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.

Apium graveolens (celery) has a long history of use as an infusion and poultice in several cultural traditions. In Chinese folk medicine, the root is boiled into a decoction to relieve stomach pain and diarrhea; this practice is documented in Li et al., 2015. Among European herbalists, dried leaves are steeped in hot water to produce a mild tea that is traditionally taken after meals to aid digestion, as described in Chevallier, 2001. The Cherokee of North America have used a maceration of fresh leaves applied as a poultice to soothe skin infections and reduce inflammation, a use recorded in the American Herbal Pharmacopoeia, 2015.

A simple, safe celery tea can be prepared by taking 5 g of dried celery leaves and adding them to 250 ml of boiling water. Let the mixture steep for 5–10 minutes, then strain and sip. This infusion delivers the plant’s diuretic and anti‑inflammatory benefits. Pregnant women should avoid large quantities of celery tea because the plant’s coumarin content can stimulate uterine contractions, and individuals taking anticoagulant medications should consult a healthcare provider due to the same coumarin compounds.

The therapeutic effects of celery are largely attributed to its well‑studied phytochemical profile. Phthalides such as butylphthalide and linalyl acetate give celery its characteristic aroma and contribute to its diuretic and smooth‑muscle‑relaxing properties. Flavonoids, including apigenin and luteolin, provide antioxidant and anti‑inflammatory activity, while the coumarin esculin has mild anticoagulant effects. Celery also supplies vitamin K, which supports blood clotting and bone health.

Today, celery extracts are marketed as weight‑loss and diuretic supplements, and ongoing research is exploring their potential anti‑cancer and neuroprotective properties. The plant remains a staple in both culinary and traditional medicinal contexts, bridging ancient wisdom with modern science.

General Uses Top

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Common products:
Celery is processed primarily as a fresh vegetable (stalks and leaves), as celery seeds (spice), and as a flavoring agent via essential oil and oleoresin (seed-origin). Processed products include dehydrated celery (powder, flakes), celery juice and concentrates, celery fiber (dietary fiber concentrate), and seed oil for flavoring. Celery salt is prepared by blending salt with ground celery seed.

Industrial and craft applications:
Dehydrated celery and fiber are used in soups, sauces, snack foods, and meat products as a flavor carrier and bulk texturant; pectin from celery pomace (a juice-processing byproduct) has gelling applications. A-cellulose isolated from celery has served in biochemical studies on plant cell wall structure.

Food and beverages (non-medicinal):
Stalks are eaten raw or cooked. Leaves provide herb flavoring. Seeds and seed extracts serve as spices and natural flavoring in condiments, meats, pickles, salad dressings, and broths. Oleoresin and essential oil are used as standardized flavor components in processed foods. Furanocoumarins present in celery can make it a known phototoxicant in handlers and processors, warranting exposure controls and labeling in workplaces; no health claims are made.

Colorants and tanning:
No established use in textiles or leather tanning is documented.

Wood and fiber:
No timber or fiber products are recorded.

Fragrance and cosmetics:
Celery seed absolute and essential oil are used in small amounts in perfumery and as flavor/fragrance notes. Standardized oleoresin is preferred for flavor use to maintain consistent levels of phthalides (e.g., sedanenolide/sedanolide).

Properties relevant to use:
The characteristic aroma derives from phthalides and related compounds in seed oil; seed oil is lipophilic and steam-distillable, making it suitable for food-grade flavoring. Celery fiber is low in fat and high in insoluble fiber; it adds bulk and moisture-holding capacity in foods.

Standards and regulation:
Fenaroli’s Handbook of Flavor Ingredients and FEMA GRAS reports provide guidance for celery seed oil, oleoresin, and absolute as food-grade flavorings. International Flavour Association (IFRA) guidelines apply to fragrance uses, and food safety systems (e.g., Hazard Analysis and Critical Control Points) govern processing and juice operations.

Sustainability and sourcing:
Seed oil yields are relatively low, favoring use as a flavoring rather than a bulk commodity. Crop residues (pomace) can supply fiber and pectin; commercial seed cultivars are widely cultivated, reducing pressure on wild collection.

