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Sideritis leucantha

Sideritis leucantha - 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
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Details Top

Internal ID UUID643fecd7120c9689170852
Scientific name Sideritis leucantha
Authority Cav.
First published in Icon. 4: 2 (1797)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sideritis angustifolia var. canescens T.Navarro & Rosua Anales Biol., Fac. Biol., Univ. Murcia 9: 51 (1986)
Sideritis leucantha subsp. albicaulis Obón & D.Rivera Anales Jard. Bot. Madrid 48: 267 (1990 publ. 1991)
Sideritis leucantha subsp. illicitana Alcaraz, T.E.Díaz, Rivas Mart. & Sánchez-Gómez Itin. Geobot. 2: 117 (1989)
Sideritis leucantha subsp. incana (Willk.) Alcaraz, Peinado, Mart.Parras, J.S.Carrion & Sánchez-Gómez Acta Bot. Malac. 12: 246. 1987
Sideritis leucantha var. meridionalis Font Quer Trab. Mus. Ci. Nat. Barcelona 5(4): 9. 1924
Sideritis leucantha var. tomentosa Font Quer ex O.Bolòs & Vigo Collect. Bot. (Barcelona) 14: 93 (1983)
Sideritis linearifolia var. incana Willk. Linnaea 25: 56 1852
Sideritis murgetana Obón & D.Rivera Anales Jard. Bot. Madrid 48: 264 (1990 publ. 1991)
Sideritis murgetana subsp. littoralis Obón & D.Rivera Anales Jard. Bot. Madrid 48: 265 (1990 publ. 1991)
Sideritis murgetana subsp. pauciflora Obón & D.Rivera Anales Jard. Bot. Madrid 48: 265 (1990 publ. 1991)

Common names Top

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Language Common/alternative name
Spanish rabo de gato

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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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-0000310221
Tropicos 17600649
KEW urn:lsid:ipni.org:names:458973-1
The Plant List kew-191429
Open Tree Of Life 5232694
Observations.org 131871
NCBI Taxonomy 1391945
IUCN Red List 203269
IPNI 458973-1
iNaturalist 443677
GBIF 7307627
Freebase /m/0v3dz70
Elurikkus 586258
USDA GRIN 407625
Wikipedia Sideritis_leucantha

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
In Vitro Propagation, Genetic Assessment, and Medium-Term Conservation of the Coastal Endangered Species Tetraclinis articulata (Vahl) Masters (Cupressaceae) from Adult Trees Juan-Vicedo J, Serrano-Martínez F, Cano-Castillo M, Casas JL Plants (Basel) 11-Jan-2022
PMCID:PMC8778163
doi:10.3390/plants11020187
PMID:35050075
Preventative and Therapeutic Potential of Flavonoids in Peptic Ulcers Zhang W, Lian Y, Li Q, Sun L, Chen R, Lai X, Lai Z, Yuan E, Sun S Molecules 11-Oct-2020
PMCID:PMC7594042
doi:10.3390/molecules25204626
PMID:33050668
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
Seasonal Variation of Free Flavone Aglycones from Sideritis leucantha (Lamiaceae) F. A. T. Barberán, F. Tomás, J. M. Núñez Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1985-11-1228
Tlc, uv and acidic treatment in the differentiation of 5,6- and 5,8-dihydroxyflavones, 3-methoxyflavones and flavonols F.A.T. Barberán, F. Ferreres, F. Tomás Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)91379-1
Two flavone glucosides from Sideritis leucantha Francisco Tomas, Federico Ferreres Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83037-8
Hypolaetin 8-glucoside from Sideritis leucantha Francisco Tomas, Bernard Voirin, Francisco A.T. Barberan, Philippe Lebreton Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81082-1
An HPLC study of flavones from some Spanish Sideritis species F Barberan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81116-4
Two flavone glycosides from Sideritis leucantha F.A.T. Barberán, F. Tomás, F. Ferreres Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85000-1
Electron impact mass spectrometric differentiation of 5,6-dihydroxy-7,8-dimethoxy- and 5,8-dihydroxy-6,7-dimethoxyflavones F.A.T. Barberan, F. Ferreres, F. Tomas, A. Guirado Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)80028-0
The essential oils of some eastern Spain Sideritis Carmen Mateo, Jesús Sanz, José Calderón Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80325-8
Anti-Inflammatory Activity of a Flavone from Sideritis leucantha. Jiménez MJ, Alcaraz MJ, Ferrandiz ML, Villar A Planta Med 01-Dec-1986
doi:10.1055/S-2007-969341
PMID:17345496

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Fenchyl acetate 107217 Click to see CC(=O)OC1C(C2CCC1(C2)C)(C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
[(E,7R)-3,7-dimethyl-9-[(1S,6S)-2,2,6-trimethylcyclohexyl]non-2-enyl] acetate 162905171 Click to see CC1CCCC(C1CCC(C)CCCC(=CCOC(=O)C)C)(C)C 336.60 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene 10899740 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4S,6Z,10Z,11aR)-6-formyl-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 101967046 Click to see CC(=C)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)C=O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,8-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162923910 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown https://doi.org/10.1016/0031-9422(80)83037-8
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,8-dimethoxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162923911 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown https://doi.org/10.1016/0031-9422(80)83037-8
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 21721963 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)O)O 522.50 unknown https://doi.org/10.1016/0031-9422(80)83037-8
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 73829941 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)O)O 522.50 unknown https://doi.org/10.1016/0031-9422(80)83037-8
5,7,3',4'-Tetrahydroxy-6,8-dimethoxyflavone 7-glucoside 44258639 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown https://doi.org/10.1016/0031-9422(80)83037-8
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,8-dihydroxychromen-4-one 162942038 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
7-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,8-dihydroxychromen-4-one 162942036 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163016227 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-8-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163016226 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
2-(3,4-Dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74977945 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85000-1
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13988639 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)81082-1
Hypolaetin 8-O-beta-D-glucoside 44258591 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)81082-1
Hypolaetin-8-glucoside 5318255 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)81082-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
https://doi.org/10.1515/ZNC-1985-11-1228
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
https://doi.org/10.1515/ZNC-1985-11-1228
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1515/ZNC-1985-11-1228
https://doi.org/10.1016/S0031-9422(00)81116-4
Leucanthogenin 15224752 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)O)OC 346.30 unknown https://doi.org/10.1016/S0040-4020(01)91379-1
https://doi.org/10.1016/0031-9422(86)80028-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
8-Methoxycirsilineol 181092 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)81116-4
https://doi.org/10.1515/ZNC-1985-11-1228
Sideritoflavone 155493 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC)OC 360.30 unknown https://doi.org/10.1515/ZNC-1985-11-1228
https://doi.org/10.1055/S-2007-969341
https://doi.org/10.1016/S0031-9422(00)81116-4
Xanthomicrol 73207 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC 344.30 unknown https://doi.org/10.1515/ZNC-1985-11-1228
https://doi.org/10.1016/S0031-9422(00)81116-4

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