Elaeagnus umbellata

Details Top

Internal ID UUID644019076b525233942975
Scientific name Elaeagnus umbellata
Authority Thunb.
First published in Syst. Veg. ed. 14 : 164 (1784)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Elaeagnus umbellata is noted in East Asian folk practice as a remedy for cough and cold symptoms, most commonly prepared as an infusion or decoction of the leaves. In the People’s Republic of China, rural households traditionally steep fresh or dried leaves in hot water to make a mild tea used for upper respiratory discomfort, a practice recorded in the classic materia medica Bencao Gangmu (Li Shizhen, 1596) and summarized in modern pharmacognosy texts such as Zhao et al. (2010) on Chinese medicinal plants. On the Korean peninsula, Park et al. (2017) document the use of leaf and young-branch infusions or decoctions for colds and as a gargle for sore throats, a pattern also described in Japanese ethnobotanical surveys (Nakanishi, 1986). Taiwanese folk medicine adds another mode: Peng et al. (2011) describe decoctions of fresh leaves as a treatment for dysentery and edema. For a simple and gentle cough tea, use roughly 5–7 g of fresh young leaves (or 2–3 g dried) and pour 250 ml of just‑boiled water over them; cover and steep for 10–15 minutes, then strain. Drink 1 cup 2–3 times daily. Moderate use is advisable for adults; avoid during pregnancy and do not use if you are known to be allergic to plants in the Elaeagnaceae family. Well‑established phytochemicals in the leaves include flavonoids (quercetin, kaempferol, rutin), phenolic acids (gallic and ellagic acids), and vitamin C; these constituents plausibly account for the reported anti‑inflammatory and mild bronchodilatory activity (Zhao et al., 2010). Today the species remains widely planted for edible fruits and erosion control, while selective research continues on its antioxidant and anti‑inflammatory chemistry, and traditional teas and decoctions remain a familiar home remedy in parts of East Asia (Park et al., 2017).

General Uses Top

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Common products:
Edible products are made from the ripe fruit (berries) in non-medicinal food and beverage applications. The fruit is used as a primary ingredient in jams, jellies, preserves, fruit leather, sauces, and syrups, and as a base for juices, concentrates, beverages, and wine. Fruit purees and concentrates are produced for flavoring and formulation in non-alcoholic and fermented beverages. Flavor descriptors typically include tart and sweet-aromatic notes associated with ripe berries.

Industrial and craft applications:
E. umbellata has roles in reforestation, soil stabilization, windbreaks, and living fence plantings. It is a nitrogen-fixing shrub used in phytostabilization and ecological restoration plantings. Its dense, thorny habit provides shelter for wildlife and is valued in hedgerows and agroforestry systems.

Food and beverages (non-medicinal):
Processed fruit products include jams, jellies, sauces, syrups, and purees used as ingredients in beverages and condiments. The fruit is used to make wine, and the processed fruit serves as a flavoring component in beverages and other food formulations. Typical product forms include whole or crushed fruit, fruit purees, and clarified or strained products for beverage applications.

Colorants and tanning:
The fruit contains anthocyanins that can function as natural colorants and pH indicators in acidic systems. Anthocyanin-rich extracts are used as natural food colorants and have been assessed for non-textile applications.

Wood and fiber:
The wood is used for small-dimension timber, fuelwood, and charcoal. Wood anatomical features consistent with hardwood species support these utility uses. The plant’s thorny, multi-stemmed growth provides material for living fences.

Fragrance and cosmetics:
The intensely fragrant, cream to yellowish flowers are used in ornamental plantings where floral scent is a desired attribute. No direct evidence of essential oil extraction or cosmetic ingredient use is documented for this species.

Properties relevant to use:
Berries are high in carotenoids and anthocyanins, supporting natural colorant applications in acidic food systems. The nitrogen-fixing capacity enables use in soil reclamation, windbreak plantings, and phytostabilization contexts. The dense, thorny shrub form contributes to functional hedgerow and living fence uses.

