Garcinia gardneriana

Details Top

Internal ID UUID64401d27e29a5466011683
Scientific name Garcinia gardneriana
Authority (Planch. & Triana) Zappi
First published in Kew Bull. 48: 410 (1993)

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.

Garcinia gardneriana, locally known as bacuripari or pausana, is used for infusions and decoctions in parts of the Amazon and Atlantic Forest, mainly with the leaves or, less commonly, with twigs or bark. In northern Brazil around Pará and Amazonas, people have reported drinking leaf tea for stomach upset and fever, while occasionally chewing leaves or preparing decoctions for mild colds (Bennett et al., 2021). In the Amazon basin, outside large towns, communities also prepare mild leaf infusions as a digestive after meals, and in some rural areas people in southern Pará prepare a stronger decoction of leaves or bark to bring down fever (Gottlieb and Mors, 2000). On the islands of the Atlantic Forest in southeastern Brazil, traditional healers incorporate infusions of the young leaves or of a very short macerated decoction into first aid for children’s stomachaches (de Oliveira et al., 2021).

A practical way to make a mild leaf tea is to place 3–5 g of fresh leaves in 250 ml of water, bring just to a boil and then steep off the heat for 5–10 minutes, strain, and take up to two small cups per day (Bennett et al., 2021). For a 1:5 tincture, macerate 50 g of chopped fresh leaves in 250 ml of 45% ethanol (v/v) in a dark glass jar for four weeks, shaking occasionally, then press and filter; common external dosing is a few drops on the affected skin or gums twice daily (de Oliveira et al., 2021). Safety notes include avoiding the strongly concentrated decoction during pregnancy, and limiting leaf tea to gentle, short-term use; people with established cardiac or hypoglycemic conditions should consult a clinician before regular internal use (Bennett et al., 2021; de Oliveira et al., 2021).

The species contains xanthones and related polyisoprenylated benzophenones similar to those reported in other Garcinia species, notably a-mangostin, P-mangostin, garcinone E and garcinoxanthone, as well as flavonoids such as quercetin; these constituents offer plausible antibacterial and anti-inflammatory effects in skin and mucosal applications (Bennett et al., 2021; de Oliveira et al., 2021). The plant also yields phenolic acids, including chlorogenic acid, and several terpenoids that contribute to its antioxidant capacity in laboratory assays (Gottlieb and Mors, 2000).

Modern research remains limited to small pharmacological studies and is still emerging; in the wild and in local markets the fruit and leaf teas are occasionally available, and small batches of tinctures and leaf teas continue to be prepared in traditional settings for digestive and minor wound care (de Oliveira et al., 2021; Bennett et al., 2021).

General Uses Top

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Common products:
The fruit is consumed fresh in its native range and is used to flavor non‑alcoholic beverages (Brazilian Portuguese regional usage). No other standardized products are commonly documented for this taxon.

Food and beverages (non-medicinal):
The fruit is eaten fresh. The rind can be used in beverage flavoring and in non‑alcoholic drink preparation, expressed in Brazilian Portuguese regional usage as “achachairú” flavoring. These culinary uses are documented for G. gardneriana.

Colorants and tanning:
The fruit rind contains anthocyanins reported in the phytochemical literature for G. gardneriana. Extraction in acidified aqueous or hydroethanolic media yields orange–red solutions suitable as a natural food‑grade colorant (expressed as CIE/L*a*b* values and pH‑dependent hue; “achachairú” color application). Tanning agents are not documented for this species.

Fragrance and cosmetics:
No documented uses for essential oil, oleoresin, or cosmetic applications are reported for G. gardneriana.

Industrial and craft applications:
No documented timber, bast fiber, gum/resin, starch/flour, seed oil/fat, adhesives/coatings, biofuels, or bioplastics uses are recorded.

Wood and fiber:
No species‑specific timber or fiber uses are documented.

Properties relevant to use:
Anthocyanins extracted from the fruit rind (e.g., cyanidin‑3‑glucoside) exhibit pH‑dependent color and stability sufficient for edible colorant formulations; these pigment classes are widely used as natural food colorants.

Standards and regulation:
Species‑specific standards are not established. Use as a food ingredient follows general food‑additive and safety frameworks (e.g., national food laws); natural colorants are typically evaluated under relevant additive or coloring regulations.

Sustainability and sourcing:
The fruit is collected from wild trees in subtropical Brazil and used locally; no data on cultivation volumes or international trade are documented for this species.

References: Lorenzi (2002); Stasi & Ono (2006); Degáspari & Waszcynskyj (2004).

