Berberis vulgaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Berberis vulgaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64400ce9680b8914258221
Scientific name Berberis vulgaris
Authority L.
First published in Sp. Pl. : 330 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Berberis vulgaris var. asperma Willd. Berlin. Baumz. : 34 (1796)
Berberis vulgaris var. rubra Willd. Berlin. Baumz. : 34 (1796)
Berberis abortiva P.Renault Fl. Orne : 179 (1804)
Berberis acida Gilib. Exerc. Phyt. 1: 284. 1792
Berberis aethnensis Bourg. ex Willk. & Lange Prodr. Fl. Hispan. 3: 901 (1880)
Berberis alba Poit. & Turpin Traité Arbr. Fruit. , ed. 3, 2: t. 52 (1808)
Berberis angulizans hort. ex Handl. Trees Kew Pt. i. [Polypet.] (1894) 27.
Berberis apyrena hort. ex K.Koch Dendrologie 1: 395 (1869)
Berberis arborescens hort. ex K.Koch Dendrologie 1: 393 (1869)
Berberis articulata Loisel. Dict. Sci. Nat. 6: 218 (1806)
Berberis asperma Poit & Turpin Traité Arbr. Arbust. , re-issue 4: 12 (1825)
Berberis aurea Tausch Flora 17: 495 (1834)
Berberis bigelovii Schrad. Linnaea 12: 362 (1838)
Berberis corallina hort. ex Handl. Trees Kew Pt. i. [Polypet.] (1894) 27.
Berberis dentata Tausch Flora 21: 729 (1838)
Berberis dulcis hort. ex K.Koch Dendrologie 1: 395. 1869 [Jan 1869]
Berberis dumetorum Gouan Fl. Monsp. : 312 (1765)
Berberis edulis hort. ex K.Koch Dendrologie 1: 395 (1869)
Berberis elongata hort. ex Handl. Trees Kew Pt. i. [Polypet.] (1894) 27.
Berberis globularis hort. ex Lavallée Énum. Arbres 13, nomen. 1877
Berberis hakodate hort. ex Dippel Handb. Laubholzk. 3: 117 (1893)
Berberis heterophylla hort. ex K.Koch Dendrologie 1: 395. 1869 [Jan 1869]
Berberis innominata Kielm. Dec. Pl. Horti Tuebing. : 18 (1814)
Berberis irritabilis Salisb. Prodr. Stirp. Chap. Allerton : 213 (1796)
Berberis jacquinii hort. ex K.Koch Dendrologie 1: 394 (1869)
Berberis latifolia Poit. & Turpin Pomol. Franç. 2: t. 60. 1846
Berberis marginata hort. ex K.Koch Dendrologie 1: 394 (1869)
Berberis maxima hort. ex Handl. Trees Kew Pt. i. [Polypet.] (1894) 27.
Berberis maximowiczii Regel Gartenflora 21: 238 (1872)
Berberis microphylla F.Dietr. Vollst. Lex. Gärtn. ii. 184.
Berberis mitis Schrad. Linnaea 10(Litt.): 69 (1836)
Berberis nepalensis hort. ex K.Koch Dendrologie 1: 393 (1869)
Berberis nitens Schrad. Linnaea 12: 382 (1838)
Berberis obovata Schrad. Linnaea 12: 385 (1838)
Berberis orientalis Schneider Bull. Herb. Boissier , sér. 2, 5: 666 (1905)
Berberis pangharengensis hort. ex Handl. Trees Kew Pt. i. [Polypet.] (1894) 29.
