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Opuntia ficus-indica

Opuntia ficus-indica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ff6d877c22883382891
Scientific name Opuntia ficus-indica
Authority (L.) Mill.
First published in Gard. Dict.: Opuntia No. 2. 1768.

Description Top

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Synonyms Top

Scientific name Authority First published in
Opuntia maxima Mill. Gard. Dict.: Opuntia No. 5. 1768.
Opuntia mexicana Pfeiff. Enum. Diagn. Cact.: 150. 1837.
Opuntia lanceolata (Haw.) Haw. Syn. Pl. Succ.: 192. 1812.
Opuntia obovata Griffiths in Bull. Torrey Bot. Club 46: 202. 1919.
Opuntia parvula Salm-Dyck Hort. Dyck.: 364. 1834.
Opuntia fusicaulis Griffiths in Rep. (Annual) Missouri Bot. Gard. 19: 271. 1908.
Opuntia glauca Pfeiff. Enum. Diagn. Cact.: 153. 1837.
Opuntia glaberrima Pfeiff. Enum. Diagn. Cact.: 158. 1837.
Opuntia elongata (Willd.) Haw. Suppl. Pl. Succ.: 81. 1819.
Opuntia ficus-barbarica A.Berger in Monatsschr. Kakteenk. 22: 181. 1912.
Opuntia labouretiana K.Schum. Gesamtbeschr. Kakt.: 717. 1898.
Opuntia undosa Griffiths in Monatsschr. Kakteenk. 23: 139. 1913.
Opuntia umbrella Steud. Nomencl. Bot. 2(2-5): 222. 1841.
Opuntia tuna-blanca Speg. in Anales Soc. Ci. Argent. 99: 107. 1925.
Opuntia tribuloides Griffiths in Monatsschr. Kakteenk. 23: 137. 1913.
Opuntia arkansana Engelm. ex Hirscht in Monatsschr. Kakteenk. 8: 115. 1898.
Opuntia decumana (Willd.) Haw. Saxifrag. Enum. 2: 71. 1821.
Opuntia alfagayucca Karw. ex Salm-Dyck Cact. Hort. Dyck.: 68. 1845.
Opuntia amyclaea Ten. Fl. Neapol. Prodr. App. 5: 15. 1826.
Opuntia ficus-indica f. amyclaea (Ten.) Schelle Handb. Kakteenkult.: 51. 1907.
Platyopuntia cordobensis (Speg.) F.Ritter Kakteen Südamerika 2: 403. 1980.
Platyopuntia ficus-indica (L.) F.Ritter Kakteen Südamerika 2: 403. 1980.
Cactus decumanus Willd. Enum. Pl., Suppl.: 84. 1814.
Cactus elongatus Willd. Enum. Pl., Suppl.: 34. 1814.
Cactus ficus Thunb. Fl. Jap.: 198. 1784.
Cactus ficus-indica L. Sp. Pl.: 468. 1753.
Cactus lanceolatus Haw. Misc. Nat.: 188. 1803.
Cactus opuntia L. Sp. Pl.: 468. 1753.
Opuntia ficus-indica var. amyclaea (Ten.) A.Berger Hort. Mortol.: 411. 1912.
Opuntia apurimacensis (F.Ritter) R.Crook & Mottram in Bradleya 13: 100. 1995.
Opuntia ficus-indica var. decumana (Willd.) Speg. in Anales Mus. Nac. Buenos Aires, ser. 3 4: 512. 1905.
Opuntia cordobensis Speg. in Anales Mus. Nac. Buenos Aires, ser. 3 4: 513. 1905.
Opuntia compressa J.F.Macbr. in Contr. Gray Herb. 65: 41. 1922.
Platyopuntia apurimacensis F.Ritter Kakteen Südamerika 4: 1257. 1981.
Cactus maximus Colla in Mem. Reale Accad. Sci. Torino 33: 140. 1826.
Opuntia paraguayensis K.Schum. in Monatsschr. Kakteenk. 9: 149. 1899.
Opuntia caespitosa Raf. in: Bull. Bot., Geneva: 216. 1830.
