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.

Agastache rugosa, known in Chinese as “Hu Qu” and in Korean as “Sang-yeong,” has a long history of use as a digestive and respiratory tonic. In traditional Chinese medicine the dried aerial parts are brewed as a tea to relieve stomach pain, abdominal distension, and cough, a practice documented in the Chinese Pharmacopoeia (2015). Among the Korean people, Kim et al. (2019) report that a decoction of the leaves is taken after meals to ease indigestion and to calm the stomach, while the Japanese folk medicine literature (Sato et al., 2020) describes a mild infusion of the herb for sore throats and mild fever. In all three cultures the same plant part—dried leaves or whole aerial parts—is used, typically steeped in hot water or boiled for a short period to extract the volatile oils and flavonoids that give the herb its characteristic aroma and therapeutic effect.

A simple, safe recipe for a stomach‑soothing tea is as follows: take 5 g of dried Agastache rugosa leaves, add 200 ml of freshly boiled water, and steep for 5–10 minutes. Strain and drink 2–3 cups per day, preferably after meals. Because the herb contains estragole and other compounds that may stimulate uterine contractions, it is advisable for pregnant women to avoid this tea or to consult a healthcare professional before use. The tea is generally well tolerated, but individuals with a history of liver disease should limit intake to no more than 3 cups daily.

The therapeutic properties of Agastache rugosa are largely attributed to its essential oil constituents. Linalool, estragole (methyl chavicol), eugenol, and camphor are the most abundant compounds identified in the leaves, and these have been shown in vitro to possess anti‑inflammatory, antispasmodic, and antimicrobial activities that align with the herb’s traditional uses for digestive discomfort and cough. Flavonoids such as quercetin and kaempferol also contribute antioxidant effects, supporting the plant’s role in soothing irritated mucous membranes.

Today Agastache rugosa is cultivated both as an ornamental plant and as a culinary herb in Asian markets. Its essential oil is extracted for use in aromatherapy and as a natural preservative, and research into its anti‑inflammatory and antimicrobial properties continues to validate the centuries‑old practices of Chinese, Korean, and Japanese healers.

General Uses Top

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Food and beverages (non-medicinal):
Leaves are used as an edible herb and seasoning in Korean cuisine (Kim et al., 2021; Perry, 1980). They are processed as a vegetable (National Institute of Horticultural & Herbal Science, 2014). Flavor profile is described as mint–licorice; leaves are eaten raw or cooked (Plants For A Future, 2012). The plant is listed as edible by the University of Illinois Extension (2021).

Properties relevant to use:
Essential oil from aerial parts is characterized by a high proportion of phenylpropanoids—primarily methyl chavicol (estragole) and estragole—typical of the Agastache rugosa chemotype (Kim et al., 2018; Zhou et al., 2016). Anethole has also been reported as a minor to moderate component (Zhou et al., 2016; Rath et al., 2022). These constituents determine a sweet–anise/licorice aroma suitable for flavor applications, while methyl chavicol/estragole content entails flavoring regulations (EFSA, 2014).

Colorants and tanning:
No reliable reports for dyes or tannins in Agastache rugosa were found in the consulted literature.

Wood and fiber:
No reliable reports for timber or fiber uses were found.

Fragrance and cosmetics:
No reliable commercial fragrance uses of the plant or essential oil were identified in the consulted literature.

Standards and regulation:
Estragole is regulated in the EU for use in flavorings (Regulation (EC) No 1334/2008; EFSA, 2014).

Sustainability and sourcing:
No specific sustainability or sourcing standards were found for Agastache rugosa products.

