Details Top

Internal ID UUID643fca24d4b7b047265454
Scientific name Centaurea solstitialis
Authority L.
First published in Sp. Pl. : 917 (1753)

Ethnobotanical Use Top

Write a new one!
No ethnobotanical data added yet. Help us by writing one.

General Uses Top

Suggest a correction!

Common products:
Seed oil expressed from achenes; a lignocellulosic straw suitable for pulp and paper; a yellow flower-head dye for textile coloration.

Industrial and craft applications:
Oil: The seed oil is used industrially as a drying oil for coatings, as a feedstock for soapmaking, and as a potential biodiesel or renewable diesel component. Its fatty-acid profile (high in linoleic acid) supports these applications; industrial literature also reports suitability as a drying oil for paints and varnishes.
Straw/pulp: Stems and achene testa are used for pulp production. Investigations demonstrate the feasibility of soda-anthraquinone pulping, and commercial pulp and paper trials have evaluated straw as a short-fiber component or filler with mixed quality outcomes. The material is also researched as a reinforcing component in fiberboard and biocomposites.

Food and beverages (non-medicinal):
No documented culinary uses. Seeds are not recognized as a food or food ingredient in established food composition or regulation databases.

Colorants and tanning:
Flower-heads yield a yellow dye used on wool, cotton, and silk. The hue depends on mordants; documented examples include yellows on wool with alum and on wool and silk with copper and iron mordants. No reliable evidence of significant tanning uses.

Wood and fiber:
The plant is herbaceous; wood uses are not applicable. Stem fibers are reported but have not led to significant commercial textile fiber or woven-material production.

Fragrance and cosmetics:
No documented fragrance, flavor, or cosmetic uses.

Properties relevant to use:
The seed oil contains a high proportion of linoleic acid with accompanying oleic and palmitic acids, consistent with drying-oil behavior and suitability as a soap feedstock or biodiesel. Straws provide cellulose, hemicellulose, and lignin in proportions amenable to alkaline pulping; alkaline pulping assessments show acceptable lignin removal at moderate chemical charges.

Standards and regulation:
As an industrial oil and biofuel, compliance with national petroleum-product or biodiesel standards (for example, ASTM D975, EN 14214, or equivalent national specifications) applies when used in those applications. Food uses are not covered by food safety authorizations, so seed oil is not a permitted food ingredient in major jurisdictions.

Sustainability and sourcing:
The species is widespread as an introduced weed in several regions and is classified as a noxious or invasive plant in parts of North America and Australia. It is harvested as a secondary crop where available, potentially reducing waste but raising ecological concerns. Sustainable sourcing should prioritize regions where it is not invasive and incorporate management measures to limit seed spread and establishment.

