Details Top

Internal ID UUID643feb7460f8f570861700
Scientific name Sabal palmetto
Authority (Walter) Lodd. ex Schult.f.
First published in Syst. Veg., ed. 15 bis [Roemer & Schultes] 7(2): 1487. 1830 [Oct-Dec 1830]

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.

Among the Seminole people of Florida, an infusion of Sabal palmetto root or root bark was taken for fever and urinary complaints (according to Morton, 1981; Austin, 2014). On the Caribbean island of St. Lucia, a decoction of the bark was used for coughs, colds, and to “strengthen the kidneys” (B. Adams, ethnobotanical compendia cited by Morton, 1981). On the Caribbean coast of Colombia, healers prepared a leaf infusion or decoction for indigestion and colic in infants (Gupta, 1995). In southern Colombia, traditional healers also used a leaf infusion or decoction for stomach pains (Ballentine, 1999). These preparations—warm water infusions, longer decoctions, and occasional poultices of fresh leaf—match the typical ethnobotanical patterns for palms used as gentle internal carminatives and urinary demulcents (Morton, 1981).

A practical recipe that reflects these historic approaches is a mild leaf infusion. Measure 3–4 fresh leaves (roughly 10–15 g of torn leaf material), add to 500 ml of just-boiled water, cover and steep for 15–20 minutes, then strain. Drink up to one cup daily as tolerated. Alternatively, a bark decoction can be prepared by simmering 10 g of bark in 500 ml of water for 20–30 minutes, cooling, and straining; limit to 250 ml per day and discontinue if stomach upset occurs. There are no well‑documented toxicities, but medical guidance should be sought by pregnant or nursing individuals and by anyone using blood‑pressure or anticoagulant medications.

Sabal palmetto contains significant amounts of lauric, myristic, and oleic acids, as well as phytosterols including beta‑sitosterol, campesterol, and stigmasterol; these unsaturated fatty acids and sterols plausibly account for the gentle emollient and anti‑inflammatory actions reported in historic use (Chevallier, 1996). Tannins in the bark may contribute to any astringent effects noted for urinary applications (Leung & Foster, 1996).

Modern relevance is modest but clear: Sabal remains a culturally important palm in the southeastern United States and the Caribbean, where small‑scale domestic use and ethnobotanical documentation continue, while North America also sees commercial production of standardized extracts (Austin, 2014).

General Uses Top

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Common products:
Timber and poles from mature trunk wood for coastal and marine structures, utility poles, docks/wharves, and general construction framing and flooring. Leaves and fibers (bast) have been used for broom bristles, thatch, basketry, and coarse brushes.

Wood and fiber:
The palm stem yields a coarse timber used in structures subject to abrasion and saltwater exposure, as well as for poles and piles. Leaf bases yield a flexible, water-tolerant bast fiber exploited in traditional brushes and thatch; fiber bundles may be mechanically processed (separated and bundled) for brooms and brushes.

Properties relevant to use:
The wood has naturally high silica and tannins that contribute to decay and insect resistance, making it suitable for exterior and marine service without heavy preservation; density and lignification are adequate for load-bearing use in poles and heavy timber. Leaf bast fibers are strong and flexible, suited for coarse brush and thatch applications.

Standards and regulation:
Softwood and hardwood timber grading rules apply to palm timber in commercial trade; for preservative-treated poles and pilings, American Wood Protection Association (AWPA) standards for utility poles (e.g., Category P) and marine pilings are relevant. Structural grading and labeling follow US Department of Commerce standards for dimension lumber and timbers (DOC PS 20).

Sustainability and sourcing:
Sabal palmetto is widely distributed in the southeastern United States and is managed as a minor timber species in hurricane-prone coastal regions; local harvesting from natural stands and managed landscapes occurs, with impacts limited by the species’ relatively slow growth but abundant presence across private and public coastal habitats.

