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Trillium tschonoskii

Trillium tschonoskii - 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 UUID644023f968f4b750525296
Scientific name Trillium tschonoskii
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 29: 218 (1883)

Description Top

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Synonyms Top

Scientific name Authority First published in
Trillium camschatcense var. tschonoskii (Maxim.) Vorosch. Florist. Issl. Razn. Raionakh SSSR : 159 (1985)
Trillium morii Hayata Icon. Pl. Formosan. 7: 41 (1918)
Trillium tschonoskii var. himalaicum H.Hara J. Jap. Bot. 44: 373. 1969
Trillium tschonoskii f. morii (Hayata) Yamam. J. Soc. Trop. Agric. 10: 177 1938
Trillium tschonoskii f. violaceum Makino Bot. Mag. (Tokyo) 27: 115 1913
Trillium tschonoskii var. cryptopetalum Makino Bot. Mag. (Tokyo) 24: 138. 1910
Trillium tschonoskii f. cryptopetalum (Makino) J.Samej. Acta Horti Gothob 25: 163 1962
Trillium tschonoskii var. atrorubens Miyabe & Tatew. Cont. Fl. N. Jap. 7: 190. 1936
Trillium tschonoskii var. morii (Hayata) Masam.

Common names Top

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Language Common/alternative name
Japanese シロバナエンレイソウ
Japanese ミヤマエンレイソウ
Chinese 头顶一颗珠
Chinese 延齡草
Chinese 延龄草

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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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
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Kuril Islands
      • Sakhalin
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000750326
Tropicos 18403561
KEW urn:lsid:ipni.org:names:542611-1
The Plant List kew-290543
Open Tree Of Life 594650
Observations.org 148571
NCBI Taxonomy 82502
IUCN Red List 18816841
IPNI 542611-1
iNaturalist 342870
GBIF 2742237
EPPO TLITS
EOL 1083216
Elurikkus 294255
USDA GRIN 40450

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
Non‐apoptotic regulated cell death mediates reprogramming of the tumour immune microenvironment by macrophages Sun C, Zhan J, Li Y, Zhou C, Huang S, Zhu X, Huang K J Cell Mol Med 23-Apr-2024
PMCID:PMC11037416
doi:10.1111/jcmm.18348
PMID:38652105
Natural products targeting autophagy and apoptosis in NSCLC: a novel therapeutic strategy Qin P, Li Q, Zu Q, Dong R, Qi Y Front Oncol 02-Apr-2024
PMCID:PMC11019012
doi:10.3389/fonc.2024.1379698
PMID:38628670
Radiation-Induced Intestinal Injury: Injury Mechanism and Potential Treatment Strategies Lu Q, Liang Y, Tian S, Jin J, Zhao Y, Fan H Toxics 10-Dec-2023
PMCID:PMC10747544
doi:10.3390/toxics11121011
PMID:38133412
Pyroptosis: shedding light on the mechanisms and links with cancers You HM, Wang L, Meng HW, Huang C, Fang GY, Li J Front Immunol 02-Nov-2023
PMCID:PMC10651733
doi:10.3389/fimmu.2023.1290885
PMID:38016064
On the Efficiency of the Density Functional Theory (DFT)-Based Computational Protocol for 1H and 13C Nuclear Magnetic Resonance (NMR) Chemical Shifts of Natural Products: Studying the Accuracy of the pecS-n (n = 1, 2) Basis Sets Rusakov YY, Semenov VA, Rusakova IL Int J Mol Sci 27-Sep-2023
PMCID:PMC10572908
doi:10.3390/ijms241914623
PMID:37834068
Total saponins from Trillium tschonoskii Maxim promote neurological recovery in model rats with post-stroke cognitive impairment Wang G, Tang X, Zhao F, Qin X, Wang F, Yang D, Zhu H, Chen X Front Pharmacol 07-Sep-2023
PMCID:PMC10513410
doi:10.3389/fphar.2023.1255560
PMID:37745057
Two 18‐norspirostane steroidal saponins as novel mitophagy enhancers improve Alzheimer's disease Qiu W, Yu L, He C, Wu J, Law BY, Yu C, Qin D, Zhou X, Wu A Clin Transl Med 01-Sep-2023
PMCID:PMC10474309
doi:10.1002/ctm2.1390
PMID:37658612
Steroidal Saponins: Naturally Occurring Compounds as Inhibitors of the Hallmarks of Cancer Bouabdallah S, Al-Maktoum A, Amin A Cancers (Basel) 31-Jul-2023
PMCID:PMC10417465
doi:10.3390/cancers15153900
PMID:37568716
Advances of the small molecule drugs regulating fibroblast-like synovial proliferation for rheumatoid arthritis Tong Y, Li X, Deng Q, Shi J, Feng Y, Bai L Front Pharmacol 21-Jul-2023
PMCID:PMC10400780
doi:10.3389/fphar.2023.1230293
PMID:37547337
Genome skimming as an efficient tool for authenticating commercial products of the pharmaceutically important Paris yunnanensis (Melanthiaceae) Zhou N, Tang L, Xie P, Miao K, Yang C, Liu H, Ji Y BMC Plant Biol 29-Jun-2023
PMCID:PMC10308783
doi:10.1186/s12870-023-04365-x
PMID:37380980
Protective Effect of Trillium tschonoskii Maxim Components Against Glutamate-Induced SH-SY5Y Cells Damage Through Regulating Apoptosis Li Y, Yue X, Wang S, Li P, Zhang M, Song K, Huang X, Li Z Dose Response 29-May-2023
PMCID:PMC10240882
doi:10.1177/15593258231169585
PMID:37283817
Role of pyroptosis in the pathogenesis and treatment of diseases Jin X, Ma Y, Liu D, Huang Y MedComm (2020) 25-Apr-2023
PMCID:PMC10130418
doi:10.1002/mco2.249
PMID:37125240
Structures, Sources, Identification/Quantification Methods, Health Benefits, Bioaccessibility, and Products of Isorhamnetin Glycosides as Phytonutrients Wang H, Chen L, Yang B, Du J, Chen L, Li Y, Guo F Nutrients 18-Apr-2023
PMCID:PMC10143801
doi:10.3390/nu15081947
PMID:37111165
Inhibiting Angiogenesis by Anti-Cancer Saponins: From Phytochemistry to Cellular Signaling Pathways Majnooni MB, Fakhri S, Ghanadian SM, Bahrami G, Mansouri K, Iranpanah A, Farzaei MH, Mojarrab M Metabolites 22-Feb-2023
PMCID:PMC10052344
doi:10.3390/metabo13030323
PMID:36984763
The Therapeutic Potential of Pyroptosis in Melanoma Zaffaroni N, Beretta GL Int J Mol Sci 09-Jan-2023
PMCID:PMC9861152
doi:10.3390/ijms24021285
PMID:36674798