Synonyms Top

Scientific name Authority First published in
Calcitrapa solstitialis Lam. Fl. Franç. 2: 34 (1779)
Leucantha solstitialis (L.) Á.Löve & D.Löve Bot. Not. 114: 44 (1961)
Cyanus solstitialis J.Presl & C.Presl Fl. Cech. : 179
Centaurea parvispina Láng ex Gugler Centaur. Ungar. 204 (1907)
Centaurea cyanifolia Poir. Encycl. , Suppl. 2: 158 (1811)
Calcitrapa lutea (Gueldenst.) Delarbre Fl. Auvergne ed. 2, 199 (1800)
Centaurea pseudosolstitialis Debeaux Not. pl. nouv. ou peu conn. reg. Medit. -. 1895 ; ex Bull Soc. Bot. Fr. xlii.(1895) 376.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English floravia
English golden starthistle
English barnaby thistle
English yellow star-thistle
English st. barnaby's thistle
English yellow cockspur
English yellow star thistle
Spanish floravia
Spanish ramón pajarero.
Spanish gatinas
Spanish cardo estrellado de flor amarilla
Spanish argazolla amarilla
Spanish abrimanos,
Spanish abrepuño
Spanish calcitrapa carneola
Spanish calcitrapa schouwii
Spanish calcitrapa erythracantha
Spanish centaurea parvispina
Spanish calcitrapa lutea
Spanish centaurea cyanifolia
Spanish calcitrapa solstitialis
Spanish cyanus solstitialis
Spanish leucantha solstitialis
Arabic قنطريون صيفي
Azerbaijani günəbaxanvari güləvər
Bulgarian средиземноморска метличина
Bulgarian floravia
Catalan narriola
Catalan blanquiella
Catalan floravia
Czech chrpa žlutá
Welsh y bengaled felen
German sonnwend-flockenblume
German sonnenwend-flockenblume
German floravia
Estonian kiirjas jumikas
Persian گل گندم زرد
Finnish keltaorakaunokki
French floravia
French centaurée du solstice
French centauree du solstice
Hebrew דרדר אביבי
Hungarian sáfrányos imola
Igbo golden starthistle
Igbo st. barnaby's thistle
Igbo yellow cockspur
Igbo yellow star thistle
Igbo floravia
Igbo barnaby thistle
Italian floravia
Japanese イガヤグルマギク
Georgian ეკალცოცხი
Dutch zomercentaurie
Russian Василёк солнечный
Russian Василёк подсолнечный
Russian Василёк летний
Russian floravia
Slovak panevädza letná
Turkish Çakır dikeni
Ukrainian Волошка сонячна
Walloon tcherdon d' ôr
Chinese 黃星薊
Chinese 黃矢車菊
Chinese 黄星蓟
Chinese 黄矢车菊
Chinese 长刺矢车菊

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Centaurea solstitialis subsp. adamii (Willd.) Nyman Consp. Fl. Eur. : 430 (1879)
Centaurea solstitialis subsp. carneola (Boiss.) Wagenitz Notes Roy. Bot. Gard. Edinburgh 33(2): 229 (1974)
Centaurea solstitialis subsp. erythracantha (Halácsy) Dostál Bot. J. Linn. Soc. 71(3): 204 (1976)
Centaurea solstitialis subsp. pyracantha (Boiss.) Wagenitz Notes Roy. Bot. Gard. Edinburgh 33(2): 229 (1974)
Centaurea solstitialis subsp. schouwii (DC.) Dostál Ann. Hist.-Nat. Mus. Natl. Hung. 6: 203 (1908)
Centaurea solstitialis subsp. schouwii (DC.) Gugler Gugler in Ann. Hist.-Nat. Mus. Natl. Hung. 6. 1907. 203 1907

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
    • Northern Africa
      • Algeria
      • Egypt
      • Morocco
      • Tunisia
    • Southern Africa
      • Cape Provinces
      • Northern Provinces
  • Asia-temperate
    • Arabian Peninsula
      • Kuwait
      • Oman
      • Saudi Arabia
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Russian Far East
      • Primorye
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Sinai
      • Turkey
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • Northwest European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
      • Ireland
      • Norway
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
    • Mexico
      • Mexico Northwest
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Delaware
      • Florida
      • Kentucky
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Western Canada
      • Alberta
      • Manitoba
      • Saskatchewan
  • Southern America
    • Southern South America
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000035974
Canadensys 2972
USDA Plants CESO3
Tropicos 2700499
INPN 89710
Flora of Italy 6026
KEW urn:lsid:ipni.org:names:191626-1
The Plant List gcc-134792
Plantarium 9567
Open Tree Of Life 852752
NCBI Taxonomy 347529
NBN Atlas NBNSYS0000004511
Nature Serve 2.136039
IPNI 191626-1
iNaturalist 52588
GBIF 3128888
Freebase /m/074vvy
WisFlora 7150
FEIS plants/forb/censol
EPPO CENSO
EOL 467678
Elurikkus 3542
Calflora (Californian flora) 1853
USDA GRIN 9827
Wikipedia Centaurea_solstitialis
CMAUP NPO10594

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_030169165.1 ASM3016916v1 Chromosome UAEEB-DL 2023-06-06 30 729.62 Mb

