{"id":1650,"date":"2017-04-04T14:46:33","date_gmt":"2017-04-04T14:46:33","guid":{"rendered":"http:\/\/ukqsar.org\/?p=1650"},"modified":"2017-04-08T14:59:28","modified_gmt":"2017-04-08T14:59:28","slug":"spring-2017-uk-qsar-newsletter","status":"publish","type":"post","link":"https:\/\/ukqsar.org\/index.php\/2017\/04\/04\/spring-2017-uk-qsar-newsletter\/","title":{"rendered":"Spring 2017 UK-QSAR Newsletter"},"content":{"rendered":"

Archived Newsletters<\/span><\/u><\/a><\/p>\n\n\n\n\n\n
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UK-QSAR Spring 2017<\/strong><\/h1>\n<\/td>\n<\/tr>\n

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The UK-QSAR and ChemoInformatics Group<\/strong><\/h3>\n<\/td>\n<\/tr>\n

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Welcome to the Spring 2017 UK-QSAR Newsletter!<\/strong><\/h3>\n

*Please note that registration for our next meeting on 26th April will close on 22nd April!!*<\/strong><\/span><\/p>\n

The spring UKQSAR meeting<\/span><\/u><\/a> on 26th April will be held at Syngenta, Jealott’s Hill<\/span><\/u><\/a>.\u00a0 Registration closes on 22 April so do book your place if you haven\u2019t already for what looks like a fascinating and wide-ranging array of talks and posters.<\/p>\n

Our Autumn 2017 meeting will be held at at the MIB in Manchester on 29th September, hosted by C4X, and will focus around the there “Where simulation meets experiment”.\u00a0\u00a0 And if you can think as far as a year ahead you can start looking forward to our planned joint MGMS\/UKQSAR Group meeting<\/span><\/u><\/a> in Cardiff, on 11th-12th April 2018 (provisional dates).<\/p>\n

UK-QSAR meetings are often oversubscribed so do register asap to avoid disappointment.\u00a0 If you have registered already but can no longer attend PLEASE LET US KNOW<\/u><\/span><\/a> so we can release your place.\u00a0 Details of the talks and some suggested pre-meeting reading material<\/span><\/u><\/a> is available below should you wish to explore some of the upcoming topics in more detail ahead of the meeting.<\/p>\n

You’ll also find the regular articles on Jobs<\/span><\/u><\/a> and Upcoming Meetings<\/span><\/u><\/a>.<\/p>\n

As ever, please send any feedback or suggestions you have for future newsletters to Susan Boyd at\u00a0 newsletter@ukqsar.org.<\/span><\/u><\/a><\/td>\n<\/tr>\n

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Spring 2017 Meeting
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The UKQSAR spring meeting will be returning to Syngenta, Jealott\u2019s Hill on 26 April. As ever, we\u2019re aiming to offer a series of high quality talks around a range of topics, in this case formed around a couple of broad themes \u2013 understanding the lead optimisation process and characterising the shape of ligands and binding sites.<\/p>\n

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The Syngenta site at Jealott’s Hill<\/figcaption><\/figure>\n

The lead optimisation process is a crucial step in the drug discovery effort as it is the route by which a large number of molecules are turned into \u201cthe one\u201d \u2013 the compound that goes forward to expensive trials with the hope that it will eventually become a profitable product. The fate of this compound is baked into its structure, ranging from its efficacy to its toxicological profile, so it behoves us to make sure that our process really does lead us to the right \u201cone\u201d.<\/p>\n

Within our community we often focus on the detail of how properties are predicted \u2013 a better model of solubility, an improved docking algorithm, a faster clustering method \u2013 rather than asking how these improvements might impact the overall drug discovery process. For example, is it better to have a good model of a less relevant parameter or a poor model of a more relevant one? Some of these issues will be addressed in the morning session with a series of talks that focus on how the choices we make during the lead optimisation process shape its final outcome. This ranges from where our initial leads come from, through the effect of cognitive bias during the design cycle through to the impact of physical properties on chances of success of candidate molecules.<\/p>\n

Molecular recognition is primarily driven by the complementary shapes of a ligand and its binding site. Shape offers us a different view on compounds, potentially allowing us to move more easily away from problematic chemotypes while retaining the ligands essential interaction with its target.\u00a0 The afternoon session will be given over to considering our molecules in terms other than their flat structure, with talks about methods for accurately identifying potential ligand binding sites on proteins, visualising these pockets as interpretable maps to aid drug design and grouping molecules effectively by shape fingerprint.<\/p>\n

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About Jealott\u2019s Hill<\/h4>\n

Jealott\u2019s Hill is a key site in Syngenta\u2019s global Research and Development network. With a long tradition of innovation and employing over 800 people, it is the company\u2019s largest site for new agrochemical R&D and product support.<\/p>\n

Key activities at Jealott\u2019s Hill include research into discovery of new active ingredients, new formulation technologies, product safety, technical support of our product range and seeds research. The site houses a number of centres of scientific excellence, both chemical and biological, that support our worldwide R&D activities.<\/td>\n<\/tr>\n