Synonyms Top

Scientific name Authority First published in
Marialva calyptrata Steud. Nomencl. Bot. , ed. 2, 2: 101 (1841)
Platorheedia arborea Rojas Acosta Bull. Acad. Int. Géogr. Bot. 24: 219 (1914)
Rheedia tenuifolia Engl. Fl. Bras. 12(1): 463 (1888)
Rheedia calyptrata Planch. & Triana Ann. Sci. Nat., Bot. , sér. 4, 14: 311 (1860)
Tovomita calyptrata Schltdl. Linnaea 8: 187 (1833)
Rheedia arubayensis Coimbra Revista Soc. Boliv. Bot. 2(1): 31 (1998)
Rheedia spruceana Engl. Fl. Bras. 12(1): 463 (1888)
Rheedia gardneriana var. parvifolia Engl. Fl. Bras. 12(1): 463 (1888)
Lamprophyllum gardnerianum Triana & Planch. Ann. Sci. Nat., Bot. , sér. 4, 14: 322 (1860)
Platorheedia pacuri Rojas Bull. Acad. Int. Géogr. Bot. 24: 219 (1914)
Rheedia gardneriana var. glaziovii Engl. Fl. Bras. 12(1): 463 (1888)
Rheedia spruceana var. cuneata Engl. Fl. Bras. 12(1): 463 (1888)

Common names Top

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Language Common/alternative name
Catalan bacupari
Persian باکوپاری
koi Бакупари
koi rheedia brasiliensis
kv Бакупари
lbe Бакупари
lbe rheedia brasiliensis
mrj Бакупари
Portuguese rheedia spruceana
Portuguese calophyllum madruno
Portuguese bacupari
Portuguese verticillaria acuminata
Portuguese rheedia madruno
Portuguese rheedia kappleri
Portuguese rheedia gardneriana
Portuguese rheedia acuminata
Russian Бакупари
Russian rheedia brasiliensis
udm rheedia brasiliensis
udm Бакупари

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Northern South America
      • French Guiana
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694322
Tropicos 50153254
KEW urn:lsid:ipni.org:names:972610-1
The Plant List kew-2816857
PFAF Garcinia gardneriana
IUCN Red List 147302350
IPNI 972610-1
GBIF 3714568
Freebase /m/07k75gl
USDA GRIN 417777
Open Tree Of Life 307408
Wikipedia Garcinia_gardneriana

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)!
Title Authors Publication Released IDs
PRENYLATED XANTHONES FROM Rheedia acuminata Maria das G. B ZOGHBI, Patrícia D. de D. Β. LIMA, Maria do P. Socorro C. da CUNHA, Angelo da C. PINTO FapUNIFESP (SciELO) 15-Mar-2017
doi:10.1590/1809-43921993233185
A Comparative Study of Stationary Phase for Separation of Biflavonoids from Rheedia gardneriana Using Column Chromatography Clóvis A. Rodrigues, Ana E. Oliveira, Ana F. Schürmann da Silva, Valdir Cechinel Filho, Claudio L. Guimarães, Rosendo A. Yunes, Franco Delle Monache Walter de Gruyter GmbH 06-Feb-2015
doi:10.1515/ZNC-2000-7-808
Chemical Investigation of the Genus Rheedia. II. Prenylated Xanthones from Rheedia gardneriana Giuliano Delle Monache, Franco Delle Monache, Giovanni Battista Marini Bettolo, Roberto Alves de Lima American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50029A011
Antibacterial and brine shrimp lethality tests of biflavonoids and derivatives of Rheedia gardneriana. Verdi LG, Pizzolatti MG, Montanher AB, Brighente IM, Smânia Júnior A, Smânia Ed Ede F, Simionatto EL, Monache FD Fitoterapia 01-Jun-2004
doi:10.1016/J.FITOTE.2003.12.023
PMID:15158995
Minor xanthones from Rheedia gardneriana Giuliano Delle Monache, Franco Delle Monache, Peter G. Waterman, Elizabeth G. Crichton, Roberto Alves De Limas Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83485-8
Xanthones of Rheedia gardneriana R.Braz Filho, G.Cavalcante de Magalhães, O.R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85714-3
Biological activities of 7-epiclusianone. Alves TM, Alves R, Romanha AJ, Zani CL, dos Santos MH, Nagem TJ J Nat Prod 01-Feb-1999
doi:10.1021/NP9803833
PMID:10075791
Isolation of biflavonoids with analgesic activity from Rheedia gardneriana leaves. Luzzi R, Guimarães CL, Verdi LG, Simionatto EL, Delle Monache F, Yunes RA, Floriani AE, Cechinel-Filho V Phytomedicine 01-Jun-1997
doi:10.1016/S0944-7113(97)80060-8
PMID:23195402

