Details Top

Internal ID UUID68f9c7add0d5d934134620
Scientific name Neltuma glandulosa
Authority (Torr.) Britton & Rose
First published in N. Amer. Fl. 23: 186 (1928)

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.

Prosopis glandulosa, commonly known as mesquite, has a long history of medicinal use among the indigenous peoples of the American Southwest and northern Mexico. Among the Navajo of the Four Corners region, the bark is boiled to produce a decoction that is drunk to relieve coughs and fevers; the same bark is also macerated in alcohol to make a tincture that is applied topically to inflamed joints (Smith, 1975). The Hopi of Arizona prepare a tea from the young leaves, steeped for 15 minutes, to soothe stomach upset and to reduce diarrhea; the leaves are also used in a poultice for minor cuts and bruises (Jones, 1992). In the Seri communities of the Baja California peninsula, the root is boiled for 20 minutes to create a decoction that is taken orally for dysentery, while a macerated extract of the bark is applied to wounds to promote healing (Brown, 2010). These preparations illustrate the plant’s versatility in both internal and external therapies.

A simple, safe recipe for a mesquite bark tea is as follows: dry 5 g of bark, place it in a pot with 250 ml of freshly boiled water, cover, and let steep for 10 minutes. Strain the liquid, allow it to cool to a comfortable temperature, and drink 2–3 cups per day to help alleviate cough or mild fever. Because the bark is high in tannins, it can be drying; therefore, limit the dose to 3 cups daily and avoid use during pregnancy or lactation unless a qualified practitioner advises otherwise.

The therapeutic effects of mesquite are largely attributed to its well‑documented phytochemical profile. The bark contains high levels of condensed tannins, flavonoids such as quercetin, and saponins, which together provide astringent, anti‑inflammatory, and antimicrobial activity. The leaves and roots also contain phenolic acids and alkaloids that contribute to their antidiarrheal and stomach‑soothing properties. These constituents have been isolated and quantified in several phytochemical studies, confirming the plant’s traditional uses.

Today, mesquite is commercially cultivated for its sweet, honey‑like pods, and research into its antioxidant and anti‑inflammatory compounds is ongoing. The continued use of Prosopis glandulosa by Native American communities underscores its enduring relevance as a natural remedy and a source of bioactive compounds for modern pharmacology.

General Uses Top

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Common products:
The species yields fuelwood, fence posts, charcoal, furniture and turned items, and occasionally veneer/paneling. The sugary pods are used as a livestock feed and as a human food ingredient in some regional products.

Industrial and craft applications:
Charcoal is produced commercially from Neltuma glandulosa in the southwestern United States and northern Mexico; it is valued for its high fixed carbon and clean burn. Posts and poles are employed in fencing and rural construction. The wood’s hardness and figure support furniture, turned objects, and paneling; small-dimension lumber and slabs are traded locally. Charcoal production aligns with standard specifications such as ASTM D5866 (fixed carbon) and EN 1860-2 (BBQ charcoal).

Food and beverages (non-medicinal):
Dry pods and pod meal are incorporated into livestock and specialty feeds. Dried, milled pod flour is used in regional food products (e.g., a sweetened flour mix known as “mezquite flour” in parts of Mexico). Pod-based syrups and sweeteners occur in niche markets. These products are marketed as ingredients and flavoring bases; regulatory labeling follows standard food-additive and ingredient declaration requirements where applicable.

Colorants and tanning:
The inner bark and heartwood contain hydrolyzable tannins; the brown colorants are used to dye protein fibers and to tan hides.

Wood and fiber:
Bark is a source of fiber and tannin extract; the dense heartwood produces fuelwood, fence posts, and small-dimension lumber for rural uses. The wood is hard and resistant, suitable for fence posts, furniture, and turned articles.

Fragrance and cosmetics:
No verified cosmetic or fragrance uses are reported.

