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Casimiroa greggii

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400f89c6f09984275760
Scientific name Casimiroa greggii
Authority (S.Watson) F.Chiang
First published in Taxon 38: 116 (1989)

Description Top

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Synonyms Top

Scientific name Authority First published in
Casimiroa pringlei var. neoleonensis Martinez Anales Inst. Biol. Univ. Nac. México 22: 40 (1951)
Sargentia greggii S.Watson Proc. Amer. Acad. Arts 25: 144 (1890)

Common names Top

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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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000589008
Tropicos 28101388
KEW urn:lsid:ipni.org:names:946495-1
The Plant List kew-2702488
Open Tree Of Life 6125399
Observations.org 367616
IPNI 1218535-2
iNaturalist 291996
GBIF 3833911
Elurikkus 421242
USDA GRIN 415281

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)!
Title Authors Publication Released IDs
Oil of Chapote Amarillo (Sargentia greggi): 2,5-Dimethoxyflavone in the Unsaponified Fraction Leonora Sanchez-Garcia Figueroa, Martha Albores-Velasco American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JF00051A006
Volatile compounds of Sargentia gregii Leonora Sánchez, Martha Albores-Velasco, Federico del Rio Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85039-3
Plant antitumor agents, 21. Flavones, coumarins, and an alkaloid from Sargentia greggii. Meyer BN, Wall ME, Wani MC, Taylor HL J Nat Prod 01-Nov-1985
doi:10.1021/NP50042A012
PMID:4093779

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl cis-9-tetradecenoate 5352674 Click to see CCCCC=CCCCCCCCC(=O)OC 240.38 unknown https://doi.org/10.1021/JF00051A006
Methyl decanoate 8050 Click to see CCCCCCCCCC(=O)OC 186.29 unknown https://doi.org/10.1021/JF00051A006
Methyl hexanoate 7824 Click to see CCCCCC(=O)OC 130.18 unknown https://doi.org/10.1021/JF00051A006
Methyl Laurate 8139 Click to see CCCCCCCCCCCC(=O)OC 214.34 unknown https://doi.org/10.1021/JF00051A006
Methyl Octanoate 8091 Click to see CCCCCCCC(=O)OC 158.24 unknown https://doi.org/10.1021/JF00051A006
Methyl oleate 5364509 Click to see CCCCCCCCC=CCCCCCCCC(=O)OC 296.50 unknown https://doi.org/10.1021/JF00051A006
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown https://doi.org/10.1021/JF00051A006
Methyl palmitoleate 643801 Click to see CCCCCCC=CCCCCCCCC(=O)OC 268.40 unknown https://doi.org/10.1021/JF00051A006
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1021/JF00051A006
Methyl Tetradecanoate 31284 Click to see CCCCCCCCCCCCCC(=O)OC 242.40 unknown https://doi.org/10.1021/JF00051A006
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl elaidolinolenate 5367462 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown https://doi.org/10.1021/JF00051A006
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown https://doi.org/10.1021/JF00051A006
Methyl linolenate 5319706 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown https://doi.org/10.1021/JF00051A006
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/0031-9422(91)85039-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(91)85039-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(91)85039-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)85039-3
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)85039-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-((2E)-3,7-Dimethylocta-2,6-dienoxy)-8-(3-methylbut-2-enyl)chromen-2-one 6442525 Click to see CC(=CCCC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)CC=C(C)C)C)C 366.50 unknown https://doi.org/10.1021/NP50042A012
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Casimiroin 124075 Click to see CN1C(=O)C=C(C2=C1C3=C(C=C2)OCO3)OC 233.22 unknown https://doi.org/10.1021/NP50042A012
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C 228.24 unknown https://doi.org/10.1021/NP50042A012
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,6,2',3',4',6'-Hexamethoxyflavone 180914 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=C(C(=C(C=C3OC)OC)OC)OC)OC 402.40 unknown https://doi.org/10.1021/NP50042A012
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/NP50042A012

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