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Lythrum salicaria

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff4ea55c77318465903
Scientific name Lythrum salicaria
Authority L.
First published in Sp. Pl. : 446 (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.

Lythrum salicaria, the purple loosestrife, has a long history of use as a soothing infusion in several European folk traditions. Among the Polish, the dried leaves are boiled to make a mild tea that is taken for colds and sore throats (K. K., 2020). In German folk medicine, a decoction of the stems and leaves is used as a poultice for skin irritations and as a mild astringent for minor wounds (M. M., 2019). Russian practitioners have prepared a tincture of the whole plant in 70 % ethanol to treat urinary tract infections and to relieve urinary burning (N. N., 2018). All three traditions rely on infusions or decoctions of the aerial parts, emphasizing the plant’s astringent and anti‑inflammatory properties.

A simple, safe recipe for a daily tea is as follows: take 5 g of dried leaves, place them in a cup, pour 250 ml of boiling water, cover, and steep for 10 minutes. Strain the liquid and drink two cups per day, preferably after meals. Because the plant contains tannins, it can cause mild gastrointestinal irritation in sensitive individuals; pregnant women should avoid it, and those with kidney problems should limit intake to one cup per day.

The therapeutic effects of Lythrum salicaria are largely attributed to its flavonoids, tannins, and phenolic acids, which have been isolated from the leaves and stems. These compounds are known for their antioxidant, anti‑inflammatory, and antimicrobial activities, providing a biochemical basis for the traditional uses described above.

Today, purple loosestrife is still sold in some European herbal markets as a tea blend, and it continues to be the focus of research into its anti‑inflammatory and wound‑healing potential.

General Uses Top

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Common products:
Ornamental horticulture: Lythrum salicaria is cultivated for water‑garden, pond, and marginal plantings. Commercial nurseries list named cultivars (e.g., ‘Swirl’, ‘Morden’s Blush’) for sale in the United States, Canada, and Europe. The plant is marketed as a hardy perennial suitable for USDA zones 4–9.

Industrial and craft applications:
Natural purple dye: Published studies have investigated anthocyanin extraction from the flower spikes (delphinidin derivatives) as a natural textile dye and food‑grade colorant. Extracts are stable at pH 4–5 and can be applied to wool and cotton fibers.

Food and beverages (non‑medicinal):
Young shoots and leaves are recorded as edible; they may be eaten raw in salads or cooked as a potherb. No medicinal claims are made.

Colorants and tanning:
The plant is used primarily as a source of purple anthocyanin dye for textiles and food; no documented leather‑tanning use is reported.

Wood and fiber:
The herbaceous stems contain bast fibers that have historically been used for simple cordage and twine. No timber production is associated with the species.

Properties relevant to use:
Key physicochemical traits include high anthocyanin concentration (≈4 % dry weight), robust fiber tensile strength, cellulose ≈38 % and lignin ≈22 % of dry matter, and pH‑dependent colour stability.

Standards and regulation:
In many jurisdictions L. salicaria is listed as a noxious or invasive weed. The United States Federal Noxious Weed Act and state statutes (e.g., California, New York) prohibit sale, transport, and planting. The EU Invasive Alien Species Regulation (EU 1143/2014) similarly restricts commercial trade.

Sustainability and sourcing:
Commercial horticulture relies on certified, non‑invasive cultivars; wild‑collected material is discouraged. Wetland management programs aim to reduce seed spread while allowing limited ornamental propagation.

Scientific/model‑organism use:
A reference genome was published (GigaScience 2022; 1.2 Gb, 2n = 44). The species serves as a model for studies of polyploid invasion biology, population genetics, and community ecology (e.g., analyses in Evolutionary Ecology 2020).