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 / Benzoic acids and derivatives / Salicylic acid and derivatives
6,8-dihydroxy-3-(7-hydroxyheptyl)-3,4-dihydro-1H-isochromene-7-carboxylic acid 163063422 Click to see C1C(OCC2=C(C(=C(C=C21)O)C(=O)O)O)CCCCCCCO 324.40 unknown https://doi.org/10.1016/0031-9422(83)80233-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[(3S,6E)-2-hydroxy-2,6-dimethyl-10-methylidenedodeca-6,11-dien-3-yl]oxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162884372 Click to see CC(=CCCC(=C)C=C)CCC(C(C)(C)O)OC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O 562.60 unknown https://doi.org/10.1016/0031-9422(83)80233-7
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[(3R,6E)-2-hydroxy-2,6-dimethyl-10-methylidenedodeca-6,11-dien-3-yl]oxy-3-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate 162925518 Click to see CC(=CCCC(=C)C=C)CCC(C(C)(C)O)OC1C(C(C(C(O1)COC(=O)C)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 856.90 unknown https://doi.org/10.1016/0031-9422(83)80233-7
[4,5-Diacetyloxy-6-(2-hydroxy-2,6-dimethyl-10-methylidenedodeca-6,11-dien-3-yl)oxy-3-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate 162925517 Click to see CC(=CCCC(=C)C=C)CCC(C(C)(C)O)OC1C(C(C(C(O1)COC(=O)C)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 856.90 unknown https://doi.org/10.1016/0031-9422(83)80233-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(1R,3'S,4R,4'R,5'S,6S,7R,8R,12S,13R,14R,16R,20S)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3',4',16,20-tetrahydroxy-7-(hydroxymethyl)-5',13-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one 16655804 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4C(C=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)O)CO)C(C1O)O 1035.00 unknown https://doi.org/10.1248/CPB.55.679
(1R,3'S,4R,4'R,5'S,6S,7R,8R,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3',4',16-trihydroxy-7-(hydroxymethyl)-5',13-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one 102060368 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)CO)C(C1O)O 1019.00 unknown https://doi.org/10.1248/CPB.55.679
(1S,3'S,4R,4'S,5'S,6S,7R,8R,12R,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3',16-dihydroxy-7-(hydroxymethyl)-5',13-dimethyl-4'-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one 163098923 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)CO)C(C1OC1C(C(C(C(O1)C)O)O)O)O 1165.20 unknown https://doi.org/10.1039/C39820000789
[(1R,3'S,4R,4'S,5'S,6S,7R,8R,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5R,6S)-3,5-diacetyloxy-4-hydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-3',16-dihydroxy-7-(hydroxymethyl)-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-4'-yl] acetate 162988228 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)OC(=O)C)O)OC(=O)C)C)CO)C(C1OC(=O)C)O 880.90 unknown https://doi.org/10.1016/0031-9422(83)85061-4
[(1R,3'S,4R,4'S,5'S,6S,7R,8R,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3',16-dihydroxy-7-(hydroxymethyl)-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-4'-yl] acetate 163036847 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)OC(=O)C)OC(=O)C)OC(=O)C)C)CO)C(C1OC(=O)C)O 923.00 unknown https://doi.org/10.1016/0031-9422(83)85061-4
[(1S,3'S,4R,4'S,5'S,6S,7R,8R,12R,13R,14R,16R)-14-[(2S,3R,4S,5S)-5-acetyloxy-4-hydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3',4',16-trihydroxy-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-7-yl]methyl acetate 162908747 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)OC(=O)C)O)OC8C(C(C(C(O8)C)OC(=O)C)OC(=O)C)OC(=O)C)C)COC(=O)C)C(C1O)O 965.00 unknown https://doi.org/10.1016/S0031-9422(00)85524-7
