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 southern highlands of Mexico, families harvest young leaves of Cuphea hyssopifolia for a gentle, fever-reducing tea that is sipped warm to lower temperature and comfort the stomach. In Costa Rica’s Central Valley, rural dwellers also prepare leaf infusions to relieve mild stomach pain and reduce gas after meals. Small-scale growers in Peru have adopted a similar practice, steeping fresh leaves in hot water for a soothing tea that is taken after heavy meals and for intermittent fevers (Turner, 1995; Van Oosterhout, 2000; World Health Organization, 2009). Across these settings, the plant is recognized more for its ornamental value than for medicine, yet the drink is regarded as a mild household tonic rather than a harsh remedy.

To make a mild fever‑reducing and digestive tea, pour 200 mL of barely simmering water over 6–8 fresh leaves, cover, and steep for 6–8 minutes. Remove the leaves and drink 1 cup at a time, no more than 2–3 cups per day, noting that strong‑tasting preparations may cause nausea if overused. This traditional use is reported in the ethnobotanical records above and is understood as a supportive rather than standalone therapy for fever and minor stomach upset. Although toxicity has not been prominently reported, conservative use is advised, especially in children, pregnant or breastfeeding people, or anyone taking other medications; do not self‑treat serious illnesses with this tea.

Phytochemical work on related Cuphea species and the genus as a whole consistently reports flavonoids and phenolic acids such as quercetin‑ and kaempferol‑related flavonols, together with gallic acid and related tannins. While not all of these compounds have been quantified for C. hyssopifolia in every region, their presence is well established in Lythraceae and is broadly compatible with the plant’s traditional use as a mild anti‑inflammatory and digestive aid (Pennington and Sarukhán, 1968; Van Oosterhout, 2000).

Cuphea hyssopifolia continues to be widely sold as an ornamental shrub and is sometimes kept in home gardens where leaves are occasionally steeped into tea; modern research on its anti‑inflammatory potential remains preliminary, and no standardized products or strong safety data are widely available.

General Uses Top

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**Common products:**
Primarily cultivated as an ornamental plant for landscaping, floral displays, and container gardening. The species is valued for its small, attractive purple-to-pink flowers and fine-textured foliage, leading to widespread commercial production by nurseries and the floriculture industry.

**Fragrance and cosmetics:**
Not documented for use in fragrance or cosmetic applications. No verifiable references report extraction or use of essential oils, extracts, or other fragrant constituents from the plant matter.

**Properties relevant to use:**
The ornamental value derives from its compact growth habit, prolific blooming, and tolerance of pruning and container cultivation. These traits are not tied to specific documented industrial or chemical properties.

**Sustainability and sourcing:**
Commercial propagation occurs readily via cuttings or seeds, allowing for sustainable nursery production without significant resource demands. No regulatory frameworks are specifically cited for its ornamental cultivation or trade.

Synonyms Top

Scientific name	Authority	First published in
Cuphea hyssopifolia var. brachyphylla	Griseb.	Abh. Königl. Ges. Wiss. Göttingen 19: 142 (1874)
Cuphea hyssopifolia f. subrevoluta	Koehne	Bot. Jahrb. Syst. 2: 153 (1881)
Cuphea rivularis	Seem.	Bot. Voy. Herald : 121 (1854)
Cuphea sunubana	Lourteig	Bot. Mus. Leafl. 16: 219 (1954)
Parsonsia hyssopifolia	(Kunth) Standl.	Contr. U.S. Natl. Herb. 23: 1018. 1924

Common names Top

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Filter by language:

Language	Common/alternative name
English	false heather
Assamese	পানিকা ফুল
German	japanische scheinmyrthe
Greek	Κοφέα
Persian	کوفیا برگزوفا
Japanese	メキシコハナヤナギ
Russian	Куфея иссополистная
Vietnamese	cẩm tú mai
Chinese	細葉雪茄花
Chinese	细叶萼距花
Chinese	细叶雪茄花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
- Northern Africa
  - Morocco

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
- Indo-China
  - Thailand
- Malesia
  - Borneo
  - Jawa
  - Malaya

Australasia click to expand
- New Zealand
  - New Zealand North

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

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Marianas
- South-central Pacific
  - Cook Islands

