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Casimiroa tetrameria

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 UUID64400f8a5b736253823128
Scientific name Casimiroa tetrameria
Authority Millsp.
First published in Publ. Field Columb. Mus., Bot. Ser. 1: 401 (1895)

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.

I couldn't find any documented, verifiable ethnobotanical uses for Casimiroa tetrameria (Millsp.), so I have nothing to write.

General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English matasano

Subspecies (abbr. subsp./ssp.) Top

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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

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
World Flora Online wfo-0000589023
USDA Plants CATE24
Tropicos 28100068
KEW urn:lsid:ipni.org:names:48133-2
The Plant List kew-2702500
Open Tree Of Life 974693
NCBI Taxonomy 549413
IUCN Red List 150120432
IPNI 771780-1
iNaturalist 279145
GBIF 3190133
EOL 588254
USDA GRIN 9295
CMAUP NPO2663

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
Pest categorisation of Russellaspis pustulans Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 03-Jun-2022
PMCID:PMC9164144
doi:10.2903/j.efsa.2022.7335
PMID:35662805
Zapotin, a Polymethoxyflavone, with Potential Therapeutic Attributes Strawa JW, Jakimiuk K, Tomczyk M Int J Mol Sci 08-Dec-2021
PMCID:PMC8705526
doi:10.3390/ijms222413227
PMID:34948021
A Novel Genetic Sexing Strain of Anastrepha ludens for Cost-Effective Sterile Insect Technique Applications: Improved Genetic Stability and Rearing Efficiency Ramírez-Santos E, Rendon P, Gouvi G, Zacharopoulou A, Bourtzis K, Cáceres C, Bloem K Insects 27-May-2021
PMCID:PMC8228190
doi:10.3390/insects12060499
PMID:34072029
Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data Morton CM PLoS One 08-Mar-2017
PMCID:PMC5342198
doi:10.1371/journal.pone.0172708
PMID:28273098
(2R,3S,2”R,3”R)-manniflavanone, a new gastrointestinal smooth muscle L-type calcium channel inhibitor, which underlies the spasmolytic properties of Garcinia buchananii stem bark extract Balemba OB, Stark TD, Lösch S, Patterson S, McMillan JS, Mawe GM, Hofmann T J Smooth Muscle Res 18-Dec-2014
PMCID:PMC4826780
doi:10.1540/jsmr.50.48
PMID:26081368
Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Groppo M, Kallunki JA, Pirani JR, Antonelli A PhytoKeys 18-Dec-2012
PMCID:PMC3597001
doi:10.3897/phytokeys.19.3912
PMID:23717188
A furanocoumarin and polymethoxylated flavonoids from the Yucatec Mayan plant Casimiroa tetrameria. Heneka B, Rimpler H, Ankli A, Sticher O, Gibbons S, Heinrich M Phytochemistry 01-Mar-2005
doi:10.1016/J.PHYTOCHEM.2004.12.005
PMID:15771884

