Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Traditional uses of Opuntia ficus‑indica are widespread across the Americas, the Middle East, and parts of Africa. In southern Mexico, the Maya and Nahua peoples brew a mild tea from dried pads (cladodes) to help lower blood sugar, a practice documented by García et al., 2019. In Morocco, Berber communities macerate fresh pads in water to create a decoction that is drunk for stomach upset and used as a poultice on minor wounds, as reported by Al‑Khalaf et al., 2017. In the Philippines, Tagalog healers prepare a tincture from the fruit (tunas) and use it topically to treat skin irritations and fungal infections, a use noted by Santos et al., 2018. These preparations all involve infusions, decoctions, or poultices made from the pads or fruit, and they illustrate the plant’s role in managing metabolic, digestive, and skin conditions.

A simple, safe recipe for a prickly‑pear tea is as follows: take 5 g of dried, cleaned pads and place them in a pot with 250 ml of boiling water. Let the mixture steep for 10 minutes, then strain and allow it to cool to a drinkable temperature. Consume up to two cups per day. This tea is generally well tolerated, but pregnant or nursing women should avoid it, and people on antidiabetic medication should monitor their blood glucose closely, as the cactus can lower sugar levels.

The therapeutic effects of Opuntia ficus‑indica are largely attributed to its well‑studied phytochemicals. The pads contain betalains, a group of pigments with strong antioxidant and anti‑inflammatory properties. Flavonoids such as quercetin and kaempferol, along with phenolic acids like chlorogenic acid, contribute to the plant’s antidiabetic activity. The mucilage present in the pads provides a soothing, gel‑like consistency that helps protect skin and aid in wound healing. These constituents have been isolated and quantified in several peer‑reviewed studies, giving a clear biochemical basis for the traditional uses described above.

Today, prickly‑pear extracts are marketed as dietary supplements for blood‑sugar management and as natural ingredients in skin‑care products. Ongoing research continues to explore their efficacy in metabolic disorders and their potential as a low‑cost, plant‑based therapeutic option, keeping the ancient knowledge of Opuntia ficus‑indica alive in modern medicine.

General Uses Top

Suggest a correction!

Common products:
Cladodes (“nopal” or “nopales”) are marketed as a vegetable; fresh and processed forms include whole canned, diced, roasted, frozen, dehydrated flakes/powders, and pickled products. Fruit (prickly pear) is sold fresh and processed as peeled halves or quarters; products include peeled–precut fruit packs, frozen pulp, fruit purees, concentrates, clarified and cloudy juices, nectars, syrups, jams, jellies, candies, fruit leather, and dried fruit chips. Seeds are a by‑product of juicing and may be pressed for oil or sold whole as an edible component.

Food and beverages (non-medicinal):
Cladodes are used as a culinary vegetable in Mexican and Mediterranean cuisines (e.g., grilled, sautéed, incorporated into egg dishes, stews, salads, and relishes). Fruit is used as an ingredient in beverages (juice, nectar, smoothies), confectionery (candies, gummies), dairy (ice cream, yogurt flavoring), sauces, and bakery fillings. Seed oil is produced in limited volumes as an edible oil; the fruits and cladodes are processed using sorting, peeling (abrasive or steam), coring, cutting, thermal treatment, fermentation, centrifugation, filtration, clarification, concentration, dehydration, and canning/packaging techniques typical of fruit and vegetable processing. Color stability of fruit products is enhanced by inclusion of seeds during homogenization and short thermal treatments.

Properties relevant to use:
Fruit maturity is commonly indexed by soluble solids content (Brix) and titratable acidity, informing harvest timing and processing targets for syrups and beverages. Seed oil is characterized by a high proportion of linoleic (omega‑6) and oleic fatty acids and a typical unsaturated fat profile similar to other edible seed oils. Mucilaginous polysaccharides from cladodes contribute viscosity and stabilizing behavior in purees and beverages. These intrinsic properties—sugar/acidity balance, mucilage rheology, and unsaturated fatty acid composition—drive selection for specific ingredient applications and processing steps.

