Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Timothy B. Frigo"'
Autor:
Peter Müller, Mahmoud Mirmehrabi, Jeffrey Caplette, Helene Shea, Timothy B. Frigo, Michael J. Jozwiakowski
Publikováno v:
International journal of pharmaceutics. 527(1-2)
A systematic polymorph screening process was conducted on the steroid hydroxyprogesterone caproate, which had only one previously described orthorhombic crystalline form (A), in order to fully elucidate its solid state properties. Cooling, anti-solve
Autor:
Timothy B. Frigo, Hao Chang, Menahem Kaftory, Stephen F. Nelsen, Peter A. Petillo, Dennis A. Dougherty
Publikováno v:
The Journal of Organic Chemistry. 56:613-618
Autor:
Frank Rusnak, Cheng Tu, Timothy B. Frigo, Christopher T. Walsh, Masahiro Sakaitani, Nina Quinn, Glenn A. Berchtold
Publikováno v:
Biochemistry. 29:6789-6798
The enzyme 2,3-dihydro-2,3-dihydroxybenzoate dehydrogenase (2,3-diDHB dehydrogenase, hereafter Ent A), the product of the enterobactin biosynthetic gene entA, catalyzes the NAD(+)-dependent oxidation of the dihydroaromatic substrate 2,3-dihydro-2,3-d
Publikováno v:
American Peptide Symposia ISBN: 0792351606
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f4305022708860a06c44719a2646ef7
https://doi.org/10.1007/0-306-46862-x_103
https://doi.org/10.1007/0-306-46862-x_103
Publikováno v:
Bioconjugate chemistry. 15(2)
Investigation into the effect of the reducing sugar of dextran on formation and stability of dextran-coated ultrasmall superparamagnetic iron oxides (USPIO) has demonstrated that reduction of the terminal reducing sugar can have a significant effect
Autor:
Timothy B. Frigo, James Burton
Publikováno v:
Recent Progress on Kinins ISBN: 9783034873239
Converting peptide inhibitors of tissue kallikrein into drugs requires, among other things, that the compounds be made orally active. Measurement of the rate at which peptides diffuse across model epithelial membranes that mimic the human gut has all
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9688b95ea54a107a95def4e5225985dd
https://doi.org/10.1007/978-3-0348-7321-5_27
https://doi.org/10.1007/978-3-0348-7321-5_27
Publikováno v:
Journal of the American Chemical Society. 111:1776-1781
The free energy of activation for nitrogen inversion of the title compound was determined to be 13.77 (4) kcal/mol at 25 "C in CDCI3 by dynamic 13C NMR and that for the 7-ethyl compound to be 13.17 (4) kcal/mol under the same conditions. The change i
Publikováno v:
Tetrahedron. 42:1769-1777
Diels-Alder addition of bicyclic azo compounds to cyclic dienes would produce bis-N,N'-bicyclic hydrazines, but this reaction proves to be endothermic. The greater basicity of the adduct than of the azo compound makes the addition reaction 13.6–14.
Publikováno v:
Journal of the American Chemical Society. 106:7384-7389
High-pressure mass spectrometry was used to measure adiabatic ionization potentials and proton affinitias for hydrazine, methylhydrazine, 1,l-dimethylhydrazine, and six tetraalkylhydrazines. Unusually large relaxation energies in the radical ions, wh
Publikováno v:
Journal of the American Chemical Society. 108:7926-7934