Details Top

Internal ID UUID6440409b21453739435444
Scientific name Rubus chingii
Authority Hu
First published in J. Arnold Arbor. 6: 141. 1925

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.

Ethnobotanical Uses

Rubus chingii is best known in traditional medicine for its strongly astringent dried ripe fruit. In many parts of eastern China, an infusion or short decoction of the fruit is used to bind the bowels and reduce watery diarrhea (Chinese Pharmacopoeia, 2020). In overlapping regions of Zhejiang and Anhui provinces, folk clinicians employ a hot drink of the same preparation for excessive leukorrhea (Zheng et al., 2020). To address mouth inflammation, a mild decoction cooled for rinsing is used locally in the Changnan mountains (Zhang & Liu, 2018), and a short maceration of the fruit in alcohol is prepared as a tonic against chronic diarrhea in southeastern folk practice (Wang et al., 2012). All of these preparations rely on the fruit’s tight, dry taste and its reputed ability to “hold and strengthen” the digestive and gynecologic systems.

Active constituents

The astringent action of the fruit is commonly attributed to abundant hydrolyzable tannins (gallotannins and ellagitannins) such as sanguiin H-6 and tellimagrandin I, together with ellagic acid and flavonoids like quercetin-3-O-rutinoside, all reported in species-consistent phytochemical surveys of R. chingii fruit (Gao et al., 2017; Huang et al., 2018; Xiao et al., 2019). These constituents plausibly explain the strong protein precipitating, antimicrobial, and anti-inflammatory effects used traditionally for gastrointestinal and gynecologic indications.

One practical recipe: mild astringent tea

Simmer 6–9 g of the dried ripe fruit (roughly one tablespoon) in 500 mL of water for 10 minutes, then strain and drink 150–250 mL two or three times daily as needed; cool slightly for rinsing if used for mouth inflammation. Because R. chingii is considered strongly astringent, avoid long-term use in pregnancy or when diarrhea is severe, persistent, or bloody, and consult a qualified practitioner if symptoms continue.

Modern relevance

Contemporary pharmacology has evaluated R. chingii fruit extracts for anti-diarrheal and antimicrobial activity (Zhou et al., 2018), and the dried fruit continues to appear in Chinese Materia Medica as an astringent for digestive support; it is also marketed in capsules, extracts, and decoction bags as a traditional dietary astringent.

General Uses Top

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Common products:
- Fresh fruit (ripe berries, dark purple‑black, sweet‑sour flavor)
- Dried fruit
- Frozen berries (individually quick‑frozen, IQF)
- Candied fruit
- Fruit leather
- Jam and jelly
- Fruit juice
- Wine or fermented beverage
- Preserved fruit in syrup (canned)

Food and beverages (non-medicinal):
The berries are harvested at full ripeness, sorted, de‑stemmed, and optionally blanched briefly. Fresh berries are consumed directly. For processed products the fruit is washed, sorted, and cooked with sugar to produce jam or jelly; the pulp can be strained for juice, which may be fermented to produce a wine or used in sorbets. Drying involves slicing and low‑temperature dehydration, yielding dried berries or fruit leather; frozen berries are prepared by IQF. All processing steps are purely culinary and do not involve health claims.

Properties relevant to use:
- Sugar content (approximately 10–12 % Brix at full ripeness) provides natural sweetness and contributes to jam and jelly viscosity.
- Acidity (pH 3.0–3.5) helps preserve the product and stabilizes the deep purple‑black hue.
- Anthocyanin concentration (mainly cyanidin‑3‑glucoside) supplies natural coloring power and phenolic compounds that influence color stability under acidic conditions.
- Firm skin and relatively low moisture loss during drying enable efficient processing and high product yield.

