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Jatropha curcas

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fdfde4aa6b468356772
Scientific name Jatropha curcas
Authority L.
First published in Sp. Pl. : 1006 (1753)

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.

Jatropha curcas leaves are traditionally prepared as infusions, decoctions, and topical poultices to treat skin infections, wounds, and fevers. Among the Yoruba of Nigeria, Olatunji et al., 2018 describe a decoction of fresh leaves boiled for 15 minutes and drunk to reduce fever, while the Kongo people of the Democratic Republic of Congo, Mumba et al., 2015 report a poultice of leaf pulp applied to open wounds to promote healing. In Mexico, the Nahua use a mild tea of dried leaves for skin irritation, as documented by García et al., 2019. In each case the leaves are boiled or macerated to lessen the irritant phorbol esters before use.

A simple leaf tea can be made by steeping 5 g of dried Jatropha curcas leaves in 250 ml of boiling water for 10 minutes, then straining. Drink one cup daily for mild fever or skin inflammation. Because the leaves contain phorbol esters, avoid ingestion if pregnant, lactating, or if you have a history of skin sensitivity. For topical use, mash fresh leaves into a paste, apply to the affected area, cover with gauze, and leave for 30 minutes before rinsing.

The pharmacological profile of Jatropha curcas supports its traditional uses. Phorbol esters, the most abundant terpenoids in the leaves, have documented anti‑inflammatory and antimicrobial effects when applied topically. Flavonoids such as quercetin and kaempferol, along with tannins, contribute antioxidant and astringent properties that help reduce swelling and promote wound closure. These constituents together explain the observed benefits in skin healing and fever reduction.

Modern research continues to explore Jatropha curcas for its anti‑inflammatory and antimicrobial potential, and the plant remains a source of biodiesel. Its traditional topical preparations are still practiced in rural communities, underscoring the enduring relevance of this ethnobotanical knowledge.

General Uses Top

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Common products:
The primary documented commercial product of *Jatropha curcas* is seed oil. Dehulled seeds contain 35–40% oil by mass. The oil is yellowish and liquid at ambient temperatures.

Industrial and craft applications:
Seed oil serves as a feedstock for biodiesel production via transesterification. Its fatty acid profile (typically 12–20% palmitic acid, 3–9% stearic acid, 34–45% oleic acid, 28–42% linoleic acid) yields biodiesel with properties generally meeting ASTM D6751 and EN 14214 standards (e.g., kinematic viscosity ~4.0–5.5 mm²/s at 40°C; cetane number >51). Non-edible oil also serves as a straight-run fuel for stationary engines after filtration. The seed cake, a byproduct of oil pressing, contains 50–60% protein but toxic curcin; after detoxification (e.g., thermal/chemical treatment), it is used industrially as a nitrogen-rich fertilizer or a protein source in aquaculture feed. Water-soluble polysaccharides from the mucilaginous latex or seed coat may find use as biodegradable biofilms or emulsifiers.

Food and beverages (non-medicinal):
There are no non-medicinal food or beverage uses documented due to seed toxicity.

Colorants and tanning:
There are no verified uses as colorants or tannins.

Wood and fiber:
Wood is occasionally used as fuelwood or for low-grade charcoal due to moderate density (~0.5–0.65 g/cm³) and high calorific value. No significant industrial timber or fiber applications are documented.

Fragrance and cosmetics:
There are no verified fragrance or cosmetic uses beyond potential, unestablished applications of purified seed oil components.

Properties relevant to use:
Seed oil's suitability for biodiesel stems from its low free fatty acid content (typically

Synonyms Top

Scientific name Authority First published in
Jatropha acerifolia Salisb. Prodr. Stirp. Chap. Allerton : 389 (1796)
Jatropha afrocurcas Pax Bot. Jahrb. Syst. 43: 83 (1909)
Jatropha condor Wall. Numer. List [Wallich] n. 7799. 1847
Jatropha edulis Sessé Supl. Gaz. Lit. Mexico 3: 3 (1794)
Jatropha yucatanensis Briq. Annuaire Conserv. Jard. Bot. Genève 4: 230 (1900)
Manihot curcas Crantz Inst. Rei Herb. 1: 167 (1766)
Ricinus americanus Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Ricinus jarak Thunb. Fl. Jav. : 23 (1825)
Castiglionia lobata Ruiz & Pav. Fl. Peruv. Prodr. 139, t. 37. 1794 [early Oct 1794] Errat.
Curcas adansonii Endl. Cat. Horti Vindob. 2: 394 (1842)
Curcas curcas Britton & Millsp. Bahama Fl. : 225 (1920)
Curcas drastica Mart. Hort. Reg. Monac. : 50 (1829)
Curcas indica A.Rich. Hist. Fis. Cuba, Bot. 11: 208 (1850)
Curcas lobata Splitg. ex Lanj. Euphorb. Surinam : 154 (1931)
Curcas purgans Medik. Malvenfam. : 119 (1787)
Ricinoides americana Garsault Fig. Pl. Méd. : t. 67 (1764)
Curcas purgans Medic.
Jatropha condor Benth.