Synonyms Top

Scientific name Authority First published in
Inodes blackburniana (Schult. & Schult.f.) O.F.Cook Bull. Torrey Bot. Club 28(10): 531. 1901 [26 Oct 1901] (blackburniana)
Inodes palmetto O.F.Cook Bull. Torrey Bot. Club 28: 532 (1901)
Inodes schwarzii O.F.Cook Bull. Torrey Bot. Club 28: 532 (1901)
Sabal bahamensis (Becc.) L.H.Bailey Gentes Herbarum 6: 417 (1944)
Sabal jamesiana Small J. New York Bot. Gard. 28: 182 (1927)
Sabal palmetto var. bahamensis Becc. Webbia 2: 38 (1907)
Sabal parviflora Becc. Webbia 2: 43 (1908)
Sabal schwarzii Becc. Webbia 2: 39 (1908)
Sabal viatoris L.H.Bailey Gentes Herbarum 6: 403 (1944)
Sabal blackburniana Schult. & Schult.f. Syst. Veg., ed. 15 bis 7: 1488 (1830)
Chamaerops palmetto (Walter) Michx. Fl. Bor.-Amer. 1: 206 (1803)
Corypha palmetto Walter Fl. Carol. : 119 (1788)
Sabal blackburniana Glazebr. Gard. Mag. & Reg. Rural Domest. Improv. 5: 52, tt. 10-13. 1829 : use S. blackburnia
Corypha umbraculifera Jacq. Fragm. Bot. 12 (1800)

Common names Top

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Language Common/alternative name
English cabbage palmetto
English palmetto palm
English cabbage palm
English palmetto
English blue palmetto
English cabbage-palm
English carolina palmetto
English common palmetto
English swamp cabbage
Spanish palma cana
Spanish sabal viatoris
Spanish sabal schwarzii
Spanish sabal parviflora
Spanish sabal jamesiana
Spanish sabal blackburniana
Spanish sabal bahamensis
Spanish inodes schwarzii
Spanish inodes palmetto
Spanish inodes blackburniana
Spanish corypha palmetto
Spanish chamaerops palmetto
Spanish cabbage palmetto
Arabic نخيل سابال
Arabic نخيل بالميتو
Arabic سبال نخيلي
Arabic سابال بالمتو
Czech palma sabalová
German palmettopalme
Persian نخل کلمی
Finnish isopalmetto
French palmier des sables
Hebrew סבל פלמטו
Hungarian közönséges szabalpálma
Japanese パルメットヤシ
Japanese キューバサバル
Turkish lahana palmiyesi
Vietnamese cọ bắp cải
Chinese 菜棕
Chinese 巴尔麦棕榈

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000299302
Florida Plant Atlas 639
Flora of Alabama 3819
USDA Plants SAPA
Tropicos 2400614
INPN 119733
KEW urn:lsid:ipni.org:names:1004566-2
The Plant List kew-181053
PFAF Sabal palmetto
PaleoBotany 8678
Open Tree Of Life 452735
Observations.org 104704
NCBI Taxonomy 54447
Nature Serve 2.149842
IUCN Red List 87709255
IPNI 669727-1
iNaturalist 123481
GBIF 4925538
Freebase /m/02r89t
FEIS plants/tree/sabpal
EPPO SABPA
EOL 1131507
Elurikkus 6985
US Library of Congress sh97001494
USDA GRIN 32594
Wikipedia Sabal_palmetto
CMAUP NPO25479

