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Internal ID UUID64400e3866a2b489687267
Scientific name Bupleurum kaoi
Authority Liu, C.Y.Chao & Chuang
First published in Quart. J. Taiwan Mus. 14: 22 (1961)

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 臺灣柴胡
Chinese 高氏柴胡
Chinese 台湾柴胡

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000575457
Tropicos 50003352
KEW urn:lsid:ipni.org:names:839214-1
The Plant List kew-2686794
Open Tree Of Life 954840
NCBI Taxonomy 270183
IPNI 839214-1
iNaturalist 708922
GBIF 3638266
EOL 2905842

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
Complete chloroplast genome of Angelica hirsutiflora Liu et al. 1961 (Apiaceae) Huang CC, Hsu TW, Hung KH, Wang WK Mitochondrial DNA B Resour 05-Apr-2024
PMCID:PMC11000599
doi:10.1080/23802359.2024.2335992
PMID:38591054
Antiviral Protein–Protein Interaction Inhibitors Marković V, Szczepańska A, Berlicki Ł J Med Chem 23-Feb-2024
PMCID:PMC10945500
doi:10.1021/acs.jmedchem.3c01543
PMID:38394369
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Recent Updates on Viral Oncogenesis: Available Preventive and Therapeutic Entities Chowdhary S, Deka R, Panda K, Kumar R, Solomon AD, Das J, Kanoujiya S, Gupta AK, Sinha S, Ruokolainen J, Kesari KK, Gupta PK Mol Pharm 24-Jul-2023
PMCID:PMC10410670
doi:10.1021/acs.molpharmaceut.2c01080
PMID:37486263
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
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC. Mao Y, Chen H, Zhao J, Li Y, Feng L, Yang Y, Zhang Y, Wei P, Hou D J Plant Biochem Biotechnol 16-Sep-2022
PMCID:PMC9483273
doi:10.1007/s13562-022-00804-2
PMID:36160316
Complete chloroplast genome and phylogenetic analysis of Bupleurum kaoi Liu, Chao, and Chuang, 1977: an endemic species in Taiwan Huang CC, Huang CL, Hsu TW, Chang LH, Hung KH, Wang WK Mitochondrial DNA B Resour 22-Aug-2022
PMCID:PMC9415577
doi:10.1080/23802359.2022.2082892
PMID:36034531
Nanoscale Technologies in the Fight against COVID-19: From Innovative Nanomaterials to Computer-Aided Discovery of Potential Antiviral Plant-Derived Drugs Iraci N, Corsaro C, Giofrè SV, Neri G, Mezzasalma AM, Vacalebre M, Speciale A, Saija A, Cimino F, Fazio E Biomolecules 30-Jul-2022
PMCID:PMC9405735
doi:10.3390/biom12081060
PMID:36008954
R2R3-MYB Transcription Factor SmMYB52 Positively Regulates Biosynthesis of Salvianolic Acid B and Inhibits Root Growth in Salvia miltiorrhiza Yang R, Wang S, Zou H, Li L, Li Y, Wang D, Xu H, Cao X Int J Mol Sci 02-Sep-2021
PMCID:PMC8431584
doi:10.3390/ijms22179538
PMID:34502445
Antiviral Activity Exerted by Natural Products against Human Viruses Musarra-Pizzo M, Pennisi R, Ben-Amor I, Mandalari G, Sciortino MT Viruses 04-May-2021
PMCID:PMC8147851
doi:10.3390/v13050828
PMID:34064347
Medicinal plants: Treasure for antiviral drug discovery Ali SI, Sheikh WM, Rather MA, Venkatesalu V, Muzamil Bashir S, Nabi SU Phytother Res 16-Feb-2021
PMCID:PMC8013762
doi:10.1002/ptr.7039
PMID:33590931
Medicinal Plants with Potential Inhibitory Bioactive Compounds against Coronaviruses Adeleye OA, Bamiro OA, Bakre LG, Odeleye FO, Adebowale MN, Okunye OL, Sodeinde MA, Adebona AC, Menaa F Adv Pharm Bull 30-Jan-2021
PMCID:PMC9012928
doi:10.34172/apb.2022.003
PMID:35517886
Regulation of Sixth Seminal Root Formation by Jasmonate in Triticum aestivum L. Pigolev A, Miroshnichenko D, Dolgov S, Savchenko T Plants (Basel) 23-Jan-2021
PMCID:PMC7911905
doi:10.3390/plants10020219
PMID:33498738

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S)-2-[(2R)-3,5-dihydroxy-2-[[(1S,4S,5R,8R,9R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyloxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 138114182 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O 781.00 unknown https://doi.org/10.1002/PTR.2650090509
(2S)-2-[(2S)-3,5-dihydroxy-2-[[(1S,4S,5R,8S,9R,13S,14R,17S,18S)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyloxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 137705034 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O 781.00 unknown https://doi.org/10.1002/PTR.2650090509
(2S)-2-[6-[[(6aS,6bS,8aS,12aS,14aR,14bS)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxy-2-[[(4S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 44202895 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(CC7)(C)C)CO)O)C)C)C)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 929.10 unknown https://doi.org/10.1002/PTR.2650090509
Saikosaponin A 167928 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O 781.00 unknown https://doi.org/10.1002/PTR.2650090509
Saikosaponin D 107793 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O 781.00 unknown https://doi.org/10.1002/PTR.2650090509

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