Serenoa repens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Serenoa repens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

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

Description Top

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Serenoa repens, also known as saw palmetto, is a small palm tree found in the subtropical and tropical regions of the Southeastern United States. It is a slow-growing and long-lived plant, with some specimens estimated to be 500-700 years old. The leaves are fan-shaped and have sharp teeth or spines, giving the plant its common name. Saw palmetto is an important food source for wildlife and has been used as a food source by humans in the past. It has also been studied for its potential medical benefits, particularly in treating prostate cancer and urinary tract symptoms. Indigenous groups have used saw palmetto for various purposes, including thatching and treating fish poisoning.

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)

Common names Top

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Language Common/alternative name
English silver saw palmetto
English scrub palmetto
English saw palmetto
Spanish diglossophyllum
Spanish diglossophyllum serrulatum
Arabic نخل قصير
Arabic بلميط منشاري
Catalan sàbal
German sägepalme
Persian نخلک ارهای
French sabal dealbata
Hebrew דקל ננסי
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
Romanian saw palmetto
Russian Сереноа
Russian Сереноа ползучая
Russian Сереноя ползучая
Russian Сереноя
Thai ปาล์มเลื้อย
Turkish cüce palmiye
Ukrainian Сереноа
Chinese 锯棕
Chinese 鉅棕櫚果
Chinese 鋸葉棕櫚
Chinese 锯叶棕
Chinese 鋸棕櫚
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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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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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

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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
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
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
Effect of St. John’s Wort (Hypericum perforatum L.) on Male Sexual and Reproductive Health: A Narrative Review Alzahrani MA, Ofisan SB, Alshumaymiri NI, Alghuwainem M, Altamimi M, Alali AY, Rabie M, AboSkena AK, Almaymuni K, Almannie R, Binsaleh S Biomedicines 16-Oct-2023
PMCID:PMC10604084
doi:10.3390/biomedicines11102800
PMID:37893173
Drug-induced immune hemolytic anemia: detection of new signals and risk assessment in a nationwide cohort study Maquet J, Lafaurie M, Michel M, Lapeyre-Mestre M, Moulis G Blood Adv 04-Oct-2023
PMCID:PMC10874903
doi:10.1182/bloodadvances.2023009801
PMID:37782770
Statistical optimization, characterization, antioxidant and antibacterial properties of silver nanoparticle biosynthesized by saw palmetto seed phenolic extract Abdel-Aty AM, Barakat AZ, Bassuiny RI, Mohamed SA Sci Rep 20-Sep-2023
PMCID:PMC10511706
doi:10.1038/s41598-023-42675-0
PMID:37731031
Two New Components from an Association of Marine Sponges Poecillastra sp. and Jaspis sp. and Their Inhibitory Effects on Biomarkers for Benign Prostatic Hyperplasia Hwang BS, Lee S, Jeong EJ, Rho JR Mar Drugs 14-Sep-2023
PMCID:PMC10532625
doi:10.3390/md21090491
PMID:37755104
mTOR signaling in hair follicle and hair diseases: recent progress Tu W, Cao YW, Sun M, Liu Q, Zhao HG Front Med (Lausanne) 04-Sep-2023
PMCID:PMC10506410
doi:10.3389/fmed.2023.1209439
PMID:37727765
Tomato lipidic extract plus selenium decrease prostatic hyperplasia, dihydrotestosterone and androgen receptor expression versus finasteride in rats Arias-Chávez DJ, Mailloux-Salinas P, Ledesma-Aparicio J, Campos-Pérez E, Medina-Campos ON, Pedraza-Chaverri J, Bravo G World J Urol 02-Sep-2023
PMCID:PMC10582118
doi:10.1007/s00345-023-04558-x
PMID:37659980
Botanical drugs for treating erectile dysfunction: clinical evidence Xu D, Zhang Y, Bai J, Yuan H, Wang T, Liu J, Song W, Ma D Front Pharmacol 16-Aug-2023
PMCID:PMC10467024
doi:10.3389/fphar.2023.1232774
PMID:37654605
Effects of Supplementation with the Standardized Extract of Saffron (affron®) on the Kynurenine Pathway and Melatonin Synthesis in Rats De la Fuente Muñoz M, Román-Carmena M, Amor S, García-Villalón ÁL, Espinel AE, González-Hedström D, Granado García M Antioxidants (Basel) 16-Aug-2023
PMCID:PMC10451224
doi:10.3390/antiox12081619
PMID:37627614
A Review on the Impact of Oxidative Stress and Medicinal Plants on Leydig Cells Monageng E, Offor U, Takalani NB, Mohlala K, Opuwari CS Antioxidants (Basel) 04-Aug-2023
PMCID:PMC10451682
doi:10.3390/antiox12081559
PMID:37627554
Fire management effects on ruminal digestibility and in vitro methane emissions of subtropical rangeland plant species Cardoso AS, Silveira ML, Vendramini JM, Moriel P, Kohmann MM, Silva HM, Izquierdo V, Lima LO, Lage Filho NM, Silva JV, Sanchez JM Transl Anim Sci 18-Jul-2023
PMCID:PMC10464713
doi:10.1093/tas/txad080
PMID:37649644

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 CCCCCCCCCCCCCCCCCCC 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 CCCCCCCCCCCCCC(=O)O 228.37 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
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
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 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 CCCCCCCCCCCCCCCC(=O)O 256.42 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
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 CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
Tridecanoic acid 12530 Click to see CCCCCCCCCCCCC(=O)O 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
Caproic Acid 8892 Click to see CCCCCC(=O)O 116.16 unknown https://doi.org/10.1021/BK-2002-0803.CH009
https://doi.org/10.1016/0021-9673(95)00734-2
https://doi.org/10.1016/S0896-8446(01)00110-3
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1016/0021-9673(95)00734-2
https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1016/S0944-7113(11)80030-9
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
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
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 CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/S0896-8446(01)00110-3
https://doi.org/10.1016/S0944-7113(11)80030-9
Octadeca-9,12,15-trienoic acid 5282822 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/S0944-7113(11)80030-9
https://doi.org/10.1016/S0896-8446(01)00110-3
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
(2r)-2,3-Dihydroxypropyl Dodecanoate 71598538 Click to see CCCCCCCCCCCC(=O)OCC(CO)O 274.40 unknown https://doi.org/10.1021/NP960552O
2,3-Dihydroxypropyl dodecanoate 14871 Click to see CCCCCCCCCCCC(=O)OCC(CO)O 274.40 unknown https://doi.org/10.1021/NP960552O
2,3-Dihydroxypropyl tetradecanoate 79050 Click to see CCCCCCCCCCCCCC(=O)OCC(CO)O 302.40 unknown https://doi.org/10.1021/NP960552O
3-Myristoyl-sn-glycerol 71598539 Click to see CCCCCCCCCCCCCC(=O)OCC(CO)O 302.40 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
[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 CCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 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
Stigmasta-5-ene-3beta-ol myristate 13828705 Click to see CCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 625.10 unknown https://doi.org/10.1002/ARDP.19893220211
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(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,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-(undecoxymethyl)oxane-3,4,5-triol 162845268 Click to see CCCCCCCCCCCOCC1C(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
[(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 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
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 CCCCCCCCCCCOCC1C(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
24-Ethylcholest-5-en-3beta-ol 22012 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
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 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
ST 29:1;O;Hex;FA 10:0 162850669 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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 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-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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)O)O)O)O)O 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1002/ARDP.19893220211
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1002/ARDP.19893220211
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 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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