Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Dona L. Bamberger"'
Autor:
Dona L. Bamberger, Jackson B. Gibbs, Oliff Allen I, Nancy E. Kohl, Samuel L. Graham, Rands E, Thorsten E. Fisher, Robert L. Smith, Scott D. Mosser, John S. Wai, David L. Pompliano
Publikováno v:
Bioorganic & Medicinal Chemistry. 2:939-947
Replacement of the central amino methylene linkage of C[psi CH2NH]A[psi CH2NH]AX tetrapeptide inhibitors with carbon tethers led to compounds with potency in the nanomolar range. Some of the more potent olefinic compounds inhibit Ras processing in in
Autor:
Jacob M. Hoffman, Barnes Jl, Clarence S. Rooney, Anthony M. Smith, Thorsten E. Fisher, James H. Jones, Dona L. Bamberger, Thomas Cm, Theresa M. Williams, John S. Wai
Publikováno v:
Journal of Medicinal Chemistry. 36:953-966
A new series of potent specific 2-pyridinone reverse transcriptase (RT) inhibitors was developed based on the preliminary development lead 3-[(phthalmido)ethyl]-5-ethyl-6-methylpyridin-2(1H)-one (3), a non-nucleoside derivative which exhibited weak a
Autor:
W. S. Saari, J. H. Nunberg, Jacob M. Hoffman, Julie A. O'Brien, P. S. Anderson, J. H. Jones, Thorsten E. Fisher, M. E. Goldman, A. M. Smith, Quintero Julio C, C. M. Thomas, C. S. Rooney, William A. Schleif, Dona L. Bamberger, John S. Wai, Emilio A. Emini
Publikováno v:
ChemInform. 24
Autor:
John S. Wai, R. J. Hudcosky, Theresa M. Williams, Jacob M. Hoffman, J. H. Nunberg, S. C. Mactough, Quintero Julio C, W. S. Saari, P. S. Anderson, M. E. Goldman, Emilio A. Emini, William A. Schleif, C. M. Thomas, C. S. Rooney, Thorsten E. Fisher, Dona L. Bamberger, Julie A. O'Brien
Publikováno v:
ChemInform. 25
Autor:
Jacob M. Hoffman, S. C. Mactough, Dona L. Bamberger, Thorsten E. Fisher, W. S. Saari, John S. Wai, Clarence S. Rooney, R. J. Hudcosky, Theresa M. Williams, Thomas Cm
Publikováno v:
Journal of medicinal chemistry. 36(2)
In an ongoing effort to develop novel nonnucleoside, specific human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) inhibitors, a series of 3-[(pyridylmethyl)amino]- and 3-[(phenylmethyl)amino]-2-pyridinone derivatives was synthesize