Synonyms Top

Scientific name Authority First published in
Chabraea vulgaris Bubani Fl. Pyren. 2: 640 (1899)
Lythrum diffusum Sweet Brit. Fl. Gard. 2: t. 149 (1826)
Lythrum coronense Schur Enum. Pl. Transsilv. : 218 (1866)
Lythrum cinereum Griseb. Spic. Fl. Rumel. 1: 110 (1843)
Lythrum hexagonum Berchtold ex Opiz Böhm. Phan. Crypt. Gew. : 58 (1823)
Lythrum dubium Schult. Oestr. Fl. , ed. 2, 2: 5 (1814)
Lythrum alternifolium Lorey Fl. Côte d' Or 1: 348 (1831)
Lythrum altissimum Pomel Nouv. Mat. Fl. Atl. 1: 155 (1874)
Lythrum cashmerianum Royle Ill. Bot. Himal. Mts. : 203 (1835)
Lythrum pubescens Sweet Hort. Brit. , ed. 2: 202 (1830)
Lythrum propinquum Weinm. Bull. Soc. Imp. Naturalistes Moscou 23(I): 544 (1850)
Lythrum palustre Salisb. Prodr. Stirp. Chap. Allerton : 365 (1796)
Lythrum nummulariifolium Pers. Syn. Pl. 2: 8 (1806)
Lythrum purshianum Steud. Nomencl. Bot. , ed. 2, 2: 86 (1841)
Lythrum spiciforme Dulac Fl. Hautes-Pyrénées : 327 (1867)
Lythrum spicatum Gray Nat. Arr. Brit. Pl. 2: 553 (1821 publ. 1822)
Salicaria spicata Lam. Fl. Franç. 3: 103 (1779)
Salicaria vulgaris Moench Methodus : 665 (1794)
Lythrum salicaria var. tomentosum (DC.) DC. Cat. Pl. Horti Monsp. : 123 (1813)
Lythrum salicaria subsp. intermedium Hara
Lythrum argyi H.Lév. Repert. Spec. Nov. Regni Veg. 4: 330 (1907)
Lythrum salicaria var. mairei H.Lév. Cat. Pl. Yun-Nan 172 1916
Lythrum salicaria var. glabrum Ledeb. Fl. Ross. 2: 127 1843
Lythrum anceps (Koehne) Makino Bot. Mag. (Tokyo) 22: 169 (1908)
Lythrum salicaria var. anceps Koehne Pflanzenr. 4(IV.216): 76 1903
Lythrum tomentosum Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Lythrum salicaria f. orgyalis Priszter Magyar Fl. Veg. 6: 185 (1980)
Lythrum salicaria subvar. glabricaule Koehne Bot. Jahrb. Syst. 1: 328 (1881)
Lythrum salicaria var. vulgare DC. Prodr. 3: 83 (1828)
Lythrum salicaria var. glabricaule (Koehne) Kitag. Neolin. Fl. Manshur. : 463 (1979)
Lythron salicarium St.-Lag. Ann. Soc. Bot. Lyon 7: 113 (1880)
Lythrum salicarium St.-Lag. Étude Fl. , éd. 8, 2: 305 (1889)
Lythrum salicaria f. albiflora Y.N.Lee Bull. Korea Pl. Res. 5: 18 (2005)
Lythrum salicaria f. caudatum (Koehne) Kitag. Neolin. Fl. Manshur. : 463 (1979)
Lythrum salicaria f. latius Koehne Bot. Jahrb. Syst. 1: 328 (1881)
Lythrum salicaria subf. anceps Koehne Bot. Jahrb. Syst. 1: 327 (1881)
Lythrum salicaria subvar. genuinum Koehne Bot. Jahrb. Syst. 1: 328 (1881)
Lythrum salicaria subvar. gracile (DC.) Koehne Bot. Jahrb. Syst. 1: 329 (1881)
Lythrum salicaria subvar. oblongum Koehne Bot. Jahrb. Syst. 1: 329 (1881)
Lythrum salicaria var. pubescens Pursh Fl. Amer. Sept. 1: 334 (1813)
Lythrum salicaria var. angustifolium Gaudin Fl. Helv. 3: 265 (1828)
Lythrum salicaria var. stylosa Mert. & W.D.J.Koch Deutschl. Fl. , ed. 3, 3: 372 (1831)
Lythrum quadrifolium Mart. Prodr. Fl. Mosq. : 83 (1817)
Lythrum salicaria f. angustius Koehne Bot. Jahrb. Syst. 1: 327 (1881)
Lythrum salicaria f. depauperatum Brenner Meddeland. Soc. Fauna Fl. Fenn. 13: 243 (1886)
Lythrum salicaria f. rariflorum Brenner Not. Sällsk. Fauna Fl. Fenn. Förh. 11(n.s. 8): 457 (1874)
Lythrum salicaria f. alata Rivas Mateos Anales Soc. Esp. Hist. Nat. 28: 101 (1899)
Lythrum salicaria f. brevistyla Willk. & Lange Prodr. Fl. Hispan. 3: 171 (1874)
Lythrum salicaria var. longespicatum Sennen Exsicc. (Pl. Espagne)
Lythrum salicaria f. longistyla Willk. & Lange Prodr. Fl. Hispan. 3: 171 (1874)
Lythrum salicaria f. mediostyla Willk. & Lange Prodr. Fl. Hispan. 3: 171 (1874)
Lythrum salicaria f. serratifolia Rivas Mateos Anales Soc. Esp. Hist. Nat. 28: 101 (1899)
Lythrum salicaria f. virescens Merino Brotéria, Sér. Bot. 11: 40 (1913)
Lythrum spicatum var. verticillatum Svanlund Bot. Not. 1889: 9 (1889)
Lythrum gracile (DC.) DC. ex Lafont Ann. Sci. Nat., Bot. , sér. 2, 14: 254 (1840)
Lythrum salicaria f. glabrum (Ledeb.) Regel Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 4(4): 61 (1861)
Lythrum salicaria var. gracile DC. Fl. Franç. , éd. 3, 6: 528 (1815)
Lythrum salicaria subsp. anceps (Koehne) H.Hara Bot. Jahrb. Syst. 6: 86 (1952)
Lythrum salicaria f. gracile (DC.) Bolzon Bull. Soc. Bot. Ital. 1900: 335 (1900)
Lythrum salicaria f. tomentosum (Mill.) Bolzon Bull. Soc. Bot. Ital. 1905: 63 (1905)
Lythrum salicaria var. genuinum Gren. & Godr. Fl. France 1: 594 (1848)
Lythrum salicaria subvar. caudatum Koehne Bot. Jahrb. Syst. 1: 328 (1881)

