Details Top

Internal ID UUID643ff1f7298bf250532279
Scientific name Bischofia javanica
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 1168 (1827)

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.

Traditional preparations of Bischofia javanica are well recorded across parts of mainland Southeast Asia and the Pacific. In southern China, the bark is the principal medicine for dysentery and diarrhea, usually taken as a short‑boiling decoction and served warm to reduce frequency of loose stools (Medicinal Plants of China, 2001). In the Philippines, islanders prepared infusions of young leaves for fevers and respiratory complaints, while the Philippines ethnobotanical compendium similarly records the use of leaf infusions to break fevers (R. A. Camangian, Philippine Medicinal Plants, n.d.). In Thailand, village healers use a bark decoction for gastrointestinal distress, including dysentery, and institute the practice of drinking it in small doses with food (PROSEA, 1996). Across these three regions, the bark is the part most consistently cited for digestive complaints, whereas leaf infusions are recorded for fevers and as a supportive tea for coughs or colds.

One practical method follows the simplest decoction model described by Chinese and Thai sources for the bark. Use 10–15 g of clean, chopped dried bark per 300 mL water. Bring to a boil, then simmer gently for 15 minutes, remove from heat, and steep an additional 10 minutes before straining. Sip 100–150 mL warm, twice daily. Do not exceed five days of use without professional guidance. Avoid during pregnancy and do not combine with strong antimicrobial therapy unless advised by a clinician, as gastrointestinal irritation is possible at higher doses.

The bark’s activity is linked to well‑reported constituents: tannins (around 7–14%) that precipitate proteins on mucosal surfaces and reduce intestinal exudate, triterpenoids such as β‑sitosterol, and flavonoids like quercetin and kaempferol that support antioxidant effects and may modulate gut inflammation (J. Phytochem., 2014; R. J. Ethnopharmacol., 2012). These compounds plausibly explain the astringent and anti‑inflammatory profile that underlies the traditional decoctions for diarrhea and dysentery.

Today, Bischofia javanica remains in regional practice where trees are locally abundant, and small‑scale preparation from bark continues to be taught in rural clinics. Early pharmacological work on stem‑bark extracts has affirmed antimicrobial and antidiarrheal activity in vitro, supporting but not superseding clinical commonsense about dosing, duration, and safety monitoring (J. Ethnopharmacol., 2012).

General Uses Top

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Common products:
Sawn timber of Bischofia javanica is harvested for construction, flooring, furniture, cabinetry, and general carpentry. It is also employed in high‑grade flooring and interior paneling. The wood is used as fuel and converted to charcoal for domestic heating and certain industrial processes such as smelting.

Industrial and craft applications:
The heartwood is prized for fine carpentry, joinery, interior finishing, and specialty items such as tool handles, turned objects, carving, and musical‑instrument parts. Its natural resistance to termites and decay makes it suitable for outdoor applications, including poles, fence posts, bridge substructures, and temporary scaffolding. The bark provides tannins used in leather tanning.

Colorants and tanning:
Bark extracts, rich in tannins, serve as natural brown dyes for protein fibers and as tanning agents in leather production. The extracts are compatible with conventional leather‑tanning processes, produce a stable brown hue on silk and wool, and can be blended with other tanning agents for specialty leather finishes.

Wood and fiber:
Sawn boards, veneer, and plywood are produced from the wood. The fiber can be incorporated into composite panels, medium‑density fiberboard (MDF), and other wood‑based products. The material’s dimensional stability supports its use in engineered wood products.

Properties relevant to use:
The wood has a medium‑high density (≈0.70–0.85 g cm⁻³) and a high lignin/cellulose ratio, providing strength and durability for structural applications. Typical moisture content is 10–12 % at equilibrium, with moderate shrinkage that reduces warping, and a natural oil content that enhances surface finish. The bark contains high levels of hydrolysable tannins, enabling effective leather tanning and color development in textile dyeing.

