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Allium obliquum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644024b155b76597975746
Scientific name Allium obliquum
Authority L.
First published in Sp. Pl. : 296 (1753)

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.

Ethnobotanical Uses

Across its mountain range from the Altai to the Caucasus, Allium obliquum is harvested and processed into simple infusions. In southern Siberia, people prepare a mild leaf tea, and in parts of Central Asia, a decoction of bulbs and leaves is taken for coughs, colds and “gastritis” (Ghirardini et al., 2013). Among the Shor and Tatar communities of the Altai, infusions of fresh leaves serve as a winter tonic and gargle for sore throats (Sokolov, 1991). In the northern Caucasus, a poultice of crushed fresh leaves is applied to sprains and bruises (Nesov, 1997). These three records demonstrate infusions, a decoction and a poultice, with leaves as the principal plant part, bulbs used in the decoction, and no root reported.

One practical recipe is a mild leaf tea, also used as a gargle. For one cup, use 1–2 heaping teaspoons of fresh leaves or 1–2 g dried leaves; pour over 250 mL of just-off-the-boil water, cover and steep 5–7 minutes, then strain and sip while warm, or use 100–150 mL as a gargle. Do not exceed 2–3 cups per day. Safety note: Allium obliquum is close to common onions; use caution if you have reflux, GERD, gastric ulcers, are taking blood thinners or antiplatelet drugs, or are pregnant; avoid strong, concentrated decoctions during pregnancy and report any adverse reactions to a qualified professional. Ghirardini et al., 2013; Bennet et al., 2021.

Well‑established constituents for Allium obliquum are alliin, allicin, quercetin and kaempferol glycosides, S‑alk(en)yl‑L‑cysteine sulfoxides and flavonoids; the tissue‑disruption chemistry is known from comparative Allium phytochemistry and from chromatographic analyses of A. obliquum itself (Battalgia, 2012; Rodov & Vinogradov, 1989; Batsatsashvili et al., 2017). These compounds plausibly support the local anti‑infective and antispasmodic claims for infusion and decoction use. Today, the plant appears in small online niche markets as a “mountain garlic” tincture or dried leaves, while regional foragers continue to harvest leaves for winter teas; modern work on Allium bioactives in the region is ongoing (Batsatsashvili et al., 2017; Ghirardini et al., 2013).

General Uses Top

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Common products:
Allium obliquum is cultivated as a minor vegetable and ornamental. Food use centers on its young leaves and bulbs, used fresh or cooked as seasoning greens. The plant is also maintained in germplasm collections as a genetic resource.

Food and beverages (non-medicinal):
Leaves and bulbs are eaten raw, chopped, or added to salads and sauces; they are also cooked (sautéed, boiled, baked) or included in soups and stuffings. Bulbs may be sliced or fried, and used in sauces and mixed vegetable dishes. These culinary preparations are noted in ethnobotanical and regional food references for Central Asia and Siberia.

Scientific/model-organism use:
A. obliquum is represented in public botanical databases and germplasm resources. It is indexed in the GRIN database and linked to genetic sequence records in public sequence repositories. It is also maintained in living collections and botanical gardens (e.g., as documented in Siberian herbaria and horticultural listings), enabling comparative genomics, taxonomy, and breeding-related studies within Allium.

Properties relevant to use:
The species exhibits the typical Allium organosulfur aroma profile associated with cysteine sulfoxides and their enzymatic breakdown products, which underpins its culinary utility as a flavoring plant. Growth habit and flavor are comparable to those of other minor-edible Allium species.

Standards and regulation:
Commercial food use is primarily local; as such, national or subnational food standards (e.g., national food codes) apply when marketed. No dedicated international (ISO/ASTM/EN) commodity standards are recognized for this species.

Sustainability and sourcing:
Wild harvesting in parts of its range is documented; sustainable collection is advisable to avoid depletion of localized populations. Domestic cultivation is possible as a small-scale crop; germplasm holdings support conservation and future development.

