Details Top

Internal ID UUID643ff680e158c760812821
Scientific name Nelumbo lutea
Authority Pers.
First published in Syn. Pl. 2: 92 (1806)

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.

Nelumbo lutea, the American lotus, is remembered in Native North American herbal practice as a calming nervine and gynecologic tonic. In the eastern Woodlands, medicine people prepared a gentle cold infusion of the dried seeds for stomach upset and nervous tension. Similar preparations were used by Mississippi River peoples as a soothing “women’s medicine” after childbirth, and in the Ozarks Appalachian infusions of the seeds served as a calming tonic for irritability and insomnia (Moerman, 1998; Kavasch, 1979; Moerman, 1986). Over a vast interior from the Midwest to the Gulf Coast, pods and seeds were also eaten as food and carried as traveler’s provisions, a pattern noted by early ethnographers in the 19th and early 20th centuries (Moerman, 1998; Swanton, 1928; Fowles, 2004). These soothing uses of the seed infusion are consistent with the plant’s later reputation in Chinese and East Asian herbal medicine (Zhao et al., 2005).

For a practical dose, cover 1 tablespoon of roughly crushed dried Nelumbo lutea seeds with 1 cup of cool water in a jar, stir, and let sit at room temperature for 6–8 hours. Strain and sip 1/2 to 1 cup over 10–12 hours. Do not exceed 2 cups per day. No specific contraindications are recorded for Nelumbo lutea seeds in the cited ethnographies; however, avoid during pregnancy unless instructed by a qualified practitioner.

Well-established seed constituents include the isoquinoline alkaloids liensinine, neferine, and nuciferine, together with flavonoids such as quercetin and kaempferol, all detected in seed extracts (Zhang et al., 2012; Liu et al., 2016). These compounds plausibly underlie the calming and gastrointestinal-relaxing effects reported in traditional infusions. While clinical trials are limited, modern research continues to explore the pharmacology of lotus seed alkaloids in vitro and in animals, and North American wild-harvested N. lutea seeds remain available through specialty seed and herbal suppliers, alongside living rhizomes for ornamental and ecological restoration plantings (McKetta & Noe, 1993).

General Uses Top

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Common products:
Rhizomes (fleshy underground stems) and seeds are the primary harvested parts. Market forms include sliced, fresh rhizomes similar in texture to celery and lotus root; sliced or wafer‑like crisps that are dried, seasoned, and fried; and popped or roasted seeds. The rhizome flesh is valued for its high starch content and crisp texture.

Food and beverages (non-medicinal):
Rhizomes are used as a fresh vegetable: sliced, battered and fried, or incorporated into soups and stir‑fries. Seeds are consumed raw, toasted, popped (producing a popcorn‑like snack), or ground into flour for baking. These uses are supported by Native American ethnobotanical documentation and modern commercial production records for the species.

Properties relevant to use:
Rhizomes contain abundant starch granules stored in parenchyma tissue, conferring a firm, starchy texture suitable for slicing and frying. Seeds are oleaginous and accumulate triacylglycerols; their oil profile has been analyzed and reported to be dominated by linoleic and oleic acids, with measured iodine values around 132 and saponification values around 190, indicating a composition suitable for edible oil applications. The roasted/fffdf seed flavor is characterized by a nut‑like aroma developed during Maillard reactions in high‑temperature drying or toasting.

Wood and fiber:
Aquatic emergent habit; no timber or conventional bast/leaf fiber uses are documented for Nelumbo lutea in reliable sources.

Industrial and craft applications:
No documented industrial uses such as tannins, dyes, gums, or fiber products are reported in the taxa‑specific literature; however, seed oil composition data imply edible use and potentially small‑scale oil milling.

Colorants and tanning:
No reliable taxon‑specific references document dye, ink, or tannin extraction from Nelumbo lutea.

Fragrance and cosmetics:
No fragrance, essential oil, or cosmetic uses are documented for this species in the cited literature.

Sustainability and sourcing:
As a wetland obligate native of North America, wild harvesting can affect local populations and aquatic habitat; commercial supply is therefore primarily from cultivated ponds and marshes. There are no taxa‑specific regulations identified for the plant or its products; edible rhizome and seed uses comply with standard domestic food handling and labeling norms.

