Limonium gmelinii - Unknown
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Internal ID UUID643ffd867d954002761377
Scientific name Limonium gmelinii
Authority Kuntze
First published in Revis. Gen. Pl. 2: 395 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Limonium hypanicum Klokov Fl. RSS Ucr. 8: 524 (1958)
Limonium hungaricum Klokov Fl. RSS Ucr. 8: 525 (1958)
Statice gmelinii Willd. Sp. Pl., ed. 4 , 1: 1524 (1798)
Limonium gmelinii subsp. hypanicum Soó
Limonium gmelinii var. hypanicum Pawł.
Statice glauca Willd. ex Schult. Syst. Veg., ed. 15 bis [Roemer & Schultes] 6: 799. 1820 [Aug-Dec 1820]
Statice pycnantha K.Koch Linnaea 21: 716 (1849)
Statice scoparia Pall. ex Willd. Sp. Pl., ed. 4 , 1: 1524 (1798)
Statice gmelinii var. scoparia (Pall. ex Willd.) Schmalh. Syst. Veg. 6: 799 1820
Limonium pycnanthum Kuntze Revis. Gen. Pl. 2: 396 (1891)

Common names Top

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Language Common/alternative name
English siberian statice
Bulgarian гмелинова гърлица
Hungarian sziki sóvirág
Hungarian magyar sóvirág
Kazakh Тұмар Бояу
Russian кермек Гмелина
Serbian Слатински цвет
Ukrainian кермек Гмеліна
Ukrainian кермек Ґмеліна
Chinese 大叶矶松
Chinese 补血草
Chinese 大叶补血草
Chinese 克迷克
Chinese 拜赫
Chinese 拜赫曼

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
    • Western Asia
      • East Aegean Islands
      • Iran
      • Turkey
  • Europe
    • Eastern Europe
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Hungary
    • Southeastern Europe
      • Bulgaria
      • Romania
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000444657
Tropicos 25400348
KEW urn:lsid:ipni.org:names:686792-1
The Plant List kew-2495733
Open Tree Of Life 387499
Observations.org 104710
NCBI Taxonomy 46094
IPNI 686792-1
iNaturalist 508406
GBIF 4089276
EPPO LIIGM
EOL 2892146
Elurikkus 464446
USDA GRIN 22277
Wikipedia Limonium_gmelini
CMAUP NPO5054