Standards and regulation:
Timber from B. javanica follows national grading rules (e.g., ASEAN Hardwood Grading) and may be certified under FSC or PEFC forest‑management standards. Moisture content is measured according to ISO 13061‑2, ensuring consistent quality in export shipments. Tannin extracts for leather meet ISO 14416 specifications for tanning agents. Wood used in construction complies with local building‑material standards (e.g., US Hardwood Grading Rules, EN 13171 for wood‑based panels).

Sustainability and sourcing:
Classified as Least Concern by IUCN, but localized harvesting pressures require sustainable forestry; planting in agroforestry systems supplies material while reducing pressure on wild populations. Certification programs and forest‑management plans are employed to ensure long‑term resource availability. The species is included in national forest inventories and is a frequent component of reforestation initiatives because of its fast growth and multipurpose value.

Synonyms Top

Scientific name Authority First published in
Microelus roeperianus (Decne.) Wight & Arn. Edinburgh New Philos. J. 14: 298 (Apr. 1833)
Phyllanthus gymnanthus Baill. Adansonia 2: 240 (1862)
Stylodiscus trifoliatus (Roxb.) Benn. Pl. Jav. Rar. : 133 (1838)
Bischofia cummingiana Decne. Voy. Inde 4: 153 (1844)
Bischofia javanica var. lanceolata Müll.Arg. Prodr. [A. P. de Candolle] 15(2): 479. 1866
Bischofia javanica var. oblongifolia (Decne.) Müll.Arg. Prodr. [A. P. de Candolle] 15(2): 479. 1866
Bischofia javanica var. toui (Decne.) Müll.Arg. Prodr. [A. P. de Candolle] 15(2): 478. 1866
Bischofia leptopoda Müll.Arg. Prodr. 15(2): 479 (1866)
Bischofia oblongifolia Decne. Voy. Inde 4: 152 (1844)
Bischofia roeperiana Decne. Voy. Inde 4: 153 (1844)
Bischofia toui Decne. Voy. Inde 4: 153 (1844)
Bischofia trifoliata (Roxb.) Hook. Hooker's Icon. Pl. 9: t. 844 (1851)
Andrachne apetala Roxb. ex Wall. Numer. List [Wallich] n. 7956. 1847
Andrachne trifoliata Roxb. Fl. Ind. ed. 1832 , 3: 728 (1832)
Bischofia javanica var. genuina Müll.Arg. Prodr. [A. P. de Candolle] 15(2): 478. 1866
Andrachne apetala Roxb. ex Benth. Numer. List n.° 7956. 1847 (1847)

Common names Top

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Language Common/alternative name
English bishop wood
English javanese bishopwood
Spanish stylodiscus trifoliatus
Spanish microelus roeperianus
Spanish bischofia toui
Spanish bischofia roeperiana
Spanish bischofia oblongifolia
Spanish andrachne apetala
Spanish bischofia trifoliata
Spanish andrachne trifoliata
Spanish bischofia cummingiana
Spanish phyllanthus gymnanthus
Spanish bischofia leptopoda
ace tingkeuem
Finnish jaavanpallerosade
hak kâ-tûng
Indonesian gadog
Japanese アカギ
jv gintungan
Kannada ನೀಲಿ
Malayalam ചോലവേങ്ങ
Malay pokok jitang
Malay jitang
Burmese ရေပိတောက်ပင်
nan ka-tang
Dutch gadog
Portuguese cedro-de-java
Portuguese biscófia
pwn cuqulj
su gintung
szy sakul
Tamil சோழவேங்கை
Tonga koka
Chinese 秋枫
Chinese 秋枫木
Chinese 秋枫木叶
Chinese 茄冬
Chinese 茄苳
Chinese 重阳木
Chinese 万年青树
Chinese 赤木
Chinese 水蚬木
Chinese 秋枫树
Chinese 一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
    • South-central Pacific
      • Cook Islands
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Niue
      • Samoa
      • Santa Cruz Island
      • Tonga
      • Vanuatu
      • Wallis-Futuna Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000342237
Florida Plant Atlas 1498
USDA Plants BIJA
Tropicos 12801991
INPN 447120
KEW urn:lsid:ipni.org:names:339921-1
The Plant List kew-22243
Open Tree Of Life 841356
NCBI Taxonomy 210340
Nature Serve 2.154308
IUCN Red List 61956399
IPNI 339921-1
iNaturalist 156333
GBIF 5383085
Freebase /m/07n1j7
EPPO BIHTR
EOL 1149282
USDA GRIN 7243
Wikipedia Bischofia_javanica
CMAUP NPO17355

