Details Top

Internal ID UUID643ff3f3bc4bb840305203
Scientific name Luffa aegyptiaca
Authority Mill.
First published in Gard. Dict. ed. 8 : s.p. (1768)

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 Mapuche of southern Chile, people steep the mature leaves in hot water as a simple, mildly bitter tea used for fevers and to promote sweating (Bennett, 2020). In the Caribbean and parts of southern Mexico and Central America, traditional healers prepare a decoction of the seeds or leaf bases and drink it as a diuretic and to “open the kidneys,” while poultices of the fresh leaves are applied to reduce inflammation of hemorrhoids and minor skin swellings (Morton, 1981; Paulig, 1973). Across Southeast Asia, where the ridged gourd (Luffa aegyptiaca) is common, infusions or warm water extracts of the fruit pulp are taken as a mild tonic for urinary complaints and to cool the body in hot climates (Trillo et al., 2010; Politi et al., 2018). In western Africa, healers also report using the seeds or immature fruits in aqueous preparations for coughs and asthma, sometimes adding a small amount of honey to the infusion (Wong & Lee, 1999).

A practical preparation is a mild “leaf tea” based on Chilean practice. Roughly 10–15 g of fresh young leaves are added to 250–300 ml of freshly boiled water, covered, and steeped for 5–8 minutes. The liquid is strained and taken in small cups over the day. The same method can be done with mature leaves; increase the steep to 8–12 minutes for a stronger brew. Do not exceed 2–3 cups per day unless advised by a practitioner. Safety notes: there is limited human data; avoid in pregnancy and while nursing unless a qualified practitioner recommends it. Because the raw fruit and seeds contain cucurbitacins that can be irritating at high doses, use only the leaves and keep to moderate, short-term doses; discontinue if you notice stomach upset or allergic reaction.

The leaves and fruit of Luffa aegyptiaca contain well-documented constituents that plausibly support the traditional activities. These include flavonoids such as quercetin and kaempferol; chlorogenic acid and related phenolic acids; triterpenes including cucurbitacins; sterols such as β‑sitosterol; and the polysaccharide pectin. These groups are broadly recognized for anti‑inflammatory, diuretic, and antioxidant actions, and they help explain the historical use of aqueous extracts for fever relief, urinary comfort, and topical soothing.

Today, ridged‑gourd leaves and immature fruits remain available as seasonal market vegetables in many regions, while a niche market for prepared “sponge gourd leaf tea” has emerged in parts of Asia and Latin America. Recent phytochemical surveys continue to profile the plant’s flavonoids and phenolic acids, confirming the chemical basis for its long‑standing use as a cooling, diuretic tonic (Politi et al., 2018; Trillo et al., 2010).

General Uses Top

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Common products:
The mature fruit yields a dried, fibrous vascular network that is used as a natural sponge for bathing and household cleaning. The same form is used as a gentle abrasive or scrubbing pad in culinary and industrial cleaning.

Food and beverages (non-medicinal):
Young, immature fruits are consumed as a vegetable, typically prepared by slicing or stir-frying in Southeast Asian and South Asian cuisines. The edible product is marketed as “luffa” or “angled loofah,” similar to other gourds.

Colorants and tanning:
Chromogenic compounds present in leaves and fruits produce brown to yellow natural dyes suitable for protein fibers such as wool and silk, traditionally used as adjunct colorants.

Wood and fiber:
The dried vascular skeleton (loofah “fiber”) consists mainly of cellulose with lignin cross-linking, conferring stiffness and resilience. It is used as a biodegradable filler and reinforcement in polymer composites, molded panels, acoustic and vibration damping mats, packaging cushioning, and biodegradable mulch films. The fiber’s absorbency and open-cell structure support these applications; no standardized fiber property values are reported in the referenced sources.

Fragrance and cosmetics:
The loofah sponge is used as an exfoliating and lathering implement in body cleansers and bath accessories, where its coarse-textured surface facilitates mechanical removal of dead skin.

Properties relevant to use:
The loofah skeleton’s high cellulose content, lignin cross-links, open-porosity, and mechanical resilience give it a balance of flexibility and durability for cleaning and composite uses. Natural pigments (e.g., flavonoids) enable colorant applications on protein fibers.

Standards and regulation:
Loofah sponges are regulated as household and cosmetic accessories; finished products sold as “bath sponges” or “cleaning sponges” must meet general consumer product safety requirements in their destination markets. Young gourds marketed as food are subject to national food-stdards for fresh produce (e.g., general market authorization, labeling, and phytosanitary controls as applicable).

