Christopher Hulme, PhD

Professor, Pharmacology and Toxicology
Director, Medicinal Chemistry
BIO5 Drug Discovery

Dr. Christopher Hulme is director of medicinal chemistry at the BIO5 Translational Drug Discovery Center and is focused on small molecule drug design and developing enabling chemical methodologies to expedite the drug discovery process. The development of small molecule inhibitors of kinases is of particular interest. Projects are highly collaborative in nature, and students are exposed to the full array of design hurdles involved in progressing molecules along the value chain to clinical evaluation.

1. Therapies for Alzheimer’s and Neurodegenerative Diseases
With 24.3 million people affected in 2005 and an estimated rise to 45 million in 2020, dementia is currently a leading unmet medical need and a costly burden on public health. Seventy percent of these cases have been attributed to Alzheimer’s disease (AD), a neurodegenerative pathology whose most evident symptom is a progressive decline in cognitive functions. Studies in the group focus on providing a significant mechanistic alternative to common approaches that solely focus on small molecule design toward APP-cleavage inhibition. In particular, ongoing efforts are aimed at the design of structurally novel small molecule inhibitors of the dual-specificity tyrosine phosphorylation–regulated kinase 1A (DYRK1A) and their evaluation of in vivo activity and measurement of in vivo tau phosphorylation and neurofibrillary tangles pathology in 3X-TgAD mouse models of AD. Moreover, DYRK1A has also been suggested to affect other cellular pathways that may be involved in mental impairment and neurodegenerative dementia.

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Studies are being conducted with a long-term collaborator (Dr. Travis Dunckley) at Translational Genomics (TGen). Inhibition of DYRK1A functioning should theoretically mitigate multiple processes underlying the progression of neurodegeneration, particularly in the AD-related therapeutic area, for which key DYRK1A substrates include: (1) tau protein, (2) amyloid precursor protein, and (3) presenilin 1 (the catalytic subunit of γ-secretase), all pointing to clear mechanisms through which elevated DYRK1A activity may be promoting AD progression. Several other AD-related kinases are targets of current interest in the group (Smith B, Medda F, Gokhale V, Dunckley T, Hulme C [2012] Recent Advances in the Design, Synthesis, and Biological Evaluation of Selective DYRK1A Inhibitors: A New Avenue for a Disease Modifying Treatment of Alzheimer’s. ACS Chem. Neurosci., DOI: 10.1021/cn300094k).

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2. Therapeutics Modulating Prostaglandin E2Production
Prostaglandin E2 (PGE2) is well known to play a pivotal role in processes associated with inflammation, pain, and pyresis and is over-expressed in various tumors where chronic inflammation has been linked to the growth of various cancerous tissues. Indeed, PGE2 has been identified as the major prostaglandin associated with the progression of various tumor malignancies, including that of the colon, lung, and breast. An ongoing project within the group is the development of novel small molecules that mitigate PGE2 production and display antitumor growth properties in vivo. Several novel series of small molecules have been developed and are under further investigation (Smith B, Chang HH, Medda F, Gokhale V, Dietrich J, Davis A, Meuillet EJ, Hulme C [2012] Synthesis and biological activity of 2-aminothiazoles as novel inhibitors of PGE2 production in cells. Bioorg. Med. Chem. Lett., 22:3567–3570).

3. Enabling Chemical Methodologies
a. Applications of Multi-Component Reactions

The group also has a long-standing interest in the development of new reactions that produce biologically relevant molecules in an efficient manner. Indeed, front-loading screening collections with molecules possessing high “iterative efficiency potential” is critical for expediting the drug discovery process. Compounds derived from multi-component reactions (MCRs) demonstrate such potential, and thus their discovery and applications are of utmost importance. Closely linked with the Molecular Libraries Small Molecule Repository, the group seeks to develop an operationally friendly chemistry that delivers products of high molecular diversity that ultimately enable library production and deposition of compounds in both national and local screening collections. A one-pot five-step transformation developed in the group is depicted (Xu Z, De Moliner F, Cappelli A, Hulme C [2012] Ugi/Aldol Sequence: Expeditious Entry to Several Families of Densely Substituted Nitrogen Heterocycles. Angewandte Chem., Int. Ed., 51:8037–8040).

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Recent discoveries in the group have facilitated a new project toward the expeditious syntheses and application of novel dendrimer families, repetitively branched molecules that show high promise in drug delivery, gene delivery, and sensor technologies.

b. New Hypervalent Iodine Methodology and Applications
Novel hypervalent iodine–mediated C-H activation methodologies and their application for the preparation of novel peptidomimetics are an active area of research.

c. Organoselenium Chemistry
A recent discovery of a new selenium dioxide–mediated oxidative amidation is driving new studies in molecular diversity generation.

Education: 

BS, Hertford College, University of Oxford, 1989
PhD, Hertford College, University of Oxford, 1992
Postdoctoral Fellow, University of Texas, Austin, 1992–1994