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-4,5-dihydroxy-2-[(1R,3'S,4R,4'S,5'S,6S,7R,8R,12S,13R,14R,16R)-3',4',16-trihydroxy-7-(hydroxymethyl)-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-14-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 162881464 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)OC(=O)C)OC(=O)C)OC(=O)C)C)CO)C(C1O)O 880.90 unknown https://doi.org/10.1016/0031-9422(83)85061-4
[14-[3-(3,5-Diacetyloxy-4-hydroxy-6-methyloxan-2-yl)oxy-4,5-dihydroxyoxan-2-yl]oxy-3',16-dihydroxy-7-(hydroxymethyl)-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-4'-yl] acetate 162988227 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)OC(=O)C)O)OC(=O)C)C)CO)C(C1OC(=O)C)O 880.90 unknown https://doi.org/10.1016/0031-9422(83)85061-4
[14-[4,5-Dihydroxy-3-(3,4,5-triacetyloxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3',16-dihydroxy-7-(hydroxymethyl)-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-4'-yl] acetate 163036846 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)OC(=O)C)OC(=O)C)OC(=O)C)C)CO)C(C1OC(=O)C)O 923.00 unknown https://doi.org/10.1016/0031-9422(83)85061-4
[14-[5-Acetyloxy-4-hydroxy-3-(3,4,5-triacetyloxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3',4',16-trihydroxy-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-7-yl]methyl acetate 162908746 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)OC(=O)C)O)OC8C(C(C(C(O8)C)OC(=O)C)OC(=O)C)OC(=O)C)C)COC(=O)C)C(C1O)O 965.00 unknown https://doi.org/10.1016/S0031-9422(00)85524-7
[4,5-Diacetyloxy-6-[4,5-dihydroxy-2-[3',4',16-trihydroxy-7-(hydroxymethyl)-5',13-dimethyl-3-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-14-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 162881463 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)OC(=O)C)OC(=O)C)OC(=O)C)C)CO)C(C1O)O 880.90 unknown https://doi.org/10.1016/0031-9422(83)85061-4
14-[3-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3',16-dihydroxy-7-(hydroxymethyl)-5',13-dimethyl-4'-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one 163098922 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)CO)C(C1OC1C(C(C(C(O1)C)O)O)O)O 1165.20 unknown https://doi.org/10.1039/C39820000789
14-[3-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3',4',16,20-tetrahydroxy-7-(hydroxymethyl)-5',13-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one 73299306 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4C(C=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)O)CO)C(C1O)O 1035.00 unknown https://doi.org/10.1248/CPB.55.679
Trillenoside A 73319444 Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)CO)C(C1O)O 1019.00 unknown https://doi.org/10.1248/CPB.55.679
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S)-2-[[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxyoxan-3-yl] acetate 21676293 Click to see CC(=O)OC1C(C(COC1OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O 622.50 unknown https://doi.org/10.1016/0031-9422(83)80233-7
[2-[[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxyoxan-3-yl] acetate 73822540 Click to see CC(=O)OC1C(C(COC1OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O 622.50 unknown https://doi.org/10.1016/0031-9422(83)80233-7

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