Castanopsis hystrix

Details Top

Internal ID UUID6440554b371d1173457730
Scientific name Castanopsis hystrix
Authority A.DC.
First published in J. Bot. 1: 182. 1863 [Jun ? 1863]

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.

An infusion of Cassia angustifolia leaves is a classic digestive remedy in the Unani tradition of the Middle East and North Africa, prepared by steeping 1–2 g of dried leaflets in 150 mL of near‑boiling water for 10–15 minutes; the dose of this “tea” is typically taken before breakfast and at bedtime, and the Unani pharmacopoeia advises limiting use to a short course due to cathartic effects. In West Africa, particularly Nigeria and Ghana, a decoction of the dried leaflets or pods in water is taken daily as a “bitter” tonic to promote regularity; Odugbemi and Akinsulire (2008) document this preparation and emphasize careful dosing to avoid griping. Across the Horn of Africa and the Arabian Peninsula, herbal practitioners likewise report short courses of strong leaf or pod infusions for occasional constipation, with the WHO monographs noting these aqueous preparations as standard practice. In both Unani and contemporary domestic settings, the leaves are most commonly used for infusions, while the mature pods are preferred for longer‑simmered decoctions.

A practical leaf tea can be made by pouring 200 mL of just‑boiled water over 1–2 g of dried Cassia angustifolia leaflets, covering and steeping 10–15 minutes, then straining. For a decoction, simmer 2 g of dried leaflets or crushed pods in 250 mL of water for 10 minutes, cool briefly, and take warm. For a tincture, a 1:5 ethanolic extract (45% alcohol) can be prepared at a common ratio such as 100 g dried leaves macerated in 500 mL solvent for two weeks with daily shaking; typical short‑course oral use is 1–2 mL once or twice daily for mild constipation. Safety notes are widely consistent: avoid continuous use beyond 7–10 days and do not use in intestinal obstruction, inflammatory bowel disease, or during pregnancy; children and those with gallstones should use under professional guidance. While tincture usage is documented in modern herbal practice, most classic and contemporary sources emphasize the infusions and decoctions.

The anthraquinone glycosides sennosides A and B, which are the principal laxative constituents in the leaves and pods, are well‑documented, and senna is recognized by WHO and the British Herbal Medicine Association for short‑term constipation relief. Other constituents, including flavonoids and mucilage, are also present and contribute to the plant’s bitterness and soothing qualities. The modern relevance is clear: senna tea remains widely available globally as a registered herbal medicinal product and dietary supplement, with ongoing research on standardization and pharmacokinetics, yet in practice, cautious short‑term use of the infusions remains common for occasional constipation.

General Uses Top

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Common products:
Edible nuts are roasted or milled into flour; tannin extracts are produced from bark and wood chips; timber yields sawnwood, plywood, and veneer; charcoal and fuelwood are produced locally.

Industrial and craft applications:
Tannin extracts are used in leather tanning and as binding agents in plywood adhesives; silica-rich bark and sapwood generate fine charcoal for metalworking and drawing. Timbers produce veneers and plywood for furniture, flooring, and joinery; sawnwood is used in construction and carpentry.

Food and beverages (non-medicinal):
Nuts are eaten roasted or as flour for noodles, confections, and baking; they are not described as staples but occasionally used as snacks. No fermented beverages are documented for this species.

Colorants and tanning:
Bark and wood yield brown tannin extracts widely used for leather tanning; tannins are of the hydrolyzable class typical of Castanopsis. Extracts produce natural brown dyes suitable for protein fibers and mordanted cellulose fibers.

Wood and fiber:
Timber is dense and strong with fine to medium texture; species-specific grading and marking for furniture-grade veneers, joinery, and interior millwork are recognized in regional trade. Fiber is used for charcoal; pulp and paper usage is not documented for the species.

Fragrance and cosmetics:
Fragrance or cosmetic uses are not documented for this species.

Properties relevant to use:
High tannin content provides reactivity and UV stability in tanning and adhesives; hydrolyzable tannins are relatively soluble and metal-ion reactive. Wood density is high and species-specific timber grading systems recognize it for furniture applications; ring-porous wood contributes to strength but higher shrinkage.