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
Palm Fungi and Their Key Role in Biodiversity Surveys: A Review Pereira DS, Phillips AJ J Fungi (Basel) 19-Nov-2023
PMCID:PMC10672035
doi:10.3390/jof9111121
PMID:37998926
How Poor Is Aphyllophoroid Fungi Diversity in the Boreal Urban Greenhouses of Eastern Europe? Shiryaev AG, Zmitrovich IV, Senator SA, Minogina EN, Tkachenko OB J Fungi (Basel) 17-Nov-2023
PMCID:PMC10672352
doi:10.3390/jof9111116
PMID:37998921
DNA degradation in Haplaxius crudus (Hemiptera: Cixiidae) and Diaphorina citri (Hemiptera: Liviidae) on yellow sticky traps in Florida Bloch M, Mou DF, Helmick EE, Pelz-Stelinski K, Bahder BW J Insect Sci 06-Oct-2023
PMCID:PMC10558400
doi:10.1093/jisesa/iead083
PMID:37802925
Identification of Green-Leaf Volatiles Released from Cabbage Palms (Sabal palmetto) Infected with the Lethal Bronzing Phytoplasma Ferreira JA, Ramos JA, Dutra DR, Di Lella B, Helmick EE, Queiroz SC, Bahder BW Plants (Basel) 30-May-2023
PMCID:PMC10255706
doi:10.3390/plants12112164
PMID:37299142
Volatile-Based Diagnosis for Pathogenic Wood-Rot Fungus Fulvifomes siamensis by Electronic Nose (E-Nose) and Solid-Phase Microextraction/Gas Chromatography/Mass Spectrometry Tan JY, Zhang Z, Izzah HJ, Fong YK, Lee D, Mutwil M, Hong Y Sensors (Basel) 06-May-2023
PMCID:PMC10181603
doi:10.3390/s23094538
PMID:37177742
A Metagenomic Survey of Wood Decay Fungi in the Urban Trees of Singapore Hong Y, Tan JY, Xue H, Chow ML, Ali M, Ng A, Leong A, Yeo J, Koh SM, Tang MS, Lee YY, Choong AM, Lee SM, Delli Ponti R, Chan PM, Lee D, Wong JY, Mutwil M, Fong YK J Fungi (Basel) 10-Apr-2023
PMCID:PMC10145048
doi:10.3390/jof9040460
PMID:37108914
Arecaceae Seeds Constitute a Healthy Source of Fatty Acids and Phenolic Compounds Rincón-Cervera MÁ, Lahlou A, Chileh-Chelh T, Lyashenko S, López-Ruiz R, Guil-Guerrero JL Plants (Basel) 04-Jan-2023
PMCID:PMC9867020
doi:10.3390/plants12020226
PMID:36678939
Responses of Caribbean Mangroves to Quaternary Climatic, Eustatic, and Anthropogenic Drivers of Ecological Change: A Review Rull V Plants (Basel) 13-Dec-2022
PMCID:PMC9786987
doi:10.3390/plants11243502
PMID:36559614
Multi-Target Mechanisms of Phytochemicals in Alzheimer’s Disease: Effects on Oxidative Stress, Neuroinflammation and Protein Aggregation Sharifi-Rad J, Rapposelli S, Sestito S, Herrera-Bravo J, Arancibia-Diaz A, Salazar LA, Yeskaliyeva B, Beyatli A, Leyva-Gómez G, González-Contreras C, Gürer ES, Martorell M, Calina D J Pers Med 15-Sep-2022
PMCID:PMC9500804
doi:10.3390/jpm12091515
PMID:36143299
Seasonal variation in space use and territoriality in a large mammal (Sus scrofa) Schlichting PE, Boughton RK, Anderson W, Wight B, VerCauteren KC, Miller RS, Lewis JS Sci Rep 07-Mar-2022
PMCID:PMC8901613
doi:10.1038/s41598-022-07297-y
PMID:35256629
Dung beetle community composition affects dung turnover in subtropical US grasslands Stanbrook R, King JR Ecol Evol 22-Feb-2022
PMCID:PMC8861836
doi:10.1002/ece3.8660
PMID:35228864
Ecological thresholds under atmospheric nitrogen deposition for 1200 herbaceous species and 24 communities across the US Wilkins K, Clark C, Aherne J Glob Chang Biol 17-Jan-2022
PMCID:PMC9770646
doi:10.1111/gcb.16076
PMID:34986509
Airborne ascospore discharge with co‐dispersal of attached epihymenial algae in some foliicolous lichens Sanders WB, Brisky BJ Am J Bot 10-Jan-2022
PMCID:PMC9303868
doi:10.1002/ajb2.1778
PMID:34636414
Mosquito Communities Vary across Landscape and Vertical Strata in Indian River County, Florida Giordano BV, Cruz A, Pérez-Ramos DW, Ramos MM, Tavares Y, Caragata EP Pathogens 03-Dec-2021
PMCID:PMC8708810
doi:10.3390/pathogens10121575
PMID:34959530
Assessment of Inoculation Methods of Thielaviopsis paradoxa (De Seynes) Höhn into Oil Palm Seedlings under Greenhouse Conditions Gaitán-Chaparro S, Navia-Rodríguez E, Romero HM J Fungi (Basel) 27-Oct-2021
PMCID:PMC8621855
doi:10.3390/jof7110910
PMID:34829199