Sustainability and sourcing:
E. umbellata is valued in reforestation, hedgerow, and soil stabilization projects and serves as a nectar source for pollinators. Its non-medicinal food use is primarily through cultivated and wild-harvested fruit in non-alcoholic and fermented beverages.

Synonyms Top

Scientific name Authority First published in
Elaeagnus coreana H.Lév. Repert. Spec. Nov. Regni Veg. 12: 101 (1913)
Elaeagnus crispa Thunb. Syst. Veg. ed. 14 : 163 (1784)
Elaeagnus crispa var. praematura Koidz.
Elaeagnus padifolia hort. ex K.Koch Dendrologie 2(1): 390 (1872)
Elaeagnus praematura (Koidz.) Araki Hokuriku J. Bot. 4: 107 (1955)
Elaeagnus umbellata f. nakaiana (Araki) H.Ohba Fl. Jap. (Iwatsuki et al., eds.) 2c: 154. 1999
Elaeagnus longipes var. crispa (Thunb.) K.Koch Wochenschr. Vereines Beförd. Gartenbaues Königl. Preuss. Staaten 14: 159 (1871)

Common names Top

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Language Common/alternative name
English autumn olive
Azerbaijani Çətirvari iydə
Czech hlošina okoličnatá
Welsh oleaster
Danish skærm-sølvblad
German korallen-Ölweide
Estonian sarik-hõbepuu
Persian نقرهتوت ژاپنی
Italian korallen-Ölweide
Japanese アキグミ
Georgian ქოლგა ფშატი
Korean 보리수나무
Polish oliwnik baldaszkowy
Russian Лох зонтичный
Serbian Штитаста дафина
Swedish koreansk silverbuske
Turkish japon iğdesi
Chinese 小叶胡颓子
Chinese 麦粒子
Chinese 甜枣
Chinese 剪子果
Chinese 小葉胡頹子
Chinese 倒卵葉胡頹子
Chinese 牛奶子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Elaeagnus umbellata var. rotundifolia Makino Bot. Mag. (Tokyo) 8: 302. 1894 (1894)
Elaeagnus umbellata var. umbellata Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Tadzhikistan
    • Western Asia
      • Afghanistan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Cambodia
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
    • 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.
      • Montana
      • Oregon
      • Washington
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000663963
Florida Plant Atlas 1557
Flora of Alabama 1714
Cornell Woody Plants 87
Canadensys 5458
USDA Plants ELUM
UConn 162
Tropicos 11600010
INPN 95841
Flora of Italy 8464
KEW urn:lsid:ipni.org:names:927281-1
The Plant List kew-2785255
Missouri Botanical Garden 365952
PFAF Elaeagnus umbellata
Open Tree Of Life 511515
Observations.org 195236
NCBI Taxonomy 43233
NBN Atlas NBNSYS0000033903
Nature Serve 2.145344
IUCN Red List 169273702
IPNI 927281-1
iNaturalist 64697
iNaturalist 240471
GBIF 3039267
Freebase /m/02jq0p
WisFlora 3473
FEIS plants/shrub/elaumb
EPPO ELGUM
EOL 582730
Elurikkus 618927
USDA GRIN 14934
Wikipedia Elaeagnus_umbellata
Plantarium 48064