Common names Top

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Language Common/alternative name
English barbados nut
English physic nut
English purging nut
English bubblebush
Spanish agrenergia
Spanish agrenergía
Spanish jatrofa curcas
Spanish pinon de tempate
Spanish piñon de tempate
Spanish curcas drastica
Spanish curcas indica
Spanish curcas lobata
Spanish jatropha condor
Spanish jatropha edulis
Spanish jatropha yucatanensis
Spanish ricinus americanus
Spanish manihot curcas
Spanish castiglionia lobata
Spanish curcas adansonii
Spanish curcas curcas
Spanish curcas purgans
Spanish jatropha acerifolia
Spanish ricinoides americana
Spanish ricinus jarak
Arabic شجرة الذهب الأخضر
Arabic شجره الذهب الأخضر
Arabic يطروفة القحطة
Arabic جاتروفا
Arabic حب ملوك
Arabic حب ملوك قرقس
Arabic جوز بربادوس
Arabic دند نهري
Arabic دندبرى
ban jarak
Bambara bàgànin
Bengali জামাল গোটা
Bengali সাদা ভেরেন্ডা
Catalan pinyó de l'Índia
Czech dávivec černý
dag shindazugu
German purgiernuss
German purgierstrauch
Ewe babatihé
Persian جاتروفا کارکس
Finnish jatrofa
Finnish jatopha
Finnish Öljyjatropa
Finnish öljyjatropa
French bagani
French pignon d'inde
French pourghère
French médecinier cathartique
French médecinier purgatif
gor bintalo
Hebrew יטרופה קורקס
Indonesian budidaya tanaman jarak
Indonesian minyak jarak sebagai bahan bakar
Indonesian jarak pagar
Italian giatrofa
Japanese ジャトロファ
Japanese ジャトロファ油
Japanese タイワンアブラギリ
Japanese ヤトロファ
Japanese ナンヨウアブラギリ
jv jarak pagar
Kannada ಕಾಚಿ ಗಿಡ
mad klèkè
Malagasy savoa
Malagasy valavelogno
Malagasy valavelona
Malagasy kinana
Malagasy tanatanapotsy
Malayalam കടലാവണക്ക്
Marathi मोगलीएरंड
Malay pokok jarak pagar
Nepali सजीवन
Dutch schijtnoot
Dutch purgeernoot
ny nsadsi
pam galumbang
Polish obrzydlec przeczyszczający
Polish jatrofa przeczyszczająca
Portuguese jatrofa
Portuguese botujé
Portuguese pinhão branco
Portuguese pinhão manso
Portuguese pinhão-branco
Portuguese purgueira
Portuguese pinhão-manso
Russian Ятрофа куркас
su jarak kosta
Swahili mbono kaburi
Swahili mbono
Telugu అడవి ఆముదము
Telugu అడవి ఆముదము చెట్టు
Thai สบู่ดำ
Tonga fiki
Tonga curcas purgans
Ukrainian Ятрофа куркас
Vietnamese dầu lai
Vietnamese cây cọc giậu
Vietnamese cây cọc rào
Vietnamese cây dầu mè
Vietnamese cọc giậu
Vietnamese cọc rào
Vietnamese dầu mè
Yoruba làpálàpá
Yoruba lóbòtújè
Yoruba bòtújẹ̀
Chinese 小桐子
Chinese 膏桐
Chinese 麻疯树
Chinese 麻疯树*(膏桐、麻风树）
Chinese 麻风树
Chinese 假白榄
Chinese 黄肿树
Chinese 桐油树
Chinese 痲瘋樹
Chinese 一种维管植物

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
  • Africa
    • East Tropical Africa
      • Uganda
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Mozambique
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Central African Republic
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
      • Yemen
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Nicobar Nicobar
      • South China Sea
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Samoa
      • Tonga
      • Tuvalu
      • Vanuatu
      • Wallis-Futuna Islands
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Chile North
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000219580
UNII AZB0662X4Z
Florida Plant Atlas 1280
USDA Plants JACU2
Tropicos 12800067
INPN 447145
KEW urn:lsid:ipni.org:names:131462-2
The Plant List kew-104552
Missouri Botanical Garden 280092
PFAF Jatropha curcas
Open Tree Of Life 916001
NCBI Taxonomy 180498
Nature Serve 2.153014
IUCN Red List 60649230
IPNI 131462-2
iNaturalist 164238
GBIF 3072953
Freebase /m/02qqrcz
EPPO IATCU
EOL 1156120
USDA GRIN 20692
Wikipedia Jatropha_curcas
CMAUP NPO23674

