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Eurycorymbus cavaleriei

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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 UUID64401bf3755a2395194978
Scientific name Eurycorymbus cavaleriei
Authority (H.Lév.) Rehder & Hand.-Mazz.
First published in J. Arnold Arbor. 15: 8 (1934)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eurycorymbus austrosinensis Hand.-Mazz. Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 59: 104 (1922)
Rhus cavaleriei H.Lév. Repert. Spec. Nov. Regni Veg. 10: 474 (1912)

Common names Top

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Language Common/alternative name
Chinese 伞花木
Chinese 賽欒華
Chinese 伞花木属
Chinese 赛栾华
Chinese 傘花木屬

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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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 South-central
      • China Southeast
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000683353
Tropicos 28601594
KEW urn:lsid:ipni.org:names:783149-1
The Plant List kew-2805155
Open Tree Of Life 844128
NCBI Taxonomy 325641
IUCN Red List 31353
IPNI 783149-1
iNaturalist 183467
GBIF 3788104
Freebase /m/02x93w1
EOL 2889064

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
Chloroplast genome assembly of Serjania erecta Raldk: comparative analysis reveals gene number variation and selection in protein-coding plastid genes of Sapindaceae Corvalán LC, Sobreiro MB, Carvalho LR, Dias RO, Braga-Ferreira RS, Targueta CP, Silva-Neto CM, Berton BW, Pereira AM, Diniz-filho JA, Telles MP, Nunes R Front Plant Sci 26-Sep-2023
PMCID:PMC10562606
doi:10.3389/fpls.2023.1258794
PMID:37822334
Phylogeographic analysis of Siraitia grosvenorii in subtropical China provides insights into the origin of cultivated monk fruit and conservation of genetic resources Xie B, Lai B, Chen L, Wei S, Tang S Ecol Evol 09-Jun-2023
PMCID:PMC10256620
doi:10.1002/ece3.10181
PMID:37304364
Morphological and physiological adaptation characteristics of lithophytic bryophytes to karst high calcium environment Meng W, Ran J, Dai Q, Tu N, Leng T, Ren Q BMC Plant Biol 25-Mar-2023
PMCID:PMC10039556
doi:10.1186/s12870-022-03980-4
PMID:36964495
Characterization of the Complete Chloroplast Genome and Phylogenetic Implications of Euonymus microcarpus (Oliv.) Sprague Li H, Chen M, Wang Z, Hao Z, Zhao X, Zhu W, Liu L, Guo W Genes (Basel) 13-Dec-2022
PMCID:PMC9778254
doi:10.3390/genes13122352
PMID:36553619
Stepped Geomorphology Shaped the Phylogeographic Structure of a Widespread Tree Species (Toxicodendron vernicifluum, Anacardiaceae) in East Asia Wang L, Li Y, Noshiro S, Suzuki M, Arai T, Kobayashi K, Xie L, Zhang M, He N, Fang Y, Zhang F Front Plant Sci 02-Jun-2022