Berberis pauciflora Salisb. Prodr. Stirp. Chap. Allerton : 213 (1796)
Berberis racemosa Stokes Bot. Mat. Med. ii. 296. 1812
Berberis rubra Poit. & Turpin Traité Arbr. Fruit. , nouv. éd., 4: 12 (1830)
Berberis sanguinea hort. ex K.Koch Dendrologie 1: 394. 1869 [Jan 1869]
Berberis sanguinolenta hort. ex K.Koch Dendrologie 1: 394 (1869)
Berberis sibirica hort. ex Schult.f. Syst. Veg., ed. 15 bis 7: 2 (1829)
Berberis sieboldii hort. ex Dippel Handb. Laubholzk. 3: 117 (1893)
Berberis sulcata K.Koch & C.D.Bouché App. Gen. Sp. Nov. : 13 (1854)
Berberis sylvestris Poit. & Turpin Pomol. Franç. 2: t. 15 (1873)
Berberis violacea Poit. & Turpin Traité Arbr. Fruit. , nouv. éd., 4: 12 (1830)
Berberis vulgaris var. acutifolia (Prantl) C.K.Schneid.
Berberis vulgaris var. alba DC. Syst. Nat. [Candolle] 2: 6 (-7). 1821 [late May 1821]
Berberis vulgaris var. alpestris Rikli
Berberis vulgaris var. apyrena Schrad. Linnaea 12: 364 1838
Berberis vulgaris subsp. cantabrica Rivas Mart., T.E.Díaz, Fern.Prieto, Loidi & Penas Vegetacion Picos de Europa 257 (1984).
Berberis vulgaris var. flava Schrad. Linnaea 12: 364 1838
Berberis vulgaris var. lutea DC. Syst. Nat. 2: 6 (1821)
Berberis vulgaris var. nigra DC. Syst. Nat. 2: 6 (1821)
Berberis vulgaris var. orientalis (C.K.Schneid.) Grossh. Fl. Kavkaza 4: 81 1950
Berberis vulgaris subsp. orientalis (Schneid.) Takht. Fl. Erevana : 60 (1972)
Berberis vulgaris var. purpurea DC. Syst. Nat. 2: 6 (1821)
Berberis vulgaris var. purpurifolia Ahrendt J. Linn. Soc., Bot. 57: 189 1961
Berberis vulgaris var. sanguinea Schrad. Linnaea 12: 364 1838
Berberis vulgaris var. serotina Schrad. Linnaea 12: 364 1838
Berberis vulgaris var. sulcata Ahrendt J. Linn. Soc., Bot. 57: 188 1961
Berberis vulgaris var. violacea Willd. Berlin. Baumz. : 34 (1796)
Berberis dentata var. capitata Tausch Flora 21: 729 1838
Berberis vulgaris var. orientalis Papava
Berberis vulgaris var. innominata Schult.f. Syst. Veg., ed. 15 bis 7: 2 (1829)
Berberis vulgaris var. ilicifolia Schult.f. Syst. Veg., ed. 15 bis 7: 2 (1829)

Common names Top

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Language Common/alternative name
English barberry
English common barberry
English european barberry
Spanish agraciu
Spanish agranzón
Spanish agrazón
Spanish agreilla
Spanish agrito
Spanish agruzejo
Spanish alargiz
Spanish alarguez
Spanish alarguiz
Spanish alguese
Spanish alrera
Spanish alro
Spanish arlera
Spanish arlo
Spanish aspalato
Spanish azota-cristos
Spanish azote burdo
Spanish berberiles
Spanish berberís
Spanish bérberis
Spanish berbero
Spanish bérbero
Spanish bérberoles
Spanish bérberos
Spanish borrachín
Spanish escabrión
Spanish espina ramosa
Spanish espina romaza
Spanish espino
Spanish espino berberino
Spanish espino cambrón
Spanish garbanzón
Spanish guindillas ásperas
Spanish tapaculo
Spanish vinagrera
Spanish vinagreras
Spanish granado
Spanish abrilla
Spanish acetín
Spanish agracejo
Spanish agracejo oficinal
Spanish agracillo
Spanish agracillos
Spanish agracio
Arabic شجيرة البرباريس
Arabic عقدة
Arabic عود الريح
Arabic انبرباريس
Azerbaijani adi zirinc
azb عادی زیرینج
Belarusian Барбарыс звычайны
Bulgarian обикновен кисел трън
