Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI054574-02
Application #
6803954
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Program Officer
Zou, Lanling
Project Start
2003-09-26
Project End
2005-12-31
Budget Start
2004-01-01
Budget End
2004-12-31
Support Year
2
Fiscal Year
2004
Total Cost
$365,000
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
Choi, Jinil; Park, Jewn Giew; Pang, Yuan-Ping (2008) Convenient Synthesis of a Library of Discrete Hydroxamic Acids Using the Hydroxythiophenol (Marshall) Resin. Tetrahedron Lett 49:1103-1106
Pang, Y P (2007) In silico drug discovery: solving the ""target-rich and lead-poor"" imbalance using the genome-to-drug-lead paradigm. Clin Pharmacol Ther 81:30-4
Tang, Jing; Park, Jewn Giew; Millard, Charles B et al. (2007) Computer-aided lead optimization: improved small-molecule inhibitor of the zinc endopeptidase of botulinum neurotoxin serotype A. PLoS One 2:e761
Wang, Qi; Pang, Yuan-Ping (2007) Normal-mode-analysis-monitored energy minimization procedure for generating small-molecule bound conformations. PLoS One 2:e1025
Park, Jewn Giew; Sill, Peter C; Makiyi, Edward F et al. (2006) Serotype-selective, small-molecule inhibitors of the zinc endopeptidase of botulinum neurotoxin serotype A. Bioorg Med Chem 14:395-408
Merino, Isidro; Thompson, Jason D; Millard, Charles B et al. (2006) Bis-imidazoles as molecular probes for peripheral sites of the zinc endopeptidase of botulinum neurotoxin serotype A. Bioorg Med Chem 14:3583-91
Park, Jewn Giew; Langenwalter, Kevin J; Weinbaum, Carolyn A et al. (2004) Improved loading and cleavage methods for solid-phase synthesis using chlorotrityl resins: synthesis and testing of a library of 144 discrete chemicals as potential farnesyltransferase inhibitors. J Comb Chem 6:407-13
Pang, Yuan-Ping (2004) Three-dimensional model of a substrate-bound SARS chymotrypsin-like cysteine proteinase predicted by multiple molecular dynamics simulations: catalytic efficiency regulated by substrate binding. Proteins 57:747-57