Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA063536-03
Application #
2105453
Study Section
Special Emphasis Panel (SRC (V1))
Project Start
1994-07-01
Project End
1998-04-30
Budget Start
1996-05-01
Budget End
1997-04-30
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Connelly, Stephen; DeMartino, Jessica K; Boger, Dale L et al. (2013) Biological and structural evaluation of 10R- and 10S-methylthio-DDACTHF reveals a new role for sulfur in inhibition of glycinamide ribonucleotide transformylase. Biochemistry 52:5133-44
DeMartino, Jessica K; Hwang, Inkyu; Connelly, Stephen et al. (2008) Asymmetric synthesis of inhibitors of glycinamide ribonucleotide transformylase. J Med Chem 51:5441-8
Xu, Lan; Chong, Youhoon; Hwang, Inkyu et al. (2007) Structure-based design, synthesis, evaluation, and crystal structures of transition state analogue inhibitors of inosine monophosphate cyclohydrolase. J Biol Chem 282:13033-46
DeMartino, Jessica K; Hwang, Inkyu; Xu, Lan et al. (2006) Discovery of a potent, nonpolyglutamatable inhibitor of glycinamide ribonucleotide transformylase. J Med Chem 49:2998-3002
Cheng, Heng; Hwang, Inkyu; Chong, Youhoon et al. (2005) Synthesis and biological evaluation of N-[4-[5-(2,4-diamino-6-oxo-1,6-dihydropyrimidin-5-yl)-2-(2,2,2-trifluoroacetyl)pentyl]benzoyl]-L-glutamic acid as a potential inhibitor of GAR Tfase and the de novo purine biosynthetic pathway. Bioorg Med Chem 13:3593-9
Cheng, Heng; Chong, Youhoon; Hwang, Inkyu et al. (2005) Design, synthesis, and biological evaluation of 10-methanesulfonyl-DDACTHF, 10-methanesulfonyl-5-DACTHF, and 10-methylthio-DDACTHF as potent inhibitors of GAR Tfase and the de novo purine biosynthetic pathway. Bioorg Med Chem 13:3577-85
Chong, Youhoon; Hwang, Inkyu; Tavassoli, Ali et al. (2005) Synthesis and biological evaluation of alpha- and gamma-carboxamide derivatives of 10-CF3CO-DDACTHF. Bioorg Med Chem 13:3587-92
Capps, Kevin J; Humiston, Jon; Dominique, Romyr et al. (2005) Discovery of AICAR Tfase inhibitors that disrupt requisite enzyme dimerization. Bioorg Med Chem Lett 15:2840-4
Vergis, James M; Beardsley, G Peter (2004) Catalytic mechanism of the cyclohydrolase activity of human aminoimidazole carboxamide ribonucleotide formyltransferase/inosine monophosphate cyclohydrolase. Biochemistry 43:1184-92
Wolan, Dennis W; Cheong, Cheom-Gil; Greasley, Samantha E et al. (2004) Structural insights into the human and avian IMP cyclohydrolase mechanism via crystal structures with the bound XMP inhibitor. Biochemistry 43:1171-83

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