Prunus pseudocerasus

Details Top

Internal ID UUID64404089e3259928285341
Scientific name Prunus pseudocerasus
Authority Lindl.
First published in ; 1826 90 1826

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.

Prunus pseudocerasus, the China or ornamental cherry, has long been drunk as a mild infusion in Chinese communities where the ripe, pitted fruits are simmered and strained to make a soothing tea. Traditional recipes describe steeping the fresh or dried arils in hot water for a few minutes; the preparation is valued more as a seasonal comfort drink than as a medicine, with both flavor and gentle astringency noted in Chinese herbal texts (Jiangsu New Medical College, 1986; Zhonghua Bencao Editorial Board, 1999). In parts of Yunnan and Sichuan, decoctions of leaves or young stems are taken for stomach upset and diarrhea, while among Hakka and Cantonese households, a decoction of the stem bark is sometimes sipped for cough relief (Guangdong Provincial Institute of Traditional Chinese Medicine, 1999; Wu et al., 2007). These preparations rely on short, gentle simmer times that concentrate fruit sugars and phenolics without extracting large amounts of seed constituents.

A simple fruit tea can be made by simmering 30–50 g of ripe P. pseudocerasus fruits (pitted, to avoid seed fragments) in 500 mL of water for 5–7 minutes, then cooling briefly and straining; this yields a sweet‑tart beverage that can be drunk warm or chilled and is traditionally taken as a 1‑cup serving 1–2 times daily in season. A stem‑bark decoction for cough is prepared by simmering 5–10 g of dried bark in 250–300 mL water for 20–30 minutes, straining, and drinking one modest cup once or twice daily as needed (Jiangsu New Medical College, 1986; Zhonghua Bencao Editorial Board, 1999). Safety notes are essential: avoid leaves, stems, or seeds in larger medicinal decoctions without professional guidance, and refrain during pregnancy; while the ripe fruit is a recognized food, seed coats contain amygdalin and should not be simmered with the beverage.

Active constituents that plausibly account for the gentle astringency and perceived soothing effect of fruit infusions include quercetin and its glycosides, catechin and epicatechin, anthocyanins such as cyanidin‑3‑O‑glucoside and pelargonidin derivatives, vitamin C, and fructose‑rich sugars. These phenolics are well documented in Prunus pseudocerasus fruits by modern phytochemical surveys (Lu et al., 2003; Jiang et al., 2022; Jiang et al., 2020), and their astringent and antioxidant properties align with traditional reports of a refreshing, comforting tea.

Today the species remains widely cultivated in China for its ornamental value and as a seasonal fruit, with community websites still sharing recipes for “ying tao cha” (cherry tea) and seasonal decoctions. Contemporary research continues to profile the fruit’s polyphenols and sugars, supporting interest in functional foods and flavor use rather than clinical medicine.

General Uses Top

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Common products:
Fruits are sold fresh and processed into juices, jams, jellies, preserves, syrups, wines, and fruit leathers. The most widely traded product is fresh fruit; processed forms include juice concentrates and puree for use in beverages, bakery fillings, and sauces.

Industrial and craft applications:
No significant industrial or craft uses are documented for Prunus pseudocerasus beyond fresh and processed food products.

Food and beverages (non-medicinal):
Fresh fruit is consumed directly; fruit products include juices (often concentrated), jams/jellies, syrups, fermented beverages (wines), candied fruit, and fruit leathers. Processed forms are utilized in bakery, confectionery, and beverage applications.

Colorants and tanning:
Not documented.

Wood and fiber:
Not utilized for timber, fiber, or dyes.

Fragrance and cosmetics:
Not documented.

Properties relevant to use:
Fruits are fleshy drupes; the mesocarp is juicy and sweet to subacid, suitable for fresh consumption and processing into preserves and beverages. Typical fruit chemistry (high sugars and organic acids) supports fermentation for wines and provides body in juices and jams.

Standards and regulation:
No specific standards are documented for this taxon. Processed products would generally follow national food standards for fruit juices, jams, and preserved fruits where applicable.

Sustainability and sourcing:
The species is cultivated in temperate East Asia, primarily in China, with primary production oriented toward fresh-market fruit and domestic processing.

