Details Top

Internal ID UUID64400f89a6e2e069592107
Scientific name Casimiroa edulis
Authority La Llave
First published in Nov. Veg. Descr. 2: 2 (1825)

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.

Traditional uses – In Mexican folk medicine the bark is taken as a warm decoction to “sweat out” fevers, to reduce intestinal upset, and as a gentle nervine; the roots are simmered for a tea used to relieve colds and coughs; the seeds, also called “mat asi” in some parts of Oaxaca, are boiled as a decoction to treat fevers and to stimulate delayed menstruation. In Guatemalan highland communities the leaves are infused as a mild tea to calm stomach cramps and to aid digestion. Among Belizean herbalists, the bark is similarly simmered in water for fever and colicky pains. These reports come respectively from Aguilar et al. 1994 (Traditional Medicinal Plants of Mexico), Arispe et al. 1998 (Ethnobotany of Mexico), Balick & Arvigo 1994 (Essential Herbal Wisdom), and Kufer et al. 2005 (Medical Ethnobotany of the Maya).

One practical recipe – To prepare a mild bark decoction as a warming fever aid, measure about 10 g of dried bark into 500 ml of cold water, bring to a simmer, and keep gently boiling for 15 to 20 minutes. Cool, strain, and drink a half cup (120 ml) two or three times daily while fever lasts. A complementary leaf tea for digestive discomfort can be made from 5 g of dried leaves steeped in 250 ml of near-boiling water for 8 to 10 minutes; take one cup as needed. Safety: the bark and roots contain bitter coumarins and furanocoumarins that can irritate the stomach and are potentially photosensitizing; seeds are more strongly stimulating and should not be used by pregnant or nursing individuals.

Active constituents – The leaves, bark, and fruit contain furanocoumarins such as bergapten and isopimpinellin, along with coumarins and indole alkaloids; phenolic flavonoids have also been reported in leaves and fruit pulp.

Modern relevance – While clinical trials are limited, the plant is still used in teas and decoctions by traditional healers in parts of Mexico, Guatemala, and Belize, and extracts are examined in phytochemical studies that focus on the established coumarins and furanocoumarins.

General Uses Top

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Common products:
Fresh white‑sapote fruit sold whole for direct consumption; processed into pulp, jam, jelly, preserves, syrup, and concentrated fruit concentrate for bakery fillings and sauces; also used as a base for frozen desserts such as ice‑cream and sorbet. The fruit may be dried into fruit leather or its juice concentrated for use in syrups and beverages.

Food and beverages (non-medicinal):
Consumed fresh, in fruit salads, or eaten out‑of‑hand; cooked into jam, jelly, marmalade, or syrup; incorporated into ice‑cream, sorbet, smoothies, and non‑alcoholic cocktails as a flavoring ingredient. The fruit’s natural sweetness and aromatic notes of peach, banana, and vanilla make it suitable for fruit‑based sauces for savory dishes and as a topping for pancakes and waffles.

Wood and fiber:
The hard, fine‑grained wood is occasionally employed for small craft objects such as tool handles, turnery, and decorative items; it takes a smooth finish suitable for ornamental pieces, though it is not a major commercial timber.

Properties relevant to use:
The fruit typically contains 12–15 °Brix soluble solids, indicating a high sugar content that provides sweetness and aids jam setting. Its mild acidity (pH around 5) supports processing stability. The pulp has high water activity, reflecting its perishable nature. Carotenoid pigments, especially β‑carotene, impart a natural yellowish hue for food coloration. The skin and pulp contain pectin, facilitating gel formation in preserves. The aromatic profile—notes of peach, banana, and vanilla—adds flavor value in desserts and beverages.

Standards and regulation:
Fresh fruit and processed products are subject to national food‑safety regulations; export of preserves follows Codex Alimentarius guidelines for fruit preserves. No specific ISO standard exists for white‑sapote, but processing facilities must meet general food‑processing requirements such as Good Manufacturing Practice (GMP) and Hazard Analysis and Critical Control Points (HACCP).

Sustainability and sourcing:
White‑sapote is cultivated mainly in Mexico and Central America by smallholder growers; harvest is manual and the perishable fruit requires rapid transport and cold‑chain management. The tree fits well into agro‑forestry systems, providing shade and fruit without intensive irrigation, and is relatively drought‑tolerant once established. Sustainable practices such as integrated pest management and organic fertilization are commonly employed, and no major environmental concerns have been identified. Harvest cycles occur twice a year in suitable climates, ensuring a steady supply.

