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.

Verbena officinalis, commonly known as vervain, has been used for centuries in European folk medicine. Among German healers, dried leaves and stems were brewed into a mild tea to soothe stomach upset and relieve colds, as recorded in Deutsche Arzneimittel, 1885. In the Mediterranean, especially Italy and Spain, the same infusion was taken as a tonic for fatigue and as a poultice of crushed roots to treat minor wounds, according to Smith, 1978. Cherokee tradition also notes a decoction of the leaves for nervousness and a macerated tincture for urinary tract infections, documented by Brown, 1995.

To make a simple vervain tea, combine 5 g of dried leaves and stems with 250 ml of boiling water. Let steep for 10 minutes, then strain. Drink 2–3 cups per day, preferably after meals. If you are pregnant or nursing, avoid this tea because vervain contains compounds that may stimulate uterine contractions. For a stronger effect, a 1:5 ethanol tincture can be prepared by soaking 30 g of fresh leaves in 150 ml of 70 % alcohol for 4 weeks, shaking daily, then filtering.

The therapeutic properties of vervain are largely attributed to its flavonoids, such as luteolin and apigenin, and the iridoid verbascoside, which have documented anti‑inflammatory and anxiolytic activity. The essential oil contains verbenone and camphor, compounds that contribute to its aromatic profile and mild antiseptic action. These constituents have been isolated in several phytochemical studies and align with the plant’s traditional uses for digestive and nervous disorders.

Recent laboratory work confirms vervain’s anti‑inflammatory and mild sedative effects, supporting its continued use in herbal teas and tinctures. Commercially available vervain products are sold in health‑food stores and online, and the plant remains a staple in contemporary herbal practice, bridging centuries of tradition with modern wellness.

General Uses Top

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Common products:
Verbena officinalis is cultivated for two principal non‑medicinal markets. The aerial parts are processed to obtain a pale yellow essential oil that is sold under the name “Verbena oil” for fragrance applications. The plant is also produced as an ornamental herb by nurseries, offered for garden borders, wild‑flower mixes, and as a nectar‑source plant for pollinators.

Food and beverages (non‑medicinal):
The dried aerial parts and the essential oil are used as flavoring agents in alcoholic beverages. French liqueurs such as “Verveine du Velay,” “Verveine de la Drôme,” and “Verveine du Velay Périgord” employ Verbena officinalis (commonly called verveine) to impart a characteristic citrus‑herbal note. The herb also appears in small quantities in bitter aperitifs and craft bitters as a flavor‑enhancing component. No health claims are associated with these uses.

Fragrance and cosmetics:
The essential oil is incorporated into perfumes, soaps, shampoos, and other personal‑care products for its bright, lemon‑like aroma. Its use as a top‑note fragrance in formulations is documented in market listings by aroma‑chemical suppliers (e.g., Mountain Rose Herbs, Lebermuth) that specify the botanical source as Verbena officinalis.

Properties relevant to use:
The oil is obtained by steam distillation of the fresh or dried herb, with yields typically below 1 % of dry weight. Analysis of the oil shows citral (neral + geranial) as the major constituent, usually 30–40 % of the oil, accompanied by geraniol, linalool, limonene, myrcene, and α‑pinene. These monoterpenes provide a strong citrus‑herbal odor profile that is valued in perfumery and flavor‑fragrance applications.

Standards and regulation:
International standards for essential oils (ISO 3215 – determination of water content by Karl Fischer method; ISO 21063 – packaging, labeling and identification) apply to verbena oil. In the European Union, the essential oil is listed as a natural flavoring substance under Regulation (EC) No 1334/2008, which permits its use in food flavoring provided the oil meets purity criteria for natural flavorings. The herb and its extracts are also covered by the EU’s General Food Law regarding the use of plant‑based flavoring substances.

Sustainability and sourcing:
Commercial verbena oil is produced mainly in Mediterranean herb farms in France, Spain, and Italy. Cultivation relies on field‑grown perennials harvested at flowering, with organic certification increasingly common. Wild harvesting still occurs in some regions, but conservation guidelines recommend sourcing from cultivated material to prevent over‑exploitation of native populations.

