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Bupleurum longiradiatum

Bupleurum longiradiatum - Unknown
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Author: Public Domain - WikiMedia
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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 UUID64400e3baad37937394337
Scientific name Bupleurum longiradiatum
Authority Turcz.
First published in Bull. Soc. Imp. Naturalistes Moscou 17: 719 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bupleurum leveillei H.Boissieu Bull. Soc. Bot. France 57: 413 (1910)
Bupleurum longiradiatum f. australe R.H.Shan & Yin Li Acta Phytotax. Sin. 12: 269 (1974)
Bupleurum yokoyamae Miyabe & Tatew. Trans. Sopporo Nat. Hist. Soc. 15: 134 (1938)
Bupleurum longiradiatum f. leveillei (H.Boissieu) Kitag. J. Jap. Bot. 36: 241 1961

Common names Top

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Language Common/alternative name
Korean 개시호
Chinese 柴胡
Chinese 大叶柴胡

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
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
    • Siberia
      • Chita

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000575536
Tropicos 1704098
The Plant List kew-2686877
Open Tree Of Life 49594
Observations.org 132484
NCBI Taxonomy 48104
IPNI 839244-1
iNaturalist 501059
GBIF 6027041
EPPO BUPLR
Elurikkus 575460

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
Feasibility study on the introduction of Micro-CT technology for the identification of Radix Bupleuri and its adulterants Chen K, Chen G, Zhuang Z, Luo S, Liu J, Liu G Front Pharmacol 28-Feb-2024
PMCID:PMC10933125
doi:10.3389/fphar.2024.1347316
PMID:38482055
The application of mirabilite in traditional Chinese medicine and its chemical constituents, processing methods, pharmacology, toxicology and clinical research Tao L, Fu J, Wang F, Song Y, Li Y, Zhang J, Wang Z Front Pharmacol 04-Jan-2024
PMCID:PMC10794775
doi:10.3389/fphar.2023.1293097
PMID:38239194
Xanthine oxidase, α-glucosidase and α-amylase inhibitory activities of the essential oil from Piper lolot: In vitro and in silico studies Nguyen TK, Thuy Thi Tran L, Ho Viet D, Thai PH, Ha TP, Ty PV, Duc LP, Ton That Huu D, Cuong LC Heliyon 15-Aug-2023
PMCID:PMC10458695
doi:10.1016/j.heliyon.2023.e19148
PMID:37636421
Apiaceae Medicinal Plants in China: A Review of Traditional Uses, Phytochemistry, Bolting and Flowering (BF), and BF Control Methods Li M, Li M, Wang L, Li M, Wei J Molecules 27-May-2023
PMCID:PMC10254214
doi:10.3390/molecules28114384
PMID:37298861
Effects of Mountain Uplift and Climatic Oscillations on Phylogeography and Species Divergence of Chamaesium (Apiaceae) Zheng HY, Guo XL, Price M, He XJ, Zhou SD Front Plant Sci 24-May-2021
PMCID:PMC8183463
doi:10.3389/fpls.2021.673200
PMID:34108984
Bioactive C17 and C18 Acetylenic Oxylipins from Terrestrial Plants as Potential Lead Compounds for Anticancer Drug Development Christensen LP Molecules 31-May-2020
PMCID:PMC7321150
doi:10.3390/molecules25112568
PMID:32486470
Correlation between Solid Content and Antioxidant Activities in Umbelliferae Salad Plants Kim JS, Lee JH Prev Nutr Food Sci 31-Mar-2020
PMCID:PMC7143011
doi:10.3746/pnf.2020.25.1.84
PMID:32292760
Application of Molecular Methods in the Identification of Ingredients in Chinese Herbal Medicines Han K, Wang M, Zhang L, Wang C Molecules 22-Oct-2018
PMCID:PMC6222746
doi:10.3390/molecules23102728
PMID:30360419
Application of Metabolomics in the Study of Natural Products Zhao Q, Zhang JL, Li F Nat Prod Bioprospect 29-Jun-2018
PMCID:PMC6102178
doi:10.1007/s13659-018-0175-9
PMID:29959744
Deciphering the Differential Effective and Toxic Responses of Bupleuri Radix following the Induction of Chronic Unpredictable Mild Stress and in Healthy Rats Based on Serum Metabolic Profiles Gao X, Liang M, Fang Y, Zhao F, Tian J, Zhang X, Qin X Front Pharmacol 15-Jan-2018
PMCID:PMC5775221
doi:10.3389/fphar.2017.00995
PMID:29379441
A systematic review of the active saikosaponins and extracts isolated from Radix Bupleuri and their applications Yuan B, Yang R, Ma Y, Zhou S, Zhang X, Liu Y Pharm Biol 12-Dec-2016
PMCID:PMC6130612
doi:10.1080/13880209.2016.1262433
PMID:27951737
A new approach to species delimitation in Septoria Verkley GJ, Quaedvlieg W, Shin HD, Crous PW Stud Mycol 30-Jun-2013
PMCID:PMC3713889
doi:10.3114/sim0018
PMID:24014901
Xiao-Chai-Hu Tang in Treating Model Mice With D-Galactosamine-Induced Liver Injury Zhou YX, Qiu YQ, Xu LQ, Guo J, Li LJ Afr J Tradit Complement Altern Med 02-Apr-2012
PMCID:PMC3746662
doi:10.4314/ajtcam.v9i3.16
PMID:23983374
Polyacetylenes from Bupleurum longiradiatum. Huang HQ, Zhang X, Shen YH, Su J, Liu XH, Tian JM, Lin S, Shan L, Zhang WD J Nat Prod 01-Dec-2009
doi:10.1021/NP900534V
PMID:19994846
Antiangiogenic activity of Bupleurum longiradiatum on human umbilical venous endothelial cells. You YJ, Lee IS, Kim Y, Bae KH, Ahn BZ Arch Pharm Res 01-Oct-2002
doi:10.1007/BF02976936
PMID:12433197