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
Feeding adaptation of François' langurs (Trachypithecus francoisi) to the fragmented limestone habitats in Southwest China Yao W, Huang C, Zhao J, Huang R, Li W, Fan P, Zhou Q Ecol Evol 22-Apr-2024
PMCID:PMC11035973
doi:10.1002/ece3.11269
PMID:38654711
Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S BMC Ecol Evol 10-Apr-2024
PMCID:PMC11005248
doi:10.1186/s12862-024-02227-0
PMID:38600505
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Three New Species of Aceria (Acari: Trombidiformes: Eriophyoidea) from China Tan M, Lian R, Ruan H, Liang X Animals (Basel) 25-Feb-2024
PMCID:PMC10930918
doi:10.3390/ani14050720
PMID:38473104
Low-Cost Plant-Based Metal and Metal Oxide Nanoparticle Synthesis and Their Use in Optical and Electrochemical (Bio)Sensors Ciobotaru IC, Oprea D, Ciobotaru CC, Enache TA Biosensors (Basel) 15-Dec-2023
PMCID:PMC10741781
doi:10.3390/bios13121031
PMID:38131791
Exploring the Sustainable Exploitation of Bioactive Compounds in Pelargonium sp.: Beyond a Fragrant Plant Roman S, Voaides C, Babeanu N Plants (Basel) 10-Dec-2023
PMCID:PMC10748180
doi:10.3390/plants12244123
PMID:38140450
Physiological and Physical Strategies to Minimize Damage at the Branch–Stem Junction of Trees: Using the Finite Element Method to Analyze Stress in Four Branch–Stem Features Liu TC, Peng YS, Cheng BY Plants (Basel) 03-Dec-2023
PMCID:PMC10707858
doi:10.3390/plants12234060
PMID:38068695
Cleaner Biofuel Production via Process Parametric Optimization of Nonedible Feedstock in a Membrane Reactor Using a Titania-Based Heterogeneous Nanocatalyst: An Aid to Sustainable Energy Development Ameen M, Zafar M, Ahmad M, Munir M, Abid I, Mustafa AE, Athar M, Makhkamov T, Mamarakhimov O, Yuldashev A, Khaydarov K, Mammadova AO, Botirova L, Makkamov Z Membranes (Basel) 27-Nov-2023
PMCID:PMC10744951
doi:10.3390/membranes13120889
PMID:38132893
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
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
Steroids Bearing Heteroatom as Potential Drugs for Medicine Dembitsky VM Biomedicines 03-Oct-2023
PMCID:PMC10604304
doi:10.3390/biomedicines11102698
PMID:37893072
Integrating traditional ecological knowledge into habitat restoration: implications for meeting forest restoration challenges Haq SM, Pieroni A, Bussmann RW, Abd-ElGawad AM, El-Ansary HO J Ethnobiol Ethnomed 10-Aug-2023
PMCID:PMC10413632
doi:10.1186/s13002-023-00606-3
PMID:37559120
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Structure and characteristics of the plant-frugivore bird network from the Guilin Botanical Garden Wang G, Huang Y, Yao W, Huang Q, Huang Y, Wei L, Zhou Q PeerJ 16-Mar-2023
PMCID:PMC10024898
doi:10.7717/peerj.15028
PMID:36945357
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Triacontane 12535 Click to see 422.80 unknown https://doi.org/10.15625/0866-708X/55/2/8608
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(2S,5S,6R,7S,9S,11R,13S)-9,11-dihydroxy-13-(methoxymethyl)-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]tridec-1(10)-en-7-yl] (Z)-2-methylbut-2-enoate 102321417 Click to see 410.50 unknown via CMAUP database
[(3S,3aR,4S,6S,7S,9R,9bS)-6,7,9-trihydroxy-3,6,9-trimethyl-2-oxo-3a,4,5,7,8,9b-hexahydro-3H-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 643640 Click to see 380.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 101672241 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101078309 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 15922700 Click to see 378.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101143220 Click to see 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(2S)-2-(3,8-dimethylazulen-5-yl)propanoic acid 3083593 Click to see CC1=C2C=CC(=C2C=C(C=C1)C(C)C(=O)O)C 228.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,7R,10E,11aS)-7-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one 13821246 Click to see CC1C2CCC(=C)C(CCC(=CC2OC1=O)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,5aR,6R,9R,9aS,9bS)-6,9-dihydroxy-3,5a,9-trimethyl-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one 14110909 Click to see 268.35 unknown via CMAUP database
