Cytochrome P450 2D6 inhibitory constituents of Lunasia amara

Author:

Subehan ,Takahashi Naoto,Kadota Shigetoshi,Tezuka Yasuhiro

Publisher

Elsevier BV

Subject

Plant Science,Agronomy and Crop Science,Biochemistry,Biotechnology

Reference33 articles.

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2. Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine: comparison with fluoxetine and quinidine;Bertelsen;Drug Metab. Dispos.,2003

3. Quinoline alkaloids—XXI1: the 13C NMR spectra of hemiterpenoid quinoline alkaloids and related prenylquinolines;Brown;Tetrahedron,1980

4. Quinoline alkaloids part XI. A study of the Claisen rearrangement of the 3,3-dimethylallyl ether of 4-hydroxy-1-methyl-2-quinolone. Synthesis of ifflaiamine and the identification of a new alkaloid from Flindersia ifflaiana F. Muell;Chamberlain;J. Chem. Soc. (C),1971

5. Human cytochromes P450 and their role in metabolism-based drug–drug interactions;Clarke,2002

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