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Tellima grandiflora

Tellima grandiflora - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fff332c394450386390
Scientific name Tellima grandiflora
Authority (Pursh) Douglas ex Lindl.
First published in Bot. Reg. 14: t. 1178. 1828 [Sep 1828]

Description Top

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Synonyms Top

Scientific name Authority First published in
Mitella grandiflora Pursh Fl. Amer. Sept. 1: 314 (1813)
Mitella acerifolia Schlecht. ex Ledeb. Fl. Ross. 2: 228 (1844)
Tellima nudicaulis Greene Pittonia 2: 162 (1891)
Tellima breviflora Rydb. N. Amer. Fl. 22: 90 (1905)
Tellima odorata Howell Fl. N.W. Amer. : 199 (1898)
Tellima grandiflora var. virescens Regel Index Seminum (LE, Petropolitanus) 1866: 100 (1867)

Common names Top

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Language Common/alternative name
English bigflower tellima

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.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Germany
    • Northern Europe
      • Denmark
      • Great Britain
      • Ireland
      • Norway
  • Northern America
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Subarctic America
      • Alaska
      • Aleutian Islands
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000459248
Canadensys 9310
USDA Plants TEGR2
Tropicos 29100773
INPN 125863
KEW urn:lsid:ipni.org:names:794860-1
The Plant List kew-2520992
Missouri Botanical Garden 286921
PFAF Tellima grandiflora
Open Tree Of Life 182588
Observations.org 17151
NCBI Taxonomy 29775
NBN Atlas NHMSYS0000464365
Nature Serve 2.152849
IPNI 794860-1
iNaturalist 51655
GBIF 3032698
Freebase /m/0dnh9t
EPPO TLLGR
EOL 583232
Calflora (Californian flora) 7931
USDA GRIN 448262

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
Rapid Detection of the Strawberry Foliar Nematode Aphelenchoides fragariae Using Recombinase Polymerase Amplification Assay with Lateral Flow Dipsticks Subbotin SA Int J Mol Sci 10-Jan-2024
PMCID:PMC10815920
doi:10.3390/ijms25020844
PMID:38255917
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Hydrolyzable tannins are incorporated into the endocarp during sclerification of the water caltrop Trapa natans Huss JC, Antreich SJ, Felhofer M, Mayer K, Eder M, Vieira Dias dos Santos AC, Ramer G, Lendl B, Gierlinger N Plant Physiol 10-Jul-2023
PMCID:PMC10762508
doi:10.1093/plphys/kiad408
PMID:37427803
Draft Genome Sequences of 9 Actinobacteria from the Family Microbacteriaceae Associated with Insect- and Nematode-Damaged Plants Tarlachkov SV, Ospennikov YV, Demidov AV, Starodumova IP, Dorofeeva LV, Prisyazhnaya NV, Chizhov VN, Subbotin SA, Evtushenko LI Microbiol Resour Announc 31-Aug-2022
PMCID:PMC9584284
doi:10.1128/mra.00487-22
PMID:36043868
Regulation of Plant Tannin Synthesis in Crop Species Mora J, Pott DM, Osorio S, Vallarino JG Front Genet 02-May-2022
PMCID:PMC9108539
doi:10.3389/fgene.2022.870976
PMID:35586570
Genomic evidence of an ancient inland temperate rainforest in the Pacific Northwest of North America Ruffley M, Smith ML, Espíndola A, Turck DF, Mitchell N, Carstens B, Sullivan J, Tank DC Mol Ecol 09-Apr-2022
PMCID:PMC9322681
doi:10.1111/mec.16431
PMID:35322900
Bioactive compounds, antioxidant and antimicrobial activities of extracts from different plant parts of two Ziziphus Mill. species Yahia Y, Benabderrahim MA, Tlili N, Bagues M, Nagaz K PLoS One 19-May-2020
PMCID:PMC7236975
doi:10.1371/journal.pone.0232599
PMID:32428000
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
Extreme diversification of floral volatiles within and among species of Lithophragma (Saxifragaceae) Friberg M, Schwind C, Guimarães PR Jr, Raguso RA, Thompson JN Proc Natl Acad Sci U S A 14-Feb-2019
PMCID:PMC6410829
doi:10.1073/pnas.1809007116
PMID:30765532
Chemical and Biological Significance of Oenothein B and Related Ellagitannin Oligomers with Macrocyclic Structure Yoshida T, Yoshimura M, Amakura Y Molecules 02-Mar-2018
PMCID:PMC6017083
doi:10.3390/molecules23030552
PMID:29498647
Biological screening of selected Pacific Northwest forest plants using the brine shrimp (Artemia salina) toxicity bioassay Karchesy YM, Kelsey RG, Constantine G, Karchesy JJ Springerplus 23-Apr-2016
PMCID:PMC4842189
doi:10.1186/s40064-016-2145-1
PMID:27186474
Parallel chemical switches underlying pollinator isolation in Asian Mitella Okamoto T, Okuyama Y, Goto R, Tokoro M, Kato M J Evol Biol 20-Feb-2015
PMCID:PMC4418413
doi:10.1111/jeb.12591
PMID:25615872
Towards an ontogenetic understanding of inflorescence diversity Claßen-Bockhoff R, Bull-Hereñu K Ann Bot 27-Feb-2013
PMCID:PMC3828942
doi:10.1093/aob/mct009
PMID:23445936
Analysis of Flavonoids from Eugenia uniflora Leaves and Its Protective Effect against Murine Sepsis Rattmann YD, de Souza LM, Malquevicz-Paiva SM, Dartora N, Sassaki GL, Gorin PA, Iacomini M Evid Based Complement Alternat Med 20-Dec-2012
PMCID:PMC3539388
doi:10.1155/2012/623940
PMID:23320032
Tannins of Constant Structure in Medicinal and Food Plants—Hydrolyzable Tannins and Polyphenols Related to Tannins Okuda T, Ito H Molecules 04-Mar-2011
PMCID:PMC6259616
doi:10.3390/molecules16032191

