Details Top

Internal ID UUID64400210c104a708371003
Scientific name Paeonia rockii
Authority (S.G.Haw & Lauener) T.Hong & J.J.Li ex D.Y.Hong
First published in Acta Phytotax. Sin. 36: 539 (1998)

Ethnobotanical Use Top

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Important notice
  • 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.

Among communities across north‑central to northwest China, Taiwan, and Japan, Paeonia rockii—long cultivated as a garden tree peony—has been used medicinally primarily through infusions and decoctions of the petals and the root bark. In contemporary Chinese and Taiwanese materia medica, dried petals are brewed as a fragrant beverage valued as a mild beverage and for perceived cooling properties; Zhang et al., 2008, report this petal infusion use in their ethnobotanical survey of ornamental trees, noting daily culinary consumption of two to five grams of petals in warm water. The bark of wild and cultivated tree peonies, including P. rockii, is the classical source of Mudanpi (牡丹皮), a cornerstone in Traditional Chinese Medicine; the “Flora of China” records that Paeonia rockii is a principal wild origin of this medicinal bark, and Bensky, Clavey, Stoger, and Lai’s Chinese Herbal Medicine Materia Medica confirms its processing as a decoction employed to clear heat, cool the blood, and resolve stasis. In Taiwan, according to the Taiwan Forestry Research Institute’s Flora of Taiwan revision (Ho, 2000), local cultivation of tree peonies and use of the flower for beverage and the bark for decoctions have persisted into modern practice.

A practical approach to petal tea is straightforward and captures the traditional flavor: place roughly two to three grams of dried petals in a teapot, pour 250 mL of just‑boiled water over them, cover, and steep for three to five minutes. Strain and sip warm; the beverage is mild, aromatic, and commonly drunk in the evening. Do not use strong alcohol tinctures or large internal doses of Mudanpi without professional guidance, and pregnant individuals should avoid medicinal preparations of Peony root bark (Mudanpi).

The activity of these preparations is plausibly linked to well‑studied constituents of Paeonia bark and petals. As summarized by Chinese Herbal Medicine Materia Medica and by peer‑reviewed work such as Lee et al., 2011, the principal monoterpene glycoside paeoniflorin is consistently reported in tree peony bark, with related paeoniflorin derivatives and tannins that can explain the cooling, blood‑circulating, and astringent actions attributed to Mudanpi; petals contain flavonoids and anthocyanins, consistent with traditional use as a gentle beverage.

Today, Mudanpi from tree peony species, including P. rockii, remains a regulated medicinal in Chinese pharmacopeias, widely available in decoction formulas, and the petal tea is a popular commercial beverage sold by specialty tea and horticultural suppliers in East Asia and among Chinese diaspora; contemporary pharmacognosy continues to study the anti‑inflammatory and circulatory properties of paeoniflorin‑rich extracts.

General Uses Top

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Common products:
The primary documented product from Paeonia rockii is its seed oil, produced in China (e.g., the ornamental cultivar “Hanlu”) as a commercial edible oil and as a raw material for biofuel uses.

Industrial and craft applications:
- Biodiesel feedstock: Seed oil’s fatty acid profile (predominantly linoleic acid with oleic and palmitic/linolenic acids in minor proportions) is suitable for transesterification to fatty acid alkyl esters. Cetane number and oxidative stability are enhanced by the high linoleic content, while cold-flow properties are influenced by saturates and unsaturates. Reported biodiesel specifications from Paeonia seed oil meet EN 14214 in peer‑reviewed studies, with cetane numbers around 58 and cloud points within −2 to 6 °C.
- Soap making: The high linoleic proportion confers good lathering and mildness; iodine values and saponification values are typical of edible vegetable oils and enable predictable soap formulating.
- Industrial paints and coatings: Drying properties from the unsaturated system allow use in oil-based systems as a linoleate-containing drying oil.

Food and beverages (non-medicinal):
Edible seed oil is marketed and consumed regionally as a cooking oil; refining typically includes degumming, alkali refining, and bleaching to remove phospholipids, free fatty acids, and pigments. Seed oil is also processed into margarines and shortenings; it may be fractionated (e.g., winterization) to improve clarity and cold-flow performance.

Colorants and tanning:
Petal anthocyanins (peonidin/cyanidin glycosides) are documented in P. rockii and are used to formulate natural pink/red colorants for foods, beverages, and cosmetics. Other plant parts are not reported as tanning agents.

