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Spring 2017 Newsletter

Spring 2017 Newsletter

 

Welcome to the Spring 2017 Newsletter from CompChem Solutions Limited.

We’re delighted to announce our new Advocate partnership with Collaborative Drug Discovery (CDD).  CDD offers a modern approach to management of discovery informatics.  More information is below.

Every so often huge strides are made in a particular therapeutic area.  One recent example of this, which has employed quite extensive use of computational structure-based design approaches, is in the area of B-cell haematological oncology.  Two newly approved drugs for CLL/SLL, ibrutinib & venetoclax, were both developed with the aid of structural design.  We feature an article on these game-changing therapies, and invite scientists working in this field to propose new targets for future therapies.  CompChem Solutions may be able to provide limited fee-free support for development of grant proposals in the haematological oncology area.

We’ve been beta-testing Cresset’s new Flare application, which now enables inclusion of proteins to Cresset’s unique field-based approach.  Their User Group Meeting is only a few weeks ago so do attend if you’d like to learn more about Flare and their other recent innovations.

The next UK-QSAR meeting is approaching fast – we hope to see you there!  Do register if you’re planning to attend as time is running out.  And it’s nearly time for the CCG UGM too if you’re up for a trip to Copenhagen next month.

Do refer to our listings of all our selected upcoming events and jobs as well as our In Brief section for a brief round-up of news items from CompChem Solutions.

 In Brief

  • Susan Boyd has recently co-authored a  publication from Cancer Research Technology on “The development of potent inhibitors of the lysophospholipase autotaxin”
  • We’ve been delighted to to take a first look at Cresset’s Flare software for modelling protein systems using their field-based approach.  Further beta testing is now underway.
  • If you need patent or chemical information searching services, do contact us!
  • Do register for the UK-QSAR Meeting if you plan to attend!  And please let us know if you’ve already registered but can no longer attend.

CompChem Solutions partners with Collaborative Drug Discovery

Susan M Boyd, CompChem Solutions Ltd

CompChem Solutions Ltd is delighted to have become an Advocate partner for Collaborative Drug Discovery (CDD).   CDD offers a modern approach to research informatics, with their Vault application hosting a secure biological & chemical database platform which is simple to use and ideally positioned for use by small and large drug discovery teams alike. Their secure web-interfaced system includes tools for molecular visualisation, an ELN, a compound inventory as well as tools for logging compound activity and registering compounds, and is designed to support ready sharing of data across sites and between teams.  Contact us for further information.

Structure-based design has helped change the landscape of B-cell targeted oncology

Susan M Boyd, CompChem Solutions Ltd

Until quite recently, the only therapies available to patients with chronic  lymphocytic leukaemia (CLL)/small lymphocytic lymphoma (SLL) were “traditional” chemotherapy approaches.  These typically involve the use of a combination of alkylating agents, antibodies and sometimes T-cell/immunosupressants.  However, the side effects of these treatments can be significant, their effects last for at best the medium term, and they may even precipitate unfavourable clonal changes in cells to predispose the patient to complications or even secondary cancers further down the line.

In 2013, the whole landscape of treatment for these B-cell cancers was revolutionised, with the FDA approval of ibrutinib.  Ibrutininb, or Imbruvica, is an irreversible inhibitor of Bruton’s Tyrosine Kinase  (BTK), and instrumental in its development was the use of computationally-driven structure-based approaches to guide compound design (Pan et al, ChemMedChem, 2, 58-61, 2007).  The drug sits in the ATP binding site of BTK, covalently bonding to C481.  Initially a homology model of activated BTK was derived based on the unphosphorylated BTK structure 1K2P and the active structure of LCK kinase 1QPE.

From this the non-catalytic cysteine was identified and analogues synthesised and subsequently optimised, resulting in the final drug compound.  The compound was FDA-approved for mantle cell lymphoma in 2013,then for specific forms of CLL/SLL in 2014.  In the UK NICE finally approved its use for specific CLL/SLL patients at the end of 2016. Clinical trials have shown remarkable efficacy.  The RESONATE trial demonstrated an over 90% response rate to ibrutinib compared with 25% rate in the standard treatment.