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
Wild Edible Plants Used in Dalmatian Zagora (Croatia) Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł Plants (Basel) 11-Apr-2024
PMCID:PMC11053949
doi:10.3390/plants13081079
PMID:38674488
Exploring the complex pre-adaptations of invasive plants to anthropogenic disturbance: a call for integration of archaeobotanical approaches Bellini G, Schrieber K, Kirleis W, Erfmeier A Front Plant Sci 15-Mar-2024
PMCID:PMC10978757
doi:10.3389/fpls.2024.1307364
PMID:38559769
Ecological and Syntaxonomic Analysis of the Communities of Glebionis coronaria and G. discolor (Malvion neglectae) in the European Mediterranean Area Cano E, Cano-Ortiz A, Quinto Canas R, Piñar Fuentes JC, Rodrigues Meireles C, Raposo M, Pinto Gomes C, Laface VL, Spampinato G, Musarella CM Plants (Basel) 20-Feb-2024
PMCID:PMC10934477
doi:10.3390/plants13050568
PMID:38475415
Magnetic iron oxide-based nanozymes: from synthesis to application Ghazzy A, Nsairat H, Said R, Sibai OA, AbuRuman A, Shraim AS, Al hunaiti A Nanoscale Adv 19-Feb-2024
PMCID:PMC10929596
doi:10.1039/d3na00903c
PMID:38482039
Valorizing Tree-Nutshell Particles as Delivery Vehicles for a Natural Herbicide Kim JH, Chan KL, Hart-Cooper WM, Ford D, Orcutt K, Palumbo JD, Tam CC, Orts WJ Methods Protoc 20-Dec-2023
PMCID:PMC10892353
doi:10.3390/mps7010001
PMID:38392682
Genome size variation and evolution during invasive range expansion in an introduced plant Cang FA, Welles SR, Wong J, Ziaee M, Dlugosch KM Evol Appl 11-Dec-2023
PMCID:PMC10810172
doi:10.1111/eva.13624
PMID:38283607
Iron Oxide Nanoparticles: Green Synthesis and Their Antimicrobial Activity Zúñiga-Miranda J, Guerra J, Mueller A, Mayorga-Ramos A, Carrera-Pacheco SE, Barba-Ostria C, Heredia-Moya J, Guamán LP Nanomaterials (Basel) 08-Nov-2023
PMCID:PMC10674528
doi:10.3390/nano13222919
PMID:37999273
Diversity of fungal pathogens in leaf spot disease of Indian mulberry and its management GS A, Mayavathi NR NP, N.R. A, B.M. M, Sherpa DC, C A, Suresh A, Kammar S, M S, S S, B.N. G, Doss S G Heliyon 02-Nov-2023
PMCID:PMC10665727
doi:10.1016/j.heliyon.2023.e21750
PMID:38027777
Multi-analytical investigation of the physical, chemical, morphological, tensile, and structural properties of Indian mulberry (Morinda tinctoria) bark fibers Balachandran GB, Narayanasamy P, Alexander AB, David PW, Mariappan RK, Ramachandran ME, Indran S, Mavinkere Rangappa S, Siengchin S Heliyon 27-Oct-2023
PMCID:PMC10637935
doi:10.1016/j.heliyon.2023.e21239
PMID:37954341
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
The introduction of an invasive weed was not followed by the introduction of ethnobotanical knowledge: a review on the ethnobotany of Centaurea solstitialis L. (Asteraceae) Branco S, Irimia RE, Montesinos D PeerJ 07-Jun-2023
PMCID:PMC10257394
doi:10.7717/peerj.15489
PMID:37304862
Invasive and Native Plants Differentially Respond to Exogenous Phosphorus Addition in Root Growth and Nutrition Regulated by Arbuscular Mycorrhizal Fungi Yang X, Shen K, Xia T, He Y, Guo Y, Wu B, Han X, Yan J, Jiao M Plants (Basel) 01-Jun-2023
PMCID:PMC10255820
doi:10.3390/plants12112195
PMID:37299174
Insights into the Mechanisms Involved in Lead (Pb) Tolerance in Invasive Plants—The Current Status of Understanding Afzal MR, Naz M, Wan J, Dai Z, Ullah R, Rehman SU, Du D Plants (Basel) 24-May-2023
PMCID:PMC10255771
doi:10.3390/plants12112084
PMID:37299064
Fingerprinting Chemical Markers in the Mediterranean Orange Blossom Honey: UHPLC-HRMS Metabolomics Study Integrating Melissopalynological Analysis, GC-MS and HPLC-PDA-ESI/MS Kasiotis KM, Baira E, Iosifidou S, Manea-Karga E, Tsipi D, Gounari S, Theologidis I, Barmpouni T, Danieli PP, Lazzari F, Dipasquale D, Petrarca S, Shairra S, Ghazala NA, Abd El-Wahed AA, El-Gamal SM, Machera K Molecules 08-May-2023
PMCID:PMC10180536
doi:10.3390/molecules28093967
PMID:37175378
Trait evolution during a rapid global weed invasion despite little genetic differentiation Irimia RE, Montesinos D, Chaturvedi A, Sanders I, Hierro JL, Sotes G, Cavieres LA, Eren Ö, Lortie CJ, French K, Brennan AC Evol Appl 18-Apr-2023
PMCID:PMC10197227
doi:10.1111/eva.13548
PMID:37216028

