The development of S-trityl L-cysteine based inhibitors of Eg5 as anticancer chemotherapeutics.

Good, James Arthur Dudley (2012) The development of S-trityl L-cysteine based inhibitors of Eg5 as anticancer chemotherapeutics. PhD thesis, University of Glasgow.

Full text available as:
[img]
Preview
PDF
Download (5MB) | Preview

Abstract

The kinesins are a class of microtubule based motor proteins which have extensive involvement in the orchestration of the mechanics of mitosis. The most studied of these is the kinesin spindle protein Eg5, which is crucially involved in the establishment of the bipolar spindle in prometaphase. Inhibition of this protein results in monopolar mitotic spindles and subsequently mitotic arrest, which can lead to apoptosis in cancer cell lines. S-Trityl L-cysteine (STLC) was identified as a selective small molecule inhibitor of Eg5 which binds to an allosteric pocket formed by the loop L5 of Eg5. In this thesis, I present the structure based design and development and optimisation of the STLC scaffold to produce orally available potential drug candidates. This was accomplished by optimising the lipophilic binding interactions of the trityl group, and investigating a number of hydrophilic optimisation vectors from the same moiety. The L-cysteine tail was optimised to improve the potency and metabolic stability, and fluorination as a means of altering the lead candidates’ drug like properties investigated. In order to improve efficacy in multi-drug resistant (MDR) cell lines overexpressing the P-glycoprotein transporter, I also investigated a number of strategies related modifying to the terminal α-carboxylic acid. The optimised candidates display growth inhibition ≤ 50 nM across multiple tumour cell lines, and possess favourable metabolic, toxicological and physicochemical attributes. Evaluation in vivo confirms their anti tumour activity, and finally strategies for the further progression and development of the lead series in targeting haematological malignancies are discussed.

Item Type: Thesis (PhD)
Qualification Level: Doctoral
Keywords: cancer, chemotherapy, anti-mitotic, kinesins, Eg5, S-trityl L-cysteine, drug discovery, medicinal chemistry
Subjects: Q Science > QD Chemistry
R Medicine > RM Therapeutics. Pharmacology
Colleges/Schools: College of Medical Veterinary and Life Sciences > Institute of Cancer Sciences
Funder's Name: UNSPECIFIED
Supervisor's Name: Kozielski, Prof. Frank
Date of Award: 2012
Depositing User: Dr James Arthur Dudley Good
Unique ID: glathesis:2012-3748
Copyright: Copyright of this thesis is held by the author.
Date Deposited: 13 Nov 2012
Last Modified: 14 Dec 2012 13:33
URI: http://theses.gla.ac.uk/id/eprint/3748

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year