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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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

Asia-temperate click to expand
- Eastern Asia
  - Korea

Northern America click to expand
- Northeastern U.S.A.
  - Vermont

Links to other databases Top

Suggest others/fix!

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

Add a new one!

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
> 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 COC1=CC(=CC(=C1OC)OC)C2=CC=CC=C2O	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 COC1=CC(=CC(=C1O)OC)C2=CC=CC=C2O	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 COC1=CC(=CC(=C1OC)OC)C2=CC=CC=C2	244.28	unknown	https://doi.org/10.1021/NP900460J
3,5-Dimethoxybiphenyl	11469945	Click to see COC1=CC(=CC(=C1)C2=CC=CC=C2)OC	214.26	unknown	https://doi.org/10.1021/NP900460J
4-(3,5-Dimethoxyphenyl)phenol	46879743	Click to see COC1=CC(=CC(=C1)C2=CC=C(C=C2)O)OC	230.26	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
Noraucuparin	44605718	Click to see COC1=CC(=CC(=C1O)O)C2=CC=CC=C2	216.23	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 COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
4-Hydroxy-3-methoxycinnamaldehyde	5280536	Click to see COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
Berfussinol	54586911	Click to see COC1=CC(=CC(=C1O)OC)C(CO)C(=O)OC	256.25	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
Goldfussinol	71460595	Click to see COC1=CC(=CC(=C1O)OC)C(CO)C(=O)OC	256.25	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds
Threo-1-(4-hydroxy-3-methoxyphenyl)-2-(4-(3-hydroxypropyl)-2-methoxyphenoxy)-1,3-propanediol	13893598	Click to see COC1=C(C=CC(=C1)CCCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O	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 COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
(-)-Lyoniresinol	9888378	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
(+)-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 COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	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-methoxybenzyl)butane-1,4-diol	586372	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
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 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
(-)-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 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
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 COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC	584.60	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
Ficusesquilignan A	54580061	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC	584.60	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
Syringaresinol	100067	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
> 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
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
Lariciresinol dimethyl ether	14237703	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
Lariciresinol, (+)-	134203	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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	345761	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O	358.40	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
Matairesinol	119205	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O	358.40	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
> Lignans, neolignans and related compounds / Lignan glycosides
(-)-Pinoresinol 4-O-glucoside	11168362	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O	520.50	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
Symplocosin	5351523	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C)C)C2C1C)C)C(=O)O	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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C=CC6=CC=C(C=C6)O)O)O)C)C)C2C1)C)C(=O)O)C	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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C=CC6=CC=C(C=C6)O)O)O)C)C)C2C1)C)C(=O)O)C	634.80	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1(C)O)C)C(=O)O	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C)C)C2C1C)C)C(=O)O	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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)COC(=O)C=CC6=CC=C(C=C6)O)O)O)C)C)C2C1)C)C(=O)O)C	634.80	unknown	https://doi.org/10.1016/J.BMCL.2010.01.156
2,3-Dihydroxyolean-12-en-28-oic acid	3694932	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
3-O-Trans-P-Coumaroyltormentic Acid	14335955	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1(C)O)C)C(=O)O	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
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	2371	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/J.BMCL.2010.01.156
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/J.BMCL.2010.01.156
CID 3838010	3838010	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
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 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone	75142	Click to see COC1=C(C=CC(=C1)C(=O)CCO)O	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 COC1=CC(=CC(=C1O)OC)C(=O)CCO	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 COC1=CC2=C(C=C1)C3=CC(=C(C(=C3O2)OC)OC)O	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 COC1=C(C(=C2C(=C1)C3=C(C=CC=C3O2)O)OC)O	260.24	unknown	https://doi.org/10.1021/NP900460J
Epsilon-Cotonefuran	10334385	Click to see COC1=C(C2=C(C=C1)C3=CC(=C(C(=C3O2)OC)OC)O)O	290.27	unknown	https://doi.org/10.1021/NP900460J
Eriobofuran	178939	Click to see COC1=C(C(=C2C(=C1)C3=CC=CC=C3O2)OC)O	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
1H-pyrrole-2,5-dicarboxylic Acid	11846406	Click to see C1=C(NC(=C1)C(=O)O)C(=O)O	155.11	unknown	https://doi.org/10.1016/0031-9422(92)83757-P
5-(methoxycarbonyl)-1H-pyrrole-2-carboxylic acid	12459972	Click to see COC(=O)C1=CC=C(N1)C(=O)O	169.13	unknown	https://doi.org/10.1016/0031-9422(92)83757-P
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
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 COC1=C(C=C(C=C1)C(C(CO)OC2=C(C=C(C=C2OC)C3C(C4=C(O3)C(=CC(=C4)CCCO)OC)CO)OC)O)OC	600.70	unknown	https://doi.org/10.1016/J.BMCL.2011.02.104
Dihydrodehydrodiconiferyl alcohol	384679	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

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Berberis koreana

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