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 / 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/10.1016/0031-9422(75)85195-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162844175 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O 616.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[(2R,3R,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 94858131 Click to see C1=CC(=CC=C1C2=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)O 600.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[(2R,3R,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 162851080 Click to see C1=CC(=C(C=C1C2=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)O)O 616.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[(2R,3S,4R,5R,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162907331 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 632.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[(2R,3S,4R,5R,6S)-6-[6,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162979891 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=CC(=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 632.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[(2S,3R,4R,5S,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 10167601 Click to see C1=CC(=CC=C1C2=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)O 600.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[(2S,3R,4R,5S,6R)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 162913899 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/10.1016/0031-9422(75)85195-8
[(2S,3R,4S,5S,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162887513 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 600.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14055723 Click to see C1=CC(=C(C=C1C2=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)O)O 616.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162844174 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O 616.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14055725 Click to see C1=CC(=CC=C1C2=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)O 600.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162887512 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 600.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[6-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162907330 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 632.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
[6-[6,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162979890 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=CC(=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 632.50 unknown https://doi.org/10.1016/0031-9422(75)85195-8
3-(6-O-Galloyl-beta-D-glucopyranosyloxy)-3',4',5,5',7-pentahydroxyflavone 5319986 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/10.1016/0031-9422(75)85195-8
> Phenylpropanoids and polyketides / Tannins
galloyl(-2)[galloyl(-3)][galloyl(-4)][galloyl(-6)]Ido(b)-O-galloyl 129508735 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)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1016/S0031-9422(03)00280-2
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11S,12R,13S,15S)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxy-2-[[(10R,11R,12S,13S,15R)-3,4,21,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-5-yl]oxy]benzoate 162962634 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)OC8=C(C(=C(C=C8C(=O)OC9C(C1C(COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)OC9OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O 1875.30 unknown https://doi.org/10.1016/S0031-9422(03)00280-2
[(10S,11S,12S,13R,15S)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-12,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 154497559 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1016/S0031-9422(03)00280-2
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 5153915 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1016/S0031-9422(00)89087-1
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxy-2-[[3,4,21,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-5-yl]oxy]benzoate 16170937 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)OC8=C(C(=C(C=C8C(=O)OC9C(C1C(COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)OC9OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O 1875.30 unknown https://doi.org/10.1016/S0031-9422(03)00280-2
1-Desgalloyleugeniin 9918701 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1016/S0031-9422(00)89087-1
CID 11766372 11766372 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1039/B006270G
cornusiin E 91820328 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)OC8=C(C(=C(C=C8C(=O)OC9C(C1C(COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)OC9OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O 1875.30 unknown https://doi.org/10.1016/S0031-9422(03)00280-2
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.013
https://doi.org/10.1016/S0031-9422(00)89087-1
https://doi.org/10.1016/S0031-9422(03)00280-2
https://doi.org/10.1039/B006270G
Tellimagrandin II 151590 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.013
https://doi.org/10.1016/S0031-9422(00)89087-1

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