REFERENCES:
EFSA (2014). Scientific Opinion on flavouring group evaluation 220 (FGE.220): Estragole (Chemotherapy). EFSA Journal 12(6):3741.
Kim, H. et al. (2018). Chemical composition and antioxidant activity of Agastache rugosa essential oil. Journal of Essential Oil Research 30(5): 380–388.
Kim, N. et al. (2021). Edible and functional plants in Korea. Korea University Press.
National Institute of Horticultural & Herbal Science (2014). Herbal food list (Korean).
Perry, L. M. (1980). Medicinal plants of East and Southeast Asia.
Plants For A Future (2012). Agastache rugosa – (Fisch. & C.A.Mey.) Kuntze. Plants for a Future Database.
Rath, P. et al. (2022). Comparative essential oil profiles in Lamiaceae (Chiang Mai University, Thesis).
University of Illinois Extension (2021). Herb gardening: Agastache rugosa (Korean mint).
Zhou, W. et al. (2016). GC–MS analysis of essential oils from Agastache rugosa. Journal of Chemical & Pharmaceutical Research 8(10): 62–69.

Synonyms Top

Scientific name	Authority	First published in
Lophanthus formosanus	Hayata	Icon. Pl. Formosan. 8: 87 (1919)
Lophanthus rugosus	Fisch. & C.A.Mey.	Index Seminum [St.Petersburg (Petropolitanus)] i. 31.
Agastache rugosa f. alba	Y.N.Lee	Bull. Korea Pl. Res. 5: 24 (2005)
Cedronella japonica	Hassk.	Acta Soc. Regiae Sci. Indo-Neêrl. 1: 37 (1856)
Agastache formosana	(Hayata) Hayata	Fl. Japan ed. 2: 1006. 1931 (1931)
Elsholtzia monostachys	H.Lév. & Vaniot	Repert. Spec. Nov. Regni Veg. 8: 424 (1910)
Lophanthus rugosus var. hypoleucus	Maxim. ex Herder	Trudy Imp. S.-Peterburgsk. Bot. Sada 10: 4 (1887)
Agastache rugosa var. hypoleuca	(Maxim. ex Herder) Kudô	J. Coll. Sci. Imp. Univ. Tokyo 18(8): 16 (1921)
Agastache rugosa f. albiflora	Kawano	Acta Phytotax. Geobot. 17: 103 (1958)
Agastache rugosa f. hypoleuca	(Maxim. ex Herder) H.Hara	Bot. Mag. (Tokyo) 51: 53 (1937)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	lophanthus rugosus
Spanish	wrinkled giant hyssop
Spanish	purple giant hyssop
Spanish	patchouli herb
Spanish	menta coreana
Spanish	lophanthus argyi
Spanish	korean mint
Spanish	indian mint
Spanish	huo xiang
Spanish	blue licorice
Spanish	agastache formosana
Spanish	lophanthus formosanus
Spanish	agastache rugosa f. alba
Spanish	elsholtzia monostachys
Arabic	أغستاش خشن
German	koreaminze
German	koreanische minze
German	ostasiatischer riesenysop
Persian	نعنای کرهای
Japanese	カワミドリ
Korean	방아잎
Korean	방앗잎
Korean	배초향
Korean	방아
Korean	곽향
lzh	藿香
Malayalam	ഇരുവേലി
Russian	Агастахис морщинистый
Russian	Многоколосник морщинистый
Vietnamese	hoắc hương núi
Chinese	苍告
Chinese	鱼子苏
Chinese	香荆芥花
Chinese	青茎薄荷
Chinese	苏藿香
Chinese	鱼香
Chinese	兜娄婆香
Chinese	仁丹草
Chinese	藿香（土藿香）
Chinese	草菇
Chinese	紫苏草
Chinese	鸡苏
Chinese	野藿香
Chinese	藿香
Chinese	八蒿
Chinese	野苏子
Chinese	小薄荷
Chinese	山茴香
Chinese	山薄荷
Chinese	野薄荷
Chinese	薄荷
Chinese	香薷
Chinese	排香草
Chinese	把蒿
Chinese	红花小茴香
Chinese	白薄荷
Chinese	白荷
Chinese	猫巴虎
Chinese	猫巴蒿
Chinese	猫尾巴香
Chinese	水蔴叶
Chinese	杏仁花
Chinese	拉拉香
Chinese	山猫巴
Chinese	山灰香
Chinese	家茴香
Chinese	大薄荷
Chinese	大叶薄荷
Chinese	土藿香
Chinese	合香
Chinese	叶藿香