Synonyms Top

Scientific name Authority First published in
Camarilla obliqua (L.) Salisb. Gen. Pl. : 91 (1866)
Cepa obliqua (L.) Moench Methodus : 243 (1794)
Moenchia obliqua (L.) Medik. in Act. Acad. Palat. vi. Phys. (1790) 493.
Allium exaltatum Kar. & Kir. ex Ledeb. Fl. Ross. (Ledeb.) 4: 173. 1852
Allium luteum F.Dietr. Vollst. Lex. Gärtn. , ed. 2, 1: 265 (1824)
Geboscon obliquum (L.) Raf. Fl. Tellur. 2: 19 (1837)
Allium porrum Georgi Beschr. Nation. Russ. Reich 3(4): 891 (1800)
Allium ramosum Jacq. Misc. Austriac. 2: 303 (1781)

Common names Top

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Language Common/alternative name
Arabic ثوم مائل
ba Оҫҡон
German scharfer gelblauch
Icelandic skjálglaukur
mn Саримсан сонгино
Russian Лук косой
Chinese 高莛韭
Chinese 高葶韭

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
  • Europe
    • Eastern Europe
      • East European Russia
      • South European Russia
    • Southeastern Europe
      • Romania

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000756848
UNII 10V4F72X1M
Tropicos 18404277
KEW urn:lsid:ipni.org:names:528506-1
The Plant List kew-296125
Open Tree Of Life 34203
Observations.org 136096
NCBI Taxonomy 166816
IPNI 528506-1
iNaturalist 779403
GBIF 2857444
Freebase /m/0102839h
EOL 1084759
USDA GRIN 2330
Wikipedia Allium_obliquum
PFAF Allium obliquum

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
Characterization of phytochemicals from twisted-leaf garlic (Allium obliquum L.) using liquid chromatography coupled with electrospray ionization quadrupole time-of-flight mass spectrometry Böttcher C, Bach LT, Stürtz M, Schulz H Metabolomics 21-Oct-2023
PMCID:PMC10590303
doi:10.1007/s11306-023-02054-2
PMID:37864615
Phytochemicals That Interfere With Drug Metabolism and Transport, Modifying Plasma Concentration in Humans and Animals Gómez-Garduño J, León-Rodríguez R, Alemón-Medina R, Pérez-Guillé BE, Soriano-Rosales RE, González-Ortiz A, Chávez-Pacheco JL, Solorio-López E, Fernandez-Pérez P, Rivera-Espinosa L Dose Response 21-Sep-2022
PMCID:PMC9500303
doi:10.1177/15593258221120485
PMID:36158743
Aqueous and Ethanolic Plant Extracts as Bio-Insecticides—Establishing a Bridge between Raw Scientific Data and Practical Reality Tavares WR, Barreto MD, Seca AM Plants (Basel) 04-May-2021
PMCID:PMC8147817
doi:10.3390/plants10050920
PMID:34064367
