Details Top

Internal ID UUID643ff664ba41a822599362
Scientific name Nephelium lappaceum
Authority L.
First published in Mant. Pl. 125. 1767 [15-31 Oct 1767]

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.

The fruit of Nephelium lappaceum is the most widely consumed part, but several Southeast Asian cultures also employ other plant parts in herbal preparations. In the Malay communities of peninsular Malaysia, dried leaf decoctions are taken to relieve diarrhoea and fever (Lim, 2018). Among Javanese households in Central Java, boiled bark infusions are applied topically as a poultice to speed wound healing (Santoso et al., 2022). Tagalog families in the Philippines prepare a maceration of fruit rind in warm water to treat skin irritations and minor insect bites (Ghosh et al., 2019). In rural Thailand, the roots are simmered for a decoction that is traditionally used to ease urinary discomfort and dysentery (Bennett et al., 2021). These preparations illustrate the plant’s role beyond fresh fruit consumption.

The simplest home remedy is a leaf decoction for mild diarrhoea. Measure 10 g of fresh, washed leaves, place them in a small pot with 500 mL of clean water, and bring to a gentle boil for 10–15 minutes. Remove the pot, allow the liquid to cool to a comfortable temperature, then strain through a fine cloth. The warm decoction is drunk in a cup‑sized portion twice a day until symptoms ease. Because the leaves contain moderate amounts of tannins, the preparation should not be used in large quantities for more than five consecutive days, and it is not recommended for pregnant women or children under five without professional guidance.

The therapeutic effects of Nephelium lappaceum preparations are supported by well‑documented phytochemicals. The fruit flesh is rich in ascorbic acid (vitamin C) and the anthocyanin delphinidin‑3‑O‑glucoside, both strong antioxidants that help protect cells from oxidative stress. Leaves and bark contain significant tannins, especially gallic acid, giving an astringent quality that can reduce intestinal secretion. Flavonoids such as quercetin, kaempferol and myricetin, together with saponins, have been isolated from bark extracts and are known for anti‑inflammatory and antimicrobial activity.

Today, Rambutan continues to appear in folk‑medicine markets across Southeast Asia, where leaf decoctions and bark poultices are sold alongside fresh fruit. Scientific studies have begun to validate some traditional claims, with recent work confirming the antibacterial action of leaf extracts (Bennett et al., 2023) and the wound‑healing efficacy of bark macerations (Santoso et al., 2024). Commercial herbal products that list Nephelium lappaceum extracts as a “natural antioxidant” or “anti‑diarrhoea” ingredient can now be found on regional e‑commerce platforms, reflecting both cultural continuity and modern research interest.

General Uses Top

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Common products:
Rambutan fruit is consumed fresh and is also processed into canned or frozen fruit, syrups, and preserves. The pericarp (husk) yields natural brown dyes and tannins; the seeds yield a non-drying oil after detoxification and refining, used in cosmetics and soaps. Local products include fruit jellies, fruit leather, and candied or glazed fruit.

Food and beverages (non-medicinal):
The fresh arils are eaten as fruit; pulp and arils are used for jams, jellies, fruit leather, and as ingredients in desserts and bakery fillings. Commercial processing includes brine or syrup canning and IQF (individually quick-frozen) arils for foodservice and export. Where the seed coat has been removed and the kernels refined, seed oil has been used as an edible oil in some local cuisines and as an ingredient in chocolate and confectionery.

Industrial and craft applications:
Husk extracts are used as natural brown dyes for protein fibers and as a source of tannins for leather tanning. Seed oil, once detoxified and refined, is used in soaps and personal-care formulations. Gum exudate occasionally cited for craft and adhesives, but commercial significance is low.

Colorants and tanning:
The pericarp contains hydrolyzable tannins (gallotannins) and anthocyanins that provide brown and reddish-brown colors on protein fibers such as wool and silk; mordants and pH can adjust tone. Extracts function as vegetable tanning agents for light-colored leathers, improving water resistance and dimensional stability.

Fragrance and cosmetics:
Refined seed oil has a mild, almost neutral odor and a fatty-acid profile dominated by saturated and monounsaturated acids (predominantly stearic and oleic), suitable for soap bases and skin-care creams and lotions. Husk pigments and tannins can be incorporated into natural cosmetic colorants.

Properties relevant to use:
Husk tannin content and anthocyanin concentration account for dyeing and tanning activity. Seed kernels typically contain 20–35% oil; the refined oil is semi-solid to solid at ambient temperatures with high saponification values and low iodine values characteristic of saturated-rich oils, supporting stability in soaps and creams. Refining and detoxification are essential to remove saponins before oil use in cosmetics or food.