Following close on the heels of ibrutinib, apoptotic regulator BCL-2 inhibitor venetoclax (aka ABT-199) was designed based on the known BCL-Xl/BCL-2 inhibitor navitoclax.  Navitoclax itself shows dose-limiting thrombocytopenia toxicity, and it was considered that this was likely due to its lack of selectivity towards BCL-Xl.  Reverse engineering of navitoclax together with peptidomimetic design studies on other hot spot regions of the BCL-2 site were used to develop the BCL-2 selective compound venetoclax (Souers et al, Nature Medicine,19(2), 202-208, 2013). 

It was approved for use in specific CLL/SLL patients by both the FDA & the EMA in 2016.  It is still under consideration by NICE in the UK but has been approved for inclusion in the Early Access to Medicines Scheme (EAMS) and has shown an over 80% overall response rate in early clinical trials, whilst showing a highly favourable safety profile.

These drugs are true game changers in this field of oncology, and other so-called “pathway” therapeutics have also emerged, such as idelalisib.  However, the future of treatment of B-cell cancers may well lie in the use of combination therapies, involving single or multiple small molecule agents combined with antibody use.  Many clinical trials are ongoing and this is a truly exciting area of research.  There has been some concern over reports that inhibitors of the PI3Kdelta pathway,  including ibrutinib itself may themselves induce increased expression of activation-induced cytosine deaminase (AID) over the long term, which may lead to genomic instability and to development of lymphoma.  Further studies are certainly needed to establish the level of resistance to these newer drugs, and to explore their long-term usage safety.  There is still a very great need for alternative and/or improved therapies.

If you have a potential drug target which might be of use in future therapies B-cell malignancies, do get in touch.  We may be able to provide limited support free of charge in terms of structural assessment of druggability of targets and to provide background information in support of grant applications.

 

 

Events

The following meetings may be of interest to our readers:

CCG UGM & Conference (Europe), 16-19 May 2017, Copenhagen

Symposium on Streamlining Drug Discovery (Optibrium, BioSolveIT, Lhasa & Takeda), 18 May 2017, Cambridge

Cambridge Chemoinformatics Forum, 24 May, Cambridge

Cresset UGM, 29-30 June 2017, Cambridge

UK QSAR & Chemoinformatics Group Autumn 2017 Meeting, 29 September 2017,  MIB, Manchester

SCI Epigenetics 2017, 7 September 2017, Windlesham, Surrey

19th RSC/SCI Cambridge MedChem Symposium, 10-13 September 2017, Churchill College, Cambridge

Jobs

Some current jobs being advertised…….

Team Leader (CADD), Charles River Laboratories, Saffron Walden, Essex

Application Scientist, Chemical Computing Group Inc, Cambridge (UK) or Cologne (Germany)

Senior Scientific Consultant, Cresset Group, Litlington, Cambridge, UK

Product Manager (API), RSC, Cambridge, UK

Chem- and Bioinformatics Scientists, Software Engineers, Machine Learning Researchers, Benevolent.ai, London, UK

CompChem Solutions Ltd teams up with Collaborative Drug Discovery

CompChem Solutions Ltd is delighted to have become an Advocate partner for Collaborative Drug Discovery (CDD).   CDD offer a modern approach to research informatics, with their Vault application hosting a secure biological & chemical database platform which is simple to use and ideally positioned for use by small and large drug discovery teams alike.  Contact us for further information.

Summer 2016 Newsletter

Summer 2016 Newsletter

Welcome to the Summer 2016 Newsletter from CompChem Solutions Limited.

Well, they say a week is a long time in politics but, boy, this last one must surely count as one of the most dramatic episodes in living memory for most of us.  What will happen next?  When will some new normality condense from the fall-out?  We may not know the answer to these, and may other key questions, for some time yet, but we kick off this time with a synopsis of how the vote has thus far affected our area of science, and what impacts the vote could have for us going forward.  Prior to the  vote, the Cresset European User Group Meeting was held near Cambridge, and here we have penned a personal perspective on the key highlights of what was an excellent meeting.   Further to the strides which have been widely reported recently in the Alzheimer’s field, we feature an article from Christina Elliott of the Killick group at KCL, who reports on the emerging role of inflammation in the condition, and how this may be a key area for development of therapeutics towards this devastating condition.   In other developments a new science park is planned around the theme of “big data” at Downham Market – evidence of the Cambridge effect spilling out into the surrounding region perhaps?  Do refer to our listings of some upcoming events and jobs which may be of interest to our readers as well as our In Brief section for a brief round-up of news items from CompChem Solutions.  But we end this time on a rather sad note, paying tribute to the great Mike Tute who sadly passed away at the end of June.