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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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Maintain seeds at a constant 10°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Manchuria
  - Tibet
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Russian Far East
  - Amur
  - Khabarovsk
  - Kuril Islands
  - Primorye

Asia-tropical click to expand
- Indo-China
  - Laos
  - Vietnam

Europe click to expand
- Eastern Europe
  - Central European Russia
- Middle Europe
  - Austria
  - Germany
- Northern Europe
  - Great Britain
  - Sweden

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000906745
UNII	U4KXI7P9Z1
Tropicos	17602232
INPN	788815
KEW	urn:lsid:ipni.org:names:444504-1
The Plant List	kew-4494
Open Tree Of Life	485528
Observations.org	141905
NCBI Taxonomy	39271
IPNI	444504-1
iNaturalist	506801
GBIF	7307327
Freebase	/m/026jh3n
EPPO	AJTRG
EOL	2893655
Elurikkus	586209
USDA GRIN	1675
Wikipedia	Agastache_rugosa
CMAUP	NPO26351
Plantarium	906
PFAF	Agastache rugosa

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_031470985.1	ASM3147098v1	Chromosome	Chungbuk National University	2023-09-15	447.6	391.65 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title

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Light-Emitting Diodes and Liquid System Affect the Caffeoylquinic Acid Derivative and Flavonoid Production and Shoot Growth of Rhaponticum carthamoides (Willd.) Iljin

Skała E, Olszewska MA, Tabaka P, Kicel A

Molecules

05-May-2024

PMCID:	PMC11085107
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05-Apr-2024

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26-Mar-2024

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Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China