Synonyms Top

Scientific name Authority First published in
Prunus cantabrigiensis Stapf Bot. Mag. 152: t. 9129 (1928)
Cerasus cantabrigiensis (Stapf) Ohle Verz. Landwirtsch. Gärtn. Kulturpfl. 1: 419 (1986)
Cerasus pseudocerasus (Lindl.) Loudon Hortus britannicus ; 1830 200 1830
Prunus saltuum Koehne Pl. Wilson. 1: 213 (1912)
Cerasus scopulorum (Koehne) T.T.Yu & C.L.Li Fl. Reipubl. Popularis Sin. 38: 61 (1986)
Prunus pauciflora Bunge Enum. Pl. China Bor. : 23 (1833)
Prunus involucrata Koehne Pl. Wilson. 1: 206 (1912)
Padus pseudocerasus (Lindl.) S.Ya.Sokolov Derev. Kustarnik. URSS 3: 763 (1954)
Cerasus pseudocerasus (Lindl.) Anon. Hort. Soc. Lond., Cat. Fr. : 28 (1826)
Prunus scopulorum Koehne Pl. Wilson. 1: 241 (1912)
Cerasus pseudocerasus unranked chinensis Anon. Wiener Ill. Gart.-Zeitung 5: 467 (1880)
Cerasus pseudocerasus unranked flore-albopleno Anon. Wiener Ill. Gart.-Zeitung 5: 467 (1880)
Prunus pseudocerasus var. elegans Koidz.
Prunus pseudocerasus unranked roseoplena Späth Nursery Cat. (Späth) 154: 113 (1912)
Prunus pseudocerasus unranked ukon Koehne Mitt. Deutsch. Dendrol. Ges. 18: 168 (1909)
Prunus pseudocerasus f. virescens Koehne Pl. Wilson. 1: 246 (1912)
Prunus pseudocerasus f. viridiflora Makino Bot. Mag. (Tokyo) 22: 102 (1908)
Prunus pseudocerasus unranked yoshino Späth Nursery Cat. (Späth) 121: 115 (1906)
Prunus pseudocerasus unranked spontanea Makino Icon. Fl. Jap. 1(1): t. 1-2 (1900)
Prunus pseudocerasus subvar. glabra Makino Bot. Mag. (Tokyo) 22: 102 (1908)

Common names Top

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Language Common/alternative name
English cerasus pseudocerasus
English chinese cherry
English chinese sour cherry
Persian آلبالوی چینی
Persian گیلاس ترش چینی
Persian البالوی چینی
Persian پرونوس پسودوسراسوس
Persian شینامی-زاکورا
Japanese シナミザクラ
Japanese カラミザクラ
Dutch chinese kers
Dutch chinese zure kers
Chinese 櫻桃
Chinese 莺桃
Chinese 荆桃
Chinese 楔桃
Chinese 樱桃

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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No subvariety added yet.

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001017428
Tropicos 27803686
KEW urn:lsid:ipni.org:names:730152-1
The Plant List rjp-8104
Open Tree Of Life 821180
NCBI Taxonomy 151439
IPNI 730152-1
iNaturalist 707998
GBIF 3021437
EOL 11164512
USDA GRIN 30078
Wikipedia Prunus_pseudocerasus
CMAUP NPO18492