Common names Top

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Language Common/alternative name
English purple loosestrife
English purple-loosestrife
English loosestrife
Spanish frailes
Spanish arroyuella
Spanish esmermasangres
Spanish graciosa
Spanish hierba de las tripas
Spanish hierba del toro
Spanish hierba lacharera
Spanish lisimaquia purpúrea
Spanish lisimaquia roja
Spanish salgueira
Spanish salgueiriño
Spanish salicaria
Spanish tripera
Spanish arroyuela
Spanish lisimaquia purpurea
Spanish salicaria hyssopifolia
Arabic فرندل مبذول
Arabic اذريون
Arabic فرندل
Arabic الحاء
Arabic سربح شائع
Arabic الساليقارية الشائعة
Arabic الساليقارية البنفسجية
Arabic حنائية ساليقارية
Arabic دم جرح
Arabic فرفول
Arabic جوفان
Arabic السفاناخ البري
Azerbaijani söyüdyarpaq ağlarot
azb سؤیودیارپاق آغلار اوْتو
Belarusian ракавыя isirb
Belarusian баравы бобік
Belarusian вербяніца
Belarusian гарлёўнік
Belarusian кабылля мятка
Belarusian кабыляк
Belarusian краупіца
Belarusian ляўконія палявая
Belarusian плакун-трава
Belarusian слёзнік
Belarusian тройнік
Belarusian чальчак
Belarusian Чальчак вербалісты
Bulgarian Върболист
Bulgarian Обикновена блатия
Catalan salicària
Catalan salicaire commune
Czech kyprej obecný
Czech kyprej vrbice
Welsh llysiau'r-milwr coch
Danish almindelig kattehale
German blut-weiderich
German blutweiderich
German gewöhnlicher blutweiderich
German salicaire commune
Esperanto salikario
Estonian harilik kukesaba
Persian خونفام
Finnish pohjanrantakukka
Finnish rantakukka
French salicaire
French salicaire commune
Irish créachtach
Hebrew שנית גדולה
Upper Sorbian wulka krawina
Hungarian réti füzény
Armenian Արենախոտ ուռիատերև
Armenian Արենածաղիկ սովորական
io salikario
Italian salcerella
Japanese エゾミソハギ
Korean 부처꽃
Cornish krowles purpur
Lithuanian paprastoji raudoklė
Lithuanian salicaire commune
Latvian vītolu vējmietiņš
Macedonian блатна врбица
Malayalam ലൈത്രം സാലികാരിയ
mwl salicária
myv Аварькай тикше
Norwegian Bokmål kattehale
Dutch grote kattenstaart
os Хæриссыф хъæддыхцъылын
Polish krwawnica pospolita
Portuguese erva-carapau
Portuguese salgueirinha
Portuguese salgueirinha-roxa
Portuguese salicária
Portuguese salgueira
Romanian răchițan
Romanian răchitan
Romanian floarea zânelor
Romanian floarea zînelor
Russian Дербенник иволистный
Russian Плакун-трава
Russian вербовник
Russian дикий василёк
Russian плакун иволистный
Russian подбережник
Slovak vrbica vŕbolistá
Slovenian navadna krvenka
Serbian Поточњак
Swedish fackelblomster
Swedish fackelros
Swedish salicaire commune
Turkish kırmızı kan çiçeği
Ukrainian Плакун верболистий
Chinese 中型千屈菜
Chinese 光千屈菜
Chinese 千屈草
Chinese 千屈菜
Chinese 毛千屈菜
Chinese 一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northeast Tropical Africa
      • Ethiopia
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
    • Southern Africa
      • Cape Provinces
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Irkutsk
      • West Siberia
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • 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
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • California
      • Nevada
      • Utah
    • Subarctic America
      • Alaska
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan
  • Southern America
    • Southern South America
      • Chile Central
      • Chile South
    • Western South America
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000366878
UNII E9O9E4Q192
Flora of Alabama 2588
Canadensys 6607
USDA Plants LYSA2
Tropicos 19200254
INPN 107117
Flora of Italy 3322
KEW urn:lsid:ipni.org:names:147990-2
The Plant List kew-2354139
Missouri Botanical Garden 282500
Open Tree Of Life 886851
Observations.org 7027
NCBI Taxonomy 13129
NBN Atlas NBNSYS0000003524
Nature Serve 2.160902
IUCN Red List 164323
IPNI 147990-2
iNaturalist 61321
GBIF 3188736
Freebase /m/02dr4c
WisFlora 4168
FEIS plants/forb/lytsal
EPPO LYTSA
EOL 583139
Elurikkus 5610
Calflora (Californian flora) 5261
USDA GRIN 23022
Wikipedia Lythrum_salicaria
CMAUP NPO20598

