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Dysphania ambrosioides

Dysphania ambrosioides - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Dysphania ambrosioides - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644018bae45ff847376590
Scientific name Dysphania ambrosioides
Authority (L.) Mosyakin & Clemants
First published in Ukrayins'k. Bot. Zhurn. 59(4): 382 (2002).

Description Top

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Synonyms Top

Scientific name Authority First published in
Orthosporum ambrosioides (L.) Kostel. Allg. Med.-Pharm. Fl. 4: 1433 (1835)
Vulvaria ambrosioides (L.) Bubani Fl. Pyren. 1: 178 (1897)
Chenopodium ambrosioides var. suffruticosum (Willd.) Graebn. Syn. Mitteleur. Fl. 5: 20 (1913)
Ambrina ambrosioides (L.) Spach Hist. Nat. Vég. 5: 297 (1836)
Ambrina ambrosioides var. anthelmintica (L.) Moldenke Phytologia 1: 274 (1938)
Ambrina anthelmintica (L.) Spach Hist. Nat. Vég. 5: 298 (1836)
Ambrina incisa (Poir.) Moq. Chenop. Monogr. Enum. : 36 (1840)
Ambrina parvula Phil. Anales Univ. Chile 91: 421 (1895)
Ambrina spathulata Moq. Chenop. Monogr. Enum. : 39 (1840)
Atriplex ambrosioides (L.) Crantz Inst. Rei Herb. 1: 207 (1766)
Atriplex anthelmintica (L.) Crantz Inst. Rei Herb. 1: 207 (1766)
Blitum ambrosioides Beck Icon. Fl. Germ. Helv. (H.G.L. Reichenbach) xxiv. 118 (1908).
Botrys ambrosioides (L.) Nieuwl. Amer. Midl. Naturalist 3: 275 (1914)
Botrys anthelmintica (L.) Nieuwl. Amer. Midl. Naturalist 3: 275 (1914)
Chenopodium album subsp. ambrosioides (L.) H.J.Coste & A.Reyn. Bull. Herb. Boissier II, 5: 979 1905
Chenopodium amboanum (Murr) Aellen Mitt. Bot. Staatssamml. München 4: 31 (1961)
Chenopodium ambrosioides L. Sp. Pl. : 219 (1753)
Chenopodium ambrosioides var. angustifolium Sieber ex Moq. Prodr. 13(2): 73 (1849)
Chenopodium ambrosioides f. angustifolium (Pav. ex Moq.) Aellen Verh. Naturf. Ges. Basel 41: 96. 1931
Chenopodium ambrosioides var. costei Aellen Acta Bot. Acad. Sci. Hung. 19: 11 (1973)
Chenopodium ambrosioides var. dentatum Fenzl Fl. Bras. 5(1): 145 (1864)
Chenopodium ambrosioides f. dentatum (Fenzl) Aellen Verh. Naturf. Ges. Basel 41: 96. 1931
Chenopodium ambrosioides var. integrifolium Fenzl Fl. Bras. 5(1): 146 (1864)
Chenopodium ambrosioides f. integrifolium (Fenzl) Aellen Amer. Midl. Naturalist 30: 52 (1943)
Chenopodium ambrosioides f. minus (Murr) Aellen Repert. Spec. Nov. Regni Veg. 26: 37. 1929
Chenopodium ambrosioides var. obovatum (Moq.) Speg. Anales Soc. Ci. Argent. 30: 52 (1943)
Chenopodium ambrosioides f. pinnatifidum (Willk.) Aellen Amer. Midl. Naturalist 30: 52 (1943)
Chenopodium ambrosioides var. pubescens Makino
Chenopodium ambrosioides var. querciforme (Murr) Aellen Repert. Spec. Nov. Regni Veg. 26: 37 (1929)