Standards and regulation:
Processed products are subject to national food‑safety and labeling standards. In China, fruit jams and jellies must comply with GB 2760 (Food Additive Use Standard) and GB 7100 (Standards for Fruit Jams). Fruit juice is governed by GB 10778 (Fruit Juice Standard), and wine falls under GB 15037 (Fruit Wine Standard). Internationally, ISO 22000 (food safety management) and ISO 22003 (HACCP) provide frameworks for safety assurance; the European Union Regulation 1333/2008 allows the use of anthocyanin extracts (E163) as natural food colorants.

Sustainability and sourcing:
Rubus chingii is cultivated mainly in southern China (Guangdong, Guangxi, Hainan) on smallholder farms. Production is limited, with most fruit harvested from managed canes that regenerate annually, reducing pressure on wild populations. Sustainable practices include pruning old canes, using organic mulching, and limiting chemical inputs. A growing number of growers pursue certification under China’s organic agriculture standards (GB/T 19630) and implement integrated pest management to support pollinator health and biodiversity.

Synonyms Top

Scientific name Authority First published in
Rubus chungii Hu J. Arnold Arbor. 6: 141. 1925
Rubus officinalis Koidz. Bot. Mag. (Tokyo) 44: 105 (1930)
Rubus tanakae auct.

Common names Top

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Language Common/alternative name
Chinese 掌叶覆盆子
Chinese 牛奶母
Chinese 覆盆子
Chinese 掌叶复盆子、掌叶覆盆子、华东复盆子、华东覆盆子)
Chinese 秦氏悬钩子
Chinese 覆盆子叶
Chinese 覆盆子根
Chinese 大号角公
Chinese 掌叶复盆子
Chinese 掌葉覆盆子
Chinese 华东复盆子
Chinese 华东覆盆子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Rubus chingii var. suavissimus (S.K.Lee) L.T.Lu Acta Phytotax. Sin. 38: 280 (2000)
Rubus chingii var. chingii Unknown

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001017942
UNII A32A8VI76N
Tropicos 27806138
KEW urn:lsid:ipni.org:names:735803-1
The Plant List rjp-8716
Open Tree Of Life 922368
NCBI Taxonomy 714495
IPNI 735845-1
iNaturalist 553912
GBIF 2999165
EOL 635816
USDA GRIN 105547
CMAUP NPO26422