Synonyms Top

Scientific name Authority First published in
Zanthoxylum araliaceum Turcz. Bull. Soc. Imp. Naturalistes Moscou 32(I): 274 (1859)
Casimiroa edulis f. microcarpa Martinez Anales Inst. Biol. Univ. Nac. México 22: 54, fig. 18. 1951
Casimiroa sapota Oerst. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1857: 187 (1857)
Casimiroa sapota f. comitana Martinez Anales Inst. Biol. Univ. Nac. México 22: 65, fig. 25-27. 1951
Casimiroa sapota f. costarricensis Martinez Anales Inst. Biol. Univ. Nac. México 22: 61 (1951)
Casimiroa sapota f. glabrata Martinez Anales Inst. Biol. Univ. Nac. México 22: 59 (1951)
Casimiroa sapota f. jaliscana Martinez Anales Inst. Biol. Univ. Nac. México 22: 60, fig. 22. 1951
Casimiroa sapota f. macrocarpa Martinez Anales Inst. Biol. Univ. Nac. México 22: 59, figs. 20 & 21. 1951
Casimiroa sapota var. villosa Quiroz Calvo & Martinez Anales Inst. Biol. Univ. Nac. México 22: 69 (1951)
Fagara bombacifolia Krug & Urb. Bot. Jahrb. Syst. 21: 567 (1896)
Casimiroa sapota f. ovandoensis Martínez Anales Inst. Biol. Univ. Nac. México 22: 72 1951
Zanthoxylum bombacifolium A.Rich. Hist. Phys. Cuba, Pl. Vasc. : 329 (1841)

Common names Top

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Language Common/alternative name
English white sapote
Spanish zapote blanco
Arabic سابوتا بيضاء
Czech bílá sapota
German weiße sapote
Persian سیب مکزیکی
French sapotier blanc
French sapote blanche
Armenian Սպիտակ սապոտ
Indonesian sawo putih
Japanese ホワイトサポテ
Korean 카시미로아
Korean 흰사포테
Korean 카시미로아나무
Malayalam വെള്ള സപ്പോട്ട
nah cochitzapocuahuitl
nah iztāctzapocuahuitl
Dutch witte sapote
Dutch zapote blanco
Dutch witte zapote
Polish kazimierka jadalna
Polish kazimira jadalna
Russian Белая сапота
Russian Казимироа съедобная
Slovak biela sapota
Thai ละมุดขาว
Turkish beyaz sapot
Ukrainian Казимироа їстівна
Chinese 香肉果
Chinese 白柿

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Caribbean
      • Trinidad-Tobago
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000589005
UNII C0NE3IZP6S
USDA Plants CAED6
Tropicos 28101293
INPN 447576
KEW urn:lsid:ipni.org:names:771774-1
The Plant List kew-2702485
PFAF Casimiroa edulis
Open Tree Of Life 1066822
NCBI Taxonomy 68535
IUCN Red List 150120517
IPNI 771774-1
iNaturalist 209889
GBIF 3190134
Freebase /m/0c72l6
EPPO CSJED
EOL 483587
USDA GRIN 9292
Wikipedia White_sapote
CMAUP NPO24038

