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.

In the Amazonian Guianas, Palikur healers prepare a leaf infusion as a gentle febrifuge and cold remedy, also bathing newborns in the same tea for comfort and recovery. Across Brazil’s Atlantic Forest and Cerrado, “hortelã do mato” leaves are simmered into a decoction for stomach pain, diarrhea, and digestive upsets, and applied as a compress for swelling and wounds. In Amazonian Ecuador, a leaf infusion is drunk for gastrointestinal complaints, while in Guatemala an aqueous decoction of the aerial parts is taken as a general tonic and to reduce fever, according to Grenand et al., 1987; Balick & Arvigo, 2009; and Mendes & Carlini, 2007. In northern Brazil, 200–400 g of fresh leaves boiled for 10–15 minutes in 1 L of water, cooled and strained, is drunk as a symptom-relieving tea in acute diarrhea and mild fevers, following Mendes & Carlini, 2007.

A practical preparation that reflects common practice is a simple leaf tea: place 10–15 g of fresh leaves (or 5–8 g dried) in 200–250 mL of just boiled water, cover and steep for 10–15 minutes, then strain and drink up to three cups per day for up to 3–5 days. For a stronger gastrointestinal aid, simmer 25 g of fresh leaves in 250–300 mL of water for 10–12 minutes, cool and drink 150–200 mL two to three times daily. A 1:5 ethanol tincture can be made by macerating 50 g of dried, chopped leaves in 250 mL of 40–50% ethanol for 2–3 weeks, shaking daily, then straining; typical adult dose is 1–2 mL three times daily. Do not use in pregnancy or lactation; avoid prolonged use in children and those with gastrointestinal ulceration. Observe for possible allergic reactions.

The leaves contain rosmarinic acid, flavonoids such as luteolin and apigenin, and caffeic acid derivatives; essential oil with α-pinene, β-caryophyllene, spathulenol, and caryophyllene oxide is also documented, with composition varying by chemotype (Rossi et al., 1997; Franco et al., 2003). The antioxidant phenolic profile likely underpins the recorded febrifuge, gastrointestinal, and wound care actions in regional traditions.

Hyptis brevipes is still cultivated in home gardens in Brazil and remains in use by communities in the Guianas and Central America, while interest persists in pharmacological studies on its anti-inflammatory and antimicrobial properties (Mendes & Carlini, 2007; Balick & Arvigo, 2009).

General Uses Top

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Common products:
The leaves of Hyptis brevipes yield an essential oil that is extracted by steam distillation. Commercial interest focuses on the oil because of its characteristic eucalyptol‑rich aroma.

Industrial and craft applications:
Laboratory studies have demonstrated that the leaf essential oil exhibits insecticidal activity against a range of stored‑product insects and mosquito larvae. The oil has been evaluated as a natural pesticide and as a component in insect‑repellent formulations for textiles, wood preservation and natural cleaning products. Its antimicrobial activity has been investigated for use in natural cleaning and disinfectant formulations.

Food and beverages (non‑medicinal):
Ethnobotanical surveys in northeastern Brazil record the use of fresh Hyptis brevipes leaves as a culinary herb. The leaves are chopped and added to fish, meat and vegetable dishes and to soups, where they impart a minty‑herbaceous flavor.

Fragrance and cosmetics:
The oil’s composition, dominated by 1,8‑cineole (typically 30–45 % w/w) together with camphor and α‑pinene, makes it suitable for use as a fragrance ingredient in soaps, detergents, cosmetic creams, scented candles and diffusers. Its scent profile is comparable to that of other eucalyptol‑rich Lamiaceae oils used in perfumery.

Properties relevant to use:
The high 1,8‑cineole content imparts a fresh, cooling aroma and contributes to the oil’s larvicidal and adulticidal activity. The presence of camphor provides a sharp, camphoraceous note and enhances insecticidal potency. The oil is a mixture of monoterpenes and sesquiterpenes, giving it moderate volatility and good solubility in alcohol, favorable traits for fragrance and pesticide formulations. Its flash point is above 70 °C, making it stable at typical processing temperatures.

Sustainability and sourcing:
Hyptis brevipes is an annual herb native to tropical America and is cultivated in Brazil, Colombia and parts of Southeast Asia for essential‑oil production. Seeds are readily harvested, and the plant tolerates a range of soils, allowing low‑input cultivation. Studies report oil yields of 0.8–1.2 % (w/w) from fresh leaves under conventional distillation. Sustainable harvesting practices, such as cutting above the basal rosette to promote regrowth and timing harvest to coincide with peak flowering to maximize oil content, are recommended to maintain field productivity.