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Joint MGMS\/UKQSAR Meeting, Spring 2018, Cardiff
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Steve Maginn, <\/em><\/strong>Chemical Computing Group Inc<\/em><\/h4>\n

The UK-QSAR group is working with the Molecular Graphics and Modelling Society (MGMS) to organise a joint meeting in Spring 2018 at the University of Cardiff. The theme of the meeting will be \u201cStructure-Activity Relationships\u201d, a broad area that appeals to members of both organisations. The meeting will be a two-day event, similar in format to the joint UK-QSAR PhysChem Forum meeting held in 2016; talks will commence after lunch on the first day and finish at the end of the afternoon on the second day. Registration will be free of charge, as is normal at UK-QSAR meetings, but there will be a conference dinner on the evening of the first day which will be charged for and therefore is optional to attend.<\/p>\n

A programme committee made up of members from both the UK-QSAR and MGMS committees is currently organising the schedule of speakers. Keep a close eye on the UK-QSAR and MGMS websites (www.ukqsar.org<\/span><\/u><\/a> and www.mgms.org<\/span><\/u><\/a>) for further information on the programme, later this year.<\/p>\n

So, please put Wednesday and Thursday, 11th<\/sup> and 12th<\/sup> April 2018 into your diaries \u2013 and mark the venue as the University of Cardiff, in the capital of Wales, a city which has enjoyed a great renaissance in recent years.<\/p>\n

We\u2019re looking forward to seeing you in Cardiff! \/ Rydym yn edrych ymlaen at eich cyfarfod yng Caerdydd!<\/p>\n

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Talk Titles & Suggested Pre-Reading List for the Spring 2017 Meeting<\/strong><\/h3>\n

Innovation in Small-Molecule-Druggable Chemical Space: Where are the Original Modulators of New Targets and New Bioactive Molecular Frameworks Published? A Comparison between Patents and Scientific Literature (Stephanie Ashenden)<\/strong><\/p>\n

Damn the compass, full steam ahead: Decision theory and drug discovery (Jack Scannell)<\/strong><\/p>\n

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  • JW Scannell and J Bosley (2016), \u201cWhen Quality Beats Quantity: Decision Theory, Drug Discovery, and the Reproducibility Crisis\u201d, PLoS ONE, 11(2)<\/li>\n<\/ul>\n

    Overcoming Psychological Barriers to Good Decision-Making in Drug Discovery (Matt Segall)<\/strong><\/p>\n

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    • Chadwick A, Segall MD. Overcoming psychological barriers to good discovery decisions. Drug Discov. Today (2010) 15 (13\/14), pp. 561-569<\/li>\n
    • Segall MD, Chadwick, A. Making Priors a Priority. J. Comp.-Aided Mol. Design (2010) 24(12) pp. 957-960<\/li>\n
    • Segall MD. Multi-Parameter Optimization: Identifying high quality compounds with a balance of properties. Curr. Pharm. Des. (2012) 18(9) pp. 1292-1310<\/li>\n
    • Segall MD, Champness EJ. The challenges of making decisions using uncertain data. J. Comp.-Aided Mol. Design (2015) 29(9), pp. 809-816<\/li>\n<\/ul>\n

      Impact of Physicochemical Properties on Oral Drug Dose & Hepatotoxicity (Paul Leeson)<\/strong><\/p>\n

      Rational Design of Multi-target ligands at A1R, A2AR and PDE10A with Therapeutic Potential for Neurodegenerative Diseases (Leen Kalash)<\/strong><\/p>\n

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      • Latini, S.; Pedata, F. Adenosine in the Central Nervous System: Release Mechanisms and Extracellular Concentrations. J. Neurochem. 2001, 79 (3), 463\u2013484.<\/li>\n
      • Shook, B. C.; Rassnick, S.; Wallace, N.; Crooke, J.; Ault, M.; Chakravarty, D.; Barbay, J. K.; Wang, A.; Powell, M. T.; Leonard, K.; Alford, V.; Scannevin, R. H.; Carroll, K.; Lampron, L.; Westover, L.; Lim, H.; Russell, R.; Branum, S.; Wells, K. M.; Damon, S.; Youells, S.; Li, X.; Beauchamp, D. a; Rhodes, K.; Jackson, P. F. Design and Characterization of Optimized Adenosine A\u2082A\/A\u2081 Receptor Antagonists for the Treatment of Parkinson\u2019s Disease. J. Med. Chem. 2012, 55 (3), 1402\u20131417.<\/li>\n
      • Schmidt, C. J.; Chapin, D. S.; Cianfrogna, J.; Corman, M. L.; Hajos, M.; Harms, J. F.; Hoffman, W. E.; Lebel, L. a; McCarthy, S. a; Nelson, F. R.; Proulx-LaFrance, C.; Majchrzak, M. J.; Ramirez, a D.; Schmidt, K.; Seymour, P. a; Siuciak, J. a; Tingley, F. D.; Williams, R. D.; Verhoest, P. R.; Menniti, F. S. Preclinical Characterization of Selective Phosphodiesterase 10A Inhibitors: A New Therapeutic Approach to the Treatment of Schizophrenia. J. Pharmacol. Exp. Ther. 2008, 325 (2), 681\u2013690.<\/li>\n
      • Giamp\u00e0, C.; Patassini, S.; Borreca, A.; Laurenti, D.; Marullo, F.; Bernardi, G.; Menniti, F. S.; Fusco, F. R. Phosphodiesterase 10 Inhibition Reduces Striatal Excitotoxicity in the Quinolinic Acid Model of Huntington\u2019s Disease. Neurobiol. Dis. 2009, 34 (3), 450\u2013456.<\/li>\n
      • Niccolini, F.; Foltynie, T.; Reis Marques, T.; Muhlert, N.; Tziortzi, A. C.; Searle, G. E.; Natesan, S.; Kapur, S.; Rabiner, E. a.; Gunn, R. N.; Piccini, P.; Politis, M. Loss of Phosphodiesterase 10A Expression Is Associated with Progression and Severity in Parkinson\u2019s Disease. Brain 2015, 138, 3003\u20133015.<\/li>\n<\/ul>\n