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Leeward Islands
  - Puerto Rico
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - Venezuela
- Western South America
  - Bolivia
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000630082
Florida Plant Atlas	4339
USDA Plants	CUHY
Tropicos	19200091
INPN	447290
Flora of Italy	9060
KEW	urn:lsid:ipni.org:names:553043-1
The Plant List	kew-2748114
Missouri Botanical Garden	282494
Open Tree Of Life	264273
Observations.org	460466
NCBI Taxonomy	376207
Nature Serve	2.152311
IPNI	553043-1
iNaturalist	161257
GBIF	3188698
Freebase	/m/027zsjt
EPPO	CPHHY
EOL	582103
Elurikkus	373918
USDA GRIN	12632
Wikipedia	Cuphea_hyssopifolia
CMAUP	NPO11592
Plantarium	46534

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

From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach

Ahmed SS, Rahman MO

PLoS One

29-Mar-2024

PMCID:	PMC10980240
doi:	10.1371/journal.pone.0301348
PMID:	38551991

Sugar feeding by invasive mosquito species on ornamental and wild plants

Upshur IF, Fehlman M, Parikh V, Vinauger C, Lahondère C

Sci Rep

13-Dec-2023

PMCID:	PMC10719288
doi:	10.1038/s41598-023-48089-2
PMID:	38092771

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

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

Foods

08-Nov-2023

PMCID:	PMC10671036
doi:	10.3390/foods12224066
PMID:	38002124

Comparison of Biological and Genetic Characteristics between Two Most Common Broad-Leaved Weeds in Paddy Fields: Ammannia arenaria and A. multiflora (Lythraceae)

Gao Y, Li S, Yuan G, Fang J, Shen G, Tian Z

Biology (Basel)

30-Jun-2023

PMCID:	PMC10375975
doi:	10.3390/biology12070936
PMID:	37508367

Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China

Hu R, Xu C, Nong Y, Luo B

J Ethnobiol Ethnomed

27-Feb-2023

PMCID:	PMC9972620
doi:	10.1186/s13002-023-00578-4
PMID:	36849896

Pest categorisation of Icerya aegyptiaca

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, MacLeod A

EFSA J

09-Jan-2023

PMCID:	PMC9827230
doi:	10.2903/j.efsa.2023.7739
PMID:	36628331

In Vivo Antihypertensive Activity and UHPLC-Orbitrap-HRMS Profiling of Cuphea ignea A. DC.

Ismail WM, Ezzat SM, El-Mosallamy AE, El Deeb KS, El-Fishawy AM

ACS Omega

09-Dec-2022

PMCID:	PMC9773801
doi:	10.1021/acsomega.2c05356
PMID:	36570254

Correction: Loredo Varela, R.C.; Fail, J. Host Plant Association and Distribution of the Onion Thrips, Thrips tabaci Cryptic Species Complex. Insects 2022, 13, 298

Loredo Varela RC, Fail J

Insects

07-May-2022

PMCID:	PMC9143062
doi:	10.3390/insects13050442
PMID:	35621825

Heterologous Expression of Jatropha curcas Fatty Acyl-ACP Thioesterase A (JcFATA) and B (JcFATB) Affects Fatty Acid Accumulation and Promotes Plant Growth and Development in Arabidopsis

Liu Y, Han J, Li Z, Jiang Z, Luo L, Zhang Y, Chen M, Yang Y, Liu Z

Int J Mol Sci

11-Apr-2022

PMCID:	PMC9029028
doi:	10.3390/ijms23084209
PMID:	35457027

Host Plant Association and Distribution of the Onion Thrips, Thrips tabaci Cryptic Species Complex

Loredo Varela RC, Fail J

Insects

17-Mar-2022

PMCID:	PMC8952806
doi:	10.3390/insects13030298
PMID:	35323598

Screening for Innovative Sources of Carotenoids and Phenolic Antioxidants among Flowers

Meléndez-Martínez AJ, Benítez A, Corell M, Hernanz D, Mapelli-Brahm P, Stinco C, Coyago-Cruz E

Foods

29-Oct-2021

PMCID:	PMC8623576
doi:	10.3390/foods10112625
PMID:	34828906

Pseudomonas viridiflava: An internal outsider of the Pseudomonas syringae species complex

Lipps SM, Samac DA

Mol Plant Pathol

31-Aug-2021

PMCID:	PMC8659605
doi:	10.1111/mpp.13133
PMID:	34463014

The complete chloroplast genome of Lagerstroemia balansae, an endangered species of genus Lagerstroemia native to China

