The white sapote, also known as casimiroa or Mexican apple, is a tropical fruit tree native to eastern Mexico and Central America. It is named after an Otomi Indian who fought in Mexico's war of independence. The tree can reach up to 16 meters tall and has palmately compound leaves. The fruit is an ovoid drupe with a thin, inedible skin and an edible pulp that can range in flavor from bland to peach or banana-like. The seeds of the fruit have been found to contain pharmacologically active compounds. Studies have shown that one of these compounds, zapotin, may have potential anticarcinogenic effects. The fruit has been thought to produce drowsiness, but this may be due to a misinterpretation of its Nahuatl name. The white sapote is a member of the Rutaceae family, unlike the mamey sapote and black sapote, which are unrelated. It is commonly grown in northern New South Wales, Australia.

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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Filter by language:

Language	Common/alternative name
English	white sapote
Spanish	zanthoxylum araliaceum
Spanish	zapote blanco
Spanish	casimiroa edulis f. microcarpa
Arabic	سابوتا بيضاء
Czech	bílá sapota
German	weiße sapote
Persian	سیب مکزیکی
French	sapotier blanc
French	sapote blanche
Armenian	Սպիտակ սապոտ
Japanese	ホワイトサポテ
Korean	카시미로아나무
Korean	흰사포테
Korean	카시미로아
Malayalam	വെള്ള സപ്പോട്ട
nah	iztāctzapocuahuitl
nah	cochitzapocuahuitl
Dutch	zapote blanco
Dutch	witte zapote
Dutch	witte sapote
Polish	kazimira jadalna
Polish	kazimierka jadalna
Russian	Казимироа съедобная
Russian	Белая сапота
Russian	casimiroa edulus
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 click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- Caribbean
  - Trinidad-Tobago
- Central America
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua

Links to other databases Top

Suggest others/fix!

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

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

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

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

Diversity of woody species in traditional agroforestry practices in Wondo district, south-central Ethiopia

Molla T, Asfaw Z, Muluneh MG, Worku BB

Heliyon

07-Feb-2023

PMCID:	PMC9941991
doi:	10.1016/j.heliyon.2023.e13549
PMID:	36825171

Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies

De S, Paul S, Manna A, Majumder C, Pal K, Casarcia N, Mondal A, Banerjee S, Nelson VK, Ghosh S, Hazra J, Bhattacharjee A, Mandal SC, Pal M, Bishayee A

Cancers (Basel)

03-Feb-2023

PMCID:	PMC9913554
doi:	10.3390/cancers15030993
PMID:	36765950

Assessment of the Molecular Responses of an Ancient Angiosperm against Atypical Insect Oviposition: The Case of Hass Avocados and the Tephritid Fly Anastrepha ludens

Aluja M, Vázquez-Rosas-Landa M, Cerqueda-García D, Monribot-Villanueva JL, Altúzar-Molina A, Ramírez-Vázquez M, Velázquez-López O, Rosas-Saito G, Alonso-Sánchez AG, Ortega-Casas R, Enríquez-Valencia AJ, Guerrero-Analco JA, Ibarra-Laclette E

Int J Mol Sci

20-Jan-2023

PMCID:	PMC9916504
doi:	10.3390/ijms24032060
PMID:	36768387

Metabolomic Profiling, Antibacterial, and Molluscicidal Properties of the Medicinal Plants Calotropis procera and Atriplex halimus: In Silico Molecular Docking Study

Morad MY, El-Sayed H, El-Khadragy MF, Abdelsalam A, Ahmed EZ, Ibrahim AM

Plants (Basel)

19-Jan-2023

PMCID:	PMC9920412
doi:	10.3390/plants12030477
PMID:	36771561

Mitigation of apoptosis-mediated neurotoxicity induced by silver nanoparticles via rutaceae nutraceuticals: P53 activation and Bax/Bcl-2 regulation