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
Diet of moulting Swainson's Thrushes (Catharus ustulatus) and Tennessee Warblers (Leiothlypis peregrina) at a stopover site during fall migration measured with fecal DNA metabarcoding Blanc-Benigeri A, Poirier V, Narango D, Elliott KH, Frei B Sci Rep 30-Apr-2024
PMCID:PMC11061280
doi:10.1038/s41598-024-59462-0
PMID:38688969
Autumn Olive (Elaeagnus umbellata Thunb.) Berries Improve Lipid Metabolism and Delay Aging in Middle-Aged Caenorhabditis elegans Kim Y, Nam S, Lim J, Jang M Int J Mol Sci 18-Mar-2024
PMCID:PMC10970442
doi:10.3390/ijms25063418
PMID:38542392
Optimization of the method of ultrasonic extraction of lycopene with a green extract from the fruit of Elaeagnus umbellata, common in Western Georgia Surmanidze N, Vanidze M, Djafaridze I, Davitadze R, Qarcivadze I, Khakhutaishvili M, Kalandia A Food Sci Nutr 21-Feb-2024
PMCID:PMC11077213
doi:10.1002/fsn3.4030
PMID:38726431
Elaeagnus umbellata Fruit Extract Protects Skin from Ultraviolet-Mediated Photoaging in Hairless Mice Park SM, Jung CJ, Lee DG, Yu YE, Ku TH, Hong MS, Lim TK, Paeng KI, Cho HK, Cho IJ, Ku SK Antioxidants (Basel) 03-Feb-2024
PMCID:PMC10885948
doi:10.3390/antiox13020195
PMID:38397793
Dietary phenolic compounds as promising therapeutic agents for diabetes and its complications: A comprehensive review Aryal D, Joshi S, Thapa NK, Chaudhary P, Basaula S, Joshi U, Bhandari D, Rogers HM, Bhattarai S, Sharma KR, Regmi BP, Parajuli N Food Sci Nutr 30-Jan-2024
PMCID:PMC11077226
doi:10.1002/fsn3.3983
PMID:38726403
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
A literature review of bioactive substances for the treatment of periodontitis: In vitro, in vivo and clinical studies Kim TH, Heo SY, Chandika P, Kim YM, Kim HW, Kang HW, Je JY, Qian ZJ, Kim N, Jung WK Heliyon 11-Jan-2024
PMCID:PMC10826675
doi:10.1016/j.heliyon.2024.e24216
PMID:38293511
Research Progress of Polysaccharide-Gold Nanocomplexes in Drug Delivery Song M, Aipire A, Dilxat E, Li J, Xia G, Jiang Z, Fan Z, Li J Pharmaceutics 09-Jan-2024
PMCID:PMC10820823
doi:10.3390/pharmaceutics16010088
PMID:38258099
Radio Telemetry and Harmonic Radar Tracking of the Spotted Lanternfly, Lycorma delicatula (White) (Hemiptera: Fulgoridae) Siderhurst MS, Murman KM, Kaye KT, Wallace MS, Cooperband MF Insects 30-Dec-2023
PMCID:PMC10816356
doi:10.3390/insects15010017
PMID:38249023
Wild Edible Fruits as a Source of Food and Medicine: A Study among Tribal Communities of Southern Khyber Pakhtunkhwa Ul Abidin SZ, Khan R, Ahmad M, Cuerrier A, Zafar M, Ullah A, Khan J, Saeed A, Al-Qahtani WH, Kazi M Plants (Basel) 21-Dec-2023
PMCID:PMC10780817
doi:10.3390/plants13010039
PMID:38202347
The Separation, Purification, Structure Identification, and Antioxidant Activity of Elaeagnus umbellata Polysaccharides Zhang J, Xu X, Liu X, Chen M, Bai B, Yang Y, Bo T, Fan S Molecules 06-Sep-2023
PMCID:PMC10534330
doi:10.3390/molecules28186468
PMID:37764243
Sequencing the chloroplast genome of a jujube genotype (Ziziphus jujuba Mill. 'Fengmiguan') uncovered a 101 bp insertion in the large-single copy region Zhang S, Li B, Han L, Yang M, Liu M Mitochondrial DNA B Resour 06-Jul-2023
PMCID:PMC10327523
doi:10.1080/23802359.2023.2231246
PMID:37426571
Chemical compositions and biological activities of Serevenia buxifolia essential oil leaves cultivated in Vietnam (Thua Thien Hue) Bui AV, Pham TV, Nguyen KN, Nguyen NT, Huynh KD, Dang V, Ruml T, Truong D Food Sci Nutr 10-May-2023
PMCID:PMC10345695
doi:10.1002/fsn3.3395
PMID:37457193
A comparison of traditional plant knowledge between Daman people and Tibetans in Gyirong River Valley, Tibet, China Guo CA, Ding X, Hu H, Zhang Y, Bianba C, Bian B, Wang Y J Ethnobiol Ethnomed 05-May-2023
PMCID:PMC10163752
doi:10.1186/s13002-023-00583-7
PMID:37147662
Elaeagnus umbellata: A miraculous shrub with potent health-promoting benefits from Northwest Himalaya Aamir Bhat M, Kumar Mishra A, Azhar Kamal M, Rahman S, Tasleem Jan A Saudi J Biol Sci 02-May-2023
PMCID:PMC10196990
doi:10.1016/j.sjbs.2023.103662
PMID:37213692