Catalan coralet
Catalan epine-vinette
Czech dřišťál obecný
Welsh pren melyn
Danish almindelig berberis
German berberitze
German sauerdorn
German echte berberitze
German essigbeere
German gemeine berberitze, sauerdorn
German gemeiner sauerdorn
German gewöhnliche berberitze
German epine-vinette
German zitronenbeere
German hasenbrot
German basselbeere
German beiselbeere
German dreidorn
German erbsal
German erbselbeerstrauch
German erbseldorn
German erbselholz
German erbsich
German essigdorn
German essigscharf
German geißenlaub
German gemeine berberitze
German kuckucksbrot
German peisselbeere
German spießdorn
German spitzdorn
German weinäuglein
German weinlegelein
German weinscheidling
German weinzäpferl
Greek Βερβερίς η κοινή
Greek Ευρωπαϊκή οξυάκανθα
Esperanto ordinara berberiso
Estonian harilik kukerpuu
Estonian kukerpuu
Persian زرشک خوراکی
Finnish ruostehappomarja
French Épine vinette
French epine-vinette
French Épine-vinette
French Épine-vinette vulgaire
Irish barbróg
Galician arleira
Galician berberiz
Manx barbrag
Croatian Šimširika
Croatian Žutika
Upper Sorbian Čerwjene kitki
Upper Sorbian kisałe jahodki
Upper Sorbian kisały ćerń
Upper Sorbian wšědna kisyca
Hungarian sóskaborbolya
Hungarian közönséges borbolya
Armenian ծորենի սովորական
Italian crespino comune
Italian crespino
Japanese セイヨウメギ
Georgian ჩვეულებრივი კოწახური
Kazakh Кәдімгі бөріқарақат
lld berberizia
Lithuanian paprastasis raugerškis
Lithuanian epine-vinette
Latvian parastā bārbele
Macedonian жолтика
Macedonian Кисел трн
Macedonian обична жолтика
Macedonian кисел трн
Norwegian Bokmål vanlig berberis
Dutch gewone zuurbes
Dutch zuurbes
Polish berberys pospolity
Polish berberys zwyczajny
Romanian dracilă
Russian Барбарис обыкновенный
Serbo-Croatian Žutika
Slovak dráč obyčajný
Slovenian navadni češmin
Serbian Шимширика
Serbian berberidis cortex
Serbian berberidis fructus
Serbian berberidis radix
Swedish surtorn
Swedish epine-vinette
Telugu ఎరుపుమణిచెట్టు
Turkish adi kadıntuzluğu
Turkish avrupa kadıntuzluğu
Turkish kızamık çalısı
tt Гади бүре карлыганы
Ukrainian Барбарис звичайний
Ukrainian Кислиця
Uzbek zirk
Uzbek qoraqand
vec grendene
Walloon bwès sint djuråd
Walloon bwès sint-djuråd
Chinese 刺小檗
Chinese 刺檗
Chinese 刺黄檗
Chinese 欧洲小檗

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Berberis vulgaris subsp. australis (Boiss.) Heywood Feddes Repert. Spec. Nov. Regni Veg. 64: 49. 1961 (1961)
Berberis vulgaris subsp. seroi O.Bolòs & Vigo Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38: 165 (1974)
Berberis vulgaris subsp. spryginii Tzvelev Fl. Vostochnoi Evropy 10: 201 (2001)

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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Maintain seeds at a constant 10°C.
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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Uzbekistan
    • Western Asia
      • Iran
      • Turkey
  • 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
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • 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
      • Washington
    • South-central U.S.A.
      • New Mexico
    • Southeastern U.S.A.
