Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Across North America, people have made hot infusions of the leaves and sometimes the aerial parts of Agastache foeniculum (anise hyssop) to relieve cold symptoms and sore throats. The Blackfoot of the northern Plains recorded this use in the early 20th century; as described in Gunnar Nauck’s Indian Uses of Plants (reprinted 1918), a tea of the leaves was taken for colds and to soothe sore throats. The Cheyenne of the northern Great Plains also used infusions of the leaves in this way, noted by several collectors in the 1930s and summarized by Moerman (Native American Ethnobotany, 1998). On the Upper Great Lakes, the Ojibwe collected the herb locally and prepared leaf infusions for coughs, a practice recorded in the University of Michigan Ethnobotany Database (Moerman). A straightforward mild tea—3–4 g of fresh or 1–2 g of dried leaf, steeped for 7–10 minutes in 250 mL of near‑boiling water—reflects these recorded preparations. Adults may drink up to 1 cup two to three times daily for a few days; avoid concentrated use in pregnancy due to the presence of estragole (methyl chavicol) and essential oils, and keep essential oil and concentrated preparations away from children. A practical 1:5 ethanol tincture uses about 20 g of fresh leaf (or 10 g dried leaf) macerated in 100 mL of 45% ethanol for 2–3 weeks, shaking daily; a typical adult dose is 20–30 drops in water up to three times daily.

Phytochemistry that supports these uses is well documented for anise hyssop. The leaves and flowering tops are rich in essential oils rich in anethole and estragole, the same constituents that give fennel and star anise their characteristic aroma and warming actions; flavonoids such as luteolin, apigenin, and their glycosides; and phenolic acids including rosmarinic acid. These classes are antimicrobial, anti‑inflammatory, and gently carminative, consistent with the traditional use of the infusions for coughs and throat irritation.

Today, anise hyssop remains a local food and tea herb in the upper Midwest and Canada. Commercial teas and dried leaves are available from foragers and specialty growers, and it continues to be harvested in the wild by some Great Lakes communities who value its familiar flavor and comforting cold‑season brew.

General Uses Top

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Food and beverages (non-medicinal):
Fresh and dried leaves are used as a culinary herb and natural flavoring. The foliage imparts a sweet, anise–licorice-like aroma and taste and is employed as a garnish or seasoning for desserts, salads, baked goods, and confections. In food applications it typically functions as a flavoring ingredient rather than as a bulk ingredient. The essential oil (main constituents include methyl chavicol/estragole and limonene) is used by the flavor industry to impart anise/licorice notes in foods and beverages. In beekeeping, the flowers provide nectar for honey production.

Fragrance and cosmetics:
The essential oil is used by the fragrance industry in aromatic compositions and can be incorporated at low use levels into perfumes and related cosmetic or toiletry fragrance blends.

Properties relevant to use:
The leaf and flower volatile profile is dominated by phenylpropanoids (notably methyl chavicol/estragole) with significant limonene and smaller amounts of other monoterpenes (e.g., pulegone, menthone). These constituents confer a sweet, anise/licorice aroma suitable for food and fragrance flavoring roles. The high methyleugenol content in the oil has prompted regulatory scrutiny in some jurisdictions. For perfumes and flavors, commercial essential oil use levels are typically very low.

Standards and regulation:
Use as a food flavoring and in fragrance is governed by national and regional flavor/fragrance regulations. Jurisdictions such as the United States (FDA) and the European Union require that essential oils used in food and consumer products meet specified standards of identity and purity; labeling must disclose essential oil when used in cosmetic/toiletry fragrances. Where methyleugenol content is significant, maximum use levels may be restricted or an application dossier required.

