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Limonium sinense

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64404b00b9f99922751427
Scientific name Limonium sinense
Authority Kuntze
First published in Revis. Gen. Pl. 2: 396 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Statice sinensis Girard Ann. Sci. Nat., Bot. , sér. 3, 2: 329 (1844)
Statice fortunei Lindl. Edwards's Bot. Reg. 31: t. 63 (1845)

Common names Top

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Language Common/alternative name
Chinese 中华补血草
Chinese 匙叶矶松
Chinese 匙叶草
Chinese 华蔓荆
Chinese 海菠菜
Chinese 海蔓
Chinese 海蔓荆
Chinese 海赤芍
Chinese 白花玉钱香
Chinese 盐云草
Chinese 补血草
Chinese 鲂仔草
Chinese 大叶矶松
Chinese 石蓯蓉
Chinese 石蓰蓉
Chinese 石苁蓉

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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 Southeast
      • Manchuria
    • Eastern Asia
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001095301
Tropicos 25400570
KEW urn:lsid:ipni.org:names:686978-1
The Plant List tro-25400570
Open Tree Of Life 244739
NCBI Taxonomy 293752
IPNI 686978-1
iNaturalist 372030
GBIF 7298115
EPPO LIISN
EOL 2892151
USDA GRIN 423454
Wikipedia Limonium_sinense
CMAUP NPO3995

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 Multiple Promoting Effects of Suaeda glauca Root Exudates on the Growth of Alfalfa under NaCl Stress Dong L, Hua Y, Gao Z, Wu H, Hou Y, Chu Y, Zhang J, Cui G Plants (Basel) 07-Mar-2024
PMCID:PMC10974879
doi:10.3390/plants13060752
PMID:38592745
The Function of Root Exudates in the Root Colonization by Beneficial Soil Rhizobacteria Chen L, Liu Y Biology (Basel) 02-Feb-2024
PMCID:PMC10886372
doi:10.3390/biology13020095
PMID:38392313
Therapeutic approaches for chronic hepatitis C: a concise review Nawaz A, Manzoor A, Ahmed S, Ahmed N, Abbas W, Mir MA, Bilal M, Sheikh A, Ahmad S, Jeelani I, Nakagawa T Front Pharmacol 12-Jan-2024
PMCID:PMC10811011
doi:10.3389/fphar.2023.1334160
PMID:38283838
Root colonization by beneficial rhizobacteria Liu Y, Xu Z, Chen L, Xun W, Shu X, Chen Y, Sun X, Wang Z, Ren Y, Shen Q, Zhang R FEMS Microbiol Rev 13-Dec-2023
PMCID:PMC10786197
doi:10.1093/femsre/fuad066
PMID:38093453
Deciphering the mechanisms, hormonal signaling, and potential applications of endophytic microbes to mediate stress tolerance in medicinal plants Pandey P, Tripathi A, Dwivedi S, Lal K, Jhang T Front Plant Sci 15-Nov-2023
PMCID:PMC10684941
doi:10.3389/fpls.2023.1250020
PMID:38034581
Integrated network pharmacology and cellular assay reveal the biological mechanisms of Limonium sinense (Girard) Kuntze against Breast cancer Zhao H, Wang S, Williamson PT, Ewing RM, Tang X, Wang J, Wang Y BMC Complement Med Ther 13-Nov-2023
PMCID:PMC10644419
doi:10.1186/s12906-023-04233-z
PMID:37957642
The halotolerant rizhobacterium Glutamicibacter sp. alleviates salt impact on Phragmites australis by producing exopolysaccharides and limiting plant sodium uptake Hidri R, Metoui‐Ben Mahmoud O, Zorrig W, Azcon R, Abdelly C, Debez A Plant Direct 26-Oct-2023
PMCID:PMC10600829
doi:10.1002/pld3.535
PMID:37901595
An in vivo and in silico evaluation of the hepatoprotective potential of Gynura procumbens: A promising agent for combating hepatotoxicity Tithi TI, Tahsin MR, Anjum J, Zaman TS, Aktar F, Bahar NB, Tasnim S, Sultana A, Jahan I, Afrin SS, Akter T, Sen P, Koly FJ, Reza MS, Chowdhury JA, Kabir S, Chowdhury AA, Amran MS PLoS One 15-Sep-2023
PMCID:PMC10503776
doi:10.1371/journal.pone.0291125
PMID:37713406
Diversity and potential plant growth promoting capacity of seed endophytic bacteria of the holoparasite Cistanche phelypaea (Orobanchaceae) Petrosyan K, Thijs S, Piwowarczyk R, Ruraż K, Kaca W, Vangronsveld J Sci Rep 22-Jul-2023
PMCID:PMC10363106
doi:10.1038/s41598-023-38899-9
PMID:37481658
Certain Tomato Root Exudates Induced by Pseudomonas stutzeri NRCB010 Enhance Its Rhizosphere Colonization Capability Zhang H, Zheng D, Hu C, Cheng W, Lei P, Xu H, Gao N Metabolites 16-May-2023
PMCID:PMC10220591
doi:10.3390/metabo13050664
PMID:37233705
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
Bacterial ACC deaminase: Insights into enzymology, biochemistry, genetics, and potential role in amelioration of environmental stress in crop plants Shahid M, Singh UB, Khan MS, Singh P, Kumar R, Singh RN, Kumar A, Singh HV Front Microbiol 27-Apr-2023
PMCID:PMC10174264
doi:10.3389/fmicb.2023.1132770
PMID:37180266
Phytochemicals as Invaluable Sources of Potent Antimicrobial Agents to Combat Antibiotic Resistance Jadimurthy R, Jagadish S, Nayak SC, Kumar S, Mohan CD, Rangappa KS Life (Basel) 04-Apr-2023
PMCID:PMC10145550
doi:10.3390/life13040948
PMID:37109477
The peanut root exudate increases the transport and metabolism of nutrients and enhances the plant growth-promoting effects of burkholderia pyrrocinia strain P10 Han L, Zhang H, Bai X, Jiang B BMC Microbiol 30-Mar-2023
PMCID:PMC10061817
doi:10.1186/s12866-023-02818-9
PMID:36991332
Chasing the mechanisms of ecologically adaptive salinity tolerance Busoms S, Fischer S, Yant L Plant Commun 07-Mar-2023
PMCID:PMC10721451
doi:10.1016/j.xplc.2023.100571
PMID:36883005

