Amaranthus hypochondriacus - Unknown
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Internal ID UUID644008bf8455c363975107
Scientific name Amaranthus hypochondriacus
Authority L.
First published in Sp. Pl. : 991 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amaranthus anardana Buch.-Ham. Numer. List [Wallich] n. 6903. 1832
Amaranthus atrosanguineus Hort.Lugd. (1838) ex Moq. in DC. Prod. xiii. II. 266.
Amaranthus aureus Besser Cat. Jard. Bot. Krzemieniec : 8 (1816)
Amaranthus bernhardii Moq. Prodr. 13(2): 258 (1849)
Amaranthus flavus L. Syst. Nat. ed. 10 , 2: 1269 (1759)
Amaranthus frumentaceus Buch.-Ham. Fl. Ind. ed. 1832 , 3: 699 (1832)
Amaranthus hybridus Vell. Fl. Flumin. Icon. 10: t. 28. 1831 [1827 publ. 29 Oct 1831]
Amaranthus hybridus var. erythrostachys Moq. Prodr. 13(2): 259 (1849)
Amaranthus hybridus f. hypochondriacus (L.) B.L.Rob. Rhodora 10: 66. 1908 [16 May 1908]
Amaranthus hybridus var. hypochondriacus (L.) B.L.Rob. Rhodora 10: 32 (1908)
Amaranthus hybridus subsp. hypochondriacus (L.) Thell. Fl. Advent. Montpellier 204. 1912
Amaranthus hypochondriacus var. macrostachys Moq. Prodr. 13(2): 256 (1849)
Amaranthus hypochondriacus var. monstrosus Moq. Prodr. 13(2): 256 (1849)
Amaranthus hypochondriacus var. racemosus Moq. Prodr. 13(2): 256 (1849)
Amaranthus hypochondriacus var. tortuosus Moq. Prodr. 13(2): 256 (1849)
Amaranthus macrostachyus Mérat ex Moq. Prodr. 13(2): 256 (1849)
Amaranthus monstrosus Cat. Hort. Div. (1837); Hort. Tonelle, ex Moq. in DC. Prod. xiii. II. 256.
Amaranthus hybridus f. hypochondiacus (L.) B.L.Rob. Rhodora 10: 66. 1908 [16 May 1908]

Common names Top

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Language Common/alternative name
English prince-of-wales feather
Spanish amaranthus flavus
Spanish amaranthus aureus
Spanish amaranthus macrostachyus
Spanish amaranthus anardana
Spanish amaranthus atrosanguineus
Spanish amaranthus bernhardii
Spanish amaranthus frumentaceus
Spanish amaranthus hybridus f. hypochondriacus
Spanish amaranthus hybridus subsp hypochondriacus
Spanish amaranthus hybridus var erythrostachys
Spanish amaranthus hybridus var. hypochondriacus
Spanish amaranthus leucospermus
Spanish amaranthus monstrosus
Spanish amaranthus leucocarpus
Spanish amaranthus hybridus var. leucocarpus
Spanish amaranthus hybridus subsp. hypochondriacus
Arabic قطيفة شبه غضروفية
Czech laskavec červenoklasý
Welsh blodyn amor pruddglwyfus
German trauer-amarant
Finnish amaranthus hybridus subsp. hypochondriacus
Finnish meksikonrevonhäntä
Finnish amarantti
Upper Sorbian Žarowacy šćěrjenc
Hungarian piros disznóparéj
Hungarian piros amaránt
Japanese アマランツス・ハイポコンドリアカス
Japanese シロミセンニンコク
Swedish toppamarant
Chinese 老枪谷子
Chinese 籽粒苋
Chinese 千穗谷

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Amaranthus hypochondriacus var. powellii (S.Watson) Pedersen Monogr. Syst. Bot. Missouri Bot. Gard. 74: 1245 (1999)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
protect from damping off; grow cool

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
    • Northeast Tropical Africa
      • Chad
    • Northern Africa
      • Algeria
      • Morocco
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Cameroon
      • Congo
      • Zaïre
  • Asia-temperate
    • Caucasus
      • North Caucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Western Asia
      • East Aegean Islands
      • Iran
      • Lebanon-Syria
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • East European Russia
      • Northwest European Russia
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Netherlands
    • Northern Europe
      • Denmark
      • Finland
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
    • Southwestern Europe
      • France
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
      • Québec
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • Wisconsin
    • Northeastern U.S.A.
      • Massachusetts
      • Michigan
      • New York
      • Pennsylvania
      • Vermont
      • West Virginia
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Florida
    • Southwestern U.S.A.
      • Arizona
      • California
      • Utah
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
  • Pacific
    • South-central Pacific
      • Cook Islands
    • Southwestern Pacific
      • Nauru
      • Vanuatu
  • Southern America
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000530285
UNII YL06Y84R9Z
Canadensys 27774
USDA Plants AMHY2
Tropicos 1100009
INPN 81994
KEW urn:lsid:ipni.org:names:10665-2
The Plant List kew-2632908
Open Tree Of Life 22343
NCBI Taxonomy 28502
NBN Atlas NBNSYS0000141566
Nature Serve 2.128128
IPNI 10665-2
iNaturalist 75396
GBIF 6109718
Freebase /m/0872cl
WisFlora 2498
EPPO AMAHP
EOL 585514
Calflora (Californian flora) 11322
USDA GRIN 2796
Wikipedia Amaranthus_hypochondriacus
CMAUP NPO623