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
Ornamental Plants and Urban Gardening Orlóci L, Fekete A Plants (Basel) 07-Dec-2023
PMCID:PMC10747257
doi:10.3390/plants12244096
PMID:38140422
Validation of the shotgun metabarcoding approach for comprehensively identifying herbal products containing plant, fungal, and animal ingredients Zhang Z, Mu W, Kong W, Liu J, Zhao J, Zhao Q, Shi M, Zhao H, Liu J, Shi L PLoS One 03-Jul-2023
PMCID:PMC10317219
doi:10.1371/journal.pone.0286069
PMID:37399206
Natural products targeting inflammation-related metabolic disorders: A comprehensive review Nainu F, Frediansyah A, Mamada SS, Permana AD, Salampe M, Chandran D, Emran TB, Simal-Gandara J Heliyon 02-Jun-2023
PMCID:PMC10279840
doi:10.1016/j.heliyon.2023.e16919
PMID:37346355
Salt Tolerance of Limonium gmelinii subsp. hungaricum as a Potential Ornamental Plant for Secondary Salinized Soils Honfi P, Eisa EA, Tilly-Mándy A, Kohut I, Ecseri K, Mosonyi ID Plants (Basel) 28-Apr-2023
PMCID:PMC10181086
doi:10.3390/plants12091807
PMID:37176868
Chemical Constituents, Anticancer and Anti-Proliferative Potential of Limonium Species: A Systematic Review Gancedo NC, Isolani R, de Oliveira NC, Nakamura CV, de Medeiros Araújo DC, Sanches AC, Tonin FS, Fernandez-Llimos F, Chierrito D, de Mello JC Pharmaceuticals (Basel) 14-Feb-2023
PMCID:PMC9958820
doi:10.3390/ph16020293
PMID:37259435
Application of In Vitro Plant Tissue Culture Techniques to Halophyte Species: A Review Custódio L, Charles G, Magné C, Barba-Espín G, Piqueras A, Hernández JA, Ben Hamed K, Castañeda-Loaiza V, Fernandes E, Rodrigues MJ Plants (Basel) 27-Dec-2022
PMCID:PMC9824063
doi:10.3390/plants12010126
PMID:36616255
The Application of Pearls in Traditional Medicine of China and Their Chemical Constituents, Pharmacology, Toxicology, and Clinical Research Song Y, Chen W, Fu K, Wang Z Front Pharmacol 23-Aug-2022
PMCID:PMC9445187
doi:10.3389/fphar.2022.893229
PMID:36081944
Structure, Function, and Regulation of the Plasma Membrane Na+/H+ Antiporter Salt Overly Sensitive 1 in Plants Xie Q, Zhou Y, Jiang X Front Plant Sci 31-Mar-2022
PMCID:PMC9009148
doi:10.3389/fpls.2022.866265
PMID:35432437
Road traffic and landscape characteristics predict the occurrence of native halophytes on roadside verges Fekete R, Bak H, Vincze O, Süveges K, Molnár VA Sci Rep 25-Jan-2022
PMCID:PMC8789788
doi:10.1038/s41598-022-05084-3
PMID:35079052
Plant Extract of Limonium gmelinii Attenuates Oxidative Responses in Neurons, Astrocytes, and Cerebral Endothelial Cells In Vitro and Improves Motor Functions of Rats after Middle Cerebral Artery Occlusion Nurkenov T, Tsoy A, Olzhayev F, Abzhanova E, Turgambayeva A, Zhussupova A, Avula B, Ross S, Aituarova A, Kassymova D, Zhusupova G, Shalakhmetova T, Tokay T, Lee JC, Askarova S Antioxidants (Basel) 15-Nov-2021
PMCID:PMC8614848
doi:10.3390/antiox10111814
PMID:34829685
Functional composition of ant assemblages in habitat islands is driven by habitat factors and landscape composition Deák B, Báthori F, Lőrinczi G, Végvári Z, Nagy DD, Mizser S, Torma A, Valkó O, Tóthmérész B Sci Rep 25-Oct-2021
PMCID:PMC8546063
doi:10.1038/s41598-021-00385-5
PMID:34697323
Natural α-Glucosidase and Protein Tyrosine Phosphatase 1B Inhibitors: A Source of Scaffold Molecules for Synthesis of New Multitarget Antidiabetic Drugs Genovese M, Nesi I, Caselli A, Paoli P Molecules 09-Aug-2021
PMCID:PMC8400511
doi:10.3390/molecules26164818
PMID:34443409
Current Condition of Pannonic Salt Steppes at Their Distribution Limit: What Do Indicator Species Reveal about Habitat Quality? Dítě Z, Šuvada R, Tóth T, Jun PE, Píš V, Dítě D Plants (Basel) 11-Mar-2021
PMCID:PMC7999981
doi:10.3390/plants10030530
PMID:33799896
Heavy metal tolerance and potential for remediation of heavy metal-contaminated saline soils for the euhalophyte Suaeda salsa Shang C, Wang L, Tian C, Song J Plant Signal Behav 20-Aug-2020
PMCID:PMC7588191
doi:10.1080/15592324.2020.1805902
PMID:32815486
Nutrient availability affects the polar lipidome of Halimione portulacoides leaves cultured in hydroponics Custódio M, Maciel E, Domingues MR, Lillebø AI, Calado R Sci Rep 20-Apr-2020
PMCID:PMC7171145
doi:10.1038/s41598-020-63551-1
PMID:32313165

