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Internal ID UUID64400cd303b67592164034
Scientific name Berberis orthobotrys
Authority Bien. ex Aitch.
First published in J. Linn. Soc., Bot. 19: 150 (1882)

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Synonyms Top

Scientific name Authority First published in
Berberis orthobotrys var. canescens Ahrendt J. Linn. Soc., Bot. 57: 144 1961
Berberis orthobotrys var. conwayi Ahrendt J. Linn. Soc., Bot. 57: 143 1961
Berberis orthobotrys var. rubicunda Ahrendt J. Linn. Soc., Bot. 57: 144. 1961 (1961)
Berberis orthobotrys var. rupestris Ahrendt J. Linn. Soc., Bot. 57: 143 1961
Berberis orthobotrys var. sinthanensis Ahrendt J. Linn. Soc., Bot. 57: 143 1961

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Berberis orthobotrys subsp. capitata Jafri Fl. W. Pakistan 87: 20 (1975)

Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Turkmenistan
    • Western Asia
      • Afghanistan
      • Iran
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000563618
Tropicos 3500321
KEW urn:lsid:ipni.org:names:106949-1
The Plant List kew-2674223
Open Tree Of Life 5727780
Observations.org 136901
NCBI Taxonomy 1433323
IPNI 106949-1
GBIF 7300242
EPPO BEBOO
EOL 2886361
Elurikkus 585074
USDA GRIN 6928
CMAUP NPO24574

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
Determination of Therapeutic and Safety Effects of Zygophyllum coccineum Extract in Induced Inflammation in Rats Yosri M, Elaasser MM, Abdel-Aziz MM, Hassan MM, Alqhtani AH, Al-Gabri N, Ali AB, Pokoo-Aikins A, Amin BH Biomed Res Int 18-Jul-2022
PMCID:PMC9314163
doi:10.1155/2022/7513155
PMID:35898689
8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities Ali G, Cuny GD Molecules 27-Jul-2021
PMCID:PMC8347945
doi:10.3390/molecules26154521
PMID:34361671
Plant diversity of Hyrcanian relict forests: An annotated checklist, chorology and threat categories of endemic and near endemic vascular plant species Ghorbanalizadeh A, Akhani H Plant Divers 27-Jul-2021
PMCID:PMC8897184
doi:10.1016/j.pld.2021.07.005
PMID:35281126
Vincetoxicum arnottianum modulates motility features and metastatic marker expression in pediatric rhabdomyosarcoma by stabilizing the actin cytoskeleton Adamus A, Ali I, Vasileiadis V, Al-Hileh L, Lisec J, Frank M, Seitz G, Engel N BMC Complement Med Ther 04-May-2021
PMCID:PMC8097906
doi:10.1186/s12906-021-03299-x
PMID:33947373
Primary Rhabdomyosarcoma of the Pleura: A Case Report and Review of the Literature Chekhlabi N, Toughza J, Dini N Cureus 05-Jan-2021
PMCID:PMC7861058
doi:10.7759/cureus.12491
PMID:33564502
Phenolic Characterization, Antioxidant Activity, and Enzyme Inhibitory Properties of Berberis thunbergii DC. Leaves: A Valuable Source of Phenolic Acids Fernández-Poyatos MD, Ruiz-Medina A, Zengin G, Llorent-Martínez EJ Molecules 17-Nov-2019
PMCID:PMC6891573
doi:10.3390/molecules24224171
PMID:31744256
Regional trade of medicinal plants has facilitated the retention of traditional knowledge: case study in Gilgit-Baltistan Pakistan Salim MA, Ranjitkar S, Hart R, Khan T, Ali S, Kiran C, Parveen A, Batool Z, Bano S, Xu J J Ethnobiol Ethnomed 28-Jan-2019
PMCID:PMC6348662
doi:10.1186/s13002-018-0281-0
PMID:30691476
Antinociceptive effect of methanolic extract and alkaloid fractions of Berberis integerrima root in animal models Hajhashemi V, Fahmideh F, Ghanadian M Avicenna J Phytomed 01-May-2018
PMCID:PMC5987437
PMID:29881708
Anti-arthritic activity of aqueous-methanolic extract and various fractions of Berberis orthobotrys Bien ex Aitch Alamgeer, Uttra AM, Hasan UH BMC Complement Altern Med 18-Jul-2017
PMCID:PMC5516381
doi:10.1186/s12906-017-1879-9
PMID:28720131
Berberis vulgaris: specifications and traditional uses Rahimi-Madiseh M, Lorigoini Z, Zamani-gharaghoshi H, Rafieian-kopaei M Iran J Basic Med Sci 01-May-2017
PMCID:PMC5478785
doi:10.22038/IJBMS.2017.8690
PMID:28656092
Antitumor evaluation of two selected Pakistani plant extracts on human bone and breast cancer cell lines Engel N, Ali I, Adamus A, Frank M, Dad A, Ali S, Nebe B, Atif M, Ismail M, Langer P, Ahmad VU BMC Complement Altern Med 26-Jul-2016
PMCID:PMC4960692
doi:10.1186/s12906-016-1215-9
PMID:27457235
A quick overview on some aspects of endocrinological and therapeutic effects of Berberis vulgaris L. Zarei A, Changizi-Ashtiyani S, Taheri S, Ramezani M Avicenna J Phytomed 01-Nov-2015
PMCID:PMC4678494
PMID:26693406
New Alkaloids From Berberis orthobotrys S. Fazal Hussain, Lajber Khan, Khalid Khan Sadozai, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50015A006