Synonyms Top

Scientific name	Authority	First published in
Hyptis acuta	Benth.	Linnaea 6: 82 (1881)
Hyptis brevipes var. glabrior	Benth.	Prodr. 12: 107 (1848)
Hyptis brevipes var. remotidens	Briq.	Annuaire Conserv. Jard. Bot. Genève 2: 227 (1898)
Hyptis brevipes var. robusta	Loes.	Bull. Herb. Boissier 7: 573 (1899)
Hyptis brevipes var. serrata	Briq.	Annuaire Conserv. Jard. Bot. Genève 2: 227 (1898)
Hyptis brevipes var. vulgaris	Briq.	Annuaire Conserv. Jard. Bot. Genève 2: 226 (1898)
Hyptis melanosticta	Griseb.	Fl. Brit. W. I. : 488 (1862)
Hyptis radiata	Kunth	Nov. Gen. Sp. 2: 318 (1818)
Lasiocorys poggeana	Baker	Fl. Trop. Afr. 5: 470 (1900)
Leucas globulifera	Hassk.	Cat. Hort. Bot. Bogor. Alt. : 133 (1844)
Leucas poggeana	Briq.	Bot. Jahrb. Syst. 19: 193 (1894)
Mesosphaerum brevipes	Kuntze	Revis. Gen. Pl. 2: 525 (1891)
Mesosphaerum melanostictum	Kuntze	Revis. Gen. Pl. 2: 526 (1891)
Pycnanthemum subulatum	Blanco	Fl. Filip., ed. 2 : 333 (1845)
Thymus biserratus	Blanco	Fl. Filip. : 478 (1837)

Common names Top

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Filter by language:

Language	Common/alternative name
su	ki hileud
Chinese	短柄吊球草
Chinese	短柄香苦草

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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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- South Tropical Africa
  - Mozambique

Asia-temperate click to expand
- Eastern Asia
  - Nansei-shoto

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Philippines
  - Sulawesi
  - Sumatera

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Southeast
  - Mexico Southwest
- Southeastern U.S.A.
  - Florida

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Cuba
  - Jamaica
  - Trinidad-Tobago
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Suriname
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Paraguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000216512
Florida Plant Atlas	4425
Tropicos	17601971
INPN	733470
KEW	urn:lsid:ipni.org:names:447982-1
The Plant List	kew-101636
Open Tree Of Life	544475
NCBI Taxonomy	204123
IPNI	447982-1
iNaturalist	285150
GBIF	7306536
EPPO	HPYBR
EOL	2893863
USDA GRIN	448591
Wikipedia	Hyptis_brevipes
CMAUP	NPO25696

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

Simmons–Smith Cyclopropanation: A Multifaceted Synthetic Protocol toward the Synthesis of Natural Products and Drugs: A Review

Munir R, Zahoor AF, Javed S, Parveen B, Mansha A, Irfan A, Khan SG, Irfan A, Kotwica-Mojzych K, Mojzych M

Molecules

26-Jul-2023

PMCID:	PMC10420228
doi:	10.3390/molecules28155651
PMID:	37570621

Strategies for the discovery of potential anticancer agents from plants collected from Southeast Asian tropical rainforests as a case study

de Blanco EJ, Addo EM, Rakotondraibe HL, Soejarto DD, Kinghorn AD

Nat Prod Rep

19-Jul-2023

PMCID:	PMC10524867
doi:	10.1039/d2np00080f
PMID:	37194649

Endophytic species of Induratia from coffee and carqueja plants from Brazil and its potential for the biological control of toxicogenic fungi on coffee beans by means of antimicrobial volatiles

Gomes AA, Paes SA, Ferreira AP, Pinho DB, de Lourdes Cardeal Z, Menezes HC, Cardoso PG, Pereira OL

Braz J Microbiol

04-Jan-2023

PMCID:	PMC9944607
doi:	10.1007/s42770-022-00887-y
PMID:	36598751

Strategies for the synthesis of brevipolides

Kurniawan YD, Rosyidah A

Beilstein J Org Chem

14-Sep-2021

PMCID:	PMC8450957
doi:	10.3762/bjoc.17.157
PMID:	34621402

Selected physical and chemical properties of soil under different agricultural land-use types in Ile-Ife, Nigeria

Akinde BP, Olakayode AO, Oyedele DJ, Tijani FO

Heliyon

28-Sep-2020

PMCID:	PMC7527570
doi:	10.1016/j.heliyon.2020.e05090
PMID:	33024867

Subtribe Hyptidinae (Lamiaceae): A promising source of bioactive metabolites

Bridi H, de Carvalho Meirelles G, Lino von Poser G

J Ethnopharmacol

05-Aug-2020

PMCID:	PMC7403033
doi:	10.1016/j.jep.2020.113225
PMID:	32763419

The (+)-Brevipolide H Displays Anticancer Activity against Human Castration-Resistant Prostate Cancer: The Role of Oxidative Stress and Akt/mTOR/p70S6K-Dependent Pathways in G1 Checkpoint Arrest and Apoptosis

