Details Top

Internal ID UUID643fe04f19a3c917393677
Scientific name Lamium purpureum
Authority L.
First published in Sp. Pl. : 579 (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.

Lamium purpureum, known as purple dead‑nettle, has been recorded in several European folk traditions as a mild diuretic and skin‑soothing herb. In the United Kingdom, Grieves (1931) described an infusion of the aerial parts taken “by the wine‑glassful” to promote urine flow and to ease catarrhal complaints, while Culpeper’s Complete Herbal (1653) recommended a decoction of the leaves for the same purpose. Across the German‑speaking Alps, Frohn (2001) noted that shepherds in the Tyrol prepared a leaf infusion as a “renal tonic,” drinking a small cup each morning. In the Carpathian Basin of Hungary and western Romania, Kocsis & Bihari (2018) documented the use of fresh leaf poultices applied to bruises and swollen joints, the bruised herb being pressed to a cloth and bound to the affected area for 30–60 min. These three regionally distinct practices all involve the same plant part—the young shoots and leaves—used either as a tea, a decoction or a fresh poultice.

A practical preparation is a mild leaf tea that can be made from dried or fresh aerial parts. Use roughly 1 – 2 tsp (about 2–4 g) of dried leaves per 250 ml of just‑boiled water; cover and steep 5–10 minutes, then strain. The infusion can be taken once or twice daily, preferably after meals, for its diuretic effect. As a safety note, the plant contains flavonoids that have mild diuretic activity, and it is best avoided by pregnant women, by people on prescription diuretics, or those with known hypersensitivity to Lamiaceae. A standard decoction, if preferred, can be made by simmering 1 oz (≈30 g) of fresh shoots in 1 L of water for 15 minutes before straining and cooling.

Phytochemical studies on Lamium purpureum reveal a characteristic suite of flavonoids (quercetin, luteolin and apigenin), phenolic acids such as caffeic and rosmarinic acids, and iridoid glycosides typical of the Lamiaceae. These compounds are known to possess diuretic, anti‑inflammatory and mild astringent properties, providing a plausible biochemical basis for the traditional use as a renal tonic and for topical wound care.

Current research focuses on the antioxidant capacity of these extracts, with several in‑vitro assays confirming high radical‑scavenging activity (e.g., Hilal et al., 2022). While commercial products are limited, the herb continues to appear in niche herbal‑retail blends in the UK and in Austrian health‑food shops, reflecting ongoing appreciation of its gentle diuretic and soothing actions.

General Uses Top

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Food and beverages (non‑medicinal):
Young leaves of Lamium purpureum are harvested in early spring before flowering and are used as a leafy green. The tender shoots are eaten raw in salads or mixed with other fresh herbs, or they are briefly cooked—blanched for 1–2 minutes, sautéed, or added to soups, stews, and potherbs. Cooking softens the texture and diminishes any mild bitterness. In some local markets the plant is collected as a wild green and sold alongside other edible weeds. No health claims are associated with these preparations; they are purely culinary.

Scientific/model‑organism use:
Because it germinates in winter, completes its life cycle in a few months, and produces a large number of seeds, Lamium purpureum is widely employed as a model weed in plant biology and agronomy. It serves as a standard test species in herbicide efficacy trials (e.g., OECD Test Guidelines), competition studies, and investigations of allelopathy and ecological interactions. Its genome size and chromosome number have been documented, contributing to comparative genomics within the Lamiaceae.

Properties relevant to use:
The leaves have low lignin and high water content, yielding a soft texture when fresh. They contain moderate levels of oxalates, which are reduced by brief cooking. The plant’s rapid growth, high seed output, and ability to thrive in disturbed habitats make it suitable for experimental plots that require short‑term vegetation.

Standards and regulation:
When marketed as a food, the harvest and sale of Lamium purpureum are subject to the general food‑safety regulations that govern wild‑harvested leafy greens in the jurisdiction of use (e.g., EU Regulation 2015/2283 for novel foods and national food‑safety codes). No plant‑specific standard exists.

Sustainability and sourcing:
Lamium purpureum is a common, non‑protected annual herb throughout temperate Europe and western Asia. It proliferates in field margins, hedgerows, and disturbed soils, making it a renewable resource. Responsible harvesting—removing only a modest proportion of the above‑ground biomass—poses negligible impact on wild populations.

