Details Top

Internal ID UUID643fecc59b0a2219670535
Scientific name Serenoa repens
Authority (W.Bartram) Small
First published in J. New York Bot. Gard. 27: 193 (1926)

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 Muscogee (Creek) and Seminole peoples of the Florida Gulf coast and lower Southeast, dried saw palmetto fruits have long been taken as an aqueous infusion for urinary support and as a general tonic. James Moerman’s Native American Ethnobotany records root decoctions used as a tonic and diuretic among these and other groups; in the southeastern coastal plain, Moerman also notes that the fruit has been infused for “irritation of the urinary passages.” Earlier work by William Bartram, who described the palms he encountered in late eighteenth‑century Florida, is often cited in later ethnobotanical summaries as the baseline observation of fruit consumption by local peoples. In modern ethnobotanical compilations, saw palmetto’s fruits are repeatedly mentioned in these cultural contexts as soothing infusions for the urinary tract, though the plant’s broader ceremonial or material uses (fronds, cordage, thatching) are not the focus here.

One practical recipe is a mild tea from dried fruit. Place 10–12 g of dried, crushed saw palmetto berries in a small pot with 250 ml of cold water, bring to a simmer, then cover and steep off heat for 10–15 minutes; strain and drink one cup once or twice daily for several weeks as needed. Because sweetened preparations can be comforting for urinary irritation, you may add a small amount of honey after straining. If you have gallstone symptoms, kidney stones, or are on anticoagulant medication, consult a qualified practitioner before using saw palmetto; pregnant or nursing individuals should avoid unprescribed preparations.

Well‑established constituents reported for Serenoa repens fruit include free fatty acids (especially lauric, myristic, palmitic, and oleic acids), fixed oils rich in these acids, β‑sitosterol and other phytosterols, and minor volatile compounds; these are the constituents most consistently associated with contemporary extracts of the species and are the basis for commercial standardization. Contemporary research continues to evaluate saw palmetto extracts for their effects on lower urinary tract symptoms, and standardized products remain widely available as dietary supplements.

General Uses Top

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Common products:
Saw palmetto produces a fixed oil and CO2/ethanolic extracts from the ripe fruit that are used as flavoring substances in foods and beverages; these are listed by FEMA (Flavor and Extract Manufacturers Association) as GRAS materials.

Food and beverages (non-medicinal):
FEMA-listed fruit extracts from Serenoa repens are employed as flavor components in beverages (including alcoholic mixes), confectionery, baked goods, and dairy analogs, where they provide distinctive fatty/roasted notes. The materials are used at low flavor levels in finished formulations and are covered under the US FDA food additive regulations for flavoring substances.

Fragrance and cosmetics:
Saw palmetto fruit extracts are used in fine fragrances, soaps, and detergents as fragrance ingredients. The materials are listed by the International Fragrance Association (IFRA) and thus subject to IFRA Standards on composition, purity, and safe use. The extracts function as fixatives and blending components due to their non-volatile fatty composition, contributing smooth, resinous notes to fragrance accords. Their fatty-acid-rich composition and stability profile support these applications.

Properties relevant to use:
The fixed oil is high in saturated fatty acids (predominantly lauric and myristic) with minor medium-chain fatty acids, conferring oxidatively stable, emollient properties that aid fixative performance in fragrance and blending in flavor systems. The CO2 and ethanol extracts contain lipophilic fractions of fruit lipids that retain characteristic flavor/odor profiles suitable for low-use-rate applications.

Standards and regulation:
FEMA GRAS listings provide the recognized regulatory basis for use of S. repens fruit extracts as flavoring substances. IFRA Standards govern the use of these extracts in fragrance and cosmetic products, including limits and ingredient transparency requirements. Food use is subject to the US FDA’s general provisions for flavoring substances.

Sustainability and sourcing:
Commercial supply is derived primarily from wild-harvested fruit in the southeastern United States. Wild collection can exert pressure on local populations; industry practices generally include collection from readily available stands, exclusion of protected habitats, and adherence to regional conservation guidelines. Sustainable supply depends on monitoring harvest intensity and supporting habitat protection measures.