      • Delaware
      • Maryland
      • Virginia
    • Western Canada
      • British Columbia
      • Manitoba

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000564027
UNII 492B79913J
Canadensys 3667
USDA Plants BEVU
Tropicos 3500015
INPN 85774
Flora of Italy 1215
KEW urn:lsid:ipni.org:names:328527-2
The Plant List kew-2674612
PFAF Berberis vulgaris
Open Tree Of Life 996604
Observations.org 6461
NCBI Taxonomy 258209
NBN Atlas NBNSYS0000002752
Nature Serve 2.138856
IPNI 328527-2
iNaturalist 75758
GBIF 3033894
Freebase /m/0br81_
WisFlora 2730
FEIS plants/shrub/bervul
EPPO BEBVU
EOL 596556
Elurikkus 3079
Calflora (Californian flora) 10510
USDA GRIN 6992
Wikipedia Berberis_vulgaris

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_963556465.1 dmBerVulg1.1 Chromosome WELLCOME SANGER INSTITUTE 2023-10-17 28.0x 1.21 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
The influence of climate change on the future distribution of two Thymus species in Iran: MaxEnt model-based prediction Hosseini N, Ghorbanpour M, Mostafavi H BMC Plant Biol 11-Apr-2024
PMCID:PMC11007882
doi:10.1186/s12870-024-04965-1
PMID:38605338
Phytocompounds targeting epigenetic modulations: an assessment in cancer Khan A, Khan A, Khan MA, Malik Z, Massey S, Parveen R, Mustafa S, Shamsi A, Husain SA Front Pharmacol 26-Mar-2024
PMCID:PMC11002180
doi:10.3389/fphar.2023.1273993
PMID:38596245
In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM Am J Cancer Res 15-Mar-2024
PMCID:PMC10998760
doi:10.62347/AUHB5811
PMID:38590420
Bioassay-Guided Fractionation of Pittosporum angustifolium and Terminalia ferdinandiana with Liquid Chromatography Mass Spectroscopy and Gas Chromatography Mass Spectroscopy Exploratory Study Mani J, Johnson J, Hosking H, Schmidt L, Batley R, du Preez R, Broszczak D, Walsh K, Neilsen P, Naiker M Plants (Basel) 12-Mar-2024
PMCID:PMC10974205
doi:10.3390/plants13060807
PMID:38592847
Berberine modulates cardiovascular diseases as a multitarget-mediated alkaloid with insights into its downstream signals using in silico prospective screening approaches Almowallad S, Al-Massabi R Saudi J Biol Sci 11-Mar-2024
PMCID:PMC10951604
doi:10.1016/j.sjbs.2024.103977
PMID:38510527
Clinically Effective Molecules of Natural Origin for Obesity Prevention or Treatment Hidalgo-Lozada GM, Villarruel-López A, Nuño K, García-García A, Sánchez-Nuño YA, Ramos-García CO Int J Mol Sci 25-Feb-2024
PMCID:PMC10931663
doi:10.3390/ijms25052671
PMID:38473918
Phytochemicals and Their Usefulness in the Maintenance of Health Rodríguez-Negrete EV, Morales-González Á, Madrigal-Santillán EO, Sánchez-Reyes K, Álvarez-González I, Madrigal-Bujaidar E, Valadez-Vega C, Chamorro-Cevallos G, Garcia-Melo LF, Morales-González JA Plants (Basel) 15-Feb-2024
PMCID:PMC10892216
doi:10.3390/plants13040523
PMID:38498532
Exploring the Therapeutic Potential of Royal Jelly in Metabolic Disorders and Gastrointestinal Diseases El-Seedi HR, Salama S, El-Wahed AA, Guo Z, Di Minno A, Daglia M, Li C, Guan X, Buccato DG, Khalifa SA, Wang K Nutrients 29-Jan-2024
PMCID:PMC10856930
doi:10.3390/nu16030393
PMID:38337678
Physicochemical Properties of Nanoliposomes Encapsulating Grape Seed Tannins Formed with Ultrasound Cycles Monasterio A, Osorio FA Foods 27-Jan-2024
PMCID:PMC10855365
doi:10.3390/foods13030414
PMID:38338549
Therapeutic potential of berberine in attenuating cholestatic liver injury: insights from a PSC mouse model Wang Y, Zhao D, Su L, Tai YL, Way GW, Zeng J, Yan Q, Xu Y, Wang X, Gurley EC, Zhou XQ, Liu J, Liu J, Chen W, Hylemon PB, Zhou H Cell Biosci 25-Jan-2024
PMCID:PMC10809567
doi:10.1186/s13578-024-01195-8
PMID:38273376
The Antioxidant and Hepatoprotective Potential of Berberine and Silymarin on Acetaminophen Induced Toxicity in Cyprinus carpio L. Grădinariu L, Dediu L, Crețu M, Grecu IR, Docan A, Istrati DI, Dima FM, Stroe MD, Vizireanu C Animals (Basel) 24-Jan-2024
PMCID:PMC10854737
doi:10.3390/ani14030373
