Echinacea pallida - Unknown
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Internal ID UUID643fc82606c9d183433705
Scientific name Echinacea pallida
Authority (Nutt.) Nutt.
First published in Trans. Amer. Philos. Soc. , ser. 2, 7: 354 (1840)

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Synonyms Top

Scientific name Authority First published in
Echinacea pallida f. albida Steyerm. Rhodora 44: 150 (1942)
Brauneria pallida (Nutt.) Britton Mem. Torrey Bot. Club 5: 333 (1894)
Rudbeckia pallida Nutt. J. Acad. Nat. Sci. Philadelphia 7: 77 (1834)

Common names Top

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Language Common/alternative name
English pale purple coneflower
Spanish equinacea palida
Spanish equinacea pálida
Spanish equinácea pálida
Arabic قنفذية شاحبة
German blasser igelkopf
German prärie-igelkopf
Persian سر خار گل
Hungarian halvány kasvirág
Chinese 淡紫松果菊

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000020152
UNII 904CK3270L
Flora of Alabama 692
Canadensys 3059
USDA Plants ECPA
Tropicos 2710005
KEW urn:lsid:ipni.org:names:202374-1
The Plant List gcc-119485
Missouri Botanical Garden 277420
PFAF Echinacea pallida
Open Tree Of Life 608924
NCBI Taxonomy 53749
Nature Serve 2.141782
IPNI 202375-1
iNaturalist 127689
GBIF 3150919
Freebase /m/02r9390
WisFlora 3460
EPPO ECEPA
EOL 467542
USDA GRIN 70237
Wikipedia Echinacea_pallida
CMAUP NPO6412

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
Study Models of Drug–Drug Interactions Involving P-Glycoprotein: The Potential Benefit of P-Glycoprotein Modulation at the Kidney and Intestinal Levels Veiga-Matos J, Morales AI, Prieto M, Remião F, Silva R Molecules 10-Nov-2023
PMCID:PMC10673607
doi:10.3390/molecules28227532
PMID:38005253
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Determination of the Bioactive Compounds from Echinacea purpurea (L.) Moench Leaves Extracts in Correlation with the Antimicrobial Activity and the In Vitro Wound Healing Potential Burlou-Nagy C, Bănică F, Negrean RA, Jurca T, Vicaș LG, Marian E, Bácskay I, Kiss R, Fehér P, Vicaș SI, Miere (Groza) F, Memete AR, Pallag A Molecules 28-Jul-2023
PMCID:PMC10420800
doi:10.3390/molecules28155711
PMID:37570681
Phenology and foraging bias contribute to sex‐specific foraging patterns in the rare declining butterfly Argynnis idalia idalia Chmielewski MW, Naya S, Borghi M, Cortese J, Fernie AR, Swartz MT, Zografou K, Sewall BJ, Spigler RB Ecol Evol 18-Jul-2023
PMCID:PMC10353922
doi:10.1002/ece3.10287
PMID:37475725
Nutraceuticals as Modulators of Immune Function: A Review of Potential Therapeutic Effects Medoro A, Davinelli S, Colletti A, Di Micoli V, Grandi E, Fogacci F, Scapagnini G, Cicero AF Prev Nutr Food Sci 30-Jun-2023
PMCID:PMC10321448
doi:10.3746/pnf.2023.28.2.89
PMID:37416796
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
Jasmonic and Salicylic Acids Enhance Biomass, Total Phenolic Content, and Antioxidant Activity of Adventitious Roots of Acmella radicans (Jacq.) R.K. Jansen Cultured in Shake Flasks Bernabé-Antonio A, Castro-Rubio C, Rodríguez-Anda R, Silva-Guzmán JA, Manríquez-González R, Hurtado-Díaz I, Sánchez-Ramos M, Hinojosa-Ventura G, Romero-Estrada A Biomolecules 26-Apr-2023
PMCID:PMC10216742
doi:10.3390/biom13050746
PMID:37238616
Evaluation of therapeutic effects of an herbal mixture (Echinacea purpurea and Glycyrrhiza glabra) for treatment of clinical coccidiosis in broilers Ghafouri SA, Ghaniei A, Tamannaei AE, Sadr S, Charbgoo A, Ghiassi S, Abuali M Vet Med Sci 17-Oct-2022
PMCID:PMC10029886
doi:10.1002/vms3.971
PMID:36253639
Medicinal Plant Growth in Heavy Metals Contaminated Soils: Responses to Metal Stress and Induced Risks to Human Health Hlihor RM, Roșca M, Hagiu-Zaleschi L, Simion IM, Daraban GM, Stoleru V Toxics 27-Aug-2022
PMCID:PMC9504071
doi:10.3390/toxics10090499
PMID:36136464
A Review with Updated Perspectives on the Antiviral Potentials of Traditional Medicinal Plants and Their Prospects in Antiviral Therapy Saifulazmi NF, Rohani ER, Harun S, Bunawan H, Hamezah HS, Nor Muhammad NA, Azizan KA, Ahmed QU, Fakurazi S, Mediani A, Sarian MN Life (Basel) 22-Aug-2022