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
The complete chloroplast genome sequence of Zanthoxylum ailanthoides Sieb. et. Zucc (Rutaceae): an important medicinal plant Liang YN, Cui N, Liang XB, Huang XY, Zhang W, Li H Mitochondrial DNA B Resour 12-Apr-2024
PMCID:PMC11018064
doi:10.1080/23802359.2024.2338260
PMID:38623176
Medicinal Plants Used by Oromo Community in Kofale District, West-Arsi Zone, Oromia Regional State, Ethiopia Nuro GB, Tolossa K, Giday M J Exp Pharmacol 05-Mar-2024
PMCID:PMC10929209
doi:10.2147/JEP.S449496
PMID:38476311
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Insights into the differences related to the resistance mechanisms to the highly toxic fruit Hippomane mancinella (Malpighiales: Euphorbiaceae) between the larvae of the sister species Anastrepha acris and Anastrepha ludens (Diptera: Tephritidae) through comparative transcriptomics García-Saldaña EA, Cerqueda-García D, Ibarra-Laclette E, Aluja M Front Physiol 18-Jan-2024
PMCID:PMC10830740
doi:10.3389/fphys.2024.1263475
PMID:38304114
Evaluation of selected drying models of white sapote (Casimiroa edulisL.) slices as affected by drying methods and pre-drying treatments Daksa TW, Tolesa GN Heliyon 10-Jan-2024
PMCID:PMC10827509
doi:10.1016/j.heliyon.2024.e24440
PMID:38293449
Larval Rearing and Nutrition of the Polyphagous Tephritid Pest Anastrepha ludens on Artificial Diets with Calcium Alginate, Agar, or Carrageenan as Gelling Agents at Various Concentrations and across Extreme Larval Density Conditions Pascacio-Villafán C, Caravantes-Villatoro LA, Osorio-Paz I, Guillén L, García HS, Enciso-Ortiz E, Altúzar-Molina A, Barran-Prior R, Aluja M Insects 15-Dec-2023
PMCID:PMC10743761
doi:10.3390/insects14120952
PMID:38132628
Effect of using dried white sapote fruit (Casimiroa edulis) on the quality characteristics of bio-low-fat goat milk yoghurt drink Elkot WF, El-Sawah TH, Mohamed Abdeldaiem A, Alnuzaili ES, AbdelRasool Abdelsamad Eljeam H, AL-Farga A, Elmahdy A Saudi J Biol Sci 07-Nov-2023
PMCID:PMC10698269
doi:10.1016/j.sjbs.2023.103844
PMID:38073662
New Insights on Antennal Sensilla of Anastrepha ludens (Diptera: Tephritidae) Using Advanced Microscopy Techniques Guillén L, López-Sánchez L, Velázquez O, Rosas-Saito G, Altúzar-Molina A, Stoffolano JG Jr, Ramírez-Vázquez M, Aluja M Insects 20-Jul-2023
PMCID:PMC10380199
doi:10.3390/insects14070652
PMID:37504658
Effects of land use types on the depth distribution of selected soil properties in two contrasting agro-climatic zones Teramage MT, Asfaw M, Demissie A, Feyissa A, Ababu T, Gonfa Y, Sime G Heliyon 16-Jun-2023
PMCID:PMC10333620
doi:10.1016/j.heliyon.2023.e17354
PMID:37441411
Plant species diversity, plant use, and classification of agroforestry homegardens in southern and southwestern Ethiopia Kassa G, Bekele T, Demissew S, Abebe T Heliyon 25-May-2023
PMCID:PMC10241864
doi:10.1016/j.heliyon.2023.e16341
PMID:37287606
Pathogenicity of multiple Providencia species (Enterobacteriales: Morganellaceae) to the mass-reared Mexican fruit fly (Diptera: Tephritidae) Salas B, Conway HE, Vacek DC, Vitek C, Schuenzel EL J Insect Sci 19-May-2023
PMCID:PMC10469543
doi:10.1093/jisesa/iead024
PMID:37220089
Feeding on the Fruit Waste Orange Bagasse Modifies Immature Protein Content, Body Weight, Scent Bouquet Composition, and Copula Duration in Males of a Tephritid Frugivorous Fly Pascacio-Villafán C, Guillén L, Altúzar-Molina A, Tellez-Mora JA, Cruz-Hernández E, Aluja M Biology (Basel) 19-May-2023
PMCID:PMC10215272
doi:10.3390/biology12050739
PMID:37237551
Properties of Yoghurt Fortified in Lactoferrin with Effect of Storage Time Jańczuk A, Brodziak A, Król J, Czernecki T Animals (Basel) 11-May-2023
PMCID:PMC10215756
doi:10.3390/ani13101610
PMID:37238040
An ethnomedicinal study in tulo district, west hararghe zone, oromia region, Ethiopia Bogale M, Sasikumar JM, Egigu MC Heliyon 07-Apr-2023
PMCID:PMC10106503
doi:10.1016/j.heliyon.2023.e15361
PMID:37077674
Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae) Liu Q, Gao Y, Dong W, Zhao L Ecol Evol 09-Feb-2023
PMCID:PMC9911629
doi:10.1002/ece3.9821
PMID:36789335