Opuntia crassa Haw. Suppl. Pl. Succ.: 81. 1819.
Opuntia gymnocarpa F.A.C.Weber Dict. Hort.: 893. 1898.
Opuntia ficus-indica var. gymnocarpa (F.A.C.Weber) Speg. in Anales Mus. Nac. Buenos Aires, ser. 3 4: 512. 1905.
Cactus opuntia var. ficus-indica (L.) DC. Cat. Pl. Horti Monsp.: 13. 1813.
Cactus opuntia var. latifolius Risso Hist. Nat. Prod. Eur. Mérid. 2: 172. 1826.
Opuntia crassa var. major Pfeiff. Enum. Diagn. Cact.: 153. 1837.
Opuntia elongata var. laevior Salm-Dyck Cact. Hort. Dyck.: 242. 1850.
Opuntia ficus-indica f. decumana (Willd.) Schelle Handb. Kakteenkult.: 51. 1907.
Opuntia ficus-indica f. gymnocarpa (F.A.C.Weber) Schelle Kakteen: 66. 1926.
Opuntia ficus-indica f. reticulata Backeb. Descr. Cact. Nov. 1: 10. 1957.
Opuntia ficus-indica var. elongata Schelle Handb. Kakteenkult.: 51. 1907.
Opuntia ficus-indica var. saboten Makino in J. Jap. Bot. 7: 6. 1931.
Opuntia leiascheinvariana Martínez-Gonz. & Gallegos in Bot. Sci. 93: 519. 2015.
Opuntia megacantha var. tenuispina Salm-Dyck Cact. Hort. Dyck.: 68. 1850.

Common names Top

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Language Common/alternative name
English indian fig
English barbary fig
English prickly pear
English tuna cactus
English indian-fig
Spanish tuna
Spanish chumbera
Spanish penca
Spanish nopal de castilla
Spanish nopal
Spanish higuera de pala
Spanish higuera de chumbo
Afrikaans turksvy
Amharic ቁልቋል
Arabic أكناري
Arabic البرشومي
Arabic التين الشوكي
Arabic برشوم
Arabic برشومي
Arabic صبير التين الهندي
Arabic تين شوكي
arq الهندية
ary الكرموس الهندي
ary الهندية
Catalan figuera de moro
co fica d'india
Czech nopál obecný
German cactus ficus-indica
Greek Μπαρμπαροσυκιά
Greek Φραγκοσυκιά
Basque indipikondo
Persian اپونیتا فیکوس ایندیکا
Finnish viikunaopuntia
French figuier de barbarie
Galician chumbeira
Hausa takalmin makka
Hebrew צבר מצוי
Croatian indijska smokva
Croatian gospina pogača
Upper Sorbian figowa opuntija
Hungarian közönséges fügekaktusz
Italian fico d'india
Italian ficodindia
Japanese オオガタホウケン
Japanese ウチワサボテン
Kabyle lkarmus
Korean 백년초
Korean 보검선인장
lad chumbero
Lithuanian figavaisė opuncija
Macedonian индиска смоква
nah nōchtli
Norwegian Bokmål fikenkaktus
Norwegian Bokmål kaktusfiken
Norwegian Nynorsk fikenkaktus
oc figuièr de barbariá
Polish opuncja figowa
Punjab کھانوالا چھتر تھور
Portuguese figueira da Índia
Quechua tuna waraqu
Russian Опунция индийская
Kinyarwanda ikimungu
sc figu morisca
scn ficu d'innia
scn ficadìnnia
scn ficudìnnia
Tachelhit taknarit
Slovenian smokvova opuncija
Albanian fiku i detit
Serbian Опунција
Swedish fikonkaktus
szl figowo uopůncyjo
Telugu భారతీయ నాగ జెముడు
Turkish hint inciri
Chinese 梨果仙人掌
Chinese 秘鲁柱
Chinese 食用仙人掌
Chinese 龙华宝剑

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.