Synonyms Top

Scientific name	Authority	First published in
Sison ruta	Burm.f.	Fl. Indica , Prodr. Fl. Cap.: 7 (1768)
Sium graveolens	Vest	Man. Bot. : 517 (1805)
Smyrnium laterale	Thunb.	Prodr. Pl. Cap. : 51 (1794)
Seseli graveolens	Scop.	Fl. Carniol. , ed. 2, 1: 215 (1771)
Apium australe var. latisectum	H.Wolff	Pflanzenr. , IV, 228(90): 32 (1927)
Apium celleri	Gaertn.	Fruct. Sem. Pl. 1: t. 22 (1788)
Apium decumbens	Eckl. & Zeyh.	Enum. Pl. Afric. Austral. : 340 (1837)
Apium dulce	Mill.	Gard. Dict. ed. 8 : n.º 5 (1768)
Apium graveolens var. bashmensis	Hosni	Taeckholmia 11: 57 (1988).
Apium graveolens var. butronensis	D.Gómez & G.Monts.	in C. Aseginolaza Iparragirre et al., Cat. Flor. Alava, Vizcaya & Guipuzcoa 512 (1984).
Apium graveolens subsp. butronensis	(D.Gómez & G.Monts.) Aizpuru	Munibe, Ci. Nat. 49: 66. 1997
Apium graveolens var. dulce	(Mill.) DC.	Prodr. [A. P. de Candolle] 4: 101. 1830 [late Sep 1830]
Apium graveolens var. lusitanicum	(Mill.) DC.	Prodr. 4: 101 (1830)
Apium graveolens f. lusitanicum	(Mill.) J.Helm	Kulturpflanze 19: 82. 1972 , as 'lustianicum'
Apium graveolens var. maritimum	Dumort.	Fl. Belg. 78 1827
Apium integrilobum	Hayata	J. Coll. Sci. Imp. Univ. Tokyo 30(1): 126 (1911)
Apium lobatum	Gilib.	Fl. Lit. Inch. ii. 41. 1782
Apium lusitanicum	Mill.	Gard. Dict. ed. 8 : n.º 7 (1768)
Apium maritimum	Salisb.	Prodr. Stirp. Chap. Allerton : 169 (1796)
Apium palustre	Thore	Essai Chloris : 109 (1803)
Apium rapaceum	Mill.	Gard. Dict. ed. 8 : n.º 6 (1768)
Apium vulgare	Bubani	Fl. Pyren. 2: 344 (1899)
Carum graveolens	(L.) Koso-Pol.	Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 199 (1915 publ. 1916)
Celeria graveolens	(L.) Britton	Ill. Fl. N. U.S. (Britton & Brown), ed. 2. 2: 660. 1913
Helosciadium graveolens	Rojas Acosta	Cat. Hist. Nat. Corrientes : 65 (1897)
Helosciadium ruta	DC.	Prodr. 4: 106 (1830)
Helosciadium rutaceum	St.-Lag.	Ann. Soc. Linn. Lyon 7: 127 (1880)
Apium graveolens subsp. rapaceum	(Mill.) P.D.Sell	Fl. Great Britain Ireland 3: 518 (2009)
Sium apium	Roth	Tent. Fl. Germ. 1: 128 (1788)
Sison trifidum	Burm. ex DC.	Prodr. [A. P. de Candolle] 4: 106. 1830 [late Sep 1830]
Selinum graveolens	(L.) E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 12: 38 (1904)
Apium graveolens var. rapaceum	(Mill.) DC.	Prodr. [A. P. de Candolle] 4: 101. 1830 [late Sep 1830]
Apium graveolens var. bashmense	Hosni	Taeckholmia 11: 57 (1988)
Apium graveolens var. butronense	D.Gómez & G.Monts.	Cat. Flor. Alava, Vizcaya & Guipuzcoa : 512 (1984)
Celeri graveolens	(L.) Britton	Ill. Fl. N. U.S. , ed. 2, 2: 660 (1913)
Apium graveolens var. silvestre	Alef.	Landw. Fl. : 150 (1866)
Apium graveolens var. album	Alef.	Landw. Fl. : 150 (1866)
Apium graveolens var. juglandinum	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. violaceum	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. aromaticum	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. secalinum	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. erfurtense	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. praecox	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. laeve	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. humile	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. crispum	Nois.	Man. Compl. Jard. 2: 421 (1825)
Apium graveolens var. venosum	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. rubrum	Alef.	Landw. Fl. : 151 (1866)
Apium graveolens var. vulgare	Nois.	Man. Compl. Jard. 2: 421 (1825)
Apium graveolens var. variegatum	Nois.	Man. Compl. Jard. 2: 422 (1825)
Apium graveolens var. latifolium	Nois.	Man. Compl. Jard. 2: 422 (1825)
Apium graveolens var. tuberosum	Nois.	Man. Compl. Jard. 2: 422 (1825)
Apium graveolens var. sativum	Gaudin	Fl. Helv. 2: 422 (1828)
Apium graveolens subsp. butronense	(D.Gómez & G.Monts.) Aizpuru	Munibe, Ci. Nat. 49: 66 (1997)
Apium graveolens var. rapaceum	(Mill.) Poir.	Encycl. 5: 195 (1804)
Apium graveolens f. rapaceum	(Mill.) Gaudin	Fl. Helv. 2: 422 (1828)
Apium graveolens var. dulce	(Mill.) Poir.	Encycl. 5: 194 (1804)
Apium graveolens subsp. rapaceum	(Mill.) Schübl. & G.Martens	Fl. Würtemberg : 191 (1834)
Apium graveolens subsp. dulce	(Mill.) Schübl. & G.Martens	Fl. Würtemberg : 191 (1834)

Common names Top

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Filter by language:

Language	Common/alternative name
English	wild celery
English	celery plant
English	celery
Spanish	apio
Afrikaans	seldery
Amharic	ሰለሪ
Arabic	الكرفس
Arabic	الكرفس النتن
Arabic	كرافس
Arabic	كرفس
Arabic	كرفس نبطي
atj	ciwapw
Azerbaijani	İyli kərəviz
azb	ایلی کرویز
ba	Сельдерей
ban	seladri
Belarusian	сельдэрэй пахучы
Bulgarian	кервиз
Bulgarian	керевиз
Bulgarian	обикновена целина
bjn	daun sop
Bengali	সেলেরি
Bengali	পাথুনি শাক
Tibetan	ལྕ་ཚལ།
br	ach
Bosnian	celer
Catalan	api-nap
Catalan	api
Czech	celer
Czech	miřík celer
Welsh	seleri
Danish	bladselleri
German	sellerie
German	staudensellerie
German	echter sellerie
Greek	Νεροσέλινο
Greek	Ραπανοσέλινο
Greek	Σέλινο
eml	sèlar
Esperanto	celerio
Estonian	seller
Estonian	aedseller
Basque	apio
Persian	کرفس
Finnish	selleri
French	céleri
French	cèleri
frr	echt silere
Irish	soilire
Irish	lus na smaileog
Irish	meirse
Irish	smaileog
Galician	apio
Manx	smullish
Hebrew	סלרי
Croatian	celer
ht	sèlri
Hungarian	kerti zeller
Hungarian	nagyszagú zeller
Hungarian	zeller
Armenian	Նեխուր բուրավետ
Indonesian	seledri
io	apio
io	celerio
Icelandic	sellerí
Icelandic	seljurót
Italian	sedano
Italian	sedano rapa
Italian	sedano da costa
Japanese	オランダミツバ
Japanese	セルリ
Japanese	セルリー
Japanese	セレリアック
Japanese	塘蒿
Japanese	清正人参
Japanese	セロリ
jv	slèdri
Georgian	ნიახური
Kazakh	Балдыркөк
Kannada	ಸೆಲರಿ
Korean	셀러리
lb	zelleri
lij	séllao
Lithuanian	salierai
Lithuanian	valgomasis salieras
Lithuanian	salieras
Latvian	lapu selerija
Latvian	sakņu selerija
Latvian	salātu selerija
Latvian	selerijas
Latvian	smaržīgā selerija
lzh	芹
Malagasy	seleria
min	saladari
Macedonian	целер
Marathi	अजमोदा
Malay	saderi
Malay	seleri
Malay	daun saderi
mt	karfus
mt	karfusa
Burmese	တရုတ်နံနံပင်
nap	accio
Norwegian Bokmål	sellerier
Norwegian Bokmål	selleristenger
Norwegian Bokmål	selleri
Dutch	selderij
Norwegian Nynorsk	selleri
Norwegian Nynorsk	selleriplante
Norwegian Nynorsk	hageselleri
nv	hazaʼaleehtsoh
oc	api
os	Маламар
os	тæфгæнæг маламар
Punjabi	ਅਜਮੋਦ
pam	kimche
pcd	chéléri
pcd	chilri
Polish	seler zwyczajny
Polish	selery zwyczajne
Punjab	اجمود
Portuguese	aipo
Quechua	apio
Quechua	kastilla raqacha
Quechua	apiyu
Romanian	Ţelina
Romanian	Ţelină
Romanian	Țelina
Romanian	Țelină
Russian	сельдерей пахучий
Russian	апиум
Russian	сельдерей душистый
Russian	сельдерей культурный
Russian	сельдерей
Kinyarwanda	seleri
sa	धान्याकपत्रम्
sa	कुस्तुम्बरीपर्णम्
sat	ᱫᱷᱩᱱᱤᱭᱟ. ᱥᱟᱠᱟᱢ
sc	appiu
scn	accia
scn	acciu
sco	celery
se	seller
Serbo-Croatian	celer
Slovak	zeler voňavý
Slovenian	zelena
Slovenian	navadna zelena
sma	seellerije
smn	seller
sms	seller
Albanian	selinoja
Serbian	целер
Serbian	биљка целера
su	salédri
Swedish	selleri
Tamil	சிவரிக்கீரை
tg	Карафс
Thai	celery
Thai	คึ่นช่าย
Thai	เซเลอรี
Thai	ขึ้นฉ่าย
Turkish	kereviz
ug	كەرەپشە(چىڭسەي)
Ukrainian	селера
Urdu	اجمود
Uzbek	keleriya
vec	sełeno
vec	sełéno
vep	hajukaz sel'derei
Vietnamese	cần tây
vls	selder
vls	seldery
Walloon	celeri
xmf	სონა
yi	סעלערי
za	ginzcaiq
Chinese	芹菜
Chinese	旱芹
Chinese	旱芹香芹菜、药芹、芹菜
Chinese	旱芹（芹菜）
Chinese	旱菜
Chinese	芹菜子
Chinese	芹菜根皮
Chinese	药芹
Chinese	香芹菜

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Cape Verde
  - Madeira
- Middle Atlantic Ocean
  - Saint Helena
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Socotra
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
- South Tropical Africa
  - Mozambique
- Southern Africa
  - Botswana
  - Cape Provinces
  - Free State
  - Kwazulu-Natal
  - Lesotho
  - Namibia
  - Northern Provinces
- West-central Tropical Africa
  - Cameroon
- Western Indian Ocean
  - Réunion

Antarctica click to expand
- Subantarctic Islands
  - Amsterdam-St.Paul Islands

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Oman
  - Saudi Arabia
  - Yemen
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Inner Mongolia
- Eastern Asia
  - Taiwan
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Siberia
  - Buryatiya
- Western Asia
  - Afghanistan
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Myanmar
  - Thailand
  - Vietnam

Australasia click to expand
- Australia
  - Norfolk Island
- New Zealand
  - Chatham Islands
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Central European Russia
  - East European Russia
  - Krym
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - Nova Scotia
- Mexico
  - Mexico Northwest
- North-central U.S.A.
  - Missouri
  - Oklahoma
  - South Dakota
- Northeastern U.S.A.
  - Connecticut
  - Massachusetts
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - West Virginia
- Northwestern U.S.A.
  - Idaho
  - Oregon
  - Washington
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Florida
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
- Southwestern U.S.A.
  - Arizona
  - California
  - Nevada
  - Utah

Pacific click to expand
- Northwestern Pacific
  - Marianas
  - Marshall Islands

Southern America click to expand
- Brazil
  - Brazil South
- Caribbean
  - Bermuda
  - Cuba
  - Dominican Republic
  - Haiti
  - Puerto Rico
  - Trinidad-Tobago
- Central America
  - Costa Rica
  - Guatemala
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Chile North
  - Chile South
  - Juan Fernández Islands
- Western South America
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000540626
Florida Plant Atlas	1396
Flora of Alabama	5565
Canadensys	2545
USDA Plants	APGR2
Tropicos	1700014
INPN	83195
Flora of Italy	3575
KEW	urn:lsid:ipni.org:names:838067-1
The Plant List	kew-2644053
Plantarium	3334
Open Tree Of Life	2472
Observations.org	2348
NCBI Taxonomy	4045
NBN Atlas	NBNSYS0000003663
Nature Serve	2.131636
IUCN Red List	164203
IPNI	838067-1
iNaturalist	58788
GBIF	5371879
Freebase	/m/01xj_
EPPO	APUGV
EOL	579558
Elurikkus	2832
Calflora (Californian flora)	423
US Library of Congress	sh85021621
USDA GRIN	300034
Wikipedia	Apium_graveolens
CMAUP	NPO26721
PFAF	Apium graveolens

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCF_009905375.1	ASM990537v1	Chromosome	North China University of Science and Technology	2021-05-17	101.61	3.10 Gb

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

Phytochemical investigation of the n-hexane-extracted oil from four umbelliferous vegetables using GC/MS analysis in the context of antibacterial activity

Baky MH, El-Taher EM, Naggar DM, Abouelela MB

Sci Rep

08-May-2024

PMCID:	PMC11079057
doi:	10.1038/s41598-024-60631-4
PMID:	38719900

Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species

Önder S, Periz ÇD, Ulusoy S, Erbaş S, Önder D, Tonguç M

Sci Rep

02-May-2024

PMCID:	PMC11066118
doi:	10.1038/s41598-024-60810-3
PMID:	38698117

Commodity risk assessment of Petunia spp. and Calibrachoa spp. unrooted cuttings from Kenya

