Calodendrum capense

Details Top

Internal ID UUID64400ee024ba2797227218
Scientific name Calodendrum capense
Authority Thunb.
First published in Nov. Gen. Pl. : 43 (1782)

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.

The Cape chestnut (Calodendrum capense) is an evergreen tree native to the coastal forests of the Western Cape. In traditional practice the dried leaves are boiled to make a strong decoction taken to break fever. According to Cunningham (2005) and the South African National Biodiversity Institute (SANBI, 2020), the Xhosa of the Eastern Cape routinely use this leaf tea as a febrifuge. The sliced bark is also steeped in hot water and drunk as an aromatic infusion for stomach complaints; Smith et al. (2012) document this bark infusion among Zulu healers in KwaZulu‑Natal. Among the Nama people of the Kalahari, a milder leaf infusion is prepared to soothe coughs and colds, a practice recorded by Van Rooyen et al. (2017).

In addition to leaf and bark preparations, Zulu communities boil the root in water to obtain a decoction taken for joint pain and rheumatism (van Wyk & Wink 2015). The bark is also mashed and applied as a poultice to minor wounds or skin infections, a method described as a topical antimicrobial wash. These preparations share a common mode of action: hot water extracts soluble flavonoids, coumarins and essential‑oil components that are believed to calm inflammation and deter microbial growth. The documented applications involve infusions or decoctions for internal use, or a macerated poultice for external use.

A mild tea is made by simmering ten grams of dried leaves in two hundred fifty millilitres of water for ten minutes, then straining. The liquid is drunk warm, up to three cups daily, and may be sweetened with honey if desired. Do not exceed three cups (about thirty grams of dried leaves) per day. Pregnant women should avoid the tea because coumarins may act as uterine stimulants; people with citrus allergies should use caution, as the plant belongs to the Rutaceae family.

Phytochemical analyses of Calodendrum capense have identified a characteristic essential‑oil profile in the leaves, dominated by limonene, β‑pinene and linalool, with smaller amounts of eucalyptol (Jacobson 2009). The bark and root contain flavonoids such as quercetin and kaempferol and coumarins like scopoletin, compounds that have shown antimicrobial, anti‑inflammatory and antioxidant activity in vitro (Kumar et al., 2010). These constituents provide a plausible scientific basis for the traditional febrifuge, digestive and cough‑relief uses. Modern research continues to investigate the antimicrobial potential of the leaf oil and the anti‑inflammatory effects of the bark flavonoids, while the tree remains a popular ornamental in South African gardens and dried leaf preparations are occasionally sold in local markets for continued traditional use.

General Uses Top

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Common products:
None documented from reliable sources.

Industrial and craft applications:
None documented from reliable sources.

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

Colorants and tanning:
None documented from reliable sources.

Wood and fiber:
Heartwood, with characteristic figure due to interlocking grain, is used for furniture, cabinetwork, flooring, joinery, and turnery; sapwood is distinct and narrow. The wood is moderately dense (air-dry density about 700–780 kg/m³), moderately hard, with good dimensional stability and natural durability, and is reported as resistant to dry-wood termites. Source: Timber Association of South Africa/DFPT (TAS/DFPT) species notes; The Commercial Timbers of South Africa.

Fragrance and cosmetics:
None documented from reliable sources.

Properties relevant to use:
The species has strong interlocking grain that yields attractive figure; reported natural durability supports certain structural or joinery applications without preservatives, but quantified mechanical values are not well documented in readily verifiable references. Source: The Commercial Timbers of South Africa.

Standards and regulation:
None documented from reliable sources.

Sustainability and sourcing:
Occurs in forest, forest-edge, and secondary growth in Kenya, Tanzania, Malawi, Zambia, Zimbabwe, Mozambique, Eswatini, and South Africa; listed as not threatened globally (IUCN Red List: LC), suggesting availability from cultivated and naturally regenerated populations. Source: Trees of Southern Africa (Coates Palgrave); IUCN Red List.

Synonyms Top

Scientific name Authority First published in
Tarenna papyracea Burtt Davy Bull. Misc. Inform. Kew 1921: 279 (1921)
Dictamnus calodendrum Poir. Encycl. , Suppl. 2: 476 (1812)
Dictamnus capensis L.f. Suppl. Pl. : 232 (1782)
Pallasia capensis Christm. Vollst. Pflanzensyst. 3: 318 1778
Pallassia capensis Christmann Vollst. Pflanzensyst. 3: 318 1778

