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Sesbania punicea

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 UUID643fd8246a6ab041796857
Scientific name Sesbania punicea
Authority (Cav.) Benth.
First published in C.F.P.von Martius & auct. suc. (eds.), Fl. Bras.15(1): 43 (1859)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Ornamental shrub – cultivated for its striking, pendulous racemes of bright red‑purple flowers; widely sold by nurseries and garden centers for landscaping, container planting, and pollinator‑friendly gardens.
- Cut‑flower material – occasionally harvested for floral arrangements because the inflorescences retain colour and last several days in water.
- Nursery propagation stock – reproduced by seed (often scarified) or semi‑hardwood cuttings; seedlings and rooted cuttings are supplied to the horticultural trade.

Industrial and craft applications:
- No documented commercial industrial uses.

Food and beverages (non‑medicinal):
- No documented food‑related uses.

Colorants and tanning:
- No documented use as a natural dye or tanning agent.

Wood and fiber:
- Fuel wood and small‑scale timber – the relatively soft, light‑density wood is sometimes used locally as firewood or for simple craft items; it is not suitable for structural timber because of low mechanical strength.

Fragrance and cosmetics:
- No documented use in perfumery or cosmetic formulations.

Properties relevant to use:
- Fast‑growing, semi‑woody habit reaching 3–5 m in height; readily establishes from seed or cuttings.
- Tolerates saline soils, moderate drought, and full sun, making it suitable for coastal and subtropical gardens.
- Nitrogen‑fixing capability (rhizobial symbiosis) improves soil fertility in cultivated settings.
- Produces abundant, long‑lasting, brightly coloured inflorescences from summer to early autumn, which attract bees and butterflies and provide visual impact throughout the growing season.
- Seed production is prolific, facilitating propagation while also posing a potential source of spread in non‑native regions.

Standards and regulation:
- Classified as a noxious or invasive species in several jurisdictions: South Africa’s National Environmental Management: Biodiversity Act (Category 1b invasive), New Zealand’s National Pest Plant Accord, and Australia’s Weeds of National Significance (WONS).
- Trade may be restricted or require permits; regulatory agencies in these regions monitor and control cultivation and sale.

Sustainability and sourcing:
- In regions where it is invasive, management typically combines mechanical removal, targeted herbicide application, and public education to limit spread.
- Cultivation is promoted in non‑invasive areas as an ornamental, with responsible propagation practices (e.g., preventing seed dispersal) encouraged to mitigate ecological risk.
- Nurseries in compatible climates supply seedlings and cuttings for landscaping, contributing to a sustainable ornamental market while maintaining awareness of its invasive potential.

Synonyms Top

Scientific name Authority First published in
Daubentonia punicea (Cav.) DC. Prodr.2: 267 (1825)
Piscidia ovalifolia Larrañaga Escritos D. A. Larrañaga2: 235 (1923)
Piscidia punicea Cav. Icon.4: 8 (1797)
Sesbania tripetii F.T.Hubb.
Aeschynomene miniata Ortega Nov. Rar. Pl. Descr. Dec.: 28 (1797)
Daubentonia tripetii Poit. Ann. Soc. Hort. Paris27: 136 (1840)
Daubentonia superbissima Haage & Schmidt ex K.Koch Wochenschr. Vereines Beförd. Gartenbaues Königl. Preuss. Staaten14: 158 (1871)
Emerus puniceus (Cav.) Kuntze Revis. Gen. Pl.1: 181 (1891)
Ormocarpum elegans G.Don Gen. Hist.2: 279 (1832)
Solulus elegans (G.Don) Kuntze Revis. Gen. Pl.1: 205 (1891)
Sesbania tripetii (Poit.) hort. ex F.T.Hubb. Stand. Cycl. Hort. 3157. 1917 [28 Mar 1917]
Sesbania tripetii (Poit.) Mouill. Traité Arbr. Arbriss.1: 581 (1894)
Piscidia ovalis Larrañaga Escritos D. A. Larrañaga : t. 95 (1927)
Daubentonia tripetiana Poit. Ann. Soc. Hort. Paris 31: 120 (1842)

