Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Paul E. Fagerness"'
Publikováno v:
Journal of the American Chemical Society. 125:7696-7703
Competition ligand-based NMR screening experiments have recently been introduced to overcome most of the problems associated with traditional ligand-based NMR screening. Molecules with marginal solubility and high affinity for a given target can be e
Autor:
Paul E Fagerness, Michael Barfield and
Publikováno v:
Journal of the American Chemical Society. 119:8699-8711
The dependence of the 13C, 15N, and 1H isotropic NMR chemical shifts on amine substitution of aromatic ring systems are examined both experimentally and by DFT/GIAO (density functional theory/gauge including atomic orbitals) methods. There are large,
Autor:
Ping Gao, Paul E. Fagerness
Publikováno v:
Pharmaceutical Research. 12:955-964
Purpose. This work describes diffusivity measurements of drug (adinazolam mesylate) and water in a variety of solutions including polymer gels.
Publikováno v:
Pharmaceutical Research. 10:75-79
Understanding how moisture interacts with a drug or formulation is a critical component of product development. This study demonstrates how water affects the 3′-gem-diol ↔ 3′-keto equilibrium in trospectomycin sulfate bulk drug and freeze-dried
Publikováno v:
Biochemical Journal. 194:627-631
The facultative anaerobes Rhodopseudomonas spheroides and Propionibacterium shermanii were grown under anaerobic and aerobic conditions. The effect of light was studied with the photosynthetic R. spheroides, and the adaptation of both species to dark
Publikováno v:
Tetrahedron. 36:2721-2725
Due to their sensitivity to light and air, porphyrinogens are not normally isolated, but are routinely analyzed by oxidation to the corresponding porphyrin. We report herein the 13 C- and 15 N-NMR spectra of uroporphyrinogens I and III in their “na
Publikováno v:
The Journal of Organic Chemistry. 43:828-834
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :1586-1591
A series of v-triazolo[4,5-b]pyridine nucleosides, which are structurally related to the biologically active 8-azapurines, has been prepared. The use of natural abundance carbon-13 n.m.r. in establishing the site of ribosylation of the nucleoside 5-a
Autor:
Yi Jin Jang, N. E. Mackenzie, J P G Malthouse, A. Brisson, Le Zong Qi, Paul E. Fagerness, A. I. Scott, Carl M. Carter, W. U. Primrose, W. Bode
Publikováno v:
Tetrahedron. 42:3269-3276
Comparison of the X-ray diffraction data and both solution and solid (CPMAS) NMR spectra for the covalent adduct of trypsin and carbobenzyloxylysyl chloromethyl ketone provides unequivocal evidence that the serine-195 hydroxyl group of the enzyme for
Autor:
John Y. Lee, Philip J. Sidebottom, Gerardo Burton, Kozo Shishido, Paul E. Fagerness, A. Ian Scott, Robert Baxter, J. Martyn Gunn
Publikováno v:
Canadian Journal of Chemistry. 58:1839-1846
Applications of 13C nmr in following the metabolism and fate of 13C enriched substrates in whole cells are described. Studies on the elaboration of coproporphyrinogens I (2a) and III (2b) from [5-13C]-δ-aminolevulinic acid (1) and [11-13C-porphobili