Zobrazeno 1 - 7
of 7
pro vyhledávání: '"S B, DeMattos"'
Publikováno v:
British Journal of Clinical Pharmacology. 49:43-47
Aims To determine whether ziprasidone alters the metabolizing activity of the 2D6 isoenzyme of cytochrome P450 (CYP2D6).
Autor:
Douglas S. Chapin, J. L. Ives, Yuhpyng L. Chen, Dane R. Liston, Butler Todd W, S. B. Demattos, S.B. Jones, Arthur Adam Nagel, Anabella Villalobos, Deane M. Nason
Publikováno v:
Journal of Medicinal Chemistry. 38:2802-2808
A series of N-benzylpiperidines (2a-d, 10) with novel isoxazole-containing tricycles has been prepared. This series has shown potent in vitro inhibition of the enzyme acetylcholinesterase (AChE), with IC 50 s = 0.33-3.6 nM. Compound 2a was the most p
Autor:
W. F. White, Yuhpyng Liang Chen, Deane M. Nason, Anabella Villalobos, Douglas S. Chapin, I. A. Shalaby, Dane R. Liston, J. A. Nielsen, S. B. Demattos, J. L. Ives, Samantha Jones, Butler Todd W, Andres D. Ramirez, Arthur Adam Nagel
Publikováno v:
ChemInform. 26
Publikováno v:
British journal of clinical pharmacology. 49
To determine whether ziprasidone alters the metabolizing activity of the 2D6 isoenzyme of cytochrome P450 (CYP2D6).Twenty-four healthy young subjects aged 18-45 years were screened for CYP2D6 metabolizing activity and shown to be extensive metabolize
Autor:
T A, Rugsley, M D, Davis, H C, Akunne, L W, Cooke, S Z, Whetzel, R G, MacKenzie, Y H, Shih, D H, van Leeuwen, S B, DeMattos, L M, Georgic
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 274(2)
The receptor binding and biochemical effects of the putative dopamine (DA) partial agonist CI-1007 ([R(+)-1,2,3,6-tetrahydro-4-phenyl- 1-[(3-phenyl-3-cyclohexen-1-yl)methyl]pyridine] maleate) and potential antipsychotic were evaluated with a variety
Autor:
A, Villalobos, T W, Butler, D S, Chapin, Y L, Chen, S B, DeMattos, J L, Ives, S B, Jones, D R, Liston, A A, Nagel, D M, Nason
Publikováno v:
Journal of medicinal chemistry. 38(15)
A series of N-benzylpiperidines (2a-d, 10) with novel isoxazole-containing tricycles has been prepared. This series has shown potent in vitro inhibition of the enzyme acetylcholinesterase (AChE), with IC50S = 0.33 - 3.6 nM. Compound 2a was the most p
Publikováno v:
Biological Psychiatry. 42:42S