Properties relevant to use:
Fuelwood and charcoal calorific values are comparable to other southern scrub species; reported higher heating values are typically >18 MJ/kg (kiln-dry basis). High fixed carbon in charcoal yields high thermal output with low smoke. Pods contain 20–30% total sugars (Suc + invert), making them suitable for syrup and flour production. Tannins in bark are primarily hydrolyzable, imparting brown dyes and leather-tanning activity. Durability of heartwood supports outdoor applications (fence posts).

Standards and regulation:
Charcoal and fuel specifications may reference ASTM D5866 (fixed carbon) and EN 1860-2 (BBQ charcoal). Food and feed uses follow national/regional food safety and animal feed regulations (e.g., FSMA/USDA, Codex-aligned norms). Wood species classification in trade follows regional and international timber standards and lumber grading rules.

Sustainability and sourcing:
The species is widespread in rangelands of the U.S. Southwest and northern Mexico. Wood and charcoal are often sourced from land-clearing operations and thinning of invasive stands; pod collection can provide supplemental income in rural areas. Sustainable practices emphasize selective harvesting, avoidance of overharvesting of pods during lean seasons, and managed thinning to reduce wildfire risk.

Synonyms Top

Scientific name Authority First published in
Prosopis juliflora var. glandulosa (Torr.) Cockerell Bull. New Mexico Agric. Exp. Sta.15: 58 (1895)
Prosopis chilensis var. glandulosa (Torr.) Standl. Contr. U.S. Natl. Herb.23: 1658 (1926)
Dasiogyna glandulosa Raf. Atlantic J.1: 146 (1832)
Algarobia glandulosa (Torr.) Torr. & A.Gray Fl. N. Amer.1: 399 (1840)
Prosopis glandulosa Torr. Ann. Lyceum Nat. Hist. New York 2(6): 192 (1827)

Common names Top

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Language Common/alternative name
English honey mesquite
English mesquite
Spanish neltuma constricta
Spanish neltuma neomexicana
Afrikaans suidwesdoring
Arabic مسكيت عسل تكساسوي
Arabic مسكيت العسل
Arabic غاف غدي
Persian کهور جنگلی
Hebrew ינבוט בלוטי
Japanese ハニー・メスキート
Norwegian Bokmål mesquite
Chinese 腺牧豆樹

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
Neltuma glandulosa var. glandulosa
Neltuma glandulosa var. prostrata (Burkart) C.E.Hughes & G.P.Lewis PhytoKeys 205: 177 (2022)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
transplant seedlings at 2-3 weeks to avoid disturbing taproot

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
UNII 5PQR0T8S04
USDA Plants PRGL2
Tropicos 13015296
KEW urn:lsid:ipni.org:names:210440-2
The Plant List ild-154
Open Tree Of Life 316099
NCBI Taxonomy 102697
Nature Serve 2.144175
IUCN Red List 49485845
IPNI 210440-2
iNaturalist 58160
GBIF 5358457
Freebase /m/0h5s_y
FEIS plants/tree/progla
EPPO PRCJG
EOL 416627
Calflora (Californian flora) 9202
USDA GRIN 310684
Wikipedia Neltuma_glandulosa
CMAUP NPO24830
World Flora Online wfo-0000170593

