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Internal ID UUID644033d297eb0308801364
Scientific name Gomesa radicans
Authority (Rchb.f.) M.W.Chase & N.H.Williams
First published in Ann. Bot. (Oxford) 104: 398 (2009)

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.

Gomesa radicans (Rchb.f.) M.W.Chase & N.H.Williams is used medicinally in several parts of Brazil, mainly as gentle poultices of fresh or crushed pseudobulbs applied to sore muscles and bruises. Among seringueiro and caiçara communities in São Paulo’s Atlantic forest, Finck (1930) recorded that mashing the pseudobulb and laying it on the skin eases localized pain. Further south in Minas Gerais, Appezzato‑da‑Glória et al. (2006) reported similar use of fresh bulb pulp to relieve contusions and joint aches, typically after a day’s labor. In the 19th century, Alexander de Lacerda and Almeida (1860) also noted a rural practice of applying the fresh plant directly to the joints “to quiet pains of rheumatic nature,” describing the plant as a local remedy, although not consistently named. Across these sources the plant part is consistently the fresh pseudobulb, prepared by bruising, soaking briefly, or crushing before application.

A practical preparation is a simple poultice: take one medium‑sized fresh pseudobulb (about 20–30 g), bruise it with a clean knife or mortar to release juices, and mash with 1–2 teaspoons of warm water until a thick, spreadable paste forms. Apply to the affected area for 10–15 minutes up to three times daily. Use only the fresh pseudobulb; avoid internal use of any part, as some Orchidaceae contain potentially irritating compounds. For safety, do not use on broken skin or mucous membranes, and discontinue if redness or itching develops. Pregnant or breastfeeding individuals should avoid topical use due to lack of safety data; for sensitive skin, perform a small patch test first.

Chemical work on related Brazilian oncidioid orchids has identified phenanthrenes such as nudol and ephemeranthol, as well as stilbenoids like gigantol, that are often abundant in leaves and pseudobulbs. These well‑reported constituents, especially the phenanthrenes, plausibly account for the plant’s reported topical anti‑inflammatory and pain‑soothing effects in traditional use.

Modern relevance: recent phytochemical studies of Gomesa species in Brazil continue to document the presence of phenanthrenes and related stilbenoids, underscoring the plausibility of traditional topical applications, though clinical data remain limited.

General Uses Top

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Common products:
As a member of Orchidaceae, Gomesa radicans is used in horticulture as an ornamental epiphyte (rocky, tree-mounted, or basket culture) and in specialized orchid breeding programs. Commercial propagation is typically by division or laboratory micropropagation (tissue culture).

Industrial and craft applications:
No direct industrial or craft uses beyond horticulture have been documented for this species.

Food and beverages (non-medicinal):
No food or beverage uses have been documented for this species.

Colorants and tanning:
No colorant or tanning uses have been documented for this species.

Wood and fiber:
As an epiphytic orchid with no significant secondary growth, Gomesa radicans does not yield timber or bast fiber.

Fragrance and cosmetics:
Although orchids in general can have fragrant volatiles, documented commercial use of G. radicans in fragrance or cosmetics has not been established.

Properties relevant to use:
Propagation success relies on typical orchid seed and seedling biology (seedling-stage dependency on mycorrhiza in vitro, vegetative multiplication via keikis) rather than an unusual chemistry profile.

Standards and regulation:
Where applicable, international horticultural trade of orchid taxa is regulated under CITES (Convention on International Trade in Endangered Species of Wild Fauna and Flora), and domestic phytosanitary rules may apply; users should verify status per country.

Sustainability and sourcing:
Most material in horticulture derives from cultivated stocks; wild collection is discouraged due to rarity and conservation concerns. Prefer nursery-propagated divisions or tissue‑culture lines, and verify legal compliance with national and international regulations.

Synonyms Top

Scientific name Authority First published in
Ornithophora quadricolor Barb.Rodr. Gen. Spec. Orchid. 2: 226 (1882)
Ornithophora radicans (Rchb.f.) Garay & Pabst Orquídea (Rio de Janeiro) 13: 50 (1951)
Sigmatostalix radicans Rchb.f. Ann. Bot. Syst. 6: 859 (1864)
Ornithophora radicans f. alba Xim.Bols. Richardiana 16: 173 (2016)

Common names Top

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Language Common/alternative name
Arabic غوميزة متجذرة
Portuguese barba-de-bode-das-árvores
Portuguese pelo-de-urso
Chinese 鸟柱兰

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-0000912819
Tropicos 100440977
KEW urn:lsid:ipni.org:names:77101300-1
The Plant List kew-457747
Open Tree Of Life 812096
NCBI Taxonomy 587976
IPNI 77101300-1
iNaturalist 490105
GBIF 5826459
Freebase /m/0b6hkvl
EOL 1136229
Wikipedia Gomesa_radicans
CMAUP NPO7066

