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)

Common names Top

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Filter by language:

Language	Common/alternative name
English	anise
English	garden myrrh
English	sweet cicely
English	cicely
Spanish	perifollo oloroso
Arabic	مرس
Arabic	مرا
Arabic	بقدونس إفرنجي
Bulgarian	смирна
Catalan	mirris
Catalan	cerfeuil musqué
Czech	čechřice vonná
Welsh	creithig bêr
Danish	sødskærm
Danish	spansk kørvel
German	süssdolde
German	süßdolde
German	cerfeuil musqué
German	myrrhenkerbel
German	echte süßdolde
Estonian	mesiputk
Persian	چتردار شیرین
Finnish	saksankirveli
French	fougère musquée
French	cerfeuil d'espagne
French	cerfeuil musqué
French	cerfeuil musque
French	cerfeuil anisé
French	gros persil
French	cerfeuil perpétuel
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	cerfeuil musqué
Lithuanian	garduoklė
Lithuanian	kvapnioji garduoklė
Norwegian Bokmål	spansk kjørvel
Dutch	roomse kervel
Norwegian Nynorsk	spansk kjørvel
Polish	marchewnik anyżowy
Polish	marchewnik wonny
Slovenian	dišeči kromač
Swedish	spansk körvel
Swedish	cerfeuil musqué
Turkish	misk maydanozu
Ukrainian	Мірис запашний
Walloon	cierfouy di pidjon
Chinese	歐洲沒藥
Chinese	欧洲没药
Chinese	甜芹
Chinese	茉莉芹

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!

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

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

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

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

Chemical Composition of the Leaf Oil of<i>Myrrhis odorata</i>(L.) Scop.

Kirill G. Tkachenko, Igor G. Zenkevich

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.1993.9698232

Other herbs and spices: mango ginger to wasabi

Ravindran PN, Pillai GS, Divakaran M

Handbook of Herbs and Spices

01-Jan-2012

PMCID:	PMC7152468
doi:	10.1533/9780857095688.557

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 CC=CC1=CC=C(C=C1)OC	148.20	unknown	https://doi.org/10.1080/10412905.1993.9698232 https://doi.org/10.1080/10412905.1999.9701174
Estragole	8815	Click to see COC1=CC=C(C=C1)CC=C	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 CC1=CCC(=CC1)C(C)C	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 CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Petroselinic acid	5281125	Click to see CCCCCCCCCCCC=CCCCCC(=O)O	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 CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
18-Nordehydroabiet-4(19)-ene	44268166	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C	254.40	unknown	via CMAUP database
7-Dehydroabietanone	11289118	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C	300.40	unknown	via CMAUP database
Abieta-8,11,13-trien-15-ol	101586702	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)C	286.50	unknown	via CMAUP database
Abieta-8,11,13-trien-7alpha-ol	21764434	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C	286.50	unknown	via CMAUP database
Abietatriene	6432211	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C	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
Anticopalic acid methyl ester	11290126	Click to see CC(=CC(=O)OC)CCC1C(=C)CCC2C1(CCCC2(C)C)C	318.50	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 CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C	272.50	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 CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C	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 CC(=CCCC(=C)C=C)C	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 CC1(C2CCC(=C)C1C2)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
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1007/BF02860485
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
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	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 CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1007/BF02860485
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698232
gamma-Terpineol	11467	Click to see CC(=C1CCC(CC1)(C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698232
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	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
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
Longifolene	289151	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)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 CC1CCC2C1C3C(C3(C)C)CCC2=C	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-ylcyclohexyl)propan-2-ol	547972	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698232
Elemol	92138	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	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 CC(=C)C1CCC2(CCCC(=C)C2C1)C	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
(24S)-Lanosta-9(11)-ene-3beta,24,25-triol	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
16-Oxo-21-episerratenediol	101280208	Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	456.70	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
21-Episerratenediol 3-methyl ether	101280203	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	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 CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CC5C6(CCC5(C4C6)C(=O)O)C)C)C)C	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
Serratenediol dimethyl ether	101280202	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C	470.80	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 CC(C)CCCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C	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 CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C	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
13-Vinyl-16,17-dinor-14-oxaabietane	102594798	Click to see CC1(CCCC2(C1CCC3C2CCC(O3)(C)C=C)C)C	276.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Peucedanin	8616	Click to see CC(C)C1=C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC	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 CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3	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 C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	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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