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_000753965.2 IBAB_Ahyp_2.0 Chromosome Institute of Bioinformatics and Applied Biotechnology 2020-10-02 25.0x 398.12 Mb

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
Simulating short-term light responses of photosynthesis and water use efficiency in sweet sorghum under varying temperature and CO2 conditions Yang XL, Ma XF, Ye ZP, Yang LS, Shi JB, Wang X, Zhou BB, Wang FB, Deng ZF Front Plant Sci 28-Mar-2024
PMCID:PMC11007071
doi:10.3389/fpls.2024.1291630
PMID:38606074
Genome-Wide Comparative Analysis of Five Amaranthaceae Species Reveals a Large Amount of Repeat Content Singh A, Maurya A, Rajkumar S, Singh AK, Bhardwaj R, Kaushik SK, Kumar S, Singh K, Singh GP, Singh R Plants (Basel) 13-Mar-2024
PMCID:PMC10975975
doi:10.3390/plants13060824
PMID:38592842
Microgreens on the rise: Expanding our horizons from farm to fork Lone JK, Pandey R, Gayacharan Heliyon 11-Feb-2024
PMCID:PMC10881865
doi:10.1016/j.heliyon.2024.e25870
PMID:38390124
New Insights into Antioxidant Peptides: An Overview of Efficient Screening, Evaluation Models, Molecular Mechanisms, and Applications Zhang Y, Li Y, Quan Z, Xiao P, Duan JA Antioxidants (Basel) 05-Feb-2024
PMCID:PMC10886007
doi:10.3390/antiox13020203
PMID:38397801
Flavonoids influence key rhizocompetence traits for early root colonization and PCB degradation potential of Paraburkholderia xenovorans LB400 Ghitti E, Rolli E, Vergani L, Borin S Front Plant Sci 02-Feb-2024
PMCID:PMC10869545
doi:10.3389/fpls.2024.1325048
PMID:38371405
1H NMR-Based Metabolomics Profile of Green and Red Amaranthus Grown in Open Field versus Greenhouse Cultivation System Nemadodzi LE, Managa GM Metabolites 28-Dec-2023
PMCID:PMC10819972
doi:10.3390/metabo14010021
PMID:38248824
Unraveling Compositional Study, Chemometric Analysis, and Cell-Based Antioxidant Potential of Selective High Nutraceutical Value Amaranth Cultivars Using a GC-MS and NMR-Based Metabolomics Approach Gupta A, Singh GD, Gautam A, Tripathi T, Taneja AK, Singh BN, Roy R, Sidhu OP, Panda SK, Bhatt A ACS Omega 05-Dec-2023
PMCID:PMC10733922
doi:10.1021/acsomega.3c05597
PMID:38144049
Insect α-Amylases and Their Application in Pest Management Wang B, Huang D, Cao C, Gong Y Molecules 01-Dec-2023
PMCID:PMC10708458
doi:10.3390/molecules28237888
PMID:38067617
Data analysis of polygalacturonase inhibiting proteins (PGIPs) from agriculturally important proteomes Acharya S, Troell HA, Billingsley RL, Lawrence KS, McKirgan DS, Alkharouf NW, Klink VP Data Brief 19-Nov-2023
PMCID:PMC10698527
doi:10.1016/j.dib.2023.109831
PMID:38076472
Replacing alfalfa hay with amaranth hay: effects on production performance, rumen fermentation, nutrient digestibility and antioxidant ability in dairy cow Ma J, Fan X, Sun G, Yin F, Zhou G, Zhao Z, Gan S Anim Biosci 01-Nov-2023
PMCID:PMC10766491
doi:10.5713/ab.23.0232
PMID:37946438
Effects of Different Proportions of Amaranthus hypochondriacus Stem and Leaf Powder Inclusions on Growth Performance, Carcass Traits, and Blood Biochemical Parameters of Broilers Ren Y, Liu L, Zhou S, Li Y, Wang Y, Yang K, Chen W, Zhao S Animals (Basel) 05-Sep-2023
PMCID:PMC10525678
doi:10.3390/ani13182818
PMID:37760218
Effect of Germination on Fatty Acid Composition in Cereal Grains Al-Taher F, Nemzer B Foods 02-Sep-2023
PMCID:PMC10487171
doi:10.3390/foods12173306
PMID:37685238
Early growth, development and allometry of glyphosate-resistant and susceptible Amaranthus palmeri in response to current and elevated temperature and CO2 de Souza Rodrigues J, Shilling D, Tishchenko V, Bowen S, Deng S, Hall DB, Grey TL Sci Rep 02-Sep-2023
PMCID:PMC10475059
doi:10.1038/s41598-023-41121-5
PMID:37660074
Editorial: Nutritional structures, growth and development processes, and responses to stresses in coarse cereals Li J, Fan Y Front Genet 31-Aug-2023
PMCID:PMC10501830
doi:10.3389/fgene.2023.1273932
PMID:37719699
Complete Chloroplast Genomes and Phylogenetic Relationships of Bougainvillea spectabilis and Bougainvillea glabra (Nyctaginaceae) Zhang H, Huang T, Zhou Q, Sheng Q, Zhu Z Int J Mol Sci 22-Aug-2023
PMCID:PMC10487864
doi:10.3390/ijms241713044
PMID:37685873

