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Inhibition of Cytochrome P450 Enzymes by Quinones and Anthraquinones
In silico docking studies and quantitative structure–activity relationship analysis of a number of in-house cytochrome P450 inhibitors have revealed important structural characteristics that are required for a molecule to function as a good inhibitor of P450 enzymes 1A1, 1A2, 2B1, and/or 2A6. These...
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| Vydáno v: | Chem Res Toxicol |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5461952/ https://ncbi.nlm.nih.gov/pubmed/22185593 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/tx2004163 |
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