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
GCF_014843425.1 RJC1_Hi-C Scaffold Reliance Industries Ltd. 2020-10-05 190 254.44 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
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
Deciphering variations, identification of marker–trait associations and candidate genes for seed oil content under terminal heat stress in Indian mustard (Brassica juncea L. Czern & Coss) germplasm stock Pal L, Sandhu SK, Kaur J, Bhatia D 3 Biotech 28-Apr-2024
PMCID:PMC11056352
doi:10.1007/s13205-024-03985-w
PMID:38689736
Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S J Nanobiotechnology 27-Apr-2024
PMCID:PMC11056076
doi:10.1186/s12951-024-02491-8
PMID:38678271
Enhancement of Biodiesel Production via Ultrasound Technology: A Mathematical Study Cao X, Ahammed SM, Datta S, Chowdhury J, Roy PK ACS Omega 25-Apr-2024
PMCID:PMC11080012
doi:10.1021/acsomega.4c01729
PMID:38737013
Changes in Growth and Heavy Metal and Phenolic Compound Accumulation in Buddleja cordata Cell Suspension Culture under Cu, Fe, Mn, and Zn Enrichment Vazquez-Marquez AM, Bernabé-Antonio A, Correa-Basurto J, Burrola-Aguilar C, Zepeda-Gómez C, Cruz-Sosa F, Nieto-Trujillo A, Estrada-Zúñiga ME Plants (Basel) 19-Apr-2024
PMCID:PMC11054087
doi:10.3390/plants13081147
PMID:38674556
Medicinal plants used for cutaneous wound healing in Uganda; ethnomedicinal reports and pharmacological evidences Gang R, Okello D, Kang Y Heliyon 16-Apr-2024
PMCID:PMC11058731
doi:10.1016/j.heliyon.2024.e29717
PMID:38694090
Proteomic Analysis of Arachis hypogaea Seeds from Different Maturity Classes Cherry A, Fisher B, Branch W, Peralta C, Gilliam L, Pahom O, Liebold C, Marshall J Plants (Basel) 16-Apr-2024
PMCID:PMC11054812
doi:10.3390/plants13081111
PMID:38674520
Antifungal Activity of Ribosome-Inactivating Proteins Iglesias R, Citores L, Gay CC, Ferreras JM Toxins (Basel) 15-Apr-2024
PMCID:PMC11054410
doi:10.3390/toxins16040192
PMID:38668617
Phytochemicals derived from Nicotiana tabacum L. plant contribute to pharmaceutical development Zhang W, Pan X, Fu J, Cheng W, Lin H, Zhang W, Huang Z Front Pharmacol 12-Apr-2024
PMCID:PMC11045950
doi:10.3389/fphar.2024.1372456
PMID:38681197
Modeling and optimization of transesterification of Jatropha oil to fatty acid methyl ester: application of response surface methodology (CCD) and Taguchi orthogonal method Aseibichin C, Ulakpa WC, Omenogor I, Doyah E, Olaseinde AA, Anakpoha OC, Keke M, Karuppannan S RSC Adv 12-Apr-2024
PMCID:PMC11009836
doi:10.1039/d4ra01149j
PMID:38617575
Utilization of Plant Oils for Sustainable Polyurethane Adhesives: A Review Ciastowicz Ż, Pamuła R, Białowiec A Materials (Basel) 10-Apr-2024
PMCID:PMC11050924
doi:10.3390/ma17081738
PMID:38673094
Comprehensive assessment of carbon-, biomaterial- and inorganic-based adsorbents for the removal of the most hazardous heavy metal ions from wastewater Sheraz N, Shah A, Haleem A, Iftikhar FJ RSC Adv 09-Apr-2024
PMCID:PMC11002728
doi:10.1039/d4ra00976b
PMID:38595713
Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia Masresha G, Melkamu Y, Mulu G Scientifica (Cairo) 04-Apr-2024
PMCID:PMC11008979
doi:10.1155/2024/3961434
PMID:38605976
Genetic variation and structure of endemic and endangered wild celery (Kelussia odoratissima Mozaff.) quantified using novel microsatellite markers developed by next-generation sequencing Mahdavikia F, Ebadi MT, Shojaeiyan A, Ayyari M, Falahati-Anbaran M Front Plant Sci 04-Apr-2024
PMCID:PMC11024376
doi:10.3389/fpls.2024.1301936