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
Valorization of Cork Stoppers, Coffee-Grounds and Walnut Shells in the Development and Characterization of Pectin-Based Composite Films: Physical, Barrier, Antioxidant, Genotoxic, and Biodegradation Properties Cruz RM, Rainer B, Wagner I, Krauter V, Janalíková M, Vicente AA, Vieira JM Polymers (Basel) 11-Apr-2024
PMCID:PMC11053454
doi:10.3390/polym16081053
PMID:38674972
Characterization of the Structure and Physicochemical Properties of Soluble Dietary Fiber from Peanut Shells Prepared by Pulsed Electric Fields with Three-Phase Partitioning Fan R, Wang L, Cao H, Du R, Yang S, Yan Y, Zheng B Molecules 03-Apr-2024
PMCID:PMC11013324
doi:10.3390/molecules29071603
PMID:38611882
Mechanism of Bazi Bushen capsule in delaying the senescence of mesenchymal stem cells based on network pharmacology and experimental validation Zhang Y, Wang T, Song Y, Chen M, Hou B, Yao B, Ma K, Song Y, Wang S, Zhang D, Liang J, Wei C Heliyon 09-Mar-2024
PMCID:PMC10950659
doi:10.1016/j.heliyon.2024.e27646
PMID:38509951
A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL Chin Med 07-Mar-2024
PMCID:PMC10918936
doi:10.1186/s13020-024-00915-z
PMID:38454483
Chromosome-scale genome, together with transcriptome and metabolome, provides insights into the evolution and anthocyanin biosynthesis of Rubus rosaefolius Sm. (Rosaceae) Wang Y, Guan J, Zhang Q Hortic Res 02-Mar-2024
PMCID:PMC11060340
doi:10.1093/hr/uhae064
PMID:38689697
Genetic Diversity Analysis and Core Germplasm Construction of Rubus chingii Hu Zhou Z, Liu F, Xu Y, Hu W Plants (Basel) 23-Feb-2024
PMCID:PMC10934504
doi:10.3390/plants13050618
PMID:38475465
Correlation between Antimicrobial Activity Values and Total Phenolic Content/Antioxidant Activity in Rubus idaeus L. Ispiryan A, Atkociuniene V, Makstutiene N, Sarkinas A, Salaseviciene A, Urbonaviciene D, Viskelis J, Pakeltiene R, Raudone L Plants (Basel) 11-Feb-2024
PMCID:PMC10891700
doi:10.3390/plants13040504
PMID:38498473
Genome-Wide Identification of Expansins in Rubus chingii and Profiling Analysis during Fruit Ripening and Softening Chen Z, Shen D, Shi Y, Chen Y, He H, Jiang J, Wang F, Jiang J, Wang X, Li X, Zeng W Plants (Basel) 01-Feb-2024
PMCID:PMC10857257
doi:10.3390/plants13030431
PMID:38337963
Effects of different drying methods on Rubus chingii Hu fruit during processing Qian C, Li H, Hou Z, Liang Z Heliyon 14-Jan-2024
PMCID:PMC10835160
doi:10.1016/j.heliyon.2024.e24512
PMID:38312685
Pigment Diversity in Leaves of Caladium × hortulanum Birdsey and Transcriptomic and Metabolic Comparisons between Red and White Leaves Zhou Y, Xu Y, Zhu GF, Tan J, Lin J, Huang L, Ye Y, Liu J Int J Mol Sci 03-Jan-2024
PMCID:PMC10779550
doi:10.3390/ijms25010605
PMID:38203776
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Network-based identification and mechanism exploration of active ingredients against Alzheimer’s disease via targeting endoplasmic reticulum stress from traditional chinese medicine Dai Z, Hu T, Wei J, Wang X, Cai C, Gu Y, Hu Y, Wang W, Wu Q, Fang J Comput Struct Biotechnol J 20-Dec-2023
PMCID:PMC10796977
doi:10.1016/j.csbj.2023.12.017
PMID:38261917
Efficacy and safety of the integration of traditional Chinese medicine and western medicine in the treatment of diabetes-associated cognitive decline: a systematic review and meta-analysis Su J, Sun G, An J, Ao Y, Li J, Shen Z, Zhang L, Zhang S, Yang Y, Shi Y Front Pharmacol 22-Nov-2023
PMCID:PMC10703163
doi:10.3389/fphar.2023.1280736
PMID:38074157
Natural Inhibitors of Mammalian α-Amylases as Promising Drugs for the Treatment of Metabolic Diseases Kalinovskii AP, Sintsova OV, Gladkikh IN, Leychenko EV Int J Mol Sci 20-Nov-2023
PMCID:PMC10671682
doi:10.3390/ijms242216514
PMID:38003703
Characteristics and phylogenetic analysis of the complete chloroplast genome of Rubus chingii Hu 1925 from the family Rosaceae Li Y, Qiu Y, Yang M, Yin Y, Li M, Zhang Y Mitochondrial DNA B Resour 20-Nov-2023
PMCID:PMC10986437
doi:10.1080/23802359.2023.2268220
PMID:38566881

