Iminolactones from Schizophyllum commune

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Standard

Iminolactones from Schizophyllum commune. / Liu, Xuemei; Frydenvang, Karla Andrea; Liu, Huizhen; Zhai, Lin; Chen, Ming; Olsen, Carl Erik; Christensen, Søren Brøgger.

I: Journal of Natural Products, Bind 78, Nr. 5, 2015, s. 1165-1168.

Publikation: Bidrag til tidsskriftTidsskriftartikelfagfællebedømt

Harvard

Liu, X, Frydenvang, KA, Liu, H, Zhai, L, Chen, M, Olsen, CE & Christensen, SB 2015, 'Iminolactones from Schizophyllum commune', Journal of Natural Products, bind 78, nr. 5, s. 1165-1168. https://doi.org/10.1021/np500836y

APA

Liu, X., Frydenvang, K. A., Liu, H., Zhai, L., Chen, M., Olsen, C. E., & Christensen, S. B. (2015). Iminolactones from Schizophyllum commune. Journal of Natural Products, 78(5), 1165-1168. https://doi.org/10.1021/np500836y

Vancouver

Liu X, Frydenvang KA, Liu H, Zhai L, Chen M, Olsen CE o.a. Iminolactones from Schizophyllum commune. Journal of Natural Products. 2015;78(5):1165-1168. https://doi.org/10.1021/np500836y

Author

Liu, Xuemei ; Frydenvang, Karla Andrea ; Liu, Huizhen ; Zhai, Lin ; Chen, Ming ; Olsen, Carl Erik ; Christensen, Søren Brøgger. / Iminolactones from Schizophyllum commune. I: Journal of Natural Products. 2015 ; Bind 78, Nr. 5. s. 1165-1168.

Bibtex

@article{5dbdaeb2770f49b3a5445c4a7f5abbc5,
title = "Iminolactones from Schizophyllum commune",
abstract = "Schizine A (1) and B (2) the first naturally occurring iminolactones (3,6-dihydro-2H-1,4-oxazin-2-one derivatives) to be reported have been isolated from the fruiting bodies of Schizophyllym commune. In principle the 2-oxazinone moiety might have been formed by a reaction between the amino acids phenylalanine or tryptophan and an α-hydroxyketomniopetal. The alkaloids are unusual in that the carboxyl group of the amino acid precursor is preserved during the biosynthesis. The compounds showed some inhibition of the growth of cancer cells.",
keywords = "Faculty of Health and Medical Sciences, Natural products, Iminolactones, Schizophyllum commune",
author = "Xuemei Liu and Frydenvang, {Karla Andrea} and Huizhen Liu and Lin Zhai and Ming Chen and Olsen, {Carl Erik} and Christensen, {S{\o}ren Br{\o}gger}",
year = "2015",
doi = "10.1021/np500836y",
language = "English",
volume = "78",
pages = "1165--1168",
journal = "Journal of Natural Products",
issn = "0974-5211",
publisher = "Journal of Natural Products",
number = "5",

}

RIS

TY - JOUR

T1 - Iminolactones from Schizophyllum commune

AU - Liu, Xuemei

AU - Frydenvang, Karla Andrea

AU - Liu, Huizhen

AU - Zhai, Lin

AU - Chen, Ming

AU - Olsen, Carl Erik

AU - Christensen, Søren Brøgger

PY - 2015

Y1 - 2015

N2 - Schizine A (1) and B (2) the first naturally occurring iminolactones (3,6-dihydro-2H-1,4-oxazin-2-one derivatives) to be reported have been isolated from the fruiting bodies of Schizophyllym commune. In principle the 2-oxazinone moiety might have been formed by a reaction between the amino acids phenylalanine or tryptophan and an α-hydroxyketomniopetal. The alkaloids are unusual in that the carboxyl group of the amino acid precursor is preserved during the biosynthesis. The compounds showed some inhibition of the growth of cancer cells.

AB - Schizine A (1) and B (2) the first naturally occurring iminolactones (3,6-dihydro-2H-1,4-oxazin-2-one derivatives) to be reported have been isolated from the fruiting bodies of Schizophyllym commune. In principle the 2-oxazinone moiety might have been formed by a reaction between the amino acids phenylalanine or tryptophan and an α-hydroxyketomniopetal. The alkaloids are unusual in that the carboxyl group of the amino acid precursor is preserved during the biosynthesis. The compounds showed some inhibition of the growth of cancer cells.

KW - Faculty of Health and Medical Sciences

KW - Natural products

KW - Iminolactones

KW - Schizophyllum commune

U2 - 10.1021/np500836y

DO - 10.1021/np500836y

M3 - Journal article

C2 - 25951057

VL - 78

SP - 1165

EP - 1168

JO - Journal of Natural Products

JF - Journal of Natural Products

SN - 0974-5211

IS - 5

ER -

ID: 137476779