Synonyms Top

Scientific name	Authority	First published in
Verbena adulterina	Hausskn. ex Nyman	Consp. Fl. Eur. Suppl. 2(1): 245. 1889 [1-15 Dec 1889]
Verbena spicata	Gilib.	Fl. Lit. Inch. 1: 92 (1782)
Verbena urticifolia var. riparia	(Raf. ex Small & A.Heller) Britton	Mem. Torrey Bot. Club 5: 276. 1894
Vitex adulterina	Hausskn.	Mitth. Thüring. Bot. Vereins n.s., x. 65 (1897), hybr.
Verbena officinalis var. ramosa	H.Lév.	Repert. Spec. Nov. Regni Veg. 10: 440. 1912
Verbena officinalis var. prostrata	Gren. & Godr.	Fl. France 2: 718. 1853
Verbena officinalis var. spuria	(L.) Hook.	Compan. Bot. Mag. 1: 176. 1836
Verbena officinalis var. grandiflora	Hausskn.	Mitth. Thüring. Bot. Vereins n.s., 10: 65. 1897

Common names Top

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Filter by language:

Language	Common/alternative name
English	herb of the cross
English	vervain
Spanish	hierba de santa isabel
Spanish	hierba de la verbena
Spanish	verbana
Spanish	yerba sagrada
ab	Адәыҳәымсаг
Arabic	نبتة الفيربينا
Arabic	رعى الحمام
Arabic	رجل الحمام
Arabic	رعي الحمام الطبي
Azerbaijani	dərman minaçiçəyi
azb	مینچیچک
Belarusian	Вербена лекавая
Bulgarian	върбинка
Catalan	berbena
Czech	sporýš lékařský
Welsh	y ferfain
Danish	lægejernurt
Danish	læge-jernurt
German	echtes eisenkraut
German	wunschkraut
German	taubenkraut
German	sagenkraut
German	katzenblutkraut
German	gewöhnliches eisenkraut
German	eisenkraut
Esperanto	oficina verbeno
Estonian	harilik raudürt
Basque	berbena
Persian	وربنا آفیسینالیس
Finnish	rohtorautayrtti
Finnish	rohtoverbena
French	verveine sauvage
French	verveine officinale
French	veine de vénus
French	herbe sacrée
French	herbe aux sorcières
frr	echt iisenkrüüs
Galician	verxebán
Manx	vervine
Upper Sorbian	prawa twjerdźenka
Hungarian	közönséges vasfű
Armenian	Աղավնիճ դեղատու
Japanese	バベンソウ
Japanese	クマツヅラ
Kazakh	Дәрілік нарқайсар
Korean	말초리풀
Korean	마편초
lb	eisekraut
lb	werbeen
lb	verveine
lmo	erba de san giuann
Lithuanian	vaistinė verbena
Macedonian	обична врбинка
Macedonian	врбинка
mt	buqexrem
Dutch	ijzerkruid
Dutch	ijzerhard
Polish	werbena pospolita
Polish	werbena lekarska
Romanian	verbina comună
Romanian	verbină
Romanian	spornic
Romanian	sporiș
Romanian	sporici
Russian	Вербена лекарственная
Kinyarwanda	umugosora
Slovak	železník lekársky
Slovenian	navadni sporiš
Swedish	järnört
Ukrainian	Вербена лікарська
Uzbek	tizimgul
Chinese	兔子草
Chinese	透骨草
Chinese	土马鞭;风须草
Chinese	鐵馬鞭
Chinese	馬鞭草
Chinese	马鞭草
Chinese	马鞭稍
Chinese	土马鞭
Chinese	粘身蓝被
Chinese	蛤蟆裸
Chinese	蜻蜓草
Chinese	蜻蜓饭
Chinese	铁马鞭
Chinese	风须草
Chinese	马鞭子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Verbena officinalis var. africana	(R.Fern. & Verdc.) Munir	J. Adelaide Bot. Gard. 20: 82 (2002)
Verbena officinalis var. officinalis		Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Macaronesia
  - Azores
  - Canary Islands
  - Cape Verde
  - Madeira
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
  - Western Sahara
- South Tropical Africa
  - Zambia
  - Zimbabwe
- Southern Africa
  - Free State
  - Kwazulu-Natal
  - Northern Provinces
- West Tropical Africa
  - Mauritania
  - Niger
- West-central Tropical Africa
  - Rwanda
  - Zaïre

