Rumex patientia - Unknown
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Internal ID UUID643ff8bbd8b7b105774533
Scientific name Rumex patientia
Authority L.
First published in Sp. Pl. : 333 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lapathum hortense Garsault Fig. Pl. Med. 3: t. 321. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 199. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 791.
Acetosa patientia (L.) M.Gómez Anales Inst. Segunda Enseñ. 2: 277 (1896)
Rumex callosus (F.Schmidt) Rech.f. Repert. Spec. Nov. Regni Veg. 31: 257 (1933)
Rumex patientia subsp. callosus (F.Schmidt ex Maxim.) Rech.f.
Rumex patientia subsp. pamiricus (Rech.f.) Rech.f. Candollea 12: 73–74 1949
Rumex patientia var. callosus F.Schmidt ex Maxim. Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 228 1859
Lapathum hortense Lam. Fl. Franç. 3: 2 (1779)
Rumex patientia subsp. tibeticus (Rech.f.) Rech.f. Candollea 12: 74 1949
Rumex patientia subsp. interruptus Rech.f. Candollea 12: 74–75 1949
Rumex interruptus Rech.f. Repert. Spec. Nov. Regni Veg. 33: 359 (1934)
Rumex patientia var. tibeticus Rech.f. Repert. Spec. Nov. Regni Veg. 31: 262 1933
Rumex tibeticus Rech.f. Repert. Spec. Nov. Regni Veg. 31: 262 (1933)

Common names Top

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Language Common/alternative name
English patience dock
Spanish rumex lonaczevskii
Spanish rumex interruptus
Spanish lapathum hortense
Spanish rumex callosus
Arabic حماض كبير
Bulgarian спанаков лапад
Czech šťovík zahradní
Welsh tafolen oddefus
German gemüse-ampfer
Estonian spinatoblikas
Persian ترشک شفادهنده
Finnish pinaattihierakka
Upper Sorbian zahrodny zdźer
ht lòzèy
Norwegian Bokmål hagesyre
Dutch spinaziezuring
Romanian Ștevie
Serbian Зеље
Swedish spenatskräppa
Chinese 西藏酸模
Chinese 牛西西叶
Chinese 牛西西
Chinese 巴天酸模
Chinese 酸模叶
Chinese 酸模
Chinese 皱叶酸模

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Rumex patientia subsp. orientalis (Bernh. ex Schult. & Schult.f.) Danser Ned. Kruidk. Arch. 1923: 281 1924
Rumex patientia subsp. recurvatus (Rech.) Rech.f. Repert. Spec. Nov. Regni Veg. 31: 252 1933

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
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Kamchatka
      • Khabarovsk
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Irkutsk
      • West Siberia
    • Western Asia
      • Afghanistan
      • Cyprus
      • Iran
      • Lebanon-Syria
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Nepal
      • Pakistan
      • West Himalaya
    • Malesia
      • Malaya
  • Europe
    • Eastern Europe
      • Central European Russia
      • Krym
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
  • Northern America
    • Eastern Canada
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southeastern U.S.A.
      • Kentucky
      • Maryland
      • North Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Utah
  • Southern America
    • Caribbean
      • Dominican Republic
      • Haiti
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000403926
Florida Plant Atlas 1978
Canadensys 8218
USDA Plants RUPA5
Tropicos 26000928
INPN 119558
KEW urn:lsid:ipni.org:names:697388-1
The Plant List kew-2424661
Plantarium 32816
Open Tree Of Life 213388
Observations.org 7377
NCBI Taxonomy 137229
NBN Atlas NBNSYS0000003786
Nature Serve 2.135906
IPNI 697388-1
iNaturalist 168248
GBIF 2889019
Freebase /m/04cs4fd
WisFlora 4923
EPPO RUMPA
EOL 585272
Elurikkus 6974
USDA GRIN 32544
Wikipedia Rumex_patientia
CMAUP NPO13107