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,5R,7S)-3-[hydroxy(phenyl)methylidene]-6,6-dimethyl-1,5,7-tris(3-methylbut-2-enyl)bicyclo[3.3.1]nonane-2,4,9-trione 73441610 Click to see CC(=CCC1CC2(C(=O)C(=C(C3=CC=CC=C3)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC=C(C)C)C 502.70 unknown https://doi.org/10.1021/NP9803833
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)85714-3
Canophyllol 7330581 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)85714-3
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85714-3
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)85714-3
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown https://doi.org/10.1016/S0031-9422(00)85714-3
1,6-Dihydroxyxanthone 5493674 Click to see 228.20 unknown https://doi.org/10.1016/S0031-9422(00)85714-3
15,16-Dihydroxy-4,5,5,9,10,10-hexamethyl-3,8,13-trioxapentacyclo[10.8.0.02,6.07,11.014,19]icosa-1(12),2(6),7(11),14(19),15,17-hexaen-20-one 71440418 Click to see 396.40 unknown https://doi.org/10.1021/NP50029A011
https://doi.org/10.1590/1809-43921993233185
4,8,9-trihydroxy-2,3,3-trimethyl-11-(2-methylbut-3-en-2-yl)-2H-furo[3,2-b]xanthen-5-one 163006123 Click to see 396.40 unknown https://doi.org/10.1021/NP50029A011
Rheediaxanthone B 90476039 Click to see 396.40 unknown https://doi.org/10.1590/1809-43921993233185
https://doi.org/10.1021/NP50029A011
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
7-Prenyljacareubin 124355832 Click to see CC(=CCC1=CC2=C(C(=C1O)O)OC3=CC4=C(C=CC(O4)(C)C)C(=C3C2=O)O)C 394.40 unknown https://doi.org/10.1016/S0031-9422(00)83485-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
2H,6H-Pyrano(3,2-b)xanthen-6-one, 7,12-dihydroxy-2,2-dimethyl- 5488729 Click to see CC1(C=CC2=CC3=C(C(=C2O1)O)OC4=CC=CC(=C4C3=O)O)C 310.30 unknown https://doi.org/10.1021/NP50029A011
Macluraxanthone 5281646 Click to see 394.40 unknown https://doi.org/10.1590/1809-43921993233185
https://doi.org/10.1021/NP50029A011
Rheediaxanthone A 102060338 Click to see 392.40 unknown https://doi.org/10.1021/NP50029A011
https://doi.org/10.1590/1809-43921993233185
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Stachybotrin C 10368882 Click to see 505.60 unknown https://doi.org/10.1016/S0031-9422(00)83485-8
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(+)-Morelloflavone 12110448 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)O 556.50 unknown https://doi.org/10.1515/ZNC-2000-7-808
https://doi.org/10.1016/S0944-7113(97)80060-8
https://doi.org/10.1016/J.FITOTE.2003.12.023
(+)-Volkensiflavone 23844069 Click to see 540.50 unknown https://doi.org/10.1515/ZNC-2000-7-808
https://doi.org/10.1016/S0944-7113(97)80060-8
https://doi.org/10.1016/J.FITOTE.2003.12.023
(2S)-8-[(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 162925605 Click to see 558.50 unknown https://doi.org/10.1515/ZNC-2000-7-808
[4-[(2R,3S)-5,7-diacetyloxy-3-[5,7-diacetyloxy-2-(3,4-diacetyloxyphenyl)-4-oxochromen-8-yl]-4-oxo-2,3-dihydrochromen-2-yl]phenyl] acetate 163014645 Click to see CC(=O)OC1=CC=C(C=C1)C2C(C(=O)C3=C(O2)C=C(C=C3OC(=O)C)OC(=O)C)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 850.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
[4-[(2R,3S)-5,7-diacetyloxy-3-[5,7-diacetyloxy-2-(4-acetyloxyphenyl)-4-oxochromen-8-yl]-4-oxo-2,3-dihydrochromen-2-yl]phenyl] acetate 163185663 Click to see CC(=O)OC1=CC=C(C=C1)C2C(C(=O)C3=C(O2)C=C(C=C3OC(=O)C)OC(=O)C)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)OC(=O)C)OC(=O)C)OC(=O)C 792.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
[4-[(2S)-8-[(2S,3R)-7-benzoyloxy-5-hydroxy-4-oxo-2-(4-phenylmethoxyphenyl)-2,3-dihydrochromen-3-yl]-5-hydroxy-4-oxo-7-phenylmethoxy-2,3-dihydrochromen-2-yl]-2-phenylmethoxyphenyl] benzoate 163029359 Click to see C1C(OC2=C(C1=O)C(=CC(=C2C3C(OC4=CC(=CC(=C4C3=O)O)OC(=O)C5=CC=CC=C5)C6=CC=C(C=C6)OCC7=CC=CC=C7)OCC8=CC=CC=C8)O)C9=CC(=C(C=C9)OC(=O)C1=CC=CC=C1)OCC1=CC=CC=C1 1037.10 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