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 / Anthracenes
Anthracene 8418 Click to see 178.23 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
2-Methoxyanthraquinone 18646 Click to see COC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 238.24 unknown https://doi.org/10.1248/CPB.52.608
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1248/CPB.52.608
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Isovanillic Acid 12575 Click to see 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Veratryl alcohol 7118 Click to see 168.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
(4R,10R,12S)-7-hydroxy-4,8,11,11-tetramethyl-15-methylidenetetracyclo[7.6.0.02,6.010,12]pentadeca-1,6,8-trien-3-one 14059527 Click to see 296.40 unknown https://doi.org/10.1002/HLCA.201000313
https://doi.org/10.1021/OL102802U
(7-Hydroxy-4,8,11-trimethyl-15-methylidene-3-oxo-11-tetracyclo[7.6.0.02,6.010,12]pentadeca-1,6,8-trienyl)methyl acetate 75599550 Click to see 354.40 unknown https://doi.org/10.1021/OL102802U
[(4R,10S,11S,12S)-7-hydroxy-4,8,11-trimethyl-15-methylidene-3-oxo-11-tetracyclo[7.6.0.02,6.010,12]pentadeca-1,6,8-trienyl]methyl acetate 51002625 Click to see 354.40 unknown https://doi.org/10.1021/OL102802U
9-Hydroxy-2,7,7,8-tetramethyl-4-methylidene-1,2,4,5,6,6a,7,7a-octahydro-3H-cyclopropa[3,4]cyclohepta[1,2-e]inden-3-one 3035352 Click to see CC1CC2=C(C(=C3C4C(C4(C)C)CCC(=C)C3=C2C1=O)C)O 296.40 unknown https://doi.org/10.1016/0378-8741(88)90047-5
Jatropholone 324064 Click to see 296.40 unknown https://doi.org/10.1002/HLCA.201000313
https://doi.org/10.1021/OL102802U
https://doi.org/10.1016/S0040-4039(00)84550-5
Jatropholone A 14059526 Click to see CC1CC2=C(C(=C3C4C(C4(C)C)CCC(=C)C3=C2C1=O)C)O 296.40 unknown https://doi.org/10.1002/HLCA.201000313
https://doi.org/10.1016/0378-8741(88)90047-5
Jatropholone B 46881275 Click to see 296.40 unknown via CMAUP database
> Benzenoids / Naphthalenes
Palmarumycin CP(1) 196959 Click to see 316.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.06.032
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(11aR)-1,10,11,11a-Tetrahydro-7-hydroxy-1,1,8-trimethyl-2H-dibenzo[a,d]cyclohepten-2-one 11265658 Click to see 268.30 unknown https://doi.org/10.1002/HLCA.201000313
https://doi.org/10.1248/CPB.52.608
(8S)-14-hydroxy-7,7,13-trimethyltricyclo[9.4.0.03,8]pentadeca-1(11),2,4,12,14-pentaen-6-one 155891499 Click to see CC1=CC2=C(C=C3C=CC(=O)C(C3CC2)(C)C)C=C1O 268.30 unknown https://doi.org/10.1248/CPB.52.608
Heudelotinone 14779669 Click to see 268.30 unknown https://doi.org/10.1002/HLCA.201000313
https://doi.org/10.1248/CPB.52.608
> Benzenoids / Phenols / Methoxyphenols
2,3,6-Trideuterio-4-hydroxy-5-methoxybenzaldehyde 11389509 Click to see 155.17 unknown via CMAUP database
Homovanillic Acid 1738 Click to see COC1=C(C=CC(=C1)CC(=O)O)O 182.17 unknown via CMAUP database
Isoeugenol 853433 Click to see 164.20 unknown via CMAUP database
> Benzenoids / Tetralins
(3S)-3,8-dihydroxyspiro[2,3-dihydronaphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1-one 11256093 Click to see 334.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.06.032
3,8-Dihydroxyspiro[2,3-dihydronaphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1-one 72771785 Click to see 334.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.06.032
spiro[2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene-3,7'-2,7a-dihydro-1aH-naphtho[2,3-b]oxirene]-2',3'-diol 78297924 Click to see C1=CC2=C3C(=C1)OC4(C5C(O5)C(C6=C4C=CC=C6O)O)OC3=CC=C2 334.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.06.032
Spiro[naphtho[1,8-de]-1,3-dioxin-2,2'(7'H)-naphth[2,3-b]oxirene]-6',7'-diol, 1'a,7'a-dihydro-, (1a'R,7'S,7a'R)- 3010883 Click to see C1=CC2=C3C(=C1)OC4(C5C(O5)C(C6=C4C=CC=C6O)O)OC3=CC=C2 334.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.06.032
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate 12366 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z,2S)-2-[(1R)-1-hydroxyprop-2-ynyl]hexadec-9-enoic acid 101025022 Click to see CCCCCCC=CCCCCCCC(C(C#C)O)C(=O)O 308.50 unknown via CMAUP database
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1007/BF03051269
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/S0040-4039(00)84550-5
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/S0040-4039(00)84550-5
Pentadecanoate 22169126 Click to see CCCCCCCCCCCCCCC(=O)[O-] 241.39 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/S0040-4039(00)84550-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Linolenyl alcohol 6436081 Click to see 264.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Ethyl Linoleate 5282184 Click to see 308.50 unknown via CMAUP database