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,3aR,5aS,6S,7S,9aR,9bS)-3-[(2R,5R)-5-ethyl-5,6-dimethylhept-6-en-2-yl]-3a,9b-dimethyl-7-prop-1-en-2-ylspiro[1,2,3,4,5,5a,7,8,9,9a-decahydrocyclopenta[a]naphthalene-6,5'-oxolane]-2'-one 162951094 Click to see 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
(3R,3aR,5aS,6S,7S,9aR,9bS)-3-[(2R,5S)-5-ethyl-5,6-dimethylhept-6-en-2-yl]-3a,9b-dimethyl-7-prop-1-en-2-ylspiro[1,2,3,4,5,5a,7,8,9,9a-decahydrocyclopenta[a]naphthalene-6,5'-oxolane]-2'-one 162951096 Click to see 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
(3R,3aR,5aS,6S,7S,9aR,9bS)-3-[(2R)-5-ethyl-5,6-dimethylhept-6-en-2-yl]-3a,9b-dimethyl-7-prop-1-en-2-ylspiro[1,2,3,4,5,5a,7,8,9,9a-decahydrocyclopenta[a]naphthalene-6,5'-oxolane]-2'-one 101735594 Click to see CCC(C)(CCC(C)C1CCC2(C1(CCC3C2CCC(C34CCC(=O)O4)C(=C)C)C)C)C(=C)C 468.80 unknown via CMAUP database
(6Z,10E,14Z,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene 25244109 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
3-(5-Ethyl-5,6-dimethylhept-6-en-2-yl)-3a,9b-dimethyl-7-prop-1-en-2-ylspiro[1,2,3,4,5,5a,7,8,9,9a-decahydrocyclopenta[a]naphthalene-6,5'-oxolane]-2'-one 85435485 Click to see 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
Squalene 638072 Click to see 410.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Di-O-Methylcrenatin 10736338 Click to see 346.33 unknown via CMAUP database
Isotachioside 15098566 Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown via CMAUP database
Multifidol glucoside 14412552 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Urolithin C 60198001 Click to see 244.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 102115501 Click to see 562.50 unknown via CMAUP database
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 101297694 Click to see 562.50 unknown via CMAUP database
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 102115500 Click to see 562.50 unknown via CMAUP database
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 102400061 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
(2R,3S)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 102400062 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown via CMAUP database
Epirobinetinidol-(4beta,8)-catechin 51042196 Click to see 578.50 unknown via CMAUP database
Fisetinidol-(4A8)-catechin 14332862 Click to see 562.50 unknown via CMAUP database
Fisetinidol-(4alpha,6)-gallocatechin 51041987 Click to see 578.50 unknown via CMAUP database
Fisetinidol-(4alpha,8)-catechin 11731408 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 562.50 unknown via CMAUP database
Robinetinidol-(4alpha->8)-catechin-(6->4alpha)-robinetinidol 442689 Click to see 866.80 unknown via CMAUP database
Robinetinidol-(4alpha,8)-catechin 70697937 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Robinetinidol-(4alpha,8)-gallocatechin 70697956 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
5-[(2R,3R)-3,7-dihydroxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,2,3-triol 101846310 Click to see 290.27 unknown via CMAUP database
Robinetinidol 12314983 Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC(=C(C(=C3)O)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Butin 92775 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
ent-Epifisetinidol-4beta-ol 44257142 Click to see 290.27 unknown via CMAUP database
Fisetinidol-4alpha-ol 164762 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown via CMAUP database
Robinetin 5281692 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
4'-O-methylrobinetinidol 3'-O-beta-D-glucopyranoside 51041986 Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C3C(CC4=C(O3)C=C(C=C4)O)O)O 466.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Fisetin 3-methyl ether 9839293 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Fisetin tetramethyl ether 631171 Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C=C3)OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database

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