التفاصيل البيبلوغرافية
| العنوان: |
Computational Prediction of Inhibitors and Inducers of the Major Isoforms of Cytochrome P450 |
| المؤلفون: |
Anastassia Rudik, Alexander Dmitriev, Alexey Lagunin, Dmitry Filimonov, Vladimir Poroikov |
| المصدر: |
Molecules; Volume 27; Issue 18; Pages: 5875 |
| بيانات النشر: |
Multidisciplinary Digital Publishing Institute |
| سنة النشر: |
2022 |
| المجموعة: |
MDPI Open Access Publishing |
| مصطلحات موضوعية: |
CYP, inhibitors, inducers, (Q)SAR models, PASS, GUSAR, drug-like compounds, metabolism, in silico prediction, P450 isoforms, 1A2, 3A4, 2D6, 2C9, 2C19 |
| جغرافية الموضوع: |
agris |
| الوصف: |
Human cytochrome P450 enzymes (CYPs) are heme-containing monooxygenases. This superfamily of drug-metabolizing enzymes is responsible for the metabolism of most drugs and other xenobiotics. The inhibition of CYPs may lead to drug–drug interactions and impair the biotransformation of drugs. CYP inducers may decrease the bioavailability and increase the clearance of drugs. Based on the freely available databases ChEMBL and PubChem, we have collected over 70,000 records containing the structures of inhibitors and inducers together with the IC50 values for the inhibitors of the five major human CYPs: 1A2, 3A4, 2D6, 2C9, and 2C19. Based on the collected data, we developed (Q)SAR models for predicting inhibitors and inducers of these CYPs using GUSAR and PASS software. The developed (Q)SAR models could be applied for assessment of the interaction of novel drug-like substances with the major human CYPs. The created (Q)SAR models demonstrated reasonable accuracy of prediction. They have been implemented in the web application P450-Analyzer that is freely available via the Internet. |
| نوع الوثيقة: |
text |
| وصف الملف: |
application/pdf |
| اللغة: |
English |
| Relation: |
Medicinal Chemistry; https://dx.doi.org/10.3390/molecules27185875 |
| DOI: |
10.3390/molecules27185875 |
| الاتاحة: |
https://doi.org/10.3390/molecules27185875 |
| Rights: |
https://creativecommons.org/licenses/by/4.0/ |
| رقم الانضمام: |
edsbas.4E06F83D |
| قاعدة البيانات: |
BASE |