HUM-MOLGEN events: Diversity-Oriented Synthesis and Natural Product Chemistry

HUM-MOLGEN -> Events -> Meetings and Conferences

Diversity-Oriented Synthesis and Natural Product Chemistry

September 12, 2003

Cambridge Healthtech Institute, Boston Park Plaza
October 9-10, 2003

Through diversity-oriented synthesis chemists are achieving more structural complexity than in the early days of combinatorial chemistry, tackling compounds with multiple stereocenters and complex, natural, product-like libraries. Preparation of structurally complex and diverse compounds results in a broader population of chemical space and facilitates effective probing of biological space. Structural complexity is very significant because many of the small molecules known to disrupt protein-protein interactions are complex, natural products or natural, product-like compounds, and have potential for therapeutic development. Attend this event to hear the latest developments in diversity-oriented synthesis and its impact on drug development.

Who Should Attend
Vice Presidents, Directors, Research Scientists in Combinatorial Chemistry, Natural Product Chemistry, Discovery Chemistry and Medicinal Chemistry

Organized by:

Cambridge Healthtech Institute

Deadline for Abstracts:

Registration:

To register visit: www.healthtech.com/2003/dos/reg.asp or call 617-630-1300.

E-mail:

chi@healthtech.com

Posted by:

Lisa Cardinale

Host:

wks140.healthtech.com