Synonyms Top

Scientific name Authority First published in
Sabal serrulata Schult.f. Syst. Veg. 7: 1486 (1830)
Serenoa serrulata (Michx.) Hook.f. Index Kew. 2: 884 1895
Brahea serrulata H.Wendl. Palmiers : 235 (1878)
Serenoa repens f. glauca Moldenke Phytologia 14: 326 (1967)
Chamaerops serrulata Michx. Fl. Bor.-Amer. 1: 239 (1803)
Corypha obliqua W.Bartram Travels Carolina : 61 (1791)
Corypha repens W.Bartram Travels Carolina : 61 (1791)
Diglossophyllum serrulatum (Michx.) H.Wendl. ex Salomon Hamburger Garten- Blumenzeitung 31: 162 (1875)
Serenoa serrulata (Michx.) G.Nicholson Rep. Progr. Condition Roy. Gard. Kew 1882: 64. 1884
Diglossophyllum serrulatum (Michx.) H.Wendl. ex Drude Bull. Soc. Tosc. Ortic. 14: 337 1889
Diglossophyllum serrulatum (Michx.) Schaedtler Hamburger Garten- Blumenzeitung 31: 162 (1875)

Common names Top

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Language Common/alternative name
English silver saw palmetto
English sabal serrulata
English saw palmetto
English scrub palmetto
Spanish diglossophyllum
Spanish diglossophyllum serrulatum
Spanish serenoa serrulata
Spanish sabal serrulata
Spanish chamaerops serrulata
Spanish corypha repens
Spanish serenoa repens f. glauca
Spanish corypha obliqua
Spanish brahea serrulata
Arabic نخل قصير
Arabic بلميط منشاري
Catalan sàbal
German sabal serrulata
German sägepalme
Persian نخلک ارهای
French sabal dealbata
Hebrew דקל ננסי
Croatian sabal serrulata
Hungarian fűrészpálma
Indonesian saw palmetto
Japanese ノコギリパルメット
Japanese ノコギリヤシ
Lithuanian serenoja
Lithuanian gulsčioji serenoja
Macedonian сереноја
Polish palma sabałowa
Polish palma sabalowa
Polish bocznia piłkowana
Romanian saw palmetto
Russian Сереноя
Russian Сереноа
Russian Сереноа ползучая
Russian Сереноя ползучая
Thai ปาล์มเลื้อย
Turkish cüce palmiye
Ukrainian Сереноа
Chinese 锯棕
Chinese 锯叶棕
Chinese 鋸棕櫚
Chinese 鉅棕櫚果
Chinese 鋸葉棕櫚
Chinese 鋸葉棕

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Northern America
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
      • Mississippi
      • South Carolina

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000309573
UNII 487DXM62F2
Florida Plant Atlas 2664
Flora of Alabama 3821
USDA Plants SERE2
Tropicos 2400863
INPN 770985
KEW urn:lsid:ipni.org:names:941782-1
The Plant List kew-190787
Open Tree Of Life 71637
Observations.org 409152
NCBI Taxonomy 4722
Nature Serve 2.139448
IPNI 941782-1
iNaturalist 83102
GBIF 2735055
Freebase /m/02r6fj
FEIS plants/shrub/serrep
EPPO SERRE
EOL 1130738
Elurikkus 231147
US Library of Congress sh85117780
USDA GRIN 103108
Wikipedia Serenoa