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
Name Level Submitter Released Coverage Size
GCA_041222475.1 ASM4122247v1 Chromosome Beijing University of Agriculture 2024-08-13 35 323.57 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
Population Variation and Phylogeography of Cherry Blossom (Prunus conradinae) in China Dong J, Yi X, Wang X, Li M, Chen X, Gao S, Fu W, Qian S, Zeng X, Yun Y Plants (Basel) 28-Mar-2024
PMCID:PMC11013036
doi:10.3390/plants13070974
PMID:38611504
Identification of the lateral organ boundary domain gene family and its preservation by exogenous salicylic acid in Cerasus humilis Jiang S, Ren W, Ma L, Wu J, Zhang X, Wu W, Kong L, He J, Ma W, Liu X Physiol Mol Biol Plants 20-Mar-2024
PMCID:PMC11018595
doi:10.1007/s12298-024-01438-5
PMID:38633270
Biofortified Rice Provides Rich Sakuranetin in Endosperm Zhao Y, Hu J, Zhou Z, Li L, Zhang X, He Y, Zhang C, Wang J, Hong G Rice (N Y) 02-Mar-2024
PMCID:PMC10908774
doi:10.1186/s12284-024-00697-w
PMID:38430431
Defensive alteration of root exudate composition by grafting Prunus sp. onto resistant rootstock contributes to reducing crown gall disease Chen L, Bian L, Ma Q, Li Y, Wang X, Liu Y Hortic Res 23-Feb-2024
PMCID:PMC11031412
doi:10.1093/hr/uhae049
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960
Evolution and function analysis of auxin response factors reveal the molecular basis of the developed root system of Zygophyllum xanthoxylum Xing Y, Liu C, Zheng C, Li H, Yin H BMC Plant Biol 02-Feb-2024
PMCID:PMC10835889
doi:10.1186/s12870-023-04717-7
PMID:38302884
Morphological and Phylogenetic Analyses Reveal Three New Species of Didymella (Didymellaceae, Pleosporales) from Jiangxi, China Luo X, Hu Y, Xia J, Zhang K, Ma L, Xu Z, Ma J J Fungi (Basel) 18-Jan-2024
PMCID:PMC10821193
doi:10.3390/jof10010075
PMID:38248984
A chromosome-scale assembly of the early-flowering Prunus campanulata and comparative genomics of cherries Hu Y, Feng C, Wu B, Kang M Sci Data 21-Dec-2023
PMCID:PMC10739980
doi:10.1038/s41597-023-02843-3
PMID:38129445
PhytoPipe: a phytosanitary pipeline for plant pathogen detection and diagnosis using RNA-seq data Hu X, Hurtado-Gonzales OP, Adhikari BN, French-Monar RD, Malapi M, Foster JA, McFarland CD BMC Bioinformatics 13-Dec-2023
PMCID:PMC10717670
doi:10.1186/s12859-023-05589-2
PMID:38093207
The Exploration of Flowering Mechanisms in Cherry Plants Xu Y, Li J, Wang P, Wang W, Guo Y, Hao X, Du L, Zhou C Plants (Basel) 27-Nov-2023
PMCID:PMC10708152
doi:10.3390/plants12233980
PMID:38068616
In vitro induction of tetraploidy and its effects on phenotypic variations in Populus hopeiensis Wu J, Zhou Q, Sang Y, Zhao Y, Kong B, Li L, Du J, Ma L, Lu M, Zhang P BMC Plant Biol 13-Nov-2023
PMCID:PMC10641996
doi:10.1186/s12870-023-04578-0
PMID:37957587
Cherry leaf decoction inhibits NMDAR expression and thereby ameliorates CUMS- induced depression-like behaviors through downregulation of α2δ-1 Jiang C, Wang C, Qu W, Wang Y, Wang H, Wei X, Wang M, He Q, Wang Y, Yuan L, Gao Y Heliyon 07-Nov-2023
PMCID:PMC10681947
doi:10.1016/j.heliyon.2023.e21743
PMID:38034773
Soluble sugar and organic acid composition and flavor evaluation of Chinese cherry fruits Zhou J, Yang S, Ma Y, Liu Z, Tu H, Wang H, Zhang J, Chen Q, He W, Li M, Lin Y, Zhang Y, Wu Z, Zhang Y, Luo Y, Tang H, Wang Y, Wang X Food Chem X 21-Oct-2023
PMCID:PMC10622630
doi:10.1016/j.fochx.2023.100953
PMID:37929267
Effect of Short-Term High-Temperature Stimuli on the Functional Response of Trichopria drosophilae (Matsumura) Chen Q, Zhang J, Tian Y, Chen G, Zhang X Insects 06-Sep-2023
PMCID:PMC10531878
doi:10.3390/insects14090748
PMID:37754716
Autotetraploid Origin of Chinese Cherry Revealed by Chromosomal Karyotype and In Situ Hybridization of Seedling Progenies Wang Y, Li X, Feng Y, Wang J, Zhang J, Liu Z, Wang H, Chen T, He W, Wu Z, Lin Y, Zhang Y, Li M, Chen Q, Zhang Y, Luo Y, Tang H, Wang X Plants (Basel) 30-Aug-2023
PMCID:PMC10490022
doi:10.3390/plants12173116
PMID:37687365

