Common products:
Sweet cicely (Myrrhis odorata) is primarily utilized as a flavoring agent and culinary herb.

Food and beverages (non-medicinal):
The plant provides fresh or dried anise-scented leaves and fruits used as a flavoring for:
* Syrups and liqueurs (e.g., alpine formulations like Génépy or SwissCH “Mys Sopra”).
* Beverages: Cordials, punches, and non-alcoholic mixes.
* Food: Salads, fruit desserts, custards, puddings, and omelettes; sweetening tart fruits (rhubarb, gooseberries) due to its mild sweetness.
* Sugar substitute: Historically, seeds or leaves macerated in sugar for imparting flavor.
Processed as a component in blended liqueurs, not as a standalone beverage.

Scientific/model-organism use:
Myrrhis odorata serves as a reference species in paleobotanical research, particularly for the study of fossilized plant silica bodies (phytoliths) diagnostic of the genus Myrrhis, aiding in paleoenvironmental reconstruction and identifying ancient agricultural or settlement sites.

Properties relevant to use:
The characteristic flavor and aroma derive from anethole, a phenylpropene compound also dominant in anise and fennel, imparting a sweet, licorice-like profile. Seed and leaf oils are cited as primary carriers of this volatile compound, contributing to the plant's utility as a flavoring agent. The dry, ribbed fruits provide a concentrated source of these flavor compounds.

Standards and regulation:
None documented specifically for this taxon.

Sustainability and sourcing:
Not documented for this species.

Synonyms Top

Scientific name	Authority	First published in
Lindera odorata	(L.) Asch.	Aschers. & Graebn., Fl. Nordostdeut. Flachl. 536.
Myrrhis iberica	Hoffm.	Gen. Pl. Umbell. : 30 (1814)
Myrrhis brevipedunculata	Hoffm.	Gen. Pl. Umbell. : 30 (1814)
Myrrhis sulcata	Lag.	Gen. Sp. Pl. : 13 (1816)
Selinum myrrhis	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 12: 68 (1904)
Scandix odorata	L.	Sp. Pl. : 257 (1753)
Chaerophyllum odoratum	Crantz	Cl. Umbell. Emend. : 75 (1767)
Myrrhis odorata var. culta	Alef.	Landw. Fl. : 164 (1866)
Myrrhis odorata var. sulcata	(Lag.) Alef.	Landw. Fl. : 164 (1866)
Myrrhis odorata subsp. sulcata	(Lag.) Nyman	Consp. Fl. Eur. : 299 (1879)

Common names Top

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Filter by language:

Language	Common/alternative name
English	cicely
English	sweet cicely
English	garden myrrh
English	anise
Spanish	chaerophyllum odoratum
Spanish	selinum myrrhis
Spanish	lindera odorata
Spanish	scandix odorata
Spanish	perifollo oloroso
Arabic	بقدونس إفرنجي
Arabic	مرس
Arabic	مرا
Bulgarian	смирна
Catalan	cerfeuil musqué
Catalan	mirris
Czech	čechřice vonná
Welsh	creithig bêr
Danish	sødskærm
Danish	spansk kørvel
German	cerfeuil musqué
German	scandix odorata
German	süßdolde
German	süssdolde
German	myrrhenkerbel
German	echte süßdolde
Estonian	mesiputk
Persian	چتردار شیرین
Finnish	saksankirveli
French	fougère musquée
French	gros persil
French	cerfeuil d'espagne
French	cerfeuil musqué
French	cerfeuil anisé
French	cerfeuil perpétuel
French	cerfeuil musque
Irish	lus áinleoige
gd	mirr
Croatian	Čehulja
Indonesian	seledri melur
Icelandic	spánarkerfill
Italian	finocchiella
Italian	mirride odorosa
Japanese	スイートシスリー
Kazakh	Миррис
Korean	시슬리
Lithuanian	garduoklė
Lithuanian	cerfeuil musqué
Lithuanian	kvapnioji garduoklė
Norwegian Bokmål	spansk kjørvel
Dutch	roomse kervel
Norwegian Nynorsk	spansk kjørvel
Polish	marchewnik anyżowy
Polish	marchewnik wonny
Slovenian	dišeči kromač
Swedish	cerfeuil musqué
Swedish	spansk körvel
Turkish	misk maydanozu
Ukrainian	Мірис запашний
Walloon	cierfouy di pidjon
Chinese	歐洲沒藥
Chinese	茉莉芹
Chinese	甜芹
Chinese	欧洲没药