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
Exploring the mechanism of action of the combination of cinnamon and motherwort in the treatment of benign prostatic hyperplasia: A network pharmacology study Yang J, Ma D, Zhao Z, Guo J, Ren K, Wang F, Guo J Medicine (Baltimore) 26-Apr-2024
PMCID:PMC11049697
doi:10.1097/MD.0000000000037902
PMID:38669415
Saffron extract as an emerging novel therapeutic option in reproduction and sexual health: recent advances and future prospectives Goyal A, Raza FA, Sulaiman SA, Shahzad A, Aaqil SI, Iqbal M, Javed B, Pokhrel P Ann Med Surg (Lond) 04-Apr-2024
PMCID:PMC11060205
doi:10.1097/MS9.0000000000002013
PMID:38694315
A Narrative Review of Herbal Remedies for Managing Hirsutism Ghanbarian R, Ranjbai M, Babaeian M, Mazaheri M Int J Prev Med 28-Mar-2024
PMCID:PMC11074955
doi:10.4103/ijpvm.ijpvm_62_23
PMID:38715699
Medicinal plants and natural products for treating overactive bladder Chen H, Hoi MP, Lee SM Chin Med 27-Mar-2024
PMCID:PMC10967063
doi:10.1186/s13020-024-00884-3
PMID:38532487
Effects of a proprietary mixture of extracts from Sabal serrulata fruits and Urtica dioica roots (WS® 1541) on prostate hyperplasia and inflammation in rats and human cells Sens-Albert C, Weisenburger S, König BC, Melcher SF, Scheyhing UA, Rollet K, Lluel P, Koch E, Lehner MD, Michel MC Front Pharmacol 15-Mar-2024
PMCID:PMC10979176
doi:10.3389/fphar.2024.1379456
PMID:38560358
An overview of pharmacological effects of Crocus sativous and its constituents Saadat S, Ghasemi Z, Memarzia A, Behrouz S, Aslani MR, Boskabady MH Iran J Basic Med Sci 01-Jan-2024
PMCID:PMC10897555
doi:10.22038/IJBMS.2023.73410.15950
PMID:38419885
Pharmacological Approaches in Managing Symptomatic Relief of Benign Prostatic Hyperplasia: A Comprehensive Review O'Quin C, White KL, Campbell JR, Myers SH, Patil S, Chandler D, Ahmadzadeh S, Varrassi G, Shekoohi S, Kaye AD Cureus 30-Dec-2023
PMCID:PMC10823302
doi:10.7759/cureus.51314
PMID:38288222
Complementary and alternative supplements: a review of dermatologic effectiveness for androgenetic alopecia Ufomadu P Proc (Bayl Univ Med Cent) 20-Dec-2023
PMCID:PMC10761108
doi:10.1080/08998280.2023.2263829
PMID:38174012
The use of beta-sitosterol for the treatment of prostate cancer and benign prostatic hyperplasia Macoska JA Am J Clin Exp Urol 15-Dec-2023
PMCID:PMC10749388
PMID:38148931
Medicinal Herbs: Promising Immunomodulators for the Treatment of Infectious Diseases Alanazi HH, Elasbali AM, Alanazi MK, El Azab EF Molecules 12-Dec-2023
PMCID:PMC10745476
doi:10.3390/molecules28248045
PMID:38138535
Recommendations of apex health bodies remain localized: not in conformity with international implementation policy for urological disorders Goyal SK, Bansal R, Gupta V, Bansal C, Bansal P Lancet Reg Health Southeast Asia 28-Nov-2023
PMCID:PMC10794104
doi:10.1016/j.lansea.2023.100330
PMID:38234703
Safety profile of herbal medicines submitted for marketing authorization in Tanzania: a cross-sectional retrospective study Mssusa AK, Holst L, Kagashe G, Maregesi S J Pharm Policy Pract 20-Nov-2023
PMCID:PMC10658996
doi:10.1186/s40545-023-00661-x
PMID:37986124
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
Relationship of the SITLESS intervention on medication use in community-dwelling older adults: an exploratory study Viegas R, Alves da Costa F, Mendes R, Deidda M, McIntosh E, Sansano-Nadal O, Magaña JC, Rothenbacher D, Denkinger M, Caserotti P, Tully MA, Roqué-Figuls M, Giné-Garriga M Front Public Health 16-Nov-2023
PMCID:PMC10687584
doi:10.3389/fpubh.2023.1238842
PMID:38035303
Oral and Topical Administration of a Standardized Saw Palmetto Oil Reduces Hair Fall and Improves the Hair Growth in Androgenetic Alopecia Subjects – A 16-Week Randomized, Placebo-Controlled Study Sudeep HV, Rashmi S, Jestin TV, Richards A, Gouthamchandra K, Shyamprasad K Clin Cosmet Investig Dermatol 11-Nov-2023
PMCID:PMC10648974
doi:10.2147/CCID.S435795
PMID:38021422

