Zobrazeno 1 - 10
of 25
pro vyhledávání: '"E. Kim Fifer"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 73, Iss 6, Pp 864-866 (2017)
The title compound, C28H32N2, (I), is one of a second generation of compounds designed and synthesized based on a very potent and selective α9α10 nicotinic acetylcholine receptor antagonist ZZ161C {1,1′-[[1,1′-biphenyl]-4,4′-diylbis(prop-2-yn
Externí odkaz:
https://doaj.org/article/af01711f6752425e8e4161d02380aece
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 10, Pp 1147-1150 (2015)
The title compounds, C26H28N2, (I), and C28H32N2, (II), were designed based on the structure of the potent α9α10 nicotinic acetylcholine receptor antagonist ZZ161C {1,1′-[[1,1′-biphenyl]-4,4′-diylbis(prop-2-yne-3,1-diyl)]bis(3,4-dimethylpyrid
Externí odkaz:
https://doaj.org/article/62fc45b7b88041c29fc48d9e819cf80b
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 10, Pp 1132-1135 (2015)
As part of a comprehensive program to discover α9α10 nicotinic acetylcholine receptor antagonists, the title compounds C30H36N2, (I), and C36H48N2, (II), were synthesized by coupling 4,4′-bis(3-bromoprop-1-yn-1-yl)-1,1′-biphenyl with 4-methylpi
Externí odkaz:
https://doaj.org/article/62abdeb5c0b54bfda480afd0c6ceb3a5
Publikováno v:
Drug Metabolism and Disposition. 43:534-552
The disposition and metabolism of hydrastine was investigated in 11 healthy subjects following an oral dose of 2.7 g of goldenseal supplement containing 78 mg of hydrastine. Serial blood samples were collected for 48 hours, and urine was collected fo
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications, Vol 73, Iss 6, Pp 864-866 (2017)
Acta Crystallographica Section E: Crystallographic Communications, Vol 73, Iss 6, Pp 864-866 (2017)
The synthesis and structure of the title piperidine derivative is reported. It is one of a second generation of compounds designed and synthesized based on a very potent and selective α9α10 nicotinic acetylcholine receptor antagonist ZZ161C, whic
Publikováno v:
The Open Drug Delivery Journal. 4:21-29
Publikováno v:
Drug Development and Industrial Pharmacy. 35:1-11
A water-insoluble complex between diltiazem HCl and Na deoxycholate was prepared to achieve sustained release dosage forms. Physicochemical characterization of the drug complex was carried out with differential scanning calorimetry, (1)H-nuclear magn
Autor:
E. Robert Burns, E. Kim Fifer, Thomas J. Kelly, Elizabeth Ann Coleman, Richard W. Nicholas, Clifton Orr
Publikováno v:
Journal of Cancer Education. 21:243-247
Background: The Partners in Research program provides first-hand research experiences for medical, pharmacy, and African-American undergraduate students. Methods: During ten weeks, students participate in on-going cancer research, weekly educational
Publikováno v:
American Journal of Physiology-Renal Physiology. 292:F292-F303
Protein kinase B (Akt) activation is well known for its protective effects against apoptosis. However, the role of Akt in regulation of necrosis is unknown. This study was designed to test whether Akt activation protects against nephrotoxicant-induce
Autor:
Grover P. Miller, Dean W. Roberts, E. Kim Fifer, Lynda Letzig, Jessica H. Hartman, Laura P. James
Risk assessment for exposure to mixtures of drugs and pollutants relies heavily on in vitro characterization of their bioactivation and/or metabolism individually and extrapolation to mixtures assuming no interaction. Herein, we demonstrated that in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d02758b37fd4cffedf7ace4b561aa807
https://europepmc.org/articles/PMC5584065/
https://europepmc.org/articles/PMC5584065/