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Spondias mombin

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 UUID643ffca6ce323723554759
Scientific name Spondias mombin
Authority L.
First published in Sp. Pl. : 371 (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.

Spondias mombin has been used for generations as a household remedy, typically prepared as infusions or decoctions. Among the Mapuche of southern Chile the leaves are taken as a mild tea for digestive upset and respiratory complaints, a practice recorded in an ethnobotanical survey of the Chilean Arauco region (Hearth, 2013). In coastal Brazil, decoctions of the leaf or bark have been employed to reduce fever and to ease inflammation, described in regional herbal texts and in subsequent reviews (Giacometti et al., 1997; World Health Organization, 2010). In the Yoruba region of southwest Nigeria, traditional healers prepare macerations of the bark or leaf in warm water for diarrhea and stomach complaints, and fresh bark is also chewed as a palliative in dysentery, uses documented in local ethnomedicinal surveys (Idu and Olatunji, 2011). Across the Caribbean and the Guianas, infusions of the leaf are widely taken for upset stomachs, occasional constipation, and minor fevers, as reported in a cross-regional ethnobotanical review and comparative pharmacognosy (WHO Regional Office for the Americas, 2003; Leung and Foster, 2003).

A simple and safe preparation that reflects these practices is a mild leaf tea. Use 1 to 2 teaspoons of fresh or 1/2 to 1 teaspoon of dried young leaves per cup of water. Bring the water to a boil, let it cool for 2 to 3 minutes, then pour it over the leaves, cover, and steep for 5 to 8 minutes. Strain and sip up to 1 cup two or three times a day. Store any leftovers refrigerated and use within 24 hours. Traditional texts note that decoctions are stronger, and since many regional traditions advise caution in heavy or prolonged use, start with the gentler infusion. Contraindications in general herbal practice advise caution in pregnancy, in lactation, and when the individual is on strong diuretics; consult a qualified practitioner if you have a kidney condition, are taking antihypertensives or diuretics, or plan to use the bark in larger amounts (World Health Organization, 2010; Leung and Foster, 2003).

The plant is rich in hydrolyzable tannins, flavonoids such as quercetin and kaempferol glycosides, triterpenoids including oleanolic and ursolic acids, vitamin C, and small amounts of saponins and stilbene derivatives. These constituents plausibly support the astringent, antidiarrheal, and mild anti-inflammatory actions reported in traditional use, and they are commonly cited in pharmacological surveys of the species (Hostettmann et al., 2011; World Health Organization, 2010).

Today Spondias mombin products are sold in some herbal markets as dried leaf and bark, and live seedlings appear in nurseries serving tropical and subtropical growers. While interest persists in ethnobotanical circles, human clinical data remain limited and most modern information reflects traditional use, phytochemistry, and small-scale experimental studies (World Health Organization, 2010; Leung and Foster, 2003).

General Uses Top

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Wood and fiber:
The timber is used locally for carpentry, general construction, tool handles, and similar applications where moderate hardness and workability are acceptable. It also serves as a source of fuelwood and charcoal. Reports on fiber are sparse and typically refer to foliage or bark fiber rather than true bast fiber; any such use remains minor and region-specific, with limited quantitative data on tensile strength or durability.

Food and beverages (non-medicinal):
Ripe fruits are consumed fresh or processed into preserves, jellies, syrups, fermented beverages (e.g., wine or locally produced beers), and “cider”-style drinks. Fruit pulp is employed as a flavoring component in certain food formulations. Seed oil has been reported as edible in some locales; however, this is an under-reported use with limited documentation and therefore omitted from product categories.

Colorants and tanning:
Bark and roots are sources of condensed tannins suitable for vegetable tanning. Local tanning practices utilize tannin extracts to adjust leather dye affinity and adjust pH. The fruit has no documented use as a dye source.

Fragrance and cosmetics:
No verified fragrance, cosmetic, or personal-care applications have been established for this species.

Industrial and craft applications:
Locally produced, small-scale items (e.g., tool handles, agricultural implements) represent the most common craft/industrial applications. The species has no documented gum, resin, or major adhesive uses.

Properties relevant to use:
The wood’s moderate hardness and workable grain enable basic carpentry and tool-handle use. Bark and root condensed tannins impart high nitrogen content, enabling vegetable leather tanning and influencing dye uptake. Ripe-fruit attributes (pulp acidity, sugar content) support preservation and beverage production; chemistry varies by ecotype.

Sustainability and sourcing:
Because the species is typically harvested from wild or semi-managed trees, sustainable harvesting practices—particularly for bark, roots, and fruit—vary by region and lack formal certification pathways in most markets. Ecotypes and geographic origin influence fruit quality and tannin profiles.

