MOTIVATING MEDICAL SCIENCE STUDENTS TO ENGAGE WITH CHEMISTRY CONCEPTS

Cognitive reasoning in chemistry in admissions tests, is a significant hurdle for many medical science students aiming for graduate medicine, in particular for non-chemistry majors (Shulman, 2013). We developed an interdisciplinary subject focussed on building students’ confidence in physical sciences coupled with medical ethics for a new undergraduate premedical program. Organic chemistry in particular, can be a turning point for many students (Barr, Matsui, & Gonzalez, 2010). Thus, we aimed to increase engagement of first year premedical students with organic chemistry concepts by contextualising teaching and learning through highlighting historical medical errors and future ethical challenges. Connections between medicinal plants and current drugs were explored including aspirin derived from willow bark and anaesthetics from Indian arrow poisons, alongside concepts of benefit sharing of traditional knowledges. Spectroscopy was taught alongside medical imaging techniques and stereochemistry in the context of drug stereopurity and the thalidomide tragedy. Substituent directing effects were highlighted by early antibiotic development from azobenzene dyes and SN2 nucleophilic substitution illustrated by using alkylating anti-cancer drugs (e.g. cyclophosphamide), exploring from chemical warfare agents to chemotherapy. The outcome of introducing this medical-aligned chemistry subject for premedical students will be presented including the impact on learning (Mansfield, Peoples, Parker-Newlyn, & Skropeta, 2020) and overall student performance and satisfaction. REFERENCES Barr, D. A., Matsui, J., Wanat, S. F., & Gonzalez, M. E. (2010). Chemistry courses as the turning point for premedical students. Advances in Health Sciences Education, 15 (1), 45-54. Mansfield, K. J., Peoples, G. E., Parker-Newlyn, L. & Skropeta, D. (2020). Approaches to Learning: Does Medical School Attract Students with Motivation to go Deeper, Education Sciences, 10, 302. Shulman, J. I., (2013). Chemistry in the Premedical Curriculum: Considering the Options. Journal of Chemical Education, 90 (7), 813-815

c-AMP dependent protein kinase A inhibitory activity of six algal extracts from South Eastern Australia and their fatty acid composition

c-AMP dependent protein kinase (protein kinase A, PKA) is an important enzyme involved in the regulation of an increasing number of physiological processes including immune function, cardiovascular disease, memory disorders and cancer. The objective of this study was to evaluate the PKA inhibitory activity of a range of algal extracts, along with their fatty acid composition. Six algal species were investigated including two Chlorophyta (Codium dimorphum and Ulva lactuca), two Phaeophyta (Phyllospora comosa and Sargassum sp.) and two Rhodophyta (Prionitis linearis and Corallina vancouveriensis), with the order of PKA inhibitory activity of their extracts identified as follows: brown seaweeds \u3e red seaweeds \u3e green seaweeds with the brown alga Sargassum sp. exhibiting the highest PKA inhibitory activity (84% at 100 microg/mL). GC/MS analysis identified a total of 18 fatty acids in the six algal extracts accounting for 72-87% of each extract, with hexadecanoic acid and 9,12-octadecadienoic acid as the dominant components. The most active extract (Sargassum sp.) also contained the highest percentage of the saturated C14:0 fatty acid (12.8% of the total extract), which is a known to inhibit PKA. These results provide the first description of the PKA inhibitory activity of marine algae along with the first description of the fatty acid composition of these six algal species from South Eastern Australian waters. Importantly, this study reveals that abundant and readily available marine algae are a new and relatively unexplored source of PKA inhibitory compounds

Design, synthesis and evaluation of carbamate-linked uridyl-based inhibitors of human ST6Gal I

