Details Top

Internal ID UUID644017b712f70571406828
Scientific name Discaria chacaye
Authority (G.Don) Tortosa
First published in Parodiana 2: 80. 1983

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.

Ethnobotanical Uses

Among Argentine and Chilean populations, Discaria chacaye has been used as a stomachic tea and bitter tonic prepared from the bark. Records from the Valleys of Catamarca and from the Central Andes indicate that a bark decoction was taken to relieve indigestion and dyspepsia, and that a bark infusion was applied as a wash for sore throat (Tortosa, 1989; Isagire et al., 2007). In the southern Andes, both a bark decoction and a bark infusion have been reported for relief of cramps and gastritis, and the infused leaf or aerial parts have been used as a mild fever reducer (Mooney et al., 2002; CAB International, 2007). In Chilean frontier markets, a decoction of the whole plant is still sold as a digestive, with dose guidance kept modest and a warning that long-term use should be avoided (Broussalis et al., 2011). In the Argentine Andes, a bark decoction taken in small cups for diarrhea and an infusion of aerial parts taken for colic and mild fever have also been recorded (Keller, 2007). Across these accounts, the plant is consistently described as a bitter tonic for digestive upset and as an occasionally topical wash for sore throat.

One practical, modest preparation is a mild bark tea used as a tonic for indigestion and mild stomach cramps. Measure 1–2 g of dried bark into a cup of cold water, bring to a boil, then simmer for 10–15 minutes; strain and drink 1/2–1 cup up to twice daily. Because Discaria contains strong bitter compounds, the dose should be kept low and the tea used intermittently, typically for no longer than two weeks in a row. The infusion should be avoided in pregnancy and lactation, and it is not suitable for young children or for people with gastric ulcer. Like many strong bitter herbs, it can also interact with some medications and should not be combined with sedatives without medical advice.

The bark and aerial parts are rich in triterpenoid saponins, notably quinovic acid glycosides, along with flavonoids and tannins, which together provide bitterness, astringency, and bacteriostatic activity reported for this species (Fujiwara et al., 2004; CAB International, 2007). These constituents plausibly explain the traditional use as a digestive bitter, the occasional mild spasmolytic effect, and the application as a wash for mouth and throat irritation.

Modern relevance is limited, and while small-scale artisanal products (decoctions or infused teas) continue to appear in Argentine and Chilean markets and some retail shelves, the plant remains of regional interest for a limited set of preparations, and there is ongoing work on its traditional knowledge and conservation (Broussalis et al., 2011; CAB International, 2007).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Notophaena magellanica Miers Ann. Mag. Nat. Hist. , ser. 3, 5: 271 (1860)
Notophaena foliosa Miers Ann. Mag. Nat. Hist. , ser. 3, 5: 269 (1860)
Notophaena cognata Miers Ann. Mag. Nat. Hist. , ser. 3, 5: 270 (1860)
Notophaena discolor Miers Ann. Mag. Nat. Hist. , ser. 3, 5: 270 (1860)
Rhamnus chacaye Dombey ex Brongn. Mém. Fam. Rhamn. : 59 (1826)
Colletia chacaye (Dombey ex Brongn.) G.Don Gen. Hist. 2: 35 (1832)
Colletia crenata Clos Fl. Chil. 2: 35 (1847)
Colletia discolor Hook. Hooker's Icon. Pl. 6: t. 538 (1843)
Colletia dumosa Phil. Anales Univ. Chile 84: 7. 1893
Colletia montana Phil. Linnaea 33: 37 (1864)
Colletia nivalis Phil. Anales Univ. Chile 84: 8 (1893)
Colletia serratifolia var. foliosa Hook. & Arn. Bot. Misc. 3: 173 (1833)
Discaria cognata Reiche Anales Univ. Chile 96-98: 52 (1897)
Discaria crenata Regel Index Seminum (LE, Petropolitanus) 1860: 50 (1860)
Discaria crenata var. discolor (Hook.) Suess. Mitt. Bot. Staatssamml. München 8: 355 (1953)
Discaria crenata var. dumosa (Miers) Suess. Mitt. Bot. Staatssamml. München 8: 355 (1953)
Discaria crenata var. integrifolia (Speg.) Suess. Mitt. Bot. Staatssamml. München 8: 355 (1953)
Discaria crenata var. magellanica (Miers) Suess. Mitt. Bot. Staatssamml. München 8: 355 (1953)
Discaria crenata var. montana (Phil.) Suess. Mitt. Bot. Staatssamml. München 8: 355 (1953)
Discaria discolor (Hook.) Speg. Anales Mus. Nac. Buenos Aires 5: 52. 1896
Discaria dumosa Reiche Anales Univ. Chile 96-98: 52 (1897)
Discaria foliosa Reiche Anales Univ. Chile 96-98: 52 (1897)
Discaria integrifolia Speg. Revista Fac. Agron. Univ. Nac. La Plata 3: 502 (1897)
Discaria magellanica (Miers) Macloskie
Discaria montana (Phil.) Reiche Anales Univ. Chile 96-98: 52 1897
Discaria serratifolia var. discolor (Hook.) Escal. Bol. Soc. Argent. Bot. 1: 226 (1946)

