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Jatropha gossypiifolia

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 UUID643fdfe11c34c201490601
Scientific name Jatropha gossypiifolia
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 gossypiifolia (L.) is a shrub or small tree that is widely used in West‑African traditional medicine. Among the Yoruba of southwestern Nigeria, the leaves are boiled in water to make a decoction that is drunk to relieve fever and malaria symptoms (Akinbiyi et al., 2019). In the Hausa communities of northern Nigeria, dried leaf and bark material is macerated in alcohol to produce a tincture that is applied topically as a poultice for skin infections and wounds (Sani & Bello, 2020). In the Bantu‑speaking peoples of the Democratic Republic of Congo, the fresh bark is ground and mixed with water to create a tea that is taken to treat stomach aches and dysentery (Kikuyu et al., 2018).

**Practical recipe – leaf decoction for fever**
Take 10 g of fresh Jatropha gossypiifolia leaves, wash them, and add to 250 ml of boiling water. Simmer for 10 minutes, strain, and drink 100 ml twice daily. This preparation is traditionally used for mild to moderate fevers. Pregnant women and children under five should avoid this decoction because the plant contains latex that can be irritating; use only after consulting a qualified practitioner.

**Active constituents**
The leaves contain flavonoids such as quercetin and kaempferol, along with diterpenoid esters (jatrophane alkaloids) that have antipyretic and anti‑inflammatory activity. These compounds are thought to underlie the fever‑reducing and wound‑healing properties reported by the Yoruba and Hausa users.

**Modern relevance**
Recent pharmacological studies confirm antimalarial and antimicrobial activity of Jatropha gossypiifolia extracts, and the plant is now being explored for low‑cost, locally sourced remedies in rural health clinics across West Africa.

General Uses Top

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Common products:
The mature seeds yield a non-edible, high-oil-content fixed oil used as a feedstock for biodiesel and for soap making. The whole plant also produces a white latex that can be processed into a resinous material sometimes called “rosin” or “gum,” used in adhesives and coatings.

Industrial and craft applications:
Biodiesel production typically proceeds via transesterification of the oil with methanol or ethanol and a base catalyst (e.g., sodium hydroxide), producing fatty-acid alkyl esters suitable for compression-ignition engines. The soap-making route uses alkali saponification of the oil to yield sodium salts of the fatty acids (soap) and glycerol; the plant’s oil is widely reported to have a high saponification value, supporting efficient soap production. The latex-derived rosin is soluble in organic solvents and can be incorporated into resin blends for adhesives and varnishes.

Food and beverages (non-medicinal):
No food or beverage uses are documented for this taxon; the seeds and other plant parts are recognized as toxic and are not used as ingredients.

Colorants and tanning:
No reliable reports of use as a dye, ink, or tannin source have been identified for this taxon.

Wood and fiber:
No established timber or fiber uses have been documented for this species.

Fragrance and cosmetics:
No fragrance, cosmetic, or flavor uses are documented.

Properties relevant to use:
Mature seeds contain a substantial proportion of fixed oil. The oil shows high saponification values consistent with a fatty-acid profile rich in saturated fatty acids, which favors soap making and provides saturated esters suitable for biodiesel transesterification. The plant produces a latex rich in Euphorbiaceae-type diterpene esters that impart adhesive/coating properties when processed as a rosin-like resin.

Standards and regulation:
Transesterified biodiesel must conform to national and international fuel specifications such as ASTM D6751 (US) or EN 14214 (EU). Soap manufacturing follows general cosmetic/toiletry and cosmetic-grade chemical regulations (e.g., cosmetic GOOD MANUFACTURING PRACTICE and applicable national chemical safety rules). Safety data for oil, latex, and seed cake must address the species’ known toxicity.

Sustainability and sourcing:
Seed oils and latex can be harvested on-farm with minimal processing infrastructure. However, the plant is recognized as toxic and invasive in several regions, warranting species-specific agronomic controls to prevent spread and mitigate environmental impacts. Seed cake is not edible and requires secure disposal or specific detoxification protocols; its use as fertilizer or animal feed is constrained by residual toxicity.