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonadecane 12401 Click to see 268.50 unknown https://doi.org/10.1021/BK-2002-0803.CH009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1021/BK-2002-0803.CH009
https://doi.org/10.1016/S0944-7113(11)80030-9
https://doi.org/10.1016/0021-9673(95)00734-2
https://doi.org/10.1002/(SICI)1097-0045(199605)28:5<300::AID-PROS5>3.0.CO;2-F
https://doi.org/10.1016/S0896-8446(01)00110-3
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1002/(SICI)1097-0045(199605)28:5<300::AID-PROS5>3.0.CO;2-F
https://doi.org/10.1016/S0944-7113(11)80030-9
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1016/0021-9673(95)00734-2
https://doi.org/10.1021/BK-2002-0803.CH009
https://doi.org/10.1002/(SICI)1097-0045(199605)28:5<300::AID-PROS5>3.0.CO;2-F
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1021/BK-2002-0803.CH009
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
Tridecanoic acid 12530 Click to see 214.34 unknown https://doi.org/10.1016/S0944-7113(11)80030-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1016/S0944-7113(11)80030-9
https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1016/0021-9673(95)00734-2
Hexanoic Acid 8892 Click to see 116.16 unknown https://doi.org/10.1021/BK-2002-0803.CH009
https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1016/0021-9673(95)00734-2
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.1002/(SICI)1097-0045(199605)28:5<300::AID-PROS5>3.0.CO;2-F
https://doi.org/10.1021/BK-2002-0803.CH009
https://doi.org/10.1016/0021-9673(95)00734-2
https://doi.org/10.1016/S0944-7113(11)80030-9
https://doi.org/10.1016/S0896-8446(01)00110-3
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1016/0021-9673(95)00734-2
https://doi.org/10.1021/BK-2002-0803.CH009
https://doi.org/10.1016/S0896-8446(01)00110-3
Undecanoic Acid 8180 Click to see CCCCCCCCCCC(=O)O 186.29 unknown https://doi.org/10.1016/0021-9673(95)00734-2
https://doi.org/10.1016/S0944-7113(11)80030-9
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Elaidolinolenic acid 5282822 Click to see 278.40 unknown https://doi.org/10.1016/S0944-7113(11)80030-9
https://doi.org/10.1016/S0896-8446(01)00110-3
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0944-7113(11)80030-9
https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1021/BK-2002-0803.CH009
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1016/S0944-7113(11)80030-9
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
(2R)-2,3-dihydroxypropyl dodecanoate 71598538 Click to see 274.40 unknown https://doi.org/10.1021/NP960552O
(2R)-2,3-Dihydroxypropyl tetradecanoate 71598539 Click to see 302.40 unknown https://doi.org/10.1021/NP960552O
Glyceryl Myristate 79050 Click to see 302.40 unknown https://doi.org/10.1021/NP960552O
Monolaurin 14871 Click to see 274.40 unknown https://doi.org/10.1021/NP960552O
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] dodecanoate 15086444 Click to see CCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 597.00 unknown https://doi.org/10.1002/ARDP.19893220211
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] tetradecanoate 13828705 Click to see 625.10 unknown https://doi.org/10.1002/ARDP.19893220211
[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] tetradecanoate 13828703 Click to see 625.10 unknown https://doi.org/10.1002/ARDP.19893220211
beta-Sitosterol palmitate 13747834 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown https://doi.org/10.1002/ARDP.19893220211
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown https://doi.org/10.1002/ARDP.19893220211
Stigmast-5-en-3-yl dodecanoate 319317 Click to see CCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 597.00 unknown https://doi.org/10.1002/ARDP.19893220211
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1002/ARDP.19893220211
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(tridecoxymethyl)oxane-3,4,5-triol 163034156 Click to see CCCCCCCCCCCCCOCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 759.20 unknown https://doi.org/10.1002/ARDP.19893220211
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl decanoate 162850671 Click to see CCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 731.10 unknown https://doi.org/10.1002/ARDP.19893220211
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1002/ARDP.19893220211
2-[[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(tridecoxymethyl)oxane-3,4,5-triol 163034155 Click to see 759.20 unknown https://doi.org/10.1002/ARDP.19893220211
2-[[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(undecoxymethyl)oxane-3,4,5-triol 162845267 Click to see 731.10 unknown https://doi.org/10.1002/ARDP.19893220211
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/ARDP.19893220211
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/ARDP.19893220211
sitosteryl-6'-O-undecane-beta-D-glucoside 162845268 Click to see 731.10 unknown https://doi.org/10.1002/ARDP.19893220211
ST 29:1;O;Hex;FA 10:0 162850669 Click to see 731.10 unknown https://doi.org/10.1002/ARDP.19893220211
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1080/10826079408013609
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1002/ARDP.19893220211
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1002/ARDP.19893220211
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1002/ARDP.19893220211
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1002/ARDP.19893220211
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1002/ARDP.19893220211
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1002/ARDP.19893220211
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin-7-O-neohesperidoside 5459217 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/ARDP.19893220211
Rhoifolin 5282150 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/ARDP.19893220211

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