Common names Top

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Language Common/alternative name
English rattlebox
Afrikaans brasiliaanse glorie-ertjie
Arabic سيسبان قرمزي
Persian لوبیای درختی چهارپر
French flamboyant d’hyères

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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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
    • South Tropical Africa
      • Malawi
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland
    • Western Indian Ocean
      • Mauritius
  • Northern America
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
      • North Carolina
      • South Carolina
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Argentina Northeast
      • Paraguay
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000178374
Florida Plant Atlas 110
Flora of Alabama 2060
USDA Plants SEPU7
Tropicos 13032916
INPN 122993
Flora of Italy 8613
KEW urn:lsid:ipni.org:names:518525-1
The Plant List ild-2444
Open Tree Of Life 1054481
Observations.org 199496
NCBI Taxonomy 543741
Nature Serve 2.159696
IUCN Red List 144292947
IPNI 518525-1
iNaturalist 79065
GBIF 2970728
Freebase /m/0j7nhp5
EPPO SEBPU
EOL 642820
Elurikkus 344546
Calflora (Californian flora) 8578
USDA GRIN 33776
Wikipedia Sesbania_punicea
CMAUP NPO28665

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
Pest categorisation of Paracoccus marginatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Mar-2023
PMCID:PMC10064853
doi:10.2903/j.efsa.2023.7899
PMID:37009439
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Three New Alien Taxa for Europe and a Chorological Update on the Alien Vascular Flora of Calabria (Southern Italy) Laface VL, Musarella CM, Cano Ortiz A, Quinto Canas R, Cannavò S, Spampinato G Plants (Basel) 11-Sep-2020
PMCID:PMC7569777
doi:10.3390/plants9091181
PMID:32932847
Assessment of Useful Alien Plant Species Cultivated and Managed in Rural Home Gardens of Limpopo Province, South Africa Silas Semenya S, Maroyi A Scientifica (Cairo) 20-Apr-2020
PMCID:PMC7204260
doi:10.1155/2020/3561306
PMID:32399313
Field data on Vegetation Structure and Effects of Human Use of the Dambos Ecosystem in Northern Mozambique Mbanze AA, Mário AM, Rivaes R, Ribeiro-Barros AI, Ribeiro NS Data Brief 12-Sep-2019
PMCID:PMC6811917
doi:10.1016/j.dib.2019.104454
PMID:31667226
Data on introduced plants in Zimbabwe: Floristic changes and patterns of collection based on historical herbarium records Maroyi A Data Brief 22-Sep-2017
PMCID:PMC5712053
doi:10.1016/j.dib.2017.09.046
PMID:29214198
Grazing limits natural biological controls of woody encroachment in Inner Mongolia Steppe Guo H, Guan L, Wang Y, Xie L, Prather CM, Liu C, Ma C Biol Open 13-Sep-2017
PMCID:PMC5665467
doi:10.1242/bio.026443
PMID:28912357
Specificity in Legume-Rhizobia Symbioses Andrews M, Andrews ME Int J Mol Sci 26-Mar-2017
PMCID:PMC5412291
doi:10.3390/ijms18040705
PMID:28346361
Medicinal Plants Cultivated in Bapedi Traditional Healers Homegardens, Limpopo Province, South Africa Semenya SS, Potgieter MJ Afr J Tradit Complement Altern Med 23-Aug-2014
PMCID:PMC4202529
doi:10.4314/ajtcam.v11i5.20
PMID:25395716
Herbal Medicines Used by Bapedi Traditional Healers to Treat Reproductive Ailments in the Limpopo Province, South Africa Semenya S, Maroyi A, Potgieter M, Erasmus L Afr J Tradit Complement Altern Med 31-Dec-2012
PMCID:PMC3746581
doi:10.4314/ajtcam.v10i2.19
PMID:24146458
Lepidopterans as Potential Agents for the Biological Control of the Invasive Plant, Miconia calvescens Morais EG, Picanço MC, Semeão AA, Barreto RW, Rosado JF, Martins JC J Insect Sci 20-May-2012
PMCID:PMC3481469
doi:10.1673/031.012.6301
PMID:22938203
Cytotoxic, Virucidal, and Antiviral Activity of South American Plant and Algae Extracts Faral-Tello P, Mirazo S, Dutra C, Pérez A, Geis-Asteggiante L, Frabasile S, Koncke E, Davyt D, Cavallaro L, Heinzen H, Arbiza J ScientificWorldJournal 24-Apr-2012
PMCID:PMC3349323
doi:10.1100/2012/174837
PMID:22619617
Evolution of petal epidermal micromorphology in Leguminosae and its use as a marker of petal identity Ojeda I, Francisco-Ortega J, Cronk QC Ann Bot 29-Sep-2009
PMCID:PMC2766202
doi:10.1093/aob/mcp211
PMID:19789174
Nodulation of Sesbania species by Rhizobium (Agrobacterium) strain IRBG74 and other rhizobia Cummings SP, Gyaneshwar P, Vinuesa P, Farruggia FT, Andrews M, Humphry D, Elliott GN, Nelson A, Orr C, Pettitt D, Shah GR, Santos SR, Krishnan HB, Odee D, Moreira FM, Sprent JI, Young JP, James EK Environ Microbiol 25-Jun-2009
PMCID:PMC7163632
doi:10.1111/j.1462-2920.2009.01975.x
PMID:19555380
Complete plastid genome sequence of the chickpea (Cicer arietinum) and the phylogenetic distribution of rps12 and clpP intron losses among legumes (Leguminosae) Jansen RK, Wojciechowski MF, Sanniyasi E, Lee SB, Daniell H Mol Phylogenet Evol 27-Jun-2008
PMCID:PMC2586962
doi:10.1016/j.ympev.2008.06.013
PMID:18638561