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

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus

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

Northern America click to expand
- Eastern Canada
  - Newfoundland
  - Nova Scotia
  - Ontario
- Northeastern U.S.A.
  - Michigan
  - New York
  - Pennsylvania
- Northwestern U.S.A.
  - Oregon
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000371898
UNII	Y4HKZ607BQ
Canadensys	2617
USDA Plants	MYOD
Tropicos	1700940
INPN	109161
Flora of Italy	3461
KEW	urn:lsid:ipni.org:names:845120-1
The Plant List	kew-2363724
Missouri Botanical Garden	276029
PFAF	Myrrhis odorata
Open Tree Of Life	105019
Observations.org	7084
NCBI Taxonomy	40880
NBN Atlas	NBNSYS0000003645
Nature Serve	2.155473
IPNI	845120-1
iNaturalist	51618
GBIF	3034681
Freebase	/m/05y18l
EPPO	MYHOD
EOL	581559
Elurikkus	5842
USDA GRIN	102117
Wikipedia	Cicely
CMAUP	NPO28932
Plantarium	24771

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
GCA_977930265.1	drMyrOdor1.hap1.1	Chromosome	WELLCOME SANGER INSTITUTE	2026-01-26	35	701.95 Mb

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

Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review

Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L

Plants (Basel)

24-Feb-2024

PMCID:	PMC10934440
doi:	10.3390/plants13050621
PMID:	38475472

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

A systematic review of the safety and efficacy on cognitive function of herbal and nutritional medicines in older adults with and without subjective cognitive impairment

Cave AE, Chang DH, Münch GW, Steiner-Lim GZ

Syst Rev

17-Aug-2023

PMCID:	PMC10433666
doi:	10.1186/s13643-023-02301-6
PMID:	37592293

Occurrence of Alkenylbenzenes in Plants: Flavours and Possibly Toxic Plant Metabolites

Götz ME, Eisenreich A, Frenzel J, Sachse B, Schäfer B

Plants (Basel)

23-May-2023

PMCID:	PMC10255789
doi:	10.3390/plants12112075
PMID:	37299054

Novel metallomic profiling and non-carcinogenic risk assessment of botanical ingredients for use in herbal, phytopharmaceutical and dietary products using HR-ICP-SFMS

Kenny CR, Ring G, Sheehan A, Mc Auliffe MA, Lucey B, Furey A

Sci Rep

20-Oct-2022

PMCID:	PMC9584900
doi:	10.1038/s41598-022-16873-1
PMID:	36266322

Long-term seed burial reveals differences in the seed-banking strategies of naturalized and invasive alien herbs

Moravcová L, Carta A, Pyšek P, Skálová H, Gioria M

Sci Rep

25-May-2022

PMCID:	PMC9132925
doi:	10.1038/s41598-022-12884-0
PMID:	35614334

β-Caryophyllene, A Natural Dietary CB2 Receptor Selective Cannabinoid can be a Candidate to Target the Trinity of Infection, Immunity, and Inflammation in COVID-19

Jha NK, Sharma C, Hashiesh HM, Arunachalam S, Meeran MN, Javed H, Patil CR, Goyal SN, Ojha S

Front Pharmacol

14-May-2021

PMCID:	PMC8163236
doi:	10.3389/fphar.2021.590201
PMID:	34054510

Phylogenetic origins and family classification of typhuloid fungi, with emphasis on Ceratellopsis, Macrotyphula and Typhula (Basidiomycota)

Olariaga I, Huhtinen S, Læssøe T, Petersen JH, Hansen K

Stud Mycol

12-Jun-2020

PMCID:	PMC7388190
doi:	10.1016/j.simyco.2020.05.003
PMID:	32774511

Natural Products as Fungicide and Their Role in Crop Protection

Santra HK, Banerjee D

Natural Bioactive Products in Sustainable Agriculture

12-May-2020

PMCID:	PMC7212785
doi:	10.1007/978-981-15-3024-1_9

A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens

Frey D, Moretti M

Data Brief

23-May-2019

PMCID:	PMC6545399
doi:	10.1016/j.dib.2019.103982
PMID:	31194048

Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention)