PMCID:PMC9201781
doi:10.3389/fpls.2022.920054
PMID:35720535
Coumarinolignans with Reactive Oxygen Species (ROS) and NF-κB Inhibitory Activities from the Roots of Waltheria indica Liu F, Mallick S, O’Donnell TJ, Rouzimaimaiti R, Luo Y, Sun R, Wall M, Wongwiwatthananukit S, Date A, Silva DK, Williams PG, Chang LC Molecules 19-May-2022
PMCID:PMC9147481
doi:10.3390/molecules27103270
PMID:35630746
Comparative genomics and phylogenetic relationships of two endemic and endangered species (Handeliodendron bodinieri and Eurycorymbus cavaleriei) of two monotypic genera within Sapindales Yang J, Hu G, Hu G BMC Genomics 06-Jan-2022
PMCID:PMC8734052
doi:10.1186/s12864-021-08259-w
PMID:34991482
Population dynamics linked to glacial cycles in Cercis chuniana F. P. Metcalf (Fabaceae) endemic to the montane regions of subtropical China Liu W, Xie J, Zhou H, Kong H, Hao G, Fritsch PW, Gong W Evol Appl 07-Oct-2021
PMCID:PMC8591333
doi:10.1111/eva.13301
PMID:34815745
Chloroplast Genome of Rambutan and Comparative Analyses in Sapindaceae Dong F, Lin Z, Lin J, Ming R, Zhang W Plants (Basel) 02-Feb-2021
PMCID:PMC7912957
doi:10.3390/plants10020283
PMID:33540810
Characterization of the complete chloroplast genome sequence of Koelreuteria bipinnata Lyu Y, Dong X, Sun H, Huang L Mitochondrial DNA B Resour 08-Sep-2020
PMCID:PMC7782333
doi:10.1080/23802359.2020.1806129
PMID:33458153
Complete chloroplast genome sequence of Acer sutchuenense subsp. tienchuanenge (Sapindaceae) Zhang W, Xia X, Chen D, Li J, He W, Ma W, Wu B, Zheng Y, Zhang C Mitochondrial DNA B Resour 20-Jul-2020
PMCID:PMC7781949
doi:10.1080/23802359.2020.1791002
PMID:33457988
Complete plastome sequence of Nephelium topengii (Merr.) H. S. Lo (Sapindaceae): an endemic species in Hainan Zhu ZX, Wang HX, Wang HF Mitochondrial DNA B Resour 11-Jul-2020
PMCID:PMC7781924
doi:10.1080/23802359.2020.1778556
PMID:33457927
Complete chloroplast genome sequence of Peganum harmala, an important medicinal plant Zha X, Zhao P, Gao F, Zhou Y Mitochondrial DNA B Resour 16-Jan-2020
PMCID:PMC7748625
doi:10.1080/23802359.2019.1711230
PMID:33366688
Complete chloroplast genome sequence of Acer ginnala, an important ornamental tree Yang H, Zha X, Cao S, Wang Y, Gao F, Zhou Y Mitochondrial DNA B Resour 14-Jan-2020
PMCID:PMC7748649
doi:10.1080/23802359.2019.1710606
PMID:33366669
Complete chloroplast genome of an endangered endemic tree, handeliodendron bodinieri (levl.) rehder (sapindaceae) from karst forests of southwest China Tian X, Li X, Miao H, Xue C, Wang B, Guo Y, Zhang G Mitochondrial DNA B Resour 27-Sep-2019
PMCID:PMC7707296
doi:10.1080/23802359.2019.1671251
PMID:33365952