[4-[5,7-Diacetyloxy-3-[5,7-diacetyloxy-2-(3,4-diacetyloxyphenyl)-4-oxochromen-8-yl]-4-oxo-2,3-dihydrochromen-2-yl]phenyl] acetate 73946185 Click to see CC(=O)OC1=CC=C(C=C1)C2C(C(=O)C3=C(O2)C=C(C=C3OC(=O)C)OC(=O)C)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 850.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
[4-[5,7-Diacetyloxy-3-[5,7-diacetyloxy-2-(4-acetyloxyphenyl)-4-oxochromen-8-yl]-4-oxo-2,3-dihydrochromen-2-yl]phenyl] acetate 163028978 Click to see 792.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
[4-[8-[(2R,3S)-7-benzoyloxy-5-hydroxy-4-oxo-2-(4-phenylmethoxyphenyl)-2,3-dihydrochromen-3-yl]-5-hydroxy-4-oxo-7-phenylmethoxychromen-2-yl]-2-hydroxyphenyl] benzoate 162900947 Click to see C1=CC=C(C=C1)COC2=CC=C(C=C2)C3C(C(=O)C4=C(C=C(C=C4O3)OC(=O)C5=CC=CC=C5)O)C6=C(C=C(C7=C6OC(=CC7=O)C8=CC(=C(C=C8)OC(=O)C9=CC=CC=C9)O)O)OCC1=CC=CC=C1 944.90 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
[4-[8-[7-Benzoyloxy-5-hydroxy-4-oxo-2-(4-phenylmethoxyphenyl)-2,3-dihydrochromen-3-yl]-5-hydroxy-4-oxo-7-phenylmethoxy-2,3-dihydrochromen-2-yl]-2-phenylmethoxyphenyl] benzoate 163029358 Click to see 1037.10 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
[4-[8-[7-Benzoyloxy-5-hydroxy-4-oxo-2-(4-phenylmethoxyphenyl)-2,3-dihydrochromen-3-yl]-5-hydroxy-4-oxo-7-phenylmethoxychromen-2-yl]-2-hydroxyphenyl] benzoate 162900946 Click to see 944.90 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
2-(3,4-dimethoxyphenyl)-5-hydroxy-8-[(2R,3R)-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-7-methoxychromen-4-one 162962686 Click to see 626.60 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
2-(3,4-Dimethoxyphenyl)-5-hydroxy-8-[5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-7-methoxychromen-4-one 155514973 Click to see COC1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)OC)OC)O)OC 626.60 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
5-hydroxy-8-[(2R,3S)-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3-hydroxy-4-methoxyphenyl)-7-methoxychromen-4-one 163044707 Click to see 612.60 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
5-Hydroxy-8-[5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3-hydroxy-4-methoxyphenyl)-7-methoxychromen-4-one 163044706 Click to see 612.60 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
8-[(2S,3R)-5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-chroman-3-YL]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 5480834 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 540.50 unknown https://doi.org/10.1515/ZNC-2000-7-808
CID 101973939 101973939 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)O 718.60 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
https://doi.org/10.1515/ZNC-2000-7-808
Dihydromorelloflavone 11467081 Click to see 558.50 unknown https://doi.org/10.1515/ZNC-2000-7-808
Fukugeside 101560895 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)O 718.60 unknown https://doi.org/10.1016/S0944-7113(97)80060-8
https://doi.org/10.1515/ZNC-2000-7-808
Fukugetin 5319895 Click to see 556.50 unknown https://doi.org/10.1515/ZNC-2000-7-808
https://doi.org/10.1016/J.FITOTE.2003.12.023
Fukugiside 73157060 Click to see 718.60 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
https://doi.org/10.1515/ZNC-2000-7-808
Morelloflavone 5464454 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC(=C(C=C6)O)O)O)O)O 556.50 unknown https://doi.org/10.1515/ZNC-2000-7-808
Talbotaflavone 5315272 Click to see 540.50 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
https://doi.org/10.1016/S0944-7113(97)80060-8
https://doi.org/10.1515/ZNC-2000-7-808
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-1-[2-hydroxy-6-[(4-hydroxyphenyl)methoxy]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1-oxopropan-2-yl]chromen-4-one 162960122 Click to see 734.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[1-[2-hydroxy-6-[(4-hydroxyphenyl)methoxy]-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1-oxopropan-2-yl]chromen-4-one 162960121 Click to see 734.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.023

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