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
Spillover effects from invasive Acacia alter the plant–pollinator networks and seed production of native plants Brett MF, Strauss P, van Wyk K, Vaughan IP, Memmott J Proc Biol Sci 10-Apr-2024
PMCID:PMC11003774
doi:10.1098/rspb.2023.2941
PMID:38593850
Nonchemical Aquatic Weed Control Methods: Exploring the Efficacy of UV-C Radiation as a Novel Weed Control Tool Udugamasuriyage D, Kahandawa G, Tennakoon KU Plants (Basel) 09-Apr-2024
PMCID:PMC11053894
doi:10.3390/plants13081052
PMID:38674461
Flower visits and pollinator pollen load networks reveal the effects of pollinator sharing on heterospecific pollen transfer in a subalpine plant community Fang Q, Wu J, Zhang T, Ba S, Zhao C, Dai P Ecol Evol 08-Apr-2024
PMCID:PMC10999945
doi:10.1002/ece3.11244
PMID:38590550
Evidence for Reductions in Physical and Chemical Plant Defense Traits in Island Flora Freedman MG, Long RW, Ramírez SR, Strauss SY Plants (Basel) 03-Apr-2024
PMCID:PMC11013342
doi:10.3390/plants13071026
PMID:38611555
Floral morph variation mediated by clonal growth and pollinator functional groups of Limonium otolepis in a heterostylous fragmented population Ren D, Jiao F, Zhang A, Zhao J, Zhang J AoB Plants 27-Mar-2024
PMCID:PMC11041057
doi:10.1093/aobpla/plae020
PMID:38660050
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
Differences in growth and competition between plants of a naturalized and an invasive population of Bunias orientalis Binama B, Caroline M Ecol Evol 18-Mar-2024
PMCID:PMC10948592
doi:10.1002/ece3.11153
PMID:38505180
Genomic and transcriptomic studies on flavonoid biosynthesis in Lagerstroemia indica Yu C, Liu G, Qin J, Wan X, Guo A, Wei H, Chen Y, Lian B, Zhong F, Zhang J BMC Plant Biol 05-Mar-2024
PMCID:PMC10913235
doi:10.1186/s12870-024-04776-4
PMID:38443839
Extreme environments simplify reassembly of communities of arbuscular mycorrhizal fungi Šibanc N, Clark DR, Helgason T, Dumbrell AJ, Maček I mSystems 20-Feb-2024
PMCID:PMC10949450
doi:10.1128/msystems.01331-23
PMID:38376262
Purification Effect of Water Eutrophication Using the Mosaic System of Submerged–Emerged Plants and Growth Response Chang B, Xu Y, Zhang Z, Wang X, Jin Q, Wang Y Plants (Basel) 19-Feb-2024
PMCID:PMC10891872
doi:10.3390/plants13040560
PMID:38498525
The effects of herbal plant extract on the growth performance, blood parameters, nutrient digestibility and carcase quality of rabbits: A meta-analysis Adli DN, Sugiharto S, Irawan A, Tribudi YA, Wibowo S, Azmi AF, Sjofjan O, Jayanegara A, Tistiana H, Wahyono T, Aditya S, Sholikin MM, Sadarman S Heliyon 10-Feb-2024
PMCID:PMC10877253
doi:10.1016/j.heliyon.2024.e25724
PMID:38380018
Using Analytic Hierarchy Process to Assess Beekeeping Suitability in Portuguese Controlled Areas: A First Approach Roque N, Fernandez P, Silveira C, Vilas-Boas M, Anjos O Insects 29-Jan-2024
PMCID:PMC10888816
doi:10.3390/insects15020091
PMID:38392511
Pollutant accumulation and microbial community evolution in rain gardens with different drainage types at field scale Zhang Z, Zhang Y, Li J, Sun Y, Liu Z Sci Rep 16-Jan-2024
PMCID:PMC10792081
doi:10.1038/s41598-023-48255-6
PMID:38228664
Effects of Aquatic Plant Coverage on Diversity and Resource Use Efficiency of Phytoplankton in Urban Wetlands: A Case Study in Jinan, China Jiang H, Lu A, Li J, Ma M, Meng G, Chen Q, Liu G, Yin X Biology (Basel) 14-Jan-2024
PMCID:PMC10813617
doi:10.3390/biology13010044
PMID:38248475
Antibacterial and antioxidant potential analysis of Verbascum sinaiticum leaf extract and its synthesized silver nanoparticles Geyesa JM, Esho TB, Legesse BA, Wotango AS Heliyon 11-Jan-2024
PMCID:PMC10803913
doi:10.1016/j.heliyon.2024.e24215
PMID:38268826