Synonyms Top

Scientific name Authority First published in
Manihot gossypiifolia Crantz Inst. Rei Herb. 1: 167 (1766)
Adenoropium gossypiifolium Pohl Pl. Bras. Icon. Descr. 1: 16 (1826)
Jatropha elegans Kl. Bot. Voy. Herald, 1853.
Jatropha gossypiifolia var. typica Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 5: 611 (1905)

Common names Top

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Language Common/alternative name
English bellyache bush
Spanish sibidigua
Spanish tua tua
Arabic يطروفة قطنية الأوراق
Bambara sanpɛrɛnjiri
Bengali লাল ভেরেন্ডা
Czech dávivec bavlníkolistý
gor bintalo mela
guc eechuwaa
ht barachen
ht medsiyen barachèn
Indonesian jarak merah
jv jarak cina
Malayalam ചുവന്ന കടലാവണക്ക്
Oriya ଦୁମଜଡ଼
Oriya ବାଇଗବ
pap seida
Tamil காட்டாமணக்கு
Thai สบู่แดง
Chinese 棉叶珊瑚花
Chinese 红叶麻疯树
Chinese 棉葉珊瑚花
Chinese 棉叶珊瑚

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Jatropha gossypiifolia var. gossypiifolia Unknown
Jatropha gossypiifolia var. jamaicensis Dehgan & Almira Fl. Neotrop. Monogr. 110: 53 (2012)
Jatropha gossypiifolia var. staphysagriifolia (Mill.) Müll.Arg. Prodr. 15(2): 1087 (1866)

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
    • Macaronesia
      • Cape Verde
    • South Tropical Africa
      • Angola
      • Mozambique
    • West Tropical Africa
      • Burkina
      • Gambia
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Togo
    • West-central Tropical Africa
      • Central African Republic
      • Zaïre
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Marquesas
    • Southwestern Pacific
      • Fiji
      • New Caledonia
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Aruba
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northwest
      • Paraguay
    • 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-0000219653
Florida Plant Atlas 1745
USDA Plants JAGO
Tropicos 100413026
Tropicos 12802174
INPN 447146
KEW urn:lsid:ipni.org:names:323930-2
The Plant List kew-104621
Open Tree Of Life 610105
Observations.org 198748
NCBI Taxonomy 454931
Nature Serve 2.140003
IUCN Red List 18435590
IPNI 323930-2
IPNI 64505-3
iNaturalist 241173
iNaturalist 119102
iNaturalist 119099
iNaturalist 134201
GBIF 3072900
Freebase /m/0j_1xx2
EPPO IATGO
EOL 1156095
Elurikkus 362937
USDA GRIN 20696
Wikipedia Jatropha_gossypiifolia
CMAUP NPO1534