Germination Successful Only with GA3: for these seeds, the use of Gibberellic Acid is not just beneficial but essential for germination to occur.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
    • Macaronesia
      • Azores
      • Canary Islands
      • Cape Verde
      • Madeira
    • Middle Atlantic Ocean
      • Saint Helena
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Sudan
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • South Tropical Africa
      • Angola
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
    • West Tropical Africa
      • Benin
      • Gambia
    • West-central Tropical Africa
      • Rwanda
      • Zaïre
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
      • Yemen
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Korea
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Victoria
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Kriti
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Spain
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
    • South-central U.S.A.
      • New Mexico
    • Southeastern U.S.A.
      • Florida
    • Southwestern U.S.A.
      • Arizona
      • California
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
    • Central America
      • El Salvador
      • Guatemala
      • Honduras
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Galápagos

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000385761
UNII 23Z87HTQ6P
Florida Plant Atlas 4393
USDA Plants OPFI
Tropicos 5100164
INPN 110758
Flora of Italy 346
KEW urn:lsid:ipni.org:names:1151735-2
The Plant List kew-2391911
Plantarium 46247
PFAF Opuntia ficus-indica
Open Tree Of Life 396274
NCBI Taxonomy 371859
Nature Serve 2.150164
IUCN Red List 151706
IPNI 1151735-2
iNaturalist 64119
GBIF 5384064
Freebase /m/07j5dt
EPPO OPUFI
EOL 479484
Calflora (Californian flora) 5938
US Library of Congress sh85106626
USDA GRIN 25840
Wikipedia Opuntia_ficus-indica

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
Profiling the chemical content of Opuntia ficus-indica flowers by HPLC–PDA-ESI-MS and GC/EIMS analyses M. De Leo, M. Bruzual De Abreu, A.M. Pawlowska, P.L. Cioni, A. Braca Elsevier BV 27-Nov-2009
doi:10.1016/J.PHYTOL.2009.11.004
The Non-volatile Acids of Succulent Plants Exhibiting a Marked Diurnal Oscillation in their Acid Content. II. Demonstration of Piscidic Acid as one of the Predominating Acids in Opuntia ficus-indica L.. Arnold Nordal, Jørgen Gether, Guri Haustveit, L. A. Kristiansen, J. Brunvoll, E. Bunnenberg, Carl Djerassi, Ruth Records Danish Chemical Society 19-Jun-2008
doi:10.3891/ACTA.CHEM.SCAND.20-1431
Betanin a betacyanin pigment purified from fruits of Opuntia ficus-indica induces apoptosis in human chronic myeloid leukemia Cell line-K562. Sreekanth D, Arunasree MK, Roy KR, Chandramohan Reddy T, Reddy GV, Reddanna P Phytomedicine 01-Nov-2007
doi:10.1016/J.PHYMED.2007.03.017
PMID:17482444
Amino and organic acids of the prickly pear cactus (<i>Opuntia ficus indica</i> L.) F. F. Feitosa Teles, J. Warren Stull, William H. Brown, Frank M. Whiting Wiley 31-Oct-2006
doi:10.1002/JSFA.2740350410
Secondary metabolites from Opuntia ficus-indica var. saboten. Saleem M, Kim HJ, Han CK, Jin C, Lee YS Phytochemistry 01-Jul-2006
doi:10.1016/J.PHYTOCHEM.2006.04.009
PMID:16762382
Volatile constituents of prickly pear (Opuntia ficus indica Mill., de Castilla variety) Robert A. Flath, Juan M. Takahashi American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JF60218A053
Chemical characterization and biological effects of Sicilian Opuntia ficus indica (L.) mill. Fruit juice: antioxidant and antiulcerogenic activity. Galati EM, Mondello MR, Giuffrida D, Dugo G, Miceli N, Pergolizzi S, Taviano MF J Agric Food Chem 13-Aug-2003
doi:10.1021/JF030123D
PMID:12903943
Antioxidant activities of sicilian prickly pear (Opuntia ficus indica) fruit extracts and reducing properties of its betalains: betanin and indicaxanthin. Butera D, Tesoriere L, Di Gaudio F, Bongiorno A, Allegra M, Pintaudi AM, Kohen R, Livrea MA J Agric Food Chem 06-Nov-2002
doi:10.1021/JF025696P
PMID:12405794
Neobetanin: A new natural plant constituent Dieter Strack, Ute Engel, Victor Wray Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84728-7