PMCID:PMC9410304
doi:10.3390/life12081287
PMID:36013466
Clinical Implications of Herbal Supplements in Conventional Medical Practice: A US Perspective Hassen G, Belete G, Carrera KG, Iriowen RO, Araya H, Alemu T, Solomon N, Bam DS, Nicola SM, Araya ME, Debele T, Zouetr M, Jain N Cureus 15-Jul-2022
PMCID:PMC9375827
doi:10.7759/cureus.26893
PMID:35978741
Chicoric Acid: Natural Occurrence, Chemical Synthesis, Biosynthesis, and Their Bioactive Effects Yang M, Wu C, Zhang T, Shi L, Li J, Liang H, Lv X, Jing F, Qin L, Zhao T, Wang C, Liu G, Feng S, Li F Front Chem 23-Jun-2022
PMCID:PMC9262330
doi:10.3389/fchem.2022.888673
PMID:35815211
Can natural products modulate cytokine storm in SARS-CoV2 patients? Abou Baker DH Biotechnol Rep (Amst) 09-Jun-2022
PMCID:PMC9181898
doi:10.1016/j.btre.2022.e00749
PMID:35702395
Echinacea purpurea (L.) Moench: Biological and Pharmacological Properties. A Review Burlou-Nagy C, Bănică F, Jurca T, Vicaș LG, Marian E, Muresan ME, Bácskay I, Kiss R, Fehér P, Pallag A Plants (Basel) 05-May-2022
PMCID:PMC9102300
doi:10.3390/plants11091244
PMID:35567246
Operational definition of complementary, alternative, and integrative medicine derived from a systematic search Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D BMC Complement Med Ther 12-Apr-2022
PMCID:PMC9006507
doi:10.1186/s12906-022-03556-7
PMID:35413882

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 / Olefins / Acyclic olefins / Alkadienes
n-Heptadecadiene 3016864 Click to see CCCCCCCCCCCCCC=CC=C 236.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<88::AID-PCA384>3.0.CO;2-4
> Lignans, neolignans and related compounds
(2R)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one 15690603 Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC 406.40 unknown via CMAUP database
(2S)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one 92466671 Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC 406.40 unknown via CMAUP database
2-Methoxy-4-[(1R,2S)-1,3-dihydroxy-2-[2-methoxy-4-(3-hydroxypropyl)phenoxy]propyl]phenol 13893597 Click to see COC1=C(C=CC(=C1)CCCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 378.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isoolivil 5316262 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
(inverted exclamation markA)-Hydnocarpin 11213425 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 464.40 unknown via CMAUP database
2-[3beta-(Hydroxymethyl)-2alpha-(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-5,7-dihydroxy-4H-1-benzopyran-4-one 10791345 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO 494.40 unknown via CMAUP database
5'-Methoxyhydnocarpin 5281879 Click to see COC1=CC(=CC2=C1OC(C(O2)C3=CC(=C(C=C3)O)OC)CO)C4=CC(=O)C5=C(C=C(C=C5O4)O)O 494.40 unknown via CMAUP database
Hydnocarpin D 11431204 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 464.40 unknown via CMAUP database
Palstatin 5323578 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C(C=C3OC)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO 524.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
2beta,5alpha-Bis(4-hydroxy-3,5-dimethoxyphenyl)tetrahydro-3alpha,4beta-furandimethanol 25136967 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO 436.50 unknown via CMAUP database
Huazhongilexin 15690604 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO 436.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Olivil 5273570 Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3S)-3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-[[4-[3-(alpha-L-rhamnopyranosyloxy)propyl]-2-methoxyphenyl]oxy]propane-1,3-diol 101606109 Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)O)O)O 554.60 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 486614 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown via CMAUP database