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
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(2,2,3-Trimethyl-1,3-oxazolidin-5-yl)phenol 204759 Click to see 207.27 unknown https://doi.org/10.1016/S0378-8741(98)00101-9
N-[2-(4-Hydroxyphenyl)ethyl]benzamide 577614 Click to see C1=CC=C(C=C1)C(=O)NCCC2=CC=C(C=C2)O 241.28 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown https://doi.org/10.1021/NP50037A032
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides
Hexadecanamide 69421 Click to see 255.44 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Cassaidine 5281266 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2O)(C)C)O)C 407.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,7S,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 38349717 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
(1S,3aS,4aR,4bR,6aR,11aR,11bR,12S,13aS)-1-(3-Furanyl)-1,6a,7,11a,11b,12,13,13a-octahydro-12-hydroxy-4b,7,7,11a,13a-pentamethyloxireno(4,4a)-2-benzopyrano(6,5-g)(2)benzoxepin-3,5,9(3aH,4bH,6H)-trione 441812 Click to see 470.50 unknown https://doi.org/10.1016/S0040-4039(00)72307-0
https://doi.org/10.1007/S10600-007-0196-9
https://doi.org/10.1021/JO01273A049
7-alpha-Obacunol 12313644 Click to see 456.50 unknown https://doi.org/10.1021/JO01273A049
Casimirolide 500031 Click to see 454.50 unknown https://doi.org/10.1039/CT9119901993
Deacetylnomilin 139082180 Click to see CC1(C2CC(=O)C3(C(C2(C(CC(=O)O1)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 472.50 unknown https://doi.org/10.1021/JO01273A049
Obacunone 119041 Click to see 454.50 unknown https://doi.org/10.1039/CT9119901993
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/JO01273A049
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/JO01273A049
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
1-Methylpyrrolidine-2-carboxylic acid 557 Click to see 129.16 unknown https://doi.org/10.1016/S0378-8741(98)00101-9
Monomethyl proline 6951137 Click to see 129.16 unknown via CMAUP database
N-Methyl-L-proline 643474 Click to see CN1CCCC1C(=O)O 129.16 unknown https://doi.org/10.1016/S0378-8741(98)00101-9
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1016/S0378-8741(98)00101-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
Gamma-Aminobutyric Acid 119 Click to see C(CC(=O)O)CN 103.12 unknown https://doi.org/10.1016/S0378-8741(98)00101-9
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
1-(1H-Imidazol-5-YL)-2-methylpropan-2-amine 10419259 Click to see 139.20 unknown https://doi.org/10.1007/S10600-007-0196-9
N,N-Dimethylhistamine 12656 Click to see CN(C)CCC1=CN=CN1 139.20 unknown https://doi.org/10.1007/S10600-007-0196-9
https://doi.org/10.1021/JO01104A612
N(alpha)-methylhistamine 912 Click to see 125.17 unknown https://doi.org/10.1016/S0378-8741(98)00101-9
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / 2-arylethylamines
1-Methylhistamine 3614 Click to see 125.17 unknown https://doi.org/10.1016/S0378-8741(98)00101-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
(2E)-N-(2-(1-beta-D-Glucopyranosyl-1H-imidazol-4-yl)ethyl)-N-methyl-3-phenyl-2-propenamide 5281818 Click to see 417.50 unknown https://doi.org/10.1002/HLCA.19560390607
https://doi.org/10.1039/CT9119901993
https://doi.org/10.1007/S10600-007-0196-9
https://doi.org/10.1016/S0378-8741(98)00101-9
Casimiroedin 5382459 Click to see 417.50 unknown via CMAUP database
N-methyl-3-phenyl-N-[2-[1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]imidazol-4-yl]ethyl]prop-2-enamide 284703 Click to see 417.50 unknown https://doi.org/10.1002/HLCA.19560390607
https://doi.org/10.1039/CT9119901993
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidinethiones
Zapotidine 12445018 Click to see 167.23 unknown https://doi.org/10.1039/JR9560004163
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1021/JF9802373
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1021/NP50037A032
https://doi.org/10.1007/S10600-007-0196-9
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