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Lacomme C, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R

EFSA J

25-Apr-2024

PMCID:	PMC11044013
doi:	10.2903/j.efsa.2024.8742
PMID:	38665158

Pharmacological Activities of Lonicerae japonicae flos and Its Derivative—“Chrysoeriol” in Skin Diseases

Law SK, Wu XX, Jiang Z, Tong CW, Chow WY, Au DC

Molecules

25-Apr-2024

PMCID:	PMC11085288
doi:	10.3390/molecules29091972
PMID:	38731465

Enrichment and Evaluation of Antitumor Properties of Total Flavonoids from Juglans mandshurica Maxim

Yang S, Chu G, Wu J, Zhang G, Du L, Lin R

Molecules

25-Apr-2024

PMCID:	PMC11085465
doi:	10.3390/molecules29091976
PMID:	38731467

Design of three-component essential oil extract mixture from Cymbopogon flexuosus, Carum carvi, and Acorus calamus with enhanced antioxidant activity

Assaggaf H, Jeddi M, Mrabti HN, Ez-zoubi A, Qasem A, Attar A, Goh BH, Tan SL, Bouyahya A, Goh KW, Hachlafi NE

Sci Rep

22-Apr-2024

PMCID:	PMC11035653
doi:	10.1038/s41598-024-59708-x
PMID:	38649707

Encapsulation of Apium graveolens essential oil into chitosan nanobiopolymer for protection of stored rice against Fusarium verticillioides and fumonisins contamination

Das S, Chaudhari AK

Heliyon

19-Apr-2024

PMCID:	PMC11061702
doi:	10.1016/j.heliyon.2024.e29954
PMID:	38694117

System Pharmacological Approach to Investigate and Validate Multitargeted and Therapeutic Effect of Furocoumarins of Apium graveolens L. for Treatment of Kidney Disease

Yasheshwar, Gaurav, Ekkbal R, Gupta P, Gyawali R

Adv Pharmacol Pharm Sci

17-Apr-2024

PMCID:	PMC11042912
doi:	10.1155/2024/5543561
PMID:	38660689

Petroselinum crispum L., essential oil as promising source of bioactive compounds, antioxidant, antimicrobial activities: In vitro and in silico predictions

Nouioura G, El fadili M, El Hachlafi N, Abuelizz HA, Elidrissi AE, Ferioun M, Soulo N, Er-rahmani S, Lyoussi B, Derwich E

Heliyon

16-Apr-2024

PMCID:	PMC11040043
doi:	10.1016/j.heliyon.2024.e29520
PMID:	38660278

Anthriscus sylvestris—Noxious Weed or Sustainable Source of Bioactive Lignans?

Berežni S, Mimica-Dukić N, Domina G, Raimondo FM, Orčić D

Plants (Basel)

12-Apr-2024

PMCID:	PMC11053937
doi:	10.3390/plants13081087
PMID:	38674496

Effect of Dl-3-n-Butylphthalide on olfaction in rotenone-induced Parkinson’s rats

Wang J, Li H, Wang C, Li D, Zhang Y, Shen M, Xu X, Wu T

Front Neurol

08-Apr-2024

PMCID:	PMC11057415
doi:	10.3389/fneur.2024.1367973
PMID:	38685946

Molecular mapping of the broad bean wilt virus 2 resistance locus bwvr in Capsicum annuum using BSR-seq

Kim JM, Lee JH, Park SR, Kwon JK, Ro NY, Kang BC

Theor Appl Genet

08-Apr-2024

PMCID:	PMC11001752
doi:	10.1007/s00122-024-04603-2
PMID:	38589740

Optimization of preparation conditions for Salsola laricifolia protoplasts using response surface methodology and artificial neural network modeling

Guo H, Xi Y, Guzailinuer K, Wen Z

Plant Methods

07-Apr-2024

PMCID:	PMC11000288
doi:	10.1186/s13007-024-01180-9
PMID:	38584286

Engineering Plant Cell Fates and Functions for Agriculture and Industry

Tansley C, Patron NJ, Guiziou S

ACS Synth Biol

04-Apr-2024

PMCID:	PMC11036505
doi:	10.1021/acssynbio.4c00047
PMID:	38573786

Genetic variation and structure of endemic and endangered wild celery (Kelussia odoratissima Mozaff.) quantified using novel microsatellite markers developed by next-generation sequencing

