The overall goal of the proposed studies is to establish the feasibility of developing therapies for brain cancers such as glioblastoma multiforme from the schweinfurthin family of antiproliferative agents. These agents are highly toxic to CNS derived tumor cell lines in vitro and more importantly appear to exhibit this activity via a novel cellular target(s). The schweinfurthins also contain chemical functional groups which should facilitate cerebrovascular barrier penetration, a very important aspect of drugs aimed at treating primary brain cancers. Phase One of these studies is comprised of three narrowly focused aims directed at proving the feasibility of finding advancing? a therapeutic lead from this family:
These aims i nclude: 1) synthesis of analogs of the schweinfurthins bearing functional groups designed to improve the """"""""drug-like"""""""" nature of the compounds; 2) improvement of the published synthesis of the hexahydroxanthene core of the 3-deoxyschweinfurthin motif to allow for more efficient and safe production of larger quantities of material for Phase Two studies; and 3) biological studies aimed at elucidation of the cellular or molecular target of the schweinfurthins.
These aims will allow a decision to be made about feasibility of studying these drugs further in pre-clinical animal models as part of Phase Two, and ultimately of bringing drugs based on this unique and potent family of compounds into use against brain cancer. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Business Technology Transfer (STTR) Grants - Phase I (R41)
Project #
1R41CA126020-01
Application #
7218415
Study Section
Special Emphasis Panel (ZRG1-ONC-T (10))
Program Officer
Haim, Todd E
Project Start
2007-09-15
Project End
2009-09-14
Budget Start
2007-09-15
Budget End
2009-09-14
Support Year
1
Fiscal Year
2007
Total Cost
$109,860
Indirect Cost
Name
Terpenoid Therapeutics, Inc.
Department
Type
DUNS #
602743903
City
Coralville
State
IA
Country
United States
Zip Code
52241
Kodet, John G; Topczewski, Joseph J; Gardner, Kevyn D et al. (2013) Electrophilic aromatic prenylation via cascade cyclization. Tetrahedron 69:9212-9218
Kodet, John G; Wiemer, David F (2013) Synthesis of indole analogues of the natural schweinfurthins. J Org Chem 78:9291-302
Kuder, Craig H; Sheehy, Ryan M; Neighbors, Jeffrey D et al. (2012) Functional evaluation of a fluorescent schweinfurthin: mechanism of cytotoxicity and intracellular quantification. Mol Pharmacol 82:9-16
Topczewski, Joseph J; Kodet, John G; Wiemer, David F (2011) Exploration of cascade cyclizations terminated by tandem aromatic substitution: total synthesis of (+)-schweinfurthin A. J Org Chem 76:909-19
Topczewski, Joseph J; Wiemer, David F (2011) First total synthesis of (+)-Vedelianin, a potent antiproliferative agent. Tetrahedron Lett 52:1628-1630
Topczewski, Joseph J; Kuder, Craig H; Neighbors, Jeffrey D et al. (2010) Fluorescent schweinfurthin B and F analogs with anti-proliferative activity. Bioorg Med Chem 18:6734-41
Ulrich, Natalie C; Kodet, John G; Mente, Nolan R et al. (2010) Structural analogues of schweinfurthin F: probing the steric, electronic, and hydrophobic properties of the D-ring substructure. Bioorg Med Chem 18:1676-83
Kuder, Craig H; Neighbors, Jeffrey D; Hohl, Raymond J et al. (2009) Synthesis and biological activity of a fluorescent schweinfurthin analogue. Bioorg Med Chem 17:4718-23