Abdel-Megeed RM, Ali SA, Khalil WB, Refaat EA, Kadry MO

Toxicol Rep

29-Nov-2022

PMCID:	PMC9742938
doi:	10.1016/j.toxrep.2022.11.009
PMID:	36518464

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(2,2,3-Trimethyl-1,3-oxazolidin-5-yl)phenol	204759	Click to see CC1(N(CC(O1)C2=CC=C(C=C2)O)C)C	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 CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	436.80	unknown	https://doi.org/10.1021/NP50037A032
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides
Hexadecanamide	69421	Click to see CCCCCCCCCCCCCCCC(=O)N	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
7-alpha-Obacunol	12313644	Click to see CC1(C2CC(C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)O)C	456.50	unknown	https://doi.org/10.1021/JO01273A049
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 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	https://doi.org/10.1039/CT9119901993
Tricoccin S3	500031	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	https://doi.org/10.1039/CT9119901993
Zapoterin	441812	Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C	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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Beta-Sitosterol	222284	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 CN1CCCC1C(=O)O	129.16	unknown	https://doi.org/10.1016/S0378-8741(98)00101-9
Monomethyl proline	6951137	Click to see C[NH+]1CCCC1C(=O)[O-]	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 CC(C)(CC1=CN=CN1)N	139.20	unknown	https://doi.org/10.1007/S10600-007-0196-9
1H-Imidazole-4-ethanamine, N-methyl-	912	Click to see CNCCC1=CN=CN1	125.17	unknown	https://doi.org/10.1016/S0378-8741(98)00101-9
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
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / 2-arylethylamines
1-Methylhistamine	3614	Click to see CN1C=C(N=C1)CCN	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
(E)-N-methyl-3-phenyl-N-[2-[1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]imidazol-4-yl]ethyl]prop-2-enamide	5382459	Click to see CN(CCC1=CN(C=N1)C2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3	417.50	unknown	via CMAUP database
Casimiroedine	5281818	Click to see CN(CCC1=CN(C=N1)C2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3	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
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 CN(CCC1=CN(C=N1)C2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3	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 CN1CCC2=CN=CN2C1=S	167.23	unknown	https://doi.org/10.1039/JR9560004163
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
gamma-Fagarine	107936	Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3	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 CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=C(C=C(C=C3)OC)O	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 CN1C2=C(C(=CC=C2)O)C(=O)C=C1C3=CC=CC=C3	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 COC1=C(C2=C(C=C1)NC(=CC2=O)C3=C(C(=CC(=C3)OC)OC)OC)OC	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 COC1=C(C(=C(C=C1)OC)OC)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC	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 COC1=C(C2=C(C=C1)NC(=CC2=O)C3=CC(=CC=C3)OC)OC	311.30	unknown	via CMAUP database
5,6-Dimethoxy-2-(3,4-dimethoxyphenyl)-1h-quinolin-4-one	11131642	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC)OC	341.40	unknown	via CMAUP database
5,8-Dimethoxy-2-(3'-methoxyphenyl)-3-propyl-1h-quinolin-4-one	24766570	Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=CC=C3)OC	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 CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=C(C=C3)OC)OC	383.40	unknown	https://doi.org/10.1007/S10600-007-0196-9
Eduleine	253834	Click to see CN1C(=CC(=O)C2=C1C=C(C=C2)OC)C3=CC=CC=C3	265.31	unknown	https://doi.org/10.1021/NP50037A032 https://doi.org/10.1007/S10600-007-0196-9 https://doi.org/10.1021/JO01273A049
Eduline	622180	Click to see CN1C2=C(C=C(C=C2)OC)C(=O)C=C1C3=CC=CC=C3	265.31	unknown	https://doi.org/10.1021/JO01273A049
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one	182073	Click to see CN1C2=CC=CC=C2C(=CC1=O)OC	189.21	unknown	https://doi.org/10.1021/JF9802373
Casimiroin	124075	Click to see CN1C(=O)C=C(C2=C1C3=C(C=C2)OCO3)OC	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 COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	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 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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten	3083726	Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)O	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 CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)CCC(C(C)(C)O)O	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 CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)CCC(C(C)(C)O)O	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 C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O	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 COC1=C(C=C2C(=C1)C=CC(=O)O2)O	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
3',5,6-Trimethoxyflavone	44257599	Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC(=CC=C3)OC)OC	312.30	unknown	https://doi.org/10.1021/JO01273A049
5,6-Dimethoxyflavone	14349486	Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3)OC	282.29	unknown	via CMAUP database
5,6,2'-Trimethoxyflavone	14484690	Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3OC)OC	312.30	unknown	https://doi.org/10.1016/0040-4020(60)80001-4 https://doi.org/10.1021/JF9802373
Zapotin	629965	Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC	342.30	unknown	https://doi.org/10.1021/JM060915+ https://doi.org/10.1021/JO01273A049 https://doi.org/10.1021/JF9802373
Zapotinin	44257595	Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3O)OC	328.30	unknown	via CMAUP database

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Casimiroa edulis

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