Echinacea angustifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Echinacea angustifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fcad242dc5588854337
Scientific name Echinacea angustifolia
Authority DC.
First published in Prodr. 5: 554 (1836)

Description Top

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Echinacea angustifolia, also known as the narrow-leaved purple coneflower, is a flowering plant native to North America. It is commonly found in the Great Plains region of central Canada and the central United States. This perennial herb has hairy stems and leaves and produces flower heads with pink or purple ray florets and orange disc florets. It typically blooms in late spring to mid-summer and thrives in dry prairies and barrens. Echinacea angustifolia has been used by many Native American groups for traditional medicine, although its effectiveness and safety for treating diseases is still debated. The plant's name is derived from the Greek word for sea urchin, due to its flower head resembling the spiny animal. It has a slow growth rate and is pollinated by bees. Echinacea angustifolia is also known for its high concentration of polyphenols and alkylamides, which are more abundant in plants growing in higher latitudes.

Synonyms Top

Scientific name Authority First published in
Echinacea pallida var. strigosa (R.L.McGregor) Gandhi
Echinacea angustifolia var. strigosa McGregor Trans. Kansas Acad. Sci. 70(3): 368 (1968)
Brauneria angustifolia (DC.) A.Heller Muhlenbergia 1: 5 (1900)
Echinacea angustifolia var. angustifolia DC.
Echinacea pallida var. angustifolia (DC.) Cronquist Vasc. Pl. Pacif. N.W. 5: 160 (1955)

Common names Top

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Language Common/alternative name
English narrow-leaved purple coneflower
English echinacea
English purple coneflower
English blacksamson echinacea
Spanish equinácea angustifolia
Arabic قنفذية رفيعة الأوراق
Catalan equinàcia
chy mo'ôhtávêheséeo'ôtse
Czech třapatka úzkolistá
German brauneria angustifolia
German schmalblättrige kegelblume
German schmalblättriger igelkopf
German schmalblättriger sonnenhut
Persian سرخارگل
Hungarian keskenylevelű kasvirág
Polish jeżówka wąskolistna
Chinese 狭叶松果菊

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • North-central U.S.A.
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Montana
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Louisiana
    • Western Canada
      • Manitoba
      • Saskatchewan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000041434
Canadensys 3058
USDA Plants ECAN2
Tropicos 2700681
KEW urn:lsid:ipni.org:names:87143-2
The Plant List gcc-140068
Missouri Botanical Garden 277183
PFAF Echinacea angustifolia
Open Tree Of Life 618371
Observations.org 117316
NCBI Taxonomy 308558
Nature Serve 2.128470
IPNI 87143-2
iNaturalist 162167
GBIF 3150933
Freebase /m/06chv_
FEIS plants/forb/echang
EPPO ECEAN
EOL 467541
USDA GRIN 14798
Wikipedia Echinacea_angustifolia
CMAUP NPO726

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
Application of Antioxidant Poly-Lactic Acid/Polyhydroxybutyrate (PLA/PHB) Films with Rice Bran Extract for the Preservation of Fresh Pork Meat Cabeza de Vaca M, Ramírez-Bernabé MR, Barrado DT, Pimienta JR, Delgado-Adámez J Foods 21-Mar-2024
PMCID:PMC10970240
doi:10.3390/foods13060972
PMID:38540962
Traditional and contemporary herbal medicines in management of cancer: A scoping review Imtiaz I, Schloss J, Bugarcic A J Ayurveda Integr Med 23-Feb-2024
PMCID:PMC10901831
doi:10.1016/j.jaim.2024.100904
PMID:38395014
The complete plastome sequences of invasive weed Parthenium hysterophorus: genome organization, evolutionary significance, structural features, and comparative analysis Lubna, Asaf S, Jan R, Asif S, Bilal S, Khan AL, Al-Rawahi AN, Kim KM, AL-Harrasi A Sci Rep 18-Feb-2024