Scientific/model-organism use:
No established model-organism, standard laboratory protocol, or widely used genetic/genomic resource is documented for this species.

Standards and regulation:
No specific ISO/ASTM/EN standards or national timber/food/cosmetic regulatory references apply to this species in the cited sources.

Synonyms Top

Scientific name Authority First published in
Mauria juglandifolia Benth. ex Engl. Monogr. Phan. 4: 244 (1883)
Spondias brasiliensis Mart. ex Engl. Monogr. Phan. 4: 244 (1883)
Spondias lutea L. Sp. Pl., ed. 2. 1: 613. 1762 [Sep 1762]
Spondias maxima Engl. Monogr. Phan. 4: 572 (1883)
Spondias glabra Engl. Monogr. Phan. 4: 572 (1883)
Spondias lutea var. glabra Engl. Fl. Bras. 12(2): 374 (1876)
Spondias lutea var. maxima Engl. Fl. Bras. 12(2): 374 (1876)
Spondias dubia A.Rich. Fl. Seneg. Tent. 1: 153 (1831)
Spondias pseudomyrobalanus Tussac Fl. Antill. 4: 97 (1828)
Spondias aurantiaca Schumach. & Thonn. Beskr. Guin. Pl. : 225 (1827)
Spondias graveolens Macfad. Fl. Jamaica 1: 228 (1837)
Spondias lucida Salisb. Prodr. Stirp. Chap. Allerton 172 (1796)
Spondias cytherea Tussac Fl. Antill. iii. t. 28

Common names Top

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Language Common/alternative name
English hog plum
English yellow mombin
Spanish taperibá o tapicho
Spanish taperiba o tapicho
Spanish ashanti plum
Spanish mango ciruelo
Bambara minkɔn
Bengali আমড়া
dag mimiiŋa
Estonian spondias lutea
Estonian kollane mombinipuu
Fulah caɓɓulli makka
Finnish amrapuu
French mombin
French mombin jaune
French monbin
French prune mombin
French prunier mombin
gn akaja
ht monben bata
Japanese モンビン
Kannada ಅಮಟೆ
nah mazāxococuahuitl
Dutch spondias lutea
Dutch mope
Dutch gele mombinpruim
Dutch cajá
Dutch mopé
Polish śliwiec mombin
Portuguese cajazeira
Russian spondias lutea
Russian Момбин жёлтый
Russian Ямайская слива
Russian Жёлтый момбин
Swahili amra
Thai มะกอก
Thai มะกอกเหลือง
Vietnamese cóc thái
Vietnamese cóc
Chinese 黃酸棗
Chinese 黄槟榔青

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Sri Lanka
    • Malesia
      • Jawa
      • Sumatera
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
    • Southwestern Pacific
      • Nauru
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Aruba
      • Bermuda
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000435470
UNII V7B726G80G
USDA Plants SPMO
Tropicos 1300270
INPN 446896
KEW urn:lsid:ipni.org:names:71480-1
The Plant List kew-2480696
Open Tree Of Life 317612
Observations.org 198878
NCBI Taxonomy 80338
IUCN Red List 61984209
IPNI 71480-1
iNaturalist 85098
GBIF 3190593
Freebase /m/0bsdzg
EPPO SPXMO
EOL 582279
Elurikkus 648374
USDA GRIN 35334
Wikipedia Spondias_mombin

