Prediction of cytochrome P450 mediated metabolism

Research

Prediction of cytochrome P450 mediated metabolism

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Prediction of cytochrome P450 mediated metabolism. / Olsen, Lars; Oostenbrink, Chris; Jørgensen, Flemming Steen.

In: Advanced Drug Delivery Reviews, Vol. 86, 06.05.2015, p. 61-71.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Olsen, L, Oostenbrink, C & Jørgensen, FS 2015, 'Prediction of cytochrome P450 mediated metabolism', Advanced Drug Delivery Reviews, vol. 86, pp. 61-71. https://doi.org/10.1016/j.addr.2015.04.020

APA

Olsen, L., Oostenbrink, C., & Jørgensen, F. S. (2015). Prediction of cytochrome P450 mediated metabolism. Advanced Drug Delivery Reviews, 86, 61-71. https://doi.org/10.1016/j.addr.2015.04.020

Vancouver

Olsen L, Oostenbrink C, Jørgensen FS. Prediction of cytochrome P450 mediated metabolism. Advanced Drug Delivery Reviews. 2015 May 6;86:61-71. https://doi.org/10.1016/j.addr.2015.04.020

Author

Olsen, Lars ; Oostenbrink, Chris ; Jørgensen, Flemming Steen. / Prediction of cytochrome P450 mediated metabolism. In: Advanced Drug Delivery Reviews. 2015 ; Vol. 86. pp. 61-71.

Bibtex

@article{8bc57d6be9274c208cedb1979d514ea2,

title = "Prediction of cytochrome P450 mediated metabolism",

abstract = "Cytochrome P450 enzymes (CYPs) form one of the most important enzyme families involved in the metabolism of xenobiotics. CYPs comprise many isoforms, which catalyze a wide variety of reactions, and potentially, a large number of different metabolites can be formed. However, it is often hard to rationalize what metabolites these enzymes generate. In recent years, many different in silico approaches have been developed to predict binding or regioselective product formation for the different CYP isoforms. These comprise ligand-based methods that are trained on experimental CYP data and structure-based methods that consider how the substrate is oriented in the active site or/and how reactive the part of the substrate that is accessible to the heme group is. We will review key aspects for various approaches that are available to predict binding and site of metabolism (SOM), what outcome can be expected from the predictions, and how they could potentially be improved.",

author = "Lars Olsen and Chris Oostenbrink and J{\o}rgensen, {Flemming Steen}",

year = "2015",

month = may,

day = "6",

doi = "10.1016/j.addr.2015.04.020",

language = "English",

volume = "86",

pages = "61--71",

journal = "Advanced Drug Delivery Reviews",

issn = "0169-409X",

publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Prediction of cytochrome P450 mediated metabolism

AU - Olsen, Lars

AU - Oostenbrink, Chris

AU - Jørgensen, Flemming Steen

PY - 2015/5/6

Y1 - 2015/5/6

N2 - Cytochrome P450 enzymes (CYPs) form one of the most important enzyme families involved in the metabolism of xenobiotics. CYPs comprise many isoforms, which catalyze a wide variety of reactions, and potentially, a large number of different metabolites can be formed. However, it is often hard to rationalize what metabolites these enzymes generate. In recent years, many different in silico approaches have been developed to predict binding or regioselective product formation for the different CYP isoforms. These comprise ligand-based methods that are trained on experimental CYP data and structure-based methods that consider how the substrate is oriented in the active site or/and how reactive the part of the substrate that is accessible to the heme group is. We will review key aspects for various approaches that are available to predict binding and site of metabolism (SOM), what outcome can be expected from the predictions, and how they could potentially be improved.

AB - Cytochrome P450 enzymes (CYPs) form one of the most important enzyme families involved in the metabolism of xenobiotics. CYPs comprise many isoforms, which catalyze a wide variety of reactions, and potentially, a large number of different metabolites can be formed. However, it is often hard to rationalize what metabolites these enzymes generate. In recent years, many different in silico approaches have been developed to predict binding or regioselective product formation for the different CYP isoforms. These comprise ligand-based methods that are trained on experimental CYP data and structure-based methods that consider how the substrate is oriented in the active site or/and how reactive the part of the substrate that is accessible to the heme group is. We will review key aspects for various approaches that are available to predict binding and site of metabolism (SOM), what outcome can be expected from the predictions, and how they could potentially be improved.

U2 - 10.1016/j.addr.2015.04.020

DO - 10.1016/j.addr.2015.04.020

M3 - Journal article

C2 - 25958010

VL - 86

SP - 61

EP - 71

JO - Advanced Drug Delivery Reviews

JF - Advanced Drug Delivery Reviews

SN - 0169-409X

ER -

ID: 140712527