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Discaria chacaye

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description 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

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
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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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 / Fatty Acyls / Fatty acid esters
(3S)-3beta,6beta,9beta-Trimethyl-4beta-(angeloyloxy)-6,7alpha-dihydroxy-9-(methoxymethyl)-2,3,3abeta,5,6,7,9,9balpha-octahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-2-one 102321417 Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(OC2O)(C)COC)(C)O 410.50 unknown via CMAUP database
2-Methyl-2-butenoic acid [(3aR)-2,3,3abeta,4,5,6,7,8,9,9balpha-decahydro-2,7-dioxo-6alpha,9beta-dihydroxy-3beta,6,9-trimethylazuleno[4,5-b]furan]-4beta-yl ester 15922700 Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(CC2=O)(C)O)(C)O 378.40 unknown via CMAUP database
8alpha-Angeloyl-2alpha,4alpha,10beta-trihydroxy-6betaH,7alphaH-1(5)-guaien-12,6alpha-olide 643640 Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(CC2O)(C)O)(C)O 380.40 unknown via CMAUP database
8alpha-Angeloyl-4alpha,10beta-dihydroxy-2-oxo-6betaH,7alphaH,11betaH-1(5)-guaien-12,6alpha-olide 101143220 Click to see CC=C(C)C(=O)OC1CC(C2=C(C3C1C(C(=O)O3)C)C(CC2=O)(C)O)(C)O 378.40 unknown via CMAUP database
Angeloylartabsin 101078309 Click to see CC=C(C)C(=O)OC1CC(C2=CCC(=C2C3C1C(C(=O)O3)C)C)(C)O 346.40 unknown via CMAUP database
Tigloylartabsin 101672241 Click to see CC=C(C)C(=O)OC1CC(C2=CCC(=C2C3C1C(C(=O)O3)C)C)(C)O 346.40 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)-3,10-Dimethyl-6-methylene-7-hydroxy-2,3,3a,4,5,6,7,8,9,11a-decahydrocyclodeca[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)-3abeta,4,5,5a,6,7,8,9,9abeta,9balpha-Decahydro-3alpha,5aalpha,9-trimethyl-6alpha,9beta-dihydroxynaphtho[1,2-b]furan-2(3H)-one 14110909 Click to see CC1C2CCC3(C(CCC(C3C2OC1=O)(C)O)O)C 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 CC1C2CCC(=CCC(C(=CC2OC1=O)C)O)C 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(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 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
(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 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
beta-Ursolic acid 220774 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
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
Ursolic Acid 64945 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
> 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
24-Ethylcholest-5-en-3beta-ol 22012 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
> 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 C[N+](C)(C)CC(=O)[O-] 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
(2S)-pyrrolidin-1-ium-2-carboxylate 6971047 Click to see C1CC([NH2+]C1)C(=O)[O-] 115.13 unknown via CMAUP database
Betonicine 164642 Click to see C[N+]1(CC(CC1C(=O)[O-])O)C 159.18 unknown via CMAUP database
Stachydrine 115244 Click to see C[N+]1(CCCC1C(=O)[O-])C 143.18 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 CC(C)CC(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC3=CC=CC=C3)C4=CC=CC=C4)N(C)C 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 CC(C)CC(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC3=CC=CC=C3)C4=CC=CC=C4)N(C)C 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 CC(C)CC(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC3=CC=CC=C3)C4=CC=CC=C4)N(C)C 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 C[N+](C)(C)CCO 104.17 unknown via CMAUP database
> Organoheterocyclic compounds / Cycloheptafurans
(3S)-2-Oxo-3beta,6,9-trimethyl-2,3,3abeta,5,6,9balpha-hexahydro-4H-cyclohepta[2,1-b:3,4-c']difuran-4beta,6alpha-diol 4-acetate 15127111 Click to see CC1C2C(CC(C3=COC(=C3C2OC1=O)C)(C)O)OC(=O)C 308.33 unknown via CMAUP database
Angeloyloxaartabsin 102008484 Click to see CC=C(C)C(=O)OC1CC(C2=COC(=C2C3C1C(C(=O)O3)C)C)(C)O 348.40 unknown via CMAUP database
Tigloyloxaartabsin 102008485 Click to see CC=C(C)C(=O)OC1CC(C2=COC(=C2C3C1C(C(=O)O3)C)C)(C)O 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
N-Methylcoclaurine 2752274 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 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 CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C 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 CC1C2C(CC(=C3C(=O)C=C(C3(C2OC1=O)O)C)C)OC(=O)C 320.30 unknown via CMAUP database
14-Deoxylactucin 156302 Click to see CC1=C2C(C3C(C(C1)O)C(=C)C(=O)O3)C(=CC2=O)C 260.28 unknown via CMAUP database
Austricin 6713966 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O 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 CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O 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
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Venoruton 24832108 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(73)80719-8
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 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 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)O 464.40 unknown via CMAUP database
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Isorhoifolin 9851181 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 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
5-Hydroxy-3,6,7,4'-tetramethoxyflavone 5318355 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown via CMAUP database
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

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