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> 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 https://doi.org/10.1055/S-2000-8547
https://doi.org/10.1055/S-2000-8540
> 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 https://doi.org/10.1055/S-2000-8540
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
CID 85150831 85150831 Click to see CC1CC2(CC(C3(O2)CCC4(C3(CCC5=C4CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)OC2C(C(C(CO2)O)O)OC2C(C(C(O2)CO)O)O)OC2C(C(C(C(O2)C)O)O)O)O)O)O)C)C)C)C)OC1=O 1353.40 unknown https://doi.org/10.1055/S-2000-8547
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(3,4-Dihydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide 54408305 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 299.32 unknown https://doi.org/10.1055/S-2000-8540
N-Caffeoyltyramine 9994897 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 299.32 unknown https://doi.org/10.1055/S-2000-8540
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1055/S-2000-8540
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(1R,9R,10R,25R,33R)-3,5,15,16,20,21,22,29,31-nonahydroxy-12-oxo-9-(3,4,5-trihydroxyphenyl)-8,11,18,26-tetraoxaheptacyclo[23.7.1.16,10.113,17.02,7.019,24.027,32]pentatriaconta-2,4,6,13,15,17(34),19,21,23,27,29,31-dodecaen-33-yl] 3,4,5-trihydroxybenzoate 154497413 Click to see C1C2C(OC3=C1C(=CC(=C3C4C(C(C5=CC(=C(C(=C5OC6=CC(=CC(=C6O)O)C(=O)O2)O)O)O)OC7=CC(=CC(=C47)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)C9=CC(=C(C(=C9)O)O)O 912.70 unknown https://doi.org/10.1055/S-2000-8540
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC127446/
Samarangenin B 85150444 Click to see C1C2C(OC3=C1C(=CC(=C3C4C(C(C5=CC(=C(C(=C5OC6=CC(=CC(=C6O)O)C(=O)O2)O)O)O)OC7=CC(=CC(=C47)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)C9=CC(=C(C(=C9)O)O)O 912.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC127446/
https://doi.org/10.1055/S-2000-8540
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4-dihydroxy-5-methoxybenzoate 10050483 Click to see COC1=CC(=CC(=C1O)O)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O 472.40 unknown https://doi.org/10.1055/S-2000-8547
[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 4-hydroxy-3,5-dimethoxybenzoate 85065894 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O 486.40 unknown https://doi.org/10.1055/S-2000-8547
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate 1287 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1055/S-2000-8547
https://doi.org/10.1055/S-2000-8540
Epigallocatechin 3-O-(3-O-methyl)gallate 9804842 Click to see COC1=CC(=CC(=C1O)O)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O 472.40 unknown https://doi.org/10.1055/S-2000-8547
Epigallocatechin 3-O-(3,5-di-O-methylgallate) 9913276 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O 486.40 unknown https://doi.org/10.1055/S-2000-8547
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1055/S-2000-8547
https://doi.org/10.1055/S-2000-8540
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2R,3S)-3,4',5,7-Tetrahydroxy-3',5'-dimethoxy-2,3-dihydroflavone 101034223 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 348.30 unknown https://doi.org/10.1055/S-2000-8540
3,5,7-Trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dihydrochromen-4-one 18798727 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 348.30 unknown https://doi.org/10.1055/S-2000-8540
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1055/S-2000-8540
Flavan-3,3',4',5,5',7-hexol 1249 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1055/S-2000-8540
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1055/S-2000-8547
(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 https://doi.org/10.1055/S-2000-8547
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 https://doi.org/10.1055/S-2000-8547
