Scientific name	Authority	First published in
Karos carvi	Nieuwl. & Lunell	Amer. Midl. Naturalist 4: 385 (1916)
Ligusticum carvi	(L.) Roth	Tent. Fl. Germ. 1: 124 (1788)
Pimpinella carvi	Jess.	Deut. Excurs.-Fl. : 191 (1879)
Sium carvi	Bernh.	Syst. Verz. Erf. : 173 (1800)
Selinum carvi	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 12: 47 (1904)
Seseli carvi	Spreng.	Syst. Veg., ed. 15 bis [Roemer & Schultes] 6: 414. 1820 [Aug-Dec 1820]
Seseli carum	Scop.	Fl. Carniol. , ed. 2, 1: 215 (1771)
Apium carvi	(L.) Crantz	Stirp. Austr. Fasc. 3: 110 (1767)
Bunium carvi	M.Bieb.	Fl. Taur.-Caucas. 1: 211 (1808)
Carum aromaticum	Salisb.	Prodr. Stirp. Chap. Allerton : 168 (1796)
Carum carvi f. gracile	(Lindl.) H.Wolff	Pflanzenr. IV, 228(90): 148 1927
Carum carvi f. rhodochranthum	A.H.Moore	Rhodora 11: 178. 1909
Carum carvi subsp. rosellum	(Woronow) Vorosch.	Florist. Issl. Razn. Raionakh SSSR : 184 (1985)
Carum carvi f. rubriflorum	H.Wolff	Acta Horti Gothob. 2: 306 1926
Carum decussatum	Gilib.	Fl. Lit. Inch. ii. 37. 1782
Carum gracile	Lindl.	Ill. Bot. Himal. Mts. : 232 (1835)
Carum officinale	Gray	Nat. Arr. Brit. Pl. 2: 515 (1821 publ. 1822)
Carum rosellum	Woronow	Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast. 1: 218 (1933)
Carum velenovskyi	Rohlena	Sitzungsber. Königl. Böhm. Ges. Wiss., Math.-Naturwiss. Cl. 17: 34 (1903)
Carvi careum	Bubani	Fl. Pyren. 2: 352 (1899)
Falcaria carvifolia	C.A.Mey.	Beitr. Pflanzenk. Russ. Reiches 1: 14 (1844)
Foeniculum carvi	Link	Enum. Hort. Berol. Alt. 1: 284 (1821)
Carum carvi var. gracile	(Lindl.) H.Wolff