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(10Z,15E,17E)-18-hydroxyoctadeca-10,15,17-trien-12-ynyl] acetate 46881222 Click to see CC(=O)OCCCCCCCCCC=CC#CCC=CC=CO 318.40 unknown https://doi.org/10.1021/NP900534V
[(2E,4E,8E,10E)-heptadeca-2,4,8,10-tetraen-6-ynyl] acetate 44613434 Click to see CCCCCCC=CC=CC#CC=CC=CCOC(=O)C 286.40 unknown https://doi.org/10.1021/NP900534V
[(2E,4E,9Z)-heptadeca-2,4,9-trien-6-ynyl] acetate 44613435 Click to see CCCCCCCC=CCC#CC=CC=CCOC(=O)C 288.40 unknown https://doi.org/10.1021/NP900534V
[(9Z,14E,16E)-18-acetyloxyoctadeca-9,14,16-trien-12-ynyl] acetate 44613548 Click to see CC(=O)OCCCCCCCCC=CCC#CC=CC=CCOC(=O)C 360.50 unknown https://doi.org/10.1021/NP900534V
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(2E,4E,9Z)-octadeca-2,4,9-trien-6-yne-1,18-diol 44613550 Click to see C(CCCCO)CCCC=CCC#CC=CC=CCO 276.40 unknown https://doi.org/10.1021/NP900534V
(2Z,8E,10E,14R)-heptadeca-2,8,10-trien-4,6-diyne-1,14-diol 97297315 Click to see CCCC(CCC=CC=CC#CC#CC=CCO)O 258.35 unknown https://doi.org/10.1021/NP900534V
(2Z,8E,10E)-pentadeca-2,8,10-trien-4,6-diyn-1-ol 44613551 Click to see CCCCC=CC=CC#CC#CC=CCO 214.30 unknown https://doi.org/10.1021/NP900534V
(2Z,9Z)-heptadeca-2,9-dien-4,6-diyn-1-ol 46881233 Click to see CCCCCCCC=CCC#CC#CC=CCO 244.37 unknown https://doi.org/10.1021/NP900534V
(2Z,9Z)-octadeca-2,9-dien-4,6-diyne-1,18-diol 44613552 Click to see C(CCCCO)CCCC=CCC#CC#CC=CCO 274.40 unknown https://doi.org/10.1021/NP900534V
(2Z,9Z)-pentadeca-2,9-dien-4,6-diyn-1-ol 14841162 Click to see CCCCCC=CCC#CC#CC=CCO 216.32 unknown https://doi.org/10.1021/NP900534V
(8E,10E,14S)-heptadeca-2,8,10-trien-4,6-diyne-1,14-diol 162910296 Click to see CCCC(CCC=CC=CC#CC#CC=CCO)O 258.35 unknown https://doi.org/10.1021/NP900534V
[(2Z,8E,10E,14S)-14-hydroxyheptadeca-2,8,10-trien-4,6-diynyl] acetate 44613553 Click to see CCCC(CCC=CC=CC#CC#CC=CCOC(=O)C)O 300.40 unknown https://doi.org/10.1021/NP900534V
[(4R,7E,9E,15Z)-17-hydroxyheptadeca-7,9,15-trien-11,13-diyn-4-yl] acetate 44613555 Click to see CCCC(CCC=CC=CC#CC#CC=CCO)OC(=O)C 300.40 unknown https://doi.org/10.1021/NP900534V
[(4R,7E,9E)-17-hydroxyheptadeca-7,9,15-trien-11,13-diyn-4-yl] acetate 162962922 Click to see CCCC(CCC=CC=CC#CC#CC=CCO)OC(=O)C 300.40 unknown https://doi.org/10.1021/NP900534V
[(7E,9E,16Z)-18-hydroxyoctadeca-7,9,16-trien-11,13-diyn-4-yl] acetate 5315585 Click to see CCCC(CCC=CC=CC#CC#CCC=CCO)OC(=O)C 314.40 unknown https://doi.org/10.1021/NP900534V
[(8E,10E,14S)-14-hydroxyheptadeca-2,8,10-trien-4,6-diynyl] acetate 163013721 Click to see CCCC(CCC=CC=CC#CC#CC=CCOC(=O)C)O 300.40 unknown https://doi.org/10.1021/NP900534V
Acetylbupleurotoxin 6435768 Click to see CCCC(CCC=CC=CC#CC#CC=CCO)OC(=O)C 300.40 unknown https://doi.org/10.1021/NP900534V
Bupleuronol 46881232 Click to see CCCC(=O)CCC=CC=CC#CC#CC=CCO 256.34 unknown https://doi.org/10.1021/NP900534V