Antarctica click to expand
- Subantarctic Islands
  - Amsterdam-St.Paul Islands
  - Tristan Da Cunha

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan
- Middle Asia
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Philippines

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - South Australia
  - Tasmania
  - Victoria
  - Western Australia
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Mexico
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
- North-central U.S.A.
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Massachusetts
  - Michigan
  - New Jersey
  - New York
  - Pennsylvania
  - Rhode Island
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Oregon
  - Washington
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Delaware
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - Arizona
  - California

Pacific click to expand
- Southwestern Pacific
  - New Caledonia
  - Niue

Southern America click to expand
- Brazil
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Bermuda
  - Cuba
  - Dominican Republic
  - Haiti
- Central America
  - Guatemala
- Southern South America
  - Chile Central
- Western South America
  - Bolivia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000332143
UNII	QT8A71T9BM
Florida Plant Atlas	3665
Flora of Alabama	3696
USDA Plants	VEOF
Tropicos	33700019
INPN	128754
Flora of Italy	4389
KEW	urn:lsid:ipni.org:names:330554-2
The Plant List	kew-212527
Open Tree Of Life	472462
Observations.org	7614
NCBI Taxonomy	79772
NBN Atlas	NBNSYS0000004191
Nature Serve	2.160656
IPNI	330554-2
iNaturalist	56163
GBIF	2925529
Freebase	/m/08yvy3
EPPO	VEBOF
EOL	579851
Calflora (Californian flora)	9424
USDA GRIN	41164
Wikipedia	Verbena_officinalis
CMAUP	NPO2838

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_958496215.1	daVerOffi1.1	Chromosome	WELLCOME SANGER INSTITUTE	2023-07-18	27	275.80 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

Exploring the Role of Apigenin in Neuroinflammation: Insights and Implications

Charrière K, Schneider V, Perrignon-Sommet M, Lizard G, Benani A, Jacquin-Piques A, Vejux A

Int J Mol Sci

06-May-2024

PMCID:	PMC11084463
doi:	10.3390/ijms25095041
PMID:	38732259

Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia

Seraw E, Melkamu Y, Masresha G

J Ethnobiol Ethnomed

17-Apr-2024

PMCID:	PMC11025143
doi:	10.1186/s13002-024-00678-9
PMID:	38632559

Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco

Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M

BMC Complement Med Ther

15-Apr-2024

PMCID:	PMC11017650
doi:	10.1186/s12906-024-04468-4
PMID:	38622669

Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential

Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR

Pharmaceutics

25-Mar-2024

PMCID:	PMC11054966
doi:	10.3390/pharmaceutics16040454
PMID:	38675115

Neuroprotective Effects of Aucubin against Cerebral Ischemia and Ischemia Injury through the Inhibition of the TLR4/NF-κB Inflammatory Signaling Pathway in Gerbils

Park JH, Lee TK, Kim DW, Ahn JH, Shin MC, Cho JH, Won MH, Kang IJ

Int J Mol Sci

19-Mar-2024

PMCID:	PMC10970631
doi:	10.3390/ijms25063461
PMID:	38542434

Uncovering the Power of GPR18 Signalling: How RvD2 and Other Ligands Could Have the Potential to Modulate and Resolve Inflammation in Various Health Disorders

Honkisz-Orzechowska E, Łażewska D, Baran G, Kieć-Kononowicz K

Molecules

12-Mar-2024

PMCID:	PMC10976181
doi:	10.3390/molecules29061258
PMID:	38542895

Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy)

Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F

J Ethnobiol Ethnomed

12-Mar-2024

PMCID:	PMC10936038
doi:	10.1186/s13002-024-00664-1
PMID:	38475780

Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia

Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A

J Ethnobiol Ethnomed

09-Mar-2024

PMCID:	PMC10924356
doi:	10.1186/s13002-024-00665-0
PMID:	38461267

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

The additive effect of herbal medicines on lifestyle modification in the treatment of non-alcoholic fatty liver disease: a systematic review and meta-analysis

Kim MH, Ahn S, Hur N, Oh SY, Son CG

Front Pharmacol

23-Feb-2024

PMCID:	PMC10920213
doi:	10.3389/fphar.2024.1362391
PMID:	38464716

Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia

Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A

J Ethnobiol Ethnomed

22-Feb-2024

PMCID:	PMC10885532
doi:	10.1186/s13002-024-00651-6
PMID:	38389077

Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches

Mazzei R, Genovese C, Magariello A, Patitucci A, Russo G, Tagarelli G

Plants (Basel)

22-Feb-2024

PMCID:	PMC10935160
doi:	10.3390/plants13050589
PMID:	38475436

Revisiting luteolin: An updated review on its anticancer potential

Rauf A, Wilairatana P, Joshi PB, Ahmad Z, Olatunde A, Hafeez N, Hemeg HA, Mubarak MS

Heliyon

20-Feb-2024

PMCID:	PMC10918152
doi:	10.1016/j.heliyon.2024.e26701
PMID:	38455556

A review of natural products targeting tumor immune microenvironments for the treatment of lung cancer

Yao P, Liang S, Liu Z, Xu C

Front Immunol

01-Feb-2024

PMCID:	PMC10867126
doi:	10.3389/fimmu.2024.1343316
PMID:	38361933

The Antimicrobial Potential of the Hop (Humulus lupulus L.) Extract against Staphylococcus aureus and Oral Streptococci

Khaliullina A, Kolesnikova A, Khairullina L, Morgatskaya O, Shakirova D, Patov S, Nekrasova P, Bogachev M, Kurkin V, Trizna E, Kayumov A

Pharmaceuticals (Basel)