Chenopodium ambrosioides f. rotundatum Aellen Amer. Midl. Naturalist 30: 52. 1943 Without locality
Chenopodium ambrosioides f. spathulatum (Moq.) Aellen Repert. Spec. Nov. Regni Veg. 26: 35. 1929
Chenopodium ambrosioides subsp. suffruticosum (Willd.) Thell. Fl. Adv. Montpellier : 191 (1912)
Chenopodium ambrosioides var. suffruticosum (Willd.) Aellen Repert. Spec. Nov. Regni Veg. 26: 35. 1929
Chenopodium ambrosioides f. suffruticosum (Willd.) Aellen Repert. Spec. Nov. Regni Veg. 26: 35 (1929)
Chenopodium ambrosioides var. vagans (Standl.) J.T.Howell Leafl. W. Bot. 5: 105. 1948
Chenopodium angustifolium Pav. ex Moq. Prodr. 13(2): 114 (1849)
Chenopodium anthelminticum L. Sp. Pl. : 220 (1753)
Chenopodium anthelminticum var. glabratum Fenzl Fl. Bras. 5(1): 149 (1864)
Chenopodium anthelminticum var. hastatum Moq. Prodr. 13(2): 74 (1849)
Chenopodium anthelminticum var. subhirsutum Fenzl Fl. Bras. 5(1): 149 (1864)
Chenopodium citriodorum Steud. Nomencl. Bot. , ed. 2, 1: 348 (1840)
Chenopodium cuneifolium Vent. ex Moq. Prodr. 13(2): 73 (1849)
Chenopodium integrifolium Vorosch. Bot. Zhurn. S.S.S.R. 27: 42, fig. 1942
Chenopodium integrifolium subsp. ramosissimum Vorosch. Bot. Zhurn. S.S.S.R. 27: 43 1942
Chenopodium opulifolium subsp. amboanum Murr
Chenopodium querciforme Murr Magyar Bot. Lapok iii. 37.
Chenopodium querciforme var. minus Murr Magyar Bot. Lapok 3: t. 1, f. 1b (1904)
Chenopodium sancta-maria Vell. Fl. Flumin. : 126 (1829)
Chenopodium spathulatum (Moq.) Sieber ex Moq. Prodr. 13(2): 73 (1849)
Chenopodium spathulatum var. platyphyllum Moq. Prodr. 13(2): 73 (1849)
Chenopodium suffruticosum Willd. Enum. Pl. : 290 (1809)
Chenopodium suffruticosum subsp. remotum Vorosch. Bot. Zhurn. S.S.S.R. 27: 44. 1942
Chenopodium vagans Standl. N. Amer. Fl. 21(1): 26. 1916 [27 Nov 1916]
Chenopodium variegatum Gouan Cat. Hort. Taur. : ? (1810)
Dysphania anthelmintica (L.) Mosyakin & Clemants Ukrayins'k. Bot. Zhurn. 59(4): 382 (2002).
Chenopodium spathulatum var. angustifolium Moq. Prodr. 13(2): 73 1849
Atriplex ambrosioides f. minus Aellen Repert. Spec. Nov. Regni Veg. 26: 37 1929
Chenopodium ambrosioides var. comosum Willk. Prodr. Fl. Hispan. 1: 271 1861
Chenopodium ambrosioides var. pinnatifidum Willk. Prodr. Fl. Hispan. 1: 271 (1861)
Chenopodium ambrosioides var. obovata (Moq.) Speg. Anales Soc. Ci. Argent. 30: 52 (1943)
Chenopodium ambrosioides var. anthelminticum (L.) Aellen Repert. Spec. Nov. Regni Veg. 26: 35. 1929
Chenopodium santamaria Vell. Fl. Flumin. 126 1825
Orthosporum suffruticosum Kostel. Allg. Med.-Pharm. Fl. 4: 1433 (1835)
Roubieva anthelmintica Hook. & Arn. Bot. Beechey Voy. : 387 (1840)
Chenopodium integrifolium subsp. ramosissimum Worosh. ex Just Bot. Zhurn. S.S.S.R. 27: 43. 1942
Teloxys ambrosioides (L.) W.A.Weber Phytologia 58(7): 477. 1985