PMCID:PMC10874969
doi:10.1038/s41598-024-54503-0
PMID:38369569
Marine Brown Algae-Derived Compounds as Potential Inhibitors of Japanese Encephalitis Virus RNA-Dependent RNA Polymerase Alshammari SO Mar Drugs 17-Feb-2024
PMCID:PMC10890675
doi:10.3390/md22020092
PMID:38393063
Importance of phytotherapy for oral health care and quality of life in adults: A scoping review Shinkai RS, Azevedo CL, de Campos TT, Michel-Crosato E, Biazevic MG J Dent Sci 24-Jan-2024
PMCID:PMC11010713
doi:10.1016/j.jds.2024.01.002
PMID:38618093
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 importance of habitat heterogeneity Quintana-Ascencio PF Proc Natl Acad Sci U S A 04-Oct-2023
PMCID:PMC10589684
doi:10.1073/pnas.2314786120
PMID:37792518
Male reproductive success is not strongly affected by phenological changes in mate availability in monoecious Sagittaria latifolia Kwok A, Stephens S, Dorken M R Soc Open Sci 27-Sep-2023
PMCID:PMC10523072
doi:10.1098/rsos.231117
PMID:37771970
Habitat fragmentation decouples fire-stimulated flowering from plant reproductive fitness Beck J, Waananen A, Wagenius S Proc Natl Acad Sci U S A 18-Sep-2023
PMCID:PMC10523459
doi:10.1073/pnas.2306967120
PMID:37722060
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
Immunomodulatory effects and mechanisms of the extracts and secondary compounds of Zingiber and Alpinia species: a review Yuandani, Jantan I, Haque MA, Rohani AS, Nugraha SE, Salim E, Septama AW, Juwita NA, Khairunnisa NA, Nasution HR, Utami DS, Ibrahim S Front Pharmacol 18-Jul-2023
PMCID:PMC10391552
doi:10.3389/fphar.2023.1222195
PMID:37533631
Echinacoside Induces UCP1- and ATP-Dependent Thermogenesis in Beige Adipocytes via the Activation of Dopaminergic Receptors Haddish K, Yun JW J Microbiol Biotechnol 17-Jul-2023
PMCID:PMC10619551
doi:10.4014/jmb.2306.06041
PMID:37463854
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
A Comprehensive Update of Various Attempts by Medicinal Chemists to Combat COVID-19 through Natural Products Rafiq A, Jabeen T, Aslam S, Ahmad M, Ashfaq UA, Mohsin NU, Zaki ME, Al-Hussain SA Molecules 20-Jun-2023
PMCID:PMC10305344
doi:10.3390/molecules28124860
PMID:37375415
Assessment of Antioxidant Stability of Meat Pâté with Allium cepa Husk Extract Chernukha I, Kupaeva N, Khvostov D, Bogdanova Y, Smirnova J, Kotenkova E Antioxidants (Basel) 16-May-2023
PMCID:PMC10215231
doi:10.3390/antiox12051103
PMID:37237969

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/0021-9673(95)00877-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/0021-9673(95)00877-2
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1055/S-0028-1097532
Dotriacontane 11008 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 450.90 unknown https://doi.org/10.1055/S-0028-1097532
Eicosane 8222 Click to see CCCCCCCCCCCCCCCCCCCC 282.50 unknown https://doi.org/10.1055/S-0028-1097532
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1055/S-0028-1097532
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1055/S-0028-1097532
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1055/S-0028-1097532
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1055/S-0028-1097532
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1055/S-0028-1097532
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1055/S-0028-1097532
Octacosane 12408 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC 394.80 unknown https://doi.org/10.1055/S-0028-1097532
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown https://doi.org/10.1055/S-0028-1097532
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1055/S-0028-1097532
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown https://doi.org/10.1055/S-0028-1097532
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1055/S-0028-1097532