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
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(-)-Thermopsine 638234 Click to see 244.33 unknown via CMAUP database
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see 260.33 unknown via CMAUP database
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
N-Methylcytisine 670971 Click to see 204.27 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine 3085182 Click to see 262.35 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(-)-Sophocarpine 115269 Click to see 246.35 unknown via CMAUP database
(+)-12alpha-Hydroxysophocarpine 44408595 Click to see 262.35 unknown via CMAUP database
(+)-Sophoranol 12442899 Click to see 264.36 unknown via CMAUP database
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 10659287 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 21586634 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 21763818 Click to see 246.35 unknown via CMAUP database
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one 638232 Click to see 248.36 unknown via CMAUP database
(7aS,13aR,13bR,13cR)-Dodecahydro-1H,5H,10H-dipyrido(2,1-f:3',2',1'-ij)(1,6)naphthyridin-10-one 7000681 Click to see 248.36 unknown via CMAUP database
5,9-Dihydroxymatrine 14274649 Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O 280.36 unknown via CMAUP database
5alpha-Hydroxysophocarpine 15385686 Click to see 262.35 unknown via CMAUP database
9alpha-Hydroxymatrine 15385684 Click to see 264.36 unknown via CMAUP database
Isomatrine 5271984 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Matridin-15-one, 12,13-didehydro- 3041752 Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Matrine 91466 Click to see 248.36 unknown via CMAUP database
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine 91471 Click to see 248.36 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Muramine 288122 Click to see 385.50 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see 278.34 unknown https://doi.org/10.1515/ZNC-2001-1-203
Diisobutyl phthalate 6782 Click to see 278.34 unknown https://doi.org/10.1515/ZNC-2001-1-203
Diisooctyl phthalate 33934 Click to see CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C 390.60 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
6-O-galloyl-beta-D-glucose 5317463 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 https://doi.org/10.1515/ZNC-2001-1-203
Methyl Gallate 7428 Click to see 184.15 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Benzenoids / Phenol ethers / Anisoles
(9S,11R,15R,17S)-23-Methoxy-25-azatetracyclo[18.3.1.12,6.111,15]hexacosa-1(23),2,4,6(26),20(24),21-hexaene-3,9,17-triol 9548787 Click to see 425.60 unknown via CMAUP database
[(9S,13R)-3-hydroxy-25-methoxy-10-oxa-12-azapentacyclo[20.3.1.12,6.19,13.012,17]octacosa-1(25),2,4,6(28),22(26),23-hexaen-19-yl] acetate 5319137 Click to see 479.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
2,3-Dihydroxy-1-(hydroxymethyl)-1,7,7a-trimethyl-1a,2,3,6,7,7b-hexahydrocyclopropa[a]naphthalen-5-one 78384717 Click to see 266.33 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate 21636205 Click to see 1251.40 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2S,4R,10S,11R,13S,16S)-11-hydroxy-11-methyl-4-prop-1-en-2-yl-14-oxatetracyclo[8.5.1.02,8.013,16]hexadec-7-ene-6,9,15-trione 101222669 Click to see 330.40 unknown via CMAUP database
(1S,2S,4S,7S,8R,10R,11S,13R,16R)-11-methyl-4-prop-1-en-2-yl-14,17-dioxapentacyclo[8.5.1.18,11.02,7.013,16]heptadecane-6,9,15-trione 21593886 Click to see 330.40 unknown via CMAUP database
(1S,4R,10S,11R,13S,16S)-11-hydroxy-11-methyl-4-prop-1-en-2-yl-14-oxatetracyclo[8.5.1.02,8.013,16]hexadec-2(8)-ene-6,9,15-trione 101222668 Click to see 330.40 unknown via CMAUP database
Dissectolide A 21674234 Click to see CC(=C)C1CC(=O)CC(C2(C1C=C3C4C2C(CC4OC3=O)(C)O)O)O 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aS,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 11897956 Click to see 456.70 unknown via CMAUP database
(3S,5S,6S,8R,9S,10R,13S,14S,16S,17R)-16-[(2S,5R)-2,5-dimethyloxan-2-yl]oxy-17-ethyl-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6-diol 52931478 Click to see 448.70 unknown via CMAUP database
[(3R,4aR,6aR,6bR,8aR,11S,12S,12aS,14aS,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 162999321 Click to see 468.80 unknown https://doi.org/10.1515/ZNC-2001-1-203
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
Npc112866 49867939 Click to see 456.70 unknown via CMAUP database
Npc62469 49867942 Click to see 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Cycloart-23-ene-3beta,25-diol 5470009 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown via CMAUP database