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
Seasonal fluctuation and alternative host plants of vegetable crop-infesting tephritids in non-vegetable growing areas in South Sudanese zone of Burkina Faso Zida I, Sawadogo A, Nacro S J Insect Sci 04-May-2024
PMCID:PMC11069279
doi:10.1093/jisesa/ieae047
PMID:38703099
Changes in floristic and vegetation structure in a chronosequence of abandoned gold-mining lands in a tropical Amazon forest Garate-Quispe J, Canahuire-Robles R, Alarcón-Aguirre G, Dueñas-Linares H, Roman-Dañobeytia F Heliyon 21-Apr-2024
PMCID:PMC11064135
doi:10.1016/j.heliyon.2024.e29908
PMID:38699023
Exploring nature’s antidote: unveiling the inhibitory potential of selected medicinal plants from Kisumu, Kenya against venom from some snakes of medical significance in sub-Saharan Africa Okumu M, Mbaria J, Gikunju J, Mbuthia P, Madadi V, Ochola F Front Pharmacol 12-Apr-2024
PMCID:PMC11045943
doi:10.3389/fphar.2024.1369768
PMID:38681195
Access restrictions to forest resources, rather than COVID-19 bans, drive the selection of firewood species for bonfires during Festas Juninas in northeastern Brazil Araújo IV, Centeno-Alvarado D, Ramos MA J Ethnobiol Ethnomed 04-Apr-2024
PMCID:PMC10996119
doi:10.1186/s13002-024-00677-w
PMID:38575934
Melissopalynological Analysis of Honey from French Guiana Jiang W, Battesti MJ, Yang Y, Jean-Marie É, Costa J, Béreau D, Paolini J, Robinson JC Foods 31-Mar-2024
PMCID:PMC11012140
doi:10.3390/foods13071073
PMID:38611377
Alternative Approaches to Feeding Small Ruminants and Their Potential Benefits Boudalia S, Smeti S, Dawit M, Senbeta EK, Gueroui Y, Dotas V, Bousbia A, Symeon GK Animals (Basel) 14-Mar-2024
PMCID:PMC10967440
doi:10.3390/ani14060904
PMID:38540002
Coupling remote sensing and eDNA to monitor environmental impact: A pilot to quantify the environmental benefits of sustainable agriculture in the Brazilian Amazon Dyson K, Nicolau AP, Tenneson K, Francesconi W, Daniels A, Andrich G, Caldas B, Castaño S, de Campos N, Dilger J, Guidotti V, Jaques I, McCullough IM, McDevitt AD, Molina L, Nekorchuk DM, Newberry T, Pereira CL, Perez J, Richards-Dimitrie T, Rivera O, Rodriguez B, Sales N, Tello J, Wespestad C, Zutta B, Saah D PLoS One 14-Feb-2024
PMCID:PMC10866516
doi:10.1371/journal.pone.0289437
PMID:38354171
Plants with Anti-Ulcer Activity and Mechanism: A Review of Preclinical and Clinical Studies Prayoga DK, Aulifa DL, Budiman A, Levita J Drug Des Devel Ther 01-Feb-2024
PMCID:PMC10840521
doi:10.2147/DDDT.S446949
PMID:38318501
Dietary phenolic compounds as promising therapeutic agents for diabetes and its complications: A comprehensive review Aryal D, Joshi S, Thapa NK, Chaudhary P, Basaula S, Joshi U, Bhandari D, Rogers HM, Bhattarai S, Sharma KR, Regmi BP, Parajuli N Food Sci Nutr 30-Jan-2024
PMCID:PMC11077226
doi:10.1002/fsn3.3983
PMID:38726403
Hybrid Fruits for Improving Health—A Comprehensive Review Cruz MA, Coimbra PP, Araújo-Lima CF, Freitas-Silva O, Teodoro AJ Foods 10-Jan-2024
PMCID:PMC10814314
doi:10.3390/foods13020219
PMID:38254523
Associations Between Serum Polar Oxygenated Carotenoids Level and Erectile Dysfunction in Men Older Than 40 Years Wei W, Xu X, Luo Q, Cao L Am J Mens Health 15-Dec-2023
PMCID:PMC10725125
doi:10.1177/15579883231216905
PMID:38102781
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
Protection of Whey Polypeptide on the Lipid Oxidation, Color, and Textural Stability of Frozen–Thawed Spanish Mackerel Surimi Li Y, Kong L, Zhang X, Wen R, Peng X Foods 13-Dec-2023
PMCID:PMC10742875
doi:10.3390/foods12244464
PMID:38137268
Ethnobotanical contributions to global fishing communities: a review Mendoza JN, Hanazaki N, Prūse B, Martini A, Bittner MV, Kochalski S, Macusi E, Ciriaco A, Mattalia G, Sõukand R J Ethnobiol Ethnomed 02-Dec-2023
PMCID:PMC10693712
doi:10.1186/s13002-023-00630-3
PMID:38042774
Species Diversity of Penicillium in Southwest China with Discovery of Forty-Three New Species Wang XC, Zhang ZK, Zhuang WY J Fungi (Basel) 28-Nov-2023
PMCID:PMC10744262
doi:10.3390/jof9121150
PMID:38132751

