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Berberis heteropoda

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400cbc37daa575032443
Scientific name Berberis heteropoda
Authority Schrenk
First published in Enum. Pl. Nov. 1: 102 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Berberis heteropoda var. sphaerocarpa (Kar. & Kir.) Ahrendt J. Linn. Soc., Bot. 57: 227 1961
Berberis sphaerocarpa Kar. & Kir. Bull. Soc. Imp. Naturalistes Moscou 14: 376 (1841)

Common names Top

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Language Common/alternative name
Azerbaijani berberis sphaerocarpa
Azerbaijani müxtəlifayaq zirinc
Kazakh Дөңгелек жемісті бөріқарақат
Russian Барбарис разноцветоножковый
Turkish karamuk
Chinese 山李子
Chinese 刺黄柏叶
Chinese 小檗实
Chinese 小檗浸膏
Chinese 异果小檗
Chinese 异果小檗(黑果小檗）
Chinese 黑果小檗

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
    • Mongolia
      • Mongolia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000563267
Tropicos 3500310
KEW urn:lsid:ipni.org:names:106735-1
The Plant List kew-2673890
Open Tree Of Life 5727764
NCBI Taxonomy 1433312
IPNI 106735-1
GBIF 3980845
EPPO BEBHP
USDA GRIN 6873

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
Evaluation of the Antioxidant and Anti-Lipoxygenase Activity of Berberis vulgaris L. Leaves, Fruits, and Stem and Their LC MS/MS Polyphenolic Profile Och A, Olech M, Bąk K, Kanak S, Cwener A, Cieśla M, Nowak R Antioxidants (Basel) 21-Jul-2023
PMCID:PMC10376855
doi:10.3390/antiox12071467
PMID:37508005
Forest stand factors determine the rainfall pattern of crown allocation of Picea schrenkiana in the northern slope of Mount Bogda, Tianshan Range, China Zhao S, Zheng XJ, Yin L, Wang Y Front Plant Sci 31-Jan-2023
PMCID:PMC9927214
doi:10.3389/fpls.2022.1113354
PMID:36798804
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
Nutritional composition and antioxidant properties of the fruit of Berberis heteropoda Schrenk Sun J, Li Q, Li J, Liu J, Xu F PLoS One 07-Apr-2022
PMCID:PMC8989241
doi:10.1371/journal.pone.0262622
PMID:35390002
Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species Hao DC, Zhang Y, He CN, Xiao PG Evid Based Complement Alternat Med 12-Jan-2022
PMCID:PMC8769838
doi:10.1155/2022/9027727
PMID:35069772
Berberine: Botanical Occurrence, Traditional Uses, Extraction Methods, and Relevance in Cardiovascular, Metabolic, Hepatic, and Renal Disorders Neag MA, Mocan A, Echeverría J, Pop RM, Bocsan CI, Crişan G, Buzoianu AD Front Pharmacol 21-Aug-2018
PMCID:PMC6111450
doi:10.3389/fphar.2018.00557
PMID:30186157
Composition and Antioxidant Activity of the Anthocyanins of the Fruit of Berberis heteropoda Schrenk Sun LL, Gao W, Zhang MM, Li C, Wang AG, Su YL, Ji TF Molecules 19-Nov-2014
PMCID:PMC6271762
doi:10.3390/molecules191119078
PMID:25415473
Über die Alkaloide von Berberis heteropoda A. Orechoff Wiley 15-Oct-2006
doi:10.1002/ARDP.19332710603
Berberis alkaloids. XVII. Investigation of the alkaloids of Berberis heteropoda M. M. Yusupov, A. Karimov, M. G. Levkovich, N. D. Abdullaev, R. Shakirov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00631012
Berberis alkaloids XIII. An investigation of the alkaloids of Berberis heteropoda A. Karimov, A. B. Butayarov, M. M. Yusupov, R. T. Mirzamatov, R. Sh. Shakirov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630680
Berberis alkaloids. XVI. Structure of berpodine A. Karimov, N. D. Abdullaev, R. Shakirov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630120

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
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/BF00631012
https://doi.org/10.1007/BF00630680
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1007/BF00631012
https://doi.org/10.1007/BF00630680
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/10.1007/BF00630680
https://doi.org/10.1007/BF00631012
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(1R,21R)-21-[[(1R,14S,21R)-1,21-dihydroxy-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-14-yl]oxy]-21-hydroxy-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-14-one 162982331 Click to see COC1=C(C2=C(C=C1)C(C3(C4=CC5=C(C=C4CCN3C2OC6(C7C8=CC9=C(C=C8CCN7C(=O)C1=C6C=CC(=C1OC)OC)OCO9)O)OCO5)O)O)OC 754.70 unknown https://doi.org/10.1007/BF00630120
21-[(1,21-Dihydroxy-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-14-yl)oxy]-1-hydroxy-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-14-one 163192687 Click to see COC1=C(C2=C(C=C1)C(C3(C4=CC5=C(C=C4CCN3C2OC6C7=C(C(=C(C=C7)OC)OC)C(=O)N8C6(C9=CC1=C(C=C9CC8)OCO1)O)OCO5)O)O)OC 754.70 unknown https://doi.org/10.1007/BF00630120
21-[(1,21-Dihydroxy-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-14-yl)oxy]-21-hydroxy-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-14-one 21627931 Click to see COC1=C(C2=C(C=C1)C(C3(C4=CC5=C(C=C4CCN3C2OC6(C7C8=CC9=C(C=C8CCN7C(=O)C1=C6C=CC(=C1OC)OC)OCO9)O)OCO5)O)O)OC 754.70 unknown https://doi.org/10.1007/BF00630120
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/10.1007/BF00631012
https://doi.org/10.1007/BF00630680
https://doi.org/10.1007/BF00630120
Canadine 34458 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.1007/BF00630680
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/10.1007/BF00631012
Pseudopalmatine 644002 Click to see COC1=C(C=C2C(=C1)CC[N+]3=CC4=CC(=C(C=C4C=C23)OC)OC)OC 352.40 unknown https://doi.org/10.1007/BF00631012
> 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/10.1007/BF00630680
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/BF00631012
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/10.1002/ARDP.19332710603
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/BF00631012
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.19332710603
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/10.1007/BF00630120
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/10.1002/ARDP.19332710603
https://doi.org/10.1007/BF00630120
https://doi.org/10.1007/BF00630680
https://doi.org/10.1007/BF00631012
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/10.1002/ARDP.19332710603
https://doi.org/10.1007/BF00630680
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-8-ol 173713 Click to see C[N+]1(CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O)C 314.40 unknown https://doi.org/10.1007/BF00630680
(R)-laudanosine 978314 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown https://doi.org/10.1007/BF00631012
(S)-Laudanosine 73397 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown https://doi.org/10.1007/BF00631012
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/BF00630680
https://doi.org/10.1007/BF00631012
https://doi.org/10.1007/BF00630120
Laudanosine 15548 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown https://doi.org/10.1007/BF00631012
Reticulin 10233 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1007/BF00630120
https://doi.org/10.1007/BF00631012
https://doi.org/10.1007/BF00630680
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1007/BF00630680
https://doi.org/10.1007/BF00630120
https://doi.org/10.1007/BF00631012
> 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/BF00631012
Oxyberberrubine 5384082 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCO5)O 337.30 unknown https://doi.org/10.1007/BF00631012

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