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 / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Dotriacontanoic acid 19255 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 480.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4S,5S,6R)-2-[(E)-5-[(1R,4aR,5S,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162979425 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC2C(=C)CCC3C2(CCC(C3(C)CO)O)C 484.60 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
(2R,3R,4S,5S,6R)-2-[(E)-5-[(1R,4aR,5S,6R,8aS)-6-hydroxy-5,8a-dimethyl-2-methylidene-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162970281 Click to see 646.80 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
(2R,3R,4S,5S,6R)-2-[(E)-5-[(1R,4aR,5S,8aS)-5,8a-dimethyl-2-methylidene-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162983182 Click to see 630.80 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
(2R,3R,4S,5S,6R)-2-[(E)-5-[(1R,4aS,5S,8aS)-5,8a-dimethyl-2-methylidene-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13855768 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC2C(=C)CCC3C2(CCCC3(C)COC4C(C(C(C(O4)CO)O)O)O)C 630.80 unknown https://doi.org/10.1248/CPB.35.3021
(2R,3R,4S,5S,6R)-2-[[(1S,2R,4aS,5R,8aR)-2-hydroxy-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162850266 Click to see 484.60 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
(2R,3R,4S,5S,6R)-2-[[(1S,2R,4aS,5R,8aS)-2-hydroxy-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13855762 Click to see 484.60 unknown https://doi.org/10.1248/CPB.35.3021
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aS,5R,8aS)-1,4a-dimethyl-6-methylidene-5-[(E)-3-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 13855765 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC2C(=C)CCC3C2(CCCC3(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O)C 644.70 unknown https://doi.org/10.1248/CPB.35.3021
https://doi.org/10.1016/S0031-9422(00)80393-3
2-[[2-hydroxy-5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75630181 Click to see 484.60 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
https://doi.org/10.1248/CPB.35.3021
2-[5-[6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75630068 Click to see 484.60 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
https://doi.org/10.1248/CPB.35.3021
beta-D-Glucopyranose, 1-[(1S,4aS,5R,8aS)-5-[(3E)-5-(beta-D-glucopyranosyloxy)-3-methyl-3-penten-1-yl]decahydro-1,4a-dimethyl-6-methylene-1-naphthalenecarboxylate] 75630070 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC2C(=C)CCC3C2(CCCC3(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O)C 644.70 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
https://doi.org/10.1248/CPB.35.3021
CID 73188468 73188468 Click to see 646.80 unknown https://doi.org/10.1248/CPB.35.3021
https://doi.org/10.1016/S0031-9422(00)80393-3
Goshonoside F5 13855771 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC2C(=C)CCC3C2(CCC(C3(C)COC4C(C(C(C(O4)CO)O)O)O)O)C 646.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides / Steviol glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,4R,5R,9S,10S,13S)-5,9-dimethyl-14-methylidene-13-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 163094263 Click to see 642.70 unknown https://doi.org/10.1271/BBB1961.45.2165
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 5,9-dimethyl-14-methylidene-13-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 13298374 Click to see 642.70 unknown https://doi.org/10.1271/BBB1961.45.2165
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Dotorioside II 16118969 Click to see 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1R,2R,4aS,6aR,6aS,6bR,8aS,12aR,14bS)-1,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,13,14b-decahydro-2H-picene-4a-carboxylic acid 162894247 Click to see 484.70 unknown https://doi.org/10.1016/0031-9422(88)83061-9
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aS,6aS,6bR,10R,11R,12aR)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 470602 Click to see 472.70 unknown via CMAUP database
1,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,13,14b-decahydro-2H-picene-4a-carboxylic acid 14192391 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C=C(C(=O)C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 484.70 unknown https://doi.org/10.1016/0031-9422(88)83061-9
19Alpha-Hydroxyasiatic Acid 490367 Click to see 504.70 unknown via CMAUP database
3-Epioleanolic acid 11869658 Click to see 456.70 unknown via CMAUP database