 In Brief

  • We’re delighted to be helping Cresset alpha and beta test their new protein modelling applications.
  • Need to outsource chemistry?  We can link you up with high quality, cost-effective offshore chemistry resource which can be project managed by UK-based medicinal chemists with extensive experience in the area.  Contact us for more information.
  • IOTA Pharmaceuticals are seeking a computational chemist for an 18-month posting based in Cambridge.  Do contact us if interested.

 

Brexit & Pharma

Susan M Boyd, CompChem Solutions Ltd

 

brexit-1024x549

 

Perhaps surprisingly, in the wake of the recent leave vote, pharmaceutical shares appear to have risen rather than plummeted – somewhat against the general trend.  Certainly investors are looking for industries where profit reliance is beyond our immediate doorstep, and they seem to have put the pharma industry into that basket.  But will this last?  The ABPI warned immediately after the result was announced that the industry faces “immediate challenges”.  Regulation of new drugs and access to the single market are, of course, key issues, but more fundamentally the level of EU funding & investment which feeds our industry is in jeopardy.  We employ many people from EU countries, and currently UK employees can be easily seconded to overseas posts within the EU, but all of this will be more difficult in the future.  Most of the leaders of our industry supported the Remain campaign and warned of the risks of Brexit.  A very nice review of some specific aspects of the probable effects can be found here.  Going forward, we must prepare for a lengthy period of uncertainty for our industry, and hope that jobs will not be put at risk.

 

 

Cresset User Group Meeting – Top Highlights (A Personal Perspective) Cresset

Susan M Boyd, CompChem Solutions Ltd

At the end of June month I enjoyed the Cresset User Group Meeting at Granta Park, Cambridge.  The well-attended meeting was competing with the England-Wales football match which was being broadcast simultaneously, but remarkably few attendees were visibly checking portable devices during the meeting – howzat for a testament to the interesting talks presented!  There were too many great talks to go through all in depth, but here are my personal highlights from the meeting:

  • Cresset protein modelling tools unveiled:  Cresset has been recognised as a leader in the field of ligand-based modelling for some time, but they are now developing pioneering approaches to apply their field-based technology to explore protein-ligand interactions.  The initial application allows visualisation of protein-ligand interactions from a field-based perspective to aid structure-based design, plus calculation of electrostatics and looking at the “happiness” of placed waters with 3D-RISM. Their collaboration with BioMolTech will allow them to link the LeadFinder docking tool into their application and initial results look very positive.  It is hoped that their protein application will be available for release in March 2017, following on from a and b-testing by experienced Cresset users.  CompChem Solutions is delighted to be helping with this testing phase over the coming months.

                                                          Cresset protein

 

  • Spark case studies: Cresset described how the ensemble of databases supplied with Spark has been expanded to include new databases such as the eMolecules reagent database and the CSD fragment database.  Some inventive uses of the tool were also described, illustrating how it can be used in fragment growing, linking, macro-cyclisation and water replacement.
  • Multidrug resistance (Mire Zloh, University of Hertforshire): Multidrug resistance is obviously a major issue in drug development.  Mire described a nice approach which looks at escort molecule/efflux pump substrate complex formation as a means to attenuate efflux action.  Potential escort molecules for known substrates were identified using a combination of molecular similarity searches and ligand-ligand docking studies.  In a validation study 3 compounds known to act synergistically with antibiotics were identified and 2 molecules which can modulate efflux with these antibiotics were discovered.
  • Prediction of cyclic peptide passive permeability (Sandeep Pal, GSK):  The passive permeability of cyclic peptides is influenced by lipophilicity and intramolecular H-bonding, which has the effect of masking some polar features of the structure.  For larger molecules it is harder to derive useful 2D descriptors of polarity due to the molecular complexity. Improvement in passive permeability and absorption is often linked to increased lipophilicity.  Sandeep described a nice PLS-DA (Partial Least Squares Discriminant Analysis) classification model based on the ChromLogD descriptor (lipophilicity) and solvation energy which can nicely predict molecules as permeable or non-permeable in tests at GSK.
  • Analysing building block diversity for DNA encoded libraries (Finton Sirockin & Nikolaus Steifl, Novartis):  Finton & Nikolaus described the use of rooted 2D fingerprints and modified invariant fingerprints, combined with Cresset’s 3D field approach and attachment point vector alignment to select diverse building blocks for DNA encoded libraries.  Clustering of the Cresset field-points was used to select reagents which spanned the available molecular space.  The approach can be used to select reagents directed at particular protein targets, and to ensure that “islands” of similar compounds exist in a library to facilitate SAR exploration post-screening.

