Sideritis syriaca - Unknown
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Internal ID UUID643fecdf6d644288017203
Scientific name Sideritis syriaca
Authority L.
First published in Sp. Pl. : 574 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Navicularia syriaca (L.) Soják Cas. Nár. Mus., Odd. Prír. 148: 79 (1979 publ. 1980)
Sideritis cretica Boiss. Fl. Orient. 4: 708 (1879)

Common names Top

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Language Common/alternative name
English ironwort
Arabic فزر سوري
Bulgarian кримски миризлив бурен
German griechischer bergtee
German malotira
German syrisches gliedkraut
French thé de crimée
French tisane strandzhan
Italian stregonia siciliana

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Sideritis syriaca subsp. nusairiensis (Post) Hub.-Mor. Bauhinia 6: 291 (1978)
Sideritis syriaca subsp. syriaca 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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

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-0000310485
Tropicos 17600670
KEW urn:lsid:ipni.org:names:459111-1
The Plant List kew-191680
Open Tree Of Life 290040
Observations.org 146857
NCBI Taxonomy 155265
IPNI 459111-1
iNaturalist 358226
GBIF 7307364
Freebase /m/011bdmyv
EPPO SIESY
USDA GRIN 411422
Wikipedia Sideritis_syriaca
CMAUP NPO1723
PFAF Sideritis syriaca

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
DNA Barcoding and Fertilization Strategies in Sideritis syriaca subsp. syriaca, a Local Endemic Plant of Crete with High Medicinal Value Paschalidis K, Fanourakis D, Tsaniklidis G, Tsichlas I, Tzanakakis VA, Bilias F, Samara E, Ipsilantis I, Grigoriadou K, Samartza I, Matsi T, Tsoktouridis G, Krigas N Int J Mol Sci 04-Feb-2024
PMCID:PMC10856587
doi:10.3390/ijms25031891
PMID:38339166
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
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
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
Determination of the Total Phenolics Content and Antioxidant Activity of Extracts from Parts of Plants from the Greek Island of Crete Kalpoutzakis E, Chatzimitakos T, Athanasiadis V, Mitakou S, Aligiannis N, Bozinou E, Gortzi O, Skaltsounis LA, Lalas SI Plants (Basel) 01-Mar-2023
PMCID:PMC10005234
doi:10.3390/plants12051092
PMID:36903954
Mediterranean Diet: The Role of Phenolic Compounds from Aromatic Plant Foods Delgado A, Gonçalves S, Romano A Foods 16-Feb-2023
PMCID:PMC9957056
doi:10.3390/foods12040840
PMID:36832914
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
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
Medicinal-Cosmetic Potential of the Local Endemic Plants of Crete (Greece), Northern Morocco and Tunisia: Priorities for Conservation and Sustainable Exploitation of Neglected and Underutilized Phytogenetic Resources Bourgou S, Ben Haj Jilani I, Karous O, Megdiche-Ksouri W, Ghrabi-Gammar Z, Libiad M, Khabbach A, El Haissoufi M, Lamchouri F, Greveniotis V, Avramakis M, Hatzilazarou S, Anestis I, Tsoktouridis G, Krigas N Biology (Basel) 16-Dec-2021
PMCID:PMC8698715
doi:10.3390/biology10121344
PMID:34943257
GIS-Facilitated Seed Germination and Multifaceted Evaluation of the Endangered Abies marocana Trab. (Pinaceae) Enabling Conservation and Sustainable Exploitation Hatzilazarou S, El Haissoufi M, Pipinis E, Kostas S, Libiad M, Khabbach A, Lamchouri F, Bourgou S, Megdiche-Ksouri W, Ghrabi-Gammar Z, Aslanidou V, Greveniotis V, Sakellariou MA, Anestis I, Tsoktouridis G, Krigas N Plants (Basel) 27-Nov-2021
PMCID:PMC8707146
doi:10.3390/plants10122606
PMID:34961077
Agro-Alimentary Potential of the Neglected and Underutilized Local Endemic Plants of Crete (Greece), Rif-Mediterranean Coast of Morocco and Tunisia: Perspectives and Challenges Libiad M, Khabbach A, El Haissoufi M, Anestis I, Lamchouri F, Bourgou S, Megdiche-Ksouri W, Ghrabi-Gammar Z, Greveniotis V, Tsiripidis I, Dariotis E, Tsiafouli MA, Krigas N Plants (Basel) 25-Aug-2021
PMCID:PMC8469186
doi:10.3390/plants10091770
PMID:34579305
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
Effect of Cocoa Bean Shell Addition on Metabolite Profile and Antioxidant Activity of Herbal Infusions Quijano-Avilés M, Chóez-Guaranda I, Viteri R, Barragán-Lucas A, Sosa D, Manzano P Int J Food Sci 06-May-2021
PMCID:PMC8121573
doi:10.1155/2021/9915797
PMID:34036096
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
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157