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.1055/S-0028-1097532
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see CC#CC#CC#CC#CC#CC=C 162.19 unknown via CMAUP database
1,11-Tridecadien-3,5,7,9-tetrayne 528754 Click to see CC=CC#CC#CC#CC#CC=C 164.20 unknown via CMAUP database
Tridec-1,3-diene-5,7,9,11-tetrayne 528755 Click to see CC#CC#CC#CC#CC=CC=C 164.20 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes
13-Methyltetradeca-2,9-diene 54332465 Click to see CC=CCCCCCC=CCCC(C)C 208.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
methyl (E)-4-(2-methylpropylamino)-4-oxobut-2-enoate 44603263 Click to see CC(C)CNC(=O)C=CC(=O)OC 185.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,10E)-N-(2-methylpropyl)dodeca-2,4,10-trien-8-ynamide 15609887 Click to see CC=CC#CCCC=CC=CC(=O)NCC(C)C 245.36 unknown https://doi.org/10.1021/JF103436P
(2E,4E,8E,10Z)-N-(2-methylpropyl)dodeca-2,4,8,10-tetraenamide 12315250 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown https://doi.org/10.1039/B615487E
https://doi.org/10.1016/S0021-9673(98)00447-6
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745817/
(2E,4E,8Z)-N-(2-methylpropyl)dodeca-2,4,8,10-tetraenamide 70693621 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
(2E,4E)-N-(2-methylpropyl)-6-oxododeca-2,4-dienamide 44556043 Click to see CCCCCCC(=O)C=CC=CC(=O)NCC(C)C 265.39 unknown via CMAUP database
(2E,4E)-N-isobutylundeca-2,4-dien-8,10-diynamide 5373537 Click to see CC(C)CNC(=O)C=CC=CCCC#CC#C 229.32 unknown https://doi.org/10.1055/S-2005-871290
(2E,4Z,10Z)-N-(2-methylpropyl)dodeca-2,4,10-trien-8-ynamide 15609888 Click to see CC=CC#CCCC=CC=CC(=O)NCC(C)C 245.36 unknown https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1055/S-2005-871290
(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/10.1177/0091270004273493
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1016/0031-9422(89)80042-1
(2E,7Z)-N-Isobutyl-2,7-tridecadiene-10,12-diynamide 15609892 Click to see CC(C)CNC(=O)C=CCCCC=CCC#CC#C 257.37 unknown https://doi.org/10.1211/0022357011776009
https://doi.org/10.1016/0031-9422(89)80042-1
(2E,9Z)-N-(2-methylpropyl)hexadeca-2,9-dien-12,14-diynamide 14259842 Click to see CC#CC#CCC=CCCCCCC=CC(=O)NCC(C)C 299.40 unknown https://doi.org/10.1016/0031-9422(89)80042-1
(2E,9Z)-N-(2-methylpropyl)pentadeca-2,9-dien-12,14-diynamide 14259840 Click to see CC(C)CNC(=O)C=CCCCCCC=CCC#CC#C 285.40 unknown https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1055/S-2005-871290
(2Z,4E,10Z)-N-Isobutyl-2,4,10-dodecatriene-8-ynamide 5326171 Click to see CC=CC#CCCC=CC=CC(=O)NCC(C)C 245.36 unknown https://doi.org/10.1021/NP040245F
(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 via CMAUP database
(2Z,4Z)-N-Isobutyl-2,4-undecadiene-8,10-diynamide 101227583 Click to see CC(C)CNC(=O)C=CC=CCCC#CC#C 229.32 unknown via CMAUP database
(E)-N-(2-methylbutyl)dodec-2-en-8,10-diynamide 14259838 Click to see CCC(C)CNC(=O)C=CCCCCC#CC#CC 259.40 unknown https://doi.org/10.1016/S0031-9422(99)00101-6
(E)-N-(2-methylpropyl)-4-oxododec-2-en-8,10-diynamide 44603265 Click to see CC#CC#CCCCC(=O)C=CC(=O)NCC(C)C 259.34 unknown via CMAUP database
(E)-N-Isobutyl-2-dodecene-8,10-diynamide 11615704 Click to see CC#CC#CCCCCC=CC(=O)NCC(C)C 245.36 unknown https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1016/J.BBRC.2007.06.073
https://doi.org/10.1177/0091270004273493
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745817/
https://doi.org/10.1055/S-0029-1214252
(Z)-N-Isobutyl-2-undecene-8,10-diynamide 14259835 Click to see CC(C)CNC(=O)C=CCCCCC#CC#C 231.33 unknown https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1016/J.BBRC.2007.06.073
2,4-Dodecadienamide, N-(2-methylpropyl)-, (2E,4E)- 6443006 Click to see CCCCCCCC=CC=CC(=O)NCC(C)C 251.41 unknown https://doi.org/10.1177/0091270004273493