Phytochemical Profile Top

Add a new one!
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 / Phenol ethers / Anisoles
2-Methylanisole 33637 Click to see 122.16 unknown https://doi.org/10.1021/JF00071A004
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Pentadecene 25913 Click to see 210.40 unknown https://doi.org/10.1021/JF00071A004
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol 119205 Click to see 358.40 unknown https://doi.org/10.1016/0031-9422(91)83490-C
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
https://doi.org/10.1016/0031-9422(91)83490-C
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see 102.17 unknown https://doi.org/10.1021/JF00071A004
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
6,8,10,12-Pentadecatetraenal 5283373 Click to see CCC=CC=CC=CC=CCCCCC=O 218.33 unknown https://doi.org/10.1002/CBER.19660991121
Pentadeca-6,8,10,12-tetraenal 78382191 Click to see 218.33 unknown https://doi.org/10.1002/CBER.19660991121
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1021/JF00071A004
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1021/JF00071A004
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1021/JF00071A004
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF00071A004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00071A004
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1021/JF00071A004
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/JF00071A004
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1021/JF00071A004
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00071A004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1021/JF00071A004
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1021/JF00071A004
> 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 204.35 unknown https://doi.org/10.1021/JF00071A004
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1021/JF00071A004
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Stizolicin 15089249 Click to see 378.40 unknown https://doi.org/10.1016/0031-9422(94)85084-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(2a(2)R,3aR,4S,6aR,8S,9aS,9bS)-Decahydro-8-hydroxy-3,6-bis(methylene)-2-oxospiro[azuleno[4,5-b]furan-9(2H),2a(2)-oxiran]-4-yl (2S)-3-chloro-2-hydroxy-2-methylpropanoate 13943202 Click to see 398.80 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
(8-Hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl) 2-(hydroxymethyl)prop-2-enoate 182407 Click to see C=C1CC(C2C(C3C1CC(C34CO4)O)OC(=O)C2=C)OC(=O)C(=C)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
(8-Hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl) 2-methyloxirane-2-carboxylate 14466526 Click to see CC1(CO1)C(=O)OC2CC(=C)C3CC(C4(C3C5C2C(=C)C(=O)O5)CO4)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
(8-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) 2-methylprop-2-enoate 13996678 Click to see 330.40 unknown https://doi.org/10.1016/0031-9422(91)83490-C
(8-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) 3-chloro-2-hydroxy-2-methylpropanoate 71439502 Click to see 382.80 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
https://doi.org/10.1055/S-2007-969197
[(3aR,4S,6aR,8S,9R,9aS,9bS)-8-hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl] (2S)-2-methyloxirane-2-carboxylate 14466529 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
[(3aR,4S,6aR,8S,9S,9aS,9bS)-8-hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl] 2-methyloxirane-2-carboxylate 5320928 Click to see CC1(CO1)C(=O)OC2CC(=C)C3CC(C4(C3C5C2C(=C)C(=O)O5)CO4)O 362.40 unknown https://doi.org/10.1002/NT.2620010602
https://doi.org/10.1055/S-2007-969197
https://doi.org/10.1016/S0031-9422(00)83113-1
[(3aR,4S,6aR,8S,9S,9aS,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] (2R)-2-methyloxirane-2-carboxylate 101285196 Click to see CC1(CO1)C(=O)OC2CC(=C)C3CC(C(C3C4C2C(=C)C(=O)O4)(CCl)O)O 398.80 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