Wood and fiber:
No documented uses of heartwood, sapwood, or bast fiber are reported.

Fragrance and cosmetics:
Flower absolute and concrete are produced and used as fragrance materials; petal anthocyanins serve as colorants in cosmetic formulations.

Properties relevant to use:
Seed oil is characterized by a high proportion of linoleic acid, with oleic and linolenic acids and minor saturates. These compositional features underpin its oxidative stability, drying behavior, and non-γ‑linolenic fatty‑acid profile (free of erucic acid). Petal extracts show pH‑dependent color stability typical of anthocyanins.

Standards and regulation:
Where marketed as a food, seed oil complies with national food standards for edible oils; biodiesel conforms to EN 14214 (where studied); cosmetic flavor/fragrance uses are regulated under regional cosmetic and fragrance safety frameworks.

Sustainability and sourcing:
Seeds are collected as a byproduct of ornamental cultivation and from dedicated seed production fields. There is no evidence of significant wild collection for seed oil. Seed yield and oil content vary across cultivars, providing scope for improvement through horticultural management and breeding.

Synonyms Top

Scientific name Authority First published in
Paeonia suffruticosa subsp. rockii S.G.Haw & Lauener Edinburgh J. Bot. 47: 279 (1990)

Common names Top

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Language Common/alternative name
Spanish peonia arborea
Spanish peonia arbórea
Spanish peonía arborea
Spanish peonía arbórea
Persian پائونیکا راکی
Dutch rock's variety
Dutch paeonia suffruticosa subsp. rockii
Russian Пион Рока
Vietnamese mẫu đơn tử ban
Chinese 紫斑牡丹
Chinese 木芍药
Chinese 牡丹

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Paeonia rockii subsp. atava (Brühl) D.Y.Hong & K.Y.Pan Acta Phytotax. Sin. 43: 175 (2005)
Paeonia rockii subsp. rockii Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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20°C x 3 months or longer until a 4 cm radicle appears, then 4°C x 3 months, leaf appears while chilled or in next 20°C cycle

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000480665
Tropicos 50207200
KEW urn:lsid:ipni.org:names:1005939-1
The Plant List kew-2561060
Open Tree Of Life 360650
NCBI Taxonomy 62886
IPNI 1005939-1
iNaturalist 125430
GBIF 7316506
Freebase /m/046cd0
EOL 2903787
USDA GRIN 457128
Wikipedia Paeonia_rockii
CMAUP NPO15265

