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Bupleurum gibraltaricum

Bupleurum gibraltaricum - Unknown
Part: Unknown
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 UUID6440470f6673a188577919
Scientific name Bupleurum gibraltaricum
Authority Lam.
First published in Encycl. 1: 520 (1785)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bupleurum arborescens Jacq. Collectanea 2: 343 (1789)
Bupleurum coriaceum L'Hér. Stirp. Nov. : 139 (1791)
Bupleurum obliquum Vahl Symb. Bot. 1: 24 (1790)
Buprestis coriacea Spreng. Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 6: 259 (1812)

Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001068441
Tropicos 1702205
KEW urn:lsid:ipni.org:names:839171-1
Open Tree Of Life 94719
NCBI Taxonomy 198841
IPNI 839171-1
iNaturalist 320781
GBIF 3638706
EPPO BUPGI

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
Salacia pallescens Oliv. (Celastraceae) Scavenges Free Radicals and Inhibits Pro-inflammatory Mediators in Lipopolysaccharide-activated RAW Cells 264.7 Macrophages ABIODUN OO, OKE TA, ADEYEMI FO, OSHINLOYE AO, AKANDE AO Turk J Pharm Sci 30-Dec-2021
PMCID:PMC8744436
doi:10.4274/tjps.galenos.2021.98623
PMID:34978399
Ethnopharmacological Potential of Aspilia africana for the Treatment of Inflammatory Diseases Okello D, Lee J, Kang Y Evid Based Complement Alternat Med 19-Jun-2020
PMCID:PMC7321516
doi:10.1155/2020/8091047
PMID:32733588
Rock climbing alters plant species composition, cover, and richness in Mediterranean limestone cliffs Lorite J, Serrano F, Lorenzo A, Cañadas EM, Ballesteros M, Peñas J PLoS One 02-Aug-2017
PMCID:PMC5540606
doi:10.1371/journal.pone.0182414
PMID:28767727
Cannabinoids in the management of difficult to treat pain Russo EB Ther Clin Risk Manag 01-Feb-2008
PMCID:PMC2503660
doi:10.2147/tcrm.s1928
PMID:18728714
Monoterpene Aldehydes from <i>Bupleurum gibraltaricum</i> Alejandro F. Barrero, Ali Haïdour, Fernando Reyes, Ahmed Sedqui, Ahmed Ibn Mansour American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960732Y
Saikosaponins from roots of Bupleurum gibraltaricum and Bupleurum spinosum. Barrero AF, Haïdour A, Sedqui A, Mansour AI, Rodríguez-Garcia I, Löpez A, Muñoz-Dorado M Phytochemistry 01-Aug-2000
doi:10.1016/S0031-9422(00)00177-1
PMID:11014258
Pharmacological activity of the essential oil of Bupleurum gibraltaricum: anti-inflammatory activity and effects on isolated rat uteri. Ocete MA, Risco S, Zarzuelo A, Jimenez J J Ethnopharmacol 01-May-1989
doi:10.1016/0378-8741(89)90036-6
PMID:2747263

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
> Benzenoids / Benzene and substituted derivatives / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown https://doi.org/10.1021/NP960732Y
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/0378-8741(89)90036-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1021/NP960732Y
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0378-8741(89)90036-6
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0378-8741(89)90036-6
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/0378-8741(89)90036-6
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/NP960732Y
> 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/NP960732Y
https://doi.org/10.1016/0378-8741(89)90036-6
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/0378-8741(89)90036-6
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP960732Y
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0378-8741(89)90036-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Cubebene 86609 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
(1R,2S,7S,8S,9S,10S)-2,6,6,9-tetramethyltetracyclo[5.4.0.02,9.08,10]undecane 98459467 Click to see CC1(CCCC2(C3C1C4C2(C4C3)C)C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1021/NP960732Y
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/NP960732Y
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/NP960732Y
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1021/NP960732Y
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Longicyclene 564934 Click to see CC1(CCCC2(C3C1C4C2(C4C3)C)C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1021/NP960732Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1021/NP960732Y
beta-Elemol 20057139 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1021/NP960732Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene 288227 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Valencene 9855795 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1021/NP960732Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1021/NP960732Y
> 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/10.1016/S0031-9422(00)00177-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2R,5S,7S,10S,11S,14S,15R,16S,17S,18S,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosane-7,18-diol 15558969 Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)O 415.70 unknown https://doi.org/10.1016/S0031-9422(00)00177-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Xylitol 6912 Click to see C(C(C(C(CO)O)O)O)O 152.15 unknown https://doi.org/10.1016/S0031-9422(00)00177-1
> Organoheterocyclic compounds / Epoxides
(1R,11S)-1,5,5,8-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 132587053 Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C 220.35 unknown https://doi.org/10.1021/NP960732Y
Humulene epoxyde 5463721 Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C 220.35 unknown https://doi.org/10.1021/NP960732Y

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