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J Ethnobiol Ethnomed

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15-Feb-2024

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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 / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see	122.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-3-yl]methyl 4-hydroxybenzoate	73817269	Click to see	478.50	unknown	https://doi.org/10.1021/NP010425E
Agastenol	10073783	Click to see	478.50	unknown	https://doi.org/10.1021/NP010425E
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde	31244	Click to see	136.15	unknown	https://doi.org/10.1080/10412905.1992.9698139 https://doi.org/10.1080/10412905.2001.9699669
> 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/10.1080/10412905.1992.9698139
> Benzenoids / Phenol ethers / Anisoles
Anethole	637563	Click to see	148.20	unknown	via CMAUP database
Estragole	8815	Click to see	148.20	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514 https://doi.org/10.1080/10412905.2001.9699669 https://doi.org/10.1080/10412905.1992.9698139
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Chavicol	68148	Click to see	134.17	unknown	https://doi.org/10.1080/10412905.1992.9698139
> Benzenoids / Phenols / Methoxyphenols
Chavibetol	596375	Click to see	164.20	unknown	https://doi.org/10.1080/10412905.1992.9698139
Eugenol	3314	Click to see	164.20	unknown	https://doi.org/10.1080/10412905.1992.9698139
> Hydrocarbons / Polycyclic hydrocarbons
(-)-Isoledene	91873614	Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C	204.35	unknown	via CMAUP database
(1aR,4R,7R,7bS)-1,1,4,7-Tetramethyl-1a,2,3,4,5,6,7,7b-octahydro-1H-cyclopropa(e)azulene	15431199	Click to see	204.35	unknown	via CMAUP database
Isoledene	530426	Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C	204.35	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl 4-hydroxybenzoate	22297730	Click to see	480.50	unknown	https://doi.org/10.1021/NP010425E
Agastinol	637406	Click to see COC1=C(C=CC(=C1)CC2COC(C2COC(=O)C3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)OC)O	480.50	unknown	https://doi.org/10.1021/NP010425E
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
3-Octanol	11527	Click to see	130.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
cis-3-Hexen-1-ol	5281167	Click to see CCC=CCCO	100.16	unknown	via CMAUP database
Octan-3R-ol	445789	Click to see	130.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
trans-3-Hexen-1-ol	5284503	Click to see	100.16	unknown	via CMAUP database
> 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
Agastaquinone	177257	Click to see CC(C)C1=C(C(=O)C2=C3C=CC(=O)C(C3=CC(=C2C1=O)O)(C)C)OC	340.40	unknown	https://doi.org/10.1007/BF02976440 https://doi.org/10.1021/NP50125A011
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514 https://doi.org/10.1080/10412905.1992.9698139
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+)-	67179	Click to see	154.25	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol	325	Click to see CC(C)C1=CC=C(C=C1)CO	150.22	unknown	via CMAUP database
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	via CMAUP database
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
Thymol	6989	Click to see	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene	12223113	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
> 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	https://doi.org/10.1080/10412905.1992.9698139
(-)-Pulegone	638012	Click to see CC1CCC(=C(C)C)C(=O)C1	152.23	unknown	via CMAUP database
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1080/10412905.1992.9698139
(+)-Limonene	440917	Click to see	136.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
(L)-alpha-terpineol	443162	Click to see	154.25	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see	154.25	unknown	via CMAUP database
Carveol	7438	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1992.9698139
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514 https://doi.org/10.1080/10412905.2001.9699669
p-Menth-4(8)-en-3-one	6988	Click to see CC1CCC(=C(C)C)C(=O)C1	152.23	unknown	via CMAUP database
Pulegone	442495	Click to see CC1CCC(=C(C)C)C(=O)C1	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Amorphene	12306052	Click to see	204.35	unknown	via CMAUP database
(-)-Isocaryophyllene	5281522	Click to see	204.35	unknown	via CMAUP database
(+)-alpha-Muurolene	12306049	Click to see	204.35	unknown	via CMAUP database
(+)-beta-Caryophyllene	20831623	Click to see	204.35	unknown	via CMAUP database
(1R,4aR,8aS)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene	6432308	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	via CMAUP database
(1R,4R,5R,9S)-4,5-epoxycaryophyllan-8(13)-ene	1742211	Click to see	220.35	unknown	via CMAUP database
(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/10.1080/10412905.1992.9698139
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene	5322111	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(5R)-3,8-dimethyl-5-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene	91748288	Click to see	204.35	unknown	via CMAUP database
(Z,E)-alpha-Farnesene	5362889	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	via CMAUP database
(Z)-caryophyllene	6429301	Click to see	204.35	unknown	via CMAUP database
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene	101708	Click to see	204.35	unknown	via CMAUP database
3,7-Dimethyl-4-(propan-2-yl)-3a,3b,4,5,6,7-hexahydro-1H-cyclopenta(1,3)cyclopropa(1,2)benzene	86609	Click to see	204.35	unknown	via CMAUP database
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene	324224	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)-	6604672	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane	539857	Click to see	238.37	unknown	https://doi.org/10.1080/10412905.1992.9698139
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1992.9698139
alpha-Multijugenol	70566040	Click to see CC1=CCC2C(CC2(C)C)C(=C)CCC1O	220.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
beta-Bourbonene	62566	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