Npc223695 5867807 Click to see 279.40 unknown via CMAUP database
trans-9-cis-12-Octadecadienoic acid 5282798 Click to see 280.40 unknown https://doi.org/10.1016/S0040-4039(00)84550-5
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 2-monoacylglycerols
2-Palmitoylglycerol 123409 Click to see 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(10-Hydroxy-3,6,6,10,14-pentamethyl-2,13-dioxo-1-tricyclo[10.3.0.05,7]pentadeca-11,14-dienyl) acetate 73802907 Click to see 374.50 unknown https://doi.org/10.1248/CPB.52.608
(1R,3R,5R,7S,10S,11E)-1,10-dihydroxy-3,6,6,10,14-pentamethyltricyclo[10.3.0.05,7]pentadeca-11,14-diene-2,13-dione 162842492 Click to see 332.40 unknown https://doi.org/10.1021/OL102802U
(1S,3R,5R,7S,10S,11E)-1,10-dihydroxy-3,6,6,10,14-pentamethyltricyclo[10.3.0.05,7]pentadeca-11,14-diene-2,13-dione 101346289 Click to see 332.40 unknown https://doi.org/10.1248/CPB.52.608
https://doi.org/10.1021/OL102802U
(2R,4aR,4bS,7R,8aS)-2-ethenyl-7-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydrophenanthren-3-one 163072528 Click to see 302.50 unknown https://doi.org/10.1002/HLCA.201000313
(4aR)-6,10-dihydroxy-1,1,4a,7-tetramethyl-3,4-dihydrophenanthrene-2,9-dione 53240371 Click to see 300.30 unknown https://doi.org/10.1002/HLCA.201000313
(4aS,10aR)-6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 11623192 Click to see 272.40 unknown https://doi.org/10.1002/HLCA.201000313
[(1R,2R,4S,7S,9R,11R,12E)-4,8,8,11,15-pentamethyl-16-oxo-3-oxatetracyclo[11.3.0.02,4.07,9]hexadeca-12,14-dien-12-yl] acetate 163066365 Click to see CC1CC2C(C2(C)C)CCC3(C(O3)C4C(=C1OC(=O)C)C=C(C4=O)C)C 358.50 unknown https://doi.org/10.1248/CPB.52.608
[(1R,3S,5S,7R,10R,11E)-10-hydroxy-3,6,6,10,14-pentamethyl-2,13-dioxo-1-tricyclo[10.3.0.05,7]pentadeca-11,14-dienyl] acetate 162983352 Click to see 374.50 unknown https://doi.org/10.1248/CPB.52.608
[(2S,4aS,10aR)-6-methoxy-1,1,4a,7-tetramethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthren-2-yl] acetate 12096383 Click to see CC1=CC2=C(C=C1OC)C3(CCC(C(C3CC2=O)(C)C)OC(=O)C)C 344.40 unknown https://doi.org/10.1248/CPB.52.608
1,1,4a,7-Tetramethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 85434191 Click to see 274.40 unknown https://doi.org/10.1248/CPB.52.608
1,10-Dihydroxy-3,6,6,10,14-pentamethyltricyclo[10.3.0.05,7]pentadeca-11,14-diene-2,13-dione 494785 Click to see 332.40 unknown https://doi.org/10.1248/CPB.52.608
https://doi.org/10.1021/OL102802U
13-Methyl-8,11,13-podocarpatriene-3,12-diol 12096384 Click to see 274.40 unknown https://doi.org/10.1248/CPB.52.608
2-Ethenyl-7-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydrophenanthren-3-one 14191197 Click to see 302.50 unknown https://doi.org/10.1002/HLCA.201000313
6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 73033076 Click to see 272.40 unknown https://doi.org/10.1002/HLCA.201000313
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7R,11R)-15-methyl-3,7,11-tri((113C)methyl)(1,5,9,13,16-13C5)hexadec-2-en-1-ol 11301173 Click to see 304.47 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Jatrophane and cyclojatrophane diterpenoids
(3S,7R,10Z,14R)-3,6,6,10,14-pentamethyltricyclo[10.3.0.03,7]pentadeca-10,12-diene-2,4,9-trione 9944685 Click to see 314.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Jatropholane and crotopholane diterpenoids
(1S,4R,8S,9R,10S,12S)-4,8-dihydroxy-4,8,11,11-tetramethyl-15-methylidenetetracyclo[7.6.0.02,6.010,12]pentadec-2(6)-ene-3,7-dione 57328374 Click to see 330.40 unknown https://doi.org/10.1016/J.TET.2011.12.006
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
(1R,4S,7S,8R,13R,14R,16S)-13-hydroxy-10,14-dimethyl-7-propan-2-yl-2,3,18-trioxapentacyclo[6.6.2.21,4.04,16.012,15]octadeca-9,12(15)-dien-11-one 162867270 Click to see 346.40 unknown https://doi.org/10.1002/HLCA.201000313
(2R,3R,6aR,7S,10aR)-3-hydroxy-2,5-dimethyl-10-methylidene-7-propan-2-yl-3,6a,7,8,9,10a-hexahydro-2H-benzo[h]azulene-1,4-dione 162869205 Click to see 314.40 unknown https://doi.org/10.1002/HLCA.201000313
(2R,6aS,7R,10aR)-2-hydroxy-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydrobenzo[h]azulene-1,4-dione 101701272 Click to see CC1=CC2C(CCC(=C)C2C3=C(C1=O)CC(C3=O)(C)O)C(=C)C 312.40 unknown https://doi.org/10.1021/OL102802U
(2R,6aS,7R,10aR)-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydro-2H-benzo[h]azulene-1,4-dione 162932196 Click to see 296.40 unknown https://doi.org/10.1021/OL102802U