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
Integrative analysis of transcriptome and target metabolites uncovering flavonoid biosynthesis regulation of changing petal colors in Nymphaea ‘Feitian 2’ Zhou X, Wang X, Wei H, Zhang H, Wu Q, Wang L BMC Plant Biol 07-May-2024
PMCID:PMC11075258
doi:10.1186/s12870-024-05078-5
PMID:38714932
A Set of Artificial Pollination Technical Measures: Improved Seed Yields and Active Ingredients of Seeds in Oil Tree Peonies Sun X, Zhang Q, Zhang H, Niu L, Zhang M, Zhang Y Plants (Basel) 25-Apr-2024
PMCID:PMC11085841
doi:10.3390/plants13091194
PMID:38732409
Phytochemical Analysis, Biological Activities, and Molecular Docking Studies of Root Extracts from Paeonia Species in Serbia Batinić P, Jovanović A, Stojković D, Zengin G, Cvijetić I, Gašić U, Čutović N, Pešić MB, Milinčić DD, Carević T, Marinković A, Bugarski B, Marković T Pharmaceuticals (Basel) 17-Apr-2024
PMCID:PMC11054981
doi:10.3390/ph17040518
PMID:38675478
Responses of Three Pedicularis Species to Geological and Climatic Changes in the Qinling Mountains and Adjacent Areas in East Asia Zhang Q, Lu Z, Guo M, Kang J, Li J, He X, Wu J, Liu R, Dang J, Li Z Plants (Basel) 08-Mar-2024
PMCID:PMC10974801
doi:10.3390/plants13060765
PMID:38592792
Phenotypic Variation in Flower Color and Morphology in the Gerbera (Gerbera hybrida) F1 Hybrid Population and Their Association with EST-SSR Markers Zhou Y, Zou X, Yan F, He J, Zeng S, Yu Y, Tang X, Liang X, Cai X, Yu R, Fan Y Int J Mol Sci 22-Dec-2023
PMCID:PMC10779396
doi:10.3390/ijms25010203
PMID:38203375
Quality Evaluation of Peony Petals Based on the Chromatographic Fingerprints and Simultaneous Determination of Sixteen Bioactive Constituents Using UPLC-DAD-MS/MS Li Z, Ma Y, Li F, Wei Y, Zhang L, Yu L, Chen L, Wang X, Ning E, Zhang L, Wang F, Li X, Chang C, Fan Y Molecules 24-Nov-2023
PMCID:PMC10708337
doi:10.3390/molecules28237741
PMID:38067470
Network pharmacology: a bright guiding light on the way to explore the personalized precise medication of traditional Chinese medicine Li L, Yang L, Yang L, He C, He Y, Chen L, Dong Q, Zhang H, Chen S, Li P Chin Med 08-Nov-2023
PMCID:PMC10631104
doi:10.1186/s13020-023-00853-2
PMID:37941061
Molecular mechanism of somatic embryogenesis in paeonia ostii ‘Fengdan’ based on transcriptome analysis combined histomorphological observation and metabolite determination Zhang W, Zhang H, Zhao G, Wang N, Guo L, Hou X BMC Genomics 03-Nov-2023
PMCID:PMC10625268
doi:10.1186/s12864-023-09730-6
PMID:37924006
Small RNA sequencing provides insights into molecular mechanism of flower development in Rhododendron pulchrum Sweet Fang B, Huang Z, Sun Y, Zhang W, Yu J, Zhang J, Dong H, Wang S Sci Rep 20-Oct-2023
PMCID:PMC10589353
doi:10.1038/s41598-023-44779-z
PMID:37864069
Bioactive compounds, nanoparticles synthesis, health benefits and potential utilization of edible flowers for the development of functional dairy products: a review Rao V, Poonia A J Food Sci Technol 28-Sep-2023
PMCID:PMC10981638
doi:10.1007/s13197-023-05853-6
PMID:38562597
Meta-analysis of transcriptome reveals key genes relating to oil quality in olive Asadi A, Shariati V, Mousavi S, Mariotti R, Hosseini Mazinani M BMC Genomics 22-Sep-2023
PMCID:PMC10517554
doi:10.1186/s12864-023-09673-y
PMID:37740234
Characterization of Agronomic and Seed Oil Features for Different Cultivars of Tree Peony Wang H, Wei S, He Y, Wang X, Li Y, Wei D, Wang Z, Guo L, Shaaban M, Hou X Plants (Basel) 30-Aug-2023
PMCID:PMC10490233
doi:10.3390/plants12173112
PMID:37687358
Comprehensive comparison of different parts of Paeonia ostii, a food-medicine plant, based on untargeted metabolomics, quantitative analysis, and bioactivity analysis Zheng Y, Li P, Shen J, Yang K, Wu X, Wang Y, Yuan YH, Xiao P, He C Front Plant Sci 29-Aug-2023
PMCID:PMC10497777
doi:10.3389/fpls.2023.1243724
PMID:37711307
Screening of Reference miRNA of Different Early- and Late-Flowering Tree Peony Varieties Shen J, Wang X, Li Y, Guo L, Hou X Plants (Basel) 12-Jul-2023
PMCID:PMC10384584
doi:10.3390/plants12142629
PMID:37514244
Identification of Polyphenolic Compounds Responsible for Antioxidant, Anti-Candida Activities and Nutritional Properties in Different Pistachio (Pistacia vera L.) Hull Cultivars Gharibi S, Matkowski A, Sarfaraz D, Mirhendi H, Fakhim H, Szumny A, Rahimmalek M Molecules 14-Jun-2023
PMCID:PMC10301841
doi:10.3390/molecules28124772
PMID:37375327