Vectors

An emerging role of inflammation in Alzheimer’s disease

Dr Christina ElliottKing’s College London, Department of Old Age Psychiatry and Dementia,  Maurice Wohl Clinical Neuroscience Institute

christina.elliott@kcl.ac.uk

Alzheimer’s disease (AD) is characterised by progressive cognitive impairment arising from synaptic dysfunction and eventual neuronal loss.  Most research has mainly focussed around the classic AD pathologies, the deposition of extracellular amyloid-β (Aβ) plaques, and the intracellular formation of neurofibrillary Tau tangles.  However, there has been a steady accumulation of circumstantial evidence highlighting a role of immune mechanisms in the development of AD, particularly the identification of TREM2 (triggering receptor expressed on myeloid cells) and other immune components in genome wide association studies in both genetic and sporadic forms of the disease.

While this provides a smoking gun, immune activation in AD has been often dismissed as merely an unfortunate consequence of the large scale death of neurons occurring within the AD brain.  However, a number of prominent papers published this year paint a more intimate picture, where immune mechanisms are closely involved in excessive synapse pruning, arguably the initial event in AD pathology.

One such mechanism is the complement cascade, a family of proteins traditionally involved in the clearance of opsonised microbes by phagocytosis.  In their paper, published in the journal Science, Hong et al. demonstrate that complement proteins are crucial for removal of synapses by tagging them for destruction by microglia phagocytosis.  Moreover, the authors show that exposure of neurons to Aβ can inappropriately activate this cascade leading to excessive synapse loss1.  It is also of note that complement mediated synapse loss has also been demonstrated in schizophrenia2.  Therefore, further elucidation of these mechanisms will be of broad significance and may provide therapeutic benefit to a number diseases underpinned by synaptic dysfunction.

Another strategy to attenuate immune mediated synapse loss is by the use of anti-inflammatory cytokines such as interleukin-33 (IL-33) as described by Fu et al. in PNAS.  In a mouse model of AD the authors show that administration of IL-33 can skew microglia towards an anti-inflammatory phenotype leading to preservation of cognition and a reduced amyloid plaque burden3.

It must be noted that the anti-inflammatory action of IL-33 has identified previously in Multiple Sclerosis (MS), a neurological disease where the immune component contributing to disease pathology has been formally demonstrated.  In fact a number of immune modulating drugs approved for the treatment of MS have been proposed to be of benefit in AD.  One such example is FTY720/Fingolimod, which has been shown to be protective against Aβ induced cognition loss in rodents4.

Together these works and many others demonstrate a crucial role for neuroinflammation entwined within the heart of AD pathology.  This provides a plethora of therapeutic opportunities from novel targeting of affected pathways to repurposing of licenced drugs currently in clinical use for other immune-linked disorders.

  1. S. Hong et al., Complement and microglia mediate early synapse loss in Alzheimer mouse models. Science 352, 712-716 (2016).
  2. A. Sekar et al., Schizophrenia risk from complex variation of complement component 4. Nature 530, 177-+ (2016).
  3. A.K. Y. Fu et al., IL-33 ameliorates Alzheimer’s disease-like pathology and cognitive decline. Proceedings of the National Academy of Sciences of the United States of America 113, E2705-E2713 (2016).
  4. M. Asle-Rousta, Z. Kolahdooz, S. Oryan, A. Ahmadiani, L. Dargahi, FTY720 (Fingolimod) Attenuates Beta-amyloid Peptide (A beta(42))-Induced Impairment of Spatial Learning and Memory in Rats. Journal of Molecular Neuroscience 50, 524-532 (2013).

