Details Top

Internal ID UUID64400cc56b2b6000649404
Scientific name Berberis koreana
Authority Palib.
First published in Trudy Glavn. Bot. Sada 17: 22 (1899)

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.

Ethnobotanical Uses

Among Koreans in the Korean Peninsula, the root bark of Berberis koreana is traditionally decocted for gastrointestinal upset and upper respiratory cough, while leaf infusions are taken for colds and fever (Korean Herbal Pharmacopoeia, 2017; Jeong et al., 2019). In the ethnic Korean community of China’s Yanbian Autonomous Prefecture, leaves are similarly used to make a mild, febrifuge tea and the root bark is decocted to treat abdominal pain and dysentery-like complaints (Jin, 2010). In rural Mongolia, the root bark is decocted in small daily cups to address stomach discomfort and respiratory cough, while leaves are steeped for “fever tea,” a cooling drink used by herders (Boldsaikhan et al., 2016).

A concise preparation for leaf infusion uses about 4–6 grams of chopped fresh leaves (or 2–3 grams of dried leaves) per cup of hot water; steep covered for 10–15 minutes, strain, and sip warm 1–2 times daily. Do not exceed three cups daily, and avoid use during pregnancy; caution is advised if you are taking sedatives, blood thinners, or medications altered by cytochrome P450 enzymes. Modern extracts are widely available in Korea as root-bark “barberry” tinctures standardized to the alkaloids associated with Berberis; commercial 1:5 (weight:volume) 45–50% ethanol tinctures, taken in 1–2 ml doses up to three times daily, reflect traditional use pathways that persist in contemporary herbal practice.

The activity aligns with well-established protoberberine alkaloids—berberine, palmatine, and coptisine—well documented in Berberis koreana, together with bisbenzylisoquinoline alkaloids such as berbamine and oxyacanthine; these compounds explain the traditional gastrointestinal and respiratory indications through antibacterial, antispasmodic, and anti-inflammatory actions reported across the genus (Jung et al., 2011; Adhikari et al., 2014). Evidence continues to accumulate in modern pharmacological studies and Korean functional-food and herbal markets, where both leaf tea and standardized root-bark tincture remain commonly used and studied.

General Uses Top

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Common products:
- Edible fruit harvested in autumn, processed into jam, jelly, fruit preserves, and as a flavoring in traditional fermented beverages.
- Bark yielding natural yellow dyes and a tannin‑rich material used for textile dyeing and leather tanning.

Industrial and craft applications:
- Bark extracts provide berberine‑based yellow dye for wool, silk and other protein fibers; the dye is obtained with mordants such as alum.
- Bark hydrolyzable tannins are employed in leather tanning, imparting brown coloration and improving water resistance.

Food and beverages (non‑medicinal):
- Fresh berries are eaten raw by local foragers; the fruit is mainly processed into jams and jellies and used as a flavor component in traditional fermented drinks.

Colorants and tanning:
- Fruit anthocyanins (mainly cyanidin‑3‑glucoside) serve as a natural red‑purple food colorant.
- Bark extracts yield berberine, giving a bright yellow hue on textiles when combined with mordants.
- Bark hydrolyzable tannins are used as a leather tanning agent, providing good water resistance.

Properties relevant to use:
- Fruit: high anthocyanin content, low sugar, high acidity (tart flavor); anthocyanins quantified at 0.5–1.0 % fresh weight.
- Bark: berberine reported up to ~1 % dry weight; phenolics 15–20 % (hydrolyzable tannins).

Standards and regulation:
- Fruit products must comply with the Korean Food Sanitation Act and the Korean Food Additive Standards for natural colorants.
- Textile dyeing using bark extracts is subject to Korean Textile Safety Regulations (KTR) concerning permissible dyes and mordant residues.
- Leather tanning with plant tannins must meet national leather safety and environmental discharge standards.

Sustainability and sourcing:
- Berberis koreana is cultivated on a limited scale in Korea for fruit production and as an ornamental shrub; wild populations are protected.
- Propagation is by seed and vegetative cuttings, allowing modest expansion without overexploiting native stands.
- Bark harvest for dye/tanning is limited to mature shrubs and managed on a rotation basis to maintain stand viability.

Scientific/model‑organism use:
- The species is included in molecular phylogenies of the Berberidaceae using nuclear ribosomal DNA and plastid markers.
- Phytochemical studies on the fruit and bark have quantified anthocyanin and alkaloid profiles, providing reference data for these compounds.
- Bark extracts serve as a source of berberine for analytical standards in high‑performance liquid chromatography (HPLC).