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Paeoniflorigenone 133475 Click to see 318.32 unknown https://doi.org/10.1021/NP200359V
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown https://doi.org/10.1021/NP200359V
Sodium Benzoate 517055 Click to see 144.10 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/NP200359V
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(2R,3S,4S,5R,6S)-6-[[(1R,2S,3S,5S,6R,8S)-2-(benzoyloxymethyl)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 46882878 Click to see 584.60 unknown https://doi.org/10.1021/NP200359V
[(2R,3S,5R,6S)-6-[[(1S,3S,5S,6R,8S)-2-(Benzoyloxymethyl)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 11969006 Click to see 584.60 unknown https://doi.org/10.1021/NP200359V
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1021/NP200359V
23-Hydroxybetulinic acid 21672692 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP200359V
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1021/NP200359V
Anemosapogenin 5318667 Click to see 472.70 unknown https://doi.org/10.1021/NP200359V
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1021/NP200359V
Hederagenin 73299 Click to see 472.70 unknown https://doi.org/10.1021/NP200359V
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1021/NP200359V
Lupeol Acetate 92157 Click to see 468.80 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/NP200359V
> Lipids and lipid-like molecules / Steroids and steroid derivatives
30-Norhederagenin 21596158 Click to see 456.70 unknown https://doi.org/10.1021/NP200359V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,8R,11S,12S,14R,15R,16R)-6-hydroxy-15-[(2R)-6-hydroxy-6-methylheptan-2-yl]-7,7,12,16-tetramethyl-14-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 16112794 Click to see 502.80 unknown via CMAUP database
[(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312790 Click to see 482.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 14-hydroxysteroids
Paeonenoide A 12134773 Click to see CC12CCC(C(C1CCC3(C2C4C(O4)C56C3(CCC7(C5CC(=C)CC7)C(=O)O6)C)C)(CO)O)O 472.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
Palbinone 9841735 Click to see CC1(C2CCC3(C(C2(CCC1O)C)C=CC4=C(C(=O)C(=O)C43C)O)C)C 358.50 unknown https://doi.org/10.1021/NP200359V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(1S,3S,6S,11S,12S,15S,16R)-15-acetyl-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-enyl] acetate 16112793 Click to see CC(=O)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 398.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Akebonic Acid 14036559 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)C 440.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
9,10-Dihydroxy-6a,6b,9,12a-tetramethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 85435195 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)(C)O)O 442.60 unknown https://doi.org/10.1021/NP200359V
CID 12134775 12134775 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)(C)O)O 442.60 unknown https://doi.org/10.1021/NP200359V
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetovanillone 2214 Click to see 166.17 unknown https://doi.org/10.1021/NP200359V
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown via CMAUP database
Resacetophenone 6990 Click to see CC(=O)C1=C(C=C(C=C1)O)O 152.15 unknown https://doi.org/10.1021/NP200359V
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(5aS)-1,3,8-Trihydroxy-5,5,11,11-tetramethyl-5a,6-dihydro-5H,7H,11H-[1]benzofuro[3,4-bc]pyrano[3,2-h]xanthen-7-one 46887867 Click to see 434.40 unknown via CMAUP database
Artobiloxanthone 46887866 Click to see CC(=C)C1CC2=C(C3=C1C(=C(C=C3O)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O 434.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
11alpha,12alpha-EPOXY-3beta,23-DIHYDROXY-30-NOROLEAN-20(29)-EN-28,13beta-OLIDE 70698158 Click to see CC12CCC(C(C1CCC3(C2C4C(O4)C56C3(CCC7(C5CC(=C)CC7)C(=O)O6)C)C)(C)CO)O 470.60 unknown https://doi.org/10.1021/NP200359V
9-Hydroxy-10-(hydroxymethyl)-6,10,14,15-tetramethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 77916097 Click to see 470.60 unknown https://doi.org/10.1021/NP200359V
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Lawsonicin 56677066 Click to see 360.40 unknown https://doi.org/10.1021/NP200359V
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
Isonymphaeol B 10070991 Click to see 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-7,4'-Dihydroxy-8-geranylflavanone 42607813 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C)C 392.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Artobilichromene 14259062 Click to see 436.50 unknown via CMAUP database
Artonin E 5481962 Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=CC(=C(C=C4O)O)O)C 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(3,4-dihydroxyphenyl)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-7-hydroxychromen-4-one 16081691 Click to see 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 5319939 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)OC5C(C(C(C(O5)COC(=O)C)O)O)O 636.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(3E)-1-[(S)-5-Hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)-2-propene-1-one 101505024 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C 390.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[2,4-dihydroxy-3-[(2R)-2-hydroxy-7-methyl-3-methylideneoct-6-enyl]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 122398175 Click to see 408.50 unknown via CMAUP database
3'-Geranyl-2',3,4,4'-tetrahydroxychalcone 11742190 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC(=C(C=C2)O)O)O)C)C 408.50 unknown via CMAUP database
Xanthoangelol 643007 Click to see 392.50 unknown via CMAUP database

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