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	caraway
English	caraway plant
English	wild caraway
Spanish	alcarabaca
Spanish	alcarahueya
Spanish	alcaravea
Spanish	alcaravia
Spanish	alcarovea
Spanish	alcarravea
Spanish	alcorobea
Spanish	caros
Spanish	carvi
Spanish	carvia
Spanish	carvía
Spanish	comino de prado
Spanish	comino de prados
Spanish	hinojo de prado
ace	jeura keusani
Afrikaans	karwy
Arabic	كراوية
Arabic	كروياء
Arabic	كوريا
Arabic	كمون أرمني
Azerbaijani	adi zirə
azb	عادی زیره
bar	kimme
Belarusian	Кмен звычайны
Bulgarian	ким
bjn	jintan
Bengali	ক্যারাম কার্ভি
Bengali	কারোয়া
Tibetan	གོ་སྙོད།
Bosnian	kim
Catalan	càrvit
Catalan	comí de prat
Catalan	matafaluga borda
Catalan	alcaravia
Czech	kmín kořenný
Czech	kmín luční
Welsh	carwy
Danish	kommen
German	wiesen-kümmel
German	wiesenkümmel
German	echter kümmel
dv	ފަރިހި ދަމުއި
Greek	αγριοκύμινο
Greek	Κιουμέλ
Esperanto	karvio
Estonian	harilik köömen
Basque	txarpoil
Persian	زیره سیاه
Persian	زیرهٔ سیاه
Persian	زیره
Finnish	maustekumina
Finnish	kumina
French	carvi
French	caraway
French	cumin des prés
French	graine de carvi
frr	bruadkrüüs
frr	seeskrüüs
frr	köömen
Irish	cearbhas
Galician	carvea
Swiss German	chümmi
Hebrew	קימל
Hebrew	כרוויה תרבותית
Hindi	शाहजीरा
Croatian	kim
Upper Sorbian	kimjelčka
Hungarian	hasznos kömény
Hungarian	keménymag
Hungarian	kerti kömény
Hungarian	kömény
Hungarian	kömény mag
Hungarian	köménymag
Hungarian	konyhakömény
Hungarian	fűszerkömény
Armenian	քիմիոն
Armenian	քիմոն սովորական
hyw	Հայկական Չաման
Indonesian	jintan
Icelandic	kúmen
Italian	carvi
Italian	cumino dei prati
Italian	cumino tedesco
Japanese	ヒメウイキョウ
Japanese	姫茴香
Japanese	キャラウェイ
jv	caraway
Georgian	ძირა
Kabyle	issamen
Korean	캐러웨이
ku	jaj
la	carvi
la	careum
lb	kümmel
lb	kimmel
Lithuanian	kmynai
Lithuanian	kmynas
Lithuanian	paprastasis kmynas
Latvian	parastā ķimene
Latvian	pļavas ķimene
mad	jhinten
Macedonian	ким
Malayalam	caraway
Malayalam	കരിം ജീരകം
Malayalam	കരിഞ്ചീരകം
Marathi	शहाजिरे
Malay	jintan
Burmese	ကရဝေး
Norwegian Bokmål	kummen
Norwegian Bokmål	kummin
Norwegian Bokmål	karve
Dutch	karwij
Dutch	kummel
Dutch	echte karwij
Dutch	karwijzaad
Norwegian Nynorsk	karve
Polish	kminek zwyczajny
Pashto	زيره
Portuguese	alcarávia
Portuguese	alcaravia
Romanian	chimen
Russian	Тмин обыкновенный
Yakutian	Анньыыс
sat	ᱡᱤᱨᱟ. ᱫᱟᱨᱮ
sat	ᱡᱤᱨᱟ.
sco	carvie
Samogitian	kvīns
Serbo-Croatian	kim
Slovak	kmín
Slovak	rasca
Slovak	rasca lúčna
Slovenian	navadna kumina
Slovenian	kumina
Albanian	qimnoni
Serbian	Ким
Swedish	brödkummin
Swedish	kummin
Telugu	కరం కరవే
tg	Карвиё
Thai	เทียนตากบ
Turkish	karaman kimyonu, frenk kimyonu, keraviye, keraviya
tt	Ак әнис
Ukrainian	Кмин звичайний
vec	kumo
Chinese	细葛缕子
Chinese	葛缕子
Chinese	葛缕子（黄蒿、藏茴香、茴香）
Chinese	藏茴香
Chinese	青海防风
Chinese	葛縷子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia

Antarctica click to expand
- Subantarctic Islands
  - South Georgia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Kamchatka
  - Khabarovsk
  - Kuril Islands
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Iraq
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - West Himalaya

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Iceland
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Eastern Canada
  - Labrador
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Minnesota
  - Missouri
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - District Of Columbia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - Virginia
- Southwestern U.S.A.
  - Utah
- Subarctic America
  - Greenland
  - Nunavut
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000588460
UNII	5TDF7P5L1D
Canadensys	2551
USDA Plants	CACA19
Tropicos	1700044
INPN	89250
Flora of Italy	3594
KEW	urn:lsid:ipni.org:names:839677-1
The Plant List	kew-2701499
PFAF	Carum carvi
Open Tree Of Life	498463
Observations.org	2419
NCBI Taxonomy	48032
NBN Atlas	NBNSYS0000003679
Nature Serve	2.147735
IPNI	839677-1
iNaturalist	123719
iNaturalist	160162
GBIF	3034714
Freebase	/m/017dpx
WisFlora	3032
EPPO	CRYCA
EOL	581712
Elurikkus	3489
USDA GRIN	9245
Wikipedia	Caraway
CMAUP	NPO12620
Plantarium	9207

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

Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco

Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M

BMC Complement Med Ther

15-Apr-2024

PMCID:	PMC11017650
doi:	10.1186/s12906-024-04468-4
PMID:	38622669

Cross-cultural ethnobotany of the Baltis and Shinas in the Kharmang district, Trans-Himalaya India-Pakistan border

Hussain B, Abbas Z, Alam J, Harun N, Khan SM, Ahmad Z, Han H, Yoo S, Raposo A

Heliyon

27-Mar-2024

PMCID:	PMC10998220
doi:	10.1016/j.heliyon.2024.e28613
PMID:	38586350

The effect of caraway oil-loaded bio-nanoemulsions on the growth and performance of barnyard grass and maize

