Language	Common/alternative name
English	spotted beebalm
Arabic	نعنع الفرس
German	pferdeminze
French	monarde punctuée
French	monarde ponctuée
nv	azeeʼ ndootʼeezhí
Russian	Монарда точечная
Ukrainian	Монарда плямиста
Chinese	斑点美国薄荷
Chinese	斑點美國薄荷

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Monarda punctata var. arkansana	(E.M.McClint. & Epling) Shinners	Field & Lab. 21: 90 (1953)
Monarda punctata var. coryi	(E.M.McClint. & Epling) Shinners	Field & Lab. 21: 90 (1953)
Monarda punctata var. intermedia	(E.M.McClint. & Epling) Waterf.	Rhodora 52: 38 (1950)
Monarda punctata var. lasiodonta	A.Gray	Syn. Fl. N. Amer. 2(1): 375 (1878)
Monarda punctata var. occidentalis	E.J.Palmer & Steyerm.	Ann. Missouri Bot. Gard. 22: 634 (1935)
Monarda punctata var. punctata		Unknown
Monarda punctata var. villicaulis	(Pennell) Shinners	Field & Lab. 21: 90 (1953)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

Northern America click to expand
- Mexico
  - Mexico Northeast
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Oklahoma
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Massachusetts
  - Michigan
  - New Jersey
  - New York
  - Pennsylvania
  - Vermont
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000245372
UNII	9Y0285U3TC
Florida Plant Atlas	3478
Flora of Alabama	2431
Canadensys	6421
USDA Plants	MOPU
Tropicos	17600171
INPN	160477
KEW	urn:lsid:ipni.org:names:452072-1
The Plant List	kew-129232
Missouri Botanical Garden	281405
Open Tree Of Life	514020
NCBI Taxonomy	182387
Nature Serve	2.149930
IPNI	452072-1
iNaturalist	118776
GBIF	5341413
Freebase	/m/0660fp8
WisFlora	4272
EPPO	MOAPU
EOL	579702
USDA GRIN	24538
Wikipedia	Monarda_punctata

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

Field Evaluation of Cotton Expressing Mpp51Aa2 as a Management Tool for Cotton Fleahoppers, Pseudatomoscelis seriatus (Reuter)

Arthur BP, Suh CP, McKnight BM, Parajulee MN, Yang F, Kerns DL

Toxins (Basel)

05-Nov-2023

PMCID:	PMC10675519
doi:	10.3390/toxins15110644
PMID:	37999507

The mint versus Covid hypothesis

Buck CB

Med Hypotheses

15-Mar-2023

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

Intracellular production of reactive oxygen species and a DAF-FM-related compound in Aspergillus fumigatus in response to antifungal agent exposure

Oiki S, Nasuno R, Urayama SI, Takagi H, Hagiwara D

Sci Rep

06-Aug-2022

PMCID:	PMC9357077
doi:	10.1038/s41598-022-17462-y
PMID:	35933435

Plant community re-organization and increased productivity due to multi-year nutrient enrichment of a coastal grassland

Brown JK, Moulton A, Zinnert JC

PLoS One

28-Jul-2022

PMCID:	PMC9333261
doi:	10.1371/journal.pone.0270798
PMID:	35901080

Effectiveness of the Influence of Selected Essential Oils on the Growth of Parasitic Fusarium Isolated from Wheat Kernels from Central Europe

Krzyśko-Łupicka T, Sokół S, Sporek M, Piekarska-Stachowiak A, Walkowiak-Lubczyk W, Sudoł A

Molecules

27-Oct-2021

PMCID:	PMC8588391
doi:	10.3390/molecules26216488
PMID:	34770893

Chromatographic profiles and antimicrobial activity of the essential oils obtained from some species and cultivars of the Mentheae tribe (Lamiaceae)

Shanaida M, Hudz N, Białoń M, Kryvtsowa M, Svydenko L, Filipska A, Paweł Wieczorek P

Saudi J Biol Sci

26-Jun-2021

PMCID:	PMC8568706
doi:	10.1016/j.sjbs.2021.06.068
PMID:	34759738

The Volatile Phytochemistry of Monarda Species Growing in South Alabama

Lawson SK, Satyal P, Setzer WN

Plants (Basel)

04-Mar-2021

PMCID:	PMC8000036
doi:	10.3390/plants10030482
PMID:	33806521

Essential Oils: Pharmaceutical Applications and Encapsulation Strategies into Lipid-Based Delivery Systems

Cimino C, Maurel OM, Musumeci T, Bonaccorso A, Drago F, Souto EM, Pignatello R, Carbone C

Pharmaceutics

03-Mar-2021

PMCID:	PMC8001530
doi:	10.3390/pharmaceutics13030327
PMID:	33802570

Are native and non‐native pollinator friendly plants equally valuable for native wild bee communities?