Common names Top

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Language Common/alternative name
English pigweed
English wormseed
English goosefoot
English lamb's quarters
English epazote
English jesuit's tea
English mexican tea
Spanish paico
Spanish epazote
Arabic أثينة عطرية
Azerbaijani ambroziyayabənzər disfaniya
Azerbaijani ambroziyaya bənzər tərə
Belarusian лебяда амброзіепадобная
Bulgarian хеноподий
Catalan te bord
Czech merlík vonný
Welsh te mecsico
German duft-drüsengänsefuß
German neobotrydium ambrosioides
German mexikanischer drüsengänsefuß
Estonian Ürt-hanemalts
Basque inurri belar
Finnish sitruunasavikka
French Épazote
gn ka'arẽ
Upper Sorbian meksikanska pólšica
ht simenkontra
Hungarian féregűző libatop
Hungarian jezsuita tea
Hungarian mirrhafű
Indonesian pasote
Japanese アリタソウ
Kannada ಕಾಡು ಓಮ
Ganda akagobadogo
Malayalam കാട്ടയമോദകം
nah epazotl
nah epazōtl
Dutch welriekende ganzenvoet
nv tséʼázhííh
Polish komosa piżmowa
Quechua payqu
Kinyarwanda kavunjahomo
Slovak mrlík voňavý
Slovenian dišeča metlika
Swedish dieselmålla
Tamil புழுக்கொல்லி
Thai เอซาโปเต
Vietnamese dầu giun
Walloon fåsse ambrôze
Chinese 臭杏
Chinese 土荊芥
Chinese 土荆芥*
Chinese 土荆芥