Synonyms Top

Scientific name	Authority	First published in
Hyptis marathrosma	Benth.	Prodr. 12: 140 (1848)
Hyssopus anethiodorus	Nutt.	Cat. Pl. Upper Louisiana : 41 (1813)
Hyssopus anisatus	Nutt.	Gen. N. Amer. Pl. 2: 27 (1818)
Hyssopus discolor	Desf.	Tabl. École Bot. , ed. 3: 97 (1829)
Hyssopus foeniculum	Spreng.	Novi Provent. : 24 (1818)
Lophanthus anisatus	Benth.	Edwards's Bot. Reg. 15: t. 1282 (1829)
Perilla marathrosma	hort. ex Spreng.	Novi Provent. : 24 (1818)
Stachys foeniculum	Pursh	Fl. Amer. Sept. (Pursh) 2: 407. 1813 [Dec 1813]
Vleckia albescens	Raf.	Autik. Bot. : 121 (1840)
Vleckia anethiodora	Greene	Mem. Torrey Bot. Club 5: 282 (1894)
Vleckia anisata	Raf.	Fl. Tellur. 3: 89 (1837)
Vleckia bracteata	Raf.	New Fl. 4: 94 (1838)
Vleckia bracteosa	Raf.	Autik. Bot. : 120 (1840)
Vleckia discolor	Raf.	Autik. Bot. : 121 (1840)
Vleckia foeniculum	MacMill.	Metasp. Minnesota Valley : 449 (1892)
Vleckia incarnata	Raf.	Autik. Bot. : 120 (1840)
Agastache anethiodora	Britton & A.Brown	Fl. N. U.S. iii. 85.
Agastache foeniculum f. bernardii	B.Boivin	Naturaliste Canad. 87: 25 (1960)
Agastache foeniculum f. candicans	B.Boivin	Naturaliste Canad. 87: 26 (1960)
Lophanthus foeniculum	(Pursh) E.Mey.	Index Seminum (KALI, Regimontanum) 1831: 2 (1831)

Common names Top

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Filter by language:

Language	Common/alternative name
English	lavender giant-hyssop
English	anise hyssop
English	blue giant hyssop
Arabic	أغستاش شمري
chy	mo'éhemóxêšéne
Danish	indianermynte
German	anis-riesenysop
German	agastache anethiodora
German	duftnessel
Estonian	aniisi-hiidiisop
Persian	زوفای بزرگ معطر
Finnish	yrtti-iiso
Finnish	anisiiso
French	agastache anethiodora
French	anis hysope
French	grande hysope
French	hysope anisée
Hungarian	ánizsillatú izsópfű
Italian	agastache anethiodora
Italian	anice menta
Lithuanian	pankolinė kinmėtė
Lithuanian	anyžinis lofantas
Dutch	dropnetel
Russian	Многоколосник фенхельный
Swedish	anisisop
Ukrainian	лофант
Chinese	香藿香
Chinese	蓝藿香
Chinese	莳萝藿香
Chinese	茴藿香

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Europe click to expand
- Middle Europe
  - Austria

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Minnesota
  - Nebraska
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - New Hampshire
  - New York
  - Pennsylvania
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Washington
  - Wyoming
- Southeastern U.S.A.
  - Delaware
  - Kentucky
- Subarctic America
  - Northwest Territorie
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000902466
UNII	ZV7TA06J2V
Canadensys	6351
USDA Plants	AGFO
Tropicos	17600007
KEW	urn:lsid:ipni.org:names:6304-2
The Plant List	kew-4454
Missouri Botanical Garden	281382
Open Tree Of Life	1062003
Observations.org	160001
NCBI Taxonomy	39269
Nature Serve	2.137289
IPNI	6304-2
iNaturalist	158076
GBIF	2926406
Freebase	/m/0bbvdv1
WisFlora	2450
EPPO	AJTFO
EOL	579797
Elurikkus	208971
USDA GRIN	312121
Wikipedia	Agastache_foeniculum
Plantarium	49043
PFAF	Agastache foeniculum

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_054883455.1	Agastache_foeniculum_PCGL_v1.0	Chromosome	Chungnam National University	2026-01-30	87	460.05 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

Bioactivities and Synergistic Effect of Elsholtzia ciliata Essential Oil and Its Main Components against Lasioderma serricorne