https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1021/JF103436P
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1211/0022357011776009
2,4-Undecadiene-8,10-diynamide, N-(2-methylpropyl)-, (2Z,4E)- 593849 Click to see CC(C)CNC(=O)C=CC=CCCC#CC#C 229.32 unknown https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1016/0031-9422(89)80042-1
2,4-Undecadiene-8,10-diynoic acid isobutylamide 15609884 Click to see CC(C)CNC(=O)C=CC=CCCC#CC#C 229.32 unknown https://doi.org/10.1016/0031-9422(89)80042-1
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/10.1016/J.BBRC.2007.06.073
https://doi.org/10.1177/0091270004273493
https://doi.org/10.1016/J.JPBA.2010.02.010
https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1111/J.1774-7909.2007.00456.X
https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1016/S0031-9422(00)80830-4
https://doi.org/10.1039/B615487E
https://doi.org/10.1080/10286020310001596015
https://doi.org/10.1021/JF103436P
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1016/J.INTIMP.2009.03.006
https://doi.org/10.1016/S0031-9422(00)83030-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745817/
https://doi.org/10.1016/J.INTIMP.2010.07.009
https://doi.org/10.1078/0944-7113-00105
https://doi.org/10.1248/CPB.29.564
Alkamide 2 15609885 Click to see CC(C)CNC(=O)C=CC=CCCC#CC#C 229.32 unknown https://doi.org/10.1002/CBER.19660991017
https://doi.org/10.1211/0022357011776009
https://doi.org/10.1016/0031-9422(89)80042-1
alpha-Sanshool 6440935 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C 247.38 unknown https://doi.org/10.1271/BBB.69.1951
https://doi.org/10.1016/0031-9422(82)80128-3
https://doi.org/10.1016/S0031-9422(96)00683-8
https://doi.org/10.1055/S-2007-969741
dodeca-2E,4E,8Z-trienoic acid isobutylamide 15609890 Click to see CCCC=CCCC=CC=CC(=O)NCC(C)C 249.39 unknown via CMAUP database
dodeca-2E,4E,8Z,10Z-tetraenoic acid isobutylamide 11413953 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown https://doi.org/10.1016/J.BBRC.2007.06.073
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147727/
https://doi.org/10.1016/J.JPBA.2010.02.010
https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1111/J.1774-7909.2007.00456.X
https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1080/08820130600745786
https://doi.org/10.1039/B615487E
https://doi.org/10.1016/S0031-9422(00)80774-8
https://doi.org/10.1016/J.INTIMP.2009.03.006
https://doi.org/10.1016/J.FITOTE.2007.07.012
https://doi.org/10.1016/J.INTIMP.2006.02.003
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745817/
https://doi.org/10.1016/J.INTIMP.2010.07.009
https://doi.org/10.1078/0944-7113-00105
https://doi.org/10.1248/CPB.29.564
Dodecadienoic acid isobutylamide 185577 Click to see CCCCCCCC=CC=CC(=O)NCC(C)C 251.41 unknown https://doi.org/10.1021/JF103436P
https://doi.org/10.1177/0091270004273493
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1211/0022357011776009
https://doi.org/10.1016/0031-9422(89)80042-1
N-(2-Methylbutyl)dodec-2-ene-8,10-diynamide 71339781 Click to see CCC(C)CNC(=O)C=CCCCCC#CC#CC 259.40 unknown https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1055/S-2005-871290
N-(2-Methylbutyl)dodeca-2,4-diene-8,10-diynamide 71339373 Click to see CCC(C)CNC(=O)C=CC=CCCC#CC#CC 257.37 unknown https://doi.org/10.1055/S-2005-871290
N-(2-methylpropyl)dodec-2-en-8,10-diynamide 73030614 Click to see CC#CC#CCCCCC=CC(=O)NCC(C)C 245.36 unknown https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1177/0091270004273493
N-(2-Methylpropyl)dodeca-2,4,10-trien-8-ynamide 71337772 Click to see CC=CC#CCCC=CC=CC(=O)NCC(C)C 245.36 unknown https://doi.org/10.1021/JF103436P
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/10.1021/JF103436P
https://doi.org/10.1177/0091270004273493