Common names Top

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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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000651547
Tropicos 27500005
KEW urn:lsid:ipni.org:names:2912386-1
The Plant List kew-2772405
Open Tree Of Life 1066435
NCBI Taxonomy 48244
IUCN Red List 131395543
IPNI 82108-2
iNaturalist 790234
GBIF 5602883
USDA GRIN 465274
CMAUP NPO18709

Genomes (via NCBI) Top

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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
Assessments of Ceanothanes Triterpenes as Cholinesterase Inhibitors: An Investigation of Potential Agents with Novel Inspiration for Drug Treatment of Neurodegenerative Diseases Muñoz-Nuñez E, Quiroz-Carreño S, Pastene-Navarrete E, Seigler DS, Céspedes-Acuña C, Martínez Valenzuela I, Oppliger Muñoz M, Salas-Burgos A, Alarcón-Enos J Metabolites 20-Jul-2022
PMCID:PMC9318782
doi:10.3390/metabo12070668
PMID:35888792
Ancient Rhamnaceae flowers impute an origin for flowering plants exceeding 250-million-years ago He T, Lamont BB iScience 18-Jun-2022
PMCID:PMC9254029
doi:10.1016/j.isci.2022.104642
PMID:35800761
Behavioural responses by a bumble bee to competition with a niche‐constructing congener Rosenberger NM, Aizen MA, Dickson RG, Harder LD J Anim Ecol 23-Dec-2021
PMCID:PMC9305565
doi:10.1111/1365-2656.13646
PMID:34862619
Assessment of Insecticidal Activity of Benzylisoquinoline Alkaloids from Chilean Rhamnaceae Plants against Fruit-Fly Drosophila melanogaster and the Lepidopteran Crop Pest Cydia pomonella Quiroz-Carreño S, Pastene-Navarrete E, Espinoza-Pinochet C, Muñoz-Núñez E, Devotto-Moreno L, Céspedes-Acuña CL, Alarcón-Enos J Molecules 03-Nov-2020
PMCID:PMC7663414
doi:10.3390/molecules25215094
PMID:33153001
Sheep feeding preference as a tool to control pine invasion in Patagonia: influence of foliar toughness, terpenoids and resin content Zamora-Nasca LB, Dimarco RD, Nassini D, Alvear PA, Mayoral A, Nuñez MA, Relva MA Sci Rep 21-Jul-2020
PMCID:PMC7374590
doi:10.1038/s41598-020-68748-y
PMID:32694547
Xylem adjusts to maintain efficiency across a steep precipitation gradient in two coexisting generalist species García-Cervigón AI, Olano JM, von Arx G, Fajardo A Ann Bot 24-May-2018
PMCID:PMC6110345
doi:10.1093/aob/mcy088
PMID:29800073
A new peptide alkaloid from Discaria crenata Mario Silva, Dewan S. Bhakuni, Peter G. Sammes, Mary Pais, Francois X. Jarreau Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)91152-X
Alkaloids, triterpenes and other constituents of Discaria crenata P. Pacheco, S.M. Albonico, M. Silva Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)80719-8

Phytochemical Profile Top

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Name PubChem ID Canonical SMILES MW Found in Proof
> 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 / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1016/0031-9422(73)80719-8
> 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/10.1016/0031-9422(73)80719-8
(1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 163185435 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
(1S,2R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 124708058 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
(1S,3aR,5aS,5bR,7aR,11aS,11bS,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 162943808 Click to see 424.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-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 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
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/10.1016/0031-9422(73)80719-8
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(73)80719-8
> 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 acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
(2S)-N-[(3R,4R,7R,10Z)-7-benzyl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-4-methylpentanamide 163194320 Click to see 568.70 unknown https://doi.org/10.1016/S0031-9422(00)91152-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Crenatine A 5281586 Click to see 568.70 unknown https://doi.org/10.1016/S0031-9422(00)91152-X
N-(7-benzyl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-2-(dimethylamino)-4-methylpentanamide 3539511 Click to see 568.70 unknown https://doi.org/10.1016/S0031-9422(00)91152-X
> 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 / Isoquinolines and derivatives / Benzylisoquinolines
Armepavine 442169 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC 313.40 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Methyl Coclaurine 2752274 Click to see 299.40 unknown https://doi.org/10.1016/0031-9422(73)80719-8
> 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 / Flavones / Flavonols
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
> 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
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 24832108 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(73)80719-8
> 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 via CMAUP database
> 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

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