(2S,3R)-3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-[[4-[3-(alpha-L-rhamnopyranosyloxy)propyl]-2-methoxyphenyl]oxy]propane-1,3-diol 15690602 Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)O)O)O 554.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(2,3,4-trimethoxyphenyl)prop-2-enoxy]oxane-3,4,5-triol 11972373 Click to see COC1=C(C(=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O)OC)OC 386.40 unknown via CMAUP database
(4S)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 38346955 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 372.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(8R,9E,13Z)-8-hydroxypentadeca-9,13-dien-11-yn-2-one 162851888 Click to see CC=CC#CC=CC(CCCCCC(=O)C)O 234.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/S0031-9422(00)82379-1
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
(E,8R)-8-hydroxypentadec-9-en-11,13-diyn-2-one 121489413 Click to see CC#CC#CC=CC(CCCCCC(=O)C)O 232.32 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/S0031-9422(00)82379-1
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1986633/
(E,8R)-8-hydroxytetradec-9-en-11,13-diyn-2-one 121490004 Click to see CC(=O)CCCCCC(C=CC#CC#C)O 218.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1986633/
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown via CMAUP database
8-Hydroxy-9-pentadecene-11,13-diyn-2-one, (9E)- 24786360 Click to see CC#CC#CC=CC(CCCCCC(=O)C)O 232.32 unknown https://doi.org/10.1055/S-2008-1034308
8-Hydroxypentadeca-9,13-dien-11-yn-2-one 86163333 Click to see CC=CC#CC=CC(CCCCCC(=O)C)O 234.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/S0031-9422(00)82379-1
https://doi.org/10.1055/S-2008-1034308
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4Z)-N-Isobutyl-2,4-dodecadiene-8,10-diynamide 11651673 Click to see CC#CC#CCCC=CC=CC(=O)NCC(C)C 243.34 unknown https://doi.org/10.1211/0022357011776009
(2Z,4E)-N-Isobutyl-2,4-dodecadiene-8,10-diynamide 11160877 Click to see CC#CC#CCCC=CC=CC(=O)NCC(C)C 243.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745817/
https://doi.org/10.1021/NP040245F
2,4,8,10-Dodecatetraenamide, N-(2-methylpropyl)-, (2E,4E,8Z,10E)- 6440539 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown https://doi.org/10.1211/0022357011776009
N-(2-Methylpropyl)dodeca-2,4,8,10-tetraenamide 156638 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown https://doi.org/10.1211/0022357011776009
N-(2-Methylpropyl)pentadeca-2,9-diene-12,14-diynamide 71412110 Click to see CC(C)CNC(=O)C=CCCCCCC=CCC#CC#C 285.40 unknown https://doi.org/10.1211/0022357011776009
N-(2-Methylpropyl)trideca-2,7-diene-10,12-diynamide 71412111 Click to see CC(C)CNC(=O)C=CCCCC=CCC#CC#C 257.37 unknown https://doi.org/10.1211/0022357011776009
Undeca-2-ene-8,10-diynoic acid isobutylamide 562564 Click to see CC(C)CNC(=O)C=CCCCCC#CC#C 231.33 unknown https://doi.org/10.1211/0022357011776009
> 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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1055/S-2006-960123
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1055/S-2006-960123
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960123
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960123
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1R)-3,3,5-Trimethyl-4-(3-oxobutyl)-4-cyclohexen-1beta-yl beta-D-glucopyranoside 101606458 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(=O)C 372.50 unknown via CMAUP database
CID 11968607 11968607 Click to see CC1=C(C(C(CC1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(=O)C 372.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1016/0031-9422(89)80321-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2006-962030
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Chicoric acid 5281764 Click to see C1=CC(=C(C=C1C=CC(=O)OC(C(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)C(=O)O)O)O 474.40 unknown https://doi.org/10.1300/J044V08N01_03
https://doi.org/10.1016/0031-9422(88)80664-2
https://doi.org/10.1055/S-2002-34397
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
(1S,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid 7067333 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1211/0022357011776009
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1016/0031-9422(88)80664-2