Sustainability and sourcing:
Mature fruits are field-dried and mechanically processed, requiring little energy and no chemical pulping. Loofah sponges are biodegradable and can replace synthetic scrubbing pads, potentially reducing petroleum-based polymer use. Production occurs in tropical and subtropical regions; however, quantitative life-cycle or yield data are not established in the available references.

Synonyms Top

Scientific name Authority First published in
Luffa subangulata Miq. Fl. Ned. Ind. 1(1): 667 (1856)
Luffa sylvestris Miq. Fl. Ned. Ind. 1(1): 666 (1856)
Luffa petola Ser. Prodr. 3: 303 (1828)
Luffa leucosperma M.Roem. Fam. Nat. Syn. Monogr. 2: 63 (1846)
Luffa pentandra Roxb. Fl. Ind. ed. 1832 , 3: 712 (1832)
Luffa fricatoria Sessé & Moc. Fl. Mexic. , ed. 2: 227 (1894)
Luffa insularum A.Gray U.S. Expl. Exped., Phan. 1: 644 (1854)
Luffa aegyptiaca var. peramara F.M.Bailey Syn. Queensl. Fl. , Suppl. 3: 29 (1890)
Momordica carinata Vell. Fl. Flumin. 10: t. 97 (1831)
Momordica reticulata Salisb. Prodr. Stirp. Chap. Allerton : 158 (1796)
Momordica luffa L. Sp. Pl. : 1009 (1753)
Poppya fabiana K.Koch Berliner Allg. Gartenzeitung 1857: 60 (1857)
Turia cordata J.F.Gmel. Syst. Nat. ed. 13[bis] : 403 (1791)
Turia cylindrica J.F.Gmel. Syst. Nat. ed. 13[bis] : 403 (1791)
Bryonia cheirophylla Wall. Numer. List : n.º 6715A (1832)
Luffa cylindrica var. insularum (A.Gray) Cogn. Monogr. Phan. 3: 459 (1881)
Melothria touchanensis H.Lév. Fl. Kouy-Tchéou : 122 (1914)

Common names Top

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Language Common/alternative name
English momordica cylindrica
English cucurbita luffa
English sponge gourd
English luffa pentandra
English momordica luffa
Arabic لوف
bcl patola
bho नेनुआ
Bambara kolanfu
Bengali ধুন্দল
Bengali ধুঁদুল
Catalan carabassera d'esponja
cdo chó̤
Czech lufa válcovitá
dag gbandɔrigu
German loofah
German schwammkürbis
German schwammgurke
German schwamm-gurke
German gurkenschwamm
Esperanto spongokukurbo
Estonian ruljas käsnkõrvits
Persian لیف
Finnish pesusienikurkku
French courge éponge
hak chhoi-koâ
Hindi घेवड़ा
Upper Sorbian lufa
Indonesian blustru
Indonesian belustru
Indonesian bestru
Japanese ヘチマ
jv bestru
kge hurung jawa
Korean 수세미오이
mad ghâluddru
mnc ᠮᡝᡳᡥᡝᡨᡠ ᡥᡝᠩᡴᡝ
Marathi घोसाळी
Marathi घोसाळे
Marathi चोपडे दोडके
Marathi घोसावळे
Marathi गिलके
Malay petola bulat
Burmese သပွတ်ပင်
Dutch sponskomkommer
Dutch zeefkomkommer
Dutch ninwa
Dutch nenwa
Polish trukwa egipska
Russian Люффа египетская
sat ᱡᱷᱤᱸᱜᱟ.
shn ၶိူဝ်းမၢၵ်ႇမူပ်ႇ
shn မၢၵ်ႇယုမ်ႁႆ
shn မၢၵ်ႇမူပ်ႇ
Serbian Луфа
su bulustru
Tamil பீர்க்கு
Tamil பீர்கங்காய்
Tamil பீரம்
tay tmi
Tonga fanguʻakumā
Urdu گھیا توری
Vietnamese mướp hương
za swhgvah
Chinese 水瓜
Chinese 天罗水
Chinese 丝瓜藤
Chinese 丝瓜蒂
Chinese 丝瓜花
Chinese 丝瓜络
Chinese 丝瓜皮
Chinese 丝瓜根
Chinese 丝瓜子胃
Chinese 丝瓜子
Chinese 丝瓜叶
Chinese 絲瓜
Chinese 丝瓜

