The objective of this proposal is to obtain funding for the purchase a Varian 400 MHz multi-nuclear NMR spectrometer as a replacement for an aging Varian Gemini 200 MHz instrument. The current spectrometer has been in continuous service since September 1988. Varian will no longer support the Gemini series of instruments. The new instrument will be the only NMR spectrometer in the Ernest Mario School of Pharmacy and will serve the needs of approximately 35-40 researchers from the Graduate Programs in Medicinal Chemistry, Pharmaceutical Science, and Pharmacology and Toxicology. These researchers have no routine access to other NMR facilities on campus. This instrument will be used to support research efforts on 13 NIH funded projects. These projects are focused largely on the design and synthesis of novel heterocyclic and macrocyclic anticancer agents, the development of new methodology for the synthesis of pharmaceutical agents, the isolation and structure elucidation of natural products having potential as anticancer or chemopreventive agents, and on the determination of the mechanisms of action of chemopreventive agents. All of these projects require ready access to a high resolution NMR spectrometer for structure determination. The Varian 400 MHz multi-nuclear NMR spectrometer for which funding is being requested will greatly enhance the cutting edge research efforts of the major users of this instrument in the areas of novel anticancer drug design, synthesis, and discovery. The research projects described in this proposal are largely targeted towards the synthesis and identification of novel anticancer agents with the potential for development into clinically-useful drugs, the isolation and structure elucidation of bioactive compounds from plants, and the determination of metabolites and activation pathways of naturally-occurring cancer-preventive agents. The availability of a high resolution multi-nuclear NMR spectrometer is an essential tool for determining the chemical structures of these compounds and advancing these research efforts. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR023698-01A1
Application #
7385164
Study Section
Special Emphasis Panel (ZRG1-BCMB-R (30))
Program Officer
Tingle, Marjorie
Project Start
2008-02-01
Project End
2009-01-31
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
1
Fiscal Year
2008
Total Cost
$351,400
Indirect Cost
Name
Rutgers University
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
001912864
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Sagong, Hye Yeon; Bauman, Joseph D; Patel, Disha et al. (2014) Phenyl substituted 4-hydroxypyridazin-3(2H)-ones and 5-hydroxypyrimidin-4(3H)-ones: inhibitors of influenza A endonuclease. J Med Chem 57:8086-98
Parhi, Ajit K; Zhang, Yongzheng; Saionz, Kurt W et al. (2013) Antibacterial activity of quinoxalines, quinazolines, and 1,5-naphthyridines. Bioorg Med Chem Lett 23:4968-74
Sagong, Hye Yeon; Parhi, Ajit; Bauman, Joseph D et al. (2013) 3-Hydroxyquinolin-2(1H)-ones As Inhibitors of Influenza A Endonuclease. ACS Med Chem Lett 4:547-50
Zhang, Yongzheng; Giurleo, Daniel; Parhi, Ajit et al. (2013) Substituted 1,6-diphenylnaphthalenes as FtsZ-targeting antibacterial agents. Bioorg Med Chem Lett 23:2001-6
Blankson, Gifty; Rzuczek, Suzanne G; Bishop, Cody et al. (2013) Macrocyclic pyridyl polyoxazoles: structure-activity studies of the aminoalkyl side-chain on G-quadruplex stabilization and cytotoxic activity. Molecules 18:11938-63
Blankson, Gifty A; Pilch, Daniel S; Liu, Angela A et al. (2013) Macrocyclic biphenyl tetraoxazoles: synthesis, evaluation as G-quadruplex stabilizers and cytotoxic activity. Bioorg Med Chem 21:4511-20
Kelley, Cody; Lu, Songfeng; Parhi, Ajit et al. (2013) Antimicrobial activity of various 4- and 5-substituted 1-phenylnaphthalenes. Eur J Med Chem 60:395-409
Parhi, Ajit; Kelley, Cody; Kaul, Malvika et al. (2012) Antibacterial activity of substituted 5-methylbenzo[c]phenanthridinium derivatives. Bioorg Med Chem Lett 22:7080-3
Parhi, Ajit; Lu, Songfeng; Kelley, Cody et al. (2012) Antibacterial activity of substituted dibenzo[a,g]quinolizin-7-ium derivatives. Bioorg Med Chem Lett 22:6962-6
Kelley, Cody; Zhang, Yongzheng; Parhi, Ajit et al. (2012) 3-Phenyl substituted 6,7-dimethoxyisoquinoline derivatives as FtsZ-targeting antibacterial agents. Bioorg Med Chem 20:7012-29

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