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(88)80664-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Icariside B2 10385469 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C 386.40 unknown via CMAUP database
Phenylethyl beta-D-glucopyranoside 11289099 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(3,5,6,7-tetramethoxy-9,10-dihydrophenanthren-2-yl)oxy]oxane-3,4,5-triol 15690608 Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 478.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 162877293 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 786.70 unknown https://doi.org/10.1211/0022357011776009
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 162996918 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)C(OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)OCCC6=CC(=C(C=C6)O)O)O)O)O)O 964.90 unknown https://doi.org/10.1211/0022357011776009
Echinacoside 5281771 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 786.70 unknown https://doi.org/10.1211/0022357011776009
https://doi.org/10.1080/13880200500408491
https://doi.org/10.1016/S0944-7113(96)80041-9
https://doi.org/10.1016/S0378-8741(01)00391-9
https://doi.org/10.1016/0031-9422(88)80664-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
(9E,13Z)-pentadeca-9,13-dien-11-yne-2,8-dione 16081693 Click to see CC=CC#CC=CC(=O)CCCCCC(=O)C 232.32 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
(E)-pentadec-9-en-11,13-diyne-2,8-dione 16081694 Click to see CC#CC#CC=CC(=O)CCCCCC(=O)C 230.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
Pentadec-9-en-11,13-diyne-2,8-dione 73236022 Click to see CC#CC#CC=CC(=O)CCCCCC(=O)C 230.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
Pentadeca-9,13-dien-11-yne-2,8-dione 73236021 Click to see CC=CC#CC=CC(=O)CCCCCC(=O)C 232.32 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
8-Tetradecene-11,13-diyn-2-one, (8Z)- 11528546 Click to see CC(=O)CCCCCC=CCC#CC#C 202.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
8,13-Pentadecadien-11-yn-2-one, (8Z,13Z)- 16046183 Click to see CC=CC#CCC=CCCCCCC(=O)C 218.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
Pentadeca-8,11-dien-2-one 71339274 Click to see CCCC=CCC=CCCCCCC(=O)C 222.37 unknown https://doi.org/10.1039/B812700J
Pentadeca-8,13-dien-11-YN-2-one 71339566 Click to see CC=CC#CCC=CCCCCCC(=O)C 218.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
Pentadeca-8Z,11Z-dien-2-on 25172308 Click to see CCCC=CCC=CCCCCCC(=O)C 222.37 unknown https://doi.org/10.1039/B812700J
Tetradeca-8-en-11,13-diyn-2-one 72996063 Click to see CC(=O)CCCCCC=CCC#CC#C 202.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
4,18-Dimethoxy-13,14-dimethyl-2,6,8,20,22-pentaoxahexacyclo[10.10.1.01,19.03,11.05,9.016,23]tricosa-3,5(9),10,15,18-pentaen-17-one 13870127 Click to see CC1C=C2C3C(C1C)C4=CC5=C(C(=C4OC36C(=C(C2=O)OC)OCO6)OC)OCO5 414.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267283/
https://doi.org/10.1016/S0031-9422(00)82379-1
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.006
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydropyrimidines
(1R,8S,9R,10S)-9-butyl-10-methyl-5,7-diazatricyclo[6.3.1.04,12]dodeca-4(12),6-dien-6-amine 162867785 Click to see CCCCC1C(CC2CCC3=C2C1N=C(N3)N)C 247.38 unknown https://doi.org/10.1211/0022357011776009
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2beta-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3alpha-methanol 10625848 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown via CMAUP database
Dihydrodehydrodiconiferyl alcohol 384679 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 11968397 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1211/0022357011776009
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/0031-9422(88)80664-2
Caftaric acid 6440397 Click to see C1=CC(=C(C=C1C=CC(=O)OC(C(C(=O)O)O)C(=O)O)O)O 312.23 unknown https://doi.org/10.1016/0031-9422(88)80664-2
https://doi.org/10.1021/JF011439T
https://doi.org/10.1021/JF001331Y
Calceolarioside A 5273566 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/0031-9422(88)80664-2