Isolation, structure and absolute configuration of indicaxanthin M. Piattelli, L. Minale, G. Prota Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)97621-5
High-performance liquid chromatographic analysis of the pigments of blood-red prickly pear (Opuntia ficus indica) Elisabetta Forni, Andrea Polesello, Dario Montefiori, Andrea Maestrelli Elsevier BV 25-Jul-2002
doi:10.1016/0021-9673(92)80284-2
Application of high-performance liquid chromatography to the characterization of the betalain pigments in prickly pear fruits. Fernández-López JA, Almela L J Chromatogr A 13-Apr-2001
doi:10.1016/S0021-9673(00)01224-3
PMID:11355839
An anti-inflammatory principle from cactus. Park EH, Kahng JH, Lee SH, Shin KH Fitoterapia 01-Mar-2001
doi:10.1016/S0367-326X(00)00287-2
PMID:11295308
Monoamine oxidase B inhibitors from the fruits of Opuntia ficus-indica var. saboten. Han YN, Choo Y, Lee YC, Moon YI, Kim SD, Choi JW Arch Pharm Res 01-Feb-2001
doi:10.1007/BF02976493
PMID:11235812
Wound healing activity of Opuntia ficus-indica. Park EH, Chun MJ Fitoterapia 01-Feb-2001
doi:10.1016/S0367-326X(00)00265-3
PMID:11223226

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
> Alkaloids and derivatives / Betalains / Betacyanins and derivatives
(2S)-1-[(2E)-2-[(2S)-2,6-dicarboxy-2,3-dihydro-1H-pyridin-4-ylidene]ethylidene]-6-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-indolin-1-ium-2-carboxylate 11953901 Click to see C1C(NC(=CC1=CC=[N+]2C(CC3=CC(=C(C=C32)O)OC4C(C(C(C(O4)CO)O)O)O)C(=O)[O-])C(=O)O)C(=O)O 550.50 unknown https://doi.org/10.1016/0021-9673(92)80284-2
https://doi.org/10.1016/S0021-9673(00)01224-3
https://doi.org/10.1021/JF025696P
https://doi.org/10.1016/S0031-9422(00)84728-7
https://doi.org/10.1016/J.PHYMED.2007.03.017
Isobetanin 6325438 Click to see C1C(NC(=CC1=CC=[N+]2C(CC3=CC(=C(C=C32)O)OC4C(C(C(C(O4)CO)O)O)O)C(=O)[O-])C(=O)O)C(=O)O 550.50 unknown https://doi.org/10.1016/S0031-9422(00)84728-7
https://doi.org/10.1016/0021-9673(92)80284-2
> Benzenoids / Benzene and substituted derivatives
Ethyl phenylacetate 7590 Click to see CCOC(=O)CC1=CC=CC=C1 164.20 unknown https://doi.org/10.1021/JF60218A053
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1021/JF60218A053
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-Phenylbutyric acid 7012 Click to see CCC(C1=CC=CC=C1)C(=O)O 164.20 unknown https://doi.org/10.1021/JF60218A053
> Benzenoids / Benzene and substituted derivatives / Toluenes
Toluene 1140 Click to see CC1=CC=CC=C1 92.14 unknown https://doi.org/10.1021/JF60218A053
> Hydrocarbons / Saturated hydrocarbons / Cycloalkanes
Methylcyclohexane 7962 Click to see CC1CCCCC1 98.19 unknown https://doi.org/10.1021/JF60218A053
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60218A053
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Diethyl succinate 31249 Click to see CCOC(=O)CCC(=O)OCC 174.19 unknown https://doi.org/10.1021/JF60218A053
Ethyl 2-methylbutyrate 24020 Click to see CCC(C)C(=O)OCC 130.18 unknown https://doi.org/10.1021/JF60218A053
Ethyl 3-hexenoate 5362622 Click to see CCC=CCC(=O)OCC 142.20 unknown https://doi.org/10.1021/JF60218A053
Ethyl butyrate 7762 Click to see CCCC(=O)OCC 116.16 unknown https://doi.org/10.1021/JF60218A053
Ethyl crotonate 429065 Click to see CCOC(=O)C=CC 114.14 unknown https://doi.org/10.1021/JF60218A053
Ethyl decanoate 8048 Click to see CCCCCCCCCC(=O)OCC 200.32 unknown https://doi.org/10.1021/JF60218A053
Ethyl dodecanoate 7800 Click to see CCCCCCCCCCCC(=O)OCC 228.37 unknown https://doi.org/10.1021/JF60218A053
Ethyl heptanoate 7797 Click to see CCCCCCC(=O)OCC 158.24 unknown https://doi.org/10.1021/JF60218A053
Ethyl hexanoate 31265 Click to see CCCCCC(=O)OCC 144.21 unknown https://doi.org/10.1021/JF60218A053
Ethyl nonanoate 31251 Click to see CCCCCCCCC(=O)OCC 186.29 unknown https://doi.org/10.1021/JF60218A053
Ethyl octanoate 7799 Click to see CCCCCCCC(=O)OCC 172.26 unknown https://doi.org/10.1021/JF60218A053
Ethyl undecanoate 12327 Click to see CCCCCCCCCCC(=O)OCC 214.34 unknown https://doi.org/10.1021/JF60218A053
Ethyl-3-hexanoate 61312 Click to see CCC=CCC(=O)OCC 142.20 unknown https://doi.org/10.1021/JF60218A053
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl decanoate 8050 Click to see CCCCCCCCCC(=O)OC 186.29 unknown https://doi.org/10.1021/JF60218A053