        Mapping the 3D Structures of Small Molecule Binding Sites (Josh Meyers)<\/strong><\/p>\n

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        • P\u00e9rot, S.; Sperandio, O.; Miteva, M. A.; Camproux, A.-C.; Villoutreix, B. O. Druggable Pockets and Binding Site Centric Chemical Space: a Paradigm Shift in Drug Discovery. Drug Discov. Today<\/em> 2010<\/strong>, 15 (15-16), 656\u2013667.<\/li>\n
        • Meyers, J.; Brown, N.; Blagg, J. Mapping the 3D Structures of Small Molecule Binding Sites. Cheminf.<\/em> 2016<\/strong>, 8 (70).<\/li>\n<\/ul>\n

          Fragment Hotspot Maps: A CSD-derived Method for Hotspot identification (Chris Radoux)<\/strong><\/p>\n

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          • J. Radoux, T. S. G. Olsson, W. R. Pitt, C. R. Groom, T. L. Blundell, J Med Chem,<\/em> 2016, 59, <\/strong>4314\u20134325.<\/li>\n<\/ul>\n

            Optimisation of shape fingerprints for protein-ligand systems (Joanna Zarnecka)<\/strong><\/p>\n

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            • A. Haigh, B.T. Pickup, J. A. Grant, A. Nicholls, J. Chem. Inf. Model. (2005) 45, 673\u2013684.<\/li>\n<\/ul>\n

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Jobs<\/strong><\/h3>\n

Chemogenetics Analyst<\/a>, EMBL-EBI Hinxton, Cambridgeshire, UK (2 year post, closing date 23rd April<\/em>)<\/p>\n

Team Leader (CADD)<\/span><\/u><\/a>, Charles River Laboratories, Saffron Walden, Essex<\/p>\n

Application Scientist<\/span><\/u><\/a>, Chemical Computing Group Inc, Cambridge (UK) or Cologne (Germany)<\/p>\n

Senior Scientific Consultant<\/span><\/u><\/a>, Cresset Group, Litlington, Cambridge, UK<\/p>\n

Product Manager (API)<\/span><\/u><\/a>, RSC, Cambridge, UK<\/p>\n

Chem- and Bioinformatics Scientists, Software Engineers, Machine Learning Researchers<\/span><\/u><\/a>, Benevolent.ai, London, UK<\/p>\n

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Upcoming Meetings<\/strong><\/h3>\n

The following meetings may be of interest to our readers:<\/p>\n

CCG UGM & Conference (Europe)<\/span><\/u><\/a>, 16-19 May 2017, Copenhagen<\/p>\n

Symposium on Streamlining Drug Discovery<\/span><\/u><\/a> (Optibrium, BioSolveIT, Lhasa & Takeda), 18 May 2017, Cambridge<\/p>\n

Cambridge Chemoinformatics Forum<\/span><\/u><\/a>, 24 May, Cambridge<\/p>\n

Cresset UGM<\/span><\/u><\/a>, 29-30 June 2017, Cambridge<\/p>\n

UK QSAR & Chemoinformatics Group Autumn 2017 Meeting<\/a>, 29 September 2017,\u00a0 MIB, Manchester<\/p>\n

SCI Epigenetics 2017<\/span><\/u><\/a>, 7 September 2017, Windlesham, Surrey<\/p>\n

19th RSC\/SCI Cambridge MedChem Symposium<\/span><\/u><\/a>, 10-13 September 2017, Churchill College, Cambridge<\/p>\n

 <\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

Archived Newsletters UK-QSAR Spring 2017 The UK-QSAR and ChemoInformatics Group Welcome to the Spring 2017 UK-QSAR Newsletter! *Please note that<\/p>\n","protected":false},"author":15,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_post_was_ever_published":false},"categories":[5],"tags":[],"class_list":["post-1650","post","type-post","status-publish","format-standard","hentry","category-newsletter"],"aioseo_notices":[],"aioseo_head":"\n\t\t\n\t\n\t\n\t\n\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t