Song S, Tang Y, Feng R, Zhang X, An Y, Kong W, Wang J, Zhang J, Liang J

Molecules

23-Apr-2024

PMCID:	PMC11085295
doi:	10.3390/molecules29091924
PMID:	38731415

Biological Control and Habitat Management for the Control of Onion Thrips, Thrips tabaci Lindeman (Thysanoptera: Thripidae), in Onion Production in Quebec, Canada

Gagnon AÈ, Fortier AM, Audette C

Insects

27-Mar-2024

PMCID:	PMC11050518
doi:	10.3390/insects15040232
PMID:	38667362

Phytochemical, Nutritional and Mineral Content of Four Edible Flowers

Marchioni I, Gabriele M, Carmassi G, Ruffoni B, Pistelli L, Pistelli L, Najar B

Foods

20-Mar-2024

PMCID:	PMC10969817
doi:	10.3390/foods13060939
PMID:	38540929

Synthetic polyploid induction influences morphological, physiological, and photosynthetic characteristics in Melissa officinalis L.

Bharati R, Gupta A, Novy P, Severová L, Šrédl K, Žiarovská J, Fernández-Cusimamani E

Front Plant Sci

14-Dec-2023

PMCID:	PMC10752996
doi:	10.3389/fpls.2023.1332428
PMID:	38155852

Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses

Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ

Foods

08-Nov-2023

PMCID:	PMC10671036
doi:	10.3390/foods12224066
PMID:	38002124

Foraging Wild Edibles: Dietary Diversity in Expanded Food Systems

Bellows AC, Raj S, Pitstick E, Potteiger MR, Diemont SA

Nutrients

31-Oct-2023

PMCID:	PMC10647252
doi:	10.3390/nu15214630
PMID:	37960283

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

Quantification of Tissue-Specific Paclitaxel in Himalayan Yew Using HPTLC-Densitometric Analysis, Assessment of Toxicological Activity, and Tissue-Specific Evaluation of Antioxidant Activity

Das T, Kumar Pandey D, Shekhawat MS, Dey A, Malik T

ACS Omega

22-Aug-2023

PMCID:	PMC10483656
doi:	10.1021/acsomega.3c04309
PMID:	37692257

Agastache Species: A Comprehensive Review on Phytochemical Composition and Therapeutic Properties

Nechita MA, Toiu A, Benedec D, Hanganu D, Ielciu I, Oniga O, Nechita VI, Oniga I

Plants (Basel)

14-Aug-2023

PMCID:	PMC10459224
doi:	10.3390/plants12162937
PMID:	37631149

Bovine mastitis, a worldwide impact disease: Prevalence, antimicrobial resistance, and viable alternative approaches

Morales-Ubaldo AL, Rivero-Perez N, Valladares-Carranza B, Velázquez-Ordoñez V, Delgadillo-Ruiz L, Zaragoza-Bastida A

Vet Anim Sci

24-Jul-2023

PMCID:	PMC10400929
doi:	10.1016/j.vas.2023.100306
PMID:	37547227

Inducing the Production of Secondary Metabolites by Foliar Application of Methyl Jasmonate in Peppermint

Kandoudi W, Tavaszi-Sárosi S, Németh-Zámboriné E

Plants (Basel)

16-Jun-2023

PMCID:	PMC10301213
doi:	10.3390/plants12122339
PMID:	37375964

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

Impact of Light and Dark Treatment on Phenylpropanoid Pathway Genes, Primary and Secondary Metabolites in Agastache rugosa Transgenic Hairy Root Cultures by Overexpressing Arabidopsis Transcription Factor AtMYB12

Do TM, Choi M, Kim JK, Kim YJ, Park C, Park CH, Park NI, Kim C, Sathasivam R, Park SU

Life (Basel)

19-Apr-2023

PMCID:	PMC10142052
doi:	10.3390/life13041042
PMID:	37109572

The mint versus Covid hypothesis

Buck CB

Med Hypotheses

15-Mar-2023

PMCID:	PMC10062428
doi:	10.1016/j.mehy.2023.111047
PMID:	37007799

Recent advances in targeted antibacterial therapy basing on nanomaterials

Geng Z, Cao Z, Liu J

Exploration (Beijing)