Standards and regulation:
Regional timber grading and export standards apply to furniture-grade and veneer timbers; national regulations govern processed tannin products used in leather; compliance with timber legality and chain-of-custody systems is common in international trade. Food uses are subject to local food safety and labeling rules where applicable.

Sustainability and sourcing:
Castanopsis hystrix has a wide East and Southeast Asian distribution and is commonly harvested from natural forests and secondary stands for tannin extracts, nuts, and timber; local management practices aim to maintain viable populations through selection cutting and regeneration measures.

Synonyms Top

Scientific name Authority First published in
Castanopsis brunnea (H.Lév.) A.Camus Les Chataigniers 482 1929

Common names Top

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Language Common/alternative name
English patle katus
Nepali पातले कटुस
Chinese 锥丝栗
Chinese 一种维管植物
Chinese 紅錐
Chinese 鉤栗
Chinese 火燒柯
Chinese 锥栗
Chinese 刺锥栗
Chinese 红㰀
Chinese 红锥栗
Chinese 椆栗
Chinese 红锥
Chinese 红椽木子
Chinese 栲树
Chinese 刺栲

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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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-0001240111
KEW urn:lsid:ipni.org:names:60450806-2
The Plant List tro-50106202
PaleoBotany 93849
Open Tree Of Life 129485
NCBI Taxonomy 167390
IPNI 295396-1
iNaturalist 544430
GBIF 5333131
Freebase /m/0271hkk
EOL 1251942
USDA GRIN 9512
Wikipedia Castanopsis_hystrix
CMAUP NPO10093

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
Provenance and family variations in early growth of Manchurian walnut (Juglans mandshurica Maxim.) and selection of superior families Zhang Q, Chen S, Qu G, Yang Y, Lu Z, Wang J, Tigabu M, Liu J, Xu L, Wang F PLoS One 07-Mar-2024
PMCID:PMC10919699
doi:10.1371/journal.pone.0298918
PMID:38451964
Community composition of phytopathogenic fungi significantly influences ectomycorrhizal fungal communities during subtropical forest succession Chen M, Yang J, Xue C, Tu T, Su Z, Feng H, Shi M, Zeng G, Zhang D, Qian X Appl Microbiol Biotechnol 10-Jan-2024
PMCID:PMC10781812
doi:10.1007/s00253-023-12992-5
PMID:38204135
Characteristics and Species Diversity of Semi-Natural Plant Communities on Langqi Island Liu Y, Huang Y, Wang Y, Wang C, Xiao Z, Shen S, Zeng J, Deng C Biology (Basel) 24-Dec-2023
PMCID:PMC10813280
doi:10.3390/biology13010011
PMID:38248442
Editorial: Highly contiguous plant genome assembly and transcriptional regulation Tian XC, Jia KH Front Plant Sci 13-Dec-2023
PMCID:PMC10751298
doi:10.3389/fpls.2023.1331498
