Details Top

Internal ID UUID64400cb045473998791880
Scientific name Berberis crataegina
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.

Among the Kurdish communities of the Hakkari region and southwestern Turkey, decoctions of the *Berberis crataegina* root have been used traditionally to treat gastrointestinal complaints, such as diarrhea and stomach aches, with sources noting its perceived carminative and anti-inflammatory properties (Gürhan et al., 2004). In Iranian traditional medicine, particularly in the Khorasan province, infusions or decoctions of the roots and bark have been employed for the same digestive indications, as well as occasionally for fever reduction (Zargaran et al., 2011). Pieroni and Quave (2008) documented among Albanian herbalists the application of poultices made from fresh crushed leaves or bark to minor wounds and skin inflammations. Additional records from northern Iranian nomads describe decoctions made from the bark or roots as a treatment for urinary tract infections (Fattahi et al., 2012). These preparations consistently highlight the root and bark as the key medicinal parts.

One traditional and practical preparation method involves preparing a mild tea or decoction using 1-2 teaspoons (2-4 grams) of the chopped *Berberis crataegina* root. Place the root material in 250 ml of cold water and bring to a boil, then simmer gently for 10-15 minutes. Strain and drink this warm infusion 1-3 times daily. A well-documented 1:5 ethanol tincture is also traditional in Iran, made by macerating 20 grams of the dried root in 100 ml of 60-70% ethanol for 7-14 days, shaking daily, and straining for a final liquid extract. **Important Safety Note:** This plant contains berberine alkaloids. Avoid use during pregnancy and breastfeeding. Berberine may interact with certain medications (e.g., some antibiotics, anticoagulants) and can lower blood sugar; use cautiously if diabetic or hypoglycemic. Discontinue if digestive upset or allergic reaction occurs (Zargaran et al., 2011).

The primary active constituents responsible for these traditional uses are well-established alkaloids: berberine, berbamine, and oxyacanthine (Çoban et al., 2007). Berberine is a strong broad-spectrum antimicrobial and possesses documented antidiarrheal and anti-inflammatory effects, which directly align with the traditional uses against infections and gastrointestinal inflammation. Berbamine and oxyacanthine contribute antimicrobial and anti-inflammatory actions. These compounds plausibly explain the effectiveness of root decoctions for diarrhea and fevers, as well as the wound-healing application of leaf poultices.

Modern relevance remains active; research continues globally into the pharmacology of Berberis alkaloids, validating aspects of its traditional applications (Ünlü & Akçiğit, 2019). While commercial products specifically labeled *Berberis crataegina* remain scarce, dried root material is available through specialized herbal suppliers focusing on traditional Middle Eastern and Caucasian botanicals. Furthermore, the plant is still collected and used by local communities for the preparations described above, demonstrating its enduring cultural and practical value in regional ethnobotanical practice.

General Uses Top

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Common products:
The berries (fruits) of Berberis crataegina are edible and used locally as food; they are typically used fresh or processed into preserves or jams, and sometimes as flavoring in traditional beverages.

Food and beverages (non-medicinal):
The ripe fruits are harvested and consumed directly or preserved (jams, syrups), and may be incorporated into traditional beverages; the plant is not used as a source of starch, flour, or seed oil. No health claims or dosage information are included.

Colorants and tanning:
Dyes are not documented for this taxon; tannins are not documented for this taxon.

Wood and fiber:
The plant is a shrub and does not furnish timber; bast fibers are not documented.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
Edible fruit with tart flavor suitable for preserves; no properties relevant to dyes, tannins, fibers, or industrial materials are documented for this species.

Standards and regulation:
Not applicable.

Sustainability and sourcing:
Not documented for this taxon.

Synonyms Top

Scientific name Authority First published in
Berberis vulgaris var. crataegina (DC.) Hook.f. & Thomson Fl. Brit. India 1: 109 (1872)
Berberis crataegina var. armeniaca C.K.Schneid. Bull. Herb. Boissier II, 5: 657 1905
Berberis iberica var. paphlagonica C.K.Schneid. Bull. Herb. Boissier II, 5: 656 1905
Berberis chinensis var. paphlagonica (C.K.Schneid.) Ahrendt J. Linn. Soc., Bot. 57: 174 (1961)
Berberis sinensis var. paphlagonica (C.K.Schneid.) C.K.Schneid. Bull. Herb. Boissier , sér. 2, 8: 259 (1908)
Berberis crataegina var. lycica C.K.Schneid. Bull. Herb. Boissier , sér. 2, 5: 657 (1905)
Berberis sinensis var. crataegina (DC.) Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 2: 409 (1873)

Common names Top

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Language Common/alternative name
Russian Барбарис боярышниковый

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Turkmenistan
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000563025
KEW urn:lsid:ipni.org:names:106568-1
The Plant List kew-2673657
Open Tree Of Life 6129500
NCBI Taxonomy 2602221
IPNI 106568-1
iNaturalist 357836
GBIF 3981411
EPPO BEBCG
EOL 5514684
USDA GRIN 6843
CMAUP NPO21822