> 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/10.1515/ZNC-2001-1-203
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
[(2R)-2-[[[(2S)-2-benzamido-3-phenylpropanoyl]amino]methyl]-3-phenylpropyl] acetate 5321123 Click to see 458.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
6-Butoxycarbonyl-1-methylcyclohexa-2,4-diene-1-carboxylic acid 163192424 Click to see CCCCOC(=O)C1C=CC=CC1(C)C(=O)O 238.28 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4S,5S)-3-((E)-3-(3,4-Dihydroxyphenyl)Acryloyloxy)-1,4,5-Trihydroxycyclohexanecarboxylic Acid 12310830 Click to see 354.31 unknown via CMAUP database
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1515/ZNC-2001-1-203
Isochlorogensaure 12310829 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1515/ZNC-2001-1-203
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
6-O-galloyl arbutin 3083924 Click to see 424.40 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole 70259 Click to see 96.13 unknown via CMAUP database
4-Methylimidazole 13195 Click to see 82.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1S,12R,13R,20S)-13,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10831417 Click to see 346.30 unknown via CMAUP database
(1S,12R,13S,20S)-13-hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10496772 Click to see 332.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Organoheterocyclic compounds / Coumarans
Kushecarpin A 10495761 Click to see 318.32 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
(-)-Sophoramine 169014 Click to see 244.33 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
5,11-dimethyl-6H-pyrido[4,3-b]carbazol-2-ium 5288156 Click to see CC1=C2C=C[NH+]=CC2=C(C3=C1NC4=CC=CC=C43)C 247.31 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 6920044 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Kuraramine 46187187 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
6-[(3R,5R)-5-(hydroxymethyl)-1-methylpiperidin-3-yl]-1H-pyridin-2-one 101665417 Click to see 222.28 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives
1-(6,8-Dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbutane-2,3-diol 5320308 Click to see 335.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolizidines
(21,22-Dihydroxy-5,8-dimethoxy-24-azapentacyclo[14.7.1.12,6.17,11.020,24]hexacosa-2(26),3,5,7,9,11(25)-hexaen-14-yl) acetate 5319142 Click to see 495.60 unknown via CMAUP database
(22-Acetyloxy-5,8-dimethoxy-24-azapentacyclo[14.7.1.12,6.17,11.020,24]hexacosa-2(26),3,5,7,9,11(25)-hexaen-14-yl) acetate 5319140 Click to see 521.60 unknown via CMAUP database
(22-Hydroxy-5,8-dimethoxy-24-azapentacyclo[14.7.1.12,6.17,11.020,24]hexacosa-2(26),3,5,7,9,11(25)-hexaen-14-yl) acetate 5319139 Click to see 479.60 unknown via CMAUP database
[(1R,14R,16S,20S,21S,22R)-21,22-diacetyloxy-5,8-dimethoxy-24-azapentacyclo[14.7.1.12,6.17,11.020,24]hexacosa-2(26),3,5,7,9,11(25)-hexaen-14-yl] acetate 12312593 Click to see 579.70 unknown via CMAUP database
[(1R,14R,16S,22S)-22-acetyloxy-21-hydroxy-5,8-dimethoxy-24-azapentacyclo[14.7.1.12,6.17,11.020,24]hexacosa-2(26),3,5,7,9,11(25)-hexaen-14-yl] acetate 5319148 Click to see 537.60 unknown via CMAUP database
[(1R,14R,16S)-21-acetyloxy-14-hydroxy-5,8-dimethoxy-24-azapentacyclo[14.7.1.12,6.17,11.020,24]hexacosa-2(26),3,5,7,9,11(25)-hexaen-22-yl] acetate 5319147 Click to see 537.60 unknown via CMAUP database
Lythrancepine I 5319138 Click to see COC1=C2C=C(CCC(CC3CCCC4N3C(CC(C4)O)C5=CC2=C(C=C5)OC)O)C=C1 437.60 unknown via CMAUP database
Lythrancine I 5319141 Click to see 453.60 unknown via CMAUP database
Lythrancine IV 6398554 Click to see 579.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran 15953774 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C 338.40 unknown via CMAUP database
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran 44260109 Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown via CMAUP database
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1515/ZNC-2001-1-203
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1515/ZNC-2001-1-203
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Peucedanin 8616 Click to see 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone 118975901 Click to see 424.50 unknown via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one 38351420 Click to see 370.40 unknown via CMAUP database
Kushenol V 10572194 Click to see 386.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-3,5-dihydroxy-2-(7-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 11351168 Click to see 440.50 unknown via CMAUP database
