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Sideritis pungens

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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 UUID643fecdc939a4331093634
Scientific name Sideritis pungens
Authority Benth.
First published in Labiat. Gen. Spec. : 579 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sideritis giennensis Pau ex Font Quer Cavanillesia 1: 40. 1928 (1928)
Sideritis gudarica Mateo, López Udias & Fabregat Anales Jard. Bot. Madrid 57: 419 (1999 publ. 2000)
Sideritis javalambrensis Pau Not. Bot. Fl. Españ. 1: 26 (1887)
Sideritis linearifolia Lag. Gen. Sp. Pl. : 18 (1816)
Sideritis pungens subsp. javalambrensis (Pau) Obón & D.Rivera Phanerog. Monogr. 21: 291 (1994)
Sideritis pungens subsp. vigoi Peris, R.Roselló & Stübing Anales Jard. Bot. Madrid 57: 416 (2000)
Sideritis linearifolia var. javalambrensis (Pau) Font Quer ex O.Bolòs & Vigo Collect. Bot. (Barcelona) 14: 93 (1983)
Fracastora linearifolia Bubani Fl. Pyren. 1: 457 (1897)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000310380
Tropicos 50194935
KEW urn:lsid:ipni.org:names:459059-1
The Plant List kew-191579
Open Tree Of Life 914854
Observations.org 132088
NCBI Taxonomy 155258
IPNI 459059-1
iNaturalist 824787
GBIF 7307469
EPPO SIEPU
Elurikkus 586231
USDA GRIN 407626

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
Essential oil of Sideritis hirsuta Carmen Mateo, Jesús Sanz, José Calderón Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80081-3
Diterpenoids from sideritis varoi José Algarra, Andrés García-Granados, Antonio Sáenz de Buruaga, Juan M.Sáenz de Buruaga Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80270-8
A manoyl oxide diterpenoid from Sideritis javalambrensis Angel Villar, Serafin Valverde, Beatriz De Las Heras, Jose M. Vivas Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)80050-3
Antioxidant activity of flavonoids from Sideritis javalambrensis. Rios JL, Mañez S, Paya M, Alcaraz MJ Phytochemistry 01-Jun-1992
doi:10.1016/0031-9422(92)80338-F
PMID:1368218
Anti-inflammatory compounds from Sideritis javalambrensis n-hexane extract. Alcaraz MJ, Jimenez MJ, Valverde S, Sanz J, Rabanal RM, Villar A J Nat Prod 01-Sep-1989
doi:10.1021/NP50065A027
PMID:2481715

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 / Kaurane diterpenoids
Siderol 12315548 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)CO)C 346.50 unknown https://doi.org/10.1016/S0031-9422(00)80270-8
> 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/10.1016/S0031-9422(00)80081-3
> 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)80081-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3S,4aS,6aR,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-2-ol 14240411 Click to see CC1(CCCC2(C1CCC3(C2CC(C(O3)(C)C=C)O)C)C)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)80270-8
(3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-2-yl) acetate 14355715 Click to see CC(=O)OC1CC2C3(CCCC(C3CCC2(OC1(C)C=C)C)(C)C)C 348.50 unknown https://doi.org/10.1016/0031-9422(93)80050-3
(3R,4aS,6aS,8R,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-ol 13970287 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC(O3)(C)C=C)C)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)80270-8
Ent-13-epi-12-acetoxymanoyl oxide 14355716 Click to see CC(=O)OC1CC2C3(CCCC(C3CCC2(OC1(C)C=C)C)(C)C)C 348.50 unknown https://doi.org/10.1016/0031-9422(93)80050-3
OH-Manoyl oxide 195370 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(CO)C=C)C)C)C 306.50 unknown https://doi.org/10.1021/NP50065A027
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl] docosanoate 163187962 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OC(=O)C(CC1=CC=C(C=C1)O)N 503.80 unknown https://doi.org/10.1021/NP50065A027
[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl] tetracosanoate 163192935 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OC(=O)C(CC1=CC=C(C=C1)O)N 531.80 unknown https://doi.org/10.1021/NP50065A027
Tyrosyl palmitate 123627724 Click to see CCCCCCCCCCCCCCCC(=O)OC(=O)C(CC1=CC=C(C=C1)O)N 419.60 unknown https://doi.org/10.1021/NP50065A027
Tyrosyl stearate 123558527 Click to see CCCCCCCCCCCCCCCCCC(=O)OC(=O)C(CC1=CC=C(C=C1)O)N 447.60 unknown https://doi.org/10.1021/NP50065A027
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6R)-6-[(2R,3R,4S,5S,6R)-2-[5,8-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162889656 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O 682.60 unknown https://doi.org/10.1016/0031-9422(92)80338-F
[(2R,3S,4R,5R,6R)-6-[(2R,3R,4S,5S,6R)-2-[5,8-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163071306 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC=C(C=C5)OC)O)CO)O)O)O)O)O 666.60 unknown https://doi.org/10.1016/0031-9422(92)80338-F
[(2R,3S,4R,5R,6R)-6-[(2S,3R,4S,5S,6R)-2-[5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162963296 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 652.60 unknown https://doi.org/10.1016/0031-9422(92)80338-F
[6-[2-[5,8-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73802680 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 652.60 unknown https://doi.org/10.1016/0031-9422(92)80338-F
[6-[2-[5,8-Dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73802681 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC=C(C=C5)OC)O)CO)O)O)O)O)O 666.60 unknown https://doi.org/10.1016/0031-9422(92)80338-F
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-5,8-dihydroxy-2-(4-methoxyphenyl)chromen-4-one 163188624 Click to see COC1=CC=C(C=C1)C2=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 624.50 unknown https://doi.org/10.1016/0031-9422(92)80338-F
7-[(2S,3S,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-5,8-dihydroxy-2-(4-methoxyphenyl)chromen-4-one 162961242 Click to see COC1=CC=C(C=C1)C2=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 624.50 unknown https://doi.org/10.1016/0031-9422(92)80338-F
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,8-dihydroxy-2-(4-methoxyphenyl)chromen-4-one 74977913 Click to see COC1=CC=C(C=C1)C2=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 624.50 unknown https://doi.org/10.1016/0031-9422(92)80338-F
8-Hydroxyhesperetin 7-[6-acetylglucosyl-(1->2)-glucoside] 74977927 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O 682.60 unknown https://doi.org/10.1016/0031-9422(92)80338-F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
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/10.1016/0031-9422(92)80338-F
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/10.1016/0031-9422(92)80338-F

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