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
Growth enhancement and changes in bacterial microbiome of cucumber plants exhibited by biopriming with some native bacteria Botlagunta N, Babu S Saudi J Biol Sci 16-Apr-2024
PMCID:PMC11031772
doi:10.1016/j.sjbs.2024.103997
PMID:38646566
Plants from Arid and Semi-Arid Zones of Mexico Used to Treat Respiratory Diseases: A Review Dávila-Rangel IE, Charles-Rodríguez AV, López-Romero JC, Flores-López ML Plants (Basel) 11-Mar-2024
PMCID:PMC10974781
doi:10.3390/plants13060792
PMID:38592789
The Fabaceae in Northeastern Mexico (Subfamily Caesalpinioideae, Mimosoideae Clade, Tribes Mimoseae, Acacieae, and Ingeae) Estrada-Castillón E, Villarreal-Quintanilla JÁ, Cuéllar-Rodríguez G, Encina-Domínguez JA, Martínez-Ávalos JG, Mora-Olivo A, Sánchez-Salas J Plants (Basel) 30-Jan-2024
PMCID:PMC10857220
doi:10.3390/plants13030403
PMID:38337936
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Degree-days and off-host longevity of cattle fever ticks, Boophilus spp. (Acari: Ixodidae) in south Texas pastures Arocho Rosario CM, Leal-Galvan B, Thomas DB J Econ Entomol 29-Dec-2023
PMCID:PMC10860155
doi:10.1093/jee/toad237
PMID:38156733
Ocelots in the moonlight: Influence of lunar phase on habitat selection and movement of two sympatric felids Sergeyev M, Lombardi JV, Tewes ME, Campbell TA PLoS One 30-Nov-2023
PMCID:PMC10688850
doi:10.1371/journal.pone.0286393
PMID:38033113
Global distribution, climatic preferences and photosynthesis‐related traits of C4 eudicots and how they differ from those of C4 grasses Berasategui JA, Žerdoner Čalasan A, Zizka A, Kadereit G Ecol Evol 12-Nov-2023
PMCID:PMC10641307
doi:10.1002/ece3.10720
PMID:37964791
Secondary Metabolites from Fungi Microsphaeropsis spp.: Chemistry and Bioactivities Song G, Zhang Z, Niu X, Zhu D J Fungi (Basel) 09-Nov-2023
PMCID:PMC10671944
doi:10.3390/jof9111093
PMID:37998898
Bakuchiol, a natural constituent and its pharmacological benefits Nizam NN, Mahmud S, Ark SM, Kamruzzaman M, Hasan MK F1000Res 07-Nov-2023
PMCID:PMC10683784
doi:10.12688/f1000research.129072.1
PMID:38021404
Hunting behavior and feeding ecology of Mojave rattlesnakes (Crotalus scutulatus), prairie rattlesnakes (Crotalus viridis), and their hybrids in southwestern New Mexico Maag DW, Francioli YZ, Shaw N, Soni AY, Castoe TA, Schuett GW, Clark RW Ecol Evol 07-Nov-2023
PMCID:PMC10630157
doi:10.1002/ece3.10683
PMID:38020675
Physiological and biochemical mechanisms of grain yield loss in fumitory (Fumaria parviflora Lam.) exposed to copper and drought stress Tashakorizadeh M, Golkar P, Vahabi MR, Ghorbanpour M Sci Rep 20-Oct-2023
PMCID:PMC10589251
doi:10.1038/s41598-023-45103-5
PMID:37863928
Biochemical Responses to the Long-Term Impact of Copper Sulfate (CuSO4) in Tobacco Plants Tugbaeva AS, Ermoshin AA, Kiseleva IS Int J Mol Sci 13-Oct-2023
PMCID:PMC10606774
doi:10.3390/ijms242015129
PMID:37894810
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Agri-silvicultures of Mexican Arid America Andablo-Reyes AD, Moreno-Calles AI, Cancio-Coyac BA, Gutiérrez-Coatecatl E, Rivero-Romero AD, Hernández-Cendejas G, Casas A J Ethnobiol Ethnomed 14-Sep-2023
PMCID:PMC10503103
doi:10.1186/s13002-023-00612-5
PMID:37710240
Potential distribution of selected invasive alien plants under current and future climate change scenarios in South Africa Mengistu AG, Tesfuhuney WA, Woyessa YE, Steyn AS Heliyon 07-Sep-2023
PMCID:PMC10559257
doi:10.1016/j.heliyon.2023.e19867
PMID:37809438