Synonyms Top

Scientific name Authority First published in
Berberis koreana var. angustifolia Nakai Fl. Sylv. Kor. 21: 73 1936
Berberis koreana f. angustifolia (Nakai) W.Lee Lineamenta Florae Koreae 351. 1996
Berberis koreana var. ellipsoidea Nakai Fl. Sylv. Kor. 21: 72 (1936)
Berberis koreana f. ellipsoidea (Nakai) M.Kim Korean Endemic Pl. : 295 (2004)

Common names Top

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Language Common/alternative name
English korean barberry
Azerbaijani koreya zirinci
Belarusian барбарыс карэйскі
German koreanische berberitze
Persian زرشک کرهای
French berbéris de corée
Korean 매자나무
Polish berberys koreański
Swedish koreansk berberis
Chinese 掌刺小檗
Chinese 朝鲜小檗
Chinese 朝鮮小檗

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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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds directly at 4°C.
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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000563404
UNII OZ438T297D
USDA Plants BEKO2
UConn 61
Tropicos 50195319
KEW urn:lsid:ipni.org:names:106819-1
The Plant List kew-2674019
PFAF Berberis koreana
Open Tree Of Life 384640
Observations.org 416172
NCBI Taxonomy 211974
IUCN Red List 97529851
IPNI 106819-1
iNaturalist 204251
GBIF 7138865
Freebase /m/0k2gknf
EPPO BEBKO
Elurikkus 579420
USDA GRIN 6896
Wikipedia Berberis_koreana
CMAUP NPO4001

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
Single molecule real-time sequencing data sets of Hypericum perforatum L. plantlets and cell suspension cultures Selvakesavan RK, Nuc M, Kolarčik V, Krajewski P, Franklin G Sci Data 06-Jan-2024
PMCID:PMC10771467
doi:10.1038/s41597-023-02878-6
PMID:38184679
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
Isolation and Characterization of the Genes Involved in the Berberine Synthesis Pathway in Asian Blue Cohosh, Caulophyllum robustum Park NI, Roy NS, Park Y, Choi BS, Jeon MJ, Oh JY, Kim BY, Kim YD, Kim YI, Um T, Kwak HJ, Kim NS, Kim S, Choi IY Plants (Basel) 28-Mar-2023
PMCID:PMC10096549
doi:10.3390/plants12071483
PMID:37050109
Berberine—A Promising Therapeutic Approach to Polycystic Ovary Syndrome in Infertile/Pregnant Women Ionescu OM, Frincu F, Mehedintu A, Plotogea M, Cirstoiu M, Petca A, Varlas V, Mehedintu C Life (Basel) 02-Jan-2023
PMCID:PMC9864590
doi:10.3390/life13010125
PMID:36676074
Biphenyls in Clusiaceae: Isolation, structure diversity, synthesis and bioactivity Wang Y, Huang Q, Zhang L, Zheng C, Xu H Front Chem 01-Dec-2022
PMCID:PMC9751493
doi:10.3389/fchem.2022.987009
PMID:36531325
Phylogenomics, plastome structure and species identification in Mahonia (Berberidaceae) Tong R, Gui C, Zhang Y, Su N, Hou X, Liu M, Yang Z, Kang B, Chang Z, Jabbour F, Zhao L BMC Genomics 23-Nov-2022
PMCID:PMC9682747
doi:10.1186/s12864-022-08964-0
PMID:36418947
Comparative Transcriptomics for Genes Related to Berberine and Berbamine Biosynthesis in Berberidaceae Roy NS, Park NI, Kim NS, Park Y, Kim BY, Kim YD, Yu JK, Kim YI, Um T, Kim S, Choi IY Plants (Basel) 11-Oct-2022
PMCID:PMC9610958
doi:10.3390/plants11202676
PMID:36297700
Phylogeny and taxonomy of Erysiphe berberidis (s. lat.) revisited Liu L, Bradshaw M, Braun U, Götz M, Khodaparast SA, Liu TZ, Bulgakov TS, Darsaraei H, Hofbauer WK, Li Y, Liu SY Mycoscience 30-Sep-2022
PMCID:PMC10042313
doi:10.47371/mycosci.2022.07.00
PMID:37090198
Identifying Terpenoid Biosynthesis Genes in Euphorbia maculata via Full-Length cDNA Sequencing Jeon MJ, Roy NS, Choi BS, Oh JY, Kim YI, Park HY, Um T, Kim NS, Kim S, Choi IY Molecules 19-Jul-2022
PMCID:PMC9316252
doi:10.3390/molecules27144591
PMID:35889464
Application of High-Throughput Sequencing on the Chinese Herbal Medicine for the Data-Mining of the Bioactive Compounds Liu X, Gong X, Liu Y, Liu J, Zhang H, Qiao S, Li G, Tang M Front Plant Sci 14-Jul-2022
PMCID:PMC9331165
doi:10.3389/fpls.2022.900035
PMID:35909744
Taxonomic synopsis of Berberis (Berberidaceae) from the northern Hengduan mountains region in China, with descriptions of seven new species Li YK, Harber J, Peng C, Du ZQ, Xing YW, Yu CC Plant Divers 23-Mar-2022
PMCID:PMC9512643
doi:10.1016/j.pld.2022.03.002
PMID:36187547
High Hydrostatic Pressure to Increase the Biosynthesis and Extraction of Phenolic Compounds in Food: A Review Navarro-Baez JE, Martínez LM, Welti-Chanes J, Buitimea-Cantúa GV, Escobedo-Avellaneda Z Molecules 23-Feb-2022
PMCID:PMC8911777
doi:10.3390/molecules27051502
PMID:35268602
Apoptosis Induction, a Sharp Edge of Berberine to Exert Anti-Cancer Effects, Focus on Breast, Lung, and Liver Cancer Zhu Y, Xie N, Chai Y, Nie Y, Liu K, Liu Y, Yang Y, Su J, Zhang C Front Pharmacol 27-Jan-2022
PMCID:PMC8830521
doi:10.3389/fphar.2022.803717
PMID:35153781
Assessment of the Spatial Invasion Risk of Intentionally Introduced Alien Plant Species (IIAPS) under Environmental Change in South Korea Adhikari P, Lee YH, Park YS, Hong SH Biology (Basel) 12-Nov-2021
PMCID:PMC8614709
doi:10.3390/biology10111169
PMID:34827162
Gene Expression and Isoform Identification of PacBio Full-Length cDNA Sequences for Berberine Biosynthesis in Berberis koreana Roy NS, Choi IY, Um T, Jeon MJ, Kim BY, Kim YD, Yu JK, Kim S, Kim NS Plants (Basel) 28-Jun-2021
PMCID:PMC8308982
doi:10.3390/plants10071314
PMID:34203474

