. Drug resistance can be a major problem in cancer therapy. The effective treatment of resistant cancer cells can be further complicated by deficiencies that inhibit the body?s own anticancer immune response. Naturally occurring chromanones can inspire the development of drugs to better target cancer resistant cancers as they can directly destroy cancer cells while simultaneously boosting the body?s own immune response. Despite their promising activity, there is a critical barrier obstructing biological studies of chromanone-based bioactive molecules. Specifically, there are limited synthetic strategies available to access these desirable targets for biological testing. As a means to overcome this barrier, the long-term goal of our research programs is to develop chemical technologies to synthesize chromanone-based therapeutic agents for biological studies. Themes directing our investigations include: (i) developing catalytic tools to enable unique, enantioselective heterocycle synthesis; (ii) streamlining access to heterocyclic bioactive targets; and (iii) exploring the biological activities of naturally-occurring chromanones and their synthetic derivatives in the context of drug discovery. This research plan is based on the central hypothesis that silanediol-catalysis is a unique chemical technology enabling access to chromanones, and related structures, that are otherwise difficult to access. The rationale for the proposed research is that the successful development of modular and efficient routes toward chromanone-based natural products, and their derivatives, will enable biological studies of these promising medicinal agents. This approach is innovative because it uses silanediol anion-binding technology to affect pharmaceutically-attractive methodologies that are inaccessible with conventional catalysts. This contribution will be significant as it will support the development of new therapeutic agents able to fight resistant cell cancer lines through unique, dual, synergistic modes of action.

Public Health Relevance

. The proposed research is relevant to public health because the new methods for drug discovery will ultimately enable access innovative, life-altering active pharmaceutical ingredients. Thus, the proposed research is relevant to the part of NIH?s mission that pertains to fostering fundamental creative discoveries and their applications as a basis for ultimately protecting and improving health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
5R35GM124804-04
Application #
9972949
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Yang, Jiong
Project Start
2017-08-15
Project End
2022-07-31
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
4
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Worcester Polytechnic Institute
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041508581
City
Worcester
State
MA
Country
United States
Zip Code
01609
Guan, Yong; Attard, Jonathan W; Visco, Michael D et al. (2018) Enantioselective Catalyst Systems from Copper(II) Triflate and BINOL-Silanediol. Chemistry 24:7123-7127