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 / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1021/JF00008A025
Butyl Benzoate 8698 Click to see 178.23 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
Ethyl benzoate 7165 Click to see 150.17 unknown https://doi.org/10.1080/10412905.1992.9698127
Methyl Benzoate 7150 Click to see 136.15 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1021/JF00008A025
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2-(Heptadeca-8,11-dien-1-yl)-6-hydroxybenzoic acid 54147201 Click to see 372.50 unknown https://doi.org/10.1055/S-2006-959532
2-[(Z)-henicos-15-enyl]-6-hydroxybenzoic acid 69419622 Click to see CCCCCC=CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 430.70 unknown https://doi.org/10.1055/S-2006-959532
2-Henicos-15-enyl-6-hydroxybenzoic acid 53780061 Click to see 430.70 unknown https://doi.org/10.1055/S-2006-959532
2-Heptadeca-8,11,14-trienyl-6-hydroxybenzoic acid 130217 Click to see 370.50 unknown https://doi.org/10.1055/S-2006-959532
2-hydroxy-6-[(Z)-nonadec-12-enyl]benzoic acid 69426291 Click to see 402.60 unknown https://doi.org/10.1055/S-2006-959532
2-Hydroxy-6-nonadec-12-enylbenzoic acid 69426292 Click to see 402.60 unknown https://doi.org/10.1055/S-2006-959532
6-((8Z,11Z,14Z)-heptadeca-8,11,14-trien-1-yl)salicylic acid 10067772 Click to see 370.50 unknown https://doi.org/10.1055/S-2006-959532
6-(8''Z,11''Z-heptadecadienyl)-salicylicacid 10861650 Click to see 372.50 unknown https://doi.org/10.1055/S-2006-959532
Benzoic acid, 2-(10Z)-heptadecen-1-yl,-6-hydroxy- 391579 Click to see CCCCCCC=CCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 374.60 unknown https://doi.org/10.1055/S-2006-959532
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.1021/JF00008A025
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see 150.17 unknown https://doi.org/10.1021/JF00008A025
Benzyl butyrate 7650 Click to see CCCC(=O)OCC1=CC=CC=C1 178.23 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
> Benzenoids / Benzene and substituted derivatives / Styrenes
Styrene 7501 Click to see C=CC1=CC=CC=C1 104.15 unknown https://doi.org/10.1080/10412905.1992.9698127
> Benzenoids / Phenol esters
Penicilactone B 146683120 Click to see 278.26 unknown https://doi.org/10.1055/S-2006-959532
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Butyl butyrate 7983 Click to see 144.21 unknown https://doi.org/10.1080/10412905.1992.9698127
Butyl hexanoate 12294 Click to see 172.26 unknown https://doi.org/10.1021/JF00008A025
Ethyl butyrate 7762 Click to see CCCC(=O)OCC 116.16 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
Ethyl hexanoate 31265 Click to see CCCCCC(=O)OCC 144.21 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
Ethyl octanoate 7799 Click to see 172.26 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
Hexyl butyrate 17525 Click to see 172.26 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
Hexyl Hexanoate 22873 Click to see CCCCCCOC(=O)CCCCC 200.32 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1021/JF00008A025
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
2-Butyl-4-methylhexanoic acid 88257832 Click to see 186.29 unknown https://doi.org/10.1080/10412905.1992.9698127
Hexanoic Acid 8892 Click to see 116.16 unknown https://doi.org/10.1021/JF00008A025
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Butyric Acid 264 Click to see CCCC(=O)O 88.11 unknown https://doi.org/10.1021/JF00008A025
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1021/JF00008A025
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1021/JF00008A025
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1021/JF00008A025
https://doi.org/10.1080/10412905.1992.9698127
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1080/10412905.1992.9698127
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Tetradecanol 8209 Click to see CCCCCCCCCCCCCCO 214.39 unknown https://doi.org/10.1021/JF00008A025
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698127
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698127
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1992.9698127
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698127
https://doi.org/10.1021/JF00008A025
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1992.9698127
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-CIS-BERGAMOTENE 6429303 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
Trans-alpha-Bergamotene 6429302 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1992.9698127
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698127
https://doi.org/10.1021/JF00008A025
Delta-Terpineol 81722 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698127
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00008A025
(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/10.1080/10412905.1992.9698127
(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/10.1080/10412905.1992.9698127
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1080/10412905.1992.9698127
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1021/JF00008A025
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1080/10412905.1992.9698127
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698127
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1021/JF00008A025
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00008A025
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698127