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
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Brevifolincarboxylic acid 9838995 Click to see 292.20 unknown https://doi.org/10.1248/CPB.47.536
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown https://doi.org/10.1248/CPB.47.536
1,6-Digalloyl-beta-D-glucopyranose 3332212 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 484.40 unknown https://doi.org/10.1248/CPB.47.536
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown https://doi.org/10.1248/CPB.47.536
(10R,11S)-11-[(10R,11R)-11-[2-[(14R,15S,19S)-14-[(10R,11R)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoyl]oxy-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid 16157358 Click to see 1871.30 unknown https://doi.org/10.1248/CPB.47.536
(10R,11S)-11-[(10R,11R)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid 16142774 Click to see 952.60 unknown https://doi.org/10.1248/CPB.47.536
https://doi.org/10.1016/S0304-3835(99)00160-3
(10R,11S)-11-[(10R,11S)-17-(6-carboxy-2,3,4-trihydroxyphenoxy)-11-[2-[(14R,15S,19S)-14-[(10R,11S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoyl]oxy-3,4,5,18,19-pentahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid 100936650 Click to see 2039.40 unknown https://doi.org/10.1248/CPB.47.536
(10S,11S)-11-[(10R,11S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid 163083929 Click to see 952.60 unknown https://doi.org/10.1248/CPB.47.536
(2R,3R)-3-[(10S,11S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3-dihydroxypropanoic acid 163193104 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C(=O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 650.50 unknown https://doi.org/10.1248/CPB.47.536
(2R,3S)-3-[(10S,11S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3-hydroxy-2-(3,4,5-trihydroxybenzoyl)oxypropanoic acid 162896278 Click to see 802.60 unknown https://doi.org/10.1248/CPB.47.536
(3,4,5,11,12,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl) 3,4,5-trihydroxybenzoate 13917511 Click to see 634.50 unknown https://doi.org/10.1248/CPB.47.536
[(10R,11R)-10-[(14R,15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 2-[(14R,15S,19S)-14-[(10R,11R)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoate 163192024 Click to see 1855.30 unknown https://doi.org/10.1248/CPB.47.536
[(10R,11R)-10-[(14R,15S,19S)-19-[(11R,12R)-12-[(10S,11R)-3,4,5,11,16,17,18-heptahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaen-10-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-6-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 162956220 Click to see 1843.30 unknown https://doi.org/10.1248/CPB.47.536
[(10R,11R)-10-[(14R,15S,19S)-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-19-[(2S,3S,4S,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 162945099 Click to see 1068.80 unknown https://doi.org/10.1248/CPB.47.536
[10-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 2-[14-[3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoate 162999883 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)C8=C(C(=C(C=C8C(=O)OC9COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)OC9C1C2C(C3=C(C(=C(C(=C3C(=O)O2)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1855.30 unknown https://doi.org/10.1248/CPB.47.536
[10-[19-[12-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-6-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 162878694 Click to see 1855.30 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1248/CPB.47.536
[10-[19-[12-(3,4,5,11,16,17,18-Heptahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaen-10-yl)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-6-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 162956219 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)C8=C(C(=C(C9=C8C(=O)OCC(C(OC(=O)C1=CC(=C(C(=C19)O)O)O)C1C(OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1843.30 unknown https://doi.org/10.1248/CPB.47.536