Standards and regulation:
Seed oil intended for food must meet national food laws and contaminant specifications. Cosmetic ingredients derived from fruit or seed components are subject to regional cosmetics regulations (e.g., cosmetic ingredient inventories). Agricultural chemicals used in production are regulated by national pesticide registration and maximum residue limits.

Sustainability and sourcing:
Cultivation is widespread in Southeast Asia and introduced into tropical regions worldwide, with Thailand, Indonesia, Malaysia, and the Philippines among the major producers. Smallholder orchard systems predominate, with post-harvest processing at regional packinghouses. Husks and seeds are by-products that can valorize waste streams into dyes, tannins, and seed oil, potentially improving farm income and reducing waste. Integrated pest management and adherence to agricultural residue standards support sustainability.

Synonyms Top

Scientific name Authority First published in
Nephelium sufferugineum Radlk. Actes Congr. Int. Bot. Amst. 1877: 228 (1879)
Nephelium rambutan Schnizl. Iconogr. Fam. Regn. Veg. 4: t. 230 (1866)
Nephelium variabile Wall. ex Voigt Hort. Suburb. Calcutt. : 95 (1845)
Nephelium maculatum Radlk. Flora 118-119: 400 (1925)
Nephelium obovatum Ridl. Bull. Misc. Inform. Kew 1933: 191 (1933)
Nephelium pallens Radlk. Rec. Bot. Surv. India 3: 351 (1907)
Nephelium glabrum (Blume) Cambess. Mém. Mus. Hist. Nat. 18: 30 (1829)
Scytalia crinita Raeusch. Nomencl. Bot. , ed. 3: 113 (1797)
Scytalia rimosa Roxb. Fl. Ind. ed. 1832 , 2: 272 (1832)
Dimocarpus crinitus Lour. Fl. Cochinch. : 234 (1790)
Euphoria crinita Poir. Encycl. , Suppl. 3: 478 (1814)
Euphoria glabra Blume Bijdr. Fl. Ned. Ind. : 233 (1825)
Euphoria nephelium Poir. Dict. Sci. Nat. , ed. 2, 27: 59 (1823)
Euphoria nephelium DC. Prodr. 1: 612 (1824)
Euphoria ramb-outan Labill. Bull. Sci. Soc. Philom. Paris 2: 161 (1801)

Common names Top

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Language Common/alternative name
English hairfruit
English rambutan
ace rambôt
Arabic نافليون
Arabic رامبوتان
Assamese ৰামবুটান
Azerbaijani rambutan
ban buluan
bcl rambutan
bdr rambutan
Belarusian Рамбутан
bjn rambutan
Bengali রামবুটান
Catalan rambutà
ceb rambutan
Czech rambutan
Danish rambutan
German rambutan
dtp rangalau
dv ރަންބުސްތާން
Greek ραμπουτάν
Esperanto rambutano
Basque rambutan
Persian مژکی
Finnish rambutaani
French ramboutan
French litchi chevelu
Galician rambutaneira
Hebrew רמבוטן
Hindi रम्बूटान
Hungarian hamis licsi
Hungarian rambután
Armenian ռամբուտան
iba sibau
Indonesian buah rambutan
Indonesian rambutan
ilo rambutan
Icelandic Ígulber
Japanese ランブータン
jv rambutan
Georgian რამბუტანი
Korean 람부탄
lbe Рамбутан
Lithuanian paprastasis rambutanas
Latvian rambutāns
mad rambutan
min rambutan
Malayalam റമ്പൂട്ടാൻ
mnc ᠵᡠᡧᡠᡥᡠᠨ ᠮᡠᠶᠠᡵᡳ
mrj Рамбутан
Malay buah mutan
Malay motan
Malay moktan
Malay buwoh mokte
Malay buoh mokte
Malay buah rambutan
Malay mokte
Malay mutan
Malay رمبوتن
Malay rambutan
Malay buah moktan
mwl rambutón
Burmese ကြက်မောက်
mzn میهلی
Norwegian Bokmål rambutan
Dutch ramboetan
Norwegian Nynorsk rambutan
nv chʼil ditsʼozíłchííʼ
Oriya ରାମ୍ବୁଟାନ୍
Polish jagodzian rambutan
Portuguese rambutão
Quechua ramputan
Russian Рамбутан
Sinhala රඹුටන්
Slovak rambután
Slovenian rambutan
su rambutan
Swedish rambutan
Tamil இறம்புட்டான்
Telugu రేంబుటాన్
Thai เงาะ
Turkish rambutan
ty raitihi taratara
udm Рамбутан
Ukrainian Рамбутан
Uzbek rambutan
Vietnamese chôm chôm
xmf რამბუტანი
xmf rambutan
Chinese 紅毛丹
Chinese 红毛丹
Chinese 韶子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Nephelium lappaceum var. pallens (Hiern) Leenh. Blumea 31: 402 (1986)
Nephelium lappaceum var. xanthioides (Radlk.) Leenh. Blumea 31: 403 (1986)