Phytochemical Profile Top

Add a new one!
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 / Benzoic acid esters
Dimethyl anthranilate 6826 Click to see CNC1=CC=CC=C1C(=O)OC 165.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see 108.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
2-M-Tolylpropene 70759 Click to see 132.20 unknown via CMAUP database
O,alpha-dimethylstyrene 81886 Click to see 132.20 unknown via CMAUP database
p-alpha-Dimethyl styrene 62385 Click to see 132.20 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(-)-Synephrine 854067 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
> Benzenoids / Phenols / 4-alkoxyphenols
4-(3-Methyl-2-butenoxy)phenol 11435274 Click to see CC(=CCOC1=CC=C(C=C1)O)C 178.23 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
6-Hexadecen-4-yne, (E)- 5367338 Click to see CCCCCCCCCC=CC#CCCC 220.39 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatetraenes
12-Methyl-1,5,9,11-tridecatetraene 564371 Click to see 190.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid 10469 Click to see 396.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Decyl acetate 8167 Click to see 200.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3R,3aS,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene-4,9-diol 101281371 Click to see 460.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
cis-alpha-Ocimene 5463455 Click to see 136.23 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Neral 643779 Click to see 152.23 unknown via CMAUP database
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
Thymol 6989 Click to see 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(+)-2-Carene 78249 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
(+)-trans-Sabinene hydrate 11228920 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown via CMAUP database
(1S,2S,3R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-diol 21626089 Click to see CC1(C2CCC1(C(C2O)O)C)C 170.25 unknown via CMAUP database
alpha-THUJENE, (+/-)- 12444324 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown via CMAUP database
Sabinene hydrate 11744854 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(5R)-5-isopropyl-2-methyl-2-cyclohexen-1-one 10888107 Click to see CC1=CCC(CC1=O)C(C)C 152.23 unknown via CMAUP database
2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enyl acetate 11333027 Click to see CC1=CCC(CC1)C(=C)COC(=O)C 194.27 unknown via CMAUP database
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethenyl)-, trans- 12618691 Click to see 152.23 unknown via CMAUP database
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, acetate, (1R-trans)- 6951358 Click to see CC1=CCC(CC1OC(=O)C)C(=C)C 194.27 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
Carvone, (-)- 439570 Click to see 150.22 unknown via CMAUP database
Perillaldehyde, (+)- 1548901 Click to see 150.22 unknown via CMAUP database
Phellandral, (R)- 12305140 Click to see 152.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
trans-1(7),8-p-Menthadien-2-ol 6428442 Click to see 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Farnesene, (3Z,6Z)- 5317320 Click to see 204.35 unknown via CMAUP database
alpha-Sinensal 5281534 Click to see CC(=CCC=C(C)C=C)CCC=C(C)C=O 218.33 unknown via CMAUP database
Farnesol 445070 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Selinene 10856614 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene 6419725 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
Asymmetrical zeta-carotene/Asym. zeta-carotene/7,8,11,12-Tetrahydrolycopene 16061252 Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C 540.90 unknown via CMAUP database
