This project is the synthetic organic chemistry component of this program project. Our tasks is the synthesis of research quantities of lead compounds. These compounds are supplied from other projects for biological testing. Amounts ranging from 100 mg to 1 g are sufficient for confirmation of initial in vitro activity and testing in secondary systems, such as mouse mammary organ culture (MMOC). If the results are promising, short-term animal testing can also be performed with these quantities of test materials, as can mechanistic evaluations. In this context, this project is also responsible for derivatization and synthetic modification of lead compounds for structure-activity relationships (SARs), which will be used for lead optimization. In addition, project 5 will perform scale-up syntheses of lead compounds for use in full-term animal studies for the assessment of chemopreventive activity. Scale-up synthesis will involve multi-step processes and possibly stereoselective transformations for quantities ranging from 500 g to 2 kg. The goal of project 5 is the efficient and timely synthesis of compounds from the discovery part of the program to the stage of complete biological evaluation. To accomplish this goal, a flexible, competent, and responsive synthetic group has been assembled. In ongoing studies, this project will focus on large scale syntheses of sulforamate, oxomate, sulforaphane, brassinin, cyclobrassinin, 4'-bromoflavone, E-resveratrol and 4'-bromorot- 2'-enonic acid for inclusion in animal carcinogenesis models (project 3). We will also continue analog syntheses of resveratrol, rotenoids and isoflavones. Thus, in a highly coordinated manner, project 5 will contribute to the further development of lead compounds that have or will emerge from this program project.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA048112-08A1
Application #
6102502
Study Section
Project Start
1999-04-01
Project End
2000-01-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
8
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Type
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
Youn, Ui Joung; Sripisut, Tawanun; Park, Eun-Jung et al. (2015) Determination of the absolute configuration of chaetoviridins and other bioactive azaphilones from the endophytic fungus Chaetomium globosum. Bioorg Med Chem Lett 25:4719-23
Chai, Xingyun; Youn, Ui Joung; Sun, Dianqing et al. (2014) Herbicidin congeners, undecose nucleosides from an organic extract of Streptomyces sp. L-9-10. J Nat Prod 77:227-33
Ihsan-ul-Haq; Mirza, Bushra; Kondratyuk, Tamara P et al. (2013) Preliminary evaluation for cancer chemopreventive and cytotoxic potential of naturally growing ethnobotanically selected plants of Pakistan. Pharm Biol 51:316-28
Ihsan-ul-Haq; Youn, Ui Joung; Chai, Xingyun et al. (2013) Biologically active withanolides from Withania coagulans. J Nat Prod 76:22-8
St John, Sarah E; Jensen, Katherine C; Kang, Soosung et al. (2013) Design, synthesis, biological and structural evaluation of functionalized resveratrol analogues as inhibitors of quinone reductase 2. Bioorg Med Chem 21:6022-37
Conda-Sheridan, Martin; Park, Eun-Jung; Beck, Daniel E et al. (2013) Design, synthesis, and biological evaluation of indenoisoquinoline rexinoids with chemopreventive potential. J Med Chem 56:2581-605
Park, Eun-Jung; Pezzuto, John M; Jang, Kyoung Hwa et al. (2012) Suppression of nitric oxide synthase by thienodolin in lipopolysaccharide-stimulated RAW 264.7 murine macrophage cells. Nat Prod Commun 7:789-94
Kondratyuk, Tamara P; Park, Eun-Jung; Yu, Rui et al. (2012) Novel marine phenazines as potential cancer chemopreventive and anti-inflammatory agents. Mar Drugs 10:451-64
Reddy, P V Narasimha; Jensen, Katherine C; Mesecar, Andrew D et al. (2012) Design, synthesis, and biological evaluation of potent quinoline and pyrroloquinoline ammosamide analogues as inhibitors of quinone reductase 2. J Med Chem 55:367-77
Mayhoub, Abdelrahman S; Marler, Laura; Kondratyuk, Tamara P et al. (2012) Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets. Bioorg Med Chem 20:510-20

Showing the most recent 10 out of 200 publications