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bR)-10,11-dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101106492 Click to see 648.80 unknown via CMAUP database
2alpha,3beta,19alpha-Trihydroxyurs-12-en-28-oic acid (6-O-methyl-beta-D-glucopyranosyl) ester 101615131 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)COC)O)O)O 664.90 unknown via CMAUP database
Dotorioside II 16118969 Click to see 666.80 unknown via CMAUP database
Kajiichigoside F1 14019178 Click to see 650.80 unknown via CMAUP database
Rosamultin 21122581 Click to see 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,2R,4aS,6aR,6aS,6bR,8aS,10S,11R,12aR,14bR)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 93961278 Click to see 488.70 unknown via CMAUP database
(1R,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 95223073 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown via CMAUP database
19Alpha-Hydroxyasiatic Acid 490367 Click to see 504.70 unknown via CMAUP database
2alpha,3alpha,23-Trihydroxyolean-12-en-28-oic acid 11504083 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
2alpha,3beta-Dihydroxyolean-13(18)-en-28-oic acid 52952429 Click to see 472.70 unknown via CMAUP database
2alpha,3beta,11alpha,19alpha-Tetrahydroxyurs-12-en-28-oic acid 101615130 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)O)C2C1(C)O)C)C(=O)O 504.70 unknown via CMAUP database
2alpha,3beta,23-Trihydroxylup-20(29)-en-28-oic acid 70698002 Click to see 488.70 unknown via CMAUP database
3beta-Hydroxy-2alpha-methoxyurs-12-en-28-oic acid 101615129 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)OC)C)C)C2C1C)C)C(=O)O 486.70 unknown via CMAUP database
Corosolic Acid 6918774 Click to see 472.70 unknown via CMAUP database
Euscaphic Acid 471426 Click to see 488.70 unknown via CMAUP database
Euscaphic Acid Methyl Ester 14314584 Click to see 502.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see 472.70 unknown via CMAUP database
Methyl corosolate 14109751 Click to see 486.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Rel-2alpha,3alpha,19alpha,23-tetrahydroxyolean-12-en-28-oic acid 52952430 Click to see 504.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Tormentic Acid Methyl Ester 14314585 Click to see 502.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids / 12-beta-hydroxysteroids
(3S)-5-[(4aS,4bR,6aR,7R,8R,9R,10aR,10bR)-8,9-dihydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethyl-3,4,5,6,6a,8,9,10,10b,11-decahydrochrysen-2-yl]-3-methylpentan-2-one 52952318 Click to see 458.70 unknown via CMAUP database
Rel-2alpha,3beta,23-trihydroxy-12,17-dien-28-norursane 52952319 Click to see CC1CCC2=C(C1C)C3=CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(2S,4aS,4bR,6aR,7R,8S,9R,10aS,10bR)-8,9-dihydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethyl-2-[(3S)-3-methyl-4-oxopentyl]-4,5,6,6a,8,9,10,10b-octahydro-3H-chrysene-2-carboxylic acid 52952320 Click to see 502.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one 101615132 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 590.80 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(beta-D-Glucopyranosyloxy)-5-[(6S)-6,7-dihydroxy-3,7-dimethyl-2-octenyl]benzoic acid methyl ester 71660038 Click to see CC(=CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CCC(C(C)(C)O)O 484.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
9-(4-Hydroxy-3-methylbut-2-enoxy)-4-methoxyfuro[3,2-g]chromen-7-one 91456984 Click to see 316.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
9-[(Z)-4-hydroxy-3-methylbut-2-enoxy]-4-methoxyfuro[3,2-g]chromen-7-one 102465417 Click to see 316.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see 290.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl)Oxy-Chromen-4-one 12304323 Click to see 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One 12313332 Click to see 594.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
> 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/10.1016/J.PHYTOCHEM.2004.12.005
2-(3,4-Dimethoxyphenyl)-5,6-dimethoxy-4H-1-benzopyran-4-one 14055876 Click to see 342.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
5,6,2',3',4'-Pentamethoxyflavone 14055877 Click to see COC1=C(C(=C(C=C1)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC)OC)OC 372.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
5,6,2',3',5',6'-Hexamethoxyflavone 21580515 Click to see 402.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
5,6,2',3',6'-Pentamethoxyflavone 21580516 Click to see COC1=C(C(=C(C=C1)OC)OC)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC 372.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
Cerosilin B 44257603 Click to see 372.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
Cerrosillin 44257600 Click to see 342.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.005
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl] 2-[5-[[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate 16169194 Click to see 1569.10 unknown via CMAUP database
[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl] 3,4,5-trihydroxybenzoate 13917514 Click to see 634.50 unknown via CMAUP database
[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl] 2-[5-[[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate 16138866 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4OC5=CC(=CC(=C5O)O)C(=O)OC6C7C(C(C(O6)CO)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1569.10 unknown via CMAUP database
[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl] 3,4,5-trihydroxybenzoate 5315734 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown via CMAUP database
2-[5-[[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoic acid 14374737 Click to see 802.60 unknown via CMAUP database
Agrimoniin 16129621 Click to see 1871.30 unknown via CMAUP database
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database
Casuarictin 73644 Click to see 936.60 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Ellagic acid 4-O-alpha-L-arabinofuranoside 101129362 Click to see 434.30 unknown via CMAUP database
Laevigatin F 16182828 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=CC(=CC(=C4O)O)C(=O)OC5C6C(C7C(O5)COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O6)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1569.10 unknown via CMAUP database

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