Rys M, Miastkowska M, Łętocha A, Wajs-Bonikowska A, Lorenzo P, Synowiec A

Sci Rep

21-Feb-2024

PMCID:	PMC10881981
doi:	10.1038/s41598-024-54721-6
PMID:	38383733

Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species

Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E

Antibiotics (Basel)

07-Feb-2024

PMCID:	PMC10885947
doi:	10.3390/antibiotics13020163
PMID:	38391549

Plant Monoterpenes and Essential Oils as Potential Anti-Ageing Agents: Insights from Preclinical Data

Zuzarte M, Sousa C, Alves-Silva J, Salgueiro L

Biomedicines

04-Feb-2024

PMCID:	PMC10886757
doi:	10.3390/biomedicines12020365
PMID:	38397967

Nutraceuticals and Pain Disorders of the Gut–Brain Interaction in Infants and Children: A Narrative Review and Practical Insights

Salvatore S, Carlino M, Sestito S, Concolino D, Agosti M, Pensabene L

Nutrients

25-Jan-2024

PMCID:	PMC10856962
doi:	10.3390/nu16030349
PMID:	38337634

Exploring the Therapeutic Potential of Natural Products in Polycystic Ovarian Syndrome (PCOS): A Mini-Review of Lipid Profile, Blood Glucose, and Ovarian Histological Improvements

Wahid S, Ramli MD, Fazleen NE, Naim RM, Mokhtar MH

Life (Basel)

19-Jan-2024

PMCID:	PMC10817691
doi:	10.3390/life14010150
PMID:	38276279

Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy

Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A

Plants (Basel)

22-Dec-2023

PMCID:	PMC10780445
doi:	10.3390/plants13010043
PMID:	38202351

Do Poisonous Plants in Pastures Communicate Their Toxicity? Meta-Study and Evaluation of Poisoning Cases in Central Europe

Aboling S

Animals (Basel)

08-Dec-2023

PMCID:	PMC10740430
doi:	10.3390/ani13243795
PMID:	38136831

Floristic–Vegetational Features of Geranium argenteum, an Alpine–Apennine Species at Its Limit of Distribution in the Apennines

Ballelli S, Tesei G, Pennesi R, Allegrezza M

Life (Basel)

28-Nov-2023

PMCID:	PMC10744573
doi:	10.3390/life13122273
PMID:	38137874

Synecology of Lagoecia cuminoides L. in Italy and evaluation of functional compounds presence in its water or hydroalcoholic extracts

Perrino EV, Mahmoud ZN, Valerio F, Tomaselli V, Wagensommer RP, Trani A

Sci Rep

27-Nov-2023

PMCID:	PMC10684886
doi:	10.1038/s41598-023-48065-w
PMID:	38017138

Antioxidant Activity of Medicinal Herbs and Spices from Plants of the Lamiaceae, Apiaceae and Asteraceae Families: Chemometric Interpretation of the Data

Ulewicz-Magulska B, Wesolowski M

Antioxidants (Basel)

24-Nov-2023

PMCID:	PMC10740862
doi:	10.3390/antiox12122039
PMID:	38136159

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Essential Oils and Their Combination with Lactic Acid Bacteria and Bacteriocins to Improve the Safety and Shelf Life of Foods: A Review

Bukvicki D, D’Alessandro M, Rossi S, Siroli L, Gottardi D, Braschi G, Patrignani F, Lanciotti R

Foods

01-Sep-2023

PMCID:	PMC10486891
doi:	10.3390/foods12173288
PMID:	37685221

Mango anthracnose disease: the current situation and direction for future research

Dofuor AK, Quartey NK, Osabutey AF, Antwi-Agyakwa AK, Asante K, Boateng BO, Ablormeti FK, Lutuf H, Osei-Owusu J, Osei JH, Ekloh W, Loh SK, Honger JO, Aidoo OF, Ninsin KD

