Marjoram is a perennial herb with a sweet pine and citrus flavor that is native to the Mediterranean region and parts of Asia. It is closely related to oregano and is sometimes referred to as pot marjoram. In ancient times, it was seen as a symbol of happiness and was used in various cultures for medicinal purposes. Today, it is primarily used for culinary purposes and is popular in low-fat and low-salt diets. Marjoram is easy to cultivate and is often grown in pots to prevent it from taking over a garden. It is used in a variety of dishes, including soups, stews, and herbal teas. Medicinally, it has been used to treat a range of ailments, and some of its uses have been scientifically proven. However, it should be used with caution by pregnant or lactating women.

Synonyms Top

Scientific name	Authority	First published in
Majorana dubia	Briq.	Nat. Pflanzenfam. 4(3a): 307 (1896)
Majorana fragrans	Raf.	Fl. Tellur. 3: 86 (1837)
Majorana hortensis	Moench	Methodus : 406 (1794)
Majorana majorana	H.Karst.	Ill. Repert. Pharm.-Med. Bot. : 999 (1886)
Majorana mexicana	M.Martens & Galeotti	Bull. Acad. Roy. Sci. Bruxelles 11(2): 191 (1844)
Majorana ovalifolia	Stokes	Bot. Mat. Med. 3: 350 (1812)
Majorana ovatifolia	Stokes	Bot. Mat. Med. 3: 351 (1812)
Majorana suffruticosa	Raf.	Fl. Tellur. 3: 86 (1837)
Majorana tenuifolia	Raf.	Fl. Tellur. 3: 86 (1837)
Majorana tenuifolia	Gray	Nat. Arr. Brit. Pl. 2: 381 (1821 publ. 1822)
Majorana uncinata	Stokes	Bot. Mat. Med. 3: 353 (1812)
Majorana vulgaris	Gray	Nat. Arr. Brit. Pl. 2: 381 (1821 publ. 1822)
Origanum confertum	Pi.Savi	Index Seminum (PI, Ticinensis) 1839: [2] (1839)
Origanum dubium	Boiss.	Fl. Orient. 4: 553 (1879)
Origanum majorana var. tenuifolium	Weston	Bot. Univ. 3: 530. 1772
Origanum majoranoides	Willd.	Sp. Pl., ed. 4 , 3: 137 (1800)
Origanum odorum	Salisb.	Prodr. Stirp. Chap. Allerton : 85 (1796)
Origanum salviifolium	Roth	Catal. Bot. 2: 48 (1800)
Thymus majorana	Kuntze	Taschen-Fl. Leipzig : 106 (1867)
Origanum majorana var. majoranoides	(Willd.) Nyman	Consp. Fl. Eur. 592. 1881
Amaracus majorana	Schinz & Thell.	Bull. Herb. Boissier , sér. 2, 7: 576 (1907)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	sweet marjoram
English	knotted marjoram
English	sweet majoram
English	sweet marjoram oil
English	marjoram
Spanish	acapuas
Spanish	almaraco
Spanish	almoradijo
Spanish	almoraduj
Spanish	almoradux casero
Spanish	almoradux morisco
Spanish	almoradux salsero
Spanish	amaraco
Spanish	amáraco
Spanish	amoradux
Spanish	anaraco
Spanish	maiorana
Spanish	mayorana
Spanish	mejorama
Spanish	mejorana bastarda
Spanish	mejorana dulce
Spanish	mejorana real
Spanish	moradux
Spanish	sampsuco
Spanish	mejorana
Afrikaans	marjolein
Arabic	مردقوش
Arabic	بردقوش
Arabic	عشبة المردكوش
Arabic	مرزجوش
Arabic	مرزنجوش
Arabic	مردكوش
Arabic	نبات البردقوش او المردقوش
Arabic	مردقوش كبير
Arabic	اذان الفأر
Arabic	العترة
Arabic	المردقوش
Arabic	برزنجوش
Arabic	سمسق
Arabic	ريحان داوود
Arabic	الدوش
Arabic	دوش
Azerbaijani	mərzə
azb	مرزه
Belarusian	мацярдушка
