Persicaria orientalis - Unknown
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Details Top

Internal ID UUID644003104b66b358083129
Scientific name Persicaria orientalis
Authority (L.) Spach
First published in Hist. Nat. Vég. 10: 537 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lagunea cochinchinensis Lour. Fl. Cochinch. : 220 (1790)
Lagunea orientalis (L.) Nakai J. Jap. Bot. 18: 112 (1942)
Polygonum amoenum Blume Bijdr. Fl. Ned. Ind. : 532 (1826)
Persicaria cochinchinensis (Lour.) Kitag. Rep. Inst. Sci. Res. Manchoukuo 3: 102 (1939)
Persicaria pilosa (Roxb.) Kitag. Neolin. Fl. Manshur. 237. 1979
Polygonum torquatum De Bruyn Pl. Jungh. : 303 (1854)
Polygonum pilosum Wall. Numer. List [Wallich] n. 1710. 1829
Polygonum cochinchinense Meisn. Monogr. Polyg. : 55 (1826)
Polygonum orientale L. Sp. Pl. : 362 (1753)
Amblygonum orientale var. pilosum (Roxb. ex Meisn.) Nakai Enum. Pl. Corea 129 1922
Amblygonum orientale Nakai Enum. Pl. Corea : 129 (1922)
Amblygonum pilosum Nakai Rigakkwai xxiv. 297 (1926); cf. Kitagawa in Rep. Inst. Sc. ResearchManchoukuo, iii. App. 1, 177 (1939), in syn.
Goniaticum solitarium Stokes Bot. Mat. Med. 2: 338 (1812)
Heptarina orientalis Raf. Fl. Tellur. 3: 15 (1837)
Polygonum orientale var. pilosum (Roxb. ex Meisn.) Meisn. Prodr. 14: 123 1856
Polygonum orientale var. discolor Benth. London J. Bot. 1: 494 1842
Polygonum cordobense Lindau Beibl. Bot. Jahrb. Syst. 48: 10 (1894)
Polygonum pilosum Roxb. Numer. List : n.º 1710 (1829)
Lagunea orientalis var. pilosa (Roxb. ex Meisn.) Nakai
Polygonum torquatum De Bruyn Pl. Jungh. : 303 (1854)

Common names Top

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Language Common/alternative name
Czech rdesno východní
German orient-knöterich
Upper Sorbian zahrodna wuroć
Hungarian pulykaorrú keserűfű
Japanese オオケタデ
Korean 노인장대
Korean 털여뀌
Swedish purpurpilört
Chinese 红蓼
Chinese 紅草
Chinese 紅蓼
Chinese 东方蓼

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
5% germination; very well drained soil

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
      • Hainan
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
    • Western Asia
      • Iraq
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
    • Papuasia
      • New Guinea
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • South Australia
      • Victoria
      • Western Australia
  • Europe
    • Eastern Europe
      • Central European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
    • Northern Europe
      • Finland
      • Great Britain
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Yugoslavia
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • Oklahoma
      • 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.
      • Oregon
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • California
  • Southern America
    • Brazil
      • Brazil South
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Chile Central
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000488434
UNII V5IV1KT5WS
Florida Plant Atlas 1963
Flora of Alabama 2934
Canadensys 8152
Tropicos 26001791
INPN 112750
Flora of Italy 378
KEW urn:lsid:ipni.org:names:60455314-2
The Plant List kew-2572578
Open Tree Of Life 19860
Observations.org 206267
NCBI Taxonomy 467334
Nature Serve 2.137974
IPNI 60455314-2
iNaturalist 78454
iNaturalist 167252
GBIF 2889229
Freebase /m/0nbgb7h
WisFlora 4586
WisFlora 13196
EPPO POLOR
EOL 585378
Elurikkus 325178
Calflora (Californian flora) 11012
USDA GRIN 409766
Wikipedia Persicaria_orientalis
CMAUP NPO25716