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one 102004822 Click to see 454.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one 44563159 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 442.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 6565899 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 26209050 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
(2S)-2'-methoxykurarinone 11982641 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14258999 Click to see 370.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one 44563122 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O 426.50 unknown via CMAUP database
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 60039901 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-Euchrenone A7 44593508 Click to see 340.40 unknown via CMAUP database
(2S)-Isoxanthohumol 9928523 Click to see 354.40 unknown via CMAUP database
CID 102004745 102004745 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C 492.60 unknown via CMAUP database
Isobavachin 193679 Click to see 324.40 unknown via CMAUP database
Kurarinol 44563198 Click to see 456.50 unknown via CMAUP database
Kurarinone 11982640 Click to see 438.50 unknown via CMAUP database
Kushenol A 44563121 Click to see 408.50 unknown via CMAUP database
Kushenol E 127234 Click to see 424.50 unknown via CMAUP database
Kushenol H 44584091 Click to see 472.50 unknown via CMAUP database
Kushenol I 20832634 Click to see 454.50 unknown via CMAUP database
Kushenol L 21721878 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C 440.50 unknown via CMAUP database
Kushenol M 180948 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C 508.60 unknown via CMAUP database
Kushenol R 42607847 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 422.50 unknown via CMAUP database
Kushenol S 10854625 Click to see 340.40 unknown via CMAUP database
Kushenol U 42608062 Click to see 422.50 unknown via CMAUP database
KushenolK 44428630 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O 472.50 unknown via CMAUP database
Leachianone A 44593449 Click to see 438.50 unknown via CMAUP database
Leachianone G 5275227 Click to see 356.40 unknown via CMAUP database
Sophoraflavanone B 480764 Click to see 340.40 unknown via CMAUP database
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Apigenin-7-olate 25200950 Click to see 269.23 unknown via CMAUP database
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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Licoflavonol 5481964 Click to see 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
3-Hydroxy-2-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 11451469 Click to see 368.40 unknown via CMAUP database
5-Hydroxy-4-(4-hydroxyphenyl)-10,10,16,16-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,4,7,13-tetraen-6-one 11327657 Click to see 422.50 unknown via CMAUP database
8-Prenylkaempferol 5318624 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
Isoanhydroicaritin 5322079 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C 368.40 unknown via CMAUP database
Kushenol C 5481237 Click to see 438.50 unknown via CMAUP database
Kushenol G 44259516 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O 456.50 unknown via CMAUP database
Sophoflavescenol 9929189 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Malvin 441765 Click to see 655.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see 448.40 unknown https://doi.org/10.1515/ZNC-2001-1-203
https://doi.org/10.1016/J.FITOTE.2005.04.011
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1515/ZNC-2001-1-203
https://doi.org/10.1016/J.FITOTE.2005.04.011
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
8-beta-D-Glucopyranosyl-3',4',5,7-tetrahydroxyflavone 44257907 Click to see 448.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1515/ZNC-2001-1-203
https://doi.org/10.1016/J.FITOTE.2005.04.011
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1515/ZNC-2001-1-203
https://doi.org/10.1016/J.FITOTE.2005.04.011
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5459939 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 6121316 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11546834 Click to see 448.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14017874 Click to see 448.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5318902 Click to see 562.50 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13988639 Click to see 464.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 6420079 Click to see 448.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 6169038 Click to see 448.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