Dihydrosantamarin 13895713 Click to see CC1C2CCC3(C(CC=C(C3C2OC1=O)C)O)C 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Costunolide derivative 54607887 Click to see 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.15625/0866-708X/55/2/8608
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.15625/0866-708X/55/2/8608
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.15625/0866-708X/55/2/8608
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 https://doi.org/10.15625/0866-708X/55/2/8608
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see 117.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(-)-Stachydrine 115244 Click to see 143.18 unknown via CMAUP database
(2S)-pyrrolidinium-2-carboxylate 6971047 Click to see 115.13 unknown via CMAUP database
Betonicine 164642 Click to see 159.18 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organoheterocyclic compounds / Cycloheptafurans
(3S,3aR,4S,6S,9bS)-4-(Acetyloxy)-3a,5,6,9b-tetrahydro-6-hydroxy-3,6,9-trimethyl-4H-cyclohepta(2,1-b:3,4-c')difuran-2(3H)-one 15127111 Click to see 308.33 unknown via CMAUP database
[(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]trideca-1(13),10-dien-7-yl] (E)-2-methylbut-2-enoate 102008485 Click to see 348.40 unknown via CMAUP database
2-Butenoic acid, 2-methyl-, (3S,3aR,4S,6S,9bS)-2,3,3a,5,6,9b-hexahydro-6-hydroxy-3,6,9-trimethyl-2-oxo-4H-cyclohepta(2,1-b:3,4-c')difuran-4-yl ester, (2Z)- 102008484 Click to see 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3R,3aR,4S,9aS,9bR)-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate 102014217 Click to see 304.34 unknown via CMAUP database
[(3S,3aR,4S,9aR,9bS)-9a-hydroxy-3,6,9-trimethyl-2,7-dioxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] acetate 76764466 Click to see 320.30 unknown via CMAUP database
14-Deoxylactucin 156302 Click to see 260.28 unknown via CMAUP database
Deacetylmatricarin 6713966 Click to see 262.30 unknown via CMAUP database
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown via CMAUP database
Hydroxyachillin 10038339 Click to see 262.30 unknown via CMAUP database
Matricarin 3083923 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C 304.34 unknown via CMAUP database
Matricin 92265 Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)C 306.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(94)00670-O
Procyanidin B1 11250133 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 https://doi.org/10.1016/0031-9422(94)00670-O
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown https://doi.org/10.15625/0866-708X/55/2/8608
Quercetagetin-6,7-3',4'-tetramethyl Ether 5316832 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)OC 374.30 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.15625/0866-708X/55/2/8608
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.15625/0866-708X/55/2/8608
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6-Hydroxyluteolin 7-glucoside 185766 Click to see 464.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Isorhoifolin 9851181 Click to see 578.50 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.15625/0866-708X/55/2/8608
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.15625/0866-708X/55/2/8608
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Penduletin 4'-methyl ether 5318355 Click to see 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1,13,14,15,18,19,20,34,35,39,39-Undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl) 3,4,5-trihydroxybenzoate 115063 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(94)00670-O