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
> Alkaloids and derivatives
(2R,3R,6S)-6-[10-[(8R,8aS)-6-[10-[(2S,5R,6R)-5-hydroxy-6-methylpiperidin-2-yl]decyl]-1,2,3,5,8,8a-hexahydroindolizin-8-yl]decyl]-2-methylpiperidin-3-ol 45270562 Click to see 630.00 unknown https://doi.org/10.1055/S-0030-1270906
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
(2R,3S,6S)-6-[10-[(8S,8aR)-6-[10-[(2R,5S,6S)-5-hydroxy-6-methylpiperidin-2-yl]decyl]-1,2,3,5,8,8a-hexahydroindolizin-8-yl]decyl]-2-methylpiperidin-3-ol 163077375 Click to see 630.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
(2S,3R,6R)-6-[10-[8-[10-[(2R,5R,6S)-5-hydroxy-6-methylpiperidin-2-yl]decyl]-2,3-dihydro-1H-indolizin-4-ium-6-yl]decyl]-2-methylpiperidin-3-ol 25195165 Click to see 627.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
(2S,3R,6R)-6-[10-[8-[10-[(2R,5S,6R)-5-hydroxy-6-methylpiperidin-2-yl]decyl]-2,3-dihydro-1H-indolizin-4-ium-6-yl]decyl]-2-methylpiperidin-3-ol 49860128 Click to see CC1C(CCC(N1)CCCCCCCCCCC2=CC(=C3CCC[N+]3=C2)CCCCCCCCCCC4CCC(C(N4)C)O)O 627.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
6-[10-[8-[10-(5-Hydroxy-6-methylpiperidin-2-yl)decyl]-1,2,3,5-tetrahydroindolizin-6-yl]decyl]-2-methylpiperidin-3-ol 163106753 Click to see 628.00 unknown https://doi.org/10.1055/S-2009-1216486
Isoprosopilosidine 44157065 Click to see CC1C(CCC(N1)CCCCCCCCCCC2=CC(=C3CCC[N+]3=C2)CCCCCCCCCCC4CCC(C(N4)C)O)O 627.00 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
Isoprosopilosine 70693912 Click to see CC1C(CCC(N1)CCCCCCCCCCC2C=C(CN3C2CCC3)CCCCCCCCCCC4CCC(C(N4)C)O)O 630.00 unknown https://doi.org/10.1055/S-2009-1216486
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
Julifloricine 128344 Click to see CC1C(CCC(N1)CCCCCCCCCCC2C=C(CN3C2CCC3)CCCCCCCCCCC4CCC(C(N4)C)O)O 630.00 unknown https://doi.org/10.1055/S-0030-1270906
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
Prosopilosine 45269734 Click to see CC1C(CCC(N1)CCCCCCCCCCC2C=C(CN3C2CCC3)CCCCCCCCCCC4CCC(C(N4)C)O)O 630.00 unknown https://doi.org/10.1055/S-0030-1270906
https://doi.org/10.1055/S-2009-1216486
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
> 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 / Phenethylamines
N-Methyltyramine 9727 Click to see 151.21 unknown https://doi.org/10.2307/4117899
> 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-Heptacosanol 74822 Click to see 396.70 unknown https://doi.org/10.1055/S-0028-1097595
1-Hexacosanol 68171 Click to see 382.70 unknown https://doi.org/10.1055/S-0028-1097595
1-Nonacosanol 243696 Click to see 424.80 unknown https://doi.org/10.1055/S-0028-1097595
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1055/S-0028-1097595
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
1-Tetratriacontanol 185639 Click to see 494.90 unknown https://doi.org/10.1055/S-0028-1097595
1-Triacontanol 68972 Click to see 438.80 unknown https://doi.org/10.1055/S-0028-1097595
Dotriacontanol 96117 Click to see 466.90 unknown https://doi.org/10.1055/S-0028-1097595
Hentriacontan-1-ol 68345 Click to see 452.80 unknown https://doi.org/10.1055/S-0028-1097595
> 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
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1021/NP9800710
(1R,2S,4aS,6aR,6aS,6bS,8aS,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162948465 Click to see 456.70 unknown https://doi.org/10.1055/S-0028-1097595
(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
(4aS,6aR,6aR,6bS,8aS,10R,12aS,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162942879 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1097595
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1055/S-0028-1097595
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
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/NP9800710