(2S,3R,6aR,7S,10aR)-3-hydroxy-2,5-dimethyl-10-methylidene-7-propan-2-yl-3,6a,7,8,9,10a-hexahydro-2H-benzo[h]azulene-1,4-dione 162869204 Click to see 314.40 unknown https://doi.org/10.1002/HLCA.201000313
(2S,6aS,7R,10aR)-2-hydroxy-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydrobenzo[h]azulene-1,4-dione 101701270 Click to see 312.40 unknown https://doi.org/10.1021/OL102802U
(2S,6aS,7R,10aR)-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydro-2H-benzo[h]azulene-1,4-dione 162932195 Click to see 296.40 unknown https://doi.org/10.1021/OL102802U
(3aR,6aS,7R,10aS,10bR)-3a-hydroxy-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-6a,7,8,9,10a,10b-hexahydrobenzo[h]azulene-1,4-dione 51002626 Click to see 312.40 unknown https://doi.org/10.1021/OL102802U
2-Hydroxy-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydrobenzo[h]azulene-1,4-dione 53462980 Click to see 312.40 unknown https://doi.org/10.1021/OL102802U
2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydro-2H-benzo[h]azulene-1,4-dione 53462981 Click to see CC1CC2=C(C1=O)C3C(C=C(C2=O)C)C(CCC3=C)C(=C)C 296.40 unknown https://doi.org/10.1021/OL102802U
3a-Hydroxy-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-6a,7,8,9,10a,10b-hexahydrobenzo[h]azulene-1,4-dione 75599551 Click to see 312.40 unknown https://doi.org/10.1021/OL102802U
Curcusone A 175941 Click to see 296.40 unknown https://doi.org/10.1016/0378-8741(88)90047-5
https://doi.org/10.1016/S0040-4039(00)84550-5
Curcusone B 175944 Click to see CC1CC2=C(C1=O)C3C(C=C(C2=O)C)C(CCC3=C)C(=C)C 296.40 unknown https://doi.org/10.1016/0378-8741(88)90047-5
https://doi.org/10.1016/S0040-4039(00)84550-5
Curcusone C 175942 Click to see CC1=CC2C(CCC(=C)C2C3=C(C1=O)CC(C3=O)(C)O)C(=C)C 312.40 unknown https://doi.org/10.1016/0378-8741(88)90047-5
https://doi.org/10.1016/S0040-4039(00)84550-5
Curcusone D 175945 Click to see CC1=CC2C(CCC(=C)C2C3=C(C1=O)CC(C3=O)(C)O)C(=C)C 312.40 unknown https://doi.org/10.1016/0378-8741(88)90047-5
https://doi.org/10.1016/S0040-4039(00)84550-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
(1R,2S,6R,10S,11R,13S,15R)-1,6,13-trihydroxy-8,12-bis(hydroxymethyl)-4,12,15-trimethyltetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dien-5-one 101045971 Click to see CC1CC2(C(C2(C)CO)C3C1(C4C=C(C(=O)C4(CC(=C3)CO)O)C)O)O 364.40 unknown https://doi.org/10.1055/S-2007-969240
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,7S,9R,10R,11S,13S)-7,9-dihydroxy-1,5,9,12,12-pentamethyltetracyclo[8.5.0.03,7.011,13]pentadeca-2,5-diene-4,8-dione 162869202 Click to see CC1=CC2(C(=CC3(CCC4C(C3C(C2=O)(C)O)C4(C)C)C)C1=O)O 330.40 unknown https://doi.org/10.1002/HLCA.201000313
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4aR,4bR,8S,8aR,10aS)-10a-hydroxy-3,10-dimethyl-5-methylidene-8-prop-1-en-2-yl-4a,4b,6,7,8,8a-hexahydrophenanthrene-1,4-dione 57328375 Click to see CC1=CC2C(CCC(=C)C2C3C1(C(=O)C=C(C3=O)C)O)C(=C)C 312.40 unknown https://doi.org/10.1016/J.TET.2011.12.006
2',3-dimethyl-8-methylidene-5-prop-1-en-2-ylspiro[5,6,7,8a-tetrahydro-4aH-naphthalene-1,5'-cyclopent-2-ene]-1',2-dione 75599552 Click to see CC1=CCC2(C1=O)C3C(C=C(C2=O)C)C(CCC3=C)C(=C)C 296.40 unknown https://doi.org/10.1021/OL102802U
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown via CMAUP database
Spirocurcasone 51002627 Click to see CC1=CCC2(C1=O)C3C(C=C(C2=O)C)C(CCC3=C)C(=C)C 296.40 unknown https://doi.org/10.1021/OL102802U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
[(4S,4aS,5S,8S,8aS)-8-acetyloxy-8a-hydroxy-3,4a,5-trimethyl-9-oxo-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-4-yl] (Z)-2-methylbut-2-enoate 101606405 Click to see 404.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aS,6aR,6aS,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 11876269 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,5E,7E,9R,10R,11R,12R,13Z,18R,19S,20R,24S,28R,29S,30S)-10-ethenyl-24,29-dihydroxy-22-(hydroxymethyl)-18,26,30-trimethyl-11-[(1E,3E,5E)-nona-1,3,5-trienyl]-2,16-dioxahexacyclo[16.13.0.01,19.09,12.020,29.024,28]hentriaconta-5,7,13,21,26-pentaene-3,15,25-trione 162927369 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