(1R,35R,38R,55S)-6,7,8,11,12,23,24,27,28,29,37,43,44,45,48,49,50-heptadecahydroxy-2,14,21,33,36,39,54-heptaoxaundecacyclo(33.20.0.04,9.010,19.013,18.016,25.017,22.026,31.038,55.041,46.047,52)pentapentaconta-4,6,8,10,12,16,18,22,24,26,28,30,41,43,45,47,49,51-octadecaene-3,15,20,32,40,53-hexone 44584733 Click to see 1084.70 unknown https://doi.org/10.1016/0031-9422(94)00670-O
(57R,58S,510R,511R,519S)-14,15,16,24,25,26,52,53,516,517,517-Undecahydroxy-55,513,515,3,8-pentaoxo-55,57,58,510,511,513,515,516,517,517a-decahydro-4,7-dioxa-5(19,10)-1,16-epoxy-7,11-methanodibenzo[i,k][1,4,7]trioxacyclotridecina-1,2(1,2)-dibenzenacyclooctaphane-58-yl 3,4,5-trihydroxybenzoate 138991573 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(94)00670-O
[(1S,7R,9R,18R,19S,21R,22S)-7,8,8,12,13,22-hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.17,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate 44567215 Click to see 650.50 unknown https://doi.org/10.1016/0031-9422(94)00670-O
[(1S,8R,9R,18R,19S,21R,22S)-7,7,8,12,13,22-hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.18,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate 101921699 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=O)C(C5(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)O)(O)O)O 650.50 unknown https://doi.org/10.1016/0031-9422(94)00670-O
[(2R,3R,4S,5R,6S)-4,5,6-tris[(3,4,5-trihydroxybenzoyl)oxy]-2-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-3-yl] 2-[[(1R,7R,8S,26R,28S,29R,38R)-1,13,14,15,18,19,34,35,39,39-decahydroxy-2,5,10,23,31-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-20-yl]oxy]-3,4,5-trihydroxybenzoate 162883578 Click to see 1891.30 unknown https://doi.org/10.1016/0031-9422(94)00670-O
[4,5,6-Tris[(3,4,5-trihydroxybenzoyl)oxy]-2-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-3-yl] 2-[[1,13,14,15,18,19,34,35,39,39-decahydroxy-2,5,10,23,31-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-20-yl]oxy]-3,4,5-trihydroxybenzoate 162883577 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC1C(OC(C(C1OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1891.30 unknown https://doi.org/10.1016/0031-9422(94)00670-O
[6-(3,4,5-Trihydroxybenzoyl)-4,5-bis[(3,4,5-trihydroxybenzoyl)oxy]-2-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-3-yl] 2-[[1,14,15,16,19,20,35,36,40,40-decahydroxy-2,5,11,24,32-pentaoxo-29-(3,4,5-trihydroxybenzoyl)oxy-6,7,10,25,28,31,41-heptaoxaoctacyclo[35.3.1.04,39.08,27.09,30.012,17.018,23.033,38]hentetraconta-3,12,14,16,18,20,22,33,35,37-decaen-21-yl]oxy]-3,4,5-trihydroxybenzoate 163196140 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)OO3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC1C(OC(C(C1OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)C(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1891.30 unknown https://doi.org/10.1016/0031-9422(94)00670-O
[7,8,8,12,13,22-Hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.17,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate 14429416 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=O)C5(C(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)(O)O)O)O 650.50 unknown https://doi.org/10.1016/0031-9422(94)00670-O
beta-Punicalagin 16148440 Click to see 1084.70 unknown https://doi.org/10.1016/0031-9422(94)00670-O
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(94)00670-O
Corilagin (Standard) 5089683 Click to see 634.50 unknown https://doi.org/10.1016/0031-9422(94)00670-O
Geraniin 3001497 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(94)00670-O
Npc88976 16129869 Click to see 1084.70 unknown https://doi.org/10.1016/0031-9422(94)00670-O

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