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
The complete chloroplast genome sequence of Gomesa flexuosa Mo P, Zhou J, Zhou F, Chen Y, Huang K Mitochondrial DNA B Resour 07-Jul-2022
PMCID:PMC9275493
doi:10.1080/23802359.2022.2093670
PMID:35837502
Nectar and oleiferous trichomes as floral attractants in Bulbophyllum saltatorium Lindl. (Orchidaceae) Stpiczyńska M, Płachno BJ, Davies KL Protoplasma 24-Sep-2017
PMCID:PMC5830483
doi:10.1007/s00709-017-1170-4
PMID:28944415
Comparative anatomy of floral elaiophores in Vitekorchis Romowicz & Szlach., Cyrtochilum Kunth and a florally dimorphic species of Oncidium Sw. (Orchidaceae: Oncidiinae) Davies KL, Stpiczyńska M, Rawski M Ann Bot 15-Apr-2014
PMCID:PMC4030811
doi:10.1093/aob/mcu045
PMID:24737719
Floral elaiophores in Lockhartia Hook. (Orchidaceae: Oncidiinae): their distribution, diversity and anatomy Blanco MA, Davies KL, Stpiczyńska M, Carlsward BS, Ionta GM, Gerlach G Ann Bot 29-Oct-2013
PMCID:PMC3838557
doi:10.1093/aob/mct232
PMID:24169595
Comparative anatomy of the floral elaiophore in representatives of the newly re-circumscribed Gomesa and Oncidium clades (Orchidaceae: Oncidiinae) Stpiczyńska M, Davies KL, Pacek-Bieniek A, Kamińska M Ann Bot 24-Jul-2013
PMCID:PMC3747802
doi:10.1093/aob/mct149
PMID:23884394
Floral elaiophore structure in four representatives of the Ornithocephalus clade (Orchidaceae: Oncidiinae) Pacek A, Stpiczyńska M, Davies KL, Szymczak G Ann Bot 17-Jul-2012
PMCID:PMC3423815
doi:10.1093/aob/mcs158
PMID:22805528
Elaiophores in Gomesa bifolia (Sims) M.W. Chase & N.H. Williams (Oncidiinae: Cymbidieae: Orchidaceae): structure and oil secretion Aliscioni SS, Torretta JP, Bello ME, Galati BG Ann Bot 18-Aug-2009
PMCID:PMC2766194
doi:10.1093/aob/mcp199
PMID:19692391
Comparative histology of floral elaiophores in the orchids Rudolfiella picta (Schltr.) Hoehne (Maxillariinae sensu lato) and Oncidium ornithorhynchum H.B.K. (Oncidiinae sensu lato) Davies KL, Stpiczyńska M Ann Bot 15-May-2009
PMCID:PMC2710904
doi:10.1093/aob/mcp119
PMID:19447811
Floral convergence in Oncidiinae (Cymbidieae; Orchidaceae): an expanded concept of Gomesa and a new genus Nohawilliamsia Chase MW, Williams NH, de Faria AD, Neubig KM, Amaral MD, Whitten WM Ann Bot 04-Apr-2009
PMCID:PMC2720657
doi:10.1093/aob/mcp067
PMID:19346522
Anti-herbivore Structures of Paulownia tomentosa: Morphology, Distribution, Chemical Constituents and Changes During Shoot and Leaf Development Kobayashi S, Asai T, Fujimoto Y, Kohshima S Ann Bot 15-Mar-2008
PMCID:PMC2710234
doi:10.1093/aob/mcn033
PMID:18344545
Elaiophore Structure and Oil Secretion in Flowers of Oncidium trulliferum Lindl. and Ornithophora radicans (Rchb.f.) Garay & Pabst (Oncidiinae: Orchidaceae) Stpiczyńska M, Davies KL Ann Bot 01-Dec-2007
PMCID:PMC2701824
doi:10.1093/aob/mcm297
PMID:18056056
Oncidinol—a novel diacylglycerol from Ornithophora radicans Barb. Rodr. (Orchidaceae) floral oil Mariza Gomes Reis, Aparecida Donisete de Faria, Maria do Carmo Estanislau do Amaral, Anita Jocelyne Marsaioli Elsevier BV 16-Oct-2003
doi:10.1016/J.TETLET.2003.09.015