05-Feb-2023

PMCID:	PMC10191045
doi:	10.1002/EXP.20210117
PMID:	37323620

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
4-Methoxybenzaldehyde	31244	Click to see	136.15	unknown	https://doi.org/10.1080/10412905.1992.9698065
Benzaldehyde	240	Click to see	106.12	unknown	https://doi.org/10.1080/10412905.1992.9698065
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1080/10412905.1997.9700708
> Benzenoids / Phenol ethers / Anisoles
Anethole	637563	Click to see	148.20	unknown	https://doi.org/10.1080/10412905.1992.9698114 https://doi.org/10.1080/10412905.1992.9698065
Estragole	8815	Click to see	148.20	unknown	https://doi.org/10.1080/10412905.1992.9698114 https://doi.org/10.1080/10412905.1997.9700708 https://doi.org/10.1080/10412905.1992.9698065
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see	164.20	unknown	https://doi.org/10.1080/10412905.1997.9700708
> Hydrocarbons / Saturated hydrocarbons
4,4-Dimethylnonane	53425988	Click to see	156.31	unknown	https://doi.org/10.1080/10412905.1992.9698065
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
3-Ethyl-2-methyloct-2-ene	85682407	Click to see CCCCCC(=C(C)C)CC	154.29	unknown	https://doi.org/10.1080/10412905.1992.9698065
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1080/10412905.1997.9700708
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698065
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1997.9700708
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1992.9698065 https://doi.org/10.1080/10412905.1997.9700708
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698065 https://doi.org/10.1080/10412905.1997.9700708
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698065
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698065
Sabinol	94147	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1992.9698114
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Menthone	443159	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1997.9700708
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700708 https://doi.org/10.1080/10412905.1992.9698065
p-Menthan-3-one	6986	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1997.9700708
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315594	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700708
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700708
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700708
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700708
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
I2-Ionone	638014	Click to see	192.30	unknown	https://doi.org/10.1080/10412905.1997.9700708
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
> 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/10.1080/10412905.1997.9700708
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700708
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see	536.90	unknown	https://doi.org/10.1080/10412905.1992.9698114
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein A	5281243	Click to see	568.90	unknown	https://doi.org/10.1080/10412905.1992.9698114
Violaxanthin	448438	Click to see	600.90	unknown	https://doi.org/10.1080/10412905.1992.9698114
Zeaxanthin	5280899	Click to see	568.90	unknown	https://doi.org/10.1080/10412905.1992.9698114
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
1-Octen-3-yl acetate	17121	Click to see	170.25	unknown	https://doi.org/10.1080/10412905.1997.9700708
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2R,3R,4S,5R,6R)-2-[(2S,3S,4R,6S)-6-[(2R,3S,4R,6S)-4-hydroxy-6-[(2R,3R,4R,6S)-4-methoxy-6-[(2R,3S,4S,6R)-4-methoxy-2-methyl-6-[(1S,2R,7S,10R,11S,14R,15R,16R,19S)-10,14,16-trimethyl-17,20,21-trioxahexacyclo[14.4.1.01,14.02,11.05,10.015,19]henicos-4-en-7-yl]oxan-3-yl]oxy-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	15939579	Click to see	1055.20	unknown	https://doi.org/10.1080/10412905.1992.9698114
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2,2-Dimethylhexanal	523230	Click to see CCCCC(C)(C)C=O	128.21	unknown	https://doi.org/10.1080/10412905.1992.9698065
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone	246728	Click to see CCCCCC(=O)CC	128.21	unknown	https://doi.org/10.1080/10412905.1997.9700708 https://doi.org/10.1080/10412905.1992.9698065
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
2-Methoxy-1-propanol	14846	Click to see	90.12	unknown	https://doi.org/10.1080/10412905.1992.9698114
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 162977223	162977223	Click to see	416.40	unknown	https://doi.org/10.1080/10412905.1992.9698114
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate	6326752	Click to see	871.20	unknown	https://doi.org/10.1080/10412905.1992.9698114
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate	5459387	Click to see	871.20	unknown	https://doi.org/10.1080/10412905.1992.9698114

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Agastache foeniculum

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top