11-[11-[2-[14-[3,4,5,17,18,19-Hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoyl]oxy-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]octadeca-1(18),2,4,6,14,16-hexaene-10-carboxylic acid 162957798 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)C8=C(C(=C(C=C8C(=O)OC9COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)OC9C1C(OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)C(=O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.47.536
14-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-2,3,4,7,8,9,19-heptahydroxy-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 14035439 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1248/CPB.47.536
2-[[(10S,11R,12R,13S,15R)-13-[2-[(14R,15S,19S)-14-[(10R,11R)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoyl]oxy-3,4,5,11,12,22,23-heptahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoic acid 16145408 Click to see 1721.20 unknown https://doi.org/10.1248/CPB.47.536
2-[[(10S,11R,12R,13S,15R)-13-[2-[(14R,15S,19S)-14-[(10R,11S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoyl]oxy-3,4,5,11,12,22,23-heptahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoic acid 100936654 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3C4C5C(OC(=O)C6=CC(=C(C(=C6C7=C(C4=C(C(=C7O)O)O)C(=O)O5)O)O)O)C8C(COC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)OC1=C(C(=C(C=C1C(=O)O)O)O)O)O)O)O)O)O 1721.20 unknown https://doi.org/10.1248/CPB.47.536
2-[[(11R,12R)-12-[(14R,15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 162936314 Click to see 1104.70 unknown https://doi.org/10.1248/CPB.47.536
2-[[(11R,12R)-12-[(14R,15S,19S)-19-[6-[[(10S,11R)-10-[(1S,2R)-2-carboxy-1-hydroxy-2-(3,4,5-trihydroxybenzoyl)oxyethyl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl]oxycarbonyl]-2,3,4-trihydroxyphenyl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 16144571 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)OC4=C(C(=C(C=C4C(=O)O)O)O)O)O)O)O)O)O)C5C6C(C7=C(C(=C(C(=C7C(=O)O6)C8=C(C(=C(C=C8C(=O)O5)O)O)O)O)O)O)C9=C(C(=C(C=C9C(=O)OC1COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)OC1C(C(C(=O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1889.30 unknown https://doi.org/10.1248/CPB.47.536
2-[[(11R,12R)-12-[(14R,15S,19S)-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-19-[(2R,3S,4S,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 162946408 Click to see 1236.90 unknown https://doi.org/10.1248/CPB.47.536
2-[[(11R,12R)-12-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 101601938 Click to see 1104.70 unknown https://doi.org/10.1248/CPB.47.536
https://doi.org/10.1016/S0304-3835(99)00160-3
2-[[(11S,12R)-12-[(14R,15S,19S)-19-[6-[[(10R,11S)-10-[(14R,15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl]oxycarbonyl]-2,3,4-trihydroxyphenyl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 100936651 Click to see 2023.40 unknown https://doi.org/10.1248/CPB.47.536
2-[[(11S,12R)-12-[(14R,15S,19S)-19-[6-[[(10R,11S)-17-(6-carboxy-2,3,4-trihydroxyphenoxy)-10-[(14R,15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,18,19-pentahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl]oxycarbonyl]-2,3,4-trihydroxyphenyl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 100936652 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)OC4=C(C(=C(C=C4C(=O)O)O)O)O)O)O)O)O)O)C5C6C(C7=C(C(=C(C(=C7C(=O)O6)C8=C(C(=C(C=C8C(=O)O5)O)O)O)O)O)O)C9=C(C(=C(C=C9C(=O)OC1COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)OC1C1C2C(C3=C(C(=C(C(=C3C(=O)O2)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)O)O)O)O)OC1=C(C(=C(C=C1C(=O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 2191.50 unknown https://doi.org/10.1248/CPB.47.536