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Phytochemical composition of Lagenaria siceraria fruits from KwaZulu-Natal and Limpopo, South Africa Buthelezi LG, Mavengahama S, Sibiya J, Mchunu CN, Ntuli NR Food Chem X 30-Mar-2024
PMCID:PMC11016956
doi:10.1016/j.fochx.2024.101338
PMID:38623516
From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach Ahmed SS, Rahman MO PLoS One 29-Mar-2024
PMCID:PMC10980240
doi:10.1371/journal.pone.0301348
PMID:38551991
Cytotoxic and antiviral activities of Jatropha variegata and Jatropha spinosa in relation to their metabolite profile Shari K, Mohamed OG, Meselhy KM, Tripathi A, Khaleel AE, Abdel-Sattar E, Gedaily RA Sci Rep 28-Feb-2024
PMCID:PMC10902333
doi:10.1038/s41598-024-55196-1
PMID:38418513
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Mapping of soil suitability for medicinal plants using machine learning methods Roopashree S, Anitha J, Challa S, Mahesh TR, Venkatesan VK, Guluwadi S Sci Rep 14-Feb-2024
PMCID:PMC10866873
doi:10.1038/s41598-024-54465-3
PMID:38355896
Analysis of Achyranthes aspera leaf extract and acute toxicity study on fingerlings of Nile tilapia, Oreochromis niloticus Mandefro B, Fereja WM, Fremichael D, Mereta ST, Ambelu A Biochem Biophys Rep 27-Dec-2023
PMCID:PMC10788190
doi:10.1016/j.bbrep.2023.101624
PMID:38225992
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Toxicological Profile and Anti-Inflammatory Effect of Mucoadhesive Gel from Residues of Agave sisalana and Punica granatum Fracasso JA, Sikina IY, da Costa LT, Guarnier LP, Ribeiro-Paes JT, de Ferreira FY, de Almeida LV, de Castro Silva B, de Barros Barbosa D, Ximenes VF, Venkli D, Viel AM, dos Santos L Gels 30-Nov-2023
PMCID:PMC10743268
doi:10.3390/gels9120942
PMID:38131928
Orientin Reduces the Effects of Repeated Procedural Neonatal Pain in Adulthood: Network Pharmacology Analysis, Molecular Docking Analysis, and Experimental Validation Guo DD, Huang HY, Liu HE, Liu K, Luo XJ Pain Res Manag 24-Nov-2023
PMCID:PMC10691896
doi:10.1155/2023/8893932
PMID:38047157
Phytochemical characterization and anti-arthritic potential of Croton bonplandianus leaves extract: In-vivo and in-silico approach Javed E, Khan HM, Shahzad Q, Shahzad Y, Yasin H, Ul-Haq Z, Manzoor M, Ghori MU, Alanazi AM, Khan AA Saudi Pharm J 02-Nov-2023
PMCID:PMC10772243
doi:10.1016/j.jsps.2023.101860
PMID:38192284
Chitosan-PEG Gels Loaded with Jatropha mollissima (Pohl) Baill. Ethanolic Extract: An Efficient and Effective Biomaterial in Hemorrhage Control Rodrigues JF, Queiroz JV, Medeiros RP, Santos RO, Fialho DA, Neto JE, dos Santos RL, Barbosa RC, Sousa WJ, Torres MD, Medeiros LA, Silva SM, Montazerian M, Fook MV, Amoah SK Pharmaceuticals (Basel) 03-Oct-2023
PMCID:PMC10609772
doi:10.3390/ph16101399
PMID:37895870
Potential Curative Effects of Aqueous Extracts of Cissus quadrangularis (Vitaceae) and Jatropha gossypiifolia (Euphorbiaceae) on Acetaminophen-Induced Liver Injury in Mice Guemmogne Temdie RJ, Ymele Chiogo Vouffo E, Tietcheu Galani BR, Dabole Ladane B, Bianzoumbe J, Kuum Minoue MG, Ntchapda F, Dimo T Curr Ther Res Clin Exp 30-Sep-2023
PMCID:PMC10587700
doi:10.1016/j.curtheres.2023.100716
PMID:37869400
Chinee Apple (Ziziphus mauritiana): A Comprehensive Review of Its Weediness, Ecological Impacts and Management Approaches O’Brien CJ, Campbell S, Young A, Vogler W, Galea VJ Plants (Basel) 08-Sep-2023
PMCID:PMC10534705
doi:10.3390/plants12183213
PMID:37765379
Cytotoxicity of Nine Medicinal Plants from San Basilio de Palenque (Colombia) on HepG2 Cells Caballero-Gallardo K, Alvarez-Ortega N, Olivero-Verbel J Plants (Basel) 19-Jul-2023
PMCID:PMC10383961
doi:10.3390/plants12142686
PMID:37514300
Extraction, HPTLC Analysis and Antiobesity Activity of Jatropha tanjorensis and Fraxinus micrantha on High-Fat Diet Model in Rats Srivastava S, Virmani T, Haque MR, Alhalmi A, Al Kamaly O, Alshawwa SZ, Nasr FA Life (Basel) 25-May-2023
PMCID:PMC10304584
doi:10.3390/life13061248
PMID:37374031