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-0000358882
UNII 38U11Z9E92
Florida Plant Atlas 178
USDA Plants LUAE
Tropicos 9200543
INPN 630065
Flora of Italy 11564
KEW urn:lsid:ipni.org:names:293060-1
Missouri Botanical Garden 364305
Open Tree Of Life 955527
Observations.org 198766
NCBI Taxonomy 3670
Nature Serve 2.132476
IPNI 105320-3
GBIF 2874599
Freebase /m/0464j9p
EOL 487006
USDA GRIN 22788
Wikipedia Luffa_aegyptiaca
CMAUP NPO1551
EOL 52202223
PFAF Luffa aegyptiaca

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_017139565.1 ASM1713956v1 Chromosome Vegetable Research Institute, Guangdong Academy of Agricultural Sciences 2021-03-09 100 625.64 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
Risk assessment of Retithrips syriacus for the EU Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, 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, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
Analyzing genetic diversity in luffa and developing a Fusarium wilt-susceptible linked SNP marker through a single plant genome-wide association (sp-GWAS) study Li YD, Liu YC, Jiang YX, Namisy A, Chung WH, Sun YH, Chen SY BMC Plant Biol 22-Apr-2024
PMCID:PMC11034075
doi:10.1186/s12870-024-05022-7
PMID:38644483
A review of the melliferous flora of Yucatan peninsula, Mexico, on the basis for the honey production cycle Zúñiga-Díaz D, Cetzal-Ix W, López-Castilla H, Noguera-Savelli E, Tamayo-Cen I, Martínez-Puc JF, Basu SK J Ethnobiol Ethnomed 25-Mar-2024
PMCID:PMC10964660
doi:10.1186/s13002-024-00681-0
PMID:38528551
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Determining soil conservation strategies: Ecological risk thresholds of arsenic and the influence of soil properties Huang Y, Zhang N, Ge Z, Lv C, Zhu L, Ding C, Liu C, Peng P, Wu T, Wang Y Eco Environ Health 12-Mar-2024
PMCID:PMC11061221
doi:10.1016/j.eehl.2024.02.007
PMID:38693960
Removing Heavy Metals: Cutting-Edge Strategies and Advancements in Biosorption Technology Staszak K, Regel-Rosocka M Materials (Basel) 01-Mar-2024
PMCID:PMC10934587
doi:10.3390/ma17051155
PMID:38473626
Comparative efficacy of non-electric cooling techniques to reduce nutrient solution temperature for the sustainable cultivation of summer vegetables in open-air hydroponics Nisar MM, Mahmood R, Tayyab S, Anees M, Nadeem F, Bibi S, Waseem F, Ahmed N, Li J, Zhao S Front Plant Sci 01-Mar-2024
PMCID:PMC10940466
doi:10.3389/fpls.2024.1340641
PMID:38495367
Microbiome structure variation and soybean’s defense responses during flooding stress and elevated CO2 Coffman L, Mejia HD, Alicea Y, Mustafa R, Ahmad W, Crawford K, Khan AL Front Plant Sci 08-Feb-2024
PMCID:PMC10882081
doi:10.3389/fpls.2023.1295674
PMID:38389716
Correction: He et al. Biology, Ecology and Management of Tephritid Fruit Flies in China: A Review. Insects 2023, 14, 196 He Y, Xu Y, Chen X Insects 31-Jan-2024
PMCID:PMC10889426
doi:10.3390/insects15020093
PMID:38392559
The complete chloroplast genome sequence of Thladiantha nudiflora Hemsl. ex F.B.Forbes & Hemsl. 1887 (Cucurbitaceae) Zhao YY, Chen MM, Duan BL, Xie QZ, Miao Q Mitochondrial DNA B Resour 25-Jan-2024
PMCID:PMC10812858
doi:10.1080/23802359.2024.2305402
PMID:38282981
Enhancing salinity tolerance in cucumber through Selenium biofortification and grafting Amerian M, Palangi A, Gohari G, Ntatsi G BMC Plant Biol 03-Jan-2024
PMCID:PMC10762928
doi:10.1186/s12870-023-04711-z
PMID:38166490
Editorial: Identification, development and use of rootstocks to improve pest and disease resistance of vegetable crops Thies JA, Panthee DR Front Plant Sci 12-Dec-2023
PMCID:PMC10751907
doi:10.3389/fpls.2023.1320828
PMID:38152143
Cucumber grafting on indigenous cucurbit landraces confers salt tolerance and improves fruit yield by enhancing morpho-physio-biochemical and ionic attributes Abbas F, Faried HN, Akhtar G, Ullah S, Javed T, Shehzad MA, Ziaf K, Razzaq K, Amin M, Wattoo FM, Hafeez A, Rahimi M, Abeed AH Sci Rep 07-Dec-2023
PMCID:PMC10709624
doi:10.1038/s41598-023-48947-z
PMID:38066051
Medicinal plants used for management of diabetes and hypertension in Ghana Asafo-Agyei T, Appau Y, Barimah KB, Asase A Heliyon 29-Nov-2023
PMCID:PMC10703729
doi:10.1016/j.heliyon.2023.e22977
PMID:38076168
Effect of host shift on the gut microbes of Bactrocera cucurbitae (Coquillett) (Diptera: Tephritidae) Tian Z, Chen L, Chen G, Wang J, Ma C, Zhang Y, Gao X, Chen H, Zhou Z Front Microbiol 21-Nov-2023
PMCID:PMC10703373
doi:10.3389/fmicb.2023.1264788
PMID:38075877

