Details Top

Internal ID UUID64402a940ff73386927416
Scientific name Castanopsis fissa
Authority Rehder & E.H.Wilson
First published in Pl. Wilson. 3: 203 (1916)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Timber: sawn wood for indoor joinery, moldings, and furniture components; utility poles and mine timbers.

Industrial and craft applications:
Plywood and laminated veneer lumber (LVL) using rotary-cut veneers; general pulpwood for kraft and neutral sulphite semi-chemical (NSSC) pulping.

Food and beverages (non-medicinal):
None documented.

Colorants and tanning:
None documented.

Wood and fiber:
Wood characteristics relevant to use: air-dry density about 690–760 kg/m³; moderate shrinkage with good dimensional stability after drying; sapwood whitish to light brown and not resistant to fungi; heartwood with reddish-brown hue and moderate natural durability; coarse to medium texture with interlocked grain; low resin content suitable for paint and varnish adhesion. Roundwood suitable for poles; veneers suitable for laminated products.

Fragrance and cosmetics:
None documented.

Properties relevant to use:
Wood density and dimensional stability support joinery and furniture use; low resin and moderate mechanical properties make it suitable for LVL/plywood and general utility applications; fiber length and lignin/cellulose ratio reported as appropriate for kraft and NSSC pulping.

Standards and regulation:
Timber quality and grading aligned with Chinese national standards for hardwood lumber and plywood.

Sustainability and sourcing:
Harvested from plantation and secondary forests in southern China and northern Vietnam; regeneration by natural seedfall with assisted natural regeneration in logged stands; demand tracked by national timber statistics; plantation rotations reported at 30–40 years for timber.

Synonyms Top

Scientific name Authority First published in
Lithocarpus fissus (Champ.) A.Camus Rev. Bot. Appl. Agric. Trop. 15: 24 (1935)
Lithocarpus fissus var. bipoupensis A.Camus Chênes Atlas 3: 115. 1948
Lithocarpus fissus subsp. tunkinensis (Drake) A.Camus Chênes Atlas 3: 114. 1948 (1948)
Quercus fissa Champ. ex Benth. Hooker's J. Bot. Kew Gard. Misc. 6: 114 (1854)
Quercus tunkinensis Drake J. Bot. (Morot) 4: 153 (1890)
Pasania fissa Oerst. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1866: 84 (1866)
Shiia fissa (Champ.) Kudô J. Soc. Trop. Agric. 3: 17 (1931)
Synaedrys fissa Koidz. Bot. Mag. (Tokyo) 30: 187 (1916)
Synaedrys tunkinensis Koidz. Bot. Mag. (Tokyo) 30: 187 (1916)
Castanea regia Hance Ann. Sci. Nat., Bot. , sér. 4, 18: 230 (1862)
Castanopsis fissoides Chun & C.C.Huang Bot. J. R.S.S.S. 1: 1000 (1965)
Castanopsis tunkinensis (Drake) Barnett Trans. & Proc. Bot. Soc. Edinburgh 34: 183 (1944)
Pasania fissa var. tunkinensis (Drake) Hickel & A.Camus Fl. Indo-Chine 5: 1006. 1930

Common names Top

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Language Common/alternative name
Chinese 大叶锥
Chinese 大叶栗
Chinese 黧蒴栲
Chinese 黧蒴锥
Chinese 大叶枹
Chinese 大叶栎
Chinese 大叶槠栗
Chinese 大吉槠栗
Chinese 裂壳锥
Chinese 黧蒴錐

Subspecies (abbr. subsp./ssp.) Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000813768
Tropicos 13100634
KEW urn:lsid:ipni.org:names:358361-1
The Plant List kew-35185
Open Tree Of Life 651161
NCBI Taxonomy 167387
IUCN Red List 138592595
IPNI 358361-1
iNaturalist 428286
GBIF 5332934
EOL 1148459
Wikipedia Castanopsis_fissa