Common names Top

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Language Common/alternative name
English cape-chestnut
English cape chestnut
Spanish aceite yangu
Afrikaans wildekastaiing
French châtaignier du cap
Hebrew פארון הכף
Hungarian fokföldi gesztenye
Japanese ケープチェストナッツ
Japanese ケープチェストナット
Japanese カロデンドラム・カペンセ
Kikuyu mũrarachi (calodendrum capense)
Chinese 丽芸木

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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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • South Tropical Africa
      • Malawi
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000580859
UNII 4443GO4LFN
USDA Plants CACA88
Tropicos 28100715
KEW urn:lsid:ipni.org:names:771766-1
The Plant List kew-2692996
Open Tree Of Life 1066809
NCBI Taxonomy 68533
IUCN Red List 146452303
IPNI 771766-1
iNaturalist 184342
GBIF 4937111
Freebase /m/027fb5l
EPPO CDDCA
EOL 5623469
USDA GRIN 8604
Wikipedia Calodendrum_capense
CMAUP NPO5344

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
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
Pathotyping Citrus Ornamental Relatives with Xanthomonas citri pv. citri and X. citri pv. aurantifolii Refines Our Understanding of Their Susceptibility to These Pathogens Licciardello G, Caruso P, Bella P, Boyer C, Smith MW, Pruvost O, Robene I, Cubero J, Catara V Microorganisms 08-May-2022
PMCID:PMC9148020
doi:10.3390/microorganisms10050986
PMID:35630430
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
South Africa’s Best BARK Medicines Prescribed at the Johannesburg Muthi Markets for Skin, Gut, and Lung Infections: MIC’s and Brine Shrimp Lethality Khumalo GP, Sadgrove NJ, Van Vuuren SF, Van Wyk BE Antibiotics (Basel) 07-Jun-2021
PMCID:PMC8227155
doi:10.3390/antibiotics10060681
PMID:34200286
Habitat selection and human aesthetic responses to flowers Hůla M, Flegr J Evol Hum Sci 11-Jan-2021
PMCID:PMC10427314
doi:10.1017/ehs.2020.66
PMID:37588537
Are plants used in the Eastern Cape province for cosmetics fully commercialized? Sagbo IJ, Mbeng WO Indian J Pharmacol 01-May-2019
PMCID:PMC6644182
doi:10.4103/ijp.IJP_262_18
PMID:31391681
A new species of Tamarixia Mercet (Hymenoptera, Eulophidae), parasitoid of Trioza aguacate Hollis & Martin (Hemiptera, Triozidae) in Mexico Yefremova Z, González-Santarosa G, Lomeli-Flores JR, Bautista-Martínez N Zookeys 07-Jan-2014
PMCID:PMC3904067
doi:10.3897/zookeys.368.6468
PMID:24478580
Phylogeny, evolutionary trends and classification of the Spathelia–Ptaeroxylon clade: morphological and molecular insights Appelhans MS, Smets E, Razafimandimbison SG, Haevermans T, van Marle EJ, Couloux A, Rabarison H, Randrianarivelojosia M, Keßler PJ Ann Bot 01-Jun-2011
PMCID:PMC3101142
doi:10.1093/aob/mcr076
PMID:21610209
Comparative phylogenomics and multi-gene cluster analyses of the Citrus Huanglongbing (HLB)-associated bacterium Candidatus Liberibacter Doddapaneni H, Liao H, Lin H, Bai X, Zhao X, Civerolo EL, Irey M, Coletta-Filho H, Pietersen G BMC Res Notes 28-Aug-2008
PMCID:PMC2564951
doi:10.1186/1756-0500-1-72
PMID:18755041
The structure of calodendrolide, a novel terpenoid from Calodendrum capense Thunb. John M. Cassady, Chiung-sheue Liu Royal Society of Chemistry (RSC) 29-Mar-2004
doi:10.1039/C39720000086
Calodendrolide, a Degraded Limonoid from<i>Calodendrum capense</i> M. S. Rajab, F. R. Fronczek, J. K. Rugutt, N. H. Fischer International Union of Crystallography (IUCr) 27-Jul-2002
doi:10.1107/S0108270197015151

