unknown https://doi.org/10.1016/0031-9422(93)85258-S
2-(Hydroxymethyl)-6-[[5-hydroxy-2-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]oxane-3,4,5-triol 14414188 Click to see CC12C3C(OC=CC3(C(C1O2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 524.50 unknown https://doi.org/10.1016/0031-9422(93)85258-S
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1248/CPB.50.1393
2-[(5,6-Dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 3512645 Click to see CC12C3C(OC=CC3(C(C1O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1016/0031-9422(92)80068-P
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-phenylmethoxyoxan-3-yl]oxyoxane-3,4,5-triol 74378451 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCC3=CC=CC=C3)CO)O)O)O)O)O 402.40 unknown https://doi.org/10.1248/CPB.50.1393
Benzyl 2-O-beta-D-xylopyranosyl-beta-D-glucopyranoside 10763616 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCC3=CC=CC=C3)CO)O)O)O)O)O 402.40 unknown https://doi.org/10.1248/CPB.50.1393
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1248/CPB.50.1393
Procumbide 21604824 Click to see CC12C3C(OC=CC3(C(C1O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1016/0031-9422(92)80214-Y
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 154497544 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1248/CPB.50.1393
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1248/CPB.50.1393
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1248/CPB.50.1393
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,5-Dimethyl-4-hydroxybenzaldehyde 75222 Click to see CC1=CC(=CC(=C1O)C)C=O 150.17 unknown https://doi.org/10.1248/CPB.50.1393
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(+)-6-Hydroxypeganine; (+)-Vasicinol; 6-Hydroxypeganine; 6-Hydroxyvasicine 4486241 Click to see C1CN2CC3=C(C=CC(=C3)O)N=C2C1O 204.22 unknown https://doi.org/10.1248/CPB.50.1393
(3S)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-ol 667496 Click to see C1CN2CC3=CC=CC=C3N=C2C1O 188.23 unknown https://doi.org/10.1016/S0021-9673(01)93059-6
1,2,3,9-Tetrahydropyrrolo(2,1-b)quinazolin-1-carboxylic acid 10965928 Click to see C1CC2=NC3=CC=CC=C3CN2C1C(=O)O 216.24 unknown https://doi.org/10.1248/CPB.50.1393
CID 776133 776133 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O 202.21 unknown https://doi.org/10.1016/S0021-9673(01)93059-6
Pyrrolo(2,1-b)quinazoline-3,7-diol, 1,2,3,9-tetrahydro-, (R)- 6452262 Click to see C1CN2CC3=C(C=CC(=C3)O)N=C2C1O 204.22 unknown https://doi.org/10.1248/CPB.50.1393
Vasicinone 442935 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C1O 202.21 unknown https://doi.org/10.1016/S0021-9673(01)93059-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(1S,2R,4S,5S,6S,10S)-6-hydroxy-2-methyl-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163193122 Click to see CC12C3C(OC=CC3(C(C1O2)OC(=O)C=CC4=CC=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O 508.50 unknown https://doi.org/10.1016/0031-9422(92)80068-P
[(1S,2R,4S,5S,6S,10S)-6-hydroxy-2-methyl-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 163193124 Click to see CC12C3C(OC=CC3(C(C1O2)OC(=O)C=CC4=CC=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O 508.50 unknown https://doi.org/10.1016/0031-9422(92)80068-P
[6-Hydroxy-2-methyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162925227 Click to see CC12C3C(OC=CC3(C(C1O2)OC(=O)C=CC4=CC=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O 508.50 unknown https://doi.org/10.1016/0031-9422(92)80068-P
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5480901 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1002/ARDP.19362740205
5-Hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 3818047 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown https://doi.org/10.1002/ARDP.19362740205
https://doi.org/10.1007/BF01522130
Linarin 5317025 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1002/ARDP.19362740205
Pectolinaroside 168849 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown https://doi.org/10.1002/ARDP.19362740205
https://doi.org/10.1007/BF01522130
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1007/BF00575036
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Glucosyringic acid 10383888 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1248/CPB.50.1393

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