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Sideritis raeseri

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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 UUID643fecdd04137099999022
Scientific name Sideritis raeseri
Authority Boiss. & Heldr.
First published in Diagn. Pl. Orient. , ser. 2, 4: 30 (1859)

Description Top

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Synonyms Top

Scientific name Authority First published in
Navicularia syriaca subsp. raeseri (Boiss. & Heldr.) Soják Cas. Nár. Mus., Odd. Prír. 148: 79 (1979 publ. 1980)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Sideritis raeseri subsp. attica (Heldr.) Papan. & Kokkini World Crops 7: 118 (1982)
Sideritis raeseri subsp. raeseri Unknown

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000310395
Tropicos 17605508
KEW urn:lsid:ipni.org:names:459065-1
The Plant List kew-191594
Open Tree Of Life 298392
NCBI Taxonomy 194203
IPNI 459065-1
iNaturalist 940263
GBIF 7307453

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
Spasmolytic Activity of Gentiana lutea L. Root Extracts on the Rat Ileum: Underlying Mechanisms of Action Kitić N, Živković J, Šavikin K, Randjelović M, Jovanović M, Kitić D, Miladinović B, Milutinović M, Stojiljković N, Branković S Plants (Basel) 04-Feb-2024
PMCID:PMC10857127
doi:10.3390/plants13030453
PMID:38337986
Characterization of the Chemical Composition and Biological Activities of Bog Bilberry (Vaccinium uliginosum L.) Leaf Extracts Obtained via Various Extraction Techniques Ștefănescu BE, Socaci SA, Fărcaș AC, Nemeș SA, Teleky BE, Martău GA, Călinoiu LF, Mitrea L, Ranga F, Grigoroaea D, Vodnar DC, Socaciu C Foods 13-Jan-2024
PMCID:PMC10814626
doi:10.3390/foods13020258
PMID:38254559
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
Chemical Composition of the Essential Oils of Three Popular Sideritis Species Cultivated in Greece Using GC-MS Analysis Kaparakou EH, Daferera D, Kanakis CD, Skotti E, Kokotou MG, Tarantilis PA Biomolecules 20-Jul-2023
PMCID:PMC10377382
doi:10.3390/biom13071157
PMID:37509192
Comparative Study on Assisted Solvent Extraction Techniques for the Extraction of Biologically Active Compounds from Sideritis raeseri and Sideritis scardica Mróz M, Malinowska-Pańczyk E, Bartoszek A, Kusznierewicz B Molecules 20-May-2023
PMCID:PMC10223660
doi:10.3390/molecules28104207
PMID:37241947
Natural Products for the Prevention and Treatment of Common Cold and Viral Respiratory Infections Mammari N, Albert Q, Devocelle M, Kenda M, Kočevar Glavač N, Sollner Dolenc M, Mercolini L, Tóth J, Milan N, Czigle S, Varbanov M Pharmaceuticals (Basel) 28-Apr-2023
PMCID:PMC10220542
doi:10.3390/ph16050662
PMID:37242445
Phylogenetic data reveal a surprising origin of Euphorbia orphanidis (Euphorbiaceae) and environmental modeling suggests that microtopology limits its distribution to small patches in Mt. Parnassus (Greece) Faltner F, Wessely J, Frajman B Front Plant Sci 16-Feb-2023
PMCID:PMC9978759
doi:10.3389/fpls.2023.1116496
PMID:36875595
Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S Biomolecules 02-Dec-2022
PMCID:PMC9775335
doi:10.3390/biom12121807
PMID:36551235
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312
Effect of heavy metals on in vitro growth and development of the Momordica cymbalaria Fenzl Chaitanya G, Pavani C, Shasthree T Int J Environ Sci Technol (Tehran) 27-Jul-2022
PMCID:PMC9326134
doi:10.1007/s13762-022-04437-9
PMID:35909798
Exploration of Lamiaceae in Cardio Vascular Diseases and Functional Foods: Medicine as Food and Food as Medicine Chakrabartty I, Mohanta YK, Nongbet A, Mohanta TK, Mahanta S, Das N, Saravanan M, Sharma N Front Pharmacol 14-Jun-2022
PMCID:PMC9237463
doi:10.3389/fphar.2022.894814
PMID:35774598
Optimization of Ultrasound-Assisted Extraction of Phenolics from Sideritis raeseri Using Response Surface Methodology Šavikin K, Živković J, Janković T, Ćujić-Nikolić N, Zdunić G, Menković N, Drinić Z Molecules 28-Jun-2021
PMCID:PMC8272202
doi:10.3390/molecules26133949
PMID:34203414
A Comparison Study on Traditional Mixtures of Herbal Teas Used in Eastern Mediterranean Area Obón C, Rivera D, Fonollá E, Alcaraz F, Attieh L Front Pharmacol 23-Apr-2021
PMCID:PMC8103161
doi:10.3389/fphar.2021.632692
PMID:33967769
Antioxidant and Cytoprotective Potential of the Essential Oil Pistacia lentiscus var. chia and Its Major Components Myrcene and α-Pinene Xanthis V, Fitsiou E, Voulgaridou GP, Bogadakis A, Chlichlia K, Galanis A, Pappa A Antioxidants (Basel) 18-Jan-2021
PMCID:PMC7830477
doi:10.3390/antiox10010127
PMID:33477450
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088

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 / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
[(2R,3R,4S,5R,6R)-6-[(2S)-4-(3,4-dimethoxyphenyl)butan-2-yl]oxy-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163195602 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC(C)CCC3=CC(=C(C=C3)OC)OC)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 680.70 unknown https://doi.org/10.1016/0031-9422(90)85149-A
[6-[4-(3,4-Dimethoxyphenyl)butan-2-yloxy]-3,5-dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 85202731 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC(C)CCC3=CC(=C(C=C3)OC)OC)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 680.70 unknown https://doi.org/10.1016/0031-9422(90)85149-A
> 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/10.1080/10412905.2002.9699891
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.2002.9699891
> Phenylpropanoids and polyketides / Flavonoids / Flavones
[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] (E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 14482780 Click to see C1=CC(=CC=C1C=CC(=O)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(90)85149-A
[5-Hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] 3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 162880485 Click to see C1=CC(=CC=C1C=CC(=O)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(90)85149-A
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/10.1016/0031-9422(90)85149-A
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/10.1016/0031-9422(90)85149-A
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(90)85149-A
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(90)85149-A

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