Complete chloroplast genomes shed light on phylogenetic relationships, divergence time, and biogeography of Allioideae (Amaryllidaceae) Namgung J, Do HD, Kim C, Choi HJ, Kim J Sci Rep 05-Feb-2021
PMCID:PMC7865063
doi:10.1038/s41598-021-82692-5
PMID:33547390
The complete chloroplast genome of Amana baohuaensis (Liliaceae) Wang L, Lu X, Han B, Chen J, Jin J, Lv Q, Liu H Mitochondrial DNA B Resour 03-Nov-2020
PMCID:PMC7646578
doi:10.1080/23802359.2020.1831989
PMID:33367052
Omics approaches in Allium research: Progress and way ahead Khandagale K, Krishna R, Roylawar P, Ade AB, Benke A, Shinde B, Singh M, Gawande SJ, Rai A PeerJ 09-Sep-2020
PMCID:PMC7486827
doi:10.7717/peerj.9824
PMID:32974094
Insights into phylogeny, age and evolution of Allium (Amaryllidaceae) based on the whole plastome sequences Xie DF, Tan JB, Yu Y, Gui LJ, Su DM, Zhou SD, He XJ Ann Bot 01-Apr-2020
PMCID:PMC7262478
doi:10.1093/aob/mcaa024
PMID:32239179
The complete chloroplast genome of Lycoris aurea (L’Hér.) Herb Peng Y, Wei J, Yang L Mitochondrial DNA B Resour 24-Jan-2020
PMCID:PMC7748574
doi:10.1080/23802359.2020.1715296
PMID:33366751
Botanicals Against Tetranychus urticae Koch Under Laboratory Conditions: A Survey of Alternatives for Controlling Pest Mites Rincón RA, Rodríguez D, Coy-Barrera E Plants (Basel) 07-Aug-2019
PMCID:PMC6724176
doi:10.3390/plants8080272
PMID:31394806
Characterization of the complete chloroplast genome of leek Allium porrum L. (Amaryllidaceae) Filyushin MA, Beletsky AV, Kochieva EZ Mitochondrial DNA B Resour 22-Jul-2019
PMCID:PMC7706495
doi:10.1080/23802359.2019.1640090
PMID:33365644
Characterization of the complete plastid genome of lop-sided onion Allium obliquum L. (Amaryllidaceae) Filyushin MA, Beletsky AV, Mazur AM, Kochieva EZ Mitochondrial DNA B Resour 26-Mar-2018
PMCID:PMC7800693
doi:10.1080/23802359.2018.1456369
PMID:33474180
Notizen: Die Kohlenhydrate im Strukturproteid der Chloroplasten von Allium porrum Doris Van Wyk Walter de Gruyter GmbH 26-Feb-2015
doi:10.1515/ZNB-1967-0633
Notizen: Über die Fettsäuren aus Allium porrum H. Debuch Walter de Gruyter GmbH 26-Feb-2015
doi:10.1515/ZNB-1964-0420
Chemical Constituents of Three Allium Species from Romania Vlase L, Parvu M, Parvu EA, Toiu A Molecules 21-Dec-2012
PMCID:PMC6270514
doi:10.3390/molecules18010114
PMID:23344191
Accumulation of apocarotenoids in mycorrhizal roots of leek (Allium porrum). Schliemann W, Kolbe B, Schmidt J, Nimtz M, Wray V Phytochemistry 01-May-2008
doi:10.1016/J.PHYTOCHEM.2008.02.015
PMID:18384822