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
> Benzenoids / Benzene and substituted derivatives
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL 5318042 Click to see CCCC=CCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-one 163195101 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3=O)(C)CO)C 302.50 unknown https://doi.org/10.1016/0031-9422(83)80158-7
Kaurane-7,18-diol, 15,16-epoxy-, (4beta,7alpha,15alpha)- 163092060 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO 320.50 unknown https://doi.org/10.1016/0031-9422(83)83060-X
Siderone 14681633 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3=O)(C)CO)C 302.50 unknown https://doi.org/10.1016/0031-9422(83)80158-7
Ucriol 12315549 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO 320.50 unknown https://doi.org/10.1016/0031-9422(83)83060-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown via CMAUP database
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin 5281238 Click to see CC1=CC(CC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C)(C)C)O 584.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
[17-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-10-methyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-13-yl]methyl acetate 14102732 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)COC(=O)C)C 480.60 unknown https://doi.org/10.1016/J.FOODCHEM.2010.05.076
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp 70680285 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O 356.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Neoamygdalin 441462 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hexenal 5281168 Click to see CCCC=CC=O 98.14 unknown via CMAUP database
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one 7057972 Click to see CCCCC1CCC(=O)O1 142.20 unknown via CMAUP database
(R)-gamma-Decalactone 183870 Click to see CCCCCCC1CCC(=O)O1 170.25 unknown via CMAUP database
2(3H)-Furanone, dihydro-5-octyl-, (5R)- 10888889 Click to see CCCCCCCCC1CCC(=O)O1 198.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol 6428573 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 73353883 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate 10723070 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)OC(=O)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)O 664.60 unknown via CMAUP database
ent-Epiafzelechin-(2alpha-O-7,4alpha-8)-ent-epiafzelechin 5317051 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Geranin A 5317050 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Mahuannin A 5317052 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
[4-[5,8-Dihydroxy-7-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-4-oxochromen-2-yl]phenyl] 3-(4-hydroxyphenyl)prop-2-enoate 162868104 Click to see C1=CC(=CC=C1C=CC(=O)OC2=CC=C(C=C2)C3=CC(=O)C4=C(O3)C(=C(C=C4O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 578.50 unknown https://doi.org/10.1016/J.FOODCHEM.2010.05.076
[5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101523766 Click to see C1=CC(=CC=C1C=CC(=O)OC2=C(C3=C(C(=C2)O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)O 432.40 unknown https://doi.org/10.1016/J.FOODCHEM.2010.05.076
[5,8-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] 3-(4-hydroxyphenyl)prop-2-enoate 163057819 Click to see C1=CC(=CC=C1C=CC(=O)OC2=C(C3=C(C(=C2)O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)O 432.40 unknown https://doi.org/10.1016/J.FOODCHEM.2010.05.076
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162916367 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(94)00634-6
[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/J.FOODCHEM.2010.05.076
7-[[2-O-(6-O-Acetyl-I(2)-D-glucopyranosyl)-I(2)-D-glucopyranosyl]oxy]-5,8-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one 101915840 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(94)00634-6
7-[2-O-(6-O-Acetyl-beta-D-allopyranosyl)-beta-D-glucopyranosyloxy]-5,8-dihydroxy-4'-methoxyflavone 21576582 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/J.FOODCHEM.2010.05.076
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(94)00634-6
Echinacin 6439941 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(94)00634-6

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