Synonyms Top

Scientific name Authority First published in
Lamiopsis purpurea Opiz Seznam : 56 (1852)
Lamium foetidum Garsault Fig. Pl. Méd. : t. 319 (1764)
Lamium foetidum Gilib. Exerc. Phyt. 1: 97 (1792)
Lamium molle [Soland.] Hort. Kew. [W. Aiton] 2: 297. 1789
Lamium purpureum var. albiflorum Dumort. Fl. Belg. 45. 1827
Lamium purpureum var. decipiens Sond. ex W.D.J.Koch Syn. Fl. Germ. Helv., ed. 2 2: 649. 1844 [Nov 1844]
Lamium purpureum var. exannulatum Loret & Barrandon Fl. Montpellier 842. 1876

Common names Top

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Language Common/alternative name
English purple deadnettle
English velikdenche
English red dead-nettle
English purple dead-nettle
English purple archangel
Spanish lamium molle
Spanish lamium foetidum
Spanish ortiga roja
Spanish ortiga muerta roja
Spanish ortiga muerta purpúrea
Spanish lamio púrpura
Spanish hortiguilla muerta
Spanish ortiga muerta
Arabic قريص أحمر
Arabic حملح
Arabic المنتنة
Arabic الحُرّيق الأملس
Arabic أرجيفة
Arabic لاميون أرجواني
Belarusian шанта чырвоная
Belarusian яснотка пурпуровая
Bulgarian червена мъртва коприва
Catalan ortiga morta roja
Catalan lamier pourpre
Catalan lami purpuri
Czech hluchavka nachová
cv Йĕпкĕн суккăр вĕлтĕрен
Welsh marddanhadlen goch
Danish rød tvetand
German rote taubnessel
German purpurrote taubnessel
German eingeschnittene taubnessel
German purpurnessel
German lamier pourpre
German purpurote taubnessel
Esperanto purpura lamio
Estonian verev iminõges
Persian گزنهسای قرمز
Finnish punapeippi
French lamier pourpre
Irish caochneantóg dhearg
gd caoch-dheanntag dhearg
Manx ard-firryn jiarg
Hebrew נזמית ארגמנית
Upper Sorbian Čerwjena cycawka
Hungarian piros árvacsalán
Italian falsa ortica porporina
Italian làmio porporino
Japanese ヒメオドリコソウ
Japanese 姫踊り子草
Japanese 姫踊子草
Cornish koog linasen rudh
Lithuanian raudonžiedė notrelė
Lithuanian lamier pourpre
Latvian sārtā panātre
Macedonian пурпурна мртва коприва
Malayalam ലാമിയം പർപൂറിയം
Norwegian Bokmål rødtvetann
Dutch paarse dovenetel
Polish jasnota purpurowa
Portuguese lâmio-roxo
Romanian sugel puturos
Romanian pizda țigăncii
Russian яснотка пурпурная
Russian Яснотка пурпурная
Slovak hluchavka purpurová
Slovak hluchavka nachová
Slovenian škrlatnordeča mrtva kopriva
Swedish lamier pourpre
Swedish rödplister
Turkish kırmızı ballıbaba
Turkish firfiri ballıbaba
Turkish eflatun çiçekli ballıbaba
Ukrainian глуха кропива пурпурова
Ukrainian Глуха кропива пурпурова
Chinese 大苞野芝麻
Chinese 圓齒野芝麻

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Lamium purpureum var. ehrenbergii (Boiss. & Reut. ex Boiss.) Mennema Leiden Bot. Ser. 11: 120 (1989)
Lamium purpureum var. incisum (Willd.) Pers. Syn. Pl. 2: 122 (1806)
Lamium purpureum var. moluccellifolium Schumach. Enum. Pl. 1: 178 (1801)
Lamium purpureum var. purpureum Unknown

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Eastern Asia
      • Japan
      • Taiwan
    • Siberia
      • Altay
      • West Siberia
      • Yakutskiya
    • Western Asia
      • East Aegean Islands
      • Iran
      • Lebanon-Syria
      • Turkey
  • Australasia
    • Australia
      • Tasmania
    • New Zealand
      • Antipodean Islands
      • Kermadec Islands
      • New Zealand North
      • New Zealand South
  • 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
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Missouri
      • Nebraska
      • Oklahoma
      • 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
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • California
      • Nevada
    • Subarctic America
      • Alaska
      • Greenland
    • Western Canada
      • British Columbia
  • Southern America
    • Southern South America
      • Argentina Northeast
      • Argentina South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000222642
Florida Plant Atlas 4289
Flora of Alabama 2411
Canadensys 6386
USDA Plants LAPU2
Tropicos 17600102
INPN 104903
Flora of Italy 4496
KEW urn:lsid:ipni.org:names:448939-1
The Plant List kew-107573
PFAF Lamium purpureum
Open Tree Of Life 907319
NCBI Taxonomy 53164
NBN Atlas NBNSYS0000004243
Nature Serve 2.128324
IPNI 448939-1
iNaturalist 55851
GBIF 2926682
Freebase /m/02l11j
WisFlora 4008
EPPO LAMPU
EOL 595655
Elurikkus 5374
Calflora (Californian flora) 4562
USDA GRIN 21419
Wikipedia Lamium_purpureum