PMID:38152147
Morphology and Molecular Phylogeny Reveal Five New Species of Laccaria (Hydnangiaceae, Agaricales) from Southern China Zhang M, Gao XL, Mu LQ, Deng WQ J Fungi (Basel) 08-Dec-2023
PMCID:PMC10744585
doi:10.3390/jof9121179
PMID:38132780
Chromosome-scale genome assembly of sweet tea (Lithocarpus polystachyus Rehder) Liu H, Zhang R, Zhou BF, Shen Z, Chen XY, Gao J, Wang B Sci Data 06-Dec-2023
PMCID:PMC10700502
doi:10.1038/s41597-023-02791-y
PMID:38057329
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945
Foraging Behaviors of Red Imported Fire Ants (Hymenoptera Formicidae) in Response to Bait Containing Different Concentrations of Fipronil, Abamectin, or Indoxacarb Du C, Lyu H, Wang L, Mao L, Li L, Yang X, Wang C Insects 31-Oct-2023
PMCID:PMC10671866
doi:10.3390/insects14110852
PMID:37999051
The complete chloroplast genome of Castanopsis hystrix Hook. f. & Thomson ex A. DC. 1863 (Fagaceae) Gui Z, Sun Y, Lin D, Zhong L, Wei Q, Zhu H, Li M Mitochondrial DNA B Resour 08-Sep-2023
PMCID:PMC10494720
doi:10.1080/23802359.2023.2253999
PMID:37701524
Changes in Soil Properties, Microbial Quantity and Enzyme Activities in Four Castanopsis hystrix Forest Types in Subtropical China Wang R, Ma J, Liang H, Zhang Y, Yang J, Chen F, Wang Y, Yan W Plants (Basel) 22-Jun-2023
PMCID:PMC10347116
doi:10.3390/plants12132411
PMID:37446972
Flying squirrels use a mortise-tenon structure to fix nuts on understory twigs Xu H, Xia L, Spence JR, Lin M, Lu C, Li Y, Chen J, Luo T, Li Y, Fang S eLife 13-Jun-2023
PMCID:PMC10328505
doi:10.7554/eLife.84967
PMID:37309191
Contrasting sap flow characteristics between pioneer and late-successional tree species in secondary tropical montane forests of Eastern Himalaya, India Kumar M, Joseph G, Bhutia Y, Krishnaswamy J J Exp Bot 08-Jun-2023
PMCID:PMC10498023
doi:10.1093/jxb/erad207
PMID:37290031
A chromosome-scale genome assembly of Castanopsis hystrix provides new insights into the evolution and adaptation of Fagaceae species Huang WC, Liao B, Liu H, Liang YY, Chen XY, Wang B, Xia H Front Plant Sci 25-Apr-2023
PMCID:PMC10197965
doi:10.3389/fpls.2023.1174972
PMID:37215286
Mixing planting with native tree species reshapes soil fungal community diversity and structure in multi-generational eucalypt plantations in southern China Li C, Xu Y, Wang Z, Zhu W, Du A Front Microbiol 22-Feb-2023
PMCID:PMC9994620
doi:10.3389/fmicb.2023.1132875
PMID:36910166
Effect of Climate Change on the Potentially Suitable Distribution Pattern of Castanopsis hystrix Miq. in China Shen L, Deng H, Zhang G, Ma A, Mo X Plants (Basel) 06-Feb-2023
PMCID:PMC9966962
doi:10.3390/plants12040717
PMID:36840065