Seitz N, vanEngelsdorp D, Leonhardt SD

Ecol Evol

13-Oct-2020

PMCID:	PMC7713930
doi:	10.1002/ece3.6826
PMID:	33304497

An online survey of personal mosquito-repellent strategies

Moore EL, Scott MA, Rodriguez SD, Mitra S, Vulcan J, Cordova JJ, Chung HN, de Souza DL, Gonzales KK, Hansen IA

PeerJ

03-Jul-2018

PMCID:	PMC6034598
doi:	10.7717/peerj.5151
PMID:	30002979

Trap Nesting Wasps and Bees in Agriculture: A Comparison of Sown Wildflower and Fallow Plots in Florida

Campbell JW, Smithers C, Irvin A, Kimmel CB, Stanley-Stahr C, Daniels JC, Ellis JD

Insects

10-Oct-2017

PMCID:	PMC5746790
doi:	10.3390/insects8040107
PMID:	28994726

Update on Monoterpenes as Antimicrobial Agents: A Particular Focus on p-Cymene

Marchese A, Arciola CR, Barbieri R, Silva AS, Nabavi SF, Tsetegho Sokeng AJ, Izadi M, Jafari NJ, Suntar I, Daglia M, Nabavi SM

Materials (Basel)

15-Aug-2017

PMCID:	PMC5578313
doi:	10.3390/ma10080947
PMID:	28809799

Nectar sampling for prairie and oak savanna butterfly restoration

Arnold PM, Michaels HJ

Appl Plant Sci

21-Jun-2017

PMCID:	PMC5499304
doi:	10.3732/apps.1600148
PMID:	28690931

Proteoform-Specific Protein Binding of Small Molecules in Complex Matrices

Gil G, Mao P, Avula B, Ali Z, Chittiboyina AG, Khan IA, Walker LA, Wang D

ACS Chem Biol

21-Dec-2016

PMCID:	PMC5315634
doi:	10.1021/acschembio.6b01018
PMID:	28001351

In Search for Symbolic Qualities of Iron: The Metal of Life

Cabantchik ZI

Front Pharmacol

03-Aug-2016

PMCID:	PMC4971804
doi:	10.3389/fphar.2016.00220
PMID:	27536239

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 / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
2-Naphthalenecarboxylic acid, 4-(3,4-dihydroxyphenyl)-6,7-dihydroxy-, (1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethyl ester	71308208	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2=CC(=C3C=C(C(=CC3=C2)O)O)C4=CC(=C(C=C4)O)O)O)O	492.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-(3,4-Dihydroxyphenyl)-2-[4-(3,4-dihydroxyphenyl)-6,7-dihydroxy-naphthalene-2-carbonyl]oxy-propanoic acid	3013628	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2=CC(=C3C=C(C(=CC3=C2)O)O)C4=CC(=C(C=C4)O)O)O)O	492.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Thymohydroquinone	95779	Click to see CC1=CC(=C(C=C1O)C(C)C)O	166.22	unknown	https://doi.org/10.1002/JPS.3080200506
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1002/JLAC.18460580107
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-[(1S,6S)-6-hydroxy-6-methyl-3-propan-2-ylcyclohex-2-en-1-yl]oxyoxane-3,4,5-triol	162961062	Click to see CC(C)C1=CC(C(CC1)(C)O)OC2C(C(C(C(O2)CO)O)O)O	332.39	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
[(2R,3R,4R,5R,6S)-3,4,5-triacetyloxy-6-[(1S,6S)-6-hydroxy-6-methyl-3-propan-2-ylcyclohex-2-en-1-yl]oxyoxan-2-yl]methyl acetate	162866025	Click to see CC(C)C1=CC(C(CC1)(C)O)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	500.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
[3,4,5-Triacetyloxy-6-(6-hydroxy-6-methyl-3-propan-2-ylcyclohex-2-en-1-yl)oxyoxan-2-yl]methyl acetate	162866024	Click to see CC(C)C1=CC(C(CC1)(C)O)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	500.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
2-(Hydroxymethyl)-6-(6-hydroxy-6-methyl-3-propan-2-ylcyclohex-2-en-1-yl)oxyoxane-3,4,5-triol	75287644	Click to see CC(C)C1=CC(C(CC1)(C)O)OC2C(C(C(C(O2)CO)O)O)O	332.39	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-oxo-3-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[(1S,6R)-6-hydroxy-6-methyl-3-propan-2-ylcyclohex-2-en-1-yl]oxyoxan-2-yl]methoxy]propanoic acid	163040301	Click to see CC(C)C1=CC(C(CC1)(C)O)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)O	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-Oxo-3-[[3,4,5-trihydroxy-6-(6-hydroxy-6-methyl-3-propan-2-ylcyclohex-2-en-1-yl)oxyoxan-2-yl]methoxy]propanoic acid	163040300	Click to see CC(C)C1=CC(C(CC1)(C)O)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)O	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(5-isopropyl-2-methylphenoxy)tetrahydro-2H-pyran-3,4,5-triol	101419546	Click to see CC1=C(C=C(C=C1)C(C)C)OC2C(C(C(C(O2)CO)O)O)O	312.36	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)-5-propan-2-ylphenoxy]oxane-3,4,5-triol	102283453	Click to see CC(C)C1=CC(=C(C=C1)CO)OC2C(C(C(C(O2)CO)O)O)O	328.36	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
2-(beta-D-Glucopyranosyloxy)-5-allylphenol	5316750	Click to see C=CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O	312.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
