Scientific name	Authority	First published in
Bupleurum insulare	Rouy & E.G.Camus	Fl. France 7: 316 (1901)
Bupleurum terminale	Salisb.	Prodr. Stirp. Chap. Allerton : 160 (1796)
Buprestis fruticosa	Spreng.	Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 6: 259 (1812)

Common names Top

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Filter by language:

Language	Common/alternative name
English	shrubby hare's ear
English	shrubby hare's-ear
Arabic	دبيق شجيري
Catalan	matabou
Welsh	llwyn paladr trwyddo
German	strauchiges hasenohr
Finnish	pensasjänönputki
Norwegian Bokmål	buskhareøre
Chinese	灌木柴胡

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

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Europe click to expand
- Eastern Europe
  - Krym
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Greece
  - Italy
  - Sicilia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001067668
Tropicos	1700032
INPN	87051
Flora of Italy	3567
KEW	urn:lsid:ipni.org:names:839164-1
Open Tree Of Life	49592
NCBI Taxonomy	48103
NBN Atlas	NBNSYS0000003656
IPNI	839164-1
iNaturalist	82601
GBIF	3638793
EPPO	BUPFR
USDA GRIN	8157
Wikipedia	Bupleurum_fruticosum

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

Apium extract alleviates indomethacin-induced gastric ulcers in rats via modulating the VEGF and IK-κB/NF-κB p65 signaling pathway: insights from in silico and in vivo investigations

Abu-Baih DH, Gomaa AA, Abdel-Wahab NM, Abdelaleem ER, Zaher AM, Hassan NF, Bringmann G, Abdelmohsen UR, Altemani FH, Algehainy NA, Mokhtar FA, Abdelwahab MF

BMC Complement Med Ther

14-Feb-2024

PMCID:	PMC10865661
doi:	10.1186/s12906-023-04333-w
PMID:	38355510

Eoscyphella luciurceolata gen. and sp. nov. (Agaricomycetes) Shed Light on Cyphellopsidaceae with a New Lineage of Bioluminescent Fungi

Silva-Filho AG, Mombert A, Nascimento CC, Nóbrega BB, Soares DM, Martins AG, Domingos AH, Santos I, Della-Torre OH, Perry BA, Desjardin DE, Stevani CV, Menolli N Jr

J Fungi (Basel)

12-Oct-2023

PMCID:	PMC10608165
doi:	10.3390/jof9101004
PMID:	37888262

A 12-Year Experimental Design to Test the Recovery of Butterfly Biodiversity in an Urban Ecosystem: Lessons from the Parc Urbain des Papillons

Deschamps-Cottin M, Jacek G, Seguinel L, Le Champion C, Robles C, Ternisien M, Duque C, Vila B

Insects

24-Sep-2023

PMCID:	PMC10607803
doi:	10.3390/insects14100780
PMID:	37887792

Phytocompounds as a source for the development of new drugs to treat respiratory viral infections

Seibert JB, Amparo TR, Almeida TC, de Souza GH, dos Santos OD

23-May-2023

PMCID:	PMC10204935
doi:	10.1016/B978-0-323-91294-5.00007-5

Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy

Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A

Plants (Basel)

18-Nov-2022

PMCID:	PMC9695302
doi:	10.3390/plants11223165
PMID:	36432894

Review of Natural Resources With Vasodilation: Traditional Medicinal Plants, Natural Products, and Their Mechanism and Clinical Efficacy

Tang F, Yan HL, Wang LX, Xu JF, Peng C, Ao H, Tan YZ

Front Pharmacol

01-Apr-2021

PMCID:	PMC8048554
doi:	10.3389/fphar.2021.627458
PMID:	33867985

The Essential Oil Compositions of Three Teucrium Taxa Growing Wild in Sicily: HCA and PCA Analyses

Catinella G, Badalamenti N, Ilardi V, Rosselli S, De Martino L, Bruno M

Molecules

26-Jan-2021

PMCID:	PMC7865755
doi:	10.3390/molecules26030643
PMID:	33530639

The Combined Effect of Mediterranean Shrubland Pasture and the Dietary Administration of Sage By-Products on the Antioxidant Status of Segureña Ewes and Lambs

Jordán MJ, Martínez-Conesa C, Bañón S, Otal J, Quílez M, García-Aledo I, Romero-Espinar P, Sánchez-Gómez P

Antioxidants (Basel)

30-Sep-2020

PMCID:	PMC7600900
doi:	10.3390/antiox9100938
PMID:	33008117

Filling the gaps: ethnobotanical study of the Garrigues district, an arid zone in Catalonia (NE Iberian Peninsula)

Gras A, Vallès J, Garnatje T

J Ethnobiol Ethnomed

09-Jun-2020

PMCID:	PMC7285587
doi:	10.1186/s13002-020-00386-0
PMID:	32517701

Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes

Lautié E, Russo O, Ducrot P, Boutin JA

Front Pharmacol

07-Apr-2020

PMCID:	PMC7154113
doi:	10.3389/fphar.2020.00397
PMID:	32317969

A Review of Resistance Mechanisms of Synthetic Insecticides and Botanicals, Phytochemicals, and Essential Oils as Alternative Larvicidal Agents Against Mosquitoes

Senthil-Nathan S

Front Physiol

25-Feb-2020

PMCID:	PMC7052130
doi:	10.3389/fphys.2019.01591
PMID:	32158396

In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant

Lijalem T, Feyissa T

J Genet Eng Biotechnol

20-Jan-2020

PMCID:	PMC6970091
doi:	10.1186/s43141-019-0017-0
PMID:	31956941

Plant-Derived Essential Oils; Their Larvicidal Properties and Potential Application for Control of Mosquito-Borne Diseases