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1016/0031-9422(89)80042-1
N-(2-methylpropyl)hexadeca-2,9-dien-12,14-diynamide 72729166 Click to see CC#CC#CCC=CCCCCCC=CC(=O)NCC(C)C 299.40 unknown https://doi.org/10.1016/0031-9422(89)80042-1
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/10.1016/0031-9422(89)80042-1
https://doi.org/10.1055/S-2005-871290
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/10.1016/0031-9422(89)80042-1
N-Isobutylundeca-2(E)-en-8,10-diynamide 5368482 Click to see CC(C)CNC(=O)C=CCCCCC#CC#C 231.33 unknown https://doi.org/10.1002/PS.2274
https://doi.org/10.1016/J.JPBA.2010.02.010
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147727/
https://doi.org/10.1016/J.INTIMP.2010.07.009
https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1021/JF103436P
https://doi.org/10.1177/0091270004273493
https://doi.org/10.1016/J.FITOTE.2007.07.012
https://doi.org/10.1016/S0031-9422(00)83030-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745817/
https://doi.org/10.1016/S0031-9422(99)00101-6
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1211/0022357011776009
https://doi.org/10.1080/08820130600745786
https://doi.org/10.1016/J.BBRC.2007.06.073
https://doi.org/10.1016/0031-9422(89)80042-1
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/10.1016/0031-9422(89)80042-1
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1177/0091270004273493
https://doi.org/10.1021/JF103436P
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids
15-Acetyloxy-2,6,12-trimethylpentacyclo[11.2.1.01,10.02,7.012,14]hexadecane-6-carboxylic acid 162846250 Click to see CC(=O)OC1C2C3C2(CC4C1(C3)C5(CCCC(C5CC4)(C)C(=O)O)C)C 360.50 unknown https://doi.org/10.1055/S-2005-871290
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,4-Dihydroxy-6-methyl-3-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]benzoic acid; Grifolic acid 85080649 Click to see CC1=CC(=C(C(=C1C(=O)O)O)CC=C(C)CCC=C(C)CCC=C(C)C)O 372.50 unknown https://doi.org/10.1016/0031-9422(89)80042-1
beta Farnesene 15228937 Click to see CCC(=C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1055/S-2006-960123
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960123
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4R,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162993931 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)O)O)O)O)O 1059.20 unknown https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1016/0031-9422(89)80042-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Propanoic acid, 2-methyl-, 3,6-bis(acetyloxy)-2,3,3a,4,5,6,6a,7,9a,9b-decahydro-3,6,9-trimethyl-2-oxoazuleno(4,5-b)furan-4-yl ester, (3S-(3alpha,3aalpha,4alpha,6beta,6abeta,9abeta,9balpha))- 155119 Click to see CC1=CCC2C1C3C(C(CC2(C)OC(=O)C)OC(=O)C(C)C)C(C(=O)O3)(C)OC(=O)C 436.50 unknown https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1016/S0031-9422(00)80830-4
https://doi.org/10.1080/10286020310001596015
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 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 / Carboximidic acids and derivatives / Carboximidic acids
(2E,4E)-N-[(2R)-2-methylbutyl]dodeca-2,4-dienamide 163191162 Click to see CCCCCCCC=CC=CC(=O)NCC(C)CC 265.40 unknown https://doi.org/10.1021/JF103436P
(2E,4Z)-N-[(2S)-2-methylbutyl]dodeca-2,4-dien-8,10-diynamide 162898450 Click to see CCC(C)CNC(=O)C=CC=CCCC#CC#CC 257.37 unknown https://doi.org/10.1055/S-2005-871290
(E)-N-[(2S)-2-methylbutyl]dodec-2-en-8,10-diynamide 162882058 Click to see CCC(C)CNC(=O)C=CCCCCC#CC#CC 259.40 unknown https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1016/0031-9422(89)80042-1
(Z)-N-(2-methylbutyl)undec-2-en-8,10-diynamide 14259837 Click to see CCC(C)CNC(=O)C=CCCCCC#CC#C 245.36 unknown https://doi.org/10.1055/S-2006-959404
https://doi.org/10.1016/0031-9422(89)80042-1