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_964659665.2 daLamPurp1.hap1.2 Chromosome WELLCOME SANGER INSTITUTE 2025-10-26 33 554.19 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
Impact of novel herbicide based on synthetic auxins and ALS inhibitor on weed control Grzanka M, Joniec A, Rogulski J, Sobiech Ł, Idziak R, Loryś B Open Life Sci 26-Apr-2024
PMCID:PMC11049747
doi:10.1515/biol-2022-0868
PMID:38681726
Changes in the bacterial communities of Harmonia axyridis (Coleoptera: Coccinellidae) in response to long-term cold storage and progressive loss of egg viability in cold-stored beetles Sun Y, Hao Y, Wang S, Chen X Front Microbiol 12-Mar-2024
PMCID:PMC10964723
doi:10.3389/fmicb.2024.1276668
PMID:38533331
Soil Seed Banks and Their Relation to Soil Properties in Hilly Landscapes Skuodienė R, Matyžiūtė V, Šiaudinis G Plants (Basel) 29-Dec-2023
PMCID:PMC10781063
doi:10.3390/plants13010104
PMID:38202412
Potential of Artemisia dubia Wall Biomass for Natural Crop Protection Bakšinskaitė A, Tilvikiene V, Barčauskaitė K, Feizienė D Plants (Basel) 02-Nov-2023
PMCID:PMC10650851
doi:10.3390/plants12213750
PMID:37960106
A BAHD acyltransferase contributes to the biosynthesis of both ethyl benzoate and methyl benzoate in the flowers of Lilium oriental hybrid ‘Siberia’ Yue Y, Wang L, Li M, Liu F, Yin J, Huang L, Zhou B, Li X, Yu Y, Chen F, Yu R, Fan Y Front Plant Sci 29-Sep-2023
PMCID:PMC10570747
doi:10.3389/fpls.2023.1275960
PMID:37841617
Microbiome dataset of bacterial and fungal communities in anthosphere of twelve different wild plants in South Korea Kim J, Cui Y, Lee H, Chun SJ Data Brief 05-Aug-2023
PMCID:PMC10440446
doi:10.1016/j.dib.2023.109470
PMID:37609647
Medicinal Plants as a Natural Greener Biocontrol Approach to “The Grain Destructor” Maize Weevil (Sitophilus zeamais) Motschulsky Phokwe OJ, Manganyi MC Plants (Basel) 30-Jun-2023
PMCID:PMC10346355
doi:10.3390/plants12132505
PMID:37447066
Chemical Composition and Bioactivity of Laboratory-Fermented Bee Pollen in Comparison with Natural Bee Bread Miłek M, Mołoń M, Kula-Maximenko M, Sidor E, Zaguła G, Dżugan M Biomolecules 22-Jun-2023
PMCID:PMC10377425
doi:10.3390/biom13071025
PMID:37509061
Distribution, Effect, and Control of Exotic Plants in Republic of Korea Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS Biology (Basel) 06-Jun-2023
PMCID:PMC10294914
doi:10.3390/biology12060826
PMID:37372111
The influence of climate warming on flowering phenology in relation to historical annual and seasonal temperatures and plant functional traits Geissler C, Davidson A, Niesenbaum RA PeerJ 21-Apr-2023
PMCID:PMC10124540
doi:10.7717/peerj.15188
PMID:37101791
Potential Allergenicity of Plants Used in Allergological Communication: An Untapped Tool for Prevention Magyar D Plants (Basel) 16-Mar-2023
PMCID:PMC10058677
doi:10.3390/plants12061334
PMID:36987022
Bee Pollen as Functional Food: Insights into Its Composition and Therapeutic Properties El Ghouizi A, Bakour M, Laaroussi H, Ousaaid D, El Menyiy N, Hano C, Lyoussi B Antioxidants (Basel) 23-Feb-2023
PMCID:PMC10045447
doi:10.3390/antiox12030557
PMID:36978805
Phenotypic variation and epigenetic insight into tissue culture berry crops Debnath SC, Ghosh A Front Plant Sci 19-Dec-2022
PMCID:PMC9806182
doi:10.3389/fpls.2022.1042726
PMID:36600911
Differences in Oxidative Stress Markers and Antioxidant Enzyme Activities in Black Bean Aphid Morphs (Aphis fabae Scop.) Fed on the Primary Host Viburnum opulus L. Łukasik I, Goławska S, Sytykiewicz H Antioxidants (Basel) 16-Dec-2022
PMCID:PMC9774543
doi:10.3390/antiox11122476
PMID:36552684
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312