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
epsilon,psi-Carotene, (6R)- 5281230 Click to see 536.90 unknown via CMAUP database
Lycopene 446925 Click to see 536.90 unknown via CMAUP database
Phytofluene 6436722 Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C 542.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1S,3S,6R)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4S,6S)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol 101341894 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown via CMAUP database
(3S,3'R,5R,6S)-beta,beta-Carotene-3,3',5,6(5H,6H)-tetrol 23258402 Click to see 602.90 unknown via CMAUP database
(3S,5R,6S)-beta-cryptoxanthin 5,6-epoxide 23256985 Click to see 568.90 unknown via CMAUP database
(3S,5R,8R,3'R)-mutatoxanthin 21765300 Click to see 584.90 unknown via CMAUP database
(8a(2)R)-Neochrome 14034169 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=C=C3C(CC(CC3(C)O)O)(C)C 600.90 unknown via CMAUP database
all-trans-Neoxanthin 5281247 Click to see 600.90 unknown via CMAUP database
beta-Cryptoxathin-5',6'-epoxide 21587177 Click to see 568.90 unknown via CMAUP database
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see 552.90 unknown via CMAUP database
Violaxanthin 448438 Click to see 600.90 unknown via CMAUP database
Zeaxanthin 5280899 Click to see 568.90 unknown via CMAUP database
Zeinoxanthin 5281234 Click to see 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2E,4E,6E,8E,10E,12E,14E,16E)-17-((4R)-4-Hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-2,6,11,15-tetramethyl-2,4,6,8,10,12,14,16-heptadecaoctaenal 9845703 Click to see 432.60 unknown via CMAUP database
(3E,5E,7E,9E,11E,13E,15E,17E,19E)-20-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-5,9,14,18-tetramethylicosa-3,5,7,9,11,13,15,17,19-nonaen-2-one 101306769 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C)C)C 472.70 unknown via CMAUP database
Apocarotenal 5478003 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C 416.60 unknown via CMAUP database
beta-Citraurinene 90429320 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C)C)C 418.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10R,13R,14R,16S,19R,20S)-19-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 98050000 Click to see 502.50 unknown via CMAUP database
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 92966492 Click to see 470.50 unknown via CMAUP database
(2'R,5aR,7aR,8R,9S,11aR,11bR)-9-[(S)-furan-3-yl-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5,5,7a,9,11b-pentamethyl-3,7-dioxospiro[6,10,11,11a-tetrahydro-5aH-benzo[g][2]benzoxepine-8,3'-oxirane]-2'-carboxylic acid 53363753 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC(C34C(O4)C(=O)O)(C)C(C5=COC=C5)OC6C(C(C(C(O6)CO)O)O)O)C)C 634.70 unknown via CMAUP database
Limonin 179651 Click to see 470.50 unknown via CMAUP database
Nomilin 72320 Click to see 514.60 unknown via CMAUP database
Obacunone 119041 Click to see 454.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5,5'-Oxybis(5-methylene-2-furaldehyde) 12366272 Click to see C1=C(OC(=C1)C=O)COCC2=CC=C(O2)C=O 234.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(R)-alpha-Citronellal 72941638 Click to see 154.25 unknown via CMAUP database
Decanal 8175 Click to see 156.26 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
Octanal 454 Click to see 128.21 unknown via CMAUP database
Undecanal 8186 Click to see CCCCCCCCCCC=O 170.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1R,4R,6S)-1-methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane 6857487 Click to see CC(=C)C1CCC2(C(C1)O2)C 152.23 unknown via CMAUP database