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Betalains / Betacyanins and derivatives
Amaranthin 6325284 Click to see C1C(NC(=CC1=CC=[N+]2C(CC3=CC(=C(C=C32)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)C(=O)[O-])C(=O)O)C(=O)O 726.60 unknown https://doi.org/10.1111/J.1745-4514.1995.TB00538.X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-phenylpropionate 7643 Click to see COC(=O)CCC1=CC=CC=C1 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4As,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 11130717 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 93233226 Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)O)C)(C)C 320.50 unknown via CMAUP database
(4aalpha)-2-Hydroxy-2beta,5,5,8abeta-tetramethyldecalin-1beta-((R)-3-methylvaleric acid) 11868539 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
Labdanolic acid 11186394 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
methyl (3S)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoate 7057547 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)OC 338.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/BF02536726
Covi-ox 6560141 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/BF02536726
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
beta-Tocotrienol 5282348 Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)O 410.60 unknown https://doi.org/10.1007/BF02536726
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledol 92812 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2-hydroxy-4,4,6a,6b,14b-pentamethyl-11-methylidene-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxane-2-carboxylic acid 163094427 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 941.10 unknown https://doi.org/10.1248/CPB.39.2609
Amaranthussaponin III 131753078 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 941.10 unknown https://doi.org/10.1248/CPB.39.2609
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Amaranthussaponin I 131753081 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 957.10 unknown https://doi.org/10.1248/CPB.39.2609
Amaranthussaponin II 131753116 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C=O)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 971.10 unknown https://doi.org/10.1248/CPB.39.2609
beta-D-Glucopyranosiduronic acid, (2beta,3beta,4alpha)-28-(beta-D-glucopyranosyloxy)-2-hydroxy-23,28-dioxoolean-12-en-3-yl 3-O-(6-deoxy-alpha-L-mannopyranosyl)- 102438527 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C=O)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 971.10 unknown https://doi.org/10.1248/CPB.39.2609
beta-D-Glucopyranosiduronic acid, (2beta,3beta)-28-(beta-D-glucopyranosyloxy)-2-hydroxy-28-oxoolean-12-en-3-yl 3-O-(6-deoxy-alpha-L-mannopyranosyl)- 102438528 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 957.10 unknown https://doi.org/10.1248/CPB.39.2609
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/S0031-9422(00)81167-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-cycloartanol 9547213 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)81167-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1002/JSFA.2740580210
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4-formyl-2-hydroxy-4,6a,6b,14b-tetramethyl-11-methylidene-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxane-2-carboxylic acid 162935175 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C=O)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 955.00 unknown https://doi.org/10.1248/CPB.39.2609
Amaranthussaponin IV 131753114 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3C(CC4(C(C3(C)C=O)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)C(=O)O)O)O)O)O 955.00 unknown https://doi.org/10.1248/CPB.39.2609
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1002/JSFA.2740580210
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
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 via CMAUP database
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 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,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(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 596.50 unknown via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown via CMAUP database
3-[(6-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)oxy]-4',5,7-trihydroxy-3'-methoxyflavone 102148697 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
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
myricetin 3-O-beta-D-glucopyranoside 5318606 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)CO)O)O)O 480.40 unknown via CMAUP database
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 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid 107 Click to see C1=CC=C(C=C1)CCC(=O)O 150.17 unknown via CMAUP database

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