Belarusian	лябёдка
Belarusian	мажэржанка
Belarusian	мар’янка
Belarusian	мацержанка
Belarusian	Маяран садовы
Belarusian	размар’ян
Belarusian	Маяран
Bulgarian	майорана
Bosnian	majoran
Bosnian	mažuran
Catalan	moraduix
Catalan	marduix
Czech	majoránka
Czech	majoránka zahradní
Welsh	penrhudd yr ardd
Welsh	mintys y graig
Danish	have-merian
German	wurstkraut
German	majoran
Greek	Μαντζουράνα
Greek	Ματζουράνα
Esperanto	majorano
Estonian	aedmajoraan
Basque	mendaro (landarea)
Persian	مرزنجوش وحشی
Finnish	maustemeirami
Finnish	meirami
French	marjolaine
French	marjolaine des jardins
frr	majoraan
Irish	oragán cumhra
Galician	maiorana
Hebrew	אֵזוֹב תַּרְבּוּתִי
Hebrew	אֲזוֹבִית תַּרְבּוּתִית
Hebrew	מָיוֹרָם
Hebrew	רוֹוח מָיוֹרָם מָתוֹק
Hebrew	מיורן
Hebrew	אזוב תרבותי
Hindi	मरुआ
Croatian	majoran
Upper Sorbian	kołbasnik
Upper Sorbian	majron
Upper Sorbian	majoran
Hungarian	kerti majoránna
Hungarian	majoranna
Hungarian	majorannae herba
Hungarian	majoránna
Indonesian	marjoram
io	majorano
Italian	maggiorana
Japanese	スイートマージョラム
Japanese	マージョラム
Japanese	マジョラム
Kazakh	Майоран
Kannada	ಮರುಗ
Korean	마조람
Cornish	organs
la	amaracus
la	sampsuchum
la	sampsuchus
la	amaracum
lb	majoran
lb	mairon
li	majoraan
lij	persa
lij	persega
Lithuanian	majorana
Lithuanian	mairūnas
Lithuanian	kvapusis mairūnas
Latvian	majorana
Latvian	majorāns
Macedonian	amaracum
Macedonian	echte marjolein
Macedonian	have-merian
Macedonian	kvapusis mairūnas
Macedonian	lebiodka majeranek
Macedonian	maghiran
Macedonian	majoraan
Macedonian	majoran
Macedonian	majorán záhradný
Macedonian	majoránka zahradní
Macedonian	majoránna
Macedonian	majorano
Macedonian	majorāns
Macedonian	manjerona
Macedonian	marduix
Macedonian	mariolinne
Macedonian	marjolaine
Macedonian	marjoram
Macedonian	mažuran
Macedonian	meirami
Macedonian	mejram
Macedonian	menton salmego
Macedonian	mikhurana
Macedonian	peperna
Macedonian	Ματζουράνα
Macedonian	Майорана
Macedonian	Мајорана
Macedonian	Маяран
Macedonian	אזוב תרבותי
Macedonian	بردقوش
Macedonian	مردقوش
Macedonian	మరువము
Macedonian	マジョラム
Macedonian	墨角蘭
Macedonian	Мајоран
Malayalam	മാർജോറം
Malay	marjoram
mt	merqtux
nap	peperna
Norwegian Bokmål	merian
Dutch	echte marjolein
Dutch	majoraan
Norwegian Nynorsk	marjoram
Norwegian Nynorsk	merian
oc	majorana
os	Майоран
Punjabi	ਮਰੂਆ
pam	marjoram
pfl	marau
Polish	majeranek
Polish	majeranek ogrodowy
Polish	lebiodka majeranek
Portuguese	manjerona
Quechua	mayorana
Quechua	mayurana
Quechua	mejorana
Quechua	mihurana
Quechua	mijurana
Quechua	mikurana
Quechua	mikhurana
Romanian	măghiran
Romanian	maghiran
Russian	Майоран садовый
Russian	Майоран
Russian	майоран
scn	maiurana
scn	majurana
sco	marjoram
Samogitian	meiruonā
Slovak	majoránka
Slovak	majorán záhradný
Slovenian	majaron
Serbian	mažuran
Swedish	mejram
Telugu	మరువకపత్రం
Telugu	మరువము
Turkish	mercanköşk
Ukrainian	Майоран
Uzbek	marjoram
vec	menton salbego
vec	menton salmego
Walloon	mariolinne
Chinese	甘牛至
Chinese	多節墨角蘭
Chinese	甜墨角蘭
Chinese	馬約蘭
Chinese	馬約蘭草
Chinese	馬鬱草
Chinese	马郁兰
Chinese	墨角蘭
Chinese	墨角兰

