Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Steven S. Bondy"'
Autor:
David A. Oare, I-hung Shih, Laura S. Lehman, Erik De Clercq, Eric Mabery, Steven S. Bondy, Weidong Zhong, Inge Vliegen, Matthew Paulson, Johan Neyts, Gerhard Pürstinger, Hans Reiser, Jan Paeshuyse, Nina Boddeker, Tine De Burghgraeve, William A. Lee
Publikováno v:
Journal of Hepatology
Background/Aims Following lead optimization, a set of substituted imidazopyridines was identified as potent and selective inhibitors of in vitro HCV replication. The particular characteristics of one of the most potent compounds in this series (5-[[3
Autor:
Maisoun Sulfab, Weidong Zhong, Vivian Randall W, Steven S. Bondy, Wanchi Fung, Hengli Tang, Uli Schmitz, Christy M. Hebner, Johan Neyts, Michelle Nash, Trenkle James D, Magdeleine Hung, Xiaohong Liu, John O. Link, Roman Sakowicz, Yang Tian, Katherine M. Brendza, Kyla Bjornson, James G. Taylor, Bin Han
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e39163 (2012)
PLoS ONE
PLoS ONE
Tegobuvir (TGV) is a novel non-nucleoside inhibitor (NNI) of HCV RNA replication with demonstrated antiviral activity in patients with genotype 1 chronic HCV infection. The mechanism of action of TGV has not been clearly defined despite the identific
Autor:
Francis Van Middlesworth, Susan A. Warne, Patricia Conard, Meheryar N. Rivetna, Anthony J. Conley, Emilio A. Emini, Richard L. Tolman, John Hannah, Catherine A. Dolan, Steven S. Bondy, Jon A. Rudbach, Victoria K. Rusiecki, J. Terry Ulrich, Stephen Marburg, William J. Leanza, Elizabeth E. Sugg
Publikováno v:
Vaccine. 12:445-451
A successful prophylactic human immunodeficiency virus type 1 (HIV-1) vaccine must elicit an immune response that will prevent establishment of the persistent viral infection. The only response shown to be effective in this regard is virus-neutralizi
Autor:
Yang Tian, Betty Peng, Weidong Zhong, Matthew Paulson, William A. Lee, Gerhard Pürstinger, Uli Schmitz, I-hung Shih, Johan Neyts, Xiaoping Qi, Tse Winston C, Steven S. Bondy, Huiling Yang, Eric Mabery, Hans Reiser, Laura S. Lehman, Jan Paeshuyse, Inge Vliegen, Martijn Fenaux, Christy M. Hebner, Gina Bahador
Publikováno v:
Antimicrobial agents and chemotherapy. 55(9)
GS-9190 (Tegobuvir) is a novel imidazopyridine inhibitor of hepatitis C virus (HCV) RNA replication in vitro and has demonstrated potent antiviral activity in patients chronically infected with genotype 1 (GT1) HCV. GS-9190 exhibits reduced activity
The inhibition of C5a receptor binding by analogs of L-156,602, a cyclic hexadepsipeptide antibiotic
Autor:
Sumire V. Kobayashi, Dana N. Cianciarulo, Thomas E. Rollins, Robert A. Zambias, Salvatore J. Siciliano, Charles G. Caldwell, Steven S. Bondy, Joung L. Goulet, Joshua S. Boger, Martin S. Springer, Milton L. Hammond, Philippe L. Durette, Joanne F. Kinneary, William K. Hagmann, Thomas J. Lanza, Ihor E. Kopka
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 2:1033-1038
The cyclic hexadepsipeptide antibiotic L-156,602 ( 1 ) was found to be an inhibitor of anaphylatoxin C5a binding to its receptor (IC 50 =1.7 μg/mL). This compound also caused nonspecific degranulation of neutrophils, but not through interactions wit
Publikováno v:
The Journal of Organic Chemistry. 55:2355-2361
The 14-carbon tetrahydropyranylpropionic acid side chain of the cyclic hexadepsipeptide antibiotic L-156,602 (1) has been prepared as the methyl ester derivative 5. Asymmetric synthesis of the key intermediate 11-carbon lactone 7 was accomplished usi
Autor:
Peter L. Barker, Thomas J. Lanza, Milton L. Hammond, Florence Baker, Steven S. Bondy, Charles G. Caldwell, Philippe L. Durette, Arsenio A. Pessolano, Joshua S. Boger
Publikováno v:
Tetrahedron Letters. 31:1237-1240
The total synthesis of the naturally occurring cyclic hexadepsipeptide antibiotic L-156,602 ( 1 ) is described.
Autor:
I-hung Shih, Gerhard Pürstinger, Johan Neyts, Leen Delang, Inge Vliegen, William A. Lee, Steven S. Bondy, Jan Paeshuyse, Weidong Zhong
Publikováno v:
Journal of Hepatology. 54:S197-S198
Autor:
Steven S. Bondy, Charles G. Caldwell
Publikováno v:
Synthesis. 1990:34-36
Both enantiomers of erythro-3-hydroxyleucine are available by asymmetric epoxidation of (E)-4-methyl-2-penten-1-ol (1) followed by ruthenium tetroxide catalyzed oxidation to the corresponding glycidic acid 3, epoxide opening by benzylamine, and hydro
Autor:
Inge Vliegen, Johan Neyts, William A. Lee, Steven S. Bondy, Weidong Zhong, I-hung Shih, Gerhard Pürstinger, Jan Paeshuyse
Publikováno v:
Antiviral Research. 90:A65