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 / Benzylethers
(2S)-2-ethoxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]acetic acid 162869208 Click to see CCOC(C1=CC(=C(C(=C1)CC=C(C)C)O)CC=C(C)C)C(=O)O 332.40 unknown https://doi.org/10.1080/10286020.2011.575068
> Lignans, neolignans and related compounds / Coumarinolignans
(2S,3S)-2-(3,4-dihydroxy-5-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 24850450 Click to see COC1=CC(=CC(=C1O)O)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO 402.40 unknown https://doi.org/10.1016/J.FITOTE.2009.04.003
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
methyl (3R,3aS,5aR,5bR,7aR,8R,9S,11aR,11bR,13R,13aR,13bS)-9,13-dihydroxy-5a,5b,8,11a,13b-pentamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-8-carboxylate 102258956 Click to see CC(=C)C1CCC2(C1CCC3(C2C(CC4C3(CCC5C4(CCC(C5(C)C(=O)OC)O)C)C)O)C)C 486.70 unknown https://doi.org/10.1002/HLCA.201000131
methyl (3R,3aS,5aR,5bR,7R,7aR,8R,9S,11aR,11bR,12S,13aR,13bS)-7-acetyloxy-9,12-dihydroxy-5a,5b,8,11a,13b-pentamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-8-carboxylate 102258957 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(CC(C5C4(CCC(C5(C)C(=O)OC)O)C)OC(=O)C)C)O)C)C 544.80 unknown https://doi.org/10.1002/HLCA.201000131
Methyl 7-acetyloxy-9,12-dihydroxy-5a,5b,8,11a,13b-pentamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-8-carboxylate 162872521 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(CC(C5C4(CCC(C5(C)C(=O)OC)O)C)OC(=O)C)C)O)C)C 544.80 unknown https://doi.org/10.1002/HLCA.201000131
Methyl 9,13-dihydroxy-5a,5b,8,11a,13b-pentamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-8-carboxylate 163020133 Click to see CC(=C)C1CCC2(C1CCC3(C2C(CC4C3(CCC5C4(CCC(C5(C)C(=O)OC)O)C)C)O)C)C 486.70 unknown https://doi.org/10.1002/HLCA.201000131
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,5R,7S,8R,9R,10S,13R,14R,17S)-17-[(5R)-5,6-dihydroxy-6-methylhept-1-en-2-yl]-3-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-7-yl] benzoate 162846634 Click to see CC1(C(CCC2(C1CC(C3(C2CCC4C3(CCC4C(=C)CCC(C(C)(C)O)O)C)C)OC(=O)C5=CC=CC=C5)C)O)C 580.80 unknown https://doi.org/10.1002/HLCA.201000131
[17-(5,6-dihydroxy-6-methylhept-1-en-2-yl)-3-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-7-yl] benzoate 75576558 Click to see CC1(C(CCC2(C1CC(C3(C2CCC4C3(CCC4C(=C)CCC(C(C)(C)O)O)C)C)OC(=O)C5=CC=CC=C5)C)O)C 580.80 unknown https://doi.org/10.1002/HLCA.201000131
> Lipids and lipid-like molecules / Saccharolipids
(3S)-3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methoxy]pentanoic acid 163002544 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C(C=C2)O)OC)O)O)O)O 446.40 unknown https://doi.org/10.1080/10286020.2011.575068
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 1-hydroxysteroids
(3R,3aS,5aR,5bR,6R,7S,7aR,9S,11aR,11bR,12R,13aR,13bS)-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-6,7,9,12-tetrol 50900109 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)O)O)C)O)C)C 458.70 unknown https://doi.org/10.1002/HLCA.201000131
5a,5b,11a,13b-Tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-6,7,9,12-tetrol 75304283 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)O)O)C)O)C)C 458.70 unknown https://doi.org/10.1002/HLCA.201000131
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 6-hydroxysteroids
(7,9,12-Trihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl) benzoate 75576509 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)O)OC(=O)C6=CC=CC=C6)C)O)C)C 562.80 unknown https://doi.org/10.1002/HLCA.201000131
[(3R,3aS,5aR,5bR,6R,7S,7aR,9S,11aR,11bR,12R,13aR,13bS)-7,9,12-trihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl] benzoate 50900206 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)O)OC(=O)C6=CC=CC=C6)C)O)C)C 562.80 unknown https://doi.org/10.1002/HLCA.201000131
[(3R,3aS,5aR,5bR,6R,7S,7aR,9S,11aR,11bR,12S,13aR,13bS)-7,9,12-trihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl] benzoate 50900207 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)O)OC(=O)C6=CC=CC=C6)C)O)C)C 562.80 unknown https://doi.org/10.1002/HLCA.201000131