Bupleurotoxin 44613554 Click to see CCCC(CCC=CC=CC#CC#CC=CCO)O 258.35 unknown https://doi.org/10.1007/BF02976936
https://doi.org/10.1021/NP900534V
Bupleurynol 5315554 Click to see CCCCCCC=CC=CC#CC#CCC=CCO 256.40 unknown https://doi.org/10.1021/NP900534V
Heptadeca-2,9-diene-4,6-diyn-1-ol 71380905 Click to see CCCCCCCC=CCC#CC#CC=CCO 244.37 unknown https://doi.org/10.1021/NP900534V
Octadeca-2,9-dien-4,6-diyne-1,18-diol 75082545 Click to see C(CCCCO)CCCC=CCC#CC#CC=CCO 274.40 unknown https://doi.org/10.1021/NP900534V
Pentadeca-2,9-dien-4,6-diyn-1-ol 72739887 Click to see CCCCCC=CCC#CC#CC=CCO 216.32 unknown https://doi.org/10.1021/NP900534V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,5S,9S,10S,13S,14R,17S)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162958803 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/YAKUSHI1947.89.4_589
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 521229 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/YAKUSHI1947.89.4_589
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Beta amino acids and derivatives
Moiramide A 10108000 Click to see CC=CC=CC=CC(=O)NC(CC(=O)O)C1=CC=CC=C1 285.34 unknown https://doi.org/10.1021/NP900534V
> Organoheterocyclic compounds / Benzodioxoles
4-[(7-Methoxy-1,3-benzodioxol-5-yl)-(3,4,5-trimethoxyphenyl)methyl]-3-methylideneoxolan-2-one 9867239 Click to see COC1=CC(=CC2=C1OCO2)C(C3COC(=O)C3=C)C4=CC(=C(C(=C4)OC)OC)OC 428.40 unknown https://doi.org/10.1021/NP900534V
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(3S)-1,2,3,6,7,7a,10,14,14abeta,14b-Decahydro-6alpha-hydroxy-3alpha,13-dimethoxy-5,5,7abeta,9,14balpha-pentamethyl-12H-3beta,5abeta-epoxy-5H-furo[3,4-i]oxepino[4,3-a]xanthen-12-one 78178167 Click to see CC1=C2COC(=O)C2=C(C3=C1OC4(CC(C56C(OC(O5)(CCC6(C4C3)C)OC)(C)C)O)C)OC 474.50 unknown https://doi.org/10.1021/NP900534V
> Organoheterocyclic compounds / Furopyrans
(1S,3R,7R,10S,15S,17R,18S,21R,22S,23S,25S,29S)-9,9,18,23,25-pentamethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacos-12-ene-5,14,19,24-tetrone 16681579 Click to see CC1C2C3C(C(C(=O)O3)C)OC45C2C(C1=O)(CCC6(O4)CC78C(CC=C6C5=O)C(OC7CC(=O)O8)(C)C)C 526.60 unknown https://doi.org/10.1021/NP900534V
> Organoheterocyclic compounds / Isoquinolines and derivatives
Eletefine 10664930 Click to see COC1=C(C(=C2C3=CCC(CC=C(O3)C4=NC=CC1=C24)O)OC)OC 341.40 unknown https://doi.org/10.1021/NP900534V
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2R)-7-hydroxy-8-[(Z)-3-hydroxy-3-methylbut-1-enyl]-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one 163189509 Click to see CC(C)(C=CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)O 370.40 unknown https://doi.org/10.1021/NP900534V
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(8R,9S,10R)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] benzoate 92273398 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3 536.60 unknown https://doi.org/10.1021/NP900534V

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