Front Microbiol

24-Aug-2023

PMCID:	PMC10484599
doi:	10.3389/fmicb.2023.1168203
PMID:	37692388

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2-Methylbenzaldehyde	10722	Click to see CC1=CC=CC=C1C=O	120.15	unknown	https://doi.org/10.1021/JF00047A021
2,3,4-Trimethylbenzaldehyde	2752597	Click to see CC1=C(C(=C(C=C1)C=O)C)C	148.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
4-Methylbenzaldehyde	7725	Click to see CC1=CC=C(C=C1)C=O	120.15	unknown	https://doi.org/10.1021/JF00047A021
> Benzenoids / Benzene and substituted derivatives / Benzylethers
(2R)-2-Methoxy-2-(4-hydroxyphenyl)ethanol	636818	Click to see COC(CO)C1=CC=C(C=C1)O	168.19	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(5-Formyl-2,4,4-trimethylcyclohexa-2,5-dien-1-yl) 4-acetyloxy-3-methylbut-2-enoate	163001686	Click to see CC1=CC(C(=CC1OC(=O)C=C(C)COC(=O)C)C=O)(C)C	306.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
(5-Formyl-2,6,6-trimethylcyclohexa-2,4-dien-1-yl) 4-acetyloxy-3-methylbut-2-enoate	163034838	Click to see CC1=CC=C(C(C1OC(=O)C=C(C)COC(=O)C)(C)C)C=O	306.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
[(1R)-5-formyl-2,4,4-trimethylcyclohexa-2,5-dien-1-yl] (E)-4-acetyloxy-3-methylbut-2-enoate	163001688	Click to see CC1=CC(C(=CC1OC(=O)C=C(C)COC(=O)C)C=O)(C)C	306.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
[(1R)-5-formyl-2,6,6-trimethylcyclohexa-2,4-dien-1-yl] (E)-4-acetyloxy-3-methylbut-2-enoate	163034839	Click to see CC1=CC=C(C(C1OC(=O)C=C(C)COC(=O)C)(C)C)C=O	306.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(E)-4-acetyloxy-3-methylbut-2-enoic acid	11768832	Click to see CC(=CC(=O)O)COC(=O)C	158.15	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
4-Acetyloxy-3-methylbut-2-enoic acid	53721650	Click to see CC(=CC(=O)O)COC(=O)C	158.15	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Octadec-6-enoic acid	11634	Click to see CCCCCCCCCCCC=CCCCCC(=O)O	282.50	unknown	https://doi.org/10.1016/J.INDCROP.2012.04.060
Petroselaidic acid	5282754	Click to see CCCCCCCCCCCC=CCCCCC(=O)O	282.50	unknown	https://doi.org/10.1016/J.INDCROP.2012.04.060
Petroselinic acid	5281125	Click to see CCCCCCCCCCCC=CCCCCC(=O)O	282.50	unknown	https://doi.org/10.1016/J.INDCROP.2012.04.060
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(3-methylbutoxy)oxane-3,4,5-triol	10848285	Click to see CC(C)CCOC1C(C(C(C(O1)CO)O)O)O	250.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/JF00047A021
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/JF00047A021
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1021/JF00047A021
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1021/JF00047A021
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/JF00047A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(+)-beta-Fenchene	12309841	Click to see CC1(CC2CC1CC2=C)C	136.23	unknown	via CMAUP database
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1021/JF00047A021
alpha-THUJENE, (+/-)-	12444324	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	via CMAUP database
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/JF00047A021
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol	330573	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1021/JF00047A021
(+)-alpha-Phellandrene	443160	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	via CMAUP database
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(1R,2R,4R,8S)-p-Menthane-1,2,8,9-tetrol	10889000	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1R,2R,4S)-4-(1-Hydroxy-1-methylethyl)-1-methyl-1,2-cyclohexanediol	21593213	Click to see CC1(CCC(CC1O)C(C)(C)O)O	188.26	unknown	via CMAUP database
(1R,2S,4R,8R)-p-Menthane-1,2,8,9-tetrol	92467558	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1R,2S,4R,8R)-p-Menthane-2,8,9-triol	21593210	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(1R,2S,4R,8S)-p-Menthane-2,8,9-triol	21593209	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(1R,2S,4R)-4-[(2S)-1,2-dihydroxypropan-2-yl]-1-methylcyclohexane-1,2-diol	15541895	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1R,2S,4S,8R)-p-Menthane-1,2,8,9-tetrol	92467559	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1R,2S,4S,8S)-p-Menthane-1,2,8,9-tetrol	92288760	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1S,2R,4R,8R)-p-Menthane-1,2,8,9-tetrol	10867427	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1S,2R,4R,8R)-p-Menthane-2,8,9-triol	21593208	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(1S,2R,4R,8S)-p-Menthane-2,8,9-triol	21593207	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(1S,2S,4R,8R)-p-Menthane-1,2,9-triol	21593214	Click to see CC(CO)C1CCC(C(C1)O)(C)O	188.26	unknown	via CMAUP database