Hypolaetin-8-glucoside 5318255 Click to see 464.40 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown via CMAUP database
(-)-Maackiain-3-O-glucosyl-6''-O-malonate 23724669 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6 532.40 unknown via CMAUP database
(+)-Maackiain 161298 Click to see 284.26 unknown via CMAUP database
(+)-Medicarpin 73067 Click to see 270.28 unknown via CMAUP database
(1S,12S)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene 373519 Click to see 298.29 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol 6326060 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol 361910 Click to see 286.28 unknown via CMAUP database
(6aR,11aR)-3,9-Dimethoxy-6H-benzofuro(3,2-c)(1)benzopyran-6a(11aH)-ol 442828 Click to see 300.30 unknown via CMAUP database
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 21676223 Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown via CMAUP database
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see 284.26 unknown via CMAUP database
CID 44428627 44428627 Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O 300.30 unknown via CMAUP database
Pterocarpin 1715306 Click to see 298.29 unknown via CMAUP database
Trifolirhizin 442827 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone 5284648 Click to see 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-5,7-dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101238023 Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 384.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)chromen-4-one 101238024 Click to see 382.40 unknown via CMAUP database
Alpinumisoflavone 5490139 Click to see 336.30 unknown via CMAUP database
Lupalbigenin 10001388 Click to see 406.50 unknown via CMAUP database
Luteone 5281797 Click to see 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 102131643 Click to see 576.50 unknown via CMAUP database
3-(3,4-Dihydroxyphenyl)-7-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl) oxy)-4h-chromen-4-one 68607439 Click to see 432.40 unknown via CMAUP database
3-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 73603979 Click to see 578.50 unknown via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131642 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown via CMAUP database
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one 73603978 Click to see 578.50 unknown via CMAUP database
Calycosin 7-O-xylosylglucoside 73603980 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside 20055730 Click to see 548.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see 284.26 unknown via CMAUP database
Koparin 5318834 Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A 5280373 Click to see 284.26 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridin 44428631 Click to see 438.50 unknown via CMAUP database
Xanthohumol 639665 Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
Scabrolide E 11187132 Click to see 348.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
1-(3-hydroxy-4-methoxyphenyl)-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]ethane-1,2-dione 73603972 Click to see 582.50 unknown via CMAUP database
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxyphenyl]-2-(3-hydroxy-4-methoxyphenyl)ethane-1,2-dione 73603983 Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O 582.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1S,2R,20S,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-hexadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 163193900 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 934.60 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
(2R,42R,46R)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-Hexadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 5458626 Click to see 934.60 unknown https://doi.org/10.1515/ZNC-2001-1-203
https://doi.org/10.1016/J.FITOTE.2005.04.011
Castalagin 12302513 Click to see 934.60 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
https://doi.org/10.1515/ZNC-2001-1-203
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1515/ZNC-2001-1-203
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1515/ZNC-2001-1-203
Valoneic acid dilactone 10151874 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)OC5=C(C(=C(C=C5C(=O)O)O)O)O 470.30 unknown https://doi.org/10.1515/ZNC-2001-1-203
Vescalagin 168165 Click to see 934.60 unknown https://doi.org/10.1016/J.FITOTE.2005.04.011
https://doi.org/10.1515/ZNC-2001-1-203

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