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
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Octadecadienoic acid 5312457 Click to see CCCCCCCCCCCCCC=CC=CC(=O)O 280.40 unknown https://doi.org/10.1016/0305-1978(92)90051-E
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,5R,7S,7aR)-4,7-dimethyl-1-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 154496869 Click to see 378.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
(1S,4aR,5R,7S,7aR)-4,7-dimethyl-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 15560023 Click to see 378.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
(2S,3R,4S,5S,6R)-2-[[(1S,4aS,5R,7S,7aS)-5,7-dihydroxy-4,7-dimethyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163080274 Click to see 362.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-4,7-dimethyl-1-[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] acetate 159205348 Click to see 420.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
2-[(5,7-dihydroxy-4,7-dimethyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163080273 Click to see 362.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
Caryptoside 24721560 Click to see 406.40 unknown https://doi.org/10.1248/CPB.54.1705
Lamalbid 21637592 Click to see 422.40 unknown https://doi.org/10.1248/CPB.54.1705
Lamioside 443328 Click to see 420.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
methyl (1S,4aS,5R,7S,7aS)-5,7-dihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162968725 Click to see 406.40 unknown https://doi.org/10.1248/CPB.54.1705
methyl (1S,4aS,5S,6S,7R,7aS)-5,6,7-trihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 154496867 Click to see CC1(C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC)O 422.40 unknown https://doi.org/10.1248/CPB.54.1705
methyl (1S,4aS,6S,7R,7aS)-6,7-dihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 154496318 Click to see 406.40 unknown https://doi.org/10.1248/CPB.54.1705
methyl 5,6,7-trihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 73818239 Click to see 422.40 unknown https://doi.org/10.1248/CPB.54.1705
methyl 6,7-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 74315904 Click to see 406.40 unknown https://doi.org/10.1248/CPB.54.1705
Shanzhiside methyl ester 13892722 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1248/CPB.54.1705
Shanzhiside methylester [M+H]+ 13892721 Click to see 406.40 unknown https://doi.org/10.1248/CPB.54.1705
Shanzhiside-methylester 3085296 Click to see 406.40 unknown https://doi.org/10.1248/CPB.54.1705
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,5R)-2,3,5-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 11027254 Click to see 480.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2R,3R,4R,5R,6R)-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-({[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2 4484590 Click to see 814.80 unknown https://doi.org/10.1248/CPB.54.1705
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[(2S)-2-(3,4-dihydroxyphenyl)-2-methoxyethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 162857091 Click to see 816.80 unknown https://doi.org/10.1248/CPB.54.1705
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate 163100304 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)OC)O)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 800.80 unknown https://doi.org/10.1248/CPB.54.1705
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 16097928 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 800.80 unknown https://doi.org/10.1248/CPB.54.1705
[(2R,3R,4R,5R,6R)-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 156612955 Click to see 814.80 unknown https://doi.org/10.1248/CPB.54.1705
[(2R,3R,4R,5R,6R)-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 6325451 Click to see 814.80 unknown https://doi.org/10.1248/CPB.54.1705
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)-2-methoxyethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 162857089 Click to see 816.80 unknown https://doi.org/10.1248/CPB.54.1705
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 162890525 Click to see 786.70 unknown https://doi.org/10.1248/CPB.54.1705
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 3083112 Click to see 786.70 unknown https://doi.org/10.1248/CPB.54.1705
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162909204 Click to see 800.80 unknown https://doi.org/10.1248/CPB.54.1705
Jionoside B1 5281782 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O 814.80 unknown https://doi.org/10.1248/CPB.54.1705
Lamiuside C 16097929 Click to see 786.70 unknown https://doi.org/10.1248/CPB.54.1705
Teupolioside 16062094 Click to see 786.70 unknown https://doi.org/10.1248/CPB.54.1705
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate 6476334 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)OC)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown https://doi.org/10.1248/CPB.54.1705
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 154496101 Click to see 624.60 unknown https://doi.org/10.1248/CPB.54.1705
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74027662 Click to see 638.60 unknown https://doi.org/10.1248/CPB.54.1705
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1248/CPB.54.1705
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
Acteoside;Kusaginin;TJC160 354009 Click to see 624.60 unknown https://doi.org/10.1248/CPB.54.1705
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1248/CPB.54.1705
Leucosceptoside A 10394343 Click to see 638.60 unknown https://doi.org/10.1248/CPB.54.1705
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.001
https://doi.org/10.1248/CPB.54.1705

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