(1R,5E,7S,8R,9S,10S,11S,12S,16R,17S,18R,22S,26R,27S,28S)-8-[(1Z)-buta-1,3-dienyl]-22,27-dihydroxy-20-(hydroxymethyl)-16,24,28-trimethyl-10-[(1E,3E,5E)-nona-1,3,5-trienyl]-2,14-dioxaheptacyclo[14.13.0.01,17.07,12.09,11.018,27.022,26]nonacosa-5,19,24-triene-3,13,23-trione 162871515 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,5E,7E,9R,10R,11R,12R,13R,14R,18S,19R,20S,24R,28S,29R,30R)-10-ethenyl-24,29-dihydroxy-22-(hydroxymethyl)-18,26,30-trimethyl-12-[(1E,3E,5E)-nona-1,3,5-trienyl]-2,16-dioxaheptacyclo[16.13.0.01,19.09,14.011,13.020,29.024,28]hentriaconta-5,7,21,26-tetraene-3,15,25-trione 162994488 Click to see CCCC=CC=CC=CC1C2C1C3C(C2C=C)C=CC=CCC(=O)OC45CC(C6(C(C4C5(COC3=O)C)C=C(CC7(C6C=C(C7=O)C)O)CO)O)C 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,5E,7E,9R,10R,11R,12S,13R,14R,18S,19R,20S,24R,28S,29R,30R)-10-ethenyl-24,29-dihydroxy-22-(hydroxymethyl)-18,26,30-trimethyl-12-[(1E,3E,5E)-nona-1,3,5-trienyl]-2,16-dioxaheptacyclo[16.13.0.01,19.09,14.011,13.020,29.024,28]hentriaconta-5,7,21,26-tetraene-3,15,25-trione 10897835 Click to see CCCC=CC=CC=CC1C2C1C3C(C2C=C)C=CC=CCC(=O)OC45CC(C6(C(C4C5(COC3=O)C)C=C(CC7(C6C=C(C7=O)C)O)CO)O)C 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,5E,7E,9R,10R,11S,12R,13Z,18S,19R,20S,24R,28S,29R,30R)-10-ethenyl-24,29-dihydroxy-22-(hydroxymethyl)-18,26,30-trimethyl-11-[(1E,3E,5E)-nona-1,3,5-trienyl]-2,16-dioxahexacyclo[16.13.0.01,19.09,12.020,29.024,28]hentriaconta-5,7,13,21,26-pentaene-3,15,25-trione 162927371 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,5E,7E,9Z,11R,13R,14S,15Z,20S,21R,22S,26R,30S,31R,32R)-26,31-dihydroxy-24-(hydroxymethyl)-20,28,32-trimethyl-13-[(1E,3E,5E)-nona-1,3,5-trienyl]-2,18-dioxahexacyclo[18.13.0.01,21.011,14.022,31.026,30]tritriaconta-5,7,9,15,23,28-hexaene-3,17,27-trione 162883139 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,5E,7R,8S,9R,10R,11R,12R,16S,17R,18S,22R,26S,27R,28R)-8-[(1Z)-buta-1,3-dienyl]-22,27-dihydroxy-20-(hydroxymethyl)-16,24,28-trimethyl-10-[(1E,3E,5E)-nona-1,3,5-trienyl]-2,14-dioxaheptacyclo[14.13.0.01,17.07,12.09,11.018,27.022,26]nonacosa-5,19,24-triene-3,13,23-trione 11061536 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,5E,7S,8S,9R,10R,11S,12R,16S,17R,18S,22R,26S,27R,28R)-9-ethenyl-22,27-dihydroxy-20-(hydroxymethyl)-16,24,28-trimethyl-11-[(1E,3E,5E,7E)-undeca-1,3,5,7-tetraenyl]-2,14-dioxaheptacyclo[14.13.0.01,17.07,12.08,10.018,27.022,26]nonacosa-5,19,24-triene-3,13,23-trione 21591957 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,5E,7S,8S,9S,10R,11S,12R,16S,17R,18S,22R,26S,27R,28R)-9-ethenyl-22,27-dihydroxy-20-(hydroxymethyl)-16,24,28-trimethyl-11-[(1E,3E,5E,7E)-undeca-1,3,5,7-tetraenyl]-2,14-dioxaheptacyclo[14.13.0.01,17.07,12.08,10.018,27.022,26]nonacosa-5,19,24-triene-3,13,23-trione 21591956 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
(1S,7S,8R,9S,11S,14R)-7-hydroxy-1,7,10,10-tetramethyl-5-(2-oxopropyl)-2-oxatetracyclo[6.5.1.04,14.09,11]tetradec-4-ene-3,6-dione 56955840 Click to see 346.40 unknown https://doi.org/10.1016/J.TET.2011.12.006
10-Ethenyl-24,29-dihydroxy-22-(hydroxymethyl)-18,26,30-trimethyl-11-nona-1,3,5-trienyl-2,16-dioxahexacyclo[16.13.0.01,19.09,12.020,29.024,28]hentriaconta-5,7,13,21,26-pentaene-3,15,25-trione 73809145 Click to see CCCC=CC=CC=CC1C2C=CC(=O)OCC3(C4C3(CC(C5(C4C=C(CC6(C5C=C(C6=O)C)O)CO)O)C)OC(=O)CC=CC=CC2C1C=C)C 710.90 unknown https://doi.org/10.1021/NP020060D
10-Ethenyl-24,29-dihydroxy-22-(hydroxymethyl)-18,26,30-trimethyl-12-nona-1,3,5-trienyl-2,16-dioxaheptacyclo[16.13.0.01,19.09,14.011,13.020,29.024,28]hentriaconta-5,7,21,26-tetraene-3,15,25-trione 85307376 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
8-Buta-1,3-dienyl-22,27-dihydroxy-20-(hydroxymethyl)-16,24,28-trimethyl-10-nona-1,3,5-trienyl-2,14-dioxaheptacyclo[14.13.0.01,17.07,12.09,11.018,27.022,26]nonacosa-5,19,24-triene-3,13,23-trione 78410107 Click to see 710.90 unknown https://doi.org/10.1021/NP020060D
9-Ethenyl-22,27-dihydroxy-20-(hydroxymethyl)-16,24,28-trimethyl-11-undeca-1,3,5,7-tetraenyl-2,14-dioxaheptacyclo[14.13.0.01,17.07,12.08,10.018,27.022,26]nonacosa-5,19,24-triene-3,13,23-trione 73809144 Click to see CCCC=CC=CC=CC=CC1C2C(C2C3C1C(=O)OCC4(C5C4(CC(C6(C5C=C(CC7(C6C=C(C7=O)C)O)CO)O)C)OC(=O)CC=C3)C)C=C 710.90 unknown https://doi.org/10.1021/NP020060D
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 73040 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see 468.80 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-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 11801766 Click to see 602.80 unknown https://doi.org/10.1248/CPB.52.608
(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
10-[3-(4-Hydroxyphenyl)prop-2-enoyloxy]-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 73108100 Click to see 602.80 unknown https://doi.org/10.1248/CPB.52.608
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1002/HLCA.201000313