Synonyms Top

Scientific name Authority First published in
Nelumbo pentapetala Fernald Rhodora 36: 23 (1934)
Nelumbium codophyllum Raf. Fl. Ludov. : 22 (1817)
Nelumbium luteum Willd. Sp. Pl., ed. 4 , 2: 1259 (1799)
Nelumbium jamaicense DC. Syst. Nat. 2: 41 (1821)
Nelumbo nucifera subsp. lutea (Willd.) T.Borsch & Barthlott Beitr. Biol. Pflanzen 68: 443 (1994 publ. 1996)
Nelumbium reniforme Willd. Sp. Pl., ed. 4 , 2: 1260 (1799)
Nelumbium pentapetalum Willd. Sp. Pl., ed. 4 , 2: 1259 (1799)
Nelumbo nucifera var. lutea Kuntze Revis. Gen. Pl. 1: 12 (1891)
Cyamus flavicomus Salisb. Ann. Bot. [König & Sims]. 2(1): 75. 1805 [1 Jun (?) 1805]
Cyamus luteus (Willd.) Nutt. Gen. N. Amer. Pl. [Nuttall]. 2: 25. 1818 [14 Jul 1818]
Cyamus mysticus Salisb. Ann. Bot. [König & Sims]. 2(1): 75. 1805 [1 Jun (?) 1805]
Cyamus nelumbo Sm. Exot. Bot. i. (1806) 59. t. 31.
Cyamus pentapetalus (Walter) Pursh Fl. Amer. Sept. (Pursh) 2: 398. 1813 [Dec 1813]
Cyamus reniformis Pursh Fl. Amer. Sept. (Pursh) 2: 398. 1813 [Dec 1813]
Nymphaea pentapetala Walter Fl. Carol. : 155 (1788)

Common names Top

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Language Common/alternative name
English volee
English volée
English american lotus
English water-chinquapin
English yellow lotus
Spanish loto americano
Arabic نيلم أصفر
Bulgarian жълт лотос
Czech lotos žlutý
German amerikanische lotosblume
German amerikanischer lotos
Persian نلومبو لوتئا
Finnish amerikanlootus
French lotus d'amérique
French lotus jaune
French lotus jaune d'amérique
Hebrew נלומבו צהוב
Croatian američki lotos
Upper Sorbian ameriska lotoska
Japanese キバナハス
Japanese 黄花蓮
Lithuanian geltonasis lotosas
Malayalam നെലംബോ ലൂട്ടിയ
Marathi अमेरिकन कमळ
Norwegian Bokmål amerikansk lotus
Punjab پیلا کنول
Russian Лотос жёлтый
Russian Лотос американский
Swedish amerikansk lotus
Vietnamese sen trắng
Chinese 美国莲
Chinese 美洲黃蓮
Chinese 黃蓮花
Chinese 黄莲花
Chinese 美國蓮
Chinese 黃蓮
Chinese 美国黄莲
Chinese 黄莲
Chinese 美洲黄莲

Subspecies (abbr. subsp./ssp.) Top

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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
  • Northern America
    • Eastern Canada
      • Ontario
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000382419
Florida Plant Atlas 2954
Flora of Alabama 2692
Canadensys 6702
USDA Plants NELU
Tropicos 22600235
KEW urn:lsid:ipni.org:names:605419-1
The Plant List kew-2384987
Missouri Botanical Garden 282906
PFAF Nelumbo lutea
Open Tree Of Life 532278
NCBI Taxonomy 4431
Nature Serve 2.135254
IUCN Red List 169072
IPNI 605419-1
iNaturalist 84160
GBIF 2882453
Freebase /m/03_mpc
WisFlora 4332
EPPO NELLU
EOL 596459
Calflora (Californian flora) 9166
USDA GRIN 320239
Wikipedia Nelumbo_lutea
PaleoBotany 86132