Carvone-5,6-oxide, cis-(-)- 11030188 Click to see 166.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-(4-Hydroxyphenyl)ethyl 3-(4-hydroxyphenyl)prop-2-enoate 86163337 Click to see 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
Xanthyletin 65188 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-5,6,7,4'-tetramethoxyflavone 24752965 Click to see 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Hesperidin 10621 Click to see 610.60 unknown via CMAUP database
Naringin 442428 Click to see 580.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Takakin 44258588 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6-dimethoxyflavone 5481646 Click to see 314.29 unknown via CMAUP database
Eupatilin 5273755 Click to see 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,6,7,4'-Tetramethoxyflavone 14887080 Click to see 342.30 unknown via CMAUP database
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone 152430 Click to see 358.30 unknown via CMAUP database
5,7,3',4',5'-Pentamethoxyflavone 493376 Click to see 372.40 unknown via CMAUP database
8-Hydroxy-4',5,7-trimethoxyflavone 5318368 Click to see 328.30 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Cirsilineol 162464 Click to see 344.30 unknown via CMAUP database
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
Salvigenin 161271 Click to see 328.30 unknown via CMAUP database
Sinensetin 145659 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-7-hydroxy-5,6,8-trimethoxy-4H-1-benzopyran-4-one 10452846 Click to see 388.40 unknown via CMAUP database
3,5,6,7,8,3',4'-Heptamethoxyflavone 150893 Click to see 432.40 unknown via CMAUP database
3'-Demethylnobiletin 183466 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O 388.40 unknown via CMAUP database
3',4'-Didemethylnobiletin 5318041 Click to see 374.30 unknown via CMAUP database
4'-Demethylnobiletin 21593928 Click to see 388.40 unknown via CMAUP database
4'-Hydroxy-5,6,7,8-Tetramethoxyflavone 3010100 Click to see 358.30 unknown via CMAUP database
4',5-Dihydroxy-3',6,7,8-tetramethoxyflavone 181092 Click to see 374.30 unknown via CMAUP database
4',5-Dihydroxy-7,8-dimethoxyflavone 14585506 Click to see 314.29 unknown via CMAUP database
5-Demethoxynobiletin 44584772 Click to see 372.40 unknown via CMAUP database
5-Demethylnobiletin 358832 Click to see 388.40 unknown via CMAUP database
5-Hydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one 14353376 Click to see 328.30 unknown via CMAUP database
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 177696 Click to see 360.30 unknown via CMAUP database
6-Demethoxytangeretin 629964 Click to see 342.30 unknown via CMAUP database
7-Hydroxy-4',5,6,8-tetramethoxyflavone 5318356 Click to see 358.30 unknown via CMAUP database
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown via CMAUP database
Gardenin D 3080750 Click to see 374.30 unknown via CMAUP database
Isosinensetin 632135 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Linderoflavone B 97151 Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4)OC)OC)OC 386.40 unknown via CMAUP database
Nobiletin 72344 Click to see 402.40 unknown via CMAUP database
Sudachitin 12443122 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O 360.30 unknown via CMAUP database
Tangeretin 68077 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4'-Hydroxy-3,6-dimethoxy-6'',6''-dimethylpyrano[2,3:7,8]flavone 44258693 Click to see 380.40 unknown via CMAUP database

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