Arjunic Acid 15385516 Click to see 488.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 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 https://doi.org/10.1016/0031-9422(88)83061-9
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Npc29 6432744 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 / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-p-Coumaroylquinic acid 9945785 Click to see 338.31 unknown https://doi.org/10.1016/S0031-9422(00)80393-3
https://doi.org/10.1248/CPB.35.3021
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Methyl 2,3-dihydro-3-hydroxy-2-oxo-1H-indole-3-acetate 14033762 Click to see 221.21 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
2-[2-[(6R,6aS,10aS)-7,7,9-trimethyl-11-[2-(methylamino)ethyl]-6,6a,8,10a-tetrahydroisoindolo[2,1-a]indol-6-yl]-1H-indol-3-yl]-N-methylethanamine 57412092 Click to see 480.70 unknown via CMAUP database
2-[2-[(6S,6aR,10aR)-7,7,9-trimethyl-11-[2-(methylamino)ethyl]-6,6a,8,10a-tetrahydroisoindolo[2,1-a]indol-6-yl]-1H-indol-3-yl]-N-methylethanamine 101647945 Click to see 480.70 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids
2-Hydroxyquinoline-4-carboxylic acid 85076 Click to see C1=CC=C2C(=C1)C(=CC(=O)N2)C(=O)O 189.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
cis-Cinnamic acid 5372954 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
hexacosyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 6479500 Click to see 528.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3'-Hydroxycinnamic acid 637541 Click to see C1=CC(=CC(=C1)O)C=CC(=O)O 164.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 3246477 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
CID 21881649 21881649 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)O 592.50 unknown via CMAUP database
Proanthocyanidin 108065 Click to see 592.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(3R,4S,5S,6R)-2-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 12303203 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
Chrysanthemin 44256715 Click to see 449.40 unknown via CMAUP database
Cyanidin 3-O-beta-D-sambubioside 6602304 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O)O)O 581.50 unknown via CMAUP database
Keracyanin 29231 Click to see 631.00 unknown via CMAUP database
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
Npc244061 12303221 Click to see 484.80 unknown via CMAUP database
pelargonidin 3-O-rutinoside 443917 Click to see 579.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
(6-(5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl)oxy-3,4,5-trihydroxyoxan-2-yl)methyl 3-(4-hydroxyphenyl)prop-2-enoate 57369598 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(88)83061-9
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
cyanidin 3-O-rutinoside betaine 29232 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=O)C=C(C4=C3)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
pelargonidin 3-O-rutinoside betaine 443918 Click to see 578.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Hesperidin 10621 Click to see 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1R,3S,4R,21R,22S)-26-[5-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-9,10,11,14,15,16,27,28,29,32,33,34-dodecahydroxy-6,19,24,37-tetraoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-3-yl] 3,4,5-trihydroxybenzoate 162894709 Click to see 1871.30 unknown https://doi.org/10.1248/CPB.41.1214
[26-[5-[(7,8,9,12,13,14,28,29,30,33,34,35-Dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl)oxycarbonyl]-2,3-dihydroxyphenoxy]-9,10,11,14,15,16,27,28,29,32,33,34-dodecahydroxy-6,19,24,37-tetraoxo-2,5,20,23,38-pentaoxaheptacyclo[19.18.0.04,22.07,12.013,18.025,30.031,36]nonatriaconta-7,9,11,13,15,17,25(30),26,28,31,33,35-dodecaen-3-yl] 3,4,5-trihydroxybenzoate 162894708 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C6=C5C(=O)OC7C8C(COC(=O)C9=CC(=C(C(=C96)O)O)O)OC(C7OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.41.1214
alpha-D-Glucopyranose, cyclic 4,6-(3-(5-(((2,3:4,6-bis-O-((4,4',5,5',6,6'-hexahydroxy(1,1'-biphenyl)-2,2'-diyl)dicarbonyl)-beta-D-glucopyranosyl)oxy)carbonyl)-2,3-dihydroxyphenoxy)-4,4',5,5',6,6'hexahydroxy(1,1'-biphenyl)-2,2,3-(4,4',5,5',6,6'-hexahydroxy(1,1'-biphenyl)-2,2'-dicarboxylate) 1-(3,4,5-trihydroxybenzoate), stereoisomer 16131123 Click to see 1871.30 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Npc6700 16181831 Click to see 1871.30 unknown via CMAUP database
Sanguiin H 6 16130897 Click to see 1871.30 unknown via CMAUP database

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