Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Norman Wideburg"'
Autor:
H. L. Sham, Kent D. Stewart, Kennan C. Marsh, Chang H. Park, Thomas Herrin, Xiang-Peng Kong, C. Zhao, Dale J. Kempf, David A. Betebenner, J. J. Plattner, Akhter Molla, T. Robins, D. W. Norbeck, Shuqun Lin, Ayda Saldivar, N. Lyons, Darold L. Madigan, W. Jun. Rosenbrook, Edith McDonald, Jon F. Denissen, Norman Wideburg, Suthida Vasavanonda
Publikováno v:
ChemInform. 27
Autor:
John Erickson, David J. Neidhart, John VanDrie, Dale J. Kempf, Xiu Chun Wang, Daniel W. Norbeck, Jacob J. Plattner, Judith W. Rittenhouse, Mary Turon, Norman Wideburg, William E. Kohlbrenner, Robert Simmer, Rosalind Helfrich, Deborah A. Paul, Mark Knigge
Publikováno v:
Science. 249:527-533
A two-fold (C2) symmetric inhibitor of the protease of human immunodeficiency virus type-1 (HIV-1) has been designed on the basis of the three-dimensional symmetry of the enzyme active site. The symmetric molecule inhibited both protease activity and
Autor:
John Hengeveld, Jack Tadanier, William Rosenbrook, David Whittern, Cheuk-Man Lee, Norman Wideburg
Publikováno v:
Carbohydrate Research. 201:209-222
Analogs of 3-deoxy- d - manno -octulosonic acid (Kdo) having the β-anomeric hydroxyl group replaced by a substituted-methyl group were prepared from Kdo. The substituted-methyl groups were derived from the carboxyl group of Kdo, whereas the carboxyl
Autor:
H. L. Sham, Sudthida Vasavanonda, Edith McDonald, J. J. Plattner, Shuqun Lin, D. W. Norbeck, Ayda Saldivar, T. Robins, K. C. Marsh, Chen Zhao, Dale J. Kempf, Norman Wideburg, David A. Betebenner
Publikováno v:
Biochemical and biophysical research communications. 211(1)
A series of novel pseudo-symmetrical and unsymmetrical inhibitors based on the backbone modification of a peptidomimetic were synthesized and found to be highly potent inhibitors of the HIV-1 protease (IC50 = 2.9 to < 0.5 nM). These compounds also po
Publikováno v:
Carbohydrate research. 201(2)
Selective C-8 modifications of 2,6-anhydro-3-deoxy-D-glycero-D-talo-octonic acid ("2,3-dideoxy-beta-D-manno-2-octulosonic acid", 1a) were effected via the protected 8-hydroxy derivatives 2d and 2e. Swern oxidation of 2d and 2e gave the aldehydes 3a a
Autor:
Lester A. Mitscher, George W. Clark. III, Gordon Bokelman, Hollis D. H. Showalter, Kunikatsu Shirahata, P. Bryan Hudson, Earl Fager, Norman Wideburg, R. Jack Theriault
Publikováno v:
HETEROCYCLES. 7:779