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Rationalization of stereospecific binding of propranolol to cytochrome P450 2D6 by free energy calculations

ABSTRACT: Cytochrome P450 2D6 is a major drug-metabolising enzyme with a wide substrate range. A single-point mutation introduced in this enzyme induces stereoselective binding of R and S-propranolol whereas the wild type has no preference. The system has previously been studied both experimentally...

詳細記述

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書誌詳細
主要な著者: Nagy, Gabor, Oostenbrink, Chris
フォーマット: Artigo
言語:Inglês
出版事項: Springer-Verlag 2012
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3509327/
https://ncbi.nlm.nih.gov/pubmed/23086294
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00249-012-0865-x
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