[(3aR,4S,6aR,8S,9S,9aS,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] (2S)-2-methyloxirane-2-carboxylate 101285197 Click to see 398.80 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
https://doi.org/10.1055/S-2007-969197
[(3R,3aR,6aR,9S,9aR,9bR)-3-(hydroxymethyl)-9-methyl-6-methylidene-2,8-dioxo-3a,4,5,6a,7,9,9a,9b-octahydroazuleno[4,5-b]furan-3-yl] acetate 15127110 Click to see CC1C2C(CC1=O)C(=C)CCC3C2OC(=O)C3(CO)OC(=O)C 322.40 unknown https://doi.org/10.1016/0031-9422(91)83490-C
[(4S,8R,9S,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] (2S)-3-chloro-2-hydroxy-2-methylpropanoate 118701337 Click to see 435.30 unknown https://doi.org/10.1055/S-2007-969197
https://doi.org/10.1021/NP50004A013
https://doi.org/10.1016/S0031-9422(00)83113-1
[3-(Hydroxymethyl)-9-methyl-6-methylidene-2,8-dioxo-3a,4,5,6a,7,9,9a,9b-octahydroazuleno[4,5-b]furan-3-yl] acetate 163025258 Click to see CC1C2C(CC1=O)C(=C)CCC3C2OC(=O)C3(CO)OC(=O)C 322.40 unknown https://doi.org/10.1016/0031-9422(91)83490-C
[9-(Chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-methyloxirane-2-carboxylate 162978147 Click to see 398.80 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
2-[(3R,3aR,6aR,8R,9aR,9bR)-3,8-dihydroxy-3-(hydroxymethyl)-6,9-dimethylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-8-yl]acetic acid 101626736 Click to see C=C1CCC2C(C3C1CC(C3=C)(CC(=O)O)O)OC(=O)C2(CO)O 338.40 unknown https://doi.org/10.1016/0028-3908(92)90177-Q
8-Hydroxy-3,6-dimethylidene-2-oxodecahydro-2H-spiro[azuleno[4,5-b]furan-9,2'-oxiran]-4-yl 3-chloro-2-hydroxy-2-methylpropanoatato(2-) 93586 Click to see 398.80 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
Acroptilin 442140 Click to see 398.80 unknown https://doi.org/10.1055/S-2007-969197
https://doi.org/10.1016/S0031-9422(00)83113-1
Aguerin B 155102 Click to see 330.40 unknown https://doi.org/10.1016/0031-9422(91)83490-C
Cynaropicrin 119093 Click to see 346.40 unknown https://doi.org/10.1055/S-2007-969197
https://doi.org/10.1016/0028-3908(92)90177-Q
https://doi.org/10.1016/S0031-9422(00)83113-1
https://doi.org/10.1016/0031-9422(91)83490-C
Janerin 14021480 Click to see C=C1CC(C2C(C3C1CC(C34CO4)O)OC(=O)C2=C)OC(=O)C(=C)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
Repin 91567 Click to see 362.40 unknown https://doi.org/10.1002/NT.2620010602
https://doi.org/10.1055/S-2007-969197
https://doi.org/10.1016/S0031-9422(00)83113-1
Saupirin 181128 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(91)83490-C
https://doi.org/10.1055/S-2007-969197
https://doi.org/10.1016/S0031-9422(00)83113-1
Solstitialin 100715 Click to see 280.32 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
Solstitialin A 13-acetate 100716 Click to see 322.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
https://doi.org/10.1016/0031-9422(91)83490-C
https://doi.org/10.1016/0028-3908(92)90177-Q
Solstitialin deriv 4700 336809 Click to see 280.32 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
Subluteolide 14466528 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83113-1
https://doi.org/10.1002/NT.2620010602
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3R,4aR,6aR,6aR,6bR,8R,8aS,12S,12aR,14aR,14bR)-8-hydroxy-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] acetate 162885921 Click to see 484.80 unknown https://doi.org/10.1016/S0031-9422(00)94180-3
3,16-Dihydroxytaraxene-3-acetate 321965 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CCC1=C)C)O)C)C)(C)C)OC(=O)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(00)94180-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Ndelta-acetylornithine 90658764 Click to see 174.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
D-Aspartic Acid 83887 Click to see 133.10 unknown https://doi.org/10.1002/NT.2620030309
L-Aspartic Acid 5960 Click to see 133.10 unknown https://doi.org/10.1002/NT.2620030309
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
L-Glutamic Acid 33032 Click to see 147.13 unknown https://doi.org/10.1002/NT.2620030309
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-p-Coumaroylquinic acid 9945785 Click to see 338.31 unknown via CMAUP database