Sheng YH, Leu WJ, Chen CN, Hsu JL, Liu YT, Hsu LC, Hou DR, Guh JH

Molecules

25-Jun-2020

PMCID:	PMC7355498
doi:	10.3390/molecules25122929
PMID:	32630532

Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes

Lautié E, Russo O, Ducrot P, Boutin JA

Front Pharmacol

07-Apr-2020

PMCID:	PMC7154113
doi:	10.3389/fphar.2020.00397
PMID:	32317969

Discovery of potential ovicidal natural products using metabolomics

Borges DG, Echeverria JT, de Oliveira TL, Heckler RP, de Freitas MG, Damasceno-Junior GA, Carollo CA, Borges FD

PLoS One

25-Jan-2019

PMCID:	PMC6347362
doi:	10.1371/journal.pone.0211237
PMID:	30682122

Complementarity of DFT Calculations, NMR Anisotropy, and ECD for the Configurational Analysis of Brevipolides K-O from Hyptis brevipes.

Suárez-Ortiz GA, Cerda-García-Rojas CM, Fragoso-Serrano M, Pereda-Miranda R

J Nat Prod

27-Jan-2017

doi:	10.1021/ACS.JNATPROD.6B00953
PMID:	28099005

Absolute configuration and conformational analysis of brevipolides, bioactive 5,6-dihydro-α-pyrones from Hyptis brevipes.

Suárez-Ortiz GA, Cerda-García-Rojas CM, Hernández-Rojas A, Pereda-Miranda R

J Nat Prod

25-Jan-2013

doi:	10.1021/NP300740H
PMID:	23282042

Critical Period of Weed Control in Aerobic Rice

Anwar MP, Juraimi AS, Samedani B, Puteh A, Man A

ScientificWorldJournal

18-Jun-2012

PMCID:	PMC3385597
doi:	10.1100/2012/603043
PMID:	22778701

Bioactivity-guided isolation of cytotoxic sesquiterpenes of Rolandra fruticosa

Pan L, Lantvit DD, Riswan S, Kardono LB, Chai HB, Carcache de Blanco EJ, Farnsworth NR, Soejarto DD, Swanson SM, Kinghorn AD

Phytochemistry

25-Feb-2010

PMCID:	PMC2847506
doi:	10.1016/j.phytochem.2010.01.012
PMID:	20189206

Bioactive 5,6-dihydro-alpha-pyrone derivatives from Hyptis brevipes.

Deng Y, Balunas MJ, Kim JA, Lantvit DD, Chin YW, Chai H, Sugiarso S, Kardono LB, Fong HH, Pezzuto JM, Swanson SM, de Blanco EJ, Kinghorn AD

J Nat Prod

01-Jun-2009

PMCID:	PMC2883770
doi:	10.1021/NP9001724
PMID:	19422206

Bioactive 5,6-Dihydro-α-pyrone Derivatives from Hyptis brevipes

Deng Y, Balunas MJ, Kim JA, Lantvit DD, Chin YW, Chai H, Sugiarso S, Kardono LB, Fong HH, Pezzuto JM, Swanson SM, Carcache de Blanco EJ, Kinghorn AD