Methyl octanoate 8091 Click to see CCCCCCCC(=O)OC 158.24 unknown https://doi.org/10.1021/JF60218A053
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
2-Ethylundecanoic acid 170754 Click to see CCCCCCCCCC(CC)C(=O)O 214.34 unknown https://doi.org/10.1021/JF60218A053
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-4-[(E,3R)-4-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one 38354073 Click to see CC1=CC(=O)CC(C1C=CC(CO)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
(4S)-4-[(E,3R)-4-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one 156012974 Click to see CC1=CC(=O)CC(C1C=CC(CO)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
4-[4-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one 72807142 Click to see CC1=CC(=O)CC(C1C=CC(CO)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Heptanol 8129 Click to see CCCCCCCO 116.20 unknown https://doi.org/10.1021/JF60218A053
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1021/JF60218A053
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1021/JF60218A053
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown https://doi.org/10.1021/JF60218A053
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/JF60218A053
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60218A053
> 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/JF60218A053
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown https://doi.org/10.1021/JF60218A053
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
2-(Hydroxymethyl)-6-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)oxane-3,4,5-triol 162907437 Click to see CC1=CC(=C(C=C1O)C(C)C)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Zataroside A 25102046 Click to see CC1=CC(=C(C=C1O)C(C)C)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0367-326X(00)00287-2
https://doi.org/10.1016/S0367-326X(00)00265-3
> 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/10.1016/S0367-326X(00)00287-2
https://doi.org/10.1016/S0367-326X(00)00265-3
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/10.1016/S0367-326X(00)00287-2
https://doi.org/10.1016/S0367-326X(00)00265-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
(2S)-2-(phenylazaniumyl)propanoate 6946449 Click to see CC(C(=O)[O-])[NH2+]C1=CC=CC=C1 165.19 unknown https://doi.org/10.1055/S-1999-14037
Alanine 5950 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1055/S-1999-14037
D-alanine 71080 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Aminobutyric acid 6657 Click to see CCC(C(=O)O)N 103.12 unknown https://doi.org/10.1055/S-1999-14037
> 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
Arginine 6322 Click to see C(CC(C(=O)O)N)CN=C(N)N 174.20 unknown https://doi.org/10.1055/S-1999-14037
Citrulline 9750 Click to see C(CC(C(=O)O)N)CNC(=O)N 175.19 unknown https://doi.org/10.1055/S-1999-14037
Glutamine 5961 Click to see C(CC(=O)N)C(C(=O)O)N 146.14 unknown https://doi.org/10.1055/S-1999-14037
Lysine 5962 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://doi.org/10.1055/S-1999-14037
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
Asparagine 6267 Click to see C(C(C(=O)O)N)C(=O)N 132.12 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
Glutamic Acid 33032 Click to see C(CC(=O)O)C(C(=O)O)N 147.13 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Histidine 6274 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
l-Isoleucine 6306 Click to see CCC(C)C(C(=O)O)N 131.17 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
D-Methionine 84815 Click to see CSCCC(C(=O)O)N 149.21 unknown https://doi.org/10.1055/S-1999-14037
Methionine 6137 Click to see CSCCC(C(=O)O)N 149.21 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
D-phenylalanine 71567 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Indicaxanthin 6096870 Click to see C1CC([N+](=CC=C2CC(NC(=C2)C(=O)O)C(=O)O)C1)C(=O)[O-] 308.29 unknown https://doi.org/10.1016/S0040-4020(01)97621-5
https://doi.org/10.1016/0021-9673(92)80284-2
https://doi.org/10.1016/S0021-9673(00)01224-3
https://doi.org/10.1021/JF025696P
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
Serine 5951 Click to see C(C(C(=O)O)N)O 105.09 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Tyrosine 6057 Click to see C1=CC(=CC=C1CC(C(=O)O)N)O 181.19 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Ethyl Acetate 8857 Click to see CCOC(=O)C 88.11 unknown https://doi.org/10.1021/JF60218A053