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!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000260658
UNII	R40XM3HU5X
USDA Plants	ORMA
Tropicos	17601585
INPN	111272
Flora of Italy	4614
KEW	urn:lsid:ipni.org:names:453303-1
The Plant List	kew-143853
Missouri Botanical Garden	281497
Open Tree Of Life	61897
Observations.org	7119
NCBI Taxonomy	268884
NBN Atlas	NBNSYS0000033782
Nature Serve	2.127949
IPNI	449785-1
iNaturalist	165925
iNaturalist	279309
GBIF	2926615
Freebase	/m/04sgp
EPPO	MAJHO
EOL	579365
Elurikkus	6005
Calflora (Californian flora)	12716
USDA GRIN	25912
Wikipedia	Marjoram

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

Alginate Nanoparticles Containing Cuminum cyminum and Zataria multiflora Essential Oils with Promising Anticancer and Antibacterial Effects

Osanloo M, Ranjbar R, Zarenezhad E

Int J Biomater

02-May-2024

PMCID:	PMC11081758
doi:	10.1155/2024/5556838
PMID:	38725434

Re‐evaluation of certain aspects of the EFSA Scientific Opinion of April 2010 on risk assessment of parasites in fishery products, based on new scientific data. Part 1: ToRs1–3

Koutsoumanis K, Allende A, Alvarez‐Ordóñez A, Bover‐Cid S, Chemaly M, De Cesare A, Herman L, Hilbert F, Lindqvist R, Nauta M, Nonno R, Peixe L, Ru G, Simmons M, Skandamis P, Suffredini E, Buchmann K, Careche M, Levsen A, Mattiucci S, Mladineo I, Santos MJ, Barcia‐Cruz R, Broglia A, Chuzhakina K, Goudjihounde SM, Guerra B, Messens W, Guajardo IM, Bolton D

EFSA J

22-Apr-2024

PMCID:	PMC11033839
doi:	10.2903/j.efsa.2024.8719
PMID:	38650612

Hymenaea courbaril resin-mediated gold nanoparticles as catalysts in organic dyes degradation and sensors in pharmaceutical pollutants

Khan N, Durrani P, Jamila N, Nishan U, Jan MI, Ullah R, Bari A, Choi JY

Heliyon

20-Apr-2024

PMCID:	PMC11063429
doi:	10.1016/j.heliyon.2024.e30105
PMID:	38699715

Sandalwood Oils of Different Origins Are Active In Vitro against Madurella mycetomatis, the Major Fungal Pathogen Responsible for Eumycetoma

Abd Algaffar SO, Seegers S, Satyal P, Setzer WN, Schmidt TJ, Khalid SA

Molecules

18-Apr-2024

PMCID:	PMC11055130
doi:	10.3390/molecules29081846
PMID:	38675665

Mitigating digestive disorders: Action mechanisms of Mediterranean herbal active compounds