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
(12-Acetyloxy-7,9-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl) benzoate 75304284 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)O)OC(=O)C6=CC=CC=C6)C)OC(=O)C)C)C 604.80 unknown https://doi.org/10.1002/HLCA.201000131
(12-Acetyloxy-7,9-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl) hexanoate 75304285 Click to see CCCCCC(=O)OC1C(C2C(=C)C(CCC2(C3C1(C4(CCC5C(CCC5(C4CC3OC(=O)C)C)C(=C)C)C)C)C)O)O 598.90 unknown https://doi.org/10.1002/HLCA.201000131
(7-Acetyloxy-9-hydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-13-yl) benzoate 75576511 Click to see CC(=C)C1CCC2(C1CCC3(C2C(CC4C3(CC(C5C4(CCC(C5=C)O)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)C)C 588.80 unknown https://doi.org/10.1002/HLCA.201000131
(7-Acetyloxy-9,12-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl) benzoate 75576510 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)OC(=O)C)OC(=O)C6=CC=CC=C6)C)O)C)C 604.80 unknown https://doi.org/10.1002/HLCA.201000131
(9,13-Dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-7-yl) acetate 162913649 Click to see CC(=C)C1CCC2(C1CCC3(C2C(CC4C3(CC(C5C4(CCC(C5=C)O)C)OC(=O)C)C)O)C)C 484.70 unknown https://doi.org/10.1002/HLCA.201000131
[(3R,3aS,5aR,5bR,6R,7S,7aR,9S,11aR,11bR,12S,13aR,13bS)-7-acetyloxy-9,12-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl] benzoate 50900208 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)OC(=O)C)OC(=O)C6=CC=CC=C6)C)O)C)C 604.80 unknown https://doi.org/10.1002/HLCA.201000131
[(3R,3aS,5aR,5bR,6R,7S,7aR,9S,11aS,11bR,12R,13aR,13bS)-12-acetyloxy-7,9-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl] benzoate 50900110 Click to see CC(=C)C1CCC2(C1CCC3(C2CC(C4C3(C(C(C5C4(CCC(C5=C)O)C)O)OC(=O)C6=CC=CC=C6)C)OC(=O)C)C)C 604.80 unknown https://doi.org/10.1002/HLCA.201000131
[(3R,3aS,5aR,5bR,6R,7S,7aR,9S,11aS,11bR,12R,13aR,13bS)-12-acetyloxy-7,9-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-6-yl] hexanoate 50900111 Click to see CCCCCC(=O)OC1C(C2C(=C)C(CCC2(C3C1(C4(CCC5C(CCC5(C4CC3OC(=O)C)C)C(=C)C)C)C)C)O)O 598.90 unknown https://doi.org/10.1002/HLCA.201000131
[(3R,3aS,5aR,5bR,7R,7aR,9S,11aR,11bR,13R,13aR,13bS)-7-acetyloxy-9-hydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-13-yl] benzoate 50900209 Click to see CC(=C)C1CCC2(C1CCC3(C2C(CC4C3(CC(C5C4(CCC(C5=C)O)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)C)C 588.80 unknown https://doi.org/10.1002/HLCA.201000131
[(3R,3aS,5aR,5bR,7R,7aR,9S,11aR,11bR,13R,13aR,13bS)-9,13-dihydroxy-5a,5b,11a,13b-tetramethyl-8-methylidene-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-7-yl] acetate 102258955 Click to see CC(=C)C1CCC2(C1CCC3(C2C(CC4C3(CC(C5C4(CCC(C5=C)O)C)OC(=O)C)C)O)C)C 484.70 unknown https://doi.org/10.1002/HLCA.201000131
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 53348662 Click to see C=C(C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)O 326.30 unknown https://doi.org/10.1080/10286020.2011.575068
4-Hydroxy-3,5-dimethoxyphenyl beta-D-glucopyranoside; (-)-3,5-Dimethoxy-4-hydroxyphenyl beta-D-glucopyranoside 73981643 Click to see COC1=CC(=CC(=C1O)OC)OC2C(C(C(C(O2)CO)O)O)O 332.30 unknown https://doi.org/10.1080/10286020.2011.575068
Koaburaside 5318820 Click to see COC1=CC(=CC(=C1O)OC)OC2C(C(C(C(O2)CO)O)O)O 332.30 unknown https://doi.org/10.1080/10286020.2011.575068
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,5-Diprenyl-4-hydroxybenzaldehyde 71519781 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C=O)C 258.35 unknown https://doi.org/10.1080/10286020.2011.575068
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid 14132336 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown https://doi.org/10.1080/10286020.2011.575068
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown https://doi.org/10.1080/10286020.2011.575068
Glucosyringic acid 10383888 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1080/10286020.2011.575068
Syringic acid-4-beta-D-glucopyranoside 14132338 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1080/10286020.2011.575068

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