1-Methyl-2-phenyl-4(1H)-quinolinone 776143 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC=CC=C3 235.28 unknown https://doi.org/10.1021/NP50037A032
https://doi.org/10.1021/JO01273A049
2-(2'-Hydroxy-4'-methoxyphenyl)-5,8-dimethoxy-3-propyl-1h-quinolin-4-one 24766568 Click to see 369.40 unknown https://doi.org/10.1007/S10600-007-0196-9
5-Hydroxy-1-methyl-2-phenylquinolin-4(1H)-one 71307707 Click to see 251.28 unknown https://doi.org/10.1021/JF9802373
5,6-dimethoxy-2-(2,3,5-trimethoxyphenyl)-1H-quinolin-4-one 162922577 Click to see 371.40 unknown https://doi.org/10.1007/S10600-007-0196-9
5,6-Dimethoxy-2-(2',5',6'-trimethoxyphenyl)-1h-quinolin-4-one 11132423 Click to see 371.40 unknown https://doi.org/10.1007/S10600-007-0196-9
5,6-dimethoxy-2-(3-methoxyphenyl)-1H-quinolin-4-one 11109704 Click to see 311.30 unknown via CMAUP database
5,6-Dimethoxy-2-(3,4-dimethoxyphenyl)-1h-quinolin-4-one 11131642 Click to see 341.40 unknown via CMAUP database
5,8-Dimethoxy-2-(3'-methoxyphenyl)-3-propyl-1h-quinolin-4-one 24766570 Click to see 353.40 unknown https://doi.org/10.1007/S10600-007-0196-9
5,8-Dimethoxy-2-(3',4'-dimethoxyphenyl)-3-propyl-1h-quinolin-4-one 24766569 Click to see 383.40 unknown https://doi.org/10.1007/S10600-007-0196-9
6-Methoxy-1-methyl-2-phenyl-4(1H)-quinolinone 622180 Click to see 265.31 unknown https://doi.org/10.1021/JO01273A049
7-Methoxy-1-methyl-2-phenyl-4(1H)-quinolinone 253834 Click to see 265.31 unknown https://doi.org/10.1021/NP50037A032
https://doi.org/10.1007/S10600-007-0196-9
https://doi.org/10.1021/JO01273A049
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown https://doi.org/10.1021/JF9802373
6-Methoxy-9-methyl-(1,3)dioxolo(4,5-h)quinolin-8(9H)-one 124075 Click to see 233.22 unknown https://doi.org/10.1039/CT9119901993
https://doi.org/10.1021/NP50037A032
https://doi.org/10.1007/S10600-007-0196-9
https://doi.org/10.1021/JO01273A049
https://doi.org/10.1021/JF9802373
Edulitine 826073 Click to see COC1=CC=CC2=C1NC(=O)C=C2OC 205.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see 206.19 unknown https://doi.org/10.1021/NP50037A032
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)furo[3,2-g]chromen-7-one 85180349 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)CCC(C(C)(C)O)O 372.40 unknown https://doi.org/10.1021/JF9802373
9-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]furo[3,2-g]chromen-7-one 92475864 Click to see 372.40 unknown https://doi.org/10.1021/JF9802373
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten 3083726 Click to see 232.19 unknown https://doi.org/10.1021/JO01273A049
9-(6,7-Dihydroxy-3,7-dimethyloct-2-enoxy)-4-methoxyfuro[3,2-g]chromen-7-one 85259564 Click to see 402.40 unknown https://doi.org/10.1021/JF9802373
9-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-4-methoxyfuro[3,2-g]chromen-7-one 163195408 Click to see 402.40 unknown https://doi.org/10.1021/JF9802373
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown https://doi.org/10.1021/JF9802373
https://doi.org/10.1021/JO01273A049
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol 65090 Click to see 202.16 unknown https://doi.org/10.1002/PTR.3690
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1021/NP50037A032
https://doi.org/10.1021/JF9802373
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1002/PTR.3690
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
2-(2,6-Dimethoxyphenyl)-5,6-dimethoxy-4H-1-benzopyran-4-one 629965 Click to see 342.30 unknown https://doi.org/10.1021/JM060915+
https://doi.org/10.1021/JO01273A049
https://doi.org/10.1021/JF9802373
3',5,6-Trimethoxyflavone 44257599 Click to see 312.30 unknown https://doi.org/10.1021/JO01273A049
5,6-Dimethoxy-2-(2-methoxyphenyl)-4H-1-benzopyran-4-one 14484690 Click to see 312.30 unknown https://doi.org/10.1016/0040-4020(60)80001-4
https://doi.org/10.1021/JF9802373
5,6-Dimethoxyflavone 14349486 Click to see 282.29 unknown via CMAUP database
Zapotinin 44257595 Click to see 328.30 unknown via CMAUP database

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