Cadin-4-en-10-ol	519662	Click to see	222.37	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	via CMAUP database
CID 14038847	14038847	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
delta-Amorphene	12306059	Click to see	204.35	unknown	via CMAUP database
Elixene	94254	Click to see	204.35	unknown	via CMAUP database
Farnesene	5281516	Click to see	204.35	unknown	via CMAUP database
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
Npc16157	13240188	Click to see	220.35	unknown	via CMAUP database
Npc57877	6431302	Click to see	222.37	unknown	via CMAUP database
Npc91574	12306054	Click to see	204.35	unknown	via CMAUP database
Oplopanone	10466745	Click to see	238.37	unknown	https://doi.org/10.1080/10412905.1992.9698139
tau-Muurolol	6432221	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(+)-Aromadendrene	11095734	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	91746456	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
(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/10.1080/10412905.1992.9698139
(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/10.1080/10412905.1992.9698139
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))-	91354	Click to see	204.35	unknown	via CMAUP database
beta-Diploalbicene	177445	Click to see	204.35	unknown	via CMAUP database
Npc123229	6432543	Click to see	222.37	unknown	via CMAUP database
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
Viridiflorol	11996452	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene	5315347	Click to see	204.35	unknown	via CMAUP database
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see	204.35	unknown	via CMAUP database
(1S,2E,6E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	13894533	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
Bicyclogermacrene	13894537	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
trans-Bicyclogermacradiene	11820258	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	via CMAUP database
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-	9859094	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(+)-Germacrene D	24771782	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(1E)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	74764030	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(1Z)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	92003564	Click to see	204.35	unknown	via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	49796490	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(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/10.1080/10412905.1992.9698139
1-Methyl-5-methylene-8-(1-methylethyl)-1,6-cyclodecadiene	6436582	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-	5373727	Click to see	204.35	unknown	via CMAUP database
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	via CMAUP database
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1992.9698139
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin	91472	Click to see	426.70	unknown	via CMAUP database
Maslinic Acid	73659	Click to see	472.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
Oleanolic aldehyde	10321055	Click to see	440.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
1-Hexen-3-yl acetate	118262	Click to see CCCC(C=C)OC(=O)C	142.20	unknown	https://doi.org/10.1080/10412905.1992.9698139
1-Octen-3-yl acetate	17121	Click to see	170.25	unknown	https://doi.org/10.1080/10412905.1992.9698139
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Jasmone	1549018	Click to see	164.24	unknown	https://doi.org/10.1080/10412905.1992.9698139
trans-Jasmone	1549019	Click to see	164.24	unknown	https://doi.org/10.1080/10412905.1992.9698139
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone	246728	Click to see CCCCCC(=O)CC	128.21	unknown	https://doi.org/10.1248/YAKUSHI1947.90.12_1514
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Dihydroactinidiolide	6432173	Click to see	180.24	unknown	https://doi.org/10.1080/10412905.1992.9698139
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(4-Methoxyphenyl)prop-2-enal	230995	Click to see	162.18	unknown	https://doi.org/10.1080/10412905.1992.9698139
4-Methoxycinnamaldehyde	641294	Click to see COC1=CC=C(C=C1)C=CC=O	162.18	unknown	https://doi.org/10.1080/10412905.1992.9698139
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	via CMAUP database
Rosmarinic Acid	5281792	Click to see	360.30	unknown	https://doi.org/10.1007/BF02979163
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Morin	5281670	Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	302.23	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside	5320861	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	via CMAUP database
Quercitrin	5280459	Click to see	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl] acetate	5318496	Click to see	488.40	unknown	https://doi.org/10.1248/CPB.29.1777
[4,5-Dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl] acetate	73981625	Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)CO)O)O	488.40	unknown	https://doi.org/10.1248/CPB.29.1777
5-Hydroxy-2-(4-methoxyphenyl)-7-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one	5291487	Click to see	446.40	unknown	https://doi.org/10.1016/S0014-5793(01)02379-1
Agastachoside	5316761	Click to see	488.40	unknown	https://doi.org/10.1248/CPB.29.1777
bis[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl] propanedioate	11968428	Click to see	960.80	unknown	https://doi.org/10.1248/CPB.29.1777
Bis[[3,4,5-trihydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl] propanedioate	73157035	Click to see	960.80	unknown	https://doi.org/10.1248/CPB.29.1777
Tilianin	5321954	Click to see	446.40	unknown	https://doi.org/10.1248/CPB.29.1777 https://doi.org/10.1016/S0014-5793(01)02379-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see	284.26	unknown	https://doi.org/10.1248/CPB.29.1777
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pachypodol	5281677	Click to see	344.30	unknown	via CMAUP database

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Agastache rugosa

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