Sideritis bourgeana

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Internal ID UUID643fecce8d224820099117
Scientific name Sideritis bourgeana
Authority Boiss. & Reut.
First published in Diagn. Pl. Orient. , ser. 2, 4: 34 (1859)

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Scientific name Authority First published in
Sideritis biflora Porta & Rigo. ex Porta Atti Accad. Agiati 9: 59 (1891 publ. 1892)
Sideritis leucantha subsp. bourgeana (Boiss.) Alcaraz, Peinado, Mart.Parras, J.S.Carrion & Sánchez-Gómez Acta Bot. Malac. 12: 246 (1987)
Sideritis leucantha var. bourgeana (Boiss. & Reut.) Font Quer Treb. Mus. Ci. Nat. Barcelona, Sèr. Bot. 5(4): 10 (1924)
Sideritis parvifolia Poir. Encycl. , Suppl. 2: 384 (1811)

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000309902
Tropicos 100258528
KEW urn:lsid:ipni.org:names:458828-1
The Plant List kew-191119
Open Tree Of Life 6081591
Open Tree Of Life 6081706
IPNI 458828-1
iNaturalist 940331
GBIF 7716674
USDA GRIN 475176

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Analysis of diterpenoids from Sideritis species by reversed-phase high-performance liquid chromatography P. Go´mez-Serranillos, O.M. Palomino, A.I. Villarrubia, M.A. Cases, E. Carretero, A. Villar Elsevier BV 24-Apr-2003
doi:10.1016/S0021-9673(97)00222-7
Epoxy-isosidol: A new diterpenoid from Sideritis biflora María C. García-Alvarez, Benjamín Rodríguez Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88871-8

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 / Diterpenoids
(1R,3S,4S,4aS,8S,8aR)-8-(Hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)decalin-1,3-diol 188448 Click to see 322.50 unknown https://doi.org/10.1016/S0021-9673(97)00222-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4S,5S,6R,9S,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 637194 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1016/S0021-9673(97)00222-7
(1R,2S,4S,5S,6R,9S,10S,13R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-2,6-diol 101316788 Click to see 320.50 unknown https://doi.org/10.1016/S0021-9673(97)00222-7
[(1R,2S,4S,5S,6R,9R,10R,13R,14S,16R)-2-hydroxy-5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-6-yl] acetate 163024885 Click to see CC(=O)OC1CCC2(C3CCC4CC3(C(CC2C1(C)CO)O)C5C4(O5)C)C 378.50 unknown https://doi.org/10.1016/S0031-9422(00)88871-8
[2-Hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 12442775 Click to see CC(=O)OC1CCC2(C3CCC4CC3(CC4=C)C(CC2C1(C)CO)O)C 362.50 unknown https://doi.org/10.1016/S0021-9673(97)00222-7
[2-Hydroxy-5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-6-yl] acetate 163024884 Click to see CC(=O)OC1CCC2(C3CCC4CC3(C(CC2C1(C)CO)O)C5C4(O5)C)C 378.50 unknown https://doi.org/10.1016/S0031-9422(00)88871-8
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 12309906 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1016/S0021-9673(97)00222-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,4R,9R,10S,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.01,10.04,9]hexadec-15-en-13-ol 101277423 Click to see CC1(CCCC2(C1CCC34C2CC(C=C3)C(C4)(CO)O)C)C 304.50 unknown https://doi.org/10.1016/S0021-9673(97)00222-7

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