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 / Acylaminobenzoic acid and derivatives
4-[(2-amino-4-oxo-1H-pteridin-6-yl)methyl-formylamino]benzoic acid 97575 Click to see 340.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic Acid 5280896 Click to see 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one 92835934 Click to see 306.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(3beta,5alpha,7alpha)-3,7-Dihydroxyandrostan-17-one 9815044 Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
(3R,5R,7S,8R,9S,10S,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one 57386710 Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
(3R,5R,8R,9S,10S,13S,14S,17S)-3,17-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one 69924431 Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3R,5R,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-7,17-dione 57386713 Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O 304.40 unknown via CMAUP database
(3R,5S,6S,8R,9S,10R,13S,14S)-3,6-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one 69766330 Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
(3S,5R,7R,8S,9S,10S,13R,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,16-triol 99574281 Click to see 308.50 unknown via CMAUP database
(3S,5R,7S,8S,9S,10S,13S,14S,16S)-3,7,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one 99572894 Click to see 322.40 unknown via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one 99573267 Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one 99573266 Click to see 306.40 unknown via CMAUP database
(3S,5S,6S,8S,9S,10R,13R,14S,16R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol 99574278 Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(C4)O)C)O 308.50 unknown via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 99571962 Click to see 306.40 unknown via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 99571961 Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3S,5S,8S,9S,10S,11R,13S,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,11,16-triol 100922640 Click to see CC12CCC(CC1CCC3C2C(CC4(C3CC(C4)O)C)O)O 308.50 unknown via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one 99601533 Click to see 306.40 unknown via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one 99575783 Click to see 306.40 unknown via CMAUP database
(5R,8S,9S,10R,13S,14S,17S)-5,17-dihydroxy-10,13-dimethyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one 10979706 Click to see 306.40 unknown via CMAUP database
(5R,8S,9S,10S,13R,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-dione 99571971 Click to see 304.40 unknown via CMAUP database
(5S,6R,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99573707 Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O 306.40 unknown via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16R)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99573706 Click to see 306.40 unknown via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99573705 Click to see 306.40 unknown via CMAUP database
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99574441 Click to see 306.40 unknown via CMAUP database
(5S,8S,9R,10S,13S,14S,16R)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione 99571360 Click to see 320.40 unknown via CMAUP database
(5S,8S,9R,10S,13S,14S,16S)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione 99571358 Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O 320.40 unknown via CMAUP database
(5S,8S,9S,10S,11R,13S,14S,16R)-11,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 100922644 Click to see 306.40 unknown via CMAUP database
(5S,8S,9S,10S,13S,14S,16R)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 99574177 Click to see 304.40 unknown via CMAUP database
(5S,8S,9S,10S,13S,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 99574175 Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C 304.40 unknown via CMAUP database
11-Hydroxyandrosterone 21139727 Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
11alpha-Hydroxy-5alpha-androstane-3,17-dione 101709630 Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4=O)C)O 304.40 unknown via CMAUP database
3beta-Hydroxy-5alpha-androstane-7,17-dione 11954160 Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O 304.40 unknown via CMAUP database
5alpha-Androstan-11-one, 3alpha,17beta-dihydroxy- 10125601 Click to see 306.40 unknown via CMAUP database
5alpha-Androstan-3-one, 11alpha,17beta-dihydroxy- 22796602 Click to see 306.40 unknown via CMAUP database
5alpha-Androstan-3beta,17beta-diol-7-one 11868973 Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
5alpha-Androstan-6-one, 3beta,17beta-dihydroxy- 11551286 Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
5alpha-Androstane-3,7,17-trione 11266632 Click to see CC12CCC(=O)CC1CC(=O)C3C2CCC4(C3CCC4=O)C 302.40 unknown via CMAUP database
7-beta-Hydroxyepiandrosterone 9836181 Click to see 306.40 unknown via CMAUP database
Androstan-3-one, 6,17-dihydroxy-, (5alpha,6alpha,17beta)- 15838416 Click to see 306.40 unknown via CMAUP database
Androstan-6-one, 3,17-dihydroxy-, (3alpha,5alpha,17beta)- 15929496 Click to see 306.40 unknown via CMAUP database
Androstane-3,11,17-triol 57396177 Click to see 308.50 unknown via CMAUP database
Androstane-3,17-dione, 6-hydroxy-, (5alpha,6alpha)- 22296022 Click to see 304.40 unknown via CMAUP database
Androstane-3,6,17-triol 170796 Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(C4)O)C)O 308.50 unknown via CMAUP database
Androstane-3,7,17-triol, (3beta,5alpha,7beta,17beta)- 68995028 Click to see 308.50 unknown via CMAUP database
Exemestane Impurity 30 15917986 Click to see 306.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
10-Hydroxy-3-oxoestr-4-en-17-yl acetate 91691749 Click to see CC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)CCC34O)C 332.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
Glutaric acid 743 Click to see C(CC(=O)O)CC(=O)O 132.11 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate 3698251 Click to see C(C(=O)[O-])[OH2+] 76.05 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids
Quininic acid 345824 Click to see 203.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3S,10S)-2,10-bis(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-8-one 10366587 Click to see 452.40 unknown https://doi.org/10.1016/0031-9422(93)85419-R
(4R,8R,9S)-4,8-bis(3,4-dihydroxyphenyl)-5,9-dihydroxy-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-2-one 100978387 Click to see 452.40 unknown https://doi.org/10.1016/0031-9422(93)85419-R
4,8-bis(3,4-dihydroxyphenyl)-5,9-dihydroxy-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-2-one 73822599 Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(93)85419-R
9,10-Dihydro-10-(3,4-dihydroxyphenyl)-pyrano(2,3-h)catechin-8-one 10343836 Click to see 452.40 unknown https://doi.org/10.1016/0031-9422(93)85419-R
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(93)85419-R

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