 

Centre for Advanced Knowledge Engineering – coming soon to Downham Market

Susan M Boyd, CompChem Solutions Ltd

Plans are well underway for a new £350M big data campus at Downham Market after a successful open consultation meeting held recently in the Town Hall.

Big Data has become big in biotech/pharma right now, with GSK already collaborating with the EBI & the Wellcome Trust Sanger Institute on a big data project to aid target validation, and many other big players (eg AstraZeneca, Sanofi, Allergan, Roche) heavily invested in the field.  Applications of big data in pharma include custom applications for specific business problems, scientific search, competitive intelligence, medical affairs and drug repositioning.  A nice article from McKinsey  describes how big data can “revolutionize big pharmceutical R & D”.

The Centre for Advanced Knowledge Engineering (CfAKE), would be at the former RAF Downham Market in Bexwell, and is expected to create more than 4,500 permanent jobs if planning permission is approved.

The development will include improved infrastructure including faster broadband, road improvements and a university technical college.  An outline planning application for the site is being submitted this month and, if permission is granted, building is expected to begin towards the end of the year.

The project is supported by Aventa Capital, a finance group who have a successful track record in long-term value through regeneration investments in the UK that generate positive economic growth and transformational social impact.

 

Mike Tute

Susan M Boyd, CompChem Solutions Ltd

It is with great sadness that I learned that Mike Tute passed away at the end of June.  Mike worked at Pfizer in Sandwich for many years and I have the privilege of sharing an office with him for a short period of his “semi-retirement” during my time there.  Mike was one of the true pioneers of our field, beginning his career as a medicinal chemist before becoming a founding member of the Pfizer UK computational chemistry team.  Mike was an approachable, warm, and incredibly talented man with genuine enthusiasm for his science.  He will be missed.

 

Events

The following meetings may be of interest to our readers:

7th Joint Sheffield Chemoinformatics Meeting, 4-6th July 2016, University of Sheffield

UK QSAR & Chemoinformatics Group Autumn 2016 Meeting, 19th October 2016, ICR Sutton

21st EuroQSAR Meeting, 4-8th September 2016, Verona, Italy

Sir Simon Campbell – Science, Art & Drug Discovery, SCI lecture (free but registration necessary), 27th September 2016, London.

SCI Cheminformatics for Drug Design: Data, Models and Tools, 12th October 2016, Duxford, UK

 

Jobs

Some current jobs being advertised…….

Experienced Computational Chemist, IOTA Pharmaceuticals Ltd, Cambridge, UK.

Senior Software Developer, Chemical Computing Group Inc, Cambridge, UK.

Application Scientist, Chemical Computing Group Inc, UK or Germany.

Senior Scientific Consultant, Cresset Discovery Services, UK.

C++ Software Engineer in Chemoinformatics, Optibrium, Cambridge, UK.

 

 

 

 

 

 

 

 

 

 

 

 

 

Winter 2016 Newsletter

Winter 2016 Newsletter

Welcome to the Winter 2016 Newsletter from CompChem Solutions Limited.

It might feel a bit like spring outside, but the year is yet young!  In our latest newsletter we look forward to the upcoming inaugural UK-QSAR/PhysChem Forum joint meeting which takes place next month and we describe some of the new products and products suites recently announced by CCDC to mark the 50th anniversary of the CSD,  As ever, do check out our listings of some upcoming events and jobs which may be of interest to our readers as well as our In Brief section for a brief round-up of news items from CompChem Solutions.

 In Brief

  • We’re looking forward to the UK-QSAR and Chemoinformatics Meeting/PhysChem Forum on 15-16th March at Stevenage.
  • Have a gap in your available resource?  We can offer interim staff across both computational chemistry and computational biology. Contact us for more information.
  • CompChem Solutions are delighted to announce the renewal of our collaborations with Cresset, CCG and CCDC which will provide us with continued access to their software tools.