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
The genus Polygonum: An updated comprehensive review of its ethnomedicinal, phytochemical, pharmacological activities, toxicology, and phytopharmaceutical formulation Idoudi S, Tourrette A, Bouajila J, Romdhane M, Elfalleh W Heliyon 06-Apr-2024
PMCID:PMC11024578
doi:10.1016/j.heliyon.2024.e28947
PMID:38638945
Tetraethylenepentamine-Grafted Amino Terephthalic Acid-Modified Activated Carbon as a Novel Adsorbent for Efficient Removal of Toxic Pb(II) from Water Alshammari MS Molecules 02-Apr-2024
PMCID:PMC11013411
doi:10.3390/molecules29071586
PMID:38611865
Soil Nitrogen and Flooding Intensity Determine the Trade-Off between Leaf and Root Traits of Riparian Plant Species Zou H, Wang W, Huang J, Li X, Ma M, Wu S, Zhao C Plants (Basel) 29-Mar-2024
PMCID:PMC11013260
doi:10.3390/plants13070978
PMID:38611507
From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach Ahmed SS, Rahman MO PLoS One 29-Mar-2024
PMCID:PMC10980240
doi:10.1371/journal.pone.0301348
PMID:38551991
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
Natural Extracts and Their Applications in Polymer-Based Active Packaging: A Review Li J, Sun H, Weng Y Polymers (Basel) 25-Feb-2024
PMCID:PMC10933866
doi:10.3390/polym16050625
PMID:38475309
Antibacterial Activity of Dihydroquercetin Separated from Fructus Polygoni orientalis against Clavibacter michiganensis subsp. sepedonicus via Damaging Cell Membrane Cai J, Wang S, Wang Q Foods 20-Dec-2023
PMCID:PMC10778462
doi:10.3390/foods13010023
PMID:38201051
Effects of Datura stramonium L. Invasion into Different Habitats on Native Plant Functional Traits and Soil Carbon, Nitrogen and Phosphorus Stoichiometric Characteristics Lv J, Wang H, Chang N, Li H, Shi C Biology (Basel) 06-Dec-2023
PMCID:PMC10740971
doi:10.3390/biology12121497
PMID:38132323
Quercetin as a Therapeutic Product: Evaluation of Its Pharmacological Action and Clinical Applications—A Review Mirza MA, Mahmood S, Hilles AR, Ali A, Khan MZ, Zaidi SA, Iqbal Z, Ge Y Pharmaceuticals (Basel) 20-Nov-2023
PMCID:PMC10674654
doi:10.3390/ph16111631
PMID:38004496
Astragalin: a food-origin flavonoid with therapeutic effect for multiple diseases Chen J, Zhong K, Qin S, Jing Y, Liu S, Li D, Peng C Front Pharmacol 18-Oct-2023
PMCID:PMC10619670
doi:10.3389/fphar.2023.1265960
PMID:37920216
Mechanistic prospective and pharmacological attributes of quercetin in attenuation of different types of arthritis Bhoi A, Dwivedi SD, Singh D, Keshavkant S, Singh MR 3 Biotech 12-Oct-2023
PMCID:PMC10570262
doi:10.1007/s13205-023-03787-6
PMID:37840879
Investigation of the Mechanism of Action of Periploca forrestii Schltr. Extract on Adjuvant Collagen Rats Based on UPLC-Q-Orbitrap-HRMS Non-Targeted Lipidomics An S, Yan X, Chen H, Zhou X Molecules 22-Sep-2023
PMCID:PMC10574421
doi:10.3390/molecules28196751
PMID:37836594
Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review Tung XY, Yip JQ, Gew LT ACS Omega 06-Sep-2023
PMCID:PMC10515176
doi:10.1021/acsomega.3c02994
PMID:37744793
An ethnobotanical survey on phytomedicines based on traditional knowledge in the Barpeta district, Assam, India Bhattacharjya DK, Akhtar J, Deka P, Bharadwaj A J Ayurveda Integr Med 19-Jul-2023
PMCID:PMC10371788
doi:10.1016/j.jaim.2023.100763
PMID:37478633
Impact of Traditional Chinese Medicine on Prognosis of Patients with Hepatocellular Carcinoma: A Retrospective Cohort Study Yuan H, Niu Q, Shang X, Zhang L, Li L, Yang H, Gou C, Li J, Li H, Li X Integr Cancer Ther 03-Jul-2023
PMCID:PMC10328175
doi:10.1177/15347354231170536
PMID:37395564