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_056320005.1 American lotus-T2T Complete Genome Wuhan Botanical Garden, Chinese Academy of Sciences 2026-03-25 100 799.62 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
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
NnARF17 and NnARF18 from lotus promote root formation and modulate stress tolerance in transgenic Arabidopsis thaliana Libao C, Shiting L, Chen Z, Shuyan L BMC Plant Biol 02-Mar-2024
PMCID:PMC10908128
doi:10.1186/s12870-024-04852-9
PMID:38431568
Lotus (Nelumbo nucifera): a multidisciplinary review of its cultural, ecological, and nutraceutical significance Yang H, He S, Feng Q, Liu Z, Xia S, Zhou Q, Wu Z, Zhang Y Bioresour Bioprocess 27-Jan-2024
PMCID:PMC10991372
doi:10.1186/s40643-024-00734-y
The bZIP Transcription Factors in Current Jasmine Genomes: Identification, Characterization, Evolution and Expressions Zhao K, Luo X, Shen M, Lei W, Lin S, Lin Y, Sun H, Ahmad S, Wang G, Liu ZJ Int J Mol Sci 29-Dec-2023
PMCID:PMC10779407
doi:10.3390/ijms25010488
PMID:38203660
Impacts of Diet on Reproductive Performance of Captive American Alligators (Alligator mississippiensis) Joanen T, Mikolajczyk AP, Staton M, Kaplan J, Holmes WE, Zappi ME Animals (Basel) 08-Dec-2023
PMCID:PMC10741023
doi:10.3390/ani13243797
PMID:38136834
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124
Analysis of bZIP gene family in lotus (Nelumbo) and functional study of NnbZIP36 in regulating anthocyanin synthesis Zhou P, Li J, Jiang H, Jin Q, Wang Y, Xu Y BMC Plant Biol 15-Sep-2023
PMCID:PMC10503039
doi:10.1186/s12870-023-04425-2
PMID:37710161
Commodity risk assessment of Acer platanoides plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323725
doi:10.2903/j.efsa.2023.8073
PMID:37427021
Commodity risk assessment of Acer campestre plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Commodity risk assessment of Acer palmatum plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323724
doi:10.2903/j.efsa.2023.8075
PMID:37427020
Commodity risk assessment of Acer pseudoplatanus plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323731
doi:10.2903/j.efsa.2023.8074
PMID:37427019
Transcription factor NnMYB5 controls petal color by regulating GLUTATHIONE S-TRANSFERASE2 in Nelumbo nucifera Liu J, Wang Y, Deng X, Zhang M, Sun H, Gao L, Song H, Xin J, Ming R, Yang D, Yang M Plant Physiol 22-Jun-2023
PMCID:PMC10517185
doi:10.1093/plphys/kiad363
PMID:37348874
Analysis of Floral Color Differences between Different Ecological Conditions of Clematis tangutica (Maxim.) Korsh Guo X, Wang G, Li J, Li J, Sun X Molecules 03-Jan-2023
PMCID:PMC9824731
doi:10.3390/molecules28010462
PMID:36615653
A lotus by any other color: Gene regulation divergence in lotus petal development Lanctot A Plant Physiol 26-Dec-2022
PMCID:PMC10022601
doi:10.1093/plphys/kiac596
PMID:36567508
Complete chloroplast genomes of 11 Sabia samples: Genomic features, comparative analysis, and phylogenetic relationship Chen Q, Chen C, Wang B, Wang Z, Xu W, Huang Y, Sun Q Front Plant Sci 16-Dec-2022
PMCID:PMC9800934
doi:10.3389/fpls.2022.1052920
PMID:36589084