(1S,2S,4R,8R)-p-Menthane-2,8,9-triol	21593212	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(1S,2S,4R,8S)-p-Menthane-1,2,8,9-tetrol	11074485	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1S,2S,4R,8S)-p-Menthane-2,8,9-triol	21593211	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(1S,2S,4R)-4-[(1R)-1,2-Dihydroxy-1-methylethyl]-1-methyl-1,2-cyclohexanediol	11106463	Click to see CC1(CCC(CC1O)C(C)(CO)O)O	204.26	unknown	via CMAUP database
(1S,2S,4R)-Limonene-1,2-diol	441246	Click to see CC(=C)C1CCC(C(C1)O)(C)O	170.25	unknown	via CMAUP database
(1S,2S,4S,8R)-p-Menthane-2,8,9-triol	21593205	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(1S,2S,4S,8S)-p-Menthane-2,8,9-triol	21593206	Click to see CC1CCC(CC1O)C(C)(CO)O	188.26	unknown	via CMAUP database
(4s,8r)-8,9-Dihydroxy-p-menth-1(6)-en-2-one	11830092	Click to see CC1=CCC(CC1=O)C(C)(CO)O	184.23	unknown	via CMAUP database
(4S,8S)-8,9-Dihydroxy-p-mentha-1(6)-ene-2-one	10877793	Click to see CC1=CCC(CC1=O)C(C)(CO)O	184.23	unknown	via CMAUP database
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol	11788398	Click to see CC(=C)C1CCC(=CC1)CO	152.23	unknown	via CMAUP database
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF00047A021
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1021/JF00047A021
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1016/0926-6690(92)90031-P https://www.ncbi.nlm.nih.gov/pmc/articles/PMC34944/ https://doi.org/10.1021/JF00047A021
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC34944/ https://doi.org/10.1021/JF00047A021
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF00047A021 https://doi.org/10.1055/S-2006-961480 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC34944/
Perillaldehyde	16441	Click to see CC(=C)C1CCC(=CC1)C=O	150.22	unknown	https://doi.org/10.1021/JF00047A021
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane	5317024	Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C	218.38	unknown	https://doi.org/10.1021/JF00047A021
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane	6432312	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	https://doi.org/10.1021/JF00047A021
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF00047A021
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1R,2S,5R)-5-[1-(Hydroxymethyl)ethenyl]-2-methylcyclohexyl beta-D-glucopyranoside	11024065	Click to see CC1CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(=C)CO	332.39	unknown	via CMAUP database
(1S,2R,4R,8S)-2-(beta-D-Glucopyranosyloxy)-p-menthane-8,9-diol	11727818	Click to see CC1CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O	350.40	unknown	via CMAUP database
(1S,2R,4R,8S)-9-(beta-D-Glucopyranosyloxy)-p-menthane-2,8-diol	21593215	Click to see CC1CCC(CC1O)C(C)(COC2C(C(C(C(O2)CO)O)O)O)O	350.40	unknown	via CMAUP database
(1S,2S,4R,8R)-2-(beta-D-Glucopyranosyloxy)-p-menthane-1,8,9-triol	10904630	Click to see CC1(CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O)O	366.40	unknown	via CMAUP database
(1S,2S,4R,8S)-2-(beta-D-Glucopyranosyloxy)-p-menthane-1,8,9-triol	11024949	Click to see CC1(CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O)O	366.40	unknown	via CMAUP database
(1S,2S,4R)-2-(beta-D-Glucopyranosyloxy)-p-mentha-8-ene-1-ol	11823766	Click to see CC(=C)C1CCC(C(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)O	332.39	unknown	via CMAUP database
(1S,2S,4R)-2-(beta-D-Glucopyranosyloxy)-p-menthane-8-ene-1,10-diol	21593218	Click to see CC1(CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(=C)CO)O	348.39	unknown	via CMAUP database
(2R,4S)-7-(beta-D-Glucopyranosyloxy)-p-mentha-1(6),8-diene-2-ol	11056604	Click to see CC(=C)C1CC=C(C(C1)O)COC2C(C(C(C(O2)CO)O)O)O	330.37	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(3S)-3-hydroxy-4,6,6-trimethylcyclohexa-1,4-diene-1-carbaldehyde	162965168	Click to see CC1=CC(C(=CC1O)C=O)(C)C	166.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
