CYP2B6
Cytochroma P450 CYP2B6 (-atis, n.) (Numerus EC: 1.14.14.1) est enzymum et haemoproteinum et pars gregis Cytochroma P450 ideo in metabolismo medicamenti chemotherapiae, ut cyclophosphamidi sive ifosfamidi, interest. Circiter centesimae quinque reactionum catabolicarum medicamentorum cum cytochromate CYP2B6 patent[1]. Variationes multae geneticae descriptae sunt.
Phaenotypicae variantia
recensereLocus geni geneticus CYP2B6 in chromosomate 19 (19q13.2) situs est[2]. Polymorphismus geneticus cum plus quam centum variationibus magnum momentum habet[1]
Pharmaca ad CYP2B6 relata
recensereSubstrati | Inhibitores[5] | Inductores[6] |
---|---|---|
|
|
|
Nexus interni
Notae
recensere- ↑ 1.0 1.1 Turpeinen M, Zanger UM (2012). "Cytochrome P450 2B6: function, genetics, and clinical relevance". Drug Metabol Drug Interact 27 (4): 185-97
- ↑ "Entrez geni: cytochromum P450 CYP2B6"
- ↑ Cozza KL, Armstrong SC (2001). The Cytochrome P450 System. Drug Interaction Principles for Medical Practice. Washington, DC: American Psychiatric Publishing
- ↑ Preskorn SH (1996). Clinical Pharmacology of Selective Serotonin Reuptake Inhibitors. 1st ed.: Professional Communications, Inc.
- ↑ Inhibitor cum subtratorum effectibus fortioribus
- ↑ Inductor cum subtratorum effectibus minoribus
- ↑ Andrade C (2017). "Ketamine for Depression, 5: Potential Pharmacokinetic and Pharmacodynamic Drug Interactions". J Clin Psychiatry 78 (7): e858-61
- ↑ Kharasch ED, Stubbert K (2013). "Role of cytochrome P4502B6 in methadone metabolism and clearance". J Clin Pharmacol 53 (3): 305-13