Synthesis and evaluation of quinoline-5,8-diones and isoquinoline-5,8-diones as anticancer agents

Show simple item record

dc.contributor.advisor McCarthy, Florence en
dc.contributor.author Kruschel, Ryan D.
dc.date.accessioned 2021-01-15T09:59:04Z
dc.date.available 2021-01-15T09:59:04Z
dc.date.issued 2020-07
dc.date.submitted 2020-07
dc.identifier.citation Kruschel, R. D. 2020. Synthesis and evaluation of quinoline-5,8-diones and isoquinoline-5,8-diones as anticancer agents. PhD Thesis, University College Cork. en
dc.identifier.endpage 457 en
dc.identifier.uri http://hdl.handle.net/10468/10919
dc.description.abstract This thesis outlines the design and synthesis of novel chemical routes towards a nascent class of functionalised quinoline-5,8-diones and isoquinoline-5,8-diones. The structured approach adopted is predicted to lead to advancements in the two frameworks, expanding the structural diversity of both the quinoline-5,8-diones and isoquinoline-5,8-diones families with bioactivity evaluation. Chapters 4, 5, 6, 7 and 8 are focused on the development and biological screening of the quinoline-5,8-dione library; Chapters 9 and 10 construct and evaluate the isoquinoline-5,8-dione library. Initial route development furnished versatile quinoline-5,8-dione and isoquinoline-5,8-dione frameworks in high yields employing robust methodologies. Synthetic exploration into the regioselective addition of carbon, nitrogen, and oxygen to the quinone moiety was investigated yielding 85 novel analogues. The use of directing group strategies, Lewis acid coordination and blocking groups provided access to regioselective reactions. Antimicrobial screening was undertaken in collaboration with the Community for Open Antimicrobial Drug Discovery (CO-ADD). The quinoline-5,8-dione library exhibited potent antibacterial and antifungal MIC values, outperforming known antimicrobial agents’ vancomycin and fluconazole, respectively. Preliminary in vitro toxicology studies revealed that all analogues are not haemolytic, and multiple analogues are not cytotoxic to the human kidney cell line HEK293. Anticancer screening was undertaken in in collaboration with the National Cancer Institute (NCI) in Maryland US. Although the quinoline-5,8-dione library were not effective anticancer agents, the isoquinoline-5,8-dione family possessed nanomolar anticancer GI50 values across multiple human tumour cell lines. Multidrug resistant ovarian cancer cell lines NCI/ADR-RES and IGROV 1 were responsive to the series in the nanomolar range. Lead isoquinoline-5,8-dione N-oxide 10.21 exhibits a mean GI50 of 0.21 μM across 60 cancer cell lines. Extended mechanistic work incorporated molecular modelling, electrochemical assays and COMPARE analysis to rationalise the potent in vitro bioactivity and identities future biological targets. en
dc.format.mimetype application/pdf en
dc.language.iso en en
dc.publisher University College Cork en
dc.rights © 2020, Ryan D. Kruschel. en
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/ en
dc.subject Anticancer en
dc.subject Antimicrobial en
dc.subject Chemistry en
dc.subject Quinone en
dc.subject Cytotoxicity en
dc.subject Bioactivity en
dc.subject Organic chemistry en
dc.subject Medicinal chemistry en
dc.subject Novel compound en
dc.subject Drug design en
dc.subject Drug discovery en
dc.title Synthesis and evaluation of quinoline-5,8-diones and isoquinoline-5,8-diones as anticancer agents en
dc.type Doctoral thesis en
dc.type.qualificationlevel Doctoral en
dc.type.qualificationname PhD - Doctor of Philosophy en
dc.internal.availability Full text not available en
dc.description.version Accepted Version en
dc.contributor.funder Irish Research Council en
dc.description.status Not peer reviewed en
dc.internal.school Chemistry en
dc.check.chapterOfThesis Full thesis will need redaction en
dc.internal.conferring Spring 2021 en
dc.internal.ricu Analytical and Biological Chemistry Research Facility en
dc.availability.bitstream restricted


Files in this item

This item appears in the following Collection(s)

Show simple item record

© 2020, Ryan D. Kruschel. Except where otherwise noted, this item's license is described as © 2020, Ryan D. Kruschel.
This website uses cookies. By using this website, you consent to the use of cookies in accordance with the UCC Privacy and Cookies Statement. For more information about cookies and how you can disable them, visit our Privacy and Cookies statement