 

The First Joint UK-QSAR Group & PhysChem Forum Meeting is Ready to Spring into Action!   qsar-logo

Susan Boyd, UK-QSAR & Chemoinformatics Group Committee Member & Newsletter Editor
 

In a departure from the usual UK-QSAR & Chemoinformatics Group Meeting format, the upcoming Spring 2016 meeting will be a foray into new territory, as the group will stage its first joint meeting with the PhysChem Forum.  The meeting will be hosted by GSK Stevenage over 15-16th March, with an optional Symposium Dinner on the evening of 15th.

Whilst the PhysChem Forum’s focus has been on physical chemistry and ADME, the UK-QSAR group has traditionally placed more emphasis on computational modelling of biological processes, but both organisations have a legacy of hosting regular free-to-attend meetings for their respective communities, focussing on the science which enables development of more effective compounds. The organisers’ hope is that this event will help deepen the understanding of each other’s science and allow cross-fertilisation of ideas. As the biotech/pharma/crop protection community’s modelling focus has broadened in recent times to encompass wider aspects of bioactive compound design, from bioinformatics through to QSPR and predictive ADMET, this joint meeting seems well placed to serve up a menu of thought-provoking talks of interest to both groups.

More information and registration information is available via the UK-QSAR group’s website, but do sign up quickly if you’d like to go as registration closes on 29th February.

 

 

CSD-System 2016:  The CSD’s 50th Birthday Present – to us!CCDC-logo

Susan M Boyd, CompChem Solutions Ltd

The Cambridge Structural Database (CSD) from CCDC celebrated its 50th birthday in 2015.  To mark the occasion, the CCDC scientists have been working away, devising a brand new format for their range of products – and have just released the new CSD-System 2016 to the community.  This new delivery of their products represents the most fundamental change in the front-end to their tools since the CSD first appeared in digital format.  The idea behind the move is to present different suites of products through a common interface – and almost as importantly, through a common licencing system – to facilitate ease-of-use, communication and presentation of results across different user communities.

Four new product suites are now on offer:  CSD-Enterprise (available to all academic users and eligible commercial users) which includes CCDC’s full range of applications; CSD-System, which covers the CSD and related analysis tools; CSD-Discovery which includes CCDC’s applications which are relevant to discovery chemistry; and CSD-Materials which includes applications relevant to materials science/crystalline form studies.

In addition to the tools many of us who work in drug discovery are familiar with, such as the CSD, GOLD, IsoStar, SuperStar and Relibase+, the new release also offers a new conformation generator which has been parameterised based on crystallographic geometrical data from the CSD, and a new ligand overlay application which uses the CSD data to help identify common binding modes, interactions and geometries of structurally diverse ligands. Both of these new applications should prove useful tools for ligand-based approaches such as pharmacophore modelling, as well as helping to determine the likely experimental conformation of ligand structures – without the need to rely on the empirically derived estimations inherent in forcefield-based calculations.

csd-discovery1 csd-discovery2

New tools: Flexibly align diverse structures (left), generate ensemble of experimentally-parameterised conformers (right).

More information on accessing the new tools can be obtained from CCDC.

 

Events

The following meetings may be of interest to our readers:

5th SCI/RSC Symposium on Ion Channels as Therapeutic Targets, 14-15th March 2016, Wellcome Trust Cambridge, UK

CCG Workshop on SBDD, 30th March 2016, Cambridge, UK (free to attend, but registration needed)

Sir Paul Nurse – The Francis Crick Institute: tackling the world’s biggest health problems faster, 30th March 2016 (evening lecture), SCI London

SCI Kinase 2016: Next Generation Inhibitors, 16-17th May 2016, BioCity, Nottingham, UK

6th SCI/RSC Symposium on GPCRs in Medicinal Chemistry, 13-15th June 2016, Aptuit, Verona, Italy

Cresset European User Group Meeting, 16th June 2016, Cambridge, UK (free to attend but registration needed)

7th Joint Sheffield Chemoinformatics Meeting, 4-6th July 2016, University of Sheffield

UK QSAR & Chemoinformatics Group Autumn 2016 Meeting, 19th October 2016, ICR Sutton

21st EuroQSAR Meeting, 4-8th September 2016, Verona, Italy

 

Jobs

Some current jobs being advertised…….

Technical Expert Chemoinformatics, Syngenta, Jealott’s Hill, Berks, UK

Scientist/Senior Scientist – Computational Chemistry, RedX, Macclesfield, UK

Developer in Chemoinformatics, