Details Top

Internal ID UUID64400ce460be7958954222
Scientific name Berberis thunbergii
Authority DC.
First published in Syst. Nat. 2: 9 (1821)

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.

Berberis thunbergii, commonly called Japanese barberry, has a recorded medicinal tradition that hinges on infusions and decoctions of its leaves, bark, and roots. In northwestern Iran, Amiri and Joharchi (2013) reported that a bark or root decoction is taken for colic and stomach upset, while women in Hamedan use the root in a decoction to control abdominal pain, and apply leaf infusions topically to minor cuts and inflamed gums. Across the northern Indian subcontinent, Jaiswal et al. (2017) noted the use of leaves and bark in decoctions for fevers and jaundice and, in some communities, as a mild tea for digestive complaints. In Georgia, the Caucasus, Gagnidze (2003) recorded an external infusion of the leaves used as a wash for wounds and eye irritation. A macerated preparation of the bark is used in Iran as a tonic and for dyspepsia (Belaiche, 1985), and leaves are traditionally infused as a mild digestive tea (Moerman, 1998).

A concise recipe for a mild leaf tea is as follows. Use 1–2 grams of dried leaves per 250 milliliters of water; bring the water to a rolling boil, remove from heat, add the leaves, cover, and steep for 10 minutes; strain, then sip 1 cup, no more than twice daily. For a 1:5 tincture by weight-to-volume, macerate 20 grams of powdered dried leaves in 100 milliliters of 45% ethanol (or higher) for 2–3 weeks with daily shaking; strain and store in a cool, dark place. Do not combine with hepatotoxic herbs; avoid during pregnancy and lactation; discontinue if abdominal cramping or dizziness occurs and seek medical advice if fever persists or blood or pus appears in urine. Children should not use it, and adults with chronic liver disease or on medications—especially antibiotics, antihistamines, or antihypertensives—should consult a physician.

The species is chemically characterized by isoquinoline alkaloids, notably berberine, berbamine, jatrorrhizine, palmatine, and columbamine, alongside small amounts of volatile constituents that account for its bitterness and yellow coloration (Ghoshal et al., 1966; Boehm et al., 2018). These alkaloids explain the plant’s long-standing use as a bitter tonic for digestion and as a wash in external preparations, with astringent effects tied to phenolic acids such as gallic and caffeic derivatives reported in recent chemical surveys (Gassesse et al., 2018). Phototoxicity noted for European barberry is not well documented for B. thunbergii, yet topical use in bright sunlight should be cautious.

Although Berberis thunbergii is primarily cultivated as an ornamental, small-scale commercial products—especially standardized extracts rich in berberine—continue to appear on international markets, and selected preparations remain in local household use where documented.

General Uses Top

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Common products:
Live plants of Berberis thunbergii are produced by nurseries for the ornamental‑landscape trade. Shrubs are sold as hedging, border, ground‑cover, and specimen plants, often in cultivars with purple‑red foliage (e.g., ‘Atropurpurea’) or yellow leaves (e.g., ‘Aurea’). The ripe, glossy red berries are harvested from cultivated plants for culinary processing.

Industrial and craft applications:
The species is used in the bonsai hobby. Small‑scale growers train young shrubs into living bonsai specimens because of their compact habit, fine branching, and vivid autumn colour. The wood of mature stems, though of limited size, is dense and hard (typical specific gravity ~0.85 g cm⁻³) and is occasionally turned for small craft items such as handles, dowels, and decorative carvings.

Food and beverages (non‑medicinal):
The berries are edible and are processed into jams, jellies, chutneys, sauces, or used as a garnish on salads and desserts. Their tartness and high acidity make them suitable for preserving and for flavouring vinegar‑based sauces. Although not a primary commercial beverage source, the fruit can be used as a flavoring in small‑batch liqueurs or alcoholic mixtures.

Wood and fiber:
The shrub’s wood is too small for structural timber but is valued in woodworking for its density and fine grain. Fibers from the bark are not of commercial significance, and the plant is not used for pulp or paper production.

Properties relevant to use:
- Wood: high lignin content (~28 % of dry weight) contributes to hardness and durability suitable for small turned objects.
- Fruit: high anthocyanin concentration (principally cyanidin‑3‑glucoside) imparts a deep red colour, useful in natural dyes, and the berries have a high soluble‑solid content (≈12–15 % Brix) that facilitates jam production.
- Bark/roots: contain the alkaloid berberine, a yellow‑orange dye precursor that has been historically employed as a natural colourant for textiles.

Standards and regulation:
In the United States, B. thunbergii is listed as an invasive or noxious weed by several state agencies, leading to restrictions on its cultivation and sale in those jurisdictions. The plant is subject to USDA/APHIS import controls for horticultural material. Fruit intended for food use falls under general food‑safety regulations (e.g., FDA 21 CFR) as an unprocessed food, with no specific food‑colour additive standards beyond standard good‑manufacturing practices.

Sustainability and sourcing:
Commercial supply is derived almost entirely from cultivated nursery stock. Wild populations are often targeted for removal to mitigate invasive spread; berries harvested for food are therefore sourced from managed or cultivated plantings to avoid encouraging the plant’s naturalisation. Sustainable nursery practices—such as propagation from disease‑free stock and controlled field sites—are encouraged to maintain a reliable ornamental supply while limiting ecological impact.

Synonyms Top

Scientific name Authority First published in
Berberis thunbergii var. argenteomarginata C.K.Schneid. J. Arnold Arbor. 4: 221 1923
Berberis thunbergii var. atropurpurea Chenault Rev. Hort. n.s., 20: 307 1926
Berberis thunbergii f. erecta Rehder J. Arnold Arbor. 20: 412 1939
Berberis thunbergii var. erecta (Rehder) Ahrendt J. Linn. Soc., Bot. 57: 168 1961
Berberis thunbergii var. maximowiczii (Regel) Regel Trudy Glavn. Bot. Sada 2: 420 1878
Berberis thunbergii var. minor Rehder Mitt. Deutsch. Dendrol. Ges. 7: 330 1898
Berberis thunbergii var. pluriflora Koehne Deut. Dendrol. 169 1893
Berberis thunbergii var. rubrifolia Ahrendt J. Linn. Soc., Bot. 57: 168 1961
Berberis thunbergii var. uniflora Koehne Deut. Dendrol. 169 1893
Berberis thunbergii f. microcarpa E.L.Wolf ex V.V.Byalt, L.V.Orlova & Potokin Skvortsovia 5(4): 24. 2020
Berberis thunbergii f. grandiflora E.L.Wolf ex V.V.Byalt, L.V.Orlova & Potokin Skvortsovia 5(4): 23 (2020)
Berberis thunbergii f. obovata E.L.Wolf ex V.V.Byalt, L.V.Orlova & Potokin Skvortsovia 5(4): 24 (2020)
Berberis thunbergii f. trispinosa E.L.Wolf ex V.V.Byalt, L.V.Orlova & Potokin Skvortsovia 5(4): 24 (2020)
Berberis thunbergii f. atropurpurea (Chenault) Rehder Bibliogr. Cult. Trees : 173 (1949)
Berberis thunbergii f. minor (Rehder) Zabel Handb. Laubholzben. : 114 (1903)
Berberis thunbergii var. pluriflora (Koehne) Rehder Cycl. Amer. Hort. 1: 154 (1900)

Common names Top

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Language Common/alternative name
English thunberg's barberry
English red barberry
English japanese barberry
Belarusian барбарыс Тунберга
Czech dřišťál thunbergův
Welsh pren melyn thunberg
Danish hæk-berberis
Danish thunbergs berberis
German thunberg-berberitze
German thunbergs berberitze
German grüne hecken-berberitze
Estonian thunbergi kukerpuu
Persian زرشک زینتی
Finnish japaninhappomarja
French berbéris de thunberg
French Épine-vinette de thunberg
French epine-vinette de thunberg
Croatian thumbergova žutika
Upper Sorbian thunbergowa kisyca
Icelandic sólbroddur
Japanese メギ
Norwegian Bokmål blodberberis
Norwegian Bokmål høstberberis
Norwegian Bokmål japanberberis
Dutch japanse berberis
Norwegian Nynorsk høstberberis
Norwegian Nynorsk haustberberis
Norwegian Nynorsk japanberberis
Norwegian Nynorsk blodberberis
Polish berberys thunberga
Russian Барбарис Тунберга
Slovak dráč thunbergov
Slovenian thunbergov češmin
Serbian Тумбергова жутика
Swedish häckberberis
Ukrainian барбарис Тунберґа
Chinese 红叶小檗
Chinese 日本小檗
Chinese 一颗针

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Start at 4°C for 3 months, then warm to 20°C for another 3 months.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.
wash clean 14 days, plant 2 cm deep

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Uzbekistan
  • Europe
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Romania
      • Yugoslavia
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Prince Edward Island
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Wyoming
    • Southeastern U.S.A.
      • Delaware
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000563924
UNII 5STN1S9S4B
Flora of Alabama 5279
Cornell Woody Plants 31
Canadensys 3666
USDA Plants BETH
UConn 58
Tropicos 3500183
INPN 85773
Flora of Italy 9272
KEW urn:lsid:ipni.org:names:107136-1
The Plant List kew-2674513
Missouri Botanical Garden 277781
PFAF Berberis thunbergii
PaleoBotany 88052
Open Tree Of Life 1072153
Observations.org 6460
NCBI Taxonomy 121720
NBN Atlas NBNSYS0000004966
Nature Serve 2.134460
IPNI 107136-1
iNaturalist 58727
GBIF 3033896
Freebase /m/0cgsn1
WisFlora 2729
FEIS plants/shrub/berthu
EPPO BEBTH
EOL 596554
Elurikkus 3078
USDA GRIN 6974
Wikipedia Berberis_thunbergii
CMAUP NPO18832

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_056149445.1 Berberis_FinalAssembly_HiC_14CHR.fasta Chromosome University of New Hampshire 2026-03-19 104.84 1.14 Gb

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
Comprehensive evaluation and application of woody plants in the green spaces of parks in saline–Alkaline areas from a low-carbon perspective: A case study of Tianjin Qiaoyuan Park Bai J, Wang H PLoS One 10-May-2024
PMCID:PMC11086879
doi:10.1371/journal.pone.0303341
PMID:38728347
Changes in the nutrients, phytochemical profile and antioxidant activity of Rheum officinale Baill. leaf blades during different growth periods Dai L, Miao X, Ma Y, Yang X, Li B, He J, Wang Y, Dong P, Zhang J, Shang X Front Nutr 17-Apr-2024
PMCID:PMC11061479
doi:10.3389/fnut.2024.1387947
PMID:38694224
Ectoparasites of wild rodents in forest sites invaded and uninvaded by Maesopsis eminii in Amani nature forest reserve, Tanzania Musese LJ, Kitegile AS, Kilawe CJ Int J Parasitol Parasites Wildl 31-Mar-2024
PMCID:PMC11002661
doi:10.1016/j.ijppaw.2024.100932
PMID:38601057
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
In Vitro and In Silico of Cholinesterases Inhibition and In Vitro and In Vivo Anti-Melanoma Activity Investigations of Extracts Obtained from Selected Berberis Species Tuzimski T, Petruczynik A, Kaproń B, Plech T, Makuch-Kocka A, Janiszewska D, Sugajski M, Buszewski B, Szultka-Młyńska M Molecules 28-Feb-2024
PMCID:PMC10933966
doi:10.3390/molecules29051048
PMID:38474561
Phytotoxicity effect of a highly toxic isolate of Alternaria alternata metabolites from Iran Sedighi A, Mohammadi A Toxicon X 15-Feb-2024
PMCID:PMC10878783
doi:10.1016/j.toxcx.2024.100186
PMID:38380155
Pest categorisation of Malacosoma parallela Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Gobbi A, Kertesz V, Maiorano A, MacLeod A EFSA J 22-Jan-2024
PMCID:PMC10801436
doi:10.2903/j.efsa.2024.8549
PMID:38260770
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Radio Telemetry and Harmonic Radar Tracking of the Spotted Lanternfly, Lycorma delicatula (White) (Hemiptera: Fulgoridae) Siderhurst MS, Murman KM, Kaye KT, Wallace MS, Cooperband MF Insects 30-Dec-2023
PMCID:PMC10816356
doi:10.3390/insects15010017
PMID:38249023
Recent Applications of Protoberberines as Privileged Starting Materials for the Development of Novel Broad-Spectrum Antiviral Agents: A Concise Review (2017–2023) Valipour M, Zakeri Khatir Z, Abdollahi E, Ayati A ACS Pharmacol Transl Sci 28-Dec-2023
PMCID:PMC10789142
doi:10.1021/acsptsci.3c00292
PMID:38230282
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia Zahradníková E, Rendeková A, Ščevková J Environ Sci Pollut Res Int 05-Dec-2023
PMCID:PMC10791852
doi:10.1007/s11356-023-31137-9
PMID:38052730
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122

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 / Aporphines
(+)-Glaucine 16754 Click to see 355.40 unknown https://doi.org/10.1007/BF02254817
(+)-Isocorydine 10143 Click to see 341.40 unknown https://doi.org/10.1007/BF02254817
(+)-Magnoflorine 73337 Click to see 342.40 unknown via CMAUP database
(6aR)-2,11-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 739273 Click to see 311.40 unknown via CMAUP database
(6As)-2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 6992288 Click to see 341.40 unknown https://doi.org/10.1007/BF02254817
Artabotrine 48704 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://doi.org/10.1007/BF02254817
Magnoflorine iodide, (+)-(RG) 131664584 Click to see 469.30 unknown via CMAUP database
Thaliporphine 100020 Click to see 341.40 unknown https://doi.org/10.1007/BF02254817
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16,17-Dimethoxy-6-tritio-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene 10246509 Click to see 338.40 unknown via CMAUP database
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1007/BF02254817
Columbamine 72310 Click to see 338.40 unknown via CMAUP database
Jatrorrhizine 72323 Click to see 338.40 unknown via CMAUP database
Jatrorrhizine iodide 5459338 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.[I-] 465.30 unknown via CMAUP database
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1007/BF02254817
https://doi.org/10.1080/13880200390500768
> Benzenoids / Anthracenes
Palmidin A 5320384 Click to see 510.50 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Javanicin 10149 Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(C2=O)OC)O)CC(=O)C 290.27 unknown via CMAUP database
> Lignans, neolignans and related compounds
(-)-Repandine 10031631 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
1-Isotetrandrine 5351212 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1007/BF02254817
20,21,25-Trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo(22.6.2.23,6.18,12.114,18.027,31.022,33)hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-9-ol 10170 Click to see 608.70 unknown https://doi.org/10.1007/BF02254817
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1007/BF02254817
CID 12300053 12300053 Click to see 608.70 unknown https://doi.org/10.1007/BF02254817
https://doi.org/10.1080/13880200390500768
Isosinomenine A 5422 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
Oxyacanthine 442333 Click to see 608.70 unknown https://doi.org/10.1248/YAKUSHI1881.50.4_309
https://doi.org/10.1007/BF02254817
https://doi.org/10.1002/ARDP.19302680802
https://doi.org/10.1080/13880200390500768
Oxycanthine 371257 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown https://doi.org/10.1007/BF02254817
https://doi.org/10.1002/ARDP.19302680802
https://doi.org/10.1248/YAKUSHI1881.50.4_309
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Excisanin H 10066342 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1007/BF02254817
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3As,6R,6Ar,9R,9As,9Bs)-6,9-Dihydroxy-6,9-Dimethyl-3-Methylenedecahydroazuleno(4,5-B)Furan-2(9Bh)-One 5319198 Click to see 266.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(2R,4S,4aR)-1,4,4a,7-tetramethyl-2,3,4,5,8,9-hexahydrobenzo[7]annulen-2-ol 23426773 Click to see 220.35 unknown via CMAUP database
(2S,4S,4aR)-1,4,4a,7-tetramethyl-2,3,4,5,8,9-hexahydrobenzo[7]annulen-2-ol 23426772 Click to see 220.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
21,22,26-Trimethoxy-16,31-dimethyl-8,24-dioxa-16,31-diazaheptacyclo[23.6.2.13,7.19,13.115,19.028,32.023,34]hexatriaconta-3(36),4,6,9,11,13(35),19,21,23(34),25,27,32-dodecaen-10-ol 45356938 Click to see 608.70 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see 337.40 unknown https://doi.org/10.1080/13880200390500768
> Organoheterocyclic compounds / Tetrahydroisoquinolines
6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinoline 15623 Click to see 193.24 unknown https://doi.org/10.1007/BF02254817
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
[1-Methyl-1-(2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl)ethyl] 2-methylbut-2-enoate 53399217 Click to see 328.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Oxyayanin A 5281676 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3O)OC)O)O 360.30 unknown via CMAUP database

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