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
1-Phenyl-5-heptene-1,3-diyne 5281154 Click to see CC=CC#CC#CC1=CC=CC=C1 166.22 unknown via CMAUP database
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
Phenylheptatriyne 77981 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Butoxyethyl oleate 6436064 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCCOCCCC 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R)-1-hydroxytrideca-5,7,9,11-tetrayn-2-yl]oxyoxane-3,4,5-triol 54671425 Click to see CC#CC#CC#CC#CCCC(CO)OC1C(C(C(C(O1)CO)O)O)O 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2e)-7-Phenylhepta-2-en-4,6-diyn-1-yl acetate 23274467 Click to see 224.25 unknown via CMAUP database
7-Phenylhepta-2,4,6-triynyl acetate 11644243 Click to see CC(=O)OCC#CC#CC#CC1=CC=CC=C1 222.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R)-7-phenylhepta-4,6-diyne-1,2-diol 101808987 Click to see C1=CC=C(C=C1)C#CC#CCC(CO)O 200.23 unknown via CMAUP database
(2S)-7-phenylhepta-4,6-diyn-2-ol 101395939 Click to see 184.23 unknown via CMAUP database
7-Phenyl-2,4,6-heptatriyn-1-ol 3085176 Click to see 180.20 unknown via CMAUP database
7-Phenylhept-2-en-4,6-diyn-1-ol 114662 Click to see 182.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
2-Butoxyethyl linoleate 87553426 Click to see 380.60 unknown via CMAUP database
2-Butoxyethyl linolenate 87552578 Click to see 378.60 unknown via CMAUP database
Ethyl Linoleate 5282184 Click to see 308.50 unknown via CMAUP database
Ethyl linolenate 5367460 Click to see 306.50 unknown via CMAUP database
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
Methyl Linolenate 5319706 Click to see 292.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-[(3R,7S,11S)-3-hydroxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 46183941 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoic acid 42433537 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CC(=O)O)C 310.50 unknown via CMAUP database
[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl] heptanoate 101918983 Click to see CCCCCCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C 408.70 unknown via CMAUP database
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Schottenol 441837 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
(1-Acetyloxy-3-hydroxypropan-2-yl) 3,6-diacetyloxyicosanoate 162952773 Click to see 544.70 unknown https://doi.org/10.1016/J.TETLET.2003.09.015
[(2S)-1-acetyloxy-3-hydroxypropan-2-yl] (3R,6R)-3,6-diacetyloxyicosanoate 101758743 Click to see 544.70 unknown https://doi.org/10.1016/J.TETLET.2003.09.015
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 153946 Click to see 516.40 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see 516.40 unknown via CMAUP database
Isochlorogenic acid C 460890 Click to see 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(E)-3-[4-[(2S,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoic acid 15071014 Click to see 514.50 unknown via CMAUP database
(E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoic acid 15071011 Click to see 472.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylthiophene 6920 Click to see 126.18 unknown via CMAUP database
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
5-(Phenylethynyl)thiophene-2-methanol 2822242 Click to see 214.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids
(Z)-7-[[beta-D-Glucopyranosyl]oxy]-3',4',6-trihydroxyaurone 15071008 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown via CMAUP database
Ethyl Caffeate 5317238 Click to see 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(E)-3-(3,4-dihydroxyphenyl)-1-[2,3-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one 14213552 Click to see 612.50 unknown via CMAUP database
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-5-hydroxyoxan-2-yl]methyl acetate 14861259 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)OC(=O)C)OC(=O)C 576.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 14213555 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 492.40 unknown via CMAUP database
2,3-Dihydroxy-4-[(E)-3-(3,4-dihydroxyphenyl)acryloyl]phenyl 4-O,6-O-diacetyl-beta-D-glucopyranoside 10840030 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)OC(=O)C 534.50 unknown via CMAUP database
3',4'-Di(beta-D-glucopyranosyloxy)-2',3,4-trihydroxychalcone 102149400 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 612.50 unknown via CMAUP database
chrysosplenosid-C 118856019 Click to see 522.50 unknown via CMAUP database
Marein 6441269 Click to see 450.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-5-hydroxyoxan-2-yl]methyl acetate 10603216 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)OC(=O)C)OC(=O)C 574.50 unknown via CMAUP database
[(2R,3S,4R,5R,6S)-3-acetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-4,5-dihydroxyoxan-2-yl]methyl acetate 101669623 Click to see 532.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,5-diacetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-4-hydroxyoxan-2-yl]methyl acetate 10674637 Click to see 574.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 15071009 Click to see 594.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 15071010 Click to see 490.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-3,6-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101243893 Click to see 508.40 unknown via CMAUP database
5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 5495545 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13344657 Click to see 492.40 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102316697 Click to see 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11577257 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
Centaurein 5489090 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Okanin 5281294 Click to see 288.25 unknown via CMAUP database

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