Alamgir AN

Therapeutic Use of Medicinal Plants and their Extracts: Volume 2

24-Jun-2018

PMCID:	PMC7123938
doi:	10.1007/978-3-319-92387-1_7

Beneficial Effects of Spices in Food Preservation and Safety

Gottardi D, Bukvicki D, Prasad S, Tyagi AK

Front Microbiol

21-Sep-2016

PMCID:	PMC5030248
doi:	10.3389/fmicb.2016.01394
PMID:	27708620

Folkbotanical classification: morphological, ecological and utilitarian characterization of plants in the Napf region, Switzerland

Poncet A, Vogl CR, Weckerle CS

J Ethnobiol Ethnomed

14-Mar-2015

PMCID:	PMC4429483
doi:	10.1186/1746-4269-11-13
PMID:	25971246

Ferula asafoetida: Traditional uses and pharmacological activity

Mahendra P, Bisht S

Pharmacogn Rev

01-Jul-2012

PMCID:	PMC3459456
doi:	10.4103/0973-7847.99948
PMID:	23055640

Essential Leaf Oil Composition of<i>Myrrhis odorata</i>(L.) Scop. Grown in Finland

Jouko S. Uusitalo, Jorma E. Jalonen, Abbas Aflatuni, Sirkka L. Luoma

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.1999.9701174

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 / Phenol ethers / Anisoles
Anethole	637563	Click to see	148.20	unknown	https://doi.org/10.1080/10412905.1999.9701174 https://doi.org/10.1080/10412905.1993.9698232
Estragole	8815	Click to see	148.20	unknown	https://doi.org/10.1007/BF02860485
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698232
> 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/10.1039/JR9520004684
Oleic Acid	445639	Click to see	282.50	unknown	via CMAUP database
Petroselinic Acid	5281125	Click to see	282.50	unknown	https://doi.org/10.1039/JR9520004684
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol	13966170	Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C	304.50	unknown	via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	11870275	Click to see	302.50	unknown	via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene	44268166	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C	254.40	unknown	via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	21764434	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C	286.50	unknown	via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol	101586702	Click to see	286.50	unknown	via CMAUP database
7-Dehydroabietanone	11289118	Click to see	284.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see	300.40	unknown	via CMAUP database
Abietatriene	6432211	Click to see	270.50	unknown	via CMAUP database
Anticopalic acid	11808890	Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C	304.50	unknown	via CMAUP database
Ethyl abietate	61182	Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C	330.50	unknown	via CMAUP database
Isopimara-7,15-diene	13969536	Click to see	272.50	unknown	via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate	11290126	Click to see	318.50	unknown	via CMAUP database
Pimarol	12314285	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
Sandaracopimaradiene	443469	Click to see	272.50	unknown	via CMAUP database
Sandaracopimarinol	12314286	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698232
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	via CMAUP database
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1007/BF02860485
(+)-3-Carene	443156	Click to see	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698232
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1007/BF02860485
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698232
d-beta-Phellandrene	442484	Click to see	136.23	unknown	via CMAUP database
gamma-Terpineol	11467	Click to see CC(=C1CCC(CC1)(C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698232
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1007/BF02860485
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
(R)-beta-bisabolene	68128	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene	289151	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
Beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
CID 16396350	16396350	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren	91746537	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol	547972	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698232
Elemol	92138	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698232
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Selinene	442393	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698232
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol	101280203	Click to see	456.70	unknown	via CMAUP database
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-8,19-dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one	101280208	Click to see	456.70	unknown	via CMAUP database
(3S,6R,8S,11R,12S,15S,16R,19S,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene	101280202	Click to see	470.80	unknown	via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol	101121169	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C	460.70	unknown	via CMAUP database
21-Episerratenediol	12309682	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	442.70	unknown	via CMAUP database
3beta-Methoxy-21-oxoserratene	14830066	Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C	454.70	unknown	via CMAUP database
Pfaffic acid	441936	Click to see	440.70	unknown	via CMAUP database
Serratenediol 3-methyl ether	21672660	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one	3034666	Click to see	382.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	12943207	Click to see	410.70	unknown	via CMAUP database
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasta-3,5-dien-7-one	12444466	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C	410.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene	102594798	Click to see	276.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Peucedanin	8616	Click to see	258.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone	6453244	Click to see	270.28	unknown	via CMAUP database
Strobopinin	442520	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin	5281954	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database

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Myrrhis odorata

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