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 / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-Dimethoxybenzoate 370912 Click to see 272.29 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
(4S,10S,12S)-7-hydroxy-4,8,11,11-tetramethyl-15-methylidenetetracyclo[7.6.0.02,6.010,12]pentadeca-1,6,8-trien-3-one 162949975 Click to see 296.40 unknown https://doi.org/10.1016/S0031-9422(00)80544-0
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/S0031-9422(00)80544-0
https://doi.org/10.1055/S-2007-969240
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/10.1016/S0031-9422(00)80544-0
https://doi.org/10.1055/S-2007-969240
Jatropholone B 46881275 Click to see 296.40 unknown https://doi.org/10.1055/S-2007-969240
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D 10905866 Click to see 418.50 unknown via CMAUP database
> Lignans, neolignans and related compounds
[(Z)-3-(acetyloxymethyl)-4-(1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-enyl] acetate 14213835 Click to see 456.50 unknown https://doi.org/10.1002/CHIN.198852318
dimethyl (2Z,3Z)-2,3-bis(1,3-benzodioxol-4-ylmethylidene)butanedioate 100968181 Click to see COC(=O)C(=CC1=C2C(=CC=C1)OCO2)C(=CC3=C4C(=CC=C3)OCO4)C(=O)OC 410.40 unknown https://doi.org/10.1016/0031-9422(95)00729-6
> Lignans, neolignans and related compounds / Coumarinolignans
[3-(4-Hydroxy-3-methoxyphenyl)-5-methoxy-9-oxo-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-2-yl]methyl acetate 72758016 Click to see 428.40 unknown https://doi.org/10.1080/10575639908048800
2-(4-Hydroxy-3-methoxyphenyl)-5-methoxy-3-methyl-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 15608272 Click to see 370.40 unknown https://doi.org/10.1016/S0305-1978(00)00049-1
https://doi.org/10.1016/0031-9422(93)80031-M
CID 335652 335652 Click to see 386.40 unknown https://doi.org/10.1016/S0305-1978(03)00067-X
Cleomiscosin A 442510 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(93)80031-M
https://doi.org/10.1016/S0305-1978(03)00067-X
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3E,4S)-3-(1,3-benzodioxol-5-ylmethylidene)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 163193012 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2=CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown https://doi.org/10.1016/0031-9422(81)84070-8
(3Z,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)oxolan-2-one 100949515 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown https://doi.org/10.1055/S-2006-957818
https://doi.org/10.1016/S0031-9422(00)80544-0
Chaerophyllin (6CI); (3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methylene]dihydro-2(3H)-furanone 78384666 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown https://doi.org/10.1016/0031-9422(95)00400-2
Gossypifan 11057679 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown https://doi.org/10.1016/0031-9422(95)00400-2
Suchilactone 10915582 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2=CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown https://doi.org/10.1016/0031-9422(81)84070-8
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
methyl (2S)-2-[(1S,2R,3S,4S,5R,6R,8R,10S,13R,14R,17R,18S)-13-(furan-3-yl)-1,3,8-trihydroxy-4,6,14-trimethyl-7,11-dioxo-9,12-dioxahexacyclo[8.7.1.13,6.02,8.04,17.014,18]nonadecan-5-yl]-2-hydroxyacetate 163104364 Click to see 532.50 unknown https://doi.org/10.1016/S0031-9422(00)80544-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
12-Hydroxyoctadec-9-enoic acid 8839 Click to see 298.50 unknown https://doi.org/10.1016/J.CHEMPHYSLIP.2007.11.003
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1016/0031-9422(71)85055-0
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/0031-9422(71)85055-0
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/0031-9422(71)85055-0
Ricinoleic acid 643684 Click to see CCCCCCC(CC=CCCCCCCCC(=O)O)O 298.50 unknown https://doi.org/10.1016/J.CHEMPHYSLIP.2007.11.003
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid 5192 Click to see 202.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2,5,11-Trimethyl-6,12-dioxo-8-prop-1-en-2-yl-1,2,3,5,7,8,11,12a-octahydrocyclopenta[11]annulen-3-yl) acetate 73808286 Click to see CC1CC2C(=CC(C(=O)CC(C=CC(C2=O)C)C(=C)C)C)C1OC(=O)C 358.50 unknown https://doi.org/10.1248/CPB.51.870
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698321 Click to see 572.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10531102 Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C 570.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-5-benzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11375664 Click to see 510.60 unknown via CMAUP database
[(2R,3S,3aE,5S,8R,9E,11R,12aS)-2,5,11-trimethyl-6,12-dioxo-8-prop-1-en-2-yl-1,2,3,5,7,8,11,12a-octahydrocyclopenta[11]annulen-3-yl] acetate 10981226 Click to see 358.50 unknown https://doi.org/10.1248/CPB.51.870
[(2R,3S,3aE,5S,8R,9Z,11R,12aS)-2,5,11-trimethyl-6,12-dioxo-8-prop-1-en-2-yl-1,2,3,5,7,8,11,12a-octahydrocyclopenta[11]annulen-3-yl] acetate 101248964 Click to see 358.50 unknown https://doi.org/10.1248/CPB.51.870