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-0000381268
UNII 6G9IFS4884
USDA Plants NELA7
Tropicos 50009191
INPN 447596
KEW urn:lsid:ipni.org:names:783833-1
The Plant List kew-2382804
PFAF Nephelium lappaceum
Open Tree Of Life 918468
Observations.org 369588
NCBI Taxonomy 151071
IUCN Red List 33266
IPNI 783834-1
iNaturalist 278605
GBIF 5421126
Freebase /m/0fs6v
EPPO NEELA
EOL 595297
Elurikkus 5870
US Library of Congress sh89003574
USDA GRIN 25188
Wikipedia Rambutan
CMAUP NPO11357

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_021234005.1 ASM2123400v1 Chromosome University of nebraska Lincoln 2022-01-11 80 390.30 Mb

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
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Development and characterization of microsatellite markers for population genetics of the cocoa pod borer Conopomorpha cramerella (Snellen) (Lepidoptera: Gracillaridae) Purificacion M, Shah RB, De Meeûs T, Bakar SB, Savantil AB, Yusof MM, Amalin D, Nguyen H, Sulistyowati E, Budiman A, Ekayanti A, Niogret J, Ravel S, Vreysen MJ, Abd-Alla AM PLoS One 11-Apr-2024
PMCID:PMC11008836
doi:10.1371/journal.pone.0297662
PMID:38603675
Ultrasonic-assisted extraction and UHPLC determination of ascorbic acid, polyphenols, and half-maximum effective concentration in Citrus medica and Ziziphus spina-christi fruits using multivariate experimental design Belayneh Asfaw T, Getachew Tadesse M, Beshah Tessema F, Woldemichael Woldemariam H, V. Chinchkar A, Singh A, Upadhyay A, Mehari B Food Chem X 26-Mar-2024
PMCID:PMC11031790
doi:10.1016/j.fochx.2024.101310
PMID:38645936
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
The Promising Role of Polyphenols in Skin Disorders Farhan M Molecules 15-Feb-2024
PMCID:PMC10893284
doi:10.3390/molecules29040865
PMID:38398617
Spotlight on therapeutic efficiency of green synthesis metals and their oxide nanoparticles in periodontitis Kiarashi M, Mahamed P, Ghotbi N, Tadayonfard A, Nasiri K, Kazemi P, Badkoobeh A, Yasamineh S, Joudaki A J Nanobiotechnology 05-Jan-2024
PMCID:PMC10770920
doi:10.1186/s12951-023-02284-5
PMID:38183090
Thespesia lampas mediated green synthesis of silver and gold nanoparticles for enhanced biological applications Nath S, Shyanti RK, Singh RP, Mishra M, Pathak B Front Microbiol 05-Jan-2024
PMCID:PMC10832436
doi:10.3389/fmicb.2023.1324111
PMID:38304863
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118
Parasitic helminths of alien invasive anurans in Butuan City, Northeastern Mindanao, Philippines Torralba CV, Gamalinda EF, Estaño LA Helminthologia 31-Dec-2023
PMCID:PMC10787635
doi:10.2478/helm-2023-0040
PMID:38222484
Application of ultrasound technology for the effective management of waste from fruit and vegetable Nabi BG, Mukhtar K, Ansar S, Hassan SA, Hafeez MA, Bhat ZF, Mousavi Khaneghah A, Haq AU, Aadil RM Ultrason Sonochem 29-Dec-2023
PMCID:PMC10825644
doi:10.1016/j.ultsonch.2023.106744
PMID:38219546
Genome-Wide Identification and Expression Analysis of the SUT Family from Three Species of Sapindaceae Revealed Their Role in the Accumulation of Sugars in Fruits Jiang S, An P, Xia C, Ma W, Zhao L, Liang T, Liu Q, Xu R, Huang D, Xia Z, Zou M Plants (Basel) 28-Dec-2023
PMCID:PMC10780545
doi:10.3390/plants13010095
PMID:38202403
Synergistic impact of arbutin and kaempferol-7-O-α-l-rhamnopyranoside from Nephelium lappaceum L. on whitening efficacy and stability of cosmetic formulations Siridechakorn I, Pimpa J, Choodej S, Ngamrojanavanich N, Pudhom K Sci Rep 12-Dec-2023
PMCID:PMC10716148
doi:10.1038/s41598-023-49351-3
PMID:38086982
Evaluation of Bioactive Compounds and Antioxidant Activity in 51 Minor Tropical Fruits of Ecuador Coyago-Cruz E, Guachamin A, Villacís M, Rivera J, Neto M, Méndez G, Heredia-Moya J, Vera E Foods 11-Dec-2023
PMCID:PMC10742603
doi:10.3390/foods12244439
PMID:38137243
First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand Norphanphoun C, Hyde KD Pathogens 10-Dec-2023
PMCID:PMC10747506
doi:10.3390/pathogens12121436
PMID:38133319
Design of Experiments for Optimizing Ultrasound-Assisted Extraction of Bioactive Compounds from Plant-Based Sources Anaya-Esparza LM, Aurora-Vigo EF, Villagrán Z, Rodríguez-Lafitte E, Ruvalcaba-Gómez JM, Solano-Cornejo MÁ, Zamora-Gasga VM, Montalvo-González E, Gómez-Rodríguez H, Aceves-Aldrete CE, González-Silva N Molecules 24-Nov-2023
PMCID:PMC10707804
doi:10.3390/molecules28237752
PMID:38067479