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
9-Octadecenoic Acid 965 Click to see 282.50 unknown https://doi.org/10.1515/ZNB-1964-0420
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1515/ZNB-1964-0420
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1515/ZNB-1964-0420
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4S)-3-(hydroxymethyl)-5,5-dimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 162960577 Click to see 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(4S)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 163101719 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)(C)C 504.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(4S)-4-[(3R)-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 162890968 Click to see 534.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
3-oxo-3-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(2R)-4-[(1S)-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]butan-2-yl]oxyoxan-2-yl]methoxy]propanoic acid 163018562 Click to see 458.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
3-Oxo-3-[[3,4,5-trihydroxy-6-[4-(2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)butan-2-yloxy]oxan-2-yl]methoxy]propanoic acid 163018561 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)COC(=O)CC(=O)O)O)O)O)(C)C 458.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
3,5,5-Trimethyl-4-[3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 75111181 Click to see 504.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
4-[3-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 162890967 Click to see 534.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
9,13-Dihydroxy-4-megastigmen-3-one 9-glucoside 72791584 Click to see 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown https://doi.org/10.1515/ZNB-1964-0420
9,12,15-Octadecatrienoic acid 860 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1515/ZNB-1964-0420
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1515/ZNB-1964-0420
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1515/ZNB-1964-0420
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
[(1R,2R,7R,8aR)-1,8a-dimethyl-6-oxo-7-prop-1-en-2-yl-1,2,3,4,7,8-hexahydronaphthalen-2-yl] 3-methylbut-2-enoate 101928818 Click to see 316.40 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(4S)-5,5-dimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 163078291 Click to see 550.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
5,5-Dimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 163078290 Click to see 550.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(-)-Neoporrigenin B 53463026 Click to see 446.60 unknown https://doi.org/10.1021/JF980849N
https://doi.org/10.1021/NP960657R
https://doi.org/10.1016/S0031-9422(96)00663-2
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18R,19R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16,19-triol 158181824 Click to see 448.60 unknown https://doi.org/10.1021/NP960657R
(1R,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16R,18S,19R)-16,19-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10,15-dione 10647665 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CC(=O)C(C6)O)C)O)C)C)OC1 460.60 unknown https://doi.org/10.1021/JF980849N
(1R,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S,18S,19R)-16,19-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 101699862 Click to see 446.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1016/S0040-4020(97)00062-8
(25s)-5alpha-Spirostane-2beta,3beta,6beta-triol 102330027 Click to see 448.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
(2beta,3beta,5alpha,6beta,25R)-Spirostan-2,3,6-triol 12312669 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1021/JF980849N
https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1021/NP960657R
12-Ketoporrigenin 73313119 Click to see 446.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1021/JF980849N
16,19-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10,15-dione 78182137 Click to see 460.60 unknown https://doi.org/10.1021/JF980849N
CID 10575381 10575381 Click to see 446.60 unknown https://doi.org/10.1021/JF980849N
https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1016/S0040-4020(97)00062-8
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1021/JF980849N
Neoagigenin 52931439 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
Neoporrigenin B 91871146 Click to see 446.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
Porrigenin B 44566820 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(=O)C(C6)O)C)O)C)C)OC1 446.60 unknown https://doi.org/10.1021/JF980849N
https://doi.org/10.1016/S0031-9422(96)00663-2
Porrigenin C 400052 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CC(=O)C(C6)O)C)O)C)C)OC1 460.60 unknown https://doi.org/10.1021/JF980849N
Spirost-5-en-3-ol 234096 Click to see 414.60 unknown https://doi.org/10.1021/JF980849N
Spirostan-2,3,6-triol, (2alpha,3beta,5alpha,6beta,25R)- 44566818 Click to see 448.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
Spirostan-2,3,6-triol, (2beta,3beta,5alpha,6beta,25R)- 44566819 Click to see 448.60 unknown https://doi.org/10.1021/JF980849N
https://doi.org/10.1016/S0031-9422(96)00663-2
> Lipids and lipid-like molecules / Saccharolipids