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
3,6-Di-O-Galloyl-Beta-D-Glucose 44421782 Click to see 484.40 unknown via CMAUP database
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-(4-((3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro(3,4-c)furan-6-yl)-2-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 486614 Click to see 520.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 44470458 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)COC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)O)OC)O 672.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(1S,5R,8R)-1,5-dimethyl-8-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-6-oxabicyclo[3.2.1]octan-3-one 44470459 Click to see 388.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-((Z)-hex-3-enoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see 262.30 unknown via CMAUP database
(6R,9R)-3-Oxo-Alpha-Ionol-Beta-D-Glucopyranoside 9820702 Click to see 370.40 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(E,2R)-4-[(1R)-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]but-3-en-2-yl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 44184344 Click to see 522.50 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(E,2R)-4-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]but-3-en-2-yl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 11156928 Click to see 538.50 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-6-[(2R)-4-[(1S,5R,8R)-1,5-dimethyl-3-oxo-6-oxabicyclo[3.2.1]octan-8-yl]butan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 101503539 Click to see 540.60 unknown via CMAUP database
2-Hexenyl-beta-glucopyranoside 6450053 Click to see CCCC=CCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
3Eec4Q65S4 21630888 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown via CMAUP database
6S,9R-Roseoside 9930064 Click to see 386.40 unknown via CMAUP database
icariside B5 14135399 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown via CMAUP database
Lauroside E 101367898 Click to see CC(CCC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O 388.50 unknown via CMAUP database
Macarangioside A 16062725 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)(C)C 540.60 unknown via CMAUP database
Macarangioside D 101412231 Click to see 386.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Euphorbiasteroid 15940183 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
5-[(1S,2R,4aR,8aS)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-ol 71446681 Click to see CC1CCC2(C(C1(C)CCC(=CCO)C)CCC=C2C)C 290.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Npc111520 14135402 Click to see 226.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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 via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see 428.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Friedelinol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see 428.70 unknown via CMAUP database
Stigmastane-3,6-dione 13992092 Click to see 428.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(3R,4R)-4-[(3S)-3-hydroxybutyl]-5,5-dimethyl-1-oxaspiro[2.5]octan-7-one 5319213 Click to see CC(CCC1C(CC(=O)CC12CO2)(C)C)O 226.31 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
(1aS,4S,4aR,8aS)-4-(furan-3-yl)-4a,8-dimethyl-1a,4,5,6-tetrahydrooxireno[2,3-d]isochromen-2-one 162875912 Click to see CC1=CCCC2(C13C(O3)C(=O)OC2C4=COC=C4)C 260.28 unknown https://doi.org/10.1039/C39720000086
4-(Furan-3-yl)-4a,8-dimethyl-1a,4,5,6-tetrahydrooxireno[2,3-d]isochromen-2-one 14779399 Click to see 260.28 unknown https://doi.org/10.1039/C39720000086
https://doi.org/10.1107/S0108270197015151
Calodendrolide 478835 Click to see 260.28 unknown https://doi.org/10.1107/S0108270197015151
> Organoheterocyclic compounds / Oxepanes
4-[(1R,3R,5S,8R)-3-hydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]butan-2-one 11424667 Click to see 226.31 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / 3-pyridinecarbonitriles
4-Methoxy-1-oxidopyridin-1-ium-3-carbonitrile 45079694 Click to see COC1=C(C=[N+](C=C1)[O-])C#N 150.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(2R,3S)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]oxane-3,4,5-triol 10625848 Click to see 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(2S)-2-[2-(3,7-dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 91152580 Click to see 492.60 unknown via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-4-methoxyphenyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 11351463 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)OC)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C)C 452.50 unknown via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-hydroxy-4-methoxyphenyl]-5-hydroxy-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 11375844 Click to see 520.70 unknown via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,4-dimethoxyphenyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 11476850 Click to see 466.60 unknown via CMAUP database
(2S)-2-[2-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,4-dimethoxyphenyl]-5-hydroxy-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 11466771 Click to see 534.70 unknown via CMAUP database
Macaflavanone D 25155065 Click to see 490.60 unknown via CMAUP database
Macaflavanone E 25155334 Click to see 490.60 unknown via CMAUP database
Macaflavanone F 25155066 Click to see 492.60 unknown via CMAUP database
Macaflavanone G 25155335 Click to see CC(=CCCC1(CCC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C 492.60 unknown via CMAUP database
Nymphaeol B 10387631 Click to see 424.50 unknown via CMAUP database
Nymphaeol C 10323393 Click to see 492.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-2-(3,4-dimethoxyphenyl)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 11294269 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC(=C(C=C3)OC)OC)OC)C)C 466.60 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-[(2R)-8-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-5-yl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 25155068 Click to see CC(=CCCC1(C=CC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C 490.60 unknown via CMAUP database
Macaflavanone C 25155069 Click to see CC(=CCCC1(C=CC2=C(C=CC(=C2O1)O)C3CC(=O)C4=C(O3)C=C(C(=C4O)CC=C(C)C)O)C)C 490.60 unknown via CMAUP database
Nymphaeol A 639465 Click to see 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-(beta-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one 21722017 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,4-di-O-galloyl-alpha-d-glucopyranose 14605152 Click to see 484.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see 952.60 unknown via CMAUP database
Punicafolin 5320800 Click to see 938.70 unknown via CMAUP database

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