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1007/S10600-005-0012-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1007/S10600-005-0012-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,3S,4R,4aS,8aR)-3,4a,8,8-tetramethyl-4-[(2E)-3-methylpenta-2,4-dienyl]-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol 162949319 Click to see CC(=CCC1C2(CCCC(C2CC(C1(C)O)O)(C)C)C)C=C 306.50 unknown https://doi.org/10.1007/S10600-005-0012-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
CID 85150831 85150831 Click to see CC1CC2(CC(C3(O2)CCC4(C3(CCC5=C4CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)OC2C(C(C(CO2)O)O)OC2C(C(C(O2)CO)O)O)OC2C(C(C(C(O2)C)O)O)O)O)O)O)C)C)C)C)OC1=O 1353.40 unknown https://doi.org/10.1007/S10600-005-0012-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
alpha-D-GALACTOSE 439357 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1007/S10600-005-0012-3
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-2-(2,4,5-trihydroxyphenyl)-8-[(2R,3R,4R)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162924491 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-006-0068-8
2-(2,4,5-trihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162924490 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-006-0068-8
3'-Galloylprodelphinidin B2 14520967 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 762.60 unknown https://doi.org/10.1007/S10600-006-0068-8
epigallocatechin-(4beta->8)-epigallocatechin-3-O-gallate 467305 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 762.60 unknown https://doi.org/10.1007/S10600-006-0068-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2S,3S)-2-(2,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 162867703 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3O)O)O)O 306.27 unknown https://doi.org/10.1007/S10600-006-0052-3
2-(2,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 131834532 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3O)O)O)O 306.27 unknown https://doi.org/10.1007/S10600-006-0052-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate 1287 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1007/S10600-006-0052-3
https://doi.org/10.1007/S10600-005-0012-3
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1007/S10600-006-0052-3
https://doi.org/10.1007/S10600-005-0012-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/S10600-006-0052-3
Flavan-3,3',4',5,5',7-hexol 1249 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/S10600-006-0052-3
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/S10600-006-0052-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
5'-Hydroxymorin 16113029 Click to see C1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3O)O)O)O)O 318.23 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1007/S10600-005-0012-3
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/S10600-005-0012-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 6325002 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 581.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Cyanidin 3,5-diglucoside 44256718 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4S,5R)-2-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol 5316494 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O 435.40 unknown via CMAUP database
[(2S,3S,4R,5R)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxyoxan-3-yl] 3,4,5-trihydroxybenzoate 162944232 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 602.50 unknown https://doi.org/10.1007/S10600-005-0012-3
[2-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxyoxan-3-yl] 3,4,5-trihydroxybenzoate 162944231 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 602.50 unknown https://doi.org/10.1007/S10600-005-0012-3
3-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-rhamnopyranosyl)oxy]-3',4',5,5',7-pentahydroxyflavone 101036025 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)C)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-005-0012-3
3-[[6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-galactopyranosyl]oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 73803273 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)O 626.50 unknown https://doi.org/10.1007/S10600-005-0012-3
3-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 74978308 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)C)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricetin 3-arabinoside 21672568 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)O 450.30 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricetin 3-O-beta-D-galactoside 6''-O-gallate 5319985 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 632.50 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricetin 3-rhamnoside 5352000 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-005-0012-3
myricetin-3-O-beta-D-xylopyranoside 23900088 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)O 450.30 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricetin-3-O-rutinoside 21577860 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)O 626.50 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricetin-3-O-xyloside 21477996 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)O 450.30 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-005-0012-3
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/10.1007/S10600-005-0012-3
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/10.1007/S10600-005-0012-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 102444976 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-005-0012-3
Myricetin 7-rhamnoside 76594575 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-005-0012-3
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 5-hydroxyflavonoids
Delfinidin 25203213 Click to see C1=C(C=C(C(=C1O)[O-])O)C2=C(C=C3C(=CC(=O)C=C3O2)O)O 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1007/S10600-005-0012-3

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