Ethyl propionate 7749 Click to see CCC(=O)OCC 102.13 unknown https://doi.org/10.1021/JF60218A053
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Malonic acid 867 Click to see C(C(=O)O)C(=O)O 104.06 unknown https://doi.org/10.1002/JSFA.2740350410
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-Hydroxy-1,1-dimethylbutane-1,2,3-tricarboxylic acid 21656358 Click to see CC(C(=O)O)C(C(=O)O)(C(C)(C)C(=O)O)O 234.20 unknown https://doi.org/10.1007/BF02976493
2-Hydroxy-2-(2-methoxy-2-oxoethyl)butanedioic acid 378532 Click to see COC(=O)CC(CC(=O)O)(C(=O)O)O 206.15 unknown https://doi.org/10.1016/S0367-326X(00)00265-3
Citric Acid 311 Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)O 192.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.20-1431
https://doi.org/10.1002/JSFA.2740350410
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
2-Hydroxysuccinic Acid Methyl Ester 12100555 Click to see COC(=O)C(CC(=O)O)O 148.11 unknown https://doi.org/10.1016/S0367-326X(00)00265-3
Ethyl 3-hydroxybutyrate 62572 Click to see CCOC(=O)CC(C)O 132.16 unknown https://doi.org/10.1021/JF60218A053
Malic Acid 525 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.20-1431
https://doi.org/10.1002/JSFA.2740350410
> Organic acids and derivatives / Organic carbonic acids and derivatives / Carbonic acid diesters
Diethyl carbonate 7766 Click to see CCOC(=O)OCC 118.13 unknown https://doi.org/10.1021/JF60218A053
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine 1123 Click to see C(CS(=O)(=O)O)N 125.15 unknown https://doi.org/10.1055/S-1999-14037
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
Carnosine 439224 Click to see C1=C(NC=N1)CC(C(=O)O)NC(=O)CCN 226.23 unknown https://doi.org/10.1055/S-1999-14037
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Pentanol 6276 Click to see CCCCCO 88.15 unknown https://doi.org/10.1021/JF60218A053
3-Methyl-2-buten-1-OL 11173 Click to see CC(=CCO)C 86.13 unknown https://doi.org/10.1021/JF60218A053
3-Penten-1-ol, (3E)- 510370 Click to see CC=CCCO 86.13 unknown https://doi.org/10.1021/JF60218A053
Cis-3-Penten-1-ol 69814 Click to see CC=CCCO 86.13 unknown https://doi.org/10.1021/JF60218A053
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown https://doi.org/10.1021/JF60218A053
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
3-Pentanol 11428 Click to see CCC(CC)O 88.15 unknown https://doi.org/10.1021/JF60218A053
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclopentanols
Cyclopentanol 7298 Click to see C1CCC(C1)O 86.13 unknown https://doi.org/10.1021/JF60218A053
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0367-326X(00)00265-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-[(E)-2-[2-carboxy-6-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroindol-1-yl]ethenyl]pyridine-2,6-dicarboxylic acid 131750867 Click to see C1C(N(C2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O)C=CC4=CC(=NC(=C4)C(=O)O)C(=O)O)C(=O)O 548.50 unknown https://doi.org/10.1016/S0031-9422(00)84728-7
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
2-Methyl-pent-2-enal 12177 Click to see CCC=C(C)C=O 98.14 unknown https://doi.org/10.1021/JF60218A053
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Pentanone 7288 Click to see CCC(=O)CC 86.13 unknown https://doi.org/10.1021/JF60218A053
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone 7410 Click to see CC(=O)C1=CC=CC=C1 120.15 unknown https://doi.org/10.1021/JF60218A053
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2R,3S,4R,5R)-2-butoxy-2-(hydroxymethyl)oxane-3,4,5-triol 50914217 Click to see CCCCOC1(C(C(C(CO1)O)O)O)CO 236.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
2-Butoxy-2-(hydroxymethyl)oxane-3,4,5-triol 13059905 Click to see CCCCOC1(C(C(C(CO1)O)O)O)CO 236.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid 54670067 Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O 176.12 unknown https://doi.org/10.1021/JF030123D
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
Dioxane 31275 Click to see C1COCCO1 88.11 unknown https://doi.org/10.1021/JF60218A053
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1055/S-1999-14037