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
A dataset for fine-grained seed recognition Yuan M, Lv N, Dong Y, Hu X, Lu F, Zhan K, Shen J, Wu X, Zhu L, Xie Y Sci Data 06-Apr-2024
PMCID:PMC10998916
doi:10.1038/s41597-024-03176-5
PMID:38582756
Cross-cultural ethnobotany of the Baltis and Shinas in the Kharmang district, Trans-Himalaya India-Pakistan border Hussain B, Abbas Z, Alam J, Harun N, Khan SM, Ahmad Z, Han H, Yoo S, Raposo A Heliyon 27-Mar-2024
PMCID:PMC10998220
doi:10.1016/j.heliyon.2024.e28613
PMID:38586350
Harmony in nature: understanding the cultural and ecological aspects of plant use in Ladakh Angmo K, Adhikari BS, Bussmann RW, Rawat GS J Ethnobiol Ethnomed 14-Mar-2024
PMCID:PMC10938689
doi:10.1186/s13002-024-00670-3
PMID:38486266
Impact of Environmental Food Intake on the Gut Microbiota of Endangered Père David’s Deer: Primary Evidence for Population Reintroduction Mo Q, Yao H, Wu H, Zhao D Animals (Basel) 27-Feb-2024
PMCID:PMC10931168
doi:10.3390/ani14050728
PMID:38473113
Modern and traditional cooking methods affect the antioxidant activity and phenolic compounds content of Trachystemon Orientalis (L.) G. Don Demirel Ozbek Y, Saral O, Turker PF PLoS One 23-Feb-2024
PMCID:PMC10890727
doi:10.1371/journal.pone.0299037
PMID:38394328
Studies on the Changes of Fermentation Metabolites and the Protective Effect of Fermented Edible Grass on Stress Injury Induced by Acetaminophen in HepG2 Cells He T, Li X, Wang Z, Mao J, Mao Y, Sha R Foods 02-Feb-2024
PMCID:PMC10855311
doi:10.3390/foods13030470
PMID:38338605
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Nutritional composition of some wild edible plants consumed in Southwest Ethiopia Yimer A, Forsido SF, Addis G, Ayelign A Heliyon 23-May-2023
PMCID:PMC10220415
doi:10.1016/j.heliyon.2023.e16541
PMID:37251480
Review on melanosis coli and anthraquinone-containing traditional Chinese herbs that cause melanosis coli Zhang R, Huang C, Wu F, Fang K, Jiang S, Zhao Y, Chen G, Dong R Front Pharmacol 04-May-2023
PMCID:PMC10193150
doi:10.3389/fphar.2023.1160480
PMID:37214441
Critical review on Rumex dentatus L. a strong pharmacophore and the future medicine: Pharmacology, phytochemical analysis and traditional uses Khaliq T, Akhter S, Sultan P, Hassan QP Heliyon 05-Mar-2023
PMCID:PMC10040524
doi:10.1016/j.heliyon.2023.e14159
PMID:36994390
Small regions as key sources of traditional knowledge: a quantitative ethnobotanical survey in the central Balkans Janaćković P, Gavrilović M, Miletić M, Radulović M, Kolašinac S, Stevanović ZD J Ethnobiol Ethnomed 05-Dec-2022
PMCID:PMC9720931
doi:10.1186/s13002-022-00566-0
PMID:36471323
Biodiversity and Spatiotemporal Distribution of Spontaneous Vegetation in Tangdao Bay National Wetland Park, Qingdao City, China Xu Y, Zhang X, Liu X, Zhang Z Int J Environ Res Public Health 16-Sep-2022
PMCID:PMC9517414
doi:10.3390/ijerph191811665
PMID:36141939
New seco-anthraquinone glucoside from the roots of Rumex crispus Li YX, Li N, Li JJ, Zhang M, Zhu HT, Wang D, Zhang YJ Nat Prod Bioprospect 03-Aug-2022
PMCID:PMC9346041
doi:10.1007/s13659-022-00350-3
PMID:35918556
Agrimonia pilosa Ledeb.: A review of its traditional uses, botany, phytochemistry, pharmacology, and toxicology Wen S, Zhang X, Wu Y, Yu S, Zhang W, Liu D, Yang K, Sun J Heliyon 21-Jul-2022
PMCID:PMC9421327
doi:10.1016/j.heliyon.2022.e09972
PMID:36046524
A De Novo Transcriptome Analysis Identifies Cold-Responsive Genes in the Seeds of Taxillus chinensis (DC.) Danser Fu J, Wan L, Song L, He L, Jiang N, Long H, Huo J, Ji X, Hu F, Wei S, Pan L Biomed Res Int 06-Jul-2022
PMCID:PMC9279050
doi:10.1155/2022/9247169
PMID:35845948