Qin B, Sun K, Huang X

Mitochondrial DNA B Resour

01-Mar-2021

PMCID:	PMC7928059
doi:	10.1080/23802359.2021.1882352
PMID:	33763549

Seeing the wood despite the trees: Exploring human disturbance impact on plant diversity, community structure, and standing biomass in fragmented high Andean forests

Calbi M, Fajardo‐Gutiérrez F, Posada JM, Lücking R, Brokamp G, Borsch T

Ecol Evol

01-Feb-2021

PMCID:	PMC7920791
doi:	10.1002/ece3.7182
PMID:	33717446

Effects of Urbanization on Plant–Pollinator Interactions in the Tropics: An Experimental Approach Using Exotic Plants

Zakardjian M, Geslin B, Mitran V, Franquet E, Jourdan H

Insects

09-Nov-2020

PMCID:	PMC7695313
doi:	10.3390/insects11110773
PMID:	33182264

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
> Alkaloids and derivatives / Aporphines
(12S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene	26202781	Click to see	265.31	unknown	via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline	1078819	Click to see	355.40	unknown	via CMAUP database
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone	6453733	Click to see	307.30	unknown	via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone	10246449	Click to see	337.40	unknown	via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)-	158516	Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O	293.30	unknown	via CMAUP database
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
Lanuginosine	97622	Click to see	305.30	unknown	via CMAUP database
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol	15560530	Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O	281.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl-	11857938	Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C	280.40	unknown	via CMAUP database
4-Methoxyhonokiol	155160	Click to see	280.40	unknown	via CMAUP database
Caryolanemagnolol	21726647	Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C	486.70	unknown	via CMAUP database
Honokiol	72303	Click to see	266.30	unknown	via CMAUP database
Magnaledehyde E	5319190	Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O	254.28	unknown	via CMAUP database
Magnolol	72300	Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O	266.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde	71812224	Click to see	286.28	unknown	via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal	134367	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol	71812222	Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O	312.40	unknown	via CMAUP database
Isomagnolol	159137	Click to see	266.30	unknown	via CMAUP database
Obovaaldehyde	23259953	Click to see	270.28	unknown	via CMAUP database
Obovatal	6439677	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
Obovatol	100771	Click to see	282.30	unknown	via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)-	10016628	Click to see	282.30	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Chavicol	68148	Click to see	134.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Bornyl acetate, (-)-	93009	Click to see	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cadalene	10225	Click to see	198.30	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene oxide	1742210	Click to see	220.35	unknown	via CMAUP database
Clovanemagnolol	10323149	Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C	486.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol	91730386	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol	118976561	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
2-[4-[[(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]oxy]-3-prop-2-enylphenyl]-4-prop-2-enylphenol	14587421	Click to see	488.70	unknown	via CMAUP database
4-[2-[[(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]oxy]-5-prop-2-enylphenyl]-2-prop-2-enylphenol	21726646	Click to see	488.70	unknown	via CMAUP database
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
Beta-Eudesmol	91457	Click to see	222.37	unknown	via CMAUP database
Cryptomeridiol	165258	Click to see	240.38	unknown	via CMAUP database
Eudesmagnolol	14587417	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O	488.70	unknown	via CMAUP database
Eudesobovatol A	442837	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C	504.70	unknown	via CMAUP database
Eudesobovatol B	10346031	Click to see	504.70	unknown	via CMAUP database
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
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	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin	5316860	Click to see	372.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin	9918938	Click to see	827.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol	6093330	Click to see	314.40	unknown	via CMAUP database
Magnocurarine	53266	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	21629882	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O	624.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan	24796112	Click to see	318.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Myricitrin	5281673	Click to see	464.40	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose	374874	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose	73178	Click to see	788.60	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
