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Pyranocoumarin

Pyranocoumarins are a class of chemical compounds that have a core structure that consists of a pyran ring fused to a coumarin. As phytochemicals, pyranocoumarins are uncommon and found mainly the plant families Apiaceae and Rutaceae.[1] For example, Citrus sinensis and Citrus limonia are sources of xanthyletin and seselin.[2]

Chemical structures of xanthyletin (top) and seselin

In the biosyntheses of pyranocoumarins, the pyran ring is formed via the methylerythritol phosphate pathway and the coumarin is derived from the shikimate pathway.[2]

See also edit

References edit

  1. ^ Khandy, Maria T.; Sofronova, Anastasia K.; Gorpenchenko, Tatiana Y.; Chirikova, Nadezhda K. (2022). "Plant Pyranocoumarins: Description, Biosynthesis, Application". Plants. 11 (22): 3135. doi:10.3390/plants11223135. PMC 9693251. PMID 36432864.
  2. ^ a b Amaral, Jéssica C.; Da Silva, Michelli M.; Da Silva, M. Fátima G. F.; Alves, Thayana C.; Ferreira, A. Gilberto; Forim, Moacir R.; Fernandes, João B.; Pina, Edieidia S.; Lopes, Adriana A.; Pereira, Ana M. S.; Novelli, Valdenice M. (2020). "Advances in the Biosynthesis of Pyranocoumarins: Isolation and 13C-Incorporation Analysis by High-Performance Liquid Chromatography–Ultraviolet–Solid-Phase Extraction–Nuclear Magnetic Resonance Data". Journal of Natural Products. 83 (5): 1409–1415. doi:10.1021/acs.jnatprod.9b00607. PMID 32372647. S2CID 218519965.

pyranocoumarin, class, chemical, compounds, that, have, core, structure, that, consists, pyran, ring, fused, coumarin, phytochemicals, pyranocoumarins, uncommon, found, mainly, plant, families, apiaceae, rutaceae, example, citrus, sinensis, citrus, limonia, so. Pyranocoumarins are a class of chemical compounds that have a core structure that consists of a pyran ring fused to a coumarin As phytochemicals pyranocoumarins are uncommon and found mainly the plant families Apiaceae and Rutaceae 1 For example Citrus sinensis and Citrus limonia are sources of xanthyletin and seselin 2 Chemical structures of xanthyletin top and seselin In the biosyntheses of pyranocoumarins the pyran ring is formed via the methylerythritol phosphate pathway and the coumarin is derived from the shikimate pathway 2 See also editFuranocoumarinReferences edit Khandy Maria T Sofronova Anastasia K Gorpenchenko Tatiana Y Chirikova Nadezhda K 2022 Plant Pyranocoumarins Description Biosynthesis Application Plants 11 22 3135 doi 10 3390 plants11223135 PMC 9693251 PMID 36432864 a b Amaral Jessica C Da Silva Michelli M Da Silva M Fatima G F Alves Thayana C Ferreira A Gilberto Forim Moacir R Fernandes Joao B Pina Edieidia S Lopes Adriana A Pereira Ana M S Novelli Valdenice M 2020 Advances in the Biosynthesis of Pyranocoumarins Isolation and 13C Incorporation Analysis by High Performance Liquid Chromatography Ultraviolet Solid Phase Extraction Nuclear Magnetic Resonance Data Journal of Natural Products 83 5 1409 1415 doi 10 1021 acs jnatprod 9b00607 PMID 32372647 S2CID 218519965 nbsp This article about an organic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Pyranocoumarin amp oldid 1157489213, wikipedia, wiki, book, books, library,

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