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Sabal palmetto

Sabal palmetto - 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 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]

Description Top

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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

Common names Top

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Language Common/alternative name
English cabbage palmetto
English common palmetto
English cabbage palm
English palmetto
English blue palmetto
English cabbage-palm
English carolina palmetto
English swamp cabbage
English palmetto palm
Spanish cabbage palmetto
Spanish palma cana
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
Vietnamese cọ bắp cải
Chinese 巴尔麦棕榈
Chinese 菜棕

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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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

Suggest others/fix!
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
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
Forest Loss is Accelerating Along the US Gulf Coast McCarthy MJ, Dimmitt B, DiGeronimo S, Muller-Karger FE Estuaries Coast 09-Sep-2021
PMCID:PMC8940792
doi:10.1007/s12237-021-01000-6
PMID:35401066
Digging Up the Roots: Taxonomic and Phylogenetic Disentanglements in Corticiaceae s.s. (Corticiales, Basidiomycota) and Evolution of Nutritional Modes Ghobad-Nejhad M, Langer E, Nakasone K, Diederich P, Nilsson RH, Rajchenberg M, Ginns J Front Microbiol 25-Aug-2021
PMCID:PMC8425454
doi:10.3389/fmicb.2021.704802
PMID:34512580
Projected Status of the Ghost Orchid (Dendrophylax lindenii) in Florida during the Next Decade Based on Temporal Dynamic Studies Spanning Six Years Mújica EB, Herdman AR, Danaher MW, González EH, Zettler LW Plants (Basel) 31-Jul-2021
PMCID:PMC8401884
doi:10.3390/plants10081579
PMID:34451624

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 COC1=CC(=CC(=C1O)OC)C(=O)O 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 CCC(C)(CCC(C)C1CCC2(C1(CCC3C2CCC(C34CCC(=O)O4)C(=C)C)C)C)C(=C)C 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 CCC(C)(CCC(C)C1CCC2(C1(CCC3C2CCC(C34CCC(=O)O4)C(=C)C)C)C)C(=C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
(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 CCC(C)(CCC(C)C1CCC2(C1(CCC3C2CCC(C34CCC(=O)O4)C(=C)C)C)C)C(=C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.02.026
Sablacaurin B 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
Squalene 638072 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 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 COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CO 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 CCC(C)C(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Urolithin C 60198001 Click to see C1=CC2=C(C=C1O)OC(=O)C3=CC(=C(C=C23)O)O 244.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
4-Epibileucofisetinidin 102115501 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O 562.50 unknown via CMAUP database
4'-Epibileucofisetinidin 102115500 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O 562.50 unknown via CMAUP database
Bileucofisetinidin 101297694 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O 562.50 unknown via CMAUP database
Epirobinetinidol-(4beta,8)-catechin 51042196 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
Fisetinidol-(4A8)-catechin 14332862 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
Fisetinidol-(4alpha,6)-gallocatechin 51041987 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 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 C1C(C(OC2=C(C(=C(C(=C21)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)C6C(C(OC7=C6C=CC(=C7)O)C8=CC(=C(C(=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O 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 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
Robinetinidol-(4beta-8)-catechin 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
Robinetinidol-(4beta-8)-gallocatechin 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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
2alpha-(3,4,5-Trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3alpha,7-diol 101846310 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
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 C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown via CMAUP database
Robinetin 5281692 Click to see C1=CC2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O 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 COC1=C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 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 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)O)O)O 484.40 unknown via CMAUP database

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