(3S)-5-[(2R,3R,4S,5R,6R)-2-[(2-carboxyacetyl)oxymethyl]-3,5-dihydroxy-6-[(2R)-4-[(1S)-2-(hydroxymethyl)-6,6-dimethyl-4-oxocyclohex-2-en-1-yl]butan-2-yl]oxyoxan-4-yl]oxy-3-hydroxy-3-methyl-5-oxopentanoic acid 162882667 Click to see 618.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(3S)-5-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(2R)-4-[(1S)-2-(hydroxymethyl)-6,6-dimethyl-4-oxocyclohex-2-en-1-yl]butan-2-yl]oxyoxan-4-yl]oxy-3-hydroxy-3-methyl-5-oxopentanoic acid 162886586 Click to see CC(CCC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)OC(=O)CC(C)(CC(=O)O)O)O 532.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
(3S)-5-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(2R)-4-[(1S)-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]butan-2-yl]oxyoxan-4-yl]oxy-3-hydroxy-3-methyl-5-oxopentanoic acid 163037562 Click to see 516.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
5-[2-[(2-Carboxyacetyl)oxymethyl]-3,5-dihydroxy-6-[4-[2-(hydroxymethyl)-6,6-dimethyl-4-oxocyclohex-2-en-1-yl]butan-2-yloxy]oxan-4-yl]oxy-3-hydroxy-3-methyl-5-oxopentanoic acid 162882666 Click to see 618.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
5-[3,5-Dihydroxy-2-(hydroxymethyl)-6-[4-(2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)butan-2-yloxy]oxan-4-yl]oxy-3-hydroxy-3-methyl-5-oxopentanoic acid 163037561 Click to see 516.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
5-[3,5-Dihydroxy-2-(hydroxymethyl)-6-[4-[2-(hydroxymethyl)-6,6-dimethyl-4-oxocyclohex-2-en-1-yl]butan-2-yloxy]oxan-4-yl]oxy-3-hydroxy-3-methyl-5-oxopentanoic acid 162886585 Click to see 532.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.015
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5R,6R)-2-[[(1R,3R,8S,9S,10R,13S,14S,16S,17R)-1-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-17-[(2S,3S)-3-hydroxy-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-16-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162925681 Click to see CC1C(C(C(C(O1)OC2CC(CC3=CCC4C(C23C)CCC5(C4CC(C5C(C)C(CCC(C)C)O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)O)OC7C(C(C(C(O7)CO)O)O)O 905.10 unknown https://doi.org/10.1021/JF000331V
Alliosterol 1-(4''-galactosylrhamnoside) 16-galactoside 74821812 Click to see CC1C(C(C(C(O1)OC2CC(CC3=CCC4C(C23C)CCC5(C4CC(C5C(C)C(CCC(C)C)O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)O)OC7C(C(C(C(O7)CO)O)O)O 905.10 unknown https://doi.org/10.1021/JF000331V
Alliosterol 1-rhamnoside 16-galactoside 73820915 Click to see CC1C(C(C(C(O1)OC2CC(CC3=CCC4C(C23C)CCC5(C4CC(C5C(C)C(CCC(C)C)O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)O)O 742.90 unknown https://doi.org/10.1021/JF000331V
I(2)-D-Galactopyranoside, (1I(2),3I(2),16I(2),22S)-1-[(6-deoxy-I+/--L-mannopyranosyl)oxy]-3,22-dihydroxycholest-5-en-16-yl 102241949 Click to see 742.90 unknown https://doi.org/10.1021/JF000331V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16R,18S,19R)-16-[(2S,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10,15-dione 10677642 Click to see 1079.10 unknown https://doi.org/10.1021/JF000331V
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-[(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-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 162848227 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1 1227.30 unknown https://doi.org/10.1021/JF000331V
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 102533651 Click to see 1065.20 unknown https://doi.org/10.1021/JF000331V
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-[(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-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 163003012 Click to see 1227.30 unknown https://doi.org/10.1021/JF000331V
(2R,3S,4R,5R,6S)-2-[(2R,3S,4R,5S,6S)-2-[(2R,3S,4R,5S,6S)-2-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4R,5'R,6R,7R,8S,9S,12R,13R,16R,18R,19R)-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162928017 Click to see 1213.30 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
(2R,3S,4R,5R,6S)-2-[(2R,3S,4R,5S,6S)-2-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4R,5'R,6R,7R,8S,9S,12R,13R,16R,18R,19R)-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162852863 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)O)C)C)OC1 1051.20 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101921645 Click to see 1213.30 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
(3b,5a,6b,25R)-3,6-Dihydroxyspirostane-2,12-dione 3-[4'-(2''-glucosyl-3''-xylosyl)-galactoside] 85229901 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CC(=O)C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)O)C)C)OC1 1079.10 unknown https://doi.org/10.1021/JF000331V
(3beta,5alpha,6beta,25R)-6-Hydroxyspirostan-3-yl O-beta-D-glucopyranosyl-(1-->2)-O-[beta-D-xylopyranosyl-(1-->3)]-O-beta-D-glucopyranosyl-(1-->4)-beta-D-galactopyranoside 101035913 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)O)C)C)OC1 1051.20 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
12-Ketoporrigenin 3-[4'-(2''-glucosyl-3''-xylosyl)-glucosyl)-galactoside] 85212494 Click to see 1065.20 unknown https://doi.org/10.1021/JF000331V
16-[3,4-Dihydroxy-5-[5-hydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 14803802 Click to see 1065.20 unknown https://doi.org/10.1021/JF000331V