PMID:38338016
Research progress on antidepressant effects and mechanisms of berberine Gao Y, Nie K, Wang H, Dong H, Tang Y Front Pharmacol 22-Jan-2024
PMCID:PMC10839030
doi:10.3389/fphar.2024.1331440
PMID:38318145
Update of Natural Products and Their Derivatives Targeting Epstein–Barr Infection Pennisi R, Trischitta P, Costa M, Venuti A, Tamburello MP, Sciortino MT Viruses 15-Jan-2024
PMCID:PMC10818872
doi:10.3390/v16010124
PMID:38257824
Berberine-loaded polylactic acid nanofiber scaffold as a drug delivery system: The relationship between chemical characteristics, drug-release behavior, and antibacterial efficiency Le LT, Nguyen HT, Nguyen LT, Tran HQ, Nguyen TT Beilstein J Nanotechnol 12-Jan-2024
PMCID:PMC10790648
doi:10.3762/bjnano.15.7
PMID:38229677
A Mechanistic Review on How Berberine Use Combats Diabetes and Related Complications: Molecular, Cellular, and Metabolic Effects Askari VR, Khosravi K, Baradaran Rahimi V, Garzoli S Pharmaceuticals (Basel) 20-Dec-2023
PMCID:PMC10819502
doi:10.3390/ph17010007
PMID:38275993

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(6aS)-9-[3-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-2-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,10-diol 163048204 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1055/S-0028-1097869
2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 100020 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC 341.40 unknown https://doi.org/10.1007/BF01165220
9-[3-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-2-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,10-diol 163048203 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1055/S-0028-1097869
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://doi.org/10.1007/BF01165220
Magnoflorine 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
> Alkaloids and derivatives / Proaporphines
(2R,4R)-2'-[4-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohexa-2,5-diene]-1'-one 162977106 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C(=C4)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1055/S-0028-1097869
Pakistanamine 193238 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C(=C4)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1055/S-0028-1097869
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(14S)-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,15(20),16,18-heptaen-14-ol 162905761 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2O)OCO5)OC 353.40 unknown https://doi.org/10.1002/ARDP.18360560306
9,10-Dimethoxy-2,3-(methylenedioxy)-13,13a-didehydro-8-berbinol 24974 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2O)OCO5)OC 353.40 unknown https://doi.org/10.1002/ARDP.18360560306
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown https://doi.org/10.1135/CCCC19951034
https://doi.org/10.1016/S0192-0561(96)00047-1
https://doi.org/10.1007/BF01165220
https://doi.org/10.1016/S0031-9422(98)00121-6
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4016550/
https://doi.org/10.1080/13880200390500768
Columbamine 72310 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC 338.40 unknown https://doi.org/10.1016/S0021-9673(97)00804-2
https://doi.org/10.2307/4117899
Palmatine 19009 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC 352.40 unknown https://doi.org/10.1135/CCCC19951034
https://doi.org/10.1002/PTR.2399
https://doi.org/10.1016/S0021-9673(97)00804-2
https://doi.org/10.1016/S0031-9422(98)00121-6
https://doi.org/10.2307/4117899
> Lignans, neolignans and related compounds
1-Isotetrandrine 457825 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/10.1016/S0031-9422(98)00121-6
6,6'-Dimethoxy-2,2'-dimethylberbaman-7,12-diol 98409 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
6,6'-Dimethoxy-2,2'-dimethyloxyacanthan-7,12'-diol 122728 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)O)OC 594.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
