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Sideritis raeseri

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
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)

Ethnobotanical Use Top

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General Uses 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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Language Common/alternative name
Chinese 拉氏铁草
Chinese 拉氏毒马草

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

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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
Design of Experiments for Optimizing Ultrasound-Assisted Extraction of Bioactive Compounds from Plant-Based Sources Anaya-Esparza LM, Aurora-Vigo EF, Villagrán Z, Rodríguez-Lafitte E, Ruvalcaba-Gómez JM, Solano-Cornejo MÁ, Zamora-Gasga VM, Montalvo-González E, Gómez-Rodríguez H, Aceves-Aldrete CE, González-Silva N Molecules 24-Nov-2023
PMCID:PMC10707804
doi:10.3390/molecules28237752
PMID:38067479
Chemical profile of the Anatolian Sideritis species with bioactivity studies Çarıkçı S, Kılıç T, Gören AC, Dirmenci T, Alim Toraman GÖ, Topçu G Pharm Biol 22-Nov-2023
PMCID:PMC11001281
doi:10.1080/13880209.2023.2280253
PMID:37990887
Development of a Holistic In Vitro Cell-Free Approach to Determine the Redox Bioactivity of Agricultural Products Skaperda Z, Tekos F, Vardakas P, Nechalioti PM, Kourti M, Patouna A, Makri S, Gkasdrogka M, Kouretas D Int J Mol Sci 17-Nov-2023
PMCID:PMC10671064
doi:10.3390/ijms242216447
PMID:38003634
Pomegranate peel, Chokeberry Leaves and Ironwort Extract as Novel Natural Inhibitors of Amylin Aggregation and Cellular Toxicity in Pancreatic β Cells Rishisree A, Mallory B, Elena K, Teodora J, Gordana Z, Katarina Š, Aleksandar J Biophys Chem 31-Oct-2023
PMCID:PMC10841580
doi:10.1016/j.bpc.2023.107130
PMID:37952497
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
Characterization of Sideritis clandestina subsp. peloponnesiaca Polar Glycosides and Phytochemical Comparison to Other Mountain Tea Populations Dimaki VD, Zeliou K, Nakka F, Stavreli M, Bakratsas I, Papaioannou L, Iatrou G, Lamari FN Molecules 06-Nov-2022
PMCID:PMC9658581
doi:10.3390/molecules27217613
PMID:36364439
Bioassay-Guided Skin-Beneficial Effects of Fractionated Sideritis raeseri subsp. raeseri Extract Krgović N, Jovanović M, Aradski AA, Janković T, Stević T, Zdunić G, Laušević SD, Šavikin K Plants (Basel) 11-Oct-2022
PMCID:PMC9609566
doi:10.3390/plants11202677
PMID:36297701

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 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 136.23 unknown https://doi.org/10.1080/10412905.2002.9699891
Beta-Pinene 14896 Click to see 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 5280704 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(90)85149-A
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(90)85149-A

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