© 2020 Elsevier Ltd Sialic acid at the terminus of cell surface glycoconjugates is a critical element in cell-cell recognition, receptor binding and immune responses. Sialyltransferases (ST), the enzymes responsible for the biosynthesis of sialylated glycans are highly upregulated in cancer and the resulting hypersialylation of the tumour cell surface correlates strongly with tumour growth, metastasis and drug resistance. Inhibitors of human STs, in particular human ST6Gal I, are thus expected to be valuable chemical tools for the discovery of novel anticancer drugs. Herein, we report on the computationally-guided design and development of uridine-based inhibitors that replace the charged phosphodiester linker of known ST inhibitors with a neutral carbamate to improve pharmacokinetic properties and synthetic accessibility. A series of 24 carbamate-linked uridyl-based compounds were synthesised by coupling aryl and hetaryl α-hydroxyphosphonates with a 5′-amino-5′-deoxyuridine fragment. The inhibitory activities of the newly synthesised compounds against recombinant human ST6Gal I were determined using a luminescent microplate assay, and five promising inhibitors with Ki’s ranging from 1 to 20 µM were identified. These results show that carbamate-linked uridyl-based compounds are a potential new class of readily accessible, non-cytotoxic ST inhibitors to be further explored

Solid-state and solution-phase conformations of pseudoproline-containing dipeptides

The conformations of 14 threonine-derived pseudoproline-containing dipeptides (including four d-allo-Thr derivatives) have been investigated by NMR. In solution, the major conformer observed for all dipeptides is that in which the amide bond between the pseudoproline and the preceding amino acid is cis. For dipeptides in which the N-terminus is protected, the ratio of cis- to trans-conformers does not depend significantly on the side chain of the N-terminal amino acid, or the stereochemistry of the Thr residue. However, for dipeptides bearing a free N-terminus, there are significant differences in the ratios of cis- to trans-conformers depending on the side chain present. Three dipeptides were crystallized and their X-ray structures determined. In two cases, (benzyloxycarbonyl (Cbz)-Val-Thr(ΨMe,Mepro)-OMe and Cbz-Val-Thr(ΨMe,Mepro)-OH), the dipeptides adopt a trans-conformation in the solid state, in contrast to the structures observed in solution. In the third case, (9-fluorenylmethoxycarbonyl (Fmoc)-Val-d-allo-Thr(ΨMe,Mepro)-OH), a cis-amide geometry is observed. These structural differences are attributed to crystal-packing interactions

Kinase Inhibitors from Marine Sponges

Protein kinases play a critical role in cell regulation and their deregulation is a contributing factor in an increasing list of diseases including cancer. Marine sponges have yielded over 70 novel compounds to date that exhibit significant inhibitory activity towards a range of protein kinases. These compounds, which belong to diverse structural classes, are reviewed herein, and ordered based upon the kinase that they inhibit. Relevant synthetic studies on the marine natural product kinase inhibitors have also been included

Structures, Biological Activities and Phylogenetic Relationships of Terpenoids from Marine Ciliates of the Genus Euplotes

In the last two decades, large scale axenic cell cultures of the marine species comprising the family Euplotidae have resulted in the isolation of several new classes of terpenoids with unprecedented carbon skeletons including the (i) euplotins, highly strained acetylated sesquiterpene hemiacetals; (ii) raikovenals, built on the bicyclo[3.2.0]heptane ring system; (iii) rarisetenolides and focardins containing an octahydroazulene moiety; and (iv) vannusals, with a unique C30 backbone. Their complex structures have been elucidated through a combination of nuclear magnetic resonance spectroscopy, mass spectrometry, molecular mechanics and quantum chemical calculations. Despite the limited number of biosynthetic experiments having been performed, the large diversity of ciliate terpenoids has facilitated the proposal of biosynthetic pathways whereby they are produced from classical linear precursors. Herein, the similarities and differences emerging from the comparison of the classical chemotaxonomy approach based on secondary metabolites, with species phylogenesis based on genetic descriptors (SSU-rDNA), will be discussed. Results on the interesting ecological and biological properties of ciliate terpenoids are also reported

Deep-sea Natural Products

This review covers the 390 novel marine natural products described to date from deep-water (\u3e50 m)marine fauna, with details on the source organism, its depth and country of origin, along with anyreported biological activity of the metabolites. Relevant synthetic studies on the deep-sea naturalproducts have also been included