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 / Anthracenes
Patientoside B 71681569 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)O)C=C(C=C3O)OC 448.40 unknown https://doi.org/10.1021/NP000549B
> Benzenoids / Anthracenes / Anthraquinones
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione 24867638 Click to see CC1=CC2C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 256.25 unknown via CMAUP database
Aloe emodin 10207 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 270.24 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Chrysophanol 8-(6-O-galloyl-beta-D-glucopyranoside) 5315852 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 568.50 unknown via CMAUP database
CID 4483734 4483734 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Clicoemodin 636641 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Emodin 6-O-|A-D-glucoside 5317038 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Glucoemodin 22297291 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Emodin(1-) 25201450 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3[O-])O 269.23 unknown via CMAUP database
Glucofrangulin 318730 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Questin 160717 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC)O 284.26 unknown via CMAUP database
Questin-2-olate 25203706 Click to see CC1=CC2=C(C(=C1)[O-])C(=O)C3=C(C2=O)C=C(C=C3OC)O 283.25 unknown via CMAUP database
Questinol 147621 Click to see COC1=CC(=CC2=C1C(=O)C3=C(C2=O)C=C(C=C3O)CO)O 300.26 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
Nepodin 100780 Click to see CC1=CC2=C(C(=CC=C2)O)C(=C1C(=O)C)O 216.23 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Orcinol 10436 Click to see CC1=CC(=CC(=C1)O)O 124.14 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
> Lignans, neolignans and related compounds / Lignan glycosides
1-[4-[3-Acetyl-4-hydroxy-2-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-1-yl]-1-hydroxy-3-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 163042090 Click to see CC1=C(C2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1C(=O)C)O)C4=C(C(=C(C5=C4C=CC=C5OC6C(C(C(C(O6)CO)O)O)O)O)C(=O)C)C 754.70 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
Labadoside 101093581 Click to see CC1=C(C2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1C(=O)C)O)C4=C(C(=C(C5=C4C=CC=C5OC6C(C(C(C(O6)CO)O)O)O)O)C(=O)C)C 754.70 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
11-Hydroxysclerosporin 45380213 Click to see CC1=CC2C(CC1)C(=CCC2C(C)(C)O)C(=O)O 250.33 unknown via CMAUP database
15-Hydroxysclerosporin 45380211 Click to see CC(C)C1CC=C(C2C1C=C(CC2)CO)C(=O)O 250.33 unknown via CMAUP database
8-Hydroxysclerosporin 45380214 Click to see CC1=CC2C(CC1)C(=CC(C2C(C)C)O)C(=O)O 250.33 unknown via CMAUP database
Sclerosporin 442392 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C(=O)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Illudanes and illudins / Melleolides and analogues
Armillaridin 51351607 Click to see CC1=C(C(=CC(=C1Cl)OC)O)C(=O)OC2CC3(C2(C(=CC4C3CC(C4)(C)C)C=O)O)C 448.90 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(5,7-dichloro-8-hydroxy-6-methylnaphthalen-1-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10894753 Click to see CC1=C(C2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1Cl)O)Cl 405.20 unknown https://doi.org/10.1021/NP000549B
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 5319972 Click to see CC1=CC2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1C(=O)C)O 378.40 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
1-[4-chloro-1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 10993336 Click to see CC1=C(C(=C2C(=C1Cl)C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)C 412.80 unknown https://doi.org/10.1021/NP000549B
1-[4-Chloro-1-hydroxy-3-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 85359141 Click to see CC1=C(C(=C2C(=C1Cl)C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)C 412.80 unknown https://doi.org/10.1021/NP000549B
1-[5-[6-acetyl-5-hydroxy-7-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-1-yl]-1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 162921574 Click to see CC1=CC2=C(C=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)C4=C5C=C(C(=C(C5=C(C=C4)OC6C(C(C(C(O6)CO)O)O)O)O)C(=O)C)C 754.70 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
1-[5-[6-Acetyl-5-hydroxy-7-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-1-yl]-1-hydroxy-3-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 162921573 Click to see CC1=CC2=C(C=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)C4=C5C=C(C(=C(C5=C(C=C4)OC6C(C(C(C(O6)CO)O)O)O)O)C(=O)C)C 754.70 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
1-[8-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-3-methylnaphthalen-2-yl]ethanone 101093582 Click to see CC1=CC2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=C1C(=O)C)O 540.50 unknown via CMAUP database
1-[8-[(2S,3S,4R,5R,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-3-methylnaphthalen-2-yl]ethanone 163191144 Click to see CC1=CC2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=C1C(=O)C)O 540.50 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
2-(5,7-Dichloro-8-hydroxy-6-methylnaphthalen-1-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 85305855 Click to see CC1=C(C2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1Cl)O)Cl 405.20 unknown https://doi.org/10.1021/NP000549B
6-acetyl-4-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-7-methylnaphthalene-2-carboxylic acid 163045467 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)O 584.50 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
6-Acetyl-4-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-7-methylnaphthalene-2-carboxylic acid 163045466 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)O 584.50 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
6-acetyl-5-hydroxy-7-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalene-2-carboxylic acid 637097 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
Orientaloside 131752151 Click to see CC1=CC2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=C1C(=O)C)O 540.50 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
Rumexoside 20979907 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
Torachrysone 8-glucoside 14345578 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC 408.40 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
Torachrysone 8-O-Glucoside 11972479 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC 408.40 unknown https://doi.org/10.1016/S0031-9422(00)00368-X
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Tocris-1610 6603986 Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C=CC4=CC=CC=C4)O)O 516.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
6-Chloro-2-(3,4-dihydroxy-phenyl)-chroman-3,5,7-triol 636642 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)Cl)O)C3=CC(=C(C=C3)O)O)O 324.71 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
6-Chlorocatechin 22297292 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)Cl)O)C3=CC(=C(C=C3)O)O)O 324.71 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(01)00337-5
> 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)85309-4
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)85309-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 https://doi.org/10.1016/0031-9422(90)85309-4
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see CC1CC2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1016/S0031-9422(01)00337-5

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