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
1-O-Methylpakistanine 181478 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1021/NP50015A006
4H-Dibenzo(de,g)quinoline-1,10-diol, 5,6,6a,7-tetrahydro-2-methoxy-6-methyl-11-(4-(((1S)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)methyl)phenoxy)-, (6aR)- 156697 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1021/NP50015A006
4H-Dibenzo(de,g)quinoline-1,10-diol, 5,6,6a,7-tetrahydro-2-methoxy-6-methyl-9-(4-(((1S)-1,2,3,4-tetrahydro-7-hydroxy-6-methoxy-2-methyl-1-isoquinolinyl)methyl)phenoxy)-, (6aR)- 157105 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown https://doi.org/10.1021/NP50015A006
9-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol 4411439 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1021/NP50015A006
9-[4-[(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 21769997 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1021/NP50015A006
9-[4-[(7-hydroxy-6-methoxy-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 53462640 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O)O)OC 594.70 unknown https://doi.org/10.1021/NP50015A006
Pakistanine 193239 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1021/NP50015A006
> Alkaloids and derivatives / Proaporphines
(2R,4R)-2'-[4-[[(1S)-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 162977104 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/10.1021/NP50015A006
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/10.1021/NP50015A006
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds
(1R,2S)-1-(3-Methoxy-4-hydroxyphenyl)-2-[2-methoxy-4-[(E)-3-hydroxy-1-propenyl]phenoxy]-1,3-propanediol 14274760 Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 376.40 unknown via CMAUP database
2-Methoxy-4-[(1R,2S)-1,3-dihydroxy-2-[2-methoxy-4-(3-hydroxypropyl)phenoxy]propyl]phenol 13893597 Click to see COC1=C(C=CC(=C1)CCCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 378.40 unknown via CMAUP database
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/10.1021/NP50015A006
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/10.1021/NP50015A006
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/10.1021/NP50015A006
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/10.1021/NP50015A006
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/10.1021/NP50015A006
Repandine 10031631 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 via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Elemacarmanin 13891365 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)CO)C=C 380.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Hemistepsin 10043230 Click to see C=C1CC2C(C(C3C1CC(C3=C)O)OC(=O)C(=C)CO)C(=C)C(=O)O2 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4S,5E,9Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 53494931 Click to see CC1=CCCC(=CC(C2C(C1)OC(=O)C2=C)OC(=O)C(=C)CO)C=O 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,6abeta,9abeta,9balpha)-Decahydro-8alpha-hydroxy-6,9-bis(methylene)-4beta-[(3-hydroxy-2-methylenepropanoyl)oxy]-3beta-methylazuleno[4,5-b]furan-2(3H)-one 71503391 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC(=O)C(=C)CO 348.40 unknown via CMAUP database
11,13-Dihydrodesacylcynaropicrin 12047617 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown via CMAUP database
Cynaropicrin 119093 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown via CMAUP database
Desacylcynaropicrin 13943205 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown via CMAUP database
Isolipidiol 14589530 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
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 via CMAUP database
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown via CMAUP database
Taraxasterol acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 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 / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown via CMAUP database
Methyl indole-3-carboxylate 589098 Click to see COC(=O)C1=CNC2=CC=CC=C21 175.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 via CMAUP database

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