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(S)-4-Nonanolide 441574 Click to see CCCCCC1CCC(=O)O1 156.22 unknown https://doi.org/10.1021/JF60218A053
gamma-Decalactone 12813 Click to see CCCCCCC1CCC(=O)O1 170.25 unknown https://doi.org/10.1021/JF60218A053
Gamma-nonalactone 7710 Click to see CCCCCC1CCC(=O)O1 156.22 unknown https://doi.org/10.1021/JF60218A053
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Ethyl 3-phenylprop-2-enoate 7649 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1021/JF60218A053
Ethyl cinnamate 637758 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1021/JF60218A053
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
https://doi.org/10.1021/JF030123D
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> 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 https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
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 https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-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]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 16081699 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)OC)COC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)O)O)O 800.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
[6-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73236024 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)OC)COC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)O)O)O 800.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one 12304323 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 https://doi.org/10.1016/J.PHYTOL.2009.11.004
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1016/J.PHYTOL.2009.11.004
3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 162895542 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)OC6C(C(C(C(O6)CO)O)O)O)O)O)O 786.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
3-[3,4-Dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 162895541 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)OC6C(C(C(C(O6)CO)O)O)O)O)O)O 786.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 124629463 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 https://doi.org/10.1016/J.PHYTOL.2009.11.004
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13245589 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.004
https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one 14749097 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.004
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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 https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 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 594.50 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.004
Astragalin 5282102 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 https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.004
CID 14353383 14353383 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
CID 44566503 44566503 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 770.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Isorhamnetin 3-galactoside 13245586 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
https://doi.org/10.1016/J.PHYTOL.2009.11.004
Isorhamnetin 3-neohesperidoside 13915237 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)OC)CO)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Isorhamnetin 3-robinobioside 6223069 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 https://doi.org/10.1016/J.PHYTOL.2009.11.004
Isorhamnetin-3-O-neohespeidoside 11664505 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)OC)CO)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Kaempferol 3-O-arabinoside 5481882 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.004
Kaempferol-3-O-rutinoside 5318767 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 594.50 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.004
https://doi.org/10.1021/JF030123D
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/10.1016/J.PHYTOL.2009.11.004
https://doi.org/10.1021/JF030123D
Vitamin P 5293655 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/10.1016/J.PHYTOL.2009.11.004
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009

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