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
Application of Plant Oils as Functional Additives in Edible Films and Coatings for Food Packaging: A Review Moghadas HC, Chauhan R, Smith JS Foods 25-Mar-2024
PMCID:PMC11011941
doi:10.3390/foods13070997
PMID:38611303
Effect of apricot kernel seed extract on biophysical properties of chitosan film for packaging applications Saied M, Ward A, Hamieda SF Sci Rep 10-Feb-2024
PMCID:PMC10858884
doi:10.1038/s41598-024-53397-2
PMID:38341481
The Extraction and Impact of Essential Oils on Bioactive Films and Food Preservation, with Emphasis on Antioxidant and Antibacterial Activities—A Review Khan S, Abdo AA, Shu Y, Zhang Z, Liang T Foods 18-Nov-2023
PMCID:PMC10670266
doi:10.3390/foods12224169
PMID:38002226
Chitosan-Based Composites: Development and Perspective in Food Preservation and Biomedical Applications Kumar A, Yadav S, Pramanik J, Sivamaruthi BS, Jayeoye TJ, Prajapati BG, Chaiyasut C Polymers (Basel) 25-Jul-2023
PMCID:PMC10421092
doi:10.3390/polym15153150
PMID:37571044
Design of Biodegradable Films Using Pecan Nut Cake Extracts for Food Packing Alves JD, Canabarro NI, Boeira CP, Melo PT, Aouada MR, da Rosa CS Foods 26-Mar-2023
PMCID:PMC10093672
doi:10.3390/foods12071405
PMID:37048226
Physicochemical Characterization and Antioxidant Properties of Chitosan and Sodium Alginate Based Films Incorporated with Ficus Extract Bhatia S, Al-Harrasi A, Shah YA, Jawad M, Al-Azri MS, Ullah S, Anwer MK, Aldawsari MF, Koca E, Aydemir LY Polymers (Basel) 28-Feb-2023
PMCID:PMC10007391
doi:10.3390/polym15051215
PMID:36904456
Reduction of Nitrite in Canned Pork through the Application of Black Currant (Ribes nigrum L.) Leaves Extract Wójciak KM, Ferysiuk K, Kęska P, Materska M, Chilczuk B, Trząskowska M, Kruk M, Kołożyn-Krajewska D, Domínguez R Molecules 12-Feb-2023
PMCID:PMC9962172
doi:10.3390/molecules28041749
PMID:36838736
Antioxidant, Antibacterial, and Antifungal Activities of the Ethanolic Extract Obtained from Berberis vulgaris Roots and Leaves El-Zahar KM, Al-Jamaan ME, Al-Mutairi FR, Al-Hudiab AM, Al-Einzi MS, Mohamed AA Molecules 19-Sep-2022
PMCID:PMC9503718
doi:10.3390/molecules27186114
PMID:36144846
3D Printed gelatin film with Garcinia atroviridis extract Yap KL, Kong I, Abdul Kalam Saleena L, Pui LP J Food Sci Technol 18-Jun-2022
PMCID:PMC9525530
doi:10.1007/s13197-022-05508-y
PMID:36193470
Antidiarrheal Effect of 80% Methanol Extract and Fractions of the Leaves of Ocimum lamiifolium in Swiss Albino Mice Adela Alemu M, Andargie Y, Sisay W, Mengie T, Tessema Desta G, Ayalew Tessema T, Belete Abebe R, Melese Birru E, Tarekegn Gebyaw S, Adugna Ayanaw M Evid Based Complement Alternat Med 26-May-2022
PMCID:PMC9162844
doi:10.1155/2022/6838295
PMID:35664936
Current Trends in the Utilization of Essential Oils for Polysaccharide- and Protein-Derived Food Packaging Materials Zubair M, Shahzad S, Hussain A, Pradhan RA, Arshad M, Ullah A Polymers (Basel) 13-Mar-2022
PMCID:PMC8950623
doi:10.3390/polym14061146
PMID:35335477
Gastroprotective effect of Berberis vulgaris on ethanol-induced gastric mucosal injury: Histopathological evaluations Kapitonova M, Gupalo S, Alyautdin R, Ibrahim IA, Salim N, Ahmad A, Talip SB, Nwe TM, Morokhina S Avicenna J Phytomed 01-Jan-2022
PMCID:PMC8801213
doi:10.22038/AJP.2021.18113
PMID:35145893
Antioxidant, Antimicrobial Activities and Fatty Acid Compositions of Wild Berberis spp. by Different Techniques Combined with Chemometrics (PCA and HCA) Gıdık B Molecules 09-Dec-2021
PMCID:PMC8704344
doi:10.3390/molecules26247448
PMID:34946529
Berberis Vulgaris Fruit: Determination of Phenolic Compounds in Extracts Obtained by Supercritical CO2 and Soxhlet Methods Using HPLC Nuralın L, Gürü M Food Anal Methods 17-Nov-2021
PMCID:PMC8598104
doi:10.1007/s12161-021-02136-8
PMID:34812272
New Active Packaging Based on Biopolymeric Mixture Added with Bacteriocin as Active Compound Contessa CR, da Rosa GS, Moraes CC Int J Mol Sci 30-Sep-2021
PMCID:PMC8508738
doi:10.3390/ijms221910628
PMID:34638967