2-(Hydroxymethyl)-6-[2-(hydroxymethyl)-5-propan-2-ylphenoxy]oxane-3,4,5-triol	162851389	Click to see CC(C)C1=CC(=C(C=C1)CO)OC2C(C(C(C(O2)CO)O)O)O	328.36	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-[[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-6-[(2-carboxyacetyl)oxymethyl]-4,5-dihydroxy-2-(2-methyl-5-propan-2-ylphenoxy)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid	49817854	Click to see CC1=C(C=C(C=C1)C(C)C)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)OC3C(C(C(C(O3)COC(=O)CC(=O)O)O)O)O	646.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-[[6-[6-[(2-Carboxyacetyl)oxymethyl]-4,5-dihydroxy-2-(2-methyl-5-propan-2-ylphenoxy)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid	75287642	Click to see CC1=C(C=C(C=C1)C(C)C)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)OC3C(C(C(C(O3)COC(=O)CC(=O)O)O)O)O	646.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-Hydroxychavicol 1-glucoside	78384828	Click to see C=CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O	312.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-(hydroxymethyl)-5-propan-2-ylphenoxy]oxan-2-yl]methoxy]propanoic acid	49817855	Click to see CC(C)C1=CC(=C(C=C1)CO)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)O	414.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-Oxo-3-[[3,4,5-trihydroxy-6-(2-methyl-5-propan-2-ylphenoxy)oxan-2-yl]methoxy]propanoic acid	75287641	Click to see CC1=C(C=C(C=C1)C(C)C)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)O	398.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-Oxo-3-[[3,4,5-trihydroxy-6-[2-(hydroxymethyl)-5-propan-2-ylphenoxy]oxan-2-yl]methoxy]propanoic acid	75287643	Click to see CC(C)C1=CC(=C(C=C1)CO)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)O	414.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Citrusin C	9945189	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Eugenyl glucoside	3084296	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Malonic acid 1-[1-O-(2-methyl-5-isopropylphenyl)-6-deoxy-beta-D-glucopyranose-6-yl] ester	49817853	Click to see CC1=C(C=C(C=C1)C(C)C)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)O	398.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid	639655	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid	5099	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-[4-hydroxy-3-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)phenyl]-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	102053278	Click to see CC1=CC(=C(C=C1O)C(C)C)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O	610.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	5387370	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)O)O)O	446.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3,4,5-Trihydroxy-6-[5-hydroxy-2-[4-hydroxy-3-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)phenyl]-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	162987342	Click to see CC1=CC(=C(C=C1O)C(C)C)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O	610.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Apigenin 7-glucuronide	5319484	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)O)O)O	446.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Breviscapine	6426802	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)O)O)O)O	462.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Chrysoeriol 7-glucuronide	14630700	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	476.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Chrysoeriol glucuronide	14630703	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	476.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Luteolin 7-glucuronide	5280601	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)O)O)O)O	462.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Luteolin-7-o-glucuronide	13607752	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)O)O)O)O	462.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Scutellarin	185617	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)O)O)O)O	462.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[[(3S,4R,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methoxy]-3-oxopropanoic acid	163062770	Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)(COC(=O)CC(=O)O)O	650.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
3-[[5-[4,5-Dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methoxy]-3-oxopropanoic acid	163062769	Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)(COC(=O)CC(=O)O)O	650.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one	5377847	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
7-(2-Apiosylglucosyl)apigenin	5840046	Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)(CO)O	564.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Apigenin 7-(6''-malonylglucoside)	5281602	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O	518.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Apigenin 7-O-(6-O-malonylglucoside)	5856141	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O	518.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Apigenin 7-O-glucoside	5385553	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Apiin	5280746	Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)(CO)O	564.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009
Isorhoifolin	9851181	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.08.009

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Monarda punctata

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