27-Jan-2024

PMCID:	PMC10893079
doi:	10.3390/ph17020162
PMID:	38399377

Phytochemical Profile Top

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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 / Catechols
4-Dodecylbenzene-1,2-diol	15667771	Click to see CCCCCCCCCCCCC1=CC(=C(C=C1)O)O	278.40	unknown	https://doi.org/10.1007/S10600-011-9920-6
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tridecane	12388	Click to see	184.36	unknown	https://doi.org/10.1007/S10600-011-9920-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
2-((2R)-2-(Acetyloxy)tridecyl)-6-methoxy-2,5-cyclohexadiene-1,4-dione	46191017	Click to see	378.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Tetracontanol	10438171	Click to see	579.10	unknown	https://doi.org/10.1007/S10600-011-9920-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-Camphor	230921	Click to see	152.23	unknown	via CMAUP database
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol	88298	Click to see CC1=CC(C2CC1C2(C)C)O	152.23	unknown	via CMAUP database
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	via CMAUP database
Camphor	2537	Click to see	152.23	unknown	via CMAUP database
Camphor, (-)-	444294	Click to see	152.23	unknown	via CMAUP database
Camphor, (1S)-	10050	Click to see	152.23	unknown	via CMAUP database
D-Camphor	159055	Click to see	152.23	unknown	via CMAUP database
Npc54264	9543187	Click to see	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2-Methyl-5-(6-methylhept-5-en-2-yl)cyclohexa-1,3-diene	521253	Click to see	204.35	unknown	via CMAUP database
Alpha-Zingiberene	11127403	Click to see	204.35	unknown	via CMAUP database
delta-Curcumene	57386731	Click to see	204.35	unknown	via CMAUP database
Zingiberene	92776	Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(-)-Nootkatone	7567181	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C	218.33	unknown	via CMAUP database
Nootkatol	182645	Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O	220.35	unknown	via CMAUP database
Nootkatone	1268142	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C	218.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S)-1-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-7beta-methylcyclopenta[c]pyran-4-carbaldehyde	4490432	Click to see	344.36	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
(2S,3R,4S,5S,6R)-2-[[(1S,4aS,7S,7aR)-4-(hydroxymethyl)-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163027189	Click to see CC1CCC2C1C(OC=C2CO)OC3C(C(C(C(O3)CO)O)O)O	346.37	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
2-(Hydroxymethyl)-6-[[4-(hydroxymethyl)-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl]oxy]oxane-3,4,5-triol	14193873	Click to see CC1CCC2C1C(OC=C2CO)OC3C(C(C(C(O3)CO)O)O)O	346.37	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
2-[(4,7-Dimethyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	4490435	Click to see	330.37	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
2-[7-methyl-5-oxo-1-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4a,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-4-yl]acetic acid	5316746	Click to see	390.40	unknown	via CMAUP database
8-Epideoxyloganin	443331	Click to see	374.40	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
Aucubin	91458	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	https://doi.org/10.1007/S10600-011-9920-6
Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-7-methyl-, methyl ester, (1S,4aS,7S,7aR)-	440906	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(00)86964-2 https://doi.org/10.1016/0031-9422(89)85017-4
Deoxyloganic acid	443322	Click to see	360.36	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
Deoxyloganic acid	4490284	Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O	360.36	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
Dihydrocornin	14193887	Click to see	390.40	unknown	https://doi.org/10.1016/0031-9422(89)85017-4 https://doi.org/10.1016/0031-9422(83)80179-4 https://doi.org/10.1016/S0031-9422(00)86964-2
Hastatoside	92043450	Click to see	404.40	unknown	https://doi.org/10.1016/0031-9422(89)85017-4 https://doi.org/10.1007/BF02496313 https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1002/1099-1565(200011/12)11:6<351::AID-PCA544>3.0.CO;2-S https://doi.org/10.1016/S0031-9422(00)81424-7 https://doi.org/10.1007/S10600-011-9920-6
Iridodial glucoside	443351	Click to see	330.37	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
Iridotrial glucoside	443335	Click to see CC1CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O	344.36	unknown	https://doi.org/10.1016/0031-9422(89)85017-4
methyl (1S,4aR,7aR)-4a,6-dihydroxy-7-methyl-5-oxo-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,7a-dihydrocyclopenta[c]pyran-4-carboxylate	101875572	Click to see	418.30	unknown	via CMAUP database
methyl (4aS,7S,7aR)-7-methyl-5-oxo-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate	17751048	Click to see	388.40	unknown	via CMAUP database
Methyl 1-(hexopyranosyloxy)-4a-hydroxy-7-methyl-5-oxo-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	599030	Click to see CC1CC(=O)C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	404.40	unknown	https://doi.org/10.1016/0031-9422(89)85017-4 https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1002/1099-1565(200011/12)11:6<351::AID-PCA544>3.0.CO;2-S https://doi.org/10.1007/S10600-011-9920-6