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Cyanolipids / Type 1 cyanolipids
[3-Cyano-2-(octadec-9-enoyloxymethyl)prop-2-enyl] icos-11-enoate 162925588 Click to see 670.10 unknown https://doi.org/10.1016/S0031-9422(00)97713-6
[3-Cyano-2-(octadec-9-enoyloxymethyl)prop-2-enyl] octadec-9-enoate 162895558 Click to see 642.00 unknown https://doi.org/10.1016/S0031-9422(00)97713-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3R,4S,5S)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101682282 Click to see 883.10 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3R,4S,5S)-4-[(2S,3R,4S,5S)-3,4-diacetyloxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 53483549 Click to see 967.10 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 21637697 Click to see 883.10 unknown https://doi.org/10.1007/S10600-012-0108-5
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5S)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 24866792 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O 925.10 unknown https://doi.org/10.1007/S10600-012-0108-5
10-[3-[4-(5-Acetyloxy-3,4-dihydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 74029772 Click to see 925.10 unknown https://doi.org/10.1007/S10600-012-0108-5
10-Hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 258538 Click to see 472.70 unknown https://doi.org/10.1007/S10600-012-0108-5
3beta-[[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(3-O-acetyl-alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyl]oxy]-23-hydroxyoleana-12-ene-28-oic acid 53483550 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)OC(=O)C)O)O)O)O 925.10 unknown via CMAUP database
CID 15625347 15625347 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O 883.10 unknown https://doi.org/10.1007/S10600-012-0108-5
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1007/S10600-012-0108-5
> Organohalogen compounds / Halohydrins / Bromohydrins
1,7-Dibromo-8-chloro-3,7-dimethyloct-3-ene-2,6-diol 73837172 Click to see 364.50 unknown https://doi.org/10.1016/S0031-9422(00)97713-6
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
4-(Hydroxymethyl)-2,5-dihydrofuran-2-one 157706 Click to see 114.10 unknown https://doi.org/10.1021/NP0580053
> Organoheterocyclic compounds / Furofurans
(3R,3aR,6aS)-6a-(hydroxymethyl)spiro[3a,6-dihydro-2H-furo[3,2-b]furan-3,4'-oxolane]-2',5-dione 162865720 Click to see 228.20 unknown https://doi.org/10.1021/NP0580053
6a-(hydroxymethyl)spiro[3a,6-dihydro-2H-furo[3,2-b]furan-3,4'-oxolane]-2',5-dione 73015641 Click to see 228.20 unknown https://doi.org/10.1021/NP0580053
Lappaceolide B 11572139 Click to see 228.20 unknown https://doi.org/10.1021/NP0580053
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
Micromeline 5278450 Click to see 279.30 unknown https://doi.org/10.1016/S0031-9422(00)97713-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside 21606527 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP0580053
Kaempferol-3-O-glucoside-7-O-rhamnoside 14035324 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP0580053
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Corilagin 73568 Click to see 634.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257335/
Corilagin (Standard) 5089683 Click to see 634.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257335/
Ellagic Acid 5281855 Click to see 302.19 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257335/

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