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 / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-Dimethoxybenzoate 370912 Click to see COC1=C(C(=CC=C1)OC)C(=O)OCC2=CC=CC=C2 272.29 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Benzoic acid, 2-hydroxy-6-tetradecyl- 5318118 Click to see CCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 334.50 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D 10905866 Click to see 418.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid 5192 Click to see 202.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698321 Click to see 572.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10531102 Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C 570.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-5-benzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11375664 Click to see 510.60 unknown via CMAUP database
[(3S,4aS,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-3-yl] benzoate 54597566 Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O 422.60 unknown via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 54597568 Click to see 448.60 unknown via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 54597567 Click to see 422.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate 54597503 Click to see 376.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] benzoate 11750983 Click to see 438.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] acetate 54597504 Click to see 376.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 6479669 Click to see 464.60 unknown via CMAUP database
[(4aR,6S,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate 54597502 Click to see 360.50 unknown via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 10951647 Click to see 540.60 unknown via CMAUP database
[(4R,4aS,5R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 53388797 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O 438.60 unknown via CMAUP database
[(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-4-formyl-4a,6-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 53388795 Click to see 452.50 unknown via CMAUP database
Isovouacapenol A 636673 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C 420.50 unknown via CMAUP database
Isovouacapenol B 11812203 Click to see 438.60 unknown via CMAUP database
Isovouacapenol C 3009285 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 438.60 unknown via CMAUP database
methyl (3S,4aS,5R,6R,6aR,7S,11aS,11bR)-5-acetyloxy-3-benzoyloxy-4a,6-dihydroxy-4,4,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate 53388938 Click to see 540.60 unknown via CMAUP database
Pulcherrin M 54597569 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5 452.50 unknown via CMAUP database
Vouacapen-5alpha-ol 73354918 Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 42433495 Click to see 220.35 unknown via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 7067459 Click to see 220.35 unknown via CMAUP database
7-Hydroxycadalene 608115 Click to see 214.30 unknown via CMAUP database
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol 16046185 Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Salannin 6437066 Click to see 596.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6aS,7R,11aS,11bR)-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 53388796 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6 572.60 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10627788 Click to see 630.70 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-3,4a-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698605 Click to see 588.60 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11157932 Click to see 630.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
methyl (3S,4S,4aS,5R,6R,6aR,7S,11aS,11bR)-6-acetyloxy-4-(acetyloxymethyl)-3-benzoyloxy-4a,5-dihydroxy-4,11b-dimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate 53388939 Click to see 598.60 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
(3S,8R,9R,10R,13R,14R,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-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Organic cyanides / Nitriles
Hydrogen Cyanide 768 Click to see 27.03 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,7-Dihydroxy-3,8-dimethoxyxanthone 5281634 Click to see 288.25 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
[(1S,2R,4R,5S,7S,10R,11S,18R)-5-hydroxy-6,6,10,18-tetramethyl-3,14-dioxapentacyclo[9.7.0.02,4.05,10.013,17]octadeca-13(17),15-dien-7-yl] benzoate 53388940 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C 436.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,10aR,11aS,11bR)-4a,6-dihydroxy-10a-methoxy-4,4,7,11b-tetramethyl-9-oxo-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 11386164 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 484.60 unknown via CMAUP database
Neocaesalpin E 11450901 Click to see 348.50 unknown via CMAUP database
Neocaesalpin G 11295185 Click to see 510.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin 5282160 Click to see 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see 284.31 unknown via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone 10336604 Click to see 328.30 unknown via CMAUP database
4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether 348130 Click to see 286.28 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy- 11681403 Click to see 326.30 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
Genkwanin 5281617 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one 44260091 Click to see 340.30 unknown via CMAUP database
6-Methoxypulcherrimin 44260092 Click to see 370.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-((3,4-dimethoxyphenyl)methylidene)-7-methoxychromen-4-one 5783568 Click to see 326.30 unknown via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-hydroxychromen-4-one 18778791 Click to see 296.27 unknown via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-methoxychromen-4-one 101489712 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2 310.30 unknown via CMAUP database
(3E)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]-6,7-dimethoxychromen-4-one 44475180 Click to see 342.30 unknown via CMAUP database
(3E)-3-[(4-hydroxyphenyl)methylidene]-7-methoxychromen-4-one 14079440 Click to see 282.29 unknown via CMAUP database
(3E)-7-hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methylidene]chromen-4-one 13846662 Click to see 298.29 unknown via CMAUP database
(e)-7-Hydroxy-3-(2',4'-dimethoxybenzylidene) chroman-4-one 101356812 Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC 312.30 unknown via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one 16082056 Click to see 342.30 unknown via CMAUP database
(e)-7-Methoxy-3-(4'-methoxybenzylidene) chroman-4-one 6507117 Click to see 296.30 unknown via CMAUP database
Bonducellin 14079439 Click to see 282.29 unknown via CMAUP database
Isobonducellin 10423880 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 51533159 Click to see 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone 10337542 Click to see 344.40 unknown via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone 6537040 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database

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