Osanloo M, Sedaghat MM, Sanei-Dehkordi A, Amani A

Galen Med J

16-Aug-2019

PMCID:	PMC8344124
doi:	10.31661/gmj.v8i0.1532
PMID:	34466524

Manipulation of Plant Growth Regulators on Phytochemical Constituents and DNA Protection Potential of the Medicinal Plant Arnebia benthamii

Parray JA, Kamili AN, Jan S, Mir MY, Shameem N, Ganai BA, Abd_Allah EF, Hashem A, Alqarawi AA

Biomed Res Int

04-Jan-2018

PMCID:	PMC5817313
doi:	10.1155/2018/6870139
PMID:	29516007

The Interplay among Acorn Abundance and Rodent Behavior Drives the Spatial Pattern of Seedling Recruitment in Mature Mediterranean Oak Forests

Sunyer P, Boixadera E, Muñoz A, Bonal R, Espelta JM

PLoS One

12-Jun-2015

PMCID:	PMC4467087
doi:	10.1371/journal.pone.0129844
PMID:	26070129

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 / Styrenes
3-Phenylprop-2-en-1-yl pentanoate	112120	Click to see CCCCC(=O)OCC=CC1=CC=CC=C1	218.29	unknown	https://doi.org/10.1080/10412905.1992.9698110
Cinnamyl isovalerate	5355855	Click to see CC(C)CC(=O)OCC=CC1=CC=CC=C1	218.29	unknown	https://doi.org/10.1080/10412905.1992.9698110
Cinnamyl valerate	5367959	Click to see CCCCC(=O)OCC=CC1=CC=CC=C1	218.29	unknown	https://doi.org/10.1080/10412905.1992.9698110
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	https://doi.org/10.1080/10412905.1992.9698110
Estragole	8815	Click to see COC1=CC=C(C=C1)CC=C	148.20	unknown	https://doi.org/10.1021/NP50062A008
> Hydrocarbons / Polycyclic hydrocarbons
Bornylene	10047	Click to see CC1(C2CCC1(C=C2)C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Hexyl 2-methylbutanoate	24838	Click to see CCCCCCOC(=O)C(C)CC	186.29	unknown	https://doi.org/10.1080/10412905.1992.9698110
Hexyl isovalerate	61455	Click to see CCCCCCOC(=O)CC(C)C	186.29	unknown	https://doi.org/10.1080/10412905.1992.9698110
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate	9017	Click to see CC(CCC=C(C)C)CCOC(=O)C	198.30	unknown	https://doi.org/10.1080/10412905.1992.9698110
Decyl acetate	8167	Click to see CCCCCCCCCCOC(=O)C	200.32	unknown	https://doi.org/10.1080/10412905.1992.9698110
Octyl acetate	8164	Click to see CCCCCCCCOC(=O)C	172.26	unknown	https://doi.org/10.1080/10412905.1992.9698110
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Decanol	8174	Click to see CCCCCCCCCCO	158.28	unknown	https://doi.org/10.1080/10412905.1992.9698110
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50062A008 https://doi.org/10.1080/10412905.1992.9698110
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1021/NP50062A008
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50062A008 https://doi.org/10.1080/10412905.1992.9698110
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1992.9698110
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1021/NP50062A008
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1021/NP50062A008
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1021/NP50062A008 https://doi.org/10.1080/10412905.1992.9698110
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/NP50062A008
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/NP50062A008 https://doi.org/10.1080/10412905.1992.9698110
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
beta-Terpinene	66841	Click to see CC(C)C1=CCC(=C)CC1	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110
Dihydrocarveol	12072	Click to see CC1CCC(CC1O)C(=C)C	154.25	unknown	https://doi.org/10.1080/10412905.1992.9698110
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698110 https://doi.org/10.1021/NP50062A008
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1021/NP50062A008
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/NP50062A008
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Buddlejasaponin IV	153940	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)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O	943.10	unknown	https://doi.org/10.1055/S-2006-959442 https://doi.org/10.1021/NP50092A009
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Erythrodiol	101761	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(96)00461-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(5S,9S,10S,13R,14R)-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	137706369	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(96)00461-X
alpha-Spinasterin	5281331	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(96)00461-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Heptyl acetate	8159	Click to see CCCCCCCOC(=O)C	158.24	unknown	https://doi.org/10.1080/10412905.1992.9698110
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
5,6,6-Trimethoxy-2-prop-2-enylcyclohexa-1,3-diene	163192813	Click to see COC1C=CC(=CC1(OC)OC)CC=C	210.27	unknown	https://doi.org/10.1016/S0031-9422(96)00461-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
6-Methoxy-7-(3-methylbut-2-enoxy)chromen-2-one	1764914	Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)C	260.28	unknown	https://doi.org/10.1016/0031-9422(95)00749-0
7-(2-Hydroxy-3-methylbut-3-enoxy)-6-methoxychromen-2-one	10636169	Click to see CC(=C)C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O	276.28	unknown	https://doi.org/10.1016/0031-9422(95)00749-0
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	https://doi.org/10.1016/0031-9422(95)00749-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Capensin	644959	Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1O)OC)C	276.28	unknown	https://doi.org/10.1016/0031-9422(95)00749-0
Prenyletin	3873459	Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)O)C	246.26	unknown	https://doi.org/10.1016/0031-9422(95)00749-0 https://doi.org/10.1021/NP50115A015
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	https://doi.org/10.1016/0031-9422(95)00749-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin	5273569	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O	208.17	unknown	https://doi.org/10.1016/0031-9422(95)00749-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1016/0031-9422(95)00749-0

Biological Material Top

Contributors Top

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Bupleurum fruticosum

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top