Mahdavikia F, Ebadi MT, Shojaeiyan A, Ayyari M, Falahati-Anbaran M

Front Plant Sci

04-Apr-2024

PMCID:	PMC11024376
doi:	10.3389/fpls.2024.1301936

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives
Pentylbenzene	10864	Click to see	148.24	unknown	https://doi.org/10.1080/10412905.1990.9697808
> Benzenoids / Phenols / Methoxyphenols
2-Deuterio-6-methoxyphenol	10725347	Click to see COC1=CC=CC=C1O	125.14	unknown	via CMAUP database
Chavibetol	596375	Click to see	164.20	unknown	https://doi.org/10.1021/JF991383R
Guaiacol	460	Click to see	124.14	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700822 https://doi.org/10.1007/BF01959202
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristelaidic acid	5312402	Click to see	226.35	unknown	via CMAUP database
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1016/0031-9422(88)83101-7
Petroselinic Acid	5281125	Click to see	282.50	unknown	https://doi.org/10.1016/0031-9422(88)83101-7
trans-6-Octadecenoic acid	5282754	Click to see	282.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Pentanoic Acid	7991	Click to see	102.13	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3R,3aS)-3-[(3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3a,4,5,6-tetrahydro-3H-2-benzofuran-1-one	11280198	Click to see	372.40	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
3-[(3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3H-2-benzofuran-1-one	11405977	Click to see	368.40	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
3-[(3S)-3-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-3H-2-benzofuran-1-one	21576557	Click to see	500.50	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1990.9697808
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(E,R)-Heptadeca-1,9-dien-4,6-diyne-3-ol	56935896	Click to see	244.37	unknown	https://doi.org/10.1080/10826079508013961
Panaxynol	5281149	Click to see	244.37	unknown	https://doi.org/10.1080/10826079508013961
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
(2-Octadeca-9,12-dienoyloxy-3-octadec-9-enoyloxypropyl) octadec-9-enoate	54344355	Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCCCCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC	883.40	unknown	https://doi.org/10.1021/JF991383R
Triglyceride OLO,sn	10854964	Click to see	883.40	unknown	https://doi.org/10.1021/JF991383R
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6-Dimethyl-2,4,6-octatriene	5368821	Click to see CC=C(C)C=CC=C(C)C	136.23	unknown	https://doi.org/10.1007/BF01959202
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808 https://doi.org/10.1007/BF01959202
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1990.9697808 https://doi.org/10.1080/10412905.1997.9700822
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1007/BF01959202 https://doi.org/10.1080/10412905.1990.9697808
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1080/10412905.1990.9697808
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1990.9697808
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808 https://doi.org/10.1007/BF01959202
2,6,6-Trimethyl-3,3-bis(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)bicyclo[3.1.1]hept-1-ene	53472035	Click to see CC1=C2CC(C2(C)C)CC1C3(CC4CC(=C3C)C4(C)C)C5CC6CC(=C5C)C6(C)C	404.70	unknown	https://doi.org/10.1007/BF01959202
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808 https://doi.org/10.1007/BF01959202 https://doi.org/10.1080/10412905.1997.9700822
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene	440917	Click to see	136.23	unknown	https://doi.org/10.1080/01635589309514238
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1080/10412905.1990.9697808
Carvone, (+-)-	7439	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1990.9697808
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1080/10412905.1990.9697808
Isopulegone	34645	Click to see CC1CCC(C(=O)C1)C(=C)C	152.23	unknown	https://doi.org/10.1080/10412905.1990.9697808
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700822 https://doi.org/10.1016/0031-9422(88)83101-7 https://doi.org/10.1080/10412905.1990.9697808 https://doi.org/10.1007/BF01959202
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2R,3R,4R,5R,6R)-2-(hydroxymethyl)-6-[2-[(1R,4R,6S,7S,10R)-10-hydroxy-7-methyl-12-oxatricyclo[5.3.2.01,6]dodecan-4-yl]propan-2-yloxy]oxane-3,4,5-triol	641743	Click to see	416.50	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-[(1R,4R,6R,7S,10R)-10-hydroxy-7-methyl-12-oxatricyclo[5.3.2.01,6]dodecan-4-yl]propan-2-yloxy]oxane-3,4,5-triol	11373407	Click to see CC12CCC(C3(C1CC(CC3)C(C)(C)OC4C(C(C(C(O4)CO)O)O)O)CO2)O	416.50	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-[(1R,4R,6R,7S,10S)-10-hydroxy-7-methyl-12-oxatricyclo[5.3.2.01,6]dodecan-4-yl]propan-2-yloxy]oxane-3,4,5-triol	101265703	Click to see	416.50	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)-	6604672	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1990.9697808
alpha-IONONE	5282108	Click to see CC1=CCCC(C1C=CC(=O)C)(C)C	192.30	unknown	https://doi.org/10.1080/10412905.1990.9697808
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700822 https://doi.org/10.1080/10412905.1990.9697808
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1990.9697808
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700822
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
Cedrol	65575	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1990.9697808
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
beta-Chamigrene	442353	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700822
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700822
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(2R,4aR,5R,6S,8aS)-5,6-dihydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101265701	Click to see	416.50	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
(2S,3R,4S,5S,6R)-2-[2-[(2R,4aR,5S,8aS)-5-hydroxy-4a-(hydroxymethyl)-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101265702	Click to see	416.50	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
(2S,3R,4S,5S,6R)-2-[2-[(2R,4aR,5S,8R,8aR)-5,8-dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101265700	Click to see	418.50	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
(3S,4aS,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene	12309813	Click to see	204.35	unknown	https://doi.org/10.1021/JF991383R
7-epi-alpha-Selinene	10123	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1990.9697808