https://doi.org/10.1016/S0021-9673(98)00447-6
(Z)-N-[(2S)-2-methylbutyl]dodec-2-en-8,10-diynamide 162882059 Click to see CCC(C)CNC(=O)C=CCCCCC#CC#CC 259.40 unknown https://doi.org/10.1016/0031-9422(89)80042-1
N-[(2R)-2-methylbutyl]dodeca-2,4-dienamide 162868763 Click to see CCCCCCCC=CC=CC(=O)NCC(C)CC 265.40 unknown https://doi.org/10.1021/JF103436P
Tetradeca-2-en-10,12-diynoic acid isobutylamide 86076154 Click to see CC#CC#CCCCCCCC=CC(=O)NCC(C)C 273.40 unknown https://doi.org/10.1055/S-2005-871290
> 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/10.1039/AN9891401021
https://doi.org/10.1016/S0305-1978(02)00029-7
Cichoric acid;Dicaffeoyltartaric acid 5134221 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/10.1211/0022357011776009
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(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 via CMAUP database
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/10.1300/J044V08N01_03
https://doi.org/10.1016/S0305-1978(02)00029-7
CID 129316856 129316856 Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 516.40 unknown https://doi.org/10.1055/S-2002-32561
https://doi.org/10.1016/0731-7085(89)80139-6
https://doi.org/10.1016/S0944-7113(96)80041-9
https://doi.org/10.1080/13880200500408491
https://doi.org/10.1211/0022357011776009
https://doi.org/10.1016/S0305-1978(02)00029-7
https://doi.org/10.1021/JF001331Y
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2S,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-[(S)-[(Z)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5-hydroxy-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 163191474 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
2-(3,4-Dihydroxyphenyl)ethyl 6-deoxyhexopyranosyl-(1->3)-[hexopyranosyl-(1->6)]-4-O-[3-(3,4-dihydroxyphenyl)prop-2-enoyl]hexopyranoside 4484390 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
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/10.1300/J044V08N01_03
https://doi.org/10.1016/0731-7085(89)80139-6
https://doi.org/10.1002/OMS.1210261107
https://doi.org/10.1021/JF001331Y
https://doi.org/10.1055/S-2002-32561
https://doi.org/10.1016/S0305-1978(02)00029-7
Maltotriose 871 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown https://doi.org/10.1016/J.CARBPOL.2006.01.012
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Tridecen-2-one 53427438 Click to see CCCCCCCCCC=CC(=O)C 196.33 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<88::AID-PCA384>3.0.CO;2-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Tridecanone 11622 Click to see CCCCCCCCCCCC(=O)C 198.34 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<88::AID-PCA384>3.0.CO;2-4
Pentadec-8-en-2-one 54551543 Click to see CCCCCCC=CCCCCCC(=O)C 224.38 unknown via CMAUP database
> 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/10.1016/0031-9422(89)80042-1
https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1177/0091270004273493
> Organoheterocyclic compounds / Isocoumarans
3-(4-Methoxy-1,3-dihydro-2-benzofuran-1-yl)-1-(3-methyloxiran-2-yl)propane-1,2-diol 76462714 Click to see CC1C(O1)C(C(CC2C3=C(CO2)C(=CC=C3)OC)O)O 280.32 unknown https://doi.org/10.1055/S-2005-871290
https://doi.org/10.1016/0031-9422(89)80042-1
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Acteoside;Kusaginin;TJC160 354009 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
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/10.1080/13880200500408491
https://doi.org/10.1016/S0305-1978(02)00029-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1039/AN9891401021
https://doi.org/10.1016/S0305-1978(02)00029-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 https://doi.org/10.1039/AN9891401021
https://doi.org/10.1076/PHBI.40.2.92.5839

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