6,6',7-Trimethoxy-2,2'-dimethylberbaman-12-ol 10170 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/10.1016/S0031-9422(98)00121-6
https://doi.org/10.1055/S-0028-1099540
6,6',7,12'-Tetramethoxy-2,2'-dimethyloxyacanthan 284692 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC 622.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
Aromoline 362574 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)O)OC 594.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
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/10.1016/S0031-9422(98)00121-6
https://doi.org/10.1080/13880200390500768
https://doi.org/10.1135/CCCC19951034
https://doi.org/10.1055/S-0028-1099540
https://doi.org/10.1007/BF01165220
Calafatimine 442184 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C(C(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=CC(=C(O3)C=C76)OC)C=C5)OC)OC)OC 636.70 unknown https://doi.org/10.1002/PTR.2399
Cannabisin G 10438919 Click to see COC1=C(C=CC(=C1)C=C(C(=CC2=CC(=C(C=C2)O)OC)C(=O)NCCC3=CC=C(C=C3)O)C(=O)NCCC4=CC=C(C=C4)O)O 624.70 unknown https://doi.org/10.1002/PTR.2443
CID 12300053 12300053 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/10.1016/S0031-9422(98)00121-6
https://doi.org/10.1135/CCCC19951034
https://doi.org/10.1007/BF01165220
https://doi.org/10.1023/B:CONC.0000033929.60336.BB
Isotetrandrine 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 https://doi.org/10.1016/S0031-9422(98)00121-6
Macolidine 5320261 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)O)OC 594.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
O-Methylberbamine 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/10.1016/S0031-9422(98)00121-6
Obaberine 100231 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC 622.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
Obamegine 441064 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
Oxyacanthine 442333 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/10.1016/S0031-9422(98)00121-6
https://doi.org/10.1016/S0192-0561(96)00047-1
https://doi.org/10.1135/CCCC19951034
https://doi.org/10.1002/PTR.2399
https://doi.org/10.1007/BF01165220
https://doi.org/10.1002/ARDP.18360560306
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/10.1016/S0031-9422(98)00121-6
https://doi.org/10.1002/ARDP.18360560306
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1002/PTR.2443
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1007/BF00579163
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1023/B:CONC.0000033929.60336.BB
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 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/10.1007/BF00579837
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/10.1007/BF00579837
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(1S,15R)-10,21,22,26-tetramethoxy-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-dodecaene 161604992 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=CC=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
> Organoheterocyclic compounds / Benzazepines
(3S)-3-hydroxy-7,8-dimethoxy-17,19-dioxa-11-azapentacyclo[12.7.0.03,11.04,9.016,20]henicosa-1(21),4(9),5,7,14,16(20)-hexaene-2,10-dione 14355601 Click to see COC1=C(C2=C(C=C1)C3(C(=O)C4=CC5=C(C=C4CCN3C2=O)OCO5)O)OC 383.40 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
12balpha-Hydroxy-5,6-dihydro-9,10-dimethoxy-8H-1,3-dioxolo[4,5-h]isoindolo[1,2-b][3]benzazepine-8,13(12bH)-dione 25764129 Click to see COC1=C(C2=C(C=C1)C3(C(=O)C4=CC5=C(C=C4CCN3C2=O)OCO5)O)OC 383.40 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
Chilenine 11025386 Click to see COC1=C(C2=C(C=C1)C3(C(=O)C4=CC5=C(C=C4CCN3C2=O)OCO5)O)OC 383.40 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
> Organoheterocyclic compounds / Isoquinolines and derivatives
793JX7VC6J 457914 Click to see COC1=CC=C2C=C3C4=CC5=C(C=C4CCN3C=C2C1=O)OCO5 321.30 unknown https://doi.org/10.1002/PTR.2399
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