2-[[(11S,12R)-12-[(14R,15S,19S)-19-[6-[[(10S,11S)-10-[(1S,2R)-2-carboxy-1-hydroxy-2-(3,4,5-trihydroxybenzoyl)oxyethyl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl]oxycarbonyl]-2,3,4-trihydroxyphenyl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 100936653 Click to see 1889.30 unknown https://doi.org/10.1248/CPB.47.536
2-[[(11S,12R)-12-[(14R,15S,19S)-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-19-[(3R,4R,5S)-2,3,4,5-tetrahydroxyoxan-2-yl]-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 100936648 Click to see C1C(C(C(C(O1)(C2C3C(OC(=O)C4=CC(=C(C(=C4C5=C(C2=C(C(=C5O)O)O)C(=O)O3)O)O)O)C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)OC9=C(C(=C(C=C9C(=O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O 1236.90 unknown https://doi.org/10.1248/CPB.47.536
2-[[12-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 16174452 Click to see 1104.70 unknown https://doi.org/10.1248/CPB.47.536
2-[[12-[19-[6-[[10-[2-Carboxy-1-hydroxy-2-(3,4,5-trihydroxybenzoyl)oxyethyl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl]oxycarbonyl]-2,3,4-trihydroxyphenyl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 162880480 Click to see 1889.30 unknown https://doi.org/10.1248/CPB.47.536
2-[[12-[2,3,4,7,8,9-Hexahydroxy-12,17-dioxo-19-(2,3,4,5-tetrahydroxyoxan-2-yl)-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,17,18,19-pentahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-5-yl]oxy]-3,4,5-trihydroxybenzoic acid 162946407 Click to see 1236.90 unknown https://doi.org/10.1248/CPB.47.536
2-[[13-[2-[14-[3,4,5,17,18,19-Hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoyl]oxy-3,4,5,11,12,22,23-heptahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoic acid 163012872 Click to see 1721.20 unknown https://doi.org/10.1248/CPB.47.536
2,3-Hexahydroxydiphenoylglucopyranose 492390 Click to see 482.30 unknown https://doi.org/10.1248/CPB.47.536
3-[3,4,5,17,18,19-Hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3-dihydroxypropanoic acid 85130969 Click to see 650.50 unknown https://doi.org/10.1248/CPB.47.536
3-[3,4,5,17,18,19-Hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3-hydroxy-2-(3,4,5-trihydroxybenzoyl)oxypropanoic acid 85105861 Click to see 802.60 unknown https://doi.org/10.1248/CPB.47.536
5-Desgalloylstachyurin 10417809 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1248/CPB.47.536
Casuariin 14035442 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1248/CPB.47.536
Elaeagnatin B 100936649 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)C8=C(C(=C(C=C8C(=O)OC9COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)OC9C1C(OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)C(=O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.47.536
Hippophaenin A 16130427 Click to see 952.60 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1248/CPB.47.536
Lagerstannin C 10394485 Click to see 650.50 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1248/CPB.47.536
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1248/CPB.47.536
https://doi.org/10.1016/S0304-3835(99)00160-3
Pterocarinin A 14731325 Click to see 1068.80 unknown https://doi.org/10.1248/CPB.47.536
Punigluconin 21637585 Click to see 802.60 unknown https://doi.org/10.1248/CPB.47.536
https://doi.org/10.1016/S0304-3835(99)00160-3
Strictinin 73330 Click to see 634.50 unknown https://doi.org/10.1248/CPB.47.536
Valoneic acid dilactone 10151874 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)OC5=C(C(=C(C=C5C(=O)O)O)O)O 470.30 unknown https://doi.org/10.1248/CPB.47.536

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