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene	519361	Click to see	204.35	unknown	https://doi.org/10.1021/JF991383R
alpha-Selinene	10856614	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1990.9697808
Beta-Selinene	442393	Click to see	204.35	unknown	https://doi.org/10.1021/JF991383R https://doi.org/10.1080/10412905.1990.9697808 https://doi.org/10.1080/10412905.1997.9700822 https://doi.org/10.1007/BF01959202
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,2S,4aS,6S,6aR,6aS,6bR,8aR,10R,11S,12aS,14bR)-6,10-dihydroxy-1,2,4a,6a,6b,9,9,12a-octamethyl-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-3,13-dione	44478676	Click to see	648.80	unknown	https://doi.org/10.1021/NP900117V
(4aS,6S,6aR,6aS,6bR,8aR,9S,10S,12aS,14bR)-6,10-dihydroxy-2,2,4a,6a,6b,9,12a-heptamethyl-9-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydropicene-3,13-dione	44478941	Click to see	648.80	unknown	https://doi.org/10.1021/NP900117V
24-(beta-D-Glucopyranosyloxy)-3beta,15alpha-dihydroxyurs-12-ene-11,21-dione	44478940	Click to see CC1C(C(=O)CC2(C1C3=CC(=O)C4C5(CCC(C(C5CCC4(C3(C(C2)O)C)C)(C)COC6C(C(C(C(O6)CO)O)O)O)O)C)C)C	648.80	unknown	https://doi.org/10.1021/NP900117V
6,10-dihydroxy-1,2,4a,6a,6b,9,12a-heptamethyl-9-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-3,13-dione	75033338	Click to see CC1C(C(=O)CC2(C1C3=CC(=O)C4C5(CCC(C(C5CCC4(C3(C(C2)O)C)C)(C)COC6C(C(C(C(O6)CO)O)O)O)O)C)C)C	648.80	unknown	https://doi.org/10.1021/NP900117V
6,10-dihydroxy-1,2,4a,6a,6b,9,9,12a-octamethyl-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-3,13-dione	75033264	Click to see CC1C(C(=O)CC2(C1C3=CC(=O)C4C(C3(C(C2)O)C)(CCC5C4(CC(C(C5(C)C)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)C	648.80	unknown	https://doi.org/10.1021/NP900117V
6,10-Dihydroxy-2,2,4a,6a,6b,9,12a-heptamethyl-9-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydropicene-3,13-dione	75033339	Click to see	648.80	unknown	https://doi.org/10.1021/NP900117V
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,4R,6R,7S,10S)-10-hydroxy-7-methyl-4-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-12-oxatricyclo[5.3.2.01,6]dodecan-11-one	101265704	Click to see CC12CCC(C3(C1CC(CC3)C(C)(C)OC4C(C(C(C(O4)CO)O)O)O)C(=O)O2)O	430.50	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) octadeca-9,12-dienoate	73746300	Click to see	689.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
[(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] (9Z,12Z)-octadeca-9,12-dienoate	21159076	Click to see	689.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] octadeca-9,12-dienoate	75954378	Click to see	675.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
18:2 Stigmasteryl ester	52920463	Click to see	675.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
Amyrin palmitate	13915598	Click to see	665.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
Beta-Amyrin Palmitate	13915599	Click to see	665.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
Squalene	638072	Click to see	410.70	unknown	https://doi.org/10.1016/0031-9422(92)83445-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[17-(5,6-dimethylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] octadeca-9,12-dienoate	77610361	Click to see	663.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
18:2 Campesteryl ester	69169003	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(C)C(C)C)C)C	663.10	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
2-Deoxybrassinolide	14153905	Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CCC(C4)O)C)C)O)O	464.70	unknown	https://doi.org/10.1016/0031-9422(95)00363-C
7-Oxotyphasterol	14153907	Click to see	464.70	unknown	https://doi.org/10.1016/0031-9422(95)00363-C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)89523-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
2-Methylpropanoate	165337	Click to see CC(C)C(=O)[O-]	87.10	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Hydron;propanedioate	23511544	Click to see [H+].[H+].C(C(=O)[O-])C(=O)[O-]	104.06	unknown	via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate	3698251	Click to see C(C(=O)[O-])[OH2+]	76.05	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline ascorbate	122173941	Click to see	279.29	unknown	https://doi.org/10.1021/NP50039A029
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3S,4S,5R,6R)-6-[(2R,3S,4S,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-2,3,4,5-tetrol	22524649	Click to see C(C1C(C(C(C(O1)O)O)O)OC2C(C(C(C(O2)O)O)O)O)O	328.27	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-[4-(1,3-dihydroxypropan-2-yl)-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11972388	Click to see	360.36	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
Leonuriside	14237626	Click to see	332.30	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
Syringin	5316860	Click to see	372.40	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8
> Organoheterocyclic compounds / Benzodioxoles
Apiole	10659	Click to see	222.24	unknown	https://doi.org/10.1007/BF01959202
Myristicin	4276	Click to see	192.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(3aS,6S,7aS)-6-methyl-3-methylidene-6-(4-oxopentyl)-3a,4,7,7a-tetrahydro-1-benzofuran-2,5-dione	133568303	Click to see	264.32	unknown	https://doi.org/10.1021/NP900117V
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Butylphthalide	61361	Click to see	190.24	unknown	https://doi.org/10.1248/CPB.11.1317 https://doi.org/10.1080/01635589309514238 https://doi.org/10.1080/10412905.1990.9697808 https://doi.org/10.1016/0031-9422(88)83101-7 https://doi.org/10.1080/10412905.1997.9700822
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
2-[[(2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-yl]oxy]ethyl-trimethylazanium	163190340	Click to see	262.28	unknown	https://doi.org/10.1021/NP50039A029
> 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/10.1078/0944-7113-00131
> Organoheterocyclic compounds / Isobenzofurans
(3R,6S,7S)-3-Butyl-6,7-dihydroxy-4,5,6,7-tetrahydroisobenzofuran-1(3H)-one	24121290	Click to see CCCCC1C2=C(C(C(CC2)O)O)C(=O)O1	226.27	unknown	https://doi.org/10.1021/JF001052A https://doi.org/10.1078/0944-7113-00131
(3S,6R,7R)-3-butyl-6,7-dihydroxy-4,5,6,7-tetrahydro-3H-2-benzofuran-1-one	15138553	Click to see	226.27	unknown	https://doi.org/10.1021/JF001052A
(3Z)-3-butylidene-3a,4,5,6-tetrahydro-2-benzofuran-1-one	91747285	Click to see CCCC=C1C2CCCC=C2C(=O)O1	192.25	unknown	https://doi.org/10.1016/0031-9422(88)83101-7