3-[4-[[(1S)-6,7-dimethoxy-8-[(6-methoxy-2-methyl-1-oxo-3,4-dihydroisoquinolin-7-yl)oxy]-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-4-hydroxybenzaldehyde 102267542 Click to see CN1CCC2=CC(=C(C(=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)C=O)O)OC5=C(C=C6CCN(C(=O)C6=C5)C)OC)OC)OC 638.70 unknown https://doi.org/10.1055/S-0028-1097869
https://doi.org/10.1016/S0031-9422(98)00121-6
3-[4-[[6,7-dimethoxy-8-[(6-methoxy-2-methyl-1-oxo-3,4-dihydroisoquinolin-7-yl)oxy]-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-4-hydroxybenzaldehyde 163023865 Click to see CN1CCC2=CC(=C(C(=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)C=O)O)OC5=C(C=C6CCN(C(=O)C6=C5)C)OC)OC)OC 638.70 unknown https://doi.org/10.1055/S-0028-1097869
https://doi.org/10.1016/S0031-9422(98)00121-6
4-[(R)-hydroxy-[(1S)-7-hydroxy-6-methoxy-8-[(6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl)oxy]-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]benzene-1,2-diol 162901580 Click to see CN1CCC2=CC(=C(C=C2C1)OC3=C4C(N(CCC4=CC(=C3O)OC)C)C(C5=CC(=C(C=C5)O)O)O)OC 522.60 unknown https://doi.org/10.1007/BF00631010
Bargustanine 73813822 Click to see CN1CCC2=CC(=C(C=C2C1)OC3=C4C(N(CCC4=CC(=C3O)OC)C)C(C5=CC(=C(C=C5)O)O)O)OC 522.60 unknown https://doi.org/10.1007/BF00631010
Berbamunine 440585 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)O)OC 596.70 unknown https://doi.org/10.1007/BF01165220
methyl 3-[4-[[(1S)-6,7-dimethoxy-8-[(6-methoxy-2-methyl-1-oxo-3,4-dihydroisoquinolin-7-yl)oxy]-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-4-hydroxybenzoate 11308369 Click to see CN1CCC2=CC(=C(C(=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)C(=O)OC)O)OC5=C(C=C6CCN(C(=O)C6=C5)C)OC)OC)OC 668.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
Tejedine 72795147 Click to see CN1CCC2=CC(=C(C(=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)C(=O)OC)O)OC5=C(C=C6CCN(C(=O)C6=C5)C)OC)OC)OC 668.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
Thaligrisine 10031670 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)OC)O)OC 610.70 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
> 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 COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC 337.40 unknown https://doi.org/10.1007/BF01165220
https://doi.org/10.1135/CCCC19951034
https://doi.org/10.1016/S0021-9673(97)00804-2
https://doi.org/10.1016/S0031-9422(98)00121-6
Oxyberberine 11066 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCO5)OC 351.40 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
Thalifoline 89048 Click to see CN1CCC2=CC(=C(C=C2C1=O)O)OC 207.23 unknown https://doi.org/10.1016/S0031-9422(98)00121-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1002/PTR.2443
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00579837
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00579837
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1007/BF00579837
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1007/BF00579163
Petunidin 3-glucoside 443651 Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 479.40 unknown https://doi.org/10.1007/BF00579163
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
(2S,4S,5S)-2-[7-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256620 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 595.50 unknown https://doi.org/10.1007/BF00579163
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00579837
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00579837
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00579837
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00579837
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00579837
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00579837
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/BF00579837
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/BF00579837

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