N-aralkylated derivatives of 1-aminobenzotriazole are potent isozyme- and lung-selective mechanism-based inhibitors of guinea pig cytochrome P-450 in vivo.

L C Knickle; R M Philpot; J R Bend

Abstract

N-aralkylated derivatives of 1-aminobenzotriazole are potent isozyme- and lung-selective mechanism-based inhibitors of guinea pig cytochrome P-450 in vivo.

L C Knickle, R M Philpot and J R Bend

Journal of Pharmacology and Experimental Therapeutics July 1994, 270 (1) 377-385;

L C Knickle

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R M Philpot

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J R Bend

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Journal of Pharmacology and Experimental Therapeutics

Vol. 270, Issue 1

1 Jul 1994

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Abstract

N-aralkylated derivatives of 1-aminobenzotriazole are potent isozyme- and lung-selective mechanism-based inhibitors of guinea pig cytochrome P-450 in vivo.

L C Knickle, R M Philpot and J R Bend

Journal of Pharmacology and Experimental Therapeutics July 1, 1994, 270 (1) 377-385;

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Abstract

N-aralkylated derivatives of 1-aminobenzotriazole are potent isozyme- and lung-selective mechanism-based inhibitors of guinea pig cytochrome P-450 in vivo.

L C Knickle, R M Philpot and J R Bend

Journal of Pharmacology and Experimental Therapeutics July 1, 1994, 270 (1) 377-385;

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N-aralkylated derivatives of 1-aminobenzotriazole are potent isozyme- and lung-selective mechanism-based inhibitors of guinea pig cytochrome P-450 in vivo.

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