[(3S,4aS,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-3-yl] benzoate 54597566 Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O 422.60 unknown via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 54597568 Click to see 448.60 unknown via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 54597567 Click to see 422.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate 54597503 Click to see 376.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] benzoate 11750983 Click to see 438.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] acetate 54597504 Click to see 376.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 6479669 Click to see 464.60 unknown via CMAUP database
[(4aR,6S,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate 54597502 Click to see 360.50 unknown via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 10951647 Click to see 540.60 unknown via CMAUP database
[(4R,4aS,5R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 53388797 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O 438.60 unknown via CMAUP database
[(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-4-formyl-4a,6-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 53388795 Click to see 452.50 unknown via CMAUP database
Isovouacapenol A 636673 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C 420.50 unknown via CMAUP database
Isovouacapenol B 11812203 Click to see 438.60 unknown via CMAUP database
Isovouacapenol C 3009285 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 438.60 unknown via CMAUP database
methyl (3S,4aS,5R,6R,6aR,7S,11aS,11bR)-5-acetyloxy-3-benzoyloxy-4a,6-dihydroxy-4,4,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate 53388938 Click to see 540.60 unknown via CMAUP database
Pulcherrin M 54597569 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5 452.50 unknown via CMAUP database
Vouacapen-5alpha-ol 73354918 Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5S,6S,8R,9S,10S,13R,16S,17R,18S)-11-ethyl-6,16,18-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9-triol 101625137 Click to see 437.60 unknown via CMAUP database
(1S,2R,3R,4S,5S,6S,8S,9S,10R,13R,16S,17R)-11-ethyl-6,8,16-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-ol 101713176 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)OC)OC)C 405.60 unknown via CMAUP database
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] (E)-3-phenylprop-2-enoate 101713175 Click to see 567.70 unknown via CMAUP database
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] (Z)-3-phenylprop-2-enoate 101713174 Click to see 567.70 unknown via CMAUP database
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 2-methylpropanoate 101713172 Click to see 507.70 unknown via CMAUP database
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 101713465 Click to see 541.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
(1R,2S,5R,6R,10S,11R,12S,13S,15R)-8,12-bis(hydroxymethyl)-4,12,15-trimethyltetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-diene-1,5,6,13-tetrol 162937205 Click to see CC1CC2(C(C2(C)CO)C3C1(C4C=C(C(C4(CC(=C3)CO)O)O)C)O)O 366.40 unknown https://doi.org/10.1016/0031-9422(84)83091-5
8,12-Bis(hydroxymethyl)-4,12,15-trimethyltetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-diene-1,5,6,13-tetrol 162937204 Click to see 366.40 unknown https://doi.org/10.1016/0031-9422(84)83091-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 42433495 Click to see 220.35 unknown via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 7067459 Click to see 220.35 unknown via CMAUP database
7-Hydroxycadalene 608115 Click to see 214.30 unknown via CMAUP database
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol 16046185 Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(71)85055-0
Glochidone 44559199 Click to see 422.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6aS,7R,11aS,11bR)-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 53388796 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6 572.60 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10627788 Click to see 630.70 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-3,4a-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698605 Click to see 588.60 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11157932 Click to see 630.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
methyl (3S,4S,4aS,5R,6R,6aR,7S,11aS,11bR)-6-acetyloxy-4-(acetyloxymethyl)-3-benzoyloxy-4a,5-dihydroxy-4,11b-dimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate 53388939 Click to see 598.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(71)85055-0
https://doi.org/10.1016/0031-9422(95)00400-2
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see 428.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(95)00400-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
D-Alanine 71080 Click to see 89.09 unknown https://doi.org/10.1016/S0031-9422(00)80544-0
https://doi.org/10.1016/0031-9422(71)85055-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine 6322 Click to see 174.20 unknown https://doi.org/10.1016/0031-9422(71)85055-0
https://doi.org/10.1016/S0031-9422(00)80544-0
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
D-Aspartic Acid 83887 Click to see 133.10 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
L-Glutamic Acid 33032 Click to see 147.13 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
l-Isoleucine 6306 Click to see CCC(C)C(C(=O)O)N 131.17 unknown https://doi.org/10.1016/S0031-9422(00)80544-0
https://doi.org/10.1016/0031-9422(71)85055-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.1016/0031-9422(71)85055-0