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000658867
UNII 4H5RSU087I
Florida Plant Atlas 1769
Flora of Alabama 1505
Canadensys 4546
USDA Plants DYAM
Tropicos 50215991
INPN 611753
Flora of Italy 455
KEW urn:lsid:ipni.org:names:1198060-2
The Plant List kew-2780223
Plantarium 10151
Open Tree Of Life 36264
NCBI Taxonomy 330163
IPNI 70029925-1
iNaturalist 76746
GBIF 5568446
Freebase /m/059zr0
WisFlora 7253
EPPO CHEAM
EOL 587524
Elurikkus 546048
Calflora (Californian flora) 10846
USDA GRIN 446530
Wikipedia Dysphania_ambrosioides

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_026401315.1 BYU_DyAmbr Chromosome Brigham Young University 2022-11-27 50.0x 447.06 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
Fabrication and characterization of gold nanoparticles using alginate: In vitro and in vivo assessment of its administration effects with swimming exercise on diabetic rats Hashemzadeh V, Hashemzadeh A, Mohebbati R, Arefi RG, Yazdi ME Open Life Sci 17-Apr-2024
PMCID:PMC11032099
doi:10.1515/biol-2022-0869
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
Molecular modelling and anticholinesterase activity of the essential oil from three chemotypes of Lippia alba (Mill.) N.E.Br. ex Britton & P. Wilson (Verbenaceae) Silva Júnior AQ, Rodrigues GD, Alcântara de Sousa K, Maduro Bouillet LE, Bianchi dos Santos G, de Sousa Barroso A, Veras Mourão RH Heliyon 03-Apr-2024
PMCID:PMC11031784
doi:10.1016/j.heliyon.2024.e29063
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
PMCID:PMC11000104
doi:10.1016/j.sjbs.2024.103983
PMID:38590389
Variation in traditional knowledge of culturally important macromycete species among three indigenous communities of Oaxaca, Mexico López-García A, Gómez-Hernández M, Gándara E J Ethnobiol Ethnomed 22-Mar-2024
PMCID:PMC10958891
doi:10.1186/s13002-024-00679-8
PMID:38519986
Analysis of Primary and Secondary Metabolites, Physical Properties, Antioxidant and Antidiabetic Activities, and Chemical Composition of Rosmarinus officinalis Essential Oils under Differential Water Stress Conditions Laftouhi A, Mahraz MA, Hmamou A, Assouguem A, Ullah R, Bari A, Lahlali R, Ercisli S, Kaur S, Idrissi AM, Eloutassi N, Rais Z, Taleb A, Taleb M ACS Omega 22-Mar-2024
PMCID:PMC11007863
doi:10.1021/acsomega.4c00653
PMID:38617605
Potential Interest of Oxalis pes-caprae L., a Wild Edible Plant, for the Food and Pharmaceutical Industries Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA Foods 12-Mar-2024
PMCID:PMC10969124
doi:10.3390/foods13060858
PMID:38540848
Chenopodium Ambrosioides Linn Mitigates Bone Loss in Rats with Periodontitis Carneiro DT, da Silva MD, Vasconcelos KV, Dias R, Costa V, Vasconcelos RF, Carneiro B, Barreto G, Marques M, Vasconcelos HC, Ribeiro Júnior HL, Gusmão JN, da Silveira H, Leitão R, Brito GA, Pereira KM, Gondim DV, Goes P J Dent (Shiraz) 01-Mar-2024
PMCID:PMC10963862
doi:10.30476/dentjods.2023.95767.1891
PMID:38544779
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
Synergistic interactions of assorted ameliorating agents to enhance the potential of heavy metal phytoremediation Sanjana S, Jazeel K, Janeeshma E, Nair SG, Shackira AM Stress Biol 16-Feb-2024
PMCID:PMC10873264
doi:10.1007/s44154-024-00153-1
PMID:38363436
Citrus limon Essential Oil: Chemical Composition and Selected Biological Properties Focusing on the Antimicrobial (In Vitro, In Situ), Antibiofilm, Insecticidal Activity and Preservative Effect against Salmonella enterica Inoculated in Carrot Kačániová M, Čmiková N, Vukovic NL, Verešová A, Bianchi A, Garzoli S, Ben Saad R, Ben Hsouna A, Ban Z, Vukic MD Plants (Basel) 15-Feb-2024
PMCID:PMC10893099
doi:10.3390/plants13040524
PMID:38498554
Chemical Profiling, Insecticidal, and Phytotoxic Effect of Essential Oils from Leaves and Inflorescence of Moroccan Chenopodium ambrosioides (L.) Kasrati A, Sakar EH, Aljaiyash A, Hirri A, Tamegart L, Abbad I, Alaoui Jamali C Plants (Basel) 08-Feb-2024
PMCID:PMC10893179
doi:10.3390/plants13040483
PMID:38498455
Haitian women in New York City use global food plants for women’s health Vardeman ET, Kennelly EJ, Vandebroek I J Ethnobiol Ethnomed 12-Jan-2024
PMCID:PMC10785501
doi:10.1186/s13002-024-00648-1
PMID:38217006
Generation of PVP Membranes Using Extracts/Phenolic Fraction of Dysphania ambrosioides, Opuntia ficus-indica, and Tradescantia pallida Zaca Moran O, García Suastegui WA, Cruz San Juan JH, López Méndez LC, López Gayou V Polymers (Basel) 15-Dec-2023
PMCID:PMC10747495
doi:10.3390/polym15244720
PMID:38139971