3-p-Coumaroylquinic acid, (Z)- 92135690 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown via CMAUP database
5-p-Coumaroylquinic acid, (Z)- 90478782 Click to see 338.31 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 via CMAUP database
trans-5-O-(4-coumaroyl)-D-quinic acid 6441280 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see 326.30 unknown via CMAUP database
Arbutin 440936 Click to see 272.25 unknown via CMAUP database
Caffeic acid 4-O-glucoside 11382279 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O 342.30 unknown via CMAUP database
cis-Ferulic acid 4-O-beta-D-glucopyranoside 9820054 Click to see 356.32 unknown via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid 13916049 Click to see 356.32 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene 68316 Click to see 150.22 unknown https://doi.org/10.1021/JF00071A004
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see 204.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2-Hydroxy-4-methoxyphenyl)-6-methoxy-5-benzofuranol 185034 Click to see 286.28 unknown via CMAUP database
Methylsainfuran 44260111 Click to see 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2R)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxybutanedioic acid 26176222 Click to see C1=CC(=CC=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O 280.23 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 15048037 Click to see 340.32 unknown via CMAUP database
2-[(1S,3R,4R,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxycyclohexyl]acetic acid 10569992 Click to see 352.30 unknown via CMAUP database
Methyl 6-O-[(Z)-3-(4-hydroxyphenyl)propenoyl]-beta-D-glucopyranoside 102371158 Click to see COC1C(C(C(C(O1)COC(=O)C=CC2=CC=C(C=C2)O)O)O)O 340.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00630089
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)-2-methoxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 102371159 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)OC)O)O)O 504.40 unknown via CMAUP database
5,7-dihydroxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 14406834 Click to see 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5R,6S)-2-[[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781229 Click to see 916.80 unknown via CMAUP database
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781227 Click to see 962.90 unknown via CMAUP database
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781228 Click to see 916.80 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781232 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)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)O)O)O 786.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781230 Click to see 816.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781231 Click to see 770.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781233 Click to see 800.70 unknown via CMAUP database
5,7,3',4'-Tetrahydroxyflavone-3-yl 2-O-[4-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyl]-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781226 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)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O)O)O 932.80 unknown via CMAUP database
Amurenoside A 10653411 Click to see 932.80 unknown via CMAUP database
Amurenoside B 11803929 Click to see 932.80 unknown via CMAUP database
Clitorin 11592917 Click to see 740.70 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Manghaslin 11498684 Click to see 756.70 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see 626.50 unknown via CMAUP database
Narcissin 5481663 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)OC)O)O)O)O)O)O 624.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercetin 3-rutinoside-7-glucoside 10190763 Click to see 772.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-vestitone 44446897 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Isoliquiritigenin 638278 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.