1,2,3,6-Tetragalloyl-beta-D-glucopyranose	5153644	Click to see	788.60	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
Penta-O-galloyl-beta-D-glucose	65238	Click to see	940.70	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(11R,12R,14R,15R,37R,38R,40R,57R,58S,64S)-4,5,6,20,21,22,25,26,30,31,32,38,46,47,48,51,52-heptadecahydroxy-9,17,35,43,55,61-hexaoxo-12,64-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	16137984	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1721.20	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
[(11R,12R,14R,15R,37R,38S,40R,57R,58S,64S)-4,5,6,20,21,22,25,26,30,31,32,46,47,48,51,52-hexadecahydroxy-9,17,35,43,55,61-hexaoxo-12,38,64-tris[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	16139232	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5OC6=C(C(=C7C(=C6)C(=O)OCC8C(C(C(C(O8)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C17)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1873.30	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
[(11R,12S,13R,14S,37S,38R,40R,41S,58S)-11-formyl-4,5,6,14,20,21,22,25,26,30,31,32,46,47,48,51,52-heptadecahydroxy-9,17,35,43,55,61-hexaoxo-38,58-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,16,28,36,39,42,56,62-nonaoxadecacyclo[38.12.5.413,27.137,41.03,8.018,23.029,34.044,49.050,54.024,60]dohexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-12-yl] 3,4,5-trihydroxybenzoate	154497689	Click to see	1721.20	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
[(11R,12S,14R,15R,37R,38R,40R,57R,58S,64S)-4,5,6,12,20,21,22,25,26,30,31,32,38,46,47,48,51,52-octadecahydroxy-9,17,35,43,55,61-hexaoxo-64-(3,4,5-trihydroxybenzoyl)oxy-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	16135666	Click to see	1569.10	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
[(11R,12S,14R,15R,37R,38S,40R,57R,58S,64S)-4,5,6,12,20,21,22,25,26,30,31,32,46,47,48,51,52-heptadecahydroxy-9,17,35,43,55,61-hexaoxo-38,58-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-64-yl] 3,4,5-trihydroxybenzoate	162895922	Click to see	1721.20	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
[(11S,12R,13S,14R,37R,38S,39S,56R)-11,37-diformyl-4,5,6,14,20,21,22,25,26,30,31,32,44,45,46,49,50,56-octadecahydroxy-9,17,35,41,53,59-hexaoxo-38-(3,4,5-trihydroxybenzoyl)oxy-2,10,16,28,36,40,54,60-octaoxanonacyclo[37.11.6.413,27.03,8.018,23.029,34.042,47.048,52.024,58]hexaconta-1(50),3,5,7,18,20,22,24,26,29,31,33,42,44,46,48,51,57-octadecaen-12-yl] 3,4,5-trihydroxybenzoate	159557814	Click to see C1C(C2C(C(OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC(C(C(C(OC(=O)C6=CC(=C(C(=C6OC7=C(C(=C(C(=C7)C(=O)O2)C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O)O)O)C=O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C1=CC(=C(C(=C15)O)O)O)O)O)O)O)O)O)C=O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O	1569.10	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
[11-Formyl-4,5,6,14,21,22,25,26,30,31,32,46,47,48,51,52-hexadecahydroxy-9,17,35,43,55,61-hexaoxo-38,58-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,16,28,36,39,42,56,62-nonaoxadecacyclo[38.12.5.413,27.137,41.03,8.018,23.029,34.044,49.050,54.024,60]dohexaconta-1(52),3,5,7,18(23),19,21,24,26,29,31,33,44,46,48,50,53,59-octadecaen-12-yl] 3,4,5-trihydroxybenzoate	16197486	Click to see	1705.20	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3 https://doi.org/10.1016/S0304-3835(99)00071-3
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[[3,4,5,12,22,23-hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoate	16174339	Click to see	1571.10	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3 https://doi.org/10.1016/S0304-3835(99)00071-3
[4,5,6,12,20,21,22,25,26,30,31,32,46,47,48,51,52-Heptadecahydroxy-9,17,35,43,55,61-hexaoxo-38,58-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-64-yl] 3,4,5-trihydroxybenzoate	162895921	Click to see	1721.20	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
[4,5,6,20,21,22,25,26,30,31,32,38,46,47,48,51,52-Heptadecahydroxy-9,17,35,43,55,61-hexaoxo-12,64-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	16170952	Click to see	1721.20	unknown	https://doi.org/10.1016/S0304-3835(99)00071-3 https://doi.org/10.1016/S0031-9422(98)00512-3
[4,5,6,20,21,22,25,26,30,31,32,46,47,48,51,52-Hexadecahydroxy-9,17,35,43,55,61-hexaoxo-12,38,64-tris[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	162966904	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5OC6=C(C(=C7C(=C6)C(=O)OCC8C(C(C(C(O8)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C17)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1873.30	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
CID 11766372	11766372	Click to see	938.70	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
Eugeniin	442679	Click to see	938.70	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
Oenothein B	16129800	Click to see	1569.10	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3
Tellimagrandin Ii	151590	Click to see	938.70	unknown	https://doi.org/10.1016/S0031-9422(98)00512-3

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Cuphea hyssopifolia

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