The goal of this program is to develop new strategies for the synthesis of bioactive molecules in the prenylated indole alkaloid family. The complex natural products that we construct, and their unique derivatives which are only accessible using our strategies, will provide small molecules that will serve as a starting point to identify anticancer compounds that function via novel mechanisms. Our synthetic studies should also lead to insights into the biosynthesis of a subset of the prenylated indole alkaloids for which the biogenesis is not established. Specifically, we intend to develop strategies to synthesize different structural classes of prenylated indole alkaloids including the citrinalins, cyclopiamine, citrinadins and the stephacidins.

Public Health Relevance

Finding new and more efficient ways to synthesize complex small molecules derived from natural products is an important pursuit that may lead to improvements in human health, especially the identification of new anticancer compounds. Our goals are to develop new strategies to efficiently construct complex natural products in the prenylated indole alkaloid family and their associated derivatives. These small molecules will positively address the treatment of cancer.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM086374-05A1
Application #
8911726
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Lees, Robert G
Project Start
2009-09-30
Project End
2019-01-31
Budget Start
2015-05-01
Budget End
2016-01-31
Support Year
5
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
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