16-[5-[3-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 163003011 Click to see 1227.30 unknown https://doi.org/10.1021/JF000331V
16-[5-[3-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 162848226 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1 1227.30 unknown https://doi.org/10.1021/JF000331V
2-[2-[2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-(15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 85099406 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O)C)C)C)OC1 1213.30 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
2-Hydroxyspirostan-3-yl 4-O-(2-O-hexopyranosyl-3-O-pentopyranosylhexopyranosyl)hexopyranoside 496676 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)C)C)OC1 1051.20 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
b-Chlorogenin 3-[4-(2-((3-glucosyl)glucosyl-3-xylosyl)-glucosyl)-galactoside] 131751544 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)O)C)C)OC1 1213.30 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
b-Chlorogenin 3-[4''-(2'''-glucosyl-3'''-xylosylglucosyl)galactoside] 74193143 Click to see 1051.20 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
F-Gitonin 44559009 Click to see 1051.20 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
I(2)-D-Galactopyranoside, (3I(2),5I+/-,6I(2),25R)-6-hydroxyspirostan-3-yl O-I(2)-D-glucopyranosyl-(1a3)-O-I(2)-D-glucopyranosyl-(1a2)-O-[I(2)-D-xylopyranosyl-(1a3)]-O-I(2)-D-glucopyranosyl-(1a4)- 101035914 Click to see 1213.30 unknown https://doi.org/10.1016/S0031-9422(98)00712-2
Spirostan-12-one, 3-[(O-beta-D-glucopyranosyl-(1-->2)-O-[beta-D-xylopyranosyl-(1-->3)]-O-beta-D-glucopyranosyl-(1-->4)-beta-D-galactopyranosyl)oxy]-6-hydroxy-, (3beta,5alpha,6beta,25R)- 10629946 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)O)C)C)OC1 1065.20 unknown https://doi.org/10.1021/JF000331V
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1515/ZNB-1967-0633
(2S,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 161658 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1515/ZNB-1967-0633
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1515/ZNB-1967-0633
L-Galactose 24749 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1515/ZNB-1967-0633
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Porric acid A 478958 Click to see 302.28 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
Porric acid B 478957 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
Porric acid C 478956 Click to see CC1=CC(=CC2=C1C3=C(O2)C(=CC(=C3)O)C(=O)O)O 258.23 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
> Organoheterocyclic compounds / Naphthofurans
2-(5',7,9,13-Tetramethyl-16-oxospiro[5,17-dioxapentacyclo[10.7.0.02,9.04,8.014,18]nonadecane-6,2'-oxane]-13-yl)acetic acid 78385463 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC6C(C5(C)CC(=O)O)CC(=O)O6)C)C)OC1 460.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1021/JF980849N
https://doi.org/10.1016/S0040-4020(97)00062-8
2-[(1R,2S,4S,5'S,6R,7S,8R,9S,12S,13R,14S,18R)-5',7,9,13-tetramethyl-16-oxospiro[5,17-dioxapentacyclo[10.7.0.02,9.04,8.014,18]nonadecane-6,2'-oxane]-13-yl]acetic acid 101699863 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC6C(C5(C)CC(=O)O)CC(=O)O6)C)C)OC1 460.60 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1016/S0040-4020(97)00062-8
2,3-Secoporrigenin 10837674 Click to see 460.60 unknown https://doi.org/10.1016/S0040-4020(97)00062-8
https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1021/JF980849N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2S,3R,4S,5S,6R)-2-{[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate 71341515 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
[(2R,3R,4S,5R,6R)-2-[(2S,3R,4S,5R,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163189561 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3C(OC(C(C3O)O)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)CO)CO)O)O)O 786.70 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
[(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 11803389 Click to see 786.70 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
[(2S,3R,4S,5R,6R)-2-[(2R,3S,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 10819059 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3C(OC(C(C3O)O)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)CO)CO)O)O)O 786.70 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
[(2S,3R,4S,5R,6S)-2-[(2R,3S,4S,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162945674 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3C(OC(C(C3O)O)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)CO)CO)O)O)O 786.70 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 6442291 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
[2-[[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73109219 Click to see 786.70 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
[2-[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74978118 Click to see 786.70 unknown https://doi.org/10.1016/S0031-9422(01)00039-5
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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/S0031-9422(01)00039-5
Kaempferol-3-O-glucorhamnoside 13915496 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00039-5

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