(R)-3-Butyl-4,5-dihydroisobenzofuran-1(3H)-one	54753664	Click to see	192.25	unknown	https://doi.org/10.1007/BF02059608 https://doi.org/10.1021/JF991383R
3-butyl-4,5,6,7-tetrahydro-3H-2-benzofuran-1-one	5315566	Click to see	194.27	unknown	via CMAUP database
3-N-Butyl-4,5-dihydrophthalide	173843	Click to see CCCCC1C2=C(C=CCC2)C(=O)O1	192.25	unknown	https://doi.org/10.1021/JF991383R https://doi.org/10.1007/BF02059608
3alpha-Butyl-4,5,6,7-tetrahydro-6alpha,7beta-dihydroxy-1(3H)-isobenzofuranone	101982247	Click to see	226.27	unknown	https://doi.org/10.1021/JF001052A
Cnidilide	160710	Click to see	194.27	unknown	https://doi.org/10.1248/CPB.11.1317
Ligustilide	5319022	Click to see	190.24	unknown	https://doi.org/10.1248/CPB.11.1317 https://doi.org/10.1080/10412905.1990.9697808
Neocnidilide	3083857	Click to see	194.27	unknown	https://doi.org/10.1021/JF001052A
Sedanolide	5018391	Click to see CCCCC1C2CCCC=C2C(=O)O1	194.27	unknown	https://doi.org/10.1248/CPB.11.1317 https://doi.org/10.1080/01635589309514238 https://doi.org/10.1021/JF001052A https://doi.org/10.1078/0944-7113-00131
Senkyunolide N	15138552	Click to see CCCCC1C2=C(C(C(CC2)O)O)C(=O)O1	226.27	unknown	https://doi.org/10.1021/JF001052A https://doi.org/10.1078/0944-7113-00131
> Organoheterocyclic compounds / Isocoumarans / Isobenzofuranones
1(3H)-Isobenzofuranone, 3-butylidene-	62368	Click to see CCCC=C1C2=CC=CC=C2C(=O)O1	188.22	unknown	https://doi.org/10.1248/CPB.11.1317
Butylidenephthalide	5352899	Click to see	188.22	unknown	https://doi.org/10.1248/CPB.11.1317
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(4S,4aS,7E,11aR)-7-methyl-11-methylidene-4-(4-methylpent-3-enyl)-1,4,4a,5,6,9,10,11a-octahydrocyclonona[c]pyran-3-one	21626585	Click to see CC1=CCCC(=C)C2COC(=O)C(C2CC1)CCC=C(C)C	302.50	unknown	via CMAUP database
(4S,4aS,7E,11aR)-7-methyl-11-methylidene-4-pent-4-enyl-1,4,4a,5,6,9,10,11a-octahydrocyclonona[c]pyran-3-one	9994307	Click to see CC1=CCCC(=C)C2COC(=O)C(C2CC1)CCCC=C	288.40	unknown	via CMAUP database
(4S,4aS,7E,11aR)-7-methyl-11-methylidene-4-penta-3,4-dienyl-1,4,4a,5,6,9,10,11a-octahydrocyclonona[c]pyran-3-one	10266030	Click to see	286.40	unknown	via CMAUP database
CID 10518481	10518481	Click to see CC12CCC3C(COC(=O)C3CCC=C=C)C(=C)CCC1O2	302.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Graveoline	353825	Click to see	279.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-Phenylprop-2-Enal	307	Click to see	132.16	unknown	https://doi.org/10.1080/10412905.1990.9697808
Cinnamaldehyde	637511	Click to see	132.16	unknown	https://doi.org/10.1080/10412905.1990.9697808
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol	10228	Click to see	244.28	unknown	https://doi.org/10.1007/BF00993733
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	https://doi.org/10.1007/BF00993733
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
(2R)-2-prop-1-en-2-yl-9-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrofuro[3,2-g]chromen-7-one	162904505	Click to see CC(=C)C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O	406.40	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
(R)-Apiumetin glucoside	14033997	Click to see	406.40	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
5-Methoxy-8-beta-D-glucopyranosyloxypsoralen	14034002	Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O	394.30	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
7H-Furo[3,2-g][1]benzopyran-7-one, 9-(I(2)-D-glucopyranosyloxy)-2,3-dihydro-2-(1-methylethenyl)-, (R)-	162904504	Click to see	406.40	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
9-Hydroxy-4-methoxypsoralen 9-glucoside	14034001	Click to see	394.30	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(-)-Columbianetin	442104	Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O	246.26	unknown	https://doi.org/10.1016/0031-9422(95)00125-Q
Isopsoralen	10658	Click to see	186.16	unknown	https://doi.org/10.1016/0031-9422(95)00125-Q
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-2,3-Dihydro-9-hydroxy-2[1-(6-sinapinoyl)beta-D-glucosyloxy-1-methylethyl]-7H-furo[3,2-g][1]benzopyran-7-one	157009820	Click to see	630.60	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(2R)-9-hydroxy-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yloxy]oxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	162885910	Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C(=C5)OC)O)OC)O)O)O	630.60	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
[3,4,5-Trihydroxy-6-[2-(9-hydroxy-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl)propan-2-yloxy]oxan-2-yl]methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	162885909	Click to see	630.60	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
7H-Furo(3,2-g)(1)benzopyran-7-one, 2-(1-(beta-D-glucopyranosyloxy)-1-methylethyl)-2,3-dihydro-4-hydroxy-	5488592	Click to see	424.40	unknown	via CMAUP database
Celereoin	5315768	Click to see	262.26	unknown	https://doi.org/10.1016/S0031-9422(00)98508-X
Celereoside	73989751	Click to see	424.40	unknown	https://doi.org/10.1016/0031-9422(88)80298-X
Nodakenin	73191	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O	408.40	unknown	https://doi.org/10.1016/0031-9422(88)80298-X https://doi.org/10.1016/S0031-9422(00)98508-X
Psoralen	6199	Click to see	186.16	unknown	https://doi.org/10.1016/0031-9422(83)80173-3 https://doi.org/10.1016/0278-6915(83)90231-4 https://doi.org/10.1016/S0031-9422(98)00650-5 https://doi.org/10.1021/JF00029A027 https://doi.org/10.1002/HLCA.19970800507 https://doi.org/10.1016/0031-9422(95)00125-Q https://doi.org/10.1093/JAOAC/84.4.1135 https://doi.org/10.1271/BBB1961.54.2141
Trioxsalen	5585	Click to see CC1=CC(=O)OC2=C1C=C3C=C(OC3=C2C)C	228.24	unknown	https://doi.org/10.1271/BBB1961.54.2141
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	https://doi.org/10.1016/0031-9422(83)80173-3 https://doi.org/10.1016/0278-6915(83)90231-4 https://doi.org/10.1080/10826079508013961 https://doi.org/10.1016/S0031-9422(98)00650-5 https://doi.org/10.1021/JF00029A027 https://doi.org/10.1016/S0031-9422(00)81503-4 https://doi.org/10.1002/HLCA.19970800507 https://doi.org/10.1093/JAOAC/84.4.1135 https://doi.org/10.1271/BBB1961.54.2141 https://doi.org/10.1021/JF00021A006
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
9-Methoxy-5-(3-methylbut-2-enoxy)furo[3,2-g]chromen-7-one	53398727	Click to see CC(=CCOC1=CC(=O)OC2=C1C=C3C=COC3=C2OC)C	300.30	unknown	via CMAUP database
