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Relevant bibliographies by topics / Narceine

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Academic literature on the topic 'Narceine'

Author: Grafiati

Published: 28 July 2024

Last updated: 31 July 2025

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Journal articles on the topic "Narceine"

1

Baggio, R., S. Baggio, M. I. Pardo, and M. V. Capparelli. "Narceine Hydrochloride Trihydrate." Acta Crystallographica Section C Crystal Structure Communications 52, no. 3 (1996): 703–5. http://dx.doi.org/10.1107/s0108270195012479.

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2

Chowdhury, Dibyendu, S. Maurya, M. B. Pandey, V. B. Pandey, B. K. Sarma, and U. P. Singh. "Antifungal Activity of Narceine Methyl Ester and Narceine Isolated fromCorydalis longipesAgainst Some Phytopathogenic Fungi." Mycobiology 33, no. 4 (2005): 206. http://dx.doi.org/10.4489/myco.2005.33.4.206.

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3

Lamblin, Marc, Axel Couture, Eric Deniau, and Pierre Grandclaudon. "A concise first total synthesis of narceine imide." Organic & Biomolecular Chemistry 5, no. 9 (2007): 1466. http://dx.doi.org/10.1039/b701661a.

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4

Proksa, B. "Reaction of (Z)-narceine imide with 1,2-epoxypropane." Monatshefte f�r Chemie Chemical Monthly 124, no. 8-9 (1993): 953–57. http://dx.doi.org/10.1007/bf00816418.

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5

Francisco Sánchez Viesca and Reina Gómez Gómez. "The mechanism of the oxidation of narceine by means of selenous acid -sulphuric acid." Magna Scientia Advanced Research and Reviews 9, no. 1 (2023): 030–33. http://dx.doi.org/10.30574/msarr.2023.9.1.0128.

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The chemistry of selenous acid was misunderstood for many years, being explained by electron back donation. In this communication we disclose the reaction mechanism of the interaction of narceine with selenous acid in sulphuric acid. Narceine is a complex molecule that displays a carboxylic acid, a tertiary amine, a ketone, three methoxy groups and a benzodioxole; so, it was necessary select the principal reaction site. Although a methoxy group can be demethylated with the employed reagent since codeine gives the same violet colour obtained with morphine. The chemical deportment of the methyle

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PROKSA, B. "ChemInform Abstract: Reaction of (Z)-Narceine Imide with 1,2-Epoxypropane." ChemInform 25, no. 21 (2010): no. http://dx.doi.org/10.1002/chin.199421241.

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7

Paulová, Hana, Jan Kovář, Jiří Plocek, and Jiří Slavík. "Inhibition of aldehyde reductase I by some isoquinoline alkaloids." Collection of Czechoslovak Chemical Communications 52, no. 9 (1987): 2338–46. http://dx.doi.org/10.1135/cccc19872338.

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Aldehyde reductase I has been found to be inhibited by certain isoquinoline alkaloids (protoberberines, protopines, benzylisoquinolines, benzyltetrahydroisoquinolines, phthalideisoquinolines, pavinanes) and narceine imide. The sensitivity of this enzyme to the compounds tested was compared with that of alcohol dehydrogenase and/or aldehyde reductase II to them; alcohol dehydrogenase proved more selective in binding the alkaloids. The kinetics of the inhibitory action of berberine and other results suggest that the binding site of aldehyde reductase I for alkaloids is relatively large, has a hy

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8

Chaudhuri, Prabir K., and Raghunath S. Thakur. "Narceinone, an alkaloid from Papaver somniferum." Phytochemistry 28, no. 7 (1989): 2002–3. http://dx.doi.org/10.1016/s0031-9422(00)97912-3.

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9

Nasir, A., M. S. Sule, A. J. Alhassan, et al. "Characterisation and Anti-diabetic Activity of Phenylquinoline, and Narceine Isolated from Ficus polita Leaf." Annual Research & Review in Biology, August 3, 2020, 102–14. http://dx.doi.org/10.9734/arrb/2020/v35i730251.

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The present study was conducted to evaluate anti-diabetic potentials of column chromatography fractions (F1-F6) of chloroform leaf extract of Ficus polita and to detect the probable bioactive compounds present in the most active fraction using spectroscopic techniques. Antidiabetic potential of the fractions (F1-F6) were tested at a dose of 50 mg/kg on wistar rats. Fraction 3 and metformin treated diabetic groups showed significant decreases in fasting blood glucose (FBS) level, ameliorate hepatic and renal damages by decreasing the levels of serum total bilirubin, direct bilirubin AST, ALT, c

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10

Nasir, A., M. S. Sule, A. J. Alhassan, et al. "Characterisation and Hypolipidaemic Activity of Phenylquinoline, and Narceine Isolated from Ficus polita Leaf." International Journal of Biochemistry Research & Review, August 4, 2020, 42–54. http://dx.doi.org/10.9734/ijbcrr/2020/v29i830211.

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Aim: To evaluate hypolipidaemic potentials of column chromatography fractions (F1 to F6) of the chloroform leaf extract of Ficus polita and to detect the bioactive compounds present in the most active fraction using spectroscopic techniques. Study Design: Fourty-five (45) wistar rats were grouped into nine groups of five rats each: normal control, hyperlipidaemic control, hyperlipidaemic administered with standard drug control/ atorvastatin (10 mg/kg body weight), and hyperlipidaemic administered groups administered with 50 mg/kg body weight of column chromatography fractions (F1, F2, F3

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Book chapters on the topic "Narceine"

1

"Narceine." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0560-3_875.

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2

"narceine, n." In Oxford English Dictionary, 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/2292004315.

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3

"Narcein, in Opium." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_312687.

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4

"narceia, n." In Oxford English Dictionary, 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/1640617861.

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Conference papers on the topic "Narceine"

1

Couture, Axel, Eric Deniau, Pierre Grandclaudon, and Marc Lamblin. "First Total Synthesis of Narceine Imide." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01386.

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