Kmail A

Open Life Sci

18-Apr-2024

PMCID:	PMC11032100
doi:	10.1515/biol-2022-0857

Emerging Approaches for Mitigating Biofilm-Formation-Associated Infections in Farm, Wild, and Companion Animals

Araújo D, Silva AR, Fernandes R, Serra P, Barros MM, Campos AM, Oliveira R, Silva S, Almeida C, Castro J

Pathogens

13-Apr-2024

PMCID:	PMC11054384
doi:	10.3390/pathogens13040320
PMID:	38668275

Effect of dietary supplementation Ampelopsis grossedentata extract on growth performance and muscle nutrition of Megalobrama hoffmanni by gut bacterial mediation

Yang Q, Wang Y, Li G, Huang X, Zheng L, Peng M, Cao Y, Wang X

Heliyon

01-Apr-2024

PMCID:	PMC11004802
doi:	10.1016/j.heliyon.2024.e29008
PMID:	38601588

The effect of dietary eugenol nano-emulsion supplementation on growth performance, serum metabolites, redox homeostasis, immunity, and pro-inflammatory responses of growing rabbits under heat stress

Alrashedi SS, Almasmoum HA, Eldiasty JG

Open Vet J

31-Mar-2024

PMCID:	PMC11052630
doi:	10.5455/OVJ.2024.v14.i3.10
PMID:	38682150

Physical Stability and Antioxidant Ability of a Sustainable Oil-in-Water Emulsion Containing Perilla Skin Extract and Upcycled Aquasoya Powder

Kang BK, Yu JC, Shin WS

Foods

29-Mar-2024

PMCID:	PMC11011918
doi:	10.3390/foods13071063
PMID:	38611367

An Exploratory Experimental Analysis Backed by Quantum Mechanical Modeling, Spectroscopic, and Surface Study for C-Steel Surface in the Presence of Hydrazone-Based Schiff Bases to Fix Corrosion Defects in Acidic Media

Moustafa AH, Abdel-Rahman HH, Barakat A, Mohamed HA, El-Kholany AS

ACS Omega

28-Mar-2024

PMCID:	PMC11007727
doi:	10.1021/acsomega.4c00199
PMID:	38617646

Simultaneous Impact of Rhizobacteria Inoculation and Leaf-Chewing Insect Herbivory on Essential Oil Production and VOC Emissions in Ocimum basilicum

Palermo TB, Cappellari LD, Palermo JS, Giordano W, Banchio E

Plants (Basel)

23-Mar-2024

PMCID:	PMC11013597
doi:	10.3390/plants13070932
PMID:	38611463

A comprehensive review of mycotoxins: Toxicology, detection, and effective mitigation approaches

Khan R, Anwar F, Ghazali FM

Heliyon

23-Mar-2024

PMCID:	PMC11019184
doi:	10.1016/j.heliyon.2024.e28361
PMID:	38628751

Effects of Seven Plant Essential Oils on the Growth, Development and Feeding Behavior of the Wingless Aphis gossypii Glover

Wang X, Zhang Y, Yuan H, Lu Y

Plants (Basel)

22-Mar-2024

PMCID:	PMC11013612
doi:	10.3390/plants13070916
PMID:	38611446

Obtaining Microbiologically Safe Hatching Eggs from Hatcheries: Using Essential Oils for Integrated Sanitization Strategies in Hatching Eggs, Poultry Houses and Poultry

Oliveira GD, McManus C, Vale IR, dos Santos VM

Pathogens

18-Mar-2024

PMCID:	PMC10974541
doi:	10.3390/pathogens13030260
PMID:	38535603

Applied insight: studying reducing the carbon footprint of the drying process and its environmental impact and financial return