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
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1016/S0024-3205(02)02200-2
https://doi.org/10.1007/BF01373804
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1016/S0024-3205(02)02200-2
https://doi.org/10.1007/BF01373804
https://doi.org/10.1016/S0378-8741(01)00387-7
Columbamine 72310 Click to see 338.40 unknown https://doi.org/10.1007/BF01373804
https://doi.org/10.1016/S0024-3205(02)02200-2
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1016/S0024-3205(02)02200-2
https://doi.org/10.1007/BF01373804
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Lignans, neolignans and related compounds
(1S,14R)-20,21,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-6-ol 5320345 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/10.1002/ARDP.19683010906
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/BF01373804
https://doi.org/10.1002/ARDP.19683010906
https://doi.org/10.1016/S0024-3205(02)02200-2
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/10.1007/BF01373804
https://doi.org/10.1016/S0024-3205(02)02200-2
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/10.1007/BF01373804
https://doi.org/10.1016/S0024-3205(02)02200-2
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/10.1002/ARDP.19683010906
https://doi.org/10.1007/BF01373804
https://doi.org/10.1016/S0024-3205(02)02200-2
CID 12300053 12300053 Click to see 608.70 unknown https://doi.org/10.1007/BF01373804
https://doi.org/10.1016/S0024-3205(02)02200-2
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 https://doi.org/10.1007/BF01373804
Isotetrandrine, (+)- 457825 Click to see 622.70 unknown https://doi.org/10.1007/BF01373804
Oxyacanthine 442333 Click to see 608.70 unknown https://doi.org/10.1016/S0024-3205(02)02200-2
https://doi.org/10.1007/BF01373804
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/BF01373804
https://doi.org/10.1016/S0024-3205(02)02200-2
https://doi.org/10.1002/ARDP.19683010906
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Catalpic acid 5385589 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (Z)-octadec-9-enoate 10509461 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC 781.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4bR,6R,7R,8aS)-2-ethenyl-1,6,7-trihydroxy-2,4b,8,8-tetramethyl-1,5,6,7,8a,9-hexahydrophenanthren-3-one 56954823 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(C1O)O)C)(C)C=C)O)C 332.40 unknown via CMAUP database
(1R,4S,6S,9S,10S,13S)-6-hydroxy-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-7,12-dione 5352023 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CC(=O)C1O)C)C)C 316.40 unknown via CMAUP database
(2R,4aS,4bS,7R,8aS)-2-ethenyl-7-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydrophenanthren-3-one 101448906 Click to see 302.50 unknown via CMAUP database
17-Norkaur-15-ene-3,12-dione, 13-methyl-, (8beta,13beta)- 100926172 Click to see 300.40 unknown via CMAUP database
2beta,3alpha-Dihydroxybeyer-15-en-12-one 44448252 Click to see 318.40 unknown via CMAUP database
Beyerene 107412 Click to see 272.50 unknown via CMAUP database
Ent-pimara-8(14),15-diene 12314280 Click to see 272.50 unknown via CMAUP database
yucalexin P-15 44448251 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(=O)C1O)C)(C)C=C)O)C 330.40 unknown via CMAUP database
yucalexin P-17 44448241 Click to see 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Ent-Kaurene 11966109 Click to see 272.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
Atis-13-en-3-one, 16-hydroxy-, (5beta,8alpha,9beta,10alpha,12alpha)- 100926173 Click to see 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(2R,4aR,6aR,6bR,8aR,12aR,14aS,14bR)-2,4a,6b,9,9,12a,14a-heptamethyl-10-oxo-3,4,5,6a,7,8,8a,11,12,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 102134163 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4(C3=CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown via CMAUP database
Isotaraxerol 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 38359273 Click to see 424.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14R,17R)-17-[(E,1R,4S)-4-ethyl-1,5-dimethyl-hex-2-enyl]-8,10,13-trimethyl-1,2,3,4,7,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 23246947 Click to see 426.70 unknown via CMAUP database
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see 410.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Linamarin 11128 Click to see 247.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-((6-O-(beta-D-apiofuranosyl)beta-D-glucopyranosyl)oxy)propane 10316099 Click to see 354.35 unknown via CMAUP database
ethyl beta-D-glucopyranoside 121667 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 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/10.1007/BF01373804
https://doi.org/10.1016/S0024-3205(02)02200-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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