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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones
Plastoquinone-1 10219885 Click to see CC1=C(C(=O)C(=CC1=O)CC=C(C)C)C 204.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxychromone 5281343 Click to see C1=COC2=CC(=CC(=C2C1=O)O)O 178.14 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+] 204.22 unknown via CMAUP database
D-Tryptophan 9060 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives
1-(6,8-Dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbutane-2,3-diol 5320308 Click to see CC(C)(C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O)O 335.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
n-cis-Feruloyltyramine 6440659 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isooxypeucedanin 625383 Click to see CC(C)C(=O)COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin 73160 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
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 via CMAUP database
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
(-)-Taxifolin 712316 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
(2r)-2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydro-4h-chromen-4-one 10185 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.4268/CJCMM20101316
(3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydro-4H-chromen-4-one 12309272 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 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 https://doi.org/10.1007/BF00564011
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
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 C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257906 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257907 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 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,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 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 https://doi.org/10.1007/BF00564011
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 40486293 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 448.40 unknown https://doi.org/10.1248/CPB.30.1163
Kaempferol 3-(2'',3''-di-(E)-p-coumaroylrhamnoside) 44258960 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O 724.70 unknown via CMAUP database
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 via CMAUP database
Quercetin 3-O-rhamnoside 5353915 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 448.40 unknown https://doi.org/10.1248/CPB.30.1163
Quercitrin 5280459 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 448.40 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/10.1007/BF00564011
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 https://doi.org/10.1016/J.JCHROMB.2014.02.055
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3,5,5',6,7,8-Hexamethoxy-3',4'-methylenedioxyflavone 15511896 Click to see COC1=CC(=CC2=C1OCO2)C3=C(C(=O)C4=C(O3)C(=C(C(=C4OC)OC)OC)OC)OC 446.40 unknown https://doi.org/10.1248/CPB.30.1163
3,5,8,3'-Tetramethoxy-6,7:4',5'-bis(methylenedioxy)flavone 44260080 Click to see COC1=CC(=CC2=C1OCO2)C3=C(C(=O)C4=C(O3)C(=C5C(=C4OC)OCO5)OC)OC 430.40 unknown https://doi.org/10.1248/CPB.30.1163
3,5,8,3',4',5'-Hexamethoxy-6,7-methylenedioxyflavone 141484234 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(O2)C(=C4C(=C3OC)OCO4)OC)OC 446.40 unknown https://doi.org/10.1248/CPB.30.1163
3'-Hydroxy-3,5,6,7,8,4',5'-heptamethoxyflavone 13983767 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC 448.40 unknown https://doi.org/10.1248/CPB.30.1163
3'-Hydroxy-3,5,8,4',5'-pentamethoxy-6,7-methylenedioxyflavone 44260079 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(O2)C(=C4C(=C3OC)OCO4)OC)OC 432.40 unknown https://doi.org/10.1248/CPB.30.1163
5-Hydroxy-3,6,7,8,3'-pentamethoxy-4',5'-methylenedioxyflavone 154804640 Click to see COC1=CC(=CC2=C1OCO2)C3=C(C(=O)C4=C(C(=C(C(=C4O3)OC)OC)OC)O)OC 432.40 unknown https://doi.org/10.1248/CPB.30.1163
5,3'-Dihydroxy-3,8,4',5'-tetramethoxy-6,7-methylenedioxyflavone 44260078 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C4=C(C(=C3O2)OC)OCO4)O)OC 418.30 unknown https://doi.org/10.1248/CPB.30.1163
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown https://doi.org/10.1248/CPB.30.1163
Exoticin 389000 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC 462.40 unknown https://doi.org/10.1248/CPB.30.1163

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