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1300/J044V07N02_02
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/NP990376U
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,1'S,5R,5'S,9S)-6',6',10,10-tetramethylspiro[6-oxatricyclo[7.1.1.02,7]undec-2(7)-ene-5,2'-bicyclo[3.1.1]heptane]-3'-one 163009492 Click to see CC1(C2CC1C3=C(C2)OC4(CC3)C5CC(C5(C)C)CC4=O)C 300.40 unknown https://doi.org/10.1248/YAKUSHI1947.75.9_1036
6',6',10,10-Tetramethylspiro[6-oxatricyclo[7.1.1.02,7]undec-2(7)-ene-5,2'-bicyclo[3.1.1]heptane]-3'-one 5320137 Click to see CC1(C2CC1C3=C(C2)OC4(CC3)C5CC(C5(C)C)CC4=O)C 300.40 unknown https://doi.org/10.1248/YAKUSHI1947.75.9_1036
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see CC(C)C1=CC(C(CC1)(C)O)O 170.25 unknown https://doi.org/10.1021/NP990376U
(1R,2S,3S,4S)-1-methyl-4-propan-2-ylcyclohexane-1,2,3,4-tetrol 102007446 Click to see CC(C)C1(CCC(C(C1O)O)(C)O)O 204.26 unknown https://doi.org/10.1021/NP990376U
(1r,2s)-3-p-Menthen-1,2-diol 14262891 Click to see CC(C)C1=CC(C(CC1)(C)O)O 170.25 unknown https://doi.org/10.1021/NP990376U
(1S,2R,3R,4R)-1-methyl-4-propan-2-ylcyclohexane-1,2,3,4-tetrol 10512390 Click to see CC(C)C1(CCC(C(C1O)O)(C)O)O 204.26 unknown https://doi.org/10.1021/NP990376U
(2S,4R)-p-Mentha-[1(7),8]-diene 2-hydroperoxide 564367 Click to see CC(=C)C1CCC(=C)C(C1)OO 168.23 unknown https://doi.org/10.1021/NP010445G
(2S,4S)-2-hydroperoxy-1-methylidene-4-prop-1-en-2-ylcyclohexane 636730 Click to see CC(=C)C1CCC(=C)C(C1)OO 168.23 unknown https://doi.org/10.1021/NP010445G
(3R,6S)-3-hydroperoxy-3-methyl-6-prop-1-en-2-ylcyclohexene 10419566 Click to see CC(=C)C1CCC(C=C1)(C)OO 168.23 unknown https://doi.org/10.1021/NP010445G
(3S,6R)-3-Hydroperoxy-3-methyl-6-(prop-1-en-2-yl)cyclohex-1-ene 538497 Click to see CC(=C)C1CCC(C=C1)(C)OO 168.23 unknown https://doi.org/10.1021/NP010445G
(3S,6S)-3-hydroperoxy-3-methyl-6-prop-1-en-2-ylcyclohexene 10329704 Click to see CC(=C)C1CCC(C=C1)(C)OO 168.23 unknown https://doi.org/10.1021/NP010445G
(E)-p-mentha-1(7),8-dien-2-hydroperoxide 10103548 Click to see CC(=C)C1CCC(=C)C(C1)OO 168.23 unknown https://doi.org/10.1021/NP010445G
1-Methyl-4-propan-2-ylcyclohexane-1,2,3,4-tetrol 74402683 Click to see CC(C)C1(CCC(C(C1O)O)(C)O)O 204.26 unknown https://doi.org/10.1021/NP990376U
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1300/J044V07N02_02
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1300/J044V07N02_02
p-Mentha-3-en-1,2-diol 14262890 Click to see CC(C)C1=CC(C(CC1)(C)O)O 170.25 unknown https://doi.org/10.1021/NP990376U
trans-Ascaridolglycol 6429171 Click to see CC(C)C1(CCC(C=C1)(C)O)O 170.25 unknown https://doi.org/10.1021/NP990376U
trans-p-Menth-2-ene-1,4-diol 300085 Click to see CC(C)C1(CCC(C=C1)(C)O)O 170.25 unknown https://doi.org/10.1021/NP990376U
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
1-(4-Methylcyclohex-2-en-1-yl)ethanone 20716808 Click to see CC1CCC(C=C1)C(=O)C 138.21 unknown https://doi.org/10.1039/CT9252701649
1-[(1R,4R)-4-methylcyclohex-2-en-1-yl]ethanone 131107899 Click to see CC1CCC(C=C1)C(=O)C 138.21 unknown https://doi.org/10.1039/CT9252701649
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(2S)-2-(2-oxopropyl)-3-propan-2-yl-2H-furan-5-one 162990180 Click to see CC(C)C1=CC(=O)OC1CC(=O)C 182.22 unknown https://doi.org/10.1021/NP990376U
2-(2-oxopropyl)-3-propan-2-yl-2H-furan-5-one 10559336 Click to see CC(C)C1=CC(=O)OC1CC(=O)C 182.22 unknown https://doi.org/10.1021/NP990376U
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
Ascaridole 10545 Click to see CC(C)C12CCC(C=C1)(OO2)C 168.23 unknown https://doi.org/10.1016/0305-1978(93)90068-3
https://doi.org/10.1300/J044V07N02_02
https://doi.org/10.1021/NP010445G
https://doi.org/10.1248/CPB.41.1309
> Organoheterocyclic compounds / Oxepanes
Isoascaridole 12314661 Click to see CC(C)C12CCC3(C(C1O2)O3)C 168.23 unknown https://doi.org/10.1300/J044V07N02_02
> 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 https://doi.org/10.1016/0031-9422(90)85389-W
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 https://doi.org/10.1016/0031-9422(90)85389-W
https://doi.org/10.1080/01811797.1985.10824657
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/10.1080/01811797.1985.10824657
https://doi.org/10.1016/0031-9422(90)85389-W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one 162919094 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)OC5C(C(C(CO5)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(90)85389-W
5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[4-[(2S,3S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one 162919093 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)OC5C(C(C(CO5)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(90)85389-W
Kaempferol 3-rhamnoside 4'-xyloside 74978072 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)OC5C(C(C(CO5)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(90)85389-W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 162993875 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(90)85389-W
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 154496822 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(90)85389-W
7-[(3R,4R,5R,6S)-3-[(3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxy-5,6-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162817386 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4=C(C(=C5C(=O)CC(OC5=C4)C6=CC=C(C=C6)O)O)O)C)O)O)C)O)O)O)O)O 726.70 unknown https://doi.org/10.1055/S-0034-1382488
7-[(3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162817384 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)O)C)O)O)O)O)O 580.50 unknown https://doi.org/10.1055/S-0034-1382488
Kaempferol 3-rhamnoside 7-xyloside 14334866 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(CO4)O)O)O)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(90)85389-W

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