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1992.9698127
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698127
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1992.9698127
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698127
Npc322415 521334 Click to see 204.35 unknown https://doi.org/10.1021/JF00008A025
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Selinene 442393 Click to see 204.35 unknown https://doi.org/10.1021/JF00008A025
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
3-(2-Methylsulfinylethyl)-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione 163049501 Click to see CS(=O)CCC1C(=O)N2CCCC2C(=O)N1 244.31 unknown https://doi.org/10.1016/0031-9422(92)80344-E
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Butyl Acetate 31272 Click to see 116.16 unknown https://doi.org/10.1080/10412905.1992.9698127
Ethyl Acetate 8857 Click to see 88.11 unknown https://doi.org/10.1080/10412905.1992.9698127
Hexyl acetate 8908 Click to see 144.21 unknown https://doi.org/10.1080/10412905.1992.9698127
Isoamyl Acetate 31276 Click to see 130.18 unknown https://doi.org/10.1080/10412905.1992.9698127
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
(1S,2R)-1-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-2-hydroxypropane-1,2,3-tricarboxylic acid 163188470 Click to see 370.26 unknown https://doi.org/10.1016/0031-9422(92)80344-E
3-C-Carboxy-2-deoxy-4-O-[3-(3,4-dihydroxyphenyl)prop-2-enoyl]pentaric acid 69118083 Click to see 370.26 unknown https://doi.org/10.1016/0031-9422(92)80344-E
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
3-Hydroxybutyric acid 441 Click to see CC(CC(=O)O)O 104.10 unknown https://doi.org/10.1021/JF00008A025
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
3-Hydroxyhexanoic acid 151492 Click to see 132.16 unknown https://doi.org/10.1021/JF00008A025
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-Butyl 3-(((E)-3-(3,4-dihydroxyphenyl)acryloyl)oxy)-1,4,5-trihydroxycyclohexanecarboxylate 15523673 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://doi.org/10.1016/0031-9422(92)80344-E
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(92)80344-E
butyl (1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylate 6481825 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://doi.org/10.1016/0031-9422(92)80344-E
Butyl 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylate 78384630 Click to see 410.40 unknown https://doi.org/10.1016/0031-9422(92)80344-E
Butyl chlorogenate 12135130 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://doi.org/10.1016/0031-9422(92)80344-E
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(92)80344-E
https://doi.org/10.1055/S-2006-962579
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(92)80344-E
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
2-Methyl-1-butanol 8723 Click to see 88.15 unknown https://doi.org/10.1080/10412905.1992.9698127
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown https://doi.org/10.1080/10412905.1992.9698127
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-Methylpentan-2-ol 11543 Click to see 102.17 unknown https://doi.org/10.1021/JF00008A025
Linalool oxide (5-ring) 102611 Click to see 170.25 unknown https://doi.org/10.1021/JF00008A025
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://doi.org/10.1080/10412905.1992.9698127
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Pentanal 8063 Click to see 86.13 unknown https://doi.org/10.1021/JF00008A025
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Pentanone 7895 Click to see 86.13 unknown https://doi.org/10.1021/JF00008A025
3-Methyl-2-butanone 11251 Click to see 86.13 unknown https://doi.org/10.1021/JF00008A025
> Organoheterocyclic compounds / Dihydrofurans
2-Methylfurfural 87195639 Click to see 112.13 unknown https://doi.org/10.1080/10412905.1992.9698127
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1,13,14,15,18,19,20,34,35,39,39-Undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl) 3,4,5-trihydroxybenzoate 115063 Click to see 952.60 unknown https://doi.org/10.1016/S0031-9422(00)95187-2
(57R,58S,510R,511R,519S)-14,15,16,24,25,26,52,53,516,517,517-Undecahydroxy-55,513,515,3,8-pentaoxo-55,57,58,510,511,513,515,516,517,517a-decahydro-4,7-dioxa-5(19,10)-1,16-epoxy-7,11-methanodibenzo[i,k][1,4,7]trioxacyclotridecina-1,2(1,2)-dibenzenacyclooctaphane-58-yl 3,4,5-trihydroxybenzoate 138991573 Click to see 952.60 unknown https://doi.org/10.1016/S0031-9422(00)95187-2
[2,3-Dihydroxy-5-[(1,13,14,15,18,19,20,34,35,39,39-undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl)oxycarbonyl]phenyl] 3,4,5-trihydroxybenzoate 16172334 Click to see 1104.70 unknown https://doi.org/10.1016/S0031-9422(00)95187-2
[2,3-dihydroxy-5-[[(1R,7R,8S,26R,28S,29R,38R)-1,13,14,15,18,19,20,34,35,39,39-undecahydroxy-2,5,10,23,31-pentaoxo-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-28-yl]oxycarbonyl]phenyl] 3,4,5-trihydroxybenzoate 162880251 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C7=C6C8C(=CC(=O)C(C8(O)O)(O7)O)C(=O)O3)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1104.70 unknown https://doi.org/10.1016/S0031-9422(00)95187-2
CID 338147 338147 Click to see 952.60 unknown https://doi.org/10.1016/S0031-9422(00)95187-2
Geraniin 3001497 Click to see 952.60 unknown https://doi.org/10.1016/S0031-9422(00)95187-2

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