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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...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer-Verlag
2012
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| 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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