Methyl 5-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	14193886	Click to see	390.40	unknown	https://doi.org/10.1016/S0031-9422(00)86964-2 https://doi.org/10.1016/0031-9422(89)85017-4
Methyl 7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	5253702	Click to see CC1CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O	374.40	unknown	https://doi.org/10.1016/S0031-9422(00)86964-2 https://doi.org/10.1016/0031-9422(89)85017-4
methyl 7-methyl-5-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate	273110	Click to see	388.40	unknown	https://doi.org/10.1016/S0040-4039(01)95971-4 https://doi.org/10.1016/0031-9422(89)85017-4 https://doi.org/10.1002/HLCA.19460290624 https://doi.org/10.1007/S10600-011-9920-6
Verbenalin	73467	Click to see	388.40	unknown	https://doi.org/10.1016/S0031-9422(00)81424-7 https://doi.org/10.1016/S0040-4039(01)95971-4 https://doi.org/10.1002/1099-1565(200011/12)11:6<351::AID-PCA544>3.0.CO;2-S https://doi.org/10.1007/S10600-011-9920-6 https://doi.org/10.1016/0031-9422(89)85017-4 https://doi.org/10.1002/HLCA.19460290624 https://doi.org/10.1007/BF02496313 https://doi.org/10.1016/S0944-7113(98)80043-3 https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1016/0031-9422(83)80179-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(97)01004-2 https://doi.org/10.1002/1099-1565(200011/12)11:6<351::AID-PCA544>3.0.CO;2-S https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1007/S10600-011-9920-6
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45358157	Click to see	456.70	unknown	via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45483617	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	45483610	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	14136880	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(97)01004-2 https://doi.org/10.1007/S10600-011-9920-6
10-Hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	258538	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(97)01004-2 https://doi.org/10.1007/S10600-011-9920-6
24-Hydroxy-3-Epi-Ursolic Acid	14136878	Click to see	472.70	unknown	https://doi.org/10.1007/S10600-011-9920-6 https://doi.org/10.1016/S0031-9422(97)01004-2
3Alpha-Hydroxyurs-12-En-28-Oic Acid	7163177	Click to see	456.70	unknown	https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G
Deoxyoleanolic acid	619168	Click to see	440.70	unknown	https://doi.org/10.1007/S10600-011-9920-6
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1007/S10600-011-9920-6
Olean-12-en-28-oic acid	14208454	Click to see	440.70	unknown	https://doi.org/10.1007/S10600-011-9920-6
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G
Scutellaric Acid	12302571	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(97)01004-2 https://doi.org/10.1007/S10600-011-9920-6
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1007/S10600-011-9920-6 https://doi.org/10.1016/S0031-9422(97)01004-2
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1016/S0031-9422(97)01004-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
5-(5,6-Dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol	633877	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	https://doi.org/10.1007/S10600-011-9920-6
Ergosterol peroxide	5351516	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	https://doi.org/10.1007/S10600-011-9920-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1007/S10600-011-9920-6
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1007/S10600-011-9920-6
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1007/S10600-011-9920-6
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1007/S10600-011-9920-6
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1007/S10600-011-9920-6 https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G
> Nucleosides, nucleotides, and analogues / Purine nucleosides
(2R,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol	54732806	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,2R,5S,6S)-3-(3-methylbut-2-enyl)-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol	101967074	Click to see	196.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[3,5-Dihydroxy-2-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol	73816059	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)OC)CO)O)O)O)O	476.50	unknown	https://doi.org/10.1007/S10600-011-9920-6
9-Hydroxysemperoside	101098710	Click to see CC1CC2C3C1(COC(C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O)O	376.36	unknown	via CMAUP database
Cistanoside E	21632979	Click to see	476.50	unknown	https://doi.org/10.1007/S10600-011-9920-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3R,4R,5R,6S)-4-acetyloxy-2-(acetyloxymethyl)-6-[[(3R,4S,4aR)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-5-hydroxyoxan-3-yl] 3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	162931102	Click to see	724.70	unknown	https://doi.org/10.1080/10286020.2010.489820
[(2R,3S,4S,5R,6S)-5-acetyloxy-6-[[(3R,4S,4aR)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-3,4-dihydroxyoxan-2-yl]methyl 2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	162879175	Click to see CC(=O)OC1C(C(C(OC1OC2C(C3CCOC(=O)C3=CO2)C=C)COC(=O)C4=C(C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O	698.60	unknown	https://doi.org/10.1080/10286020.2010.489820
[4-acetyloxy-2-(acetyloxymethyl)-6-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-5-hydroxyoxan-3-yl] 3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	162931101	Click to see	724.70	unknown	https://doi.org/10.1080/10286020.2010.489820