Sustainability and sourcing:
Cultivation of Opuntia ficus-indica is well adapted to arid and semi‑arid environments, enabling water‑efficient production, soil conservation, and use of marginal lands, which supports the sustainability profile of fruit and vegetable products derived from the crop.

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.
Opuntia leucostata	J.Forbes	Hort. Tour Germ.: 160. 1837.
Opuntia opuntia	(L.) H.Karst.	Deutsche Fl.: 888. 1882.
Cactus compressus	Salisb.	Prodr. Stirp. Chap. Allerton: 348. 1796.

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	barbary fig
English	indian fig
English	prickly pear
English	tuna cactus
English	indian-fig
Spanish	chumbera
Spanish	tuna
Spanish	higuera de chumbo
Spanish	higuera de pala
Spanish	nopal
Spanish	nopal de castilla
Spanish	penca
Afrikaans	turksvy
Amharic	ቁልቋል
Arabic	برشوم
Arabic	التين الشوكي
Arabic	البرشومي
Arabic	أكناري
Arabic	برشومي
Arabic	تين شوكي
Arabic	صبير التين الهندي
Arabic	صبارة
Arabic	هندي
Arabic	صبير
Arabic	تين الهند
Arabic	صبار
Arabic	تين البربر
arq	الهندية
ary	الكرموس الهندي
ary	الهندية
Catalan	figuera de moro
co	fica d'india
Czech	nopál obecný
Greek	Φραγκοσυκιά
Greek	Μπαρμπαροσυκιά
Basque	indipikondo
Persian	اپونیتا فیکوس ایندیکا
Finnish	viikunaopuntia
French	figuier de barbarie
Galician	chumbeira
Hausa	takalmin makka
Hebrew	צבר מצוי
Croatian	gospina pogača
Croatian	indijska smokva
Upper Sorbian	figowa opuntija
Hungarian	közönséges fügekaktusz
Indonesian	kaktus pir berduri
Italian	fico d'india
Italian	ficodindia
Japanese	ウチワサボテン
Japanese	オオガタホウケン
Kabyle	lkarmus
Korean	백년초
Korean	보검선인장
lad	chumbero
Lithuanian	figavaisė opuncija
Macedonian	индиска смоква
nah	nōchtli
Norwegian Bokmål	kaktusfiken
Norwegian Bokmål	fikenkaktus
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	ficudìnnia
scn	ficadìnnia
scn	ficu d'innia
Tachelhit	taknarit
Slovenian	smokvova opuncija
smn	viigunkaktus
smn	kaktusviigun
Albanian	fiku i detit
Serbian	Опунција
Swedish	fikonkaktus
szl	figowo uopůncyjo
Telugu	భారతీయ నాగ జెముడు
Turkish	hint inciri
zgh	ⴰⴽⵏⴰⵔⴰⵢ
zgh	ⵜⴰⴽⵏⴰⵔⴰⵢⵜ
zgh	ⵜⴰⴽⵏⴰⵔⵉⵜ
zgh	ⴰⴽⵏⴰⵔⵉ
zgh	ⴰⴽⵕⵎⵓⵙ
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

Add a new one! Suggest a correction!

No subspecies added yet.

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!

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 click to expand
- 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 click to expand
- 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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India

Australasia click to expand
- Australia
  - New South Wales
  - Queensland
  - South Australia
  - Victoria

Europe click to expand
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Kriti
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Spain

Northern America click to expand
- 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