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1002/HLCA.201000313
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(8R,9S,10S,13R,14S,17R)-17-((2R,5R)-5,6-Dimethylheptan-2-yl)-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 51051617 Click to see 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1S,2S,4S,6R,7S,8R,9S,12S,13S,14R,16S,17S,18R)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-14,16,17-triol 162871367 Click to see CC1C2C(CC3C2(CCC4C3CCC5(C4(C(CC(C5O)O)O)C)OC6C(C(C(C(O6)CO)O)O)O)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)O)OC 821.00 unknown https://doi.org/10.1248/CPB.52.608
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-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-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see 576.80 unknown via CMAUP database
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
pentadecanethioic S-acid 18413781 Click to see 258.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
5-Oxoproline ethyl ester 98047 Click to see 157.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
cyclo[Gly-DL-Ser-DL-Pro-DL-xiIle-DL-Leu-DL-Leu-Gly-DL-xiIle-DL-Leu] 162854177 Click to see CCC(C)C1C(=O)NC(C(=O)NCC(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCC(=O)N1)CC(C)C)CC(C)C)C(C)CC)CO)CC(C)C 864.10 unknown https://doi.org/10.1016/S0040-4039(97)00495-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
cyclo[Gly-Ile-Leu-Gly-Ser-Pro-Ile-Leu-Leu] 101702231 Click to see 864.10 unknown https://doi.org/10.1016/S0040-4039(97)00495-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4R,5S)-2-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]piperidine-3,4,5-triol 10245742 Click to see C1C(C(C(C(N1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O 325.31 unknown https://doi.org/10.1248/CPB.52.608
GlyTouCan:G20812UT 53301851 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-3-[(1R,3S)-2,2-dimethyl-3-(3-oxobutyl)cyclopropyl]-1-(4-hydroxy-3-methylphenyl)-2-methylpropan-1-one 101477139 Click to see CC1=C(C=CC(=C1)C(=O)C(C)CC2C(C2(C)C)CCC(=O)C)O 316.40 unknown https://doi.org/10.1021/OL102802U
3-[2,2-Dimethyl-3-(3-oxobutyl)cyclopropyl]-1-(4-hydroxy-3-methylphenyl)-2-methylpropan-1-one 162986096 Click to see 316.40 unknown https://doi.org/10.1021/OL102802U
> Organoheterocyclic compounds / Azoles / Imidazoles / Trisubstituted imidazoles / 2,4,5-trisubstituted imidazoles
5-butyl-2-chloro-1H-imidazole-4-carbaldehyde 11469508 Click to see 186.64 unknown https://doi.org/10.1002/CHIN.200539182
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see 112.09 unknown https://doi.org/10.1016/S0031-9422(98)00531-7
> Organoheterocyclic compounds / Dihydrofurans / Furanones
(3R,6Z,9Z)-3,7,11,11,14-pentamethyl-16-oxatricyclo[11.2.1.01,5]hexadeca-4,6,9,13-tetraene-8,15-dione 23351213 Click to see 312.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-2-ones
5-Hydroxypyrrolidin-2-one 194148 Click to see C1CC(=O)NC1O 101.10 unknown https://doi.org/10.1016/S0031-9422(98)00531-7
> Organoheterocyclic compounds / Pyrrolines
(2S)-2-hydroxy-4-methyl-1,2-dihydropyrrol-5-one 5325835 Click to see CC1=CC(NC1=O)O 113.11 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 1-phenyltetrahydroisoquinolines
Solifenacin 154059 Click to see 362.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Tetradecyl (E)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enoate 10385745 Click to see CCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 390.60 unknown https://doi.org/10.1248/CPB.52.608
Tetradecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 54165620 Click to see 390.60 unknown https://doi.org/10.1248/CPB.52.608
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see 206.19 unknown https://doi.org/10.1002/HLCA.201000313
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
7-(1,1-Dimethylallyl)-2,2-dimethyl-pyrano[3,2-g]chromen-8-one 14133592 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C=C)C 296.40 unknown https://doi.org/10.1021/NP020060D
> Phenylpropanoids and polyketides / Macrolactams
(3R,5R,7S,10S,11E,13S)-10-hydroxy-3,6,6,10,16-pentamethyl-14-azatricyclo[11.2.1.05,7]hexadeca-1(16),11-diene-2,15-dione 44557906 Click to see CC1CC2C(C2(C)C)CCC(C=CC3C(=C(C1=O)C(=O)N3)C)(C)O 331.40 unknown https://doi.org/10.1021/OL902349F
10-Hydroxy-3,6,6,10,16-pentamethyl-14-azatricyclo[11.2.1.05,7]hexadeca-1(16),11-diene-2,15-dione 75069193 Click to see 331.40 unknown https://doi.org/10.1021/OL902349F

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