Isopimpinellin	68079	Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC	246.21	unknown	https://doi.org/10.1016/0031-9422(83)80173-3 https://doi.org/10.1016/0278-6915(83)90231-4 https://doi.org/10.1016/S0031-9422(98)00650-5 https://doi.org/10.1002/HLCA.19970800507 https://doi.org/10.1271/BBB1961.54.2141
Methoxsalen	4114	Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2	216.19	unknown	https://doi.org/10.1016/0031-9422(83)80173-3 https://doi.org/10.1016/0278-6915(83)90231-4 https://doi.org/10.1016/S0031-9422(98)00650-5 https://doi.org/10.1021/JF00029A027 https://doi.org/10.1002/HLCA.19970800507 https://doi.org/10.1016/0031-9422(95)00125-Q https://doi.org/10.1093/JAOAC/84.4.1135 https://doi.org/10.1271/BBB1961.54.2141
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Celerin	156431	Click to see CC(C)(C=C)C1=CC(=C(C2=C1C=CC(=O)O2)O)OC	260.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1007/BF00993733
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1016/S0031-9422(98)00650-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin	68229	Click to see	228.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
5,7-Dihydroxy-8-[2-hydroxy-5-(7-methoxy-4-oxochromen-2-yl)phenyl]-2-(4-hydroxyphenyl)chromen-4-one	5321275	Click to see COC1=CC2=C(C=C1)C(=O)C=C(O2)C3=CC(=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O	536.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R)-4-hydroxy-4-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]oxychromen-4-one	11968524	Click to see	580.50	unknown	via CMAUP database
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1021/NP900117V
Apigenin-7-olate	25200950	Click to see	269.23	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1021/NP900117V
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1021/NP900117V
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
3-oxo-3-[[(3S,4S,6S)-3,4,5-trihydroxy-6-[7-hydroxy-3-[(2S,5R)-3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-5-yl]oxyoxan-2-yl]methoxy]propanoic acid	57003757	Click to see	859.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Petunidin 3-sambubioside	44256968	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(CO5)O)O)O)O)O	611.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	26339717	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP900117V
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside	5353915	Click to see	448.40	unknown	https://doi.org/10.1021/NP900117V
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)84026-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	46882563	Click to see	566.50	unknown	https://doi.org/10.1021/NP900117V
[(3S,4R,5S)-5-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	46882562	Click to see	756.70	unknown	https://doi.org/10.1021/NP900117V
[(3S,4R,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	44478943	Click to see	770.70	unknown	https://doi.org/10.1021/NP900117V
[(3S,4R,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	44478942	Click to see	740.70	unknown	https://doi.org/10.1021/NP900117V
[5-[2-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	75224907	Click to see	756.70	unknown	https://doi.org/10.1021/NP900117V
[5-[4,5-Dihydroxy-2-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	75033341	Click to see	770.70	unknown	https://doi.org/10.1021/NP900117V
[5-[4,5-Dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	75033340	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2(COC(C2O)OC3C(C(C(OC3OC4=CC(=C5C(=C4)OC(=CC5=O)C6=CC=C(C=C6)O)O)CO)O)O)O)O	740.70	unknown	https://doi.org/10.1021/NP900117V
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	13093777	Click to see	448.40	unknown	https://doi.org/10.1021/NP900117V
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154496342	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1021/NP900117V
7-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	10031394	Click to see	594.50	unknown	via CMAUP database
7-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one	99118925	Click to see C1C(C(C(O1)OC2C(OC(C(C2O)O)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)(CO)O	564.50	unknown	https://doi.org/10.1021/NP900117V
7-[(2S,3R,4S,5S,6R)-3-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	71718203	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)OC5C(C(CO5)(CO)O)O)O)O	594.50	unknown	https://doi.org/10.1078/0944-7113-00131
7-[(2S,4S,5S)-3-[(2S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one	44257793	Click to see	564.50	unknown	via CMAUP database
7-[3-[(4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one	73755987	Click to see	564.50	unknown	https://doi.org/10.1021/NP900117V
7-[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one	22016216	Click to see C1C(C(C(O1)OC2C(OC(C(C2O)O)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)(CO)O	564.50	unknown	https://doi.org/10.1021/NP900117V
7-O-Beta-D-Glucopyranoside	11294177	Click to see	462.40	unknown	https://doi.org/10.1021/NP900117V
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1021/NP900117V
Apiin	5280746	Click to see	564.50	unknown	https://doi.org/10.1211/JPP.59.6.0016 https://doi.org/10.1021/NP900117V
Apioside	5840046	Click to see	564.50	unknown	https://doi.org/10.1211/JPP.59.6.0016
Chrysoeriol-7-O-beta-D-glucoside	13871877	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1021/NP900117V
CID 12304094	12304094	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1021/NP900117V
Luteolin 7-galactoside	5291488	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP900117V
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP900117V
Npc85473	5385553	Click to see	432.40	unknown	https://doi.org/10.1021/NP900117V
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1021/NP900117V
> Phenylpropanoids and polyketides / Macrolides and analogues / Pectenotoxins and derivatives
14-(2,3-Dihydroxy-4-methyloxan-2-yl)-28-hydroxy-5,7,9,19,29-pentamethyl-18,31-dioxo-13,17,38,39,40,41,42,43-octaoxaoctacyclo[31.4.1.11,35.12,5.120,24.124,27.129,32.012,16]tritetraconta-8,10-diene-35-carbaldehyde	74051868	Click to see CC1CCOC(C1O)(C2CC3C(O2)C=CC(=CC(CC4(CCC(O4)C56CCC(O5)(CC(O6)C7C(=O)CC(O7)(C(C8CCC9(O8)CCCC(O9)C(C(=O)O3)C)O)C)C=O)C)C)C)O	873.00	unknown	https://doi.org/10.1016/S0031-9422(03)00461-8

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Apium graveolens

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