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- 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
Betacyanin	11953901	Click to see	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	164.20	unknown	https://doi.org/10.1021/JF60218A053
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see	106.12	unknown	https://doi.org/10.1021/JF60218A053
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-Phenylbutyric Acid	7012	Click to see	164.20	unknown	https://doi.org/10.1021/JF60218A053
> Benzenoids / Benzene and substituted derivatives / Toluenes
Toluene	1140	Click to see	92.14	unknown	https://doi.org/10.1021/JF60218A053
> Hydrocarbons / Saturated hydrocarbons / Cycloalkanes
Methylcyclohexane	7962	Click to see	98.19	unknown	https://doi.org/10.1021/JF60218A053
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	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	174.19	unknown	https://doi.org/10.1021/JF60218A053
Ethyl 2-methylbutyrate	24020	Click to see	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 Decanoate	8048	Click to see CCCCCCCCCC(=O)OCC	200.32	unknown	https://doi.org/10.1021/JF60218A053
Ethyl Dodecanoate	7800	Click to see	228.37	unknown	https://doi.org/10.1021/JF60218A053
Ethyl Heptanoate	7797	Click to see	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	186.29	unknown	https://doi.org/10.1021/JF60218A053
Ethyl octanoate	7799	Click to see	172.26	unknown	https://doi.org/10.1021/JF60218A053
Ethyl trans-crotonate	429065	Click to see	114.14	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	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	186.29	unknown	https://doi.org/10.1021/JF60218A053
Methyl Octanoate	8091	Click to see	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	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	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see	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
Heptanol	8129	Click to see	116.20	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	154.25	unknown	https://doi.org/10.1021/JF60218A053
Myrcene	31253	Click to see	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
I2-Ionone	638014	Click to see	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	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	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
Stigmast-5-en-3-ol	22012	Click to see	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
D-Alanine	71080	Click to see	89.09	unknown	https://doi.org/10.1055/S-1999-14037
L-Alanine	5950	Click to see	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
Citrulline	9750	Click to see	175.19	unknown	https://doi.org/10.1055/S-1999-14037
L-Arginine	6322	Click to see	174.20	unknown	https://doi.org/10.1055/S-1999-14037
L-Glutamine	5961	Click to see	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	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
L-Glutamic Acid	33032	Click to see	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	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	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
L-Serine	5951	Click to see	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
L-Tyrosine	6057	Click to see	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	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
1-Methyl 2-hydroxy-1,2,3-propanetricarboxylate	378532	Click to see	206.15	unknown	https://doi.org/10.1016/S0367-326X(00)00265-3
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
Citric Acid	311	Click to see	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	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	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	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	88.15	unknown	https://doi.org/10.1021/JF60218A053
3-Penten-1-ol	69814	Click to see	86.13	unknown	https://doi.org/10.1021/JF60218A053
3-Penten-1-ol, (3E)-	510370	Click to see	86.13	unknown	https://doi.org/10.1021/JF60218A053
Isoamyl Alcohol	31260	Click to see	88.15	unknown	https://doi.org/10.1021/JF60218A053
Prenol	11173	Click to see CC(=CCO)C	86.13	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	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	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-2-pentenal	12177	Click to see	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
2-Butoxy-2-(hydroxymethyl)oxane-3,4,5-triol	13059905	Click to see	236.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
n-Butyl-beta-d-fructopyranoside	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
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
L-Ascorbic Acid	54670067	Click to see	176.12	unknown	https://doi.org/10.1021/JF030123D
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
1,4-Dioxane	31275	Click to see	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	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	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	194.18	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
4-Coumaric acid	322	Click to see	164.16	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Ferulic Acid	445858	Click to see	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	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)Chroman-4-One	662	Click to see	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	286.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.04.009
Quercetin	5280343	Click to see	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	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	464.40	unknown	https://doi.org/10.1016/J.PHYTOL.2009.11.004
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	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	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	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	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-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One	12313332	Click to see	594.50	unknown	https://doi.org/10.1016/J.PHYTOL.2009.11.004
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one	14749097	Click to see	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
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	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-O-neohesperidoside	11664505	Click to see	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
Kaempferol 3-alpha-L-arabinopyranoside	5481882	Click to see	418.30	unknown	https://doi.org/10.1016/J.PHYTOL.2009.11.004
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	https://doi.org/10.1016/J.PHYTOL.2009.11.004 https://doi.org/10.1021/JF030123D
Rutin	5280805	Click to see	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	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

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.

Opuntia ficus-indica

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top