Ibrahim A, Amer A, Elsebaee I, Sabahe A, Amer MA

Front Bioeng Biotechnol

14-Mar-2024

PMCID:	PMC10979823
doi:	10.3389/fbioe.2024.1355133
PMID:	38558793

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 / Phenols / Benzenediols / Hydroquinones
Hydroquinone	785	Click to see C1=CC(=CC=C1O)O	110.11	unknown	https://doi.org/10.1055/S-2006-962734
> Benzenoids / Phenols / Methoxyphenols
Mequinol	9015	Click to see COC1=CC=C(C=C1)O	124.14	unknown	https://doi.org/10.1055/S-2006-962734
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/JF00083A023 https://doi.org/10.1055/S-2006-960024
> 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/10.1055/S-2006-960024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	https://doi.org/10.1055/S-2006-960024
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-960024
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1055/S-2006-960024 https://doi.org/10.1080/10412905.1997.9700757
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1055/S-2006-960024
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1055/S-2006-960024
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-960024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698294
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1055/S-2006-960024 https://doi.org/10.1021/JF00083A023
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700757 https://doi.org/10.1080/10412905.1993.9698294
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/JF00083A023
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-960024
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1055/S-2006-960024
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1055/S-2006-960024
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1055/S-2006-960024
beta-Thujone	91456	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1055/S-2006-960024
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1055/S-2006-960024
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1055/S-2006-960024
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1055/S-2006-960024
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-960024
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1055/S-2006-960024
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/JF00083A023 https://doi.org/10.1055/S-2006-960024
Thujone	261491	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1055/S-2006-960024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/CBER.189903201156
4-Methoxy-1-methyl-4-(propan-2-yl)cyclohex-1-ene	71330304	Click to see CC1=CCC(CC1)(C(C)C)OC	168.28	unknown	https://doi.org/10.1021/JF00083A023
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/JF00083A023 https://doi.org/10.1080/10412905.1997.9700757 https://doi.org/10.1055/S-2006-960024
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1055/S-2006-960024
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/JF00083A023
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1055/S-2006-960024 https://doi.org/10.1002/CBER.189903201156
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1055/S-2006-960024
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1055/S-2006-960024
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1055/S-2006-960024
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
(+)-Gamma-cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
(1E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene	134687947	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol	6097621	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1055/S-2006-960024
(E,Z)-farnesol	1549109	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	https://doi.org/10.1055/S-2006-960024
(R)-beta-bisabolene	68128	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
8-Isopropyl-2,5-dimethyl-1,2,3,4-tetrahydronaphthalene	518975	Click to see CC1CCC2=C(C=CC(=C2C1)C(C)C)C	202.33	unknown	https://doi.org/10.1055/S-2006-960024
alpha-Bisabolol	10586	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1055/S-2006-960024
alpha-Cadinol #1	6431302	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1055/S-2006-960024
beta Farnesene	15228937	Click to see CCC(=C)CCC=C(C)CCC=C(C)C	206.37	unknown	https://doi.org/10.1055/S-2006-960024
Beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1055/S-2006-960024
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1055/S-2006-960024
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
Farnesol	3327	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	https://doi.org/10.1055/S-2006-960024
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-960024
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol	346	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	https://doi.org/10.1055/S-2006-962734
Arbutin	440936	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	https://doi.org/10.1055/S-2006-962734
Methylarbutin	80131	Click to see COC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	286.28	unknown	https://doi.org/10.1055/S-2006-962734
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1016/B978-0-12-818162-1.00043-2
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/10.1016/B978-0-12-818162-1.00043-2
Scutellarein	5281697	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O	286.24	unknown	https://doi.org/10.1271/BBB.67.445
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/B978-0-12-818162-1.00043-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[5,6-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	101237094	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1271/BBB.67.445
[6-[5,6-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	163031924	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1271/BBB.67.445
5,6-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	14332446	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)O	448.40	unknown	https://doi.org/10.1271/BBB.67.445
Plantaginin	5320623	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)O	448.40	unknown	https://doi.org/10.1271/BBB.67.445
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Thymonin	442662	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)O	360.30	unknown	https://doi.org/10.1016/0031-9422(84)83061-7

Biological Material Top

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.

Origanum majorana

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top