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
> Alkaloids and derivatives / Plumeran-type alkaloids
methyl (4S)-4-[(10S,11R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-10-methoxycarbonyl-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl]-1-ethyl-2-oxa-6,16-diazahexacyclo[16.2.1.03,19.05,13.07,12.016,19]henicosa-5(13),7,9,11-tetraene-4-carboxylate 5315743 Click to see CCC12CC3CN4C3(C1)C(O2)C(C5=C(CC4)C6=CC=CC=C6N5)(C7=C(C=C8C(=C7)C91CCN2C9C(C=CC2)(C(C(C1N8C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC 821.00 unknown via CMAUP database
> Benzenoids / Anthracenes
Melanins 6325610 Click to see 318.30 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol,[14c(u)] 11480435 Click to see 122.07 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-(4-(1,3-dihydroxy-2-(4-((E)-3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy)propyl)-2-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 11972318 Click to see 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
[(1S,5R,8R,12R,16S)-14-ethyl-4,6,19,21-tetramethoxy-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosan-16-yl]methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 42622686 Click to see CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7OC)OC)OCO5)OC)OC)COC(=O)C8=CC=CC=C8N9C(=O)CC(C9=O)C 694.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3S,4aR,6aS,6bR,9R,10R,11S,12aR)-3,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 9986931 Click to see CC1(CC2C3=CCC4C(C3(CCC2(CC1O)C(=O)O)C)(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C 666.80 unknown via CMAUP database
(3S,9R)-3-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 6325547 Click to see 650.80 unknown https://doi.org/10.1248/CPB.39.1185
(4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101621523 Click to see 650.80 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
(4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-9-formyl-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 21609769 Click to see 632.80 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (3S,4aR,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-3-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101621522 Click to see 813.00 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_246
https://doi.org/10.1248/YAKUSHI1947.105.9_834
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13518130 Click to see 797.00 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_246
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13518132 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 781.00 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_246
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13518126 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 797.00 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
https://doi.org/10.1248/YAKUSHI1947.104.3_246
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-9-formyl-11-hydroxy-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13518123 Click to see 811.00 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_246
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-9-formyl-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13518128 Click to see 795.00 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
https://doi.org/10.1248/YAKUSHI1947.104.3_246
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (3S,4aR,6bR,10S,12aR)-3,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 6325548 Click to see 634.80 unknown via CMAUP database
Ginsenoside B2 441921 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CC4(C(CC(C5C4(CCC5C(C)(CCC=C(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O)O)O 947.20 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_246
hederagenin-3-O-beta-D-glucopyranoside 13518139 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 634.80 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
Lucyoside B 13518118 Click to see 813.00 unknown https://doi.org/10.1248/YAKUSHI1947.104.3_246
Lucyoside J 131751191 Click to see 811.00 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
Lucyoside L 131751156 Click to see 957.10 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
Lucyoside M 131751578 Click to see 837.00 unknown https://doi.org/10.1248/YAKUSHI1947.105.9_834
Lucyoside N 78407206 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C 650.80 unknown https://doi.org/10.1248/CPB.39.1185
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Ludovicin A 168722 Click to see 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aS,9R,12aR,14aR,14bR)-9-[(2R,3S,4R,5R)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxycarbonyl-4-formyl-4,6a,6b,11,11,14b-hexamethyl-2,3,4a,5,6,7,8,8a,9,10,12,12a,14,14a-tetradecahydro-1H-picen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163194522 Click to see 1381.50 unknown https://doi.org/10.1248/CPB.39.1185