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(-)-N-nornuciferine 624491 Click to see 281.30 unknown https://doi.org/10.1002/JPS.2600661132
(12S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene 26202781 Click to see 265.31 unknown https://doi.org/10.1002/JPS.2600661132
(R)-1-Methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-2-ol 91746555 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)OC)O 281.30 unknown https://doi.org/10.1002/JPS.2600661132
(R)-Roemerine 235224 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1002/JPS.2600661132
1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 3108374 Click to see 295.40 unknown https://doi.org/10.1002/JPS.2600661132
1,2-Methylenedioxynoraporphine 3462225 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1002/JPS.2600661132
2-Hydroxy-1-methoxyaporphine 5319512 Click to see 281.30 unknown https://doi.org/10.1002/JPS.2600661132
Aprphine, 1,2-dimethoxy-, (+-)- 22156 Click to see 295.40 unknown https://doi.org/10.1002/JPS.2600661132
Nornuciferine 41169 Click to see 281.30 unknown https://doi.org/10.1002/JPS.2600661132
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1002/JPS.2600661132
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
3-Methyl-2-propylphenol 19370693 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1991.9697932
> Benzenoids / Naphthalenes
1-Methylnaphthalene 7002 Click to see 142.20 unknown https://doi.org/10.1080/10412905.1991.9697932
1,2-Dimethylnaphthalene 11317 Click to see CC1=C(C2=CC=CC=C2C=C1)C 156.22 unknown https://doi.org/10.1080/10412905.1991.9697932
Naphthalene 931 Click to see C1=CC=C2C=CC=CC2=C1 128.17 unknown https://doi.org/10.1080/10412905.1991.9697932
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1080/10412905.1991.9697932
Dotriacontane 11008 Click to see 450.90 unknown https://doi.org/10.1080/10412905.1991.9697932
Eicosane 8222 Click to see 282.50 unknown https://doi.org/10.1080/10412905.1991.9697932
Heneicosane 12403 Click to see 296.60 unknown https://doi.org/10.1080/10412905.1991.9697932
Hentriacontane 12410 Click to see 436.80 unknown https://doi.org/10.1080/10412905.1991.9697932
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1080/10412905.1991.9697932
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1080/10412905.1991.9697932
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1080/10412905.1991.9697932
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1080/10412905.1991.9697932
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1080/10412905.1991.9697932
Nonadecane 12401 Click to see 268.50 unknown https://doi.org/10.1080/10412905.1991.9697932
Octacosane 12408 Click to see 394.80 unknown https://doi.org/10.1080/10412905.1991.9697932
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://doi.org/10.1080/10412905.1991.9697932
Pentacosane 12406 Click to see 352.70 unknown https://doi.org/10.1080/10412905.1991.9697932
Pentadecane 12391 Click to see 212.41 unknown https://doi.org/10.1080/10412905.1991.9697932
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1080/10412905.1991.9697932
Triacontane 12535 Click to see 422.80 unknown https://doi.org/10.1080/10412905.1991.9697932
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1080/10412905.1991.9697932
Tridecane 12388 Click to see 184.36 unknown https://doi.org/10.1080/10412905.1991.9697932
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.1080/10412905.1991.9697932
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697932
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes
n-Heptadecadiene 3016864 Click to see CCCCCCCCCCCCCC=CC=C 236.40 unknown https://doi.org/10.1080/10412905.1991.9697932
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Eicosene 18936 Click to see CCCCCCCCCCCCCCCCCCC=C 280.50 unknown https://doi.org/10.1080/10412905.1991.9697932
1-Hentriacontene 528988 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C 434.80 unknown https://doi.org/10.1080/10412905.1991.9697932
1-Heptacosene 528971 Click to see 378.70 unknown https://doi.org/10.1080/10412905.1991.9697932
1-Hexadecene 12395 Click to see 224.42 unknown https://doi.org/10.1080/10412905.1991.9697932
1-Nonacosene 156989 Click to see 406.80 unknown https://doi.org/10.1080/10412905.1991.9697932
1-Nonadecene 29075 Click to see 266.50 unknown https://doi.org/10.1080/10412905.1991.9697932
1-Pentacosene 528972 Click to see 350.70 unknown https://doi.org/10.1080/10412905.1991.9697932
1-Tricosene 181154 Click to see CCCCCCCCCCCCCCCCCCCCCC=C 322.60 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl hexanoate 31265 Click to see CCCCCC(=O)OCC 144.21 unknown https://doi.org/10.1080/10412905.1991.9697932
Ethyl stearate 8122 Click to see 312.50 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl arachidate 14259 Click to see 326.60 unknown https://doi.org/10.1080/10412905.1991.9697932
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.1080/10412905.1991.9697932
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1080/10412905.1991.9697932
Methyl tricosanoate 75519 Click to see CCCCCCCCCCCCCCCCCCCCCCC(=O)OC 368.60 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1080/10412905.1991.9697932
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(10E)-2,6,11,15-tetramethylhexadeca-2,7,10,14-tetraen-6-ol 129661573 Click to see 290.50 unknown https://doi.org/10.1080/10412905.1991.9697932
2,6,11,15-Tetramethylhexadeca-2,7,10,14-tetraen-6-ol 71317439 Click to see 290.50 unknown https://doi.org/10.1080/10412905.1991.9697932
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1991.9697932
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697932
Linalyl hexanoate 564550 Click to see CCCCCC(=O)OC(C)(CCC=C(C)C)C=C 252.39 unknown https://doi.org/10.1080/10412905.1991.9697932
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697932
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697932
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1991.9697932
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1991.9697932
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1991.9697932
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1991.9697932
beta-Cadinene 10657 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1991.9697932
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1991.9697932
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1991.9697932
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697932
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1991.9697932
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel- 10583 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1991.9697932
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Jasmone 1549018 Click to see 164.24 unknown https://doi.org/10.1080/10412905.1991.9697932
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(+/-)-Armepavine 98348 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC 313.40 unknown https://doi.org/10.1002/JPS.2600661132
https://doi.org/10.1016/0040-4020(63)80025-3
Armepavine 442169 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC 313.40 unknown https://doi.org/10.1016/0040-4020(63)80025-3
https://doi.org/10.1002/JPS.2600661132
dl-N-Norarmepavine 317405 Click to see 299.40 unknown https://doi.org/10.1002/JPS.2600661132
L-(-)-N-norarmepavine 6999736 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)OC 299.40 unknown https://doi.org/10.1002/JPS.2600661132

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