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1055/S-2000-8547
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1055/S-2000-8547
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 https://doi.org/10.1055/S-2000-8547
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1055/S-2000-8540
https://doi.org/10.1055/S-2000-8547
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1055/S-2000-8547
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5R,6S)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 5316590 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown https://doi.org/10.1055/S-2000-8547
[(2S,3R,4R,5R,6S)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 4-hydroxybenzoate 101044324 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)OC(=O)C5=CC=C(C=C5)O)O)O 584.50 unknown https://doi.org/10.1055/S-2000-8547
[(2S,3R,4S,5R,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 5316591 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)OC(=O)C5=CC(=C(C(=C5)O)O)O 616.50 unknown https://doi.org/10.1055/S-2000-8547
[(2S,3S,4S,5R,6S)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 4-hydroxybenzoate 162959551 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)OC(=O)C5=CC=C(C=C5)O)O)O 584.50 unknown https://doi.org/10.1055/S-2000-8547
[2-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 13888666 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 600.50 unknown https://doi.org/10.1055/S-2000-8547
[2-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 59386481 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown https://doi.org/10.1055/S-2000-8547
[2-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 4-hydroxybenzoate 74978312 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)OC(=O)C5=CC=C(C=C5)O)O)O 584.50 unknown https://doi.org/10.1055/S-2000-8547
[6-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 73981560 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)OC(=O)C5=CC(=C(C(=C5)O)O)O 616.50 unknown https://doi.org/10.1055/S-2000-8547
2''-O-Galloylquercitrin 10031482 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 600.50 unknown https://doi.org/10.1055/S-2000-8547
3-O-Galloylmucic acid 74978303 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 616.50 unknown https://doi.org/10.1055/S-2000-8547
3''-O-Galloylmyricitrin 101248998 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 616.50 unknown https://doi.org/10.1055/S-2000-8547
5,7-dihydroxy-3-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 162915546 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown https://doi.org/10.1055/S-2000-8547
Myricetin 3-(6''-galloylgalactoside) 5319985 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 632.50 unknown https://doi.org/10.1055/S-2000-8547
Myricetin 3-beta-D-glucopyranoside 12311099 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1055/S-2000-8547
Myricetin 3-galactoside 5491408 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1055/S-2000-8547
Myricetin 3-rhamnoside 5352000 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 https://doi.org/10.1055/S-2000-8547
https://doi.org/10.1055/S-2000-8540
Myricetin-3-O-xyloside 21477996 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown https://doi.org/10.1055/S-2000-8547
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 https://doi.org/10.1055/S-2000-8540
https://doi.org/10.1055/S-2000-8547
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/10.1055/S-2000-8540
https://doi.org/10.1055/S-2000-8547
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 https://doi.org/10.1055/S-2000-8547
https://doi.org/10.1055/S-2000-8540
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one 12310452 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1055/S-2000-8547
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1055/S-2000-8547

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