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
Mixing with native broadleaf trees modified soil microbial communities of Cunninghamia lanceolata monocultures in South China Zheng F, Gu J, Lu D, Yang J, Shuai X, Li C, Chen H Front Microbiol 05-Mar-2024
PMCID:PMC10949948
doi:10.3389/fmicb.2024.1372128
PMID:38505544
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Comprehensive Proteomic Analysis of Common Bean (Phaseolus vulgaris L.) Seeds Reveal Shared and Unique Proteins Involved in Terminal Drought Stress Response in Tolerant and Sensitive Genotypes Subramani M, Urrea CA, Tamatamu SR, Sripathi VR, Williams K, Chintapenta LK, Todd A, Ozbay G Biomolecules 15-Jan-2024
PMCID:PMC10813106
doi:10.3390/biom14010109
PMID:38254709
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
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
Host Recognition and Specific Infection of Endomelanconiopsis endophytica during Early Infection Xie Y, Shi L, Cheng K, Li Y, Yu S J Fungi (Basel) 23-Oct-2023
PMCID:PMC10607883
doi:10.3390/jof9101040
PMID:37888296
Litter decomposition and nutrient release are faster under secondary forests than under Chinese fir plantations with forest development Li S, Xu Z, Yu Z, Fu Y, Su X, Zou B, Wang S, Huang Z, Wan X Sci Rep 05-Oct-2023
PMCID:PMC10555996
doi:10.1038/s41598-023-44042-5
PMID:37798470
Phosphorus Addition Reduces Seedling Growth and Survival for the Arbuscular Mycorrhizal Tree Cinnamomum camphora (Lauraceae) and Ectomycorrhizal Tree Castanopsis sclerophylla (Fagaceae) in Fragmented Forests in Eastern China Liu J, Zhou M, Li X, Li T, Jiang H, Zhao L, Chen S, Tian J, Han W Plants (Basel) 15-Aug-2023
PMCID:PMC10458558
doi:10.3390/plants12162946
PMID:37631158
Physiological and proteomic changes of Castanopsis fissa in response to drought stress Li C, Chen S, Wang Y Sci Rep 02-Aug-2023
PMCID:PMC10397200
doi:10.1038/s41598-023-39235-x
PMID:37532761
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
Updated taxonomy of Chinese Cantharellus subgenera Afrocantharellus and Magni (Hydnaceae, Cantharellales): Three new taxa and amended descriptions of one previous species Zhang YZ, Qin HZ, Chen ZH, Lin WF, Liang ZQ, Jiang S, Zeng NK Front Microbiol 17-Mar-2023
PMCID:PMC10064096
doi:10.3389/fmicb.2023.1109831
PMID:37007503
Dynamic changes of the contents of photoprotective substances and photosynthetic maturation during leaf development of evergreen tree species in subtropical forests Yu ZC, Lin W, He W, Yan GZ, Zheng XT, Luo YN, Zhu H, Peng CL Tree Physiol 02-Mar-2023
PMCID:PMC10785039
doi:10.1093/treephys/tpad026
PMID:36864631
Response of Rhizosphere Bacterial Communities to Near-Natural Forest Management and Tree Species within Chinese Fir Plantations Lei J, Wu H, Li X, Guo W, Duan A, Zhang J Microbiol Spectr 23-Jan-2023
PMCID:PMC9927156
doi:10.1128/spectrum.02328-22
PMID:36688690
Forest Carbon Reserve Calculation and Comprehensive Economic Value Evaluation: A Forest Management Model Based on Both Biomass Expansion Factor Method and Total Forest Value Zhao J, Hu H, Wang J Int J Environ Res Public Health 29-Nov-2022
PMCID:PMC9736741
doi:10.3390/ijerph192315925
PMID:36497999
An Efficient Time-Domain End-to-End Single-Channel Bird Sound Separation Network Zhang C, Chen Y, Hao Z, Gao X Animals (Basel) 11-Nov-2022
PMCID:PMC9686777
doi:10.3390/ani12223117
PMID:36428345