[5-acetyloxy-6-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-3,4-dihydroxyoxan-2-yl]methyl 2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate	162879174	Click to see	698.60	unknown	https://doi.org/10.1080/10286020.2010.489820
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Oxyphyllenone A	10262534	Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O	210.27	unknown	via CMAUP database
Oxyphyllenone B	44310512	Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O	210.27	unknown	via CMAUP database
Panepoxydione	11948666	Click to see CC(=CC(C1=CC(=O)C2C(C1=O)O2)O)C	208.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3R,4S)-6-methoxy-2,2-dimethyl-3,4-dihydrochromene-3,4-diol	11206858	Click to see	224.25	unknown	via CMAUP database
(3S,4S)-6-methoxy-2,2-dimethyl-3,4-dihydrochromene-3,4-diol	11310639	Click to see CC1(C(C(C2=C(O1)C=CC(=C2)OC)O)O)C	224.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
Panepophenanthrin	10432257	Click to see CC1(C2C=C3C(C4C2(C(O1)(C5C(C4O)O5)O)C=CC(C)(C)O)C(C6C(C3=O)O6)O)C	420.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole	2758	Click to see	154.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1S,3E,4S,5S,6S)-4,5-dihydroxy-3-(3-methylbut-2-enylidene)-7-oxabicyclo[4.1.0]heptan-2-one	101306865	Click to see	210.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Verbeofflin I	101875571	Click to see	240.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	73323377	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1007/S10600-011-9920-6
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside	132274946	Click to see	624.60	unknown	https://doi.org/10.1007/BF02496313 https://doi.org/10.1002/1099-1565(200011/12)11:6<351::AID-PCA544>3.0.CO;2-S https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1021/NP50035A033
Acteoside;Kusaginin;TJC160	354009	Click to see	624.60	unknown	https://doi.org/10.1002/ARDP.19863190306 https://doi.org/10.1007/S10600-011-9920-6
Isoacteoside	6476333	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1007/S10600-011-9920-6
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1002/1099-1565(200011/12)11:6<351::AID-PCA544>3.0.CO;2-S https://doi.org/10.1365/S10337-004-0359-9 https://doi.org/10.1007/S10600-011-9920-6 https://doi.org/10.1002/ARDP.19863190306 https://doi.org/10.1002/1099-1573(200009)14:6<463::AID-PTR611>3.0.CO;2-G https://doi.org/10.1021/NP50035A033
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one	6440365	Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O	310.40	unknown	via CMAUP database
Yakuchinone A	133145	Click to see	312.40	unknown	via CMAUP database
> 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/10.1007/S10600-011-9920-6
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/10.1007/S10600-011-9920-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see	316.26	unknown	via CMAUP database
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin(1-)	49852298	Click to see	447.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
8-beta-D-Glucopyranosyl-3',4',5,7-tetrahydroxyflavone	44257907	Click to see	448.40	unknown	via CMAUP database
Vitexin-7-olate	49791957	Click to see	431.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Clerodendrin	5488004	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O	622.50	unknown	https://doi.org/10.1365/S10337-004-0359-9
Luteolin 7-diglucuronide	5282153	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O	638.50	unknown	https://doi.org/10.1055/S-2006-958152
Luteolin 7-O-diglucuronide	157009729	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O)O)O)O	638.50	unknown	https://doi.org/10.1365/S10337-004-0359-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44258067	Click to see	448.40	unknown	https://doi.org/10.1016/S0305-1978(99)00114-3
7-[(2S,4S,5S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one	44258083	Click to see	594.50	unknown	https://doi.org/10.1016/S0305-1978(99)00114-3
7-[(2S,4S,5S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one	44258230	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O	608.50	unknown	https://doi.org/10.1016/S0305-1978(99)00114-3
7-[(3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one	25246223	Click to see	594.50	unknown	https://doi.org/10.1016/S0305-1978(99)00114-3
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1016/S0305-1978(99)00114-3
Chrysoeriol-7-O-beta-D-glucopyranoside	13871880	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0305-1978(99)00114-3
Hesperetin7-O-glucoside	11155451	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0305-1978(99)00114-3
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=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/10.1016/S0305-1978(99)00114-3
Luteolin-7-O-galactoside	5488493	Click to see C1=CC(=C(C=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/10.1016/S0305-1978(99)00114-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	https://doi.org/10.1007/S10600-011-9920-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4'-Hydroxywogonin	5322078	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
6,9-Dihydroxy-5-methoxy-16-oxa-24-azapentacyclo[15.7.1.18,12.02,7.019,24]hexacosa-2(7),3,5,8,10,12(26)-hexaen-15-one	5316747	Click to see	423.50	unknown	via CMAUP database

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Verbena officinalis

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