Synthesis and evaluation of the antidepressant activity of the enantiomers of bupropion

التفاصيل البيبلوغرافية
العنوان: Synthesis and evaluation of the antidepressant activity of the enantiomers of bupropion
المؤلفون: Bernard T. Kenney, Robert M. Ferris, Nariman B. Mehta, F. E. Soroko, Elizabeth B. Hollingsworth, David Lee Musso
المصدر: Chirality. 5:495-500
بيانات النشر: Wiley, 1993.
سنة النشر: 1993
مصطلحات موضوعية: Male, Biogenic Amines, Serotonin, Dopamine, Sedation, Tetrabenazine, Hypothalamus, Mice, Inbred Strains, Pharmacology, Chemical synthesis, Catalysis, Analytical Chemistry, Mice, Norepinephrine, Structure-Activity Relationship, In vivo, Biogenic amine, Drug Discovery, medicine, Animals, Bupropion, Spectroscopy, chemistry.chemical_classification, Chemistry, fungi, Organic Chemistry, Stereoisomerism, Corpus Striatum, Antidepressant, Indicators and Reagents, medicine.symptom, Enantiomer, Reuptake inhibitor, Synaptosomes, medicine.drug
الوصف: The synthesis of the enantiomers of bupropion, (rac)-2-tert-butylamino-3′-chloropropiophenone 1 (Wellbutrin®) is described. The enantiomers were compared with the racemate in both the tetrabenazine-induced sedation model and the inhibition of uptake of biogenic amine assay. No significant differences were found in their potencies to reverse tetrabenazine-induced sedation in mice or in their IC50 values as inhibitors of biogenic amine uptake into nerve endings obtained from mouse brain. © 1993 Wiley-Liss, Inc.
تدمد: 1520-636X
0899-0042
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18518f98e7a8951a6d8c0c468f0ef3b7
https://doi.org/10.1002/chir.530050704
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....18518f98e7a8951a6d8c0c468f0ef3b7
قاعدة البيانات: OpenAIRE