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/0031-9422(88)80664-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1080/13880200500408491
> Phenylpropanoids and polyketides / Coumarins and derivatives
6-Demethoxycapillarisin 5316511 Click to see C1=CC(=CC=C1O)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O 286.24 unknown via CMAUP database
Demethoxy-7-O-methylcapillarisin 71391689 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)OC3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
> 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 via CMAUP database
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 via CMAUP database
> 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 / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1016/0031-9422(89)80321-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2''-O-alpha-L-Rhamnopyranostylquercitrin 10698716 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)C)O)O)O)O)O 594.50 unknown via CMAUP database
2'',4''-Di-O-(E-p-Coumaroyl)afzelin 11765457 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
3-[2-O-(4-Hydroxy-cis-cinnamoyl)-4-O-(4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone 11700461 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
3-[2-O-(4-Hydroxy-trans-cinnamoyl)-4-O-(4-hydroxy-cis-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone 49822437 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
3-[3-O-(4-Hydroxy-cis-cinnamoyl)-4-O-(4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone 45783016 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
3'',4''-Di-O-p-coumaroylafzelin 51136469 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown via CMAUP database
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
Baohuoside I 5488822 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)OC)O)O)O 514.50 unknown via CMAUP database
Baohuoside II 5481982 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)O)O)O 500.50 unknown via CMAUP database
Hyperoside 5281643 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
Kaempferol 3-(2-rhamnopyranosylrhamnopyranoside) 10721917 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)C)O)O)O)O)O 578.50 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Baohuoside V 25087702 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)C)O)O)O)O)O 808.80 unknown via CMAUP database
Epimedin A 13916051 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)O)O 838.80 unknown via CMAUP database
Epimedin A1 92043273 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)OC6C(C(C(C(O6)CO)O)O)O)O 838.80 unknown via CMAUP database
Epimedin B 5748393 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)OC6C(C(C(CO6)O)O)O)O)O 808.80 unknown via CMAUP database
Epimedin C 5748394 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)OC)C)O)O)O)O)O 822.80 unknown via CMAUP database
Epimedokoreanoside I 87759921 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)OC6C(C(C(C(O6)COC(=O)C)O)O)O)OC(=O)C 922.90 unknown via CMAUP database
Epimedoside A 5317093 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 662.60 unknown via CMAUP database
Icariin 5318997 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 unknown via CMAUP database
Icariside I 5745470 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)OC)O)OC4C(C(C(C(O4)CO)O)O)O)C 530.50 unknown via CMAUP database
Sagittasine B 101437361 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C=C6)OC)O)C)O)O)O)O)O 838.80 unknown via CMAUP database
Sagittasine C 101437362 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)OC)O)O)O)O 692.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-methyltricetin 11267045 Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 316.26 unknown via CMAUP database
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-(1,3-Benzodioxol-5-yl)-5-hydroxy-6,7-dimethoxychromen-4-one 5321057 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC4=C(C=C3)OCO4)O)OC 342.30 unknown via CMAUP database

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