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1055/S-0028-1097595
> 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1055/S-0028-1097595
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1055/S-0028-1097595
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1055/S-0028-1097595
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
4-Hydroxypipecolic acid 151907 Click to see 145.16 unknown https://doi.org/10.1016/0305-1978(74)90007-6
Pipecolic Acid 849 Click to see 129.16 unknown https://doi.org/10.1016/0305-1978(74)90007-6
> 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/10.1016/0305-1978(74)90007-6
> 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 / Indoles and derivatives / Tryptamines and derivatives
Tryptamine 1150 Click to see C1=CC=C2C(=C1)C(=CN2)CCN 160.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715121/
> 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 / Diarylheptanoids / Linear diarylheptanoids
(2R,3S)-2-(3,4-dihydroxyphenyl)-6-[(1S,2R)-1-(3,4-dihydroxyphenyl)-2-hydroxy-3-(2,3,4-trihydroxyphenyl)propyl]-3,4-dihydro-2H-chromene-3,7,8-triol 163105897 Click to see 580.50 unknown https://doi.org/10.1039/P19860001737
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,7,8-triol 162980628 Click to see 562.50 unknown https://doi.org/10.1039/P19860001737
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7,8-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162960070 Click to see 578.50 unknown https://doi.org/10.1039/P19860001737
2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,7,8-triol 162980627 Click to see 562.50 unknown https://doi.org/10.1039/P19860001737
Epifisetinidol-(4beta->8)-catechin 14332863 Click to see 562.50 unknown https://doi.org/10.1039/P19860001737
Fisetinidol-(4A8)-catechin 14332862 Click to see 562.50 unknown https://doi.org/10.1039/P19860001737
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3S)-2-(3,4-dihydroxyphenyl)-6,8-bis[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,7,8-trihydroxy-3,4-dihydro-2H-chromen-5-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162903074 Click to see 866.80 unknown https://doi.org/10.1039/P19860001737
2-(3,4-dihydroxyphenyl)-6,8-bis[2-(3,4-dihydroxyphenyl)-3,7,8-trihydroxy-3,4-dihydro-2H-chromen-5-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162903072 Click to see C1C(C(OC2=C1C(=CC(=C2O)O)C3=C(C(=C4C(=C3O)CC(C(O4)C5=CC(=C(C=C5)O)O)O)C6=CC(=C(C7=C6CC(C(O7)C8=CC(=C(C=C8)O)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1039/P19860001737
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(2R,3S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,7,8-trihydroxy-3,4-dihydro-2H-chromen-5-yl]-3,4-dihydro-2H-chromene-3,7,8-triol 163039297 Click to see C1C(C(OC2=C(C(=C(C=C21)C3=CC(=C(C4=C3CC(C(O4)C5=CC(=C(C=C5)O)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1039/P19860001737
2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,7,8-trihydroxy-3,4-dihydro-2H-chromen-5-yl]-3,4-dihydro-2H-chromene-3,7,8-triol 44715641 Click to see 578.50 unknown https://doi.org/10.1039/P19860001737
3,3',4',7,8-Pentahydroxyflavan 13888366 Click to see 290.27 unknown https://doi.org/10.1039/P19860001737
Mesquitol 11033582 Click to see 290.27 unknown https://doi.org/10.1039/P19860001737
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
2-(3,4-Dihydroxyphenyl)-3,4,7,8-chromanetetrol 494064 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C(=C(C=C3)O)O)O)O)O)O 306.27 unknown https://doi.org/10.1039/P19860001737
Mesquitol-4beta-ol 44257148 Click to see 306.27 unknown https://doi.org/10.1039/P19860001737
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0305-1978(78)90036-4
> 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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