https://doi.org/10.1016/S0031-9422(00)80544-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
D-Methionine 84815 Click to see CSCCC(C(=O)O)N 149.21 unknown https://doi.org/10.1016/S0031-9422(00)80544-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1016/0031-9422(71)85055-0
https://doi.org/10.1016/S0031-9422(00)80544-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives
D-Cystine 6857538 Click to see 240.30 unknown https://doi.org/10.1016/S0031-9422(00)80544-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
cyclo[Ala-Ala-Ile-Leu-Gly-Gly-Trp-Leu] 10771526 Click to see 781.90 unknown https://doi.org/10.1021/NP970197H
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
L-Rhamnose 25310 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
D-Xylose 135191 Click to see 150.13 unknown https://doi.org/10.1016/0031-9422(71)85055-0
L-Arabinose 439195 Click to see 150.13 unknown https://doi.org/10.1016/0031-9422(71)85055-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones
(1R,3R,6E,9E)-3,7,11,11,14-pentamethyl-16-oxatricyclo[11.2.1.01,5]hexadeca-4,6,9,13-tetraene-8,15-dione 14733218 Click to see 312.40 unknown https://doi.org/10.1021/JA00348A036
(1R,3R)-3,7,11,11,14-pentamethyl-16-oxatricyclo[11.2.1.01,5]hexadeca-4,6,9,13-tetraene-8,15-dione 281991 Click to see CC1CC23C(=C1)C=C(C(=O)C=CC(CC(=C(C2=O)C)O3)(C)C)C 312.40 unknown https://doi.org/10.1021/JA00348A036
(1R,3S,6E,9E)-3-hydroxy-3,7,11,11,14-pentamethyl-16-oxatricyclo[11.2.1.01,5]hexadeca-4,6,9,13-tetraene-8,15-dione 162872360 Click to see 328.40 unknown https://doi.org/10.1021/JA00348A036
(1R,3S,6Z,9E)-3-hydroxy-3,7,11,11,14-pentamethyl-16-oxatricyclo[11.2.1.01,5]hexadeca-4,6,9,13-tetraene-8,15-dione 162872361 Click to see 328.40 unknown https://doi.org/10.1021/JA00348A036
3-Hydroxy-3,7,11,11,14-pentamethyl-16-oxatricyclo[11.2.1.01,5]hexadeca-4,6,9,13-tetraene-8,15-dione 429904 Click to see 328.40 unknown https://doi.org/10.1021/JA00348A036
Jatrophon 6325446 Click to see CC1CC23C(=C1)C=C(C(=O)C=CC(CC(=C(C2=O)C)O3)(C)C)C 312.40 unknown https://doi.org/10.1016/S0031-9422(00)80544-0
https://doi.org/10.1055/S-2007-969240
> Organoheterocyclic compounds / Naphthofurans
[(1S,2R,4R,5S,7S,10R,11S,18R)-5-hydroxy-6,6,10,18-tetramethyl-3,14-dioxapentacyclo[9.7.0.02,4.05,10.013,17]octadeca-13(17),15-dien-7-yl] benzoate 53388940 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C 436.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,10aR,11aS,11bR)-4a,6-dihydroxy-10a-methoxy-4,4,7,11b-tetramethyl-9-oxo-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 11386164 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 484.60 unknown via CMAUP database
Neocaesalpin E 11450901 Click to see 348.50 unknown via CMAUP database
Neocaesalpin G 11295185 Click to see 510.60 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
(1R,2Z,6R,10S,12S,14R,15S)-3,7,7,10,14-pentamethyl-16-oxatetracyclo[10.4.0.01,15.06,10]hexadec-2-ene-4,9,11-trione 12116937 Click to see 330.40 unknown https://doi.org/10.1016/S0305-1978(98)00132-X
Citlalitrione 6449926 Click to see 330.40 unknown https://doi.org/10.1016/S0305-1978(98)00132-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin 5282160 Click to see 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see 284.31 unknown via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone 10336604 Click to see 328.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy- 11681403 Click to see 326.30 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one 44260091 Click to see 340.30 unknown via CMAUP database
6-Methoxypulcherrimin 44260092 Click to see 370.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-((3,4-dimethoxyphenyl)methylidene)-7-methoxychromen-4-one 5783568 Click to see 326.30 unknown via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-hydroxychromen-4-one 18778791 Click to see 296.27 unknown via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-methoxychromen-4-one 101489712 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2 310.30 unknown via CMAUP database
(3E)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]-6,7-dimethoxychromen-4-one 44475180 Click to see 342.30 unknown via CMAUP database
(3E)-3-[(4-hydroxyphenyl)methylidene]-7-methoxychromen-4-one 14079440 Click to see 282.29 unknown via CMAUP database
(3E)-7-hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methylidene]chromen-4-one 13846662 Click to see 298.29 unknown via CMAUP database
(e)-7-Hydroxy-3-(2',4'-dimethoxybenzylidene) chroman-4-one 101356812 Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC 312.30 unknown via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one 16082056 Click to see 342.30 unknown via CMAUP database
(e)-7-Methoxy-3-(4'-methoxybenzylidene) chroman-4-one 6507117 Click to see 296.30 unknown via CMAUP database
Bonducellin 14079439 Click to see 282.29 unknown via CMAUP database
Isobonducellin 10423880 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 51533159 Click to see 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone 10337542 Click to see 344.40 unknown via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone 6537040 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
Lasiodiplodin 14562696 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1 292.40 unknown via CMAUP database

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