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
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> 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 https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
[(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 4-hydroxybenzoate 162953529 Click to see 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Benzenoids / Benzene and substituted derivatives / Styrenes
Di-(p-hydroxy-cis-styryl)methane 102326871 Click to see 252.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Benzenoids / Phenols / Benzenetriols and derivatives / Hydroxyquinols and derivatives
3-[(E)-[(2S,4aR,8aS)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-ylidene]methyl]-2,4,5-trihydroxybenzaldehyde 163188988 Click to see 358.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,5S,8aS)-5-[(3S)-4-carboxy-3-methylbutyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 124820803 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O 336.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethylhexadec-2-en-1-ol 145386 Click to see 296.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(5aR,5bR,7aS,9R,11aR,11bR,13aS,13bR)-5a,5b,8,8,11a,13b-hexamethyl-3-propan-2-yl-1,2,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydrocyclopenta[a]chrysen-9-ol 162969544 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)86842-9
5a,5b,8,8,11a,13b-Hexamethyl-3-propan-2-yl-1,2,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydrocyclopenta[a]chrysen-9-ol 124222311 Click to see CC(C)C1=C2CCC3(C(C2(CC1)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)86842-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
[(3aS,6aR,8S,9aR,9bS)-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl] (2R)-2-methylbutanoate 162997599 Click to see 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5320146 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
hyptatic acid B 12305222 Click to see 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[10,13-dimethyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13991204 Click to see 440.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
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 https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
4-Amino-1-pentofuranosyl-2(1H)-pyrimidinone 596 Click to see 243.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Cytidine 6175 Click to see C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O 243.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-1,3-dihydroxy-4,5-bis[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 13270012 Click to see 496.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
1,3,4-Trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid 4486613 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 344.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 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 https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
5-Galloylquinic acid 14520970 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 344.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
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 https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
CID 13270011 13270011 Click to see 496.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives / O-galloylquinic acids and derivatives
(1R,3R,4S,5R)-3,4-dihydroxy-1,5-bis[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 10696579 Click to see 496.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
3-Hydroxy-1,4,5-tris[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 14653355 Click to see 648.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
3,4-Dihydroxy-1,5-bis[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 85236078 Click to see 496.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
3,5-Dihydroxy-1,4-bis[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 78189359 Click to see 496.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Benzoic acid, 3,4,5-trihydroxy-, 4-carboxy-6-hydroxy-1,2,4-cyclohexanetriyl ester, (1R-(1alpha,2beta,4alpha,6alpha)-)- 452237 Click to see 648.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see 174.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4S,5S,6R)-2-[(1S,6R)-4-hydroxy-2,6-dimethoxycyclohexa-2,4-dien-1-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162928429 Click to see 334.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
2-Methyl-6-[(3,4,5-trihydroxy-6-phenylmethoxyoxan-2-yl)methoxy]oxane-3,4,5-triol 14682781 Click to see 416.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
hydrangeifolin I 10549806 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 416.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid 53669481 Click to see 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
4-Hydroxy-3,5-dimethoxyphenyl beta-D-glucopyranoside; (-)-3,5-Dimethoxy-4-hydroxyphenyl beta-D-glucopyranoside 73981643 Click to see COC1=CC(=CC(=C1O)OC)OC2C(C(C(C(O2)CO)O)O)O 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Benzoic acid + 2O, O-Hex 76211590 Click to see 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Gentisic Acid 5-O-Beta-Dglucopyranoside 10914066 Click to see 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Koaburaside 5318820 Click to see 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4Z)-4-ethylidene-3,5,5-trimethylcyclohex-2-en-1-one 14759603 Click to see 164.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
4-Ethylidene-3,5,5-trimethylcyclohex-2-en-1-one 72739000 Click to see CC=C1C(=CC(=O)CC1(C)C)C 164.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
1-(6-Oxo-2,3-dihydropyran-2-yl)hept-4-en-2-yl acetate 162908381 Click to see CCC=CCC(CC1CC=CC(=O)O1)OC(=O)C 252.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavamine 27443 Click to see CCN(CC)CC1=CC2=C(C=C1)OC(=C(C2=O)C)C3=CC=CC=C3 321.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One 5352000 Click to see 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Myricitrin 5281673 Click to see 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose 374874 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
[5-Hydroxy-3,4,6-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14188629 Click to see 788.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
1,2,3,6-Tetragalloyl-beta-D-glucopyranose 5153644 Click to see 788.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
1,3,4,6-Tetra-O-Galloyl-Beta-D-Glucopyranoside 471531 Click to see 788.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
(10S,11R,12R,13R,15R)-3,4,5,11,12,13,21,22,23-nonahydroxy-9,14,17-trioxatetracyclo(17.4.0.02,7.010,15)tricosa-1(23),2,4,6,19,21-hexaene-8,18-dione 14035459 Click to see 482.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
2,3-Di-O-methylellagic acid 5316858 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4O)O)C(=O)O2)OC 330.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
2,3-Hexahydroxydiphenoylglucopyranose 492390 Click to see 482.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
3-O-MethylduchesideA 10457042 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)OC5C(C(C(CO5)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
3,3'-di-O-Methylellagic acid 5488919 Click to see 330.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
6,13-dihydroxy-7-methoxy-14-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 162852512 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC5C(C(C(CO5)O)O)O)O)O 448.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Casuarictin 73644 Click to see 936.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
CID 14463056 14463056 Click to see 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Ducheside A 5316973 Click to see 448.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Eugeniin 442679 Click to see 938.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Pedunculagin I 492391 Click to see 784.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Potentillin 452242 Click to see 936.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007
Tellimagrandin Ii 151590 Click to see 938.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.007

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