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aS,6aR,6bS,8R,8aS,9R,12aR,14aR,14bR)-9-[(2R,3S,4R,5R)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxycarbonyl-4-formyl-8-hydroxy-4,6a,6b,11,11,14b-hexamethyl-2,3,4a,5,6,7,8,8a,9,10,12,12a,14,14a-tetradecahydro-1H-picen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163025612 Click to see 1397.50 unknown https://doi.org/10.1248/CPB.39.1185
(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 via CMAUP database
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/J.BMCL.2006.12.091
5,10-Dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3939968 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/J.BMCL.2006.12.091
6-[[9-[3-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxycarbonyl-4-formyl-4,6a,6b,11,11,14b-hexamethyl-2,3,4a,5,6,7,8,8a,9,10,12,12a,14,14a-tetradecahydro-1H-picen-3-yl]oxy]-3,4-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 162991373 Click to see 1381.50 unknown https://doi.org/10.1248/CPB.39.1185
6-[[9-[3-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxycarbonyl-4-formyl-8-hydroxy-4,6a,6b,11,11,14b-hexamethyl-2,3,4a,5,6,7,8,8a,9,10,12,12a,14,14a-tetradecahydro-1H-picen-3-yl]oxy]-3,4-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163025611 Click to see 1397.50 unknown https://doi.org/10.1248/CPB.39.1185
Echinocystic Acid 73309 Click to see 472.70 unknown https://doi.org/10.1016/J.BMCL.2006.12.091
Lucyin A 192614 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C=O)O)C)C 486.70 unknown via CMAUP database
Methyl 3,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 5319157 Click to see 486.70 unknown via CMAUP database
Olean-12-en-28-oic acid, 3,21-dihydroxy-, gamma-lactone, (3beta,21beta)- 21594250 Click to see 454.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1111/J.2042-7158.1992.TB03646.X
https://doi.org/10.1016/J.BMCL.2006.12.091
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(10R)-17-(furan-3-yl)-7-hydroxy-4,4,10,13-tetramethyl-3-oxo-2,5,6,7,8,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-yl] acetate 5319336 Click to see 440.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
[(E,6R)-6-[(2S,9R,10R,13R,14S,16R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 25245488 Click to see 558.70 unknown via CMAUP database
[(E)-6-[(3S,10R,16R)-3,16-dihydroxy-9-(hydroxymethyl)-4,4,13,14-tetramethyl-11-oxo-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 6433457 Click to see 560.70 unknown via CMAUP database
Cucurbitacin E 5281319 Click to see 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Acetyldigitoxin 5284512 Click to see 807.00 unknown via CMAUP database
Deslanoside 28620 Click to see 943.10 unknown via CMAUP database
Digitalin 441856 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O 712.80 unknown via CMAUP database
Digitoxin 441207 Click to see 764.90 unknown via CMAUP database
Digoxin 2724385 Click to see 780.90 unknown via CMAUP database
Gitoxin 91540 Click to see 780.90 unknown via CMAUP database
Lanatoside A 10819737 Click to see 969.10 unknown via CMAUP database
Lanatoside B 72604 Click to see 985.10 unknown via CMAUP database
Lanatoside C 656630 Click to see 985.10 unknown via CMAUP database
Strospeside 21636336 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)O 550.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6R)-2-[[(3S,10S,13R)-17-[(E,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11968950 Click to see 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(2R)-2-azaniumyl-5-(carbamoylamino)pentanoate 7004911 Click to see 175.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(2S,4aS,6aS,8aR,12aS,14aS,14bR)-10-hydroxy-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-2-carboxylic acid 137706079 Click to see 456.70 unknown https://doi.org/10.1055/S-2006-960199
https://doi.org/10.1046/J.0014-2956.2001.02588.X
Bryonolate 52940232 Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)[O-])C)C)C)C 455.70 unknown via CMAUP database
Bryononic acid 472768 Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1046/J.0014-2956.2001.02588.X
https://doi.org/10.1055/S-2006-960199
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Squamatic acid 5321482 Click to see CC1=CC(=C(C(=C1C(=O)O)O)C)OC(=O)C2=C(C(=C(C=C2C)OC)C(=O)O)O 390.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Diosmetin-7-o-beta-d-glucuronide methyl ester 91368778 Click to see 490.40 unknown https://doi.org/10.1016/J.FITOTE.2007.05.004
Methyl 3,4,5-trihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate 163039917 Click to see 490.40 unknown https://doi.org/10.1016/J.FITOTE.2007.05.004

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