(5R)-5-hydroxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde	163026355	Click to see CC1=CC=C(C(C1O)(C)C)C=O	166.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
1-Deoxy-d-ribitol	270738	Click to see CC(C(C(CO)O)O)O	136.15	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
3-Formyl-4,4,6-trimethylcyclohexa-2,5-dienol	12309880	Click to see CC1=CC(C(=CC1O)C=O)(C)C	166.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
5-Deoxyribitol	166761	Click to see CC(C(C(CO)O)O)O	136.15	unknown	via CMAUP database
5-Hydroxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde	101410434	Click to see CC1=CC=C(C(C1O)(C)C)C=O	166.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,2R,4S)-8-(beta-D-Glucopyranosyloxy)-p-menthane-1,2-diol	21593216	Click to see CC1(CCC(CC1O)C(C)(C)OC2C(C(C(C(O2)CO)O)O)O)O	350.40	unknown	via CMAUP database
(4S)-8-(beta-D-Glucopyranosyloxy)-p-mentha-1-ene-7-ol	10592670	Click to see CC(C)(C1CCC(=CC1)CO)OC2C(C(C(C(O2)CO)O)O)O	332.39	unknown	via CMAUP database
Benzyl beta-d-glucopyranoside	188977	Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O	270.28	unknown	via CMAUP database
Benzyl-beta-d-glucopyranoside	13254166	Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Grycerol 2-O-fucopyranoside	101159096	Click to see CC1C(C(C(C(O1)OC(CO)CO)O)O)O	238.23	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Phenylethyl beta-D-glucopyranoside	11289099	Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O	284.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Coniferin	5280372	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O	342.34	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Junipediol A 4-O-beta-D-glucopyranoside	11972388	Click to see COC1=C(C=CC(=C1)C(CO)CO)OC2C(C(C(C(O2)CO)O)O)O	360.36	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
beta-D-Fructopyranose	24310	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	via CMAUP database
D-(-)-Fructose	5984	Click to see C(C(C(C(C(=O)CO)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
D-Fructose	2723872	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
1-Deoxy-d-glucitol	10678630	Click to see CC(C(C(C(CO)O)O)O)O	166.17	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Hexane-1,2,3,4,5-pentol	3429	Click to see CC(C(C(C(CO)O)O)O)O	166.17	unknown	via CMAUP database
L-Fucitol	445724	Click to see CC(C(C(C(CO)O)O)O)O	166.17	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Butane-1,2,3,4-tetrol	8998	Click to see C(C(C(CO)O)O)O	122.12	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
D-Threitol	169019	Click to see C(C(C(CO)O)O)O	122.12	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Erythritol	222285	Click to see C(C(C(CO)O)O)O	122.12	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Galactitol	11850	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
L-Apiitol	10820745	Click to see C(C(C(CO)(CO)O)O)O	152.15	unknown	via CMAUP database
Mannitol	6251	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
Sorbitol	5780	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1016/S0031-9422(02)00288-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal	8175	Click to see CCCCCCCCCC=O	156.26	unknown	https://doi.org/10.1021/JF00047A021
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
1,9-Heptadecadiene-4,6-diyne-3,8-dione, (Z)-	15559227	Click to see CCCCCCCC=CC(=O)C#CC#CC(=O)C=C	256.34	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
4,6,6-Trimethyl-3-oxocyclohexa-1,4-diene-1-carbaldehyde	129716150	Click to see CC1=CC(C(=CC1=O)C=O)(C)C	164.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
4,6,6-Trimethyl-5-oxocyclohexa-1,3-diene-1-carbaldehyde	130025349	Click to see CC1=CC=C(C(C1=O)(C)C)C=O	164.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
(3S)-3-methoxy-4,6,6-trimethylcyclohexa-1,4-diene-1-carbaldehyde	162858747	Click to see CC1=CC(C(=CC1OC)C=O)(C)C	180.24	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995
3-Methoxy-4,6,6-trimethylcyclohexa-1,4-diene-1-carbaldehyde	101142129	Click to see CC1=CC(C(=CC1OC)C=O)(C)C	180.24	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.25-0995

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Carum carvi

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