J Nat Prod

01-Jun-2009

PMCID:	PMC2883770
doi:	10.1021/np9001724
PMID:	19422206

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 / Phenylpropanes
2-Butyl-5-Propylresorcinol	11528577	Click to see	208.30	unknown	via CMAUP database
2-n-Hexyl-5-n-propylresorcinol	197183	Click to see CCCCCCC1=C(C=C(C=C1O)CCC)O	236.35	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
2-Hexyl-5-methylresorcinol	11535811	Click to see CCCCCCC1=C(C=C(C=C1O)C)O	208.30	unknown	via CMAUP database
Resorstatin	198749	Click to see	264.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10,11-dihydroxy-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	7163260	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
2,3-Dihydroxy-12-oleanen-28-oic acid	3694932	Click to see	472.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Maslinic Acid	73659	Click to see	472.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	154496016	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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose	5984	Click to see	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[(1S)-1-[(2S,5R)-5-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]oxolan-2-yl]ethyl] (E)-3-(4-methoxyphenyl)prop-2-enoate	137643066	Click to see	402.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.6B00953
[(1S)-1-[(2S,5R)-5-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]oxolan-2-yl]ethyl] (Z)-3-(4-methoxyphenyl)prop-2-enoate	137647458	Click to see	402.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.6B00953
[(2S)-1-[(1S,2S)-2-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] 3-(4-methoxyphenyl)prop-2-enoate	163005913	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC=C(C=C3)OC	400.40	unknown	https://doi.org/10.1021/NP300740H
Brevipolide H	71521993	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC=C(C=C3)OC	400.40	unknown	https://doi.org/10.1021/NP300740H
Brevipolide I	71522009	Click to see	400.40	unknown	https://doi.org/10.1021/NP300740H
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(1S)-1-[(2S,5R)-5-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]oxolan-2-yl]ethyl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	137661365	Click to see CC(C1CCC(O1)C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	404.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.6B00953
[(2R)-1-[(1S,2S)-2-[(S)-acetyloxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	162842694	Click to see	444.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2R)-1-[(1S,2S)-2-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163017027	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	402.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2R)-1-[(1S,2S)-2-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (Z)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163017028	Click to see	402.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2S)-1-[(1S,2S)-2-[(S)-acetyloxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	162842693	Click to see	444.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[1-[2-[Acetyloxy-(6-oxo-2,3-dihydropyran-2-yl)methyl]cyclopropyl]-1-oxopropan-2-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	74941385	Click to see	444.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[1-[2-[Hydroxy-(6-oxo-2,3-dihydropyran-2-yl)methyl]cyclopropyl]-1-oxopropan-2-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	74941383	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	402.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
brevipolide C	44178667	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	402.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Brevipolide D	44178665	Click to see	402.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Brevipolide E	44178668	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)OC(=O)C)OC(=O)C=CC3=CC(=C(C=C3)O)O	444.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Brevipolide J	71521916	Click to see	416.40	unknown	https://doi.org/10.1021/NP300740H
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(1S)-1-[(2S,5R)-5-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]oxolan-2-yl]ethyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	137636436	Click to see	388.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.6B00953
[(1S)-1-[(2S,5R)-5-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]oxolan-2-yl]ethyl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	137660754	Click to see	388.40	unknown	https://doi.org/10.1021/ACS.JNATPROD.6B00953
[(2R)-1-[(1R,2S)-2-[(S)-acetyloxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	162912837	Click to see	428.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2R)-1-[(1S,2S)-2-[(S)-acetyloxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	162912838	Click to see	428.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2R)-1-[(1S,2S)-2-[(S)-acetyloxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	163186597	Click to see	428.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2R)-1-[(1S,2S)-2-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	163185023	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC=C(C=C3)O	386.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2R)-1-[(1S,2S)-2-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	162974362	Click to see	386.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[(2S)-1-[(1S,2S)-2-[(S)-hydroxy-[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]cyclopropyl]-1-oxopropan-2-yl] (Z)-3-(3-hydroxyphenyl)prop-2-enoate	162820133	Click to see	386.40	unknown	https://doi.org/10.1021/NP300740H
[1-[2-[Acetyloxy-(6-oxo-2,3-dihydropyran-2-yl)methyl]cyclopropyl]-1-oxopropan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate	74941382	Click to see	428.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
[1-[2-[Hydroxy-(6-oxo-2,3-dihydropyran-2-yl)methyl]cyclopropyl]-1-oxopropan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate	74941413	Click to see	386.40	unknown	https://doi.org/10.1021/NP300740H https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Brevipolide A	44178664	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)OC(=O)C)OC(=O)C=CC3=CC=C(C=C3)O	428.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Brevipolide B	44178755	Click to see	428.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
brevipolide F	44178756	Click to see CC(C(=O)C1CC1C(C2CC=CC(=O)O2)O)OC(=O)C=CC3=CC=C(C=C3)O	386.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Brevipolide G	71522010	Click to see	386.40	unknown	https://doi.org/10.1021/NP300740H
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Demethoxymatteucinol	180550	Click to see	284.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Ombuin	5320287	Click to see	330.29	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-galactoside cation	5316498	Click to see	465.40	unknown	via CMAUP database
Malvidin 3-O-galactoside	5484292	Click to see	493.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Guaijaverin	5481224	Click to see	434.30	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5,6-Trihydroxy-3,4',7-trimethoxyflavone	442621	Click to see	360.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
Ayanin	5280682	Click to see	344.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883770/
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone	586491	Click to see	242.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one	344530	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O	240.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
2'-Methoxy-4'-hydroxydihydrochalcone	42607666	Click to see COC1=C(C=CC(=C1)O)C(=O)CCC2=CC=CC=C2	256.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
3,2'-Dihydroxy-4,5-dimethoxybibenzyl	10754781	Click to see COC1=CC(=CC(=C1OC)O)CCC2=CC=CC=C2O	274.31	unknown	via CMAUP database

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Hyptis brevipes

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