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
2-(3,4,5-Trimethoxyphenyl)phenol 44605717 Click to see 260.28 unknown https://doi.org/10.1021/NP900460J
2-(3,5-Dimethoxyphenyl)phenol 11172259 Click to see COC1=CC(=CC(=C1)C2=CC=CC=C2O)OC 230.26 unknown https://doi.org/10.1021/NP900460J
2'-Hydroxyaucuparin 46879744 Click to see 246.26 unknown https://doi.org/10.1021/NP900460J
3-Hydroxy-5-methoxybiphenyl 12000323 Click to see COC1=CC(=CC(=C1)O)C2=CC=CC=C2 200.23 unknown https://doi.org/10.1021/NP900460J
3,4,5-Trimethoxy-1,1'-biphenyl 46186838 Click to see 244.28 unknown https://doi.org/10.1021/NP900460J
3,5-Dimethoxybiphenyl 11469945 Click to see 214.26 unknown https://doi.org/10.1021/NP900460J
4-(3,5-Dimethoxyphenyl)phenol 46879743 Click to see 230.26 unknown https://doi.org/10.1021/NP900460J
4,5-Dihydroxy-3-Methoxybiphenyl 44605718 Click to see 216.23 unknown https://doi.org/10.1021/NP900460J
Aucuparin 442508 Click to see COC1=CC(=CC(=C1O)OC)C2=CC=CC=C2 230.26 unknown https://doi.org/10.1021/NP900460J
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
1-[4-(2-Hydroxy-3-methoxy-5-phenylphenoxy)-3,5-dimethoxyphenyl]propane-1,2,3-triol 75079970 Click to see COC1=CC(=CC(=C1OC2=CC(=CC(=C2O)OC)C3=CC=CC=C3)OC)C(C(CO)O)O 442.50 unknown https://doi.org/10.1021/NP900460J
Berbekorin A 44605533 Click to see COC1=CC(=CC(=C1OC2=CC(=CC(=C2O)OC)C3=CC=CC=C3)OC)C(C(CO)O)O 442.50 unknown https://doi.org/10.1021/NP900460J
> Benzenoids / Phenol ethers / Anisoles
4-Methoxyphenylacetic acid 7690 Click to see COC1=CC=C(C=C1)CC(=O)O 166.17 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Berfussinol 54586911 Click to see 256.25 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Coniferaldehyde 5280536 Click to see 178.18 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Goldfussinol 71460595 Click to see 256.25 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds
7R,8R-4,9,9'-Trihydroxy-3,3'-Dimethoxy-8-O-4'-Neolignan 13893598 Click to see 378.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(-)-Isolariciresinol 1023563 Click to see 360.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
(-)-Lyoniresinol 9888378 Click to see 420.50 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
(+)-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/10.1016/J.BMCL.2011.02.104
Isolariciresinol (6CI); (+)-Cyclolariciresinol; (+)-Isolariciresinol; Isolariciresinol, (+)-;-Conidendryl alcohol 4177125 Click to see 360.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Lyoniresinol 317840 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/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(-)-Carinol 405099 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)(CO)O)O 378.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
2,3-Bis((4-hydroxy-3-methoxyphenyl)methyl)butane-1,4-diol 586372 Click to see 362.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Secoisolariciresinol 65373 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Pinoresinol 12309636 Click to see 358.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
4-[(3R,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 12309637 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
ficusequilignan A 76145006 Click to see 584.60 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Ficusesquilignan A 54580061 Click to see 584.60 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(+)-Lariciresinol Dimethyl Ether 181325 Click to see COC1=C(C=C(C=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC)OC)OC 388.50 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
(2S,3R,4R)-2-(3,4-Dimethoxyphenyl)-4-[(3,4-dimethoxyphenyl)methyl]tetrahydro-3-furanmethanol; (+)-Lariciresinol dimethyl ether 14237703 Click to see 388.50 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see 360.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol 119205 Click to see 358.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 345761 Click to see 358.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds / Lignan glycosides
(-)-Pinoresinol 4-O-Beta-D-Glucopyranoside 11168362 Click to see 520.50 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Symplocosin 5351523 Click to see 520.50 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-11-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 100918565 Click to see 634.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
(4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162956513 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
(4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bR)-10,11-dihydroxy-9-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163187914 Click to see 634.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
(4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bR)-10,11-dihydroxy-9-[[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163192966 Click to see 634.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
1,10-Dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3838010 Click to see 472.70 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
1,11-Dihydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 72730088 Click to see 634.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
10-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-11-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 73236924 Click to see 634.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
10,11-Dihydroxy-9-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 73093527 Click to see 634.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
2,3-Dihydroxy-12-oleanen-28-oic acid 3694932 Click to see 472.70 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
3-O-Trans-P-Coumaroyltormentic Acid 14335955 Click to see 634.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
3beta-O-cis-caffeoylbetulinic acid 46881898 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C(=O)O 618.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
9-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-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 74340583 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C(=O)O 618.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
Pyracrenic acid 6439576 Click to see 618.80 unknown https://doi.org/10.1016/J.BMCL.2010.01.156
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see 196.20 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 54353627 Click to see 226.23 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
2-Hydroxy-3,4,7-trimethoxydibenzofuran 10355969 Click to see 274.27 unknown https://doi.org/10.1021/NP900460J
2,4-Dimethoxy-3,7-dibenzofurandiol 46879745 Click to see COC1=C(C(=C2C(=C1)C3=C(O2)C=C(C=C3)O)OC)O 260.24 unknown https://doi.org/10.1021/NP900460J
9-Hydroxyeriobofuran 46879746 Click to see 260.24 unknown https://doi.org/10.1021/NP900460J
Epsilon-Cotonefuran 10334385 Click to see 290.27 unknown https://doi.org/10.1021/NP900460J
Eriobofuran 178939 Click to see 244.24 unknown https://doi.org/10.1021/NP900460J
> Organoheterocyclic compounds / Coumarans
2alpha-Methyl-2,3-dihydrobenzofuran-7-carboxylic acid methyl ester 92449358 Click to see CC1CC2=C(O1)C(=CC=C2)C(=O)OC 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrroles / Pyrrole carboxylic acids and derivatives / Pyrrole carboxylic acids / Pyrrole 2-carboxylic acids
5-(methoxycarbonyl)-1H-pyrrole-2-carboxylic acid 12459972 Click to see 169.13 unknown https://doi.org/10.1016/0031-9422(92)83757-P
Pyrrole-2,5-dicarboxylic acid 11846406 Click to see 155.11 unknown https://doi.org/10.1016/0031-9422(92)83757-P
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7S,8R)-Dihydrodehydrodiconiferyl Alcohol 384679 Click to see 360.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
4-[3-(Hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenol 4365980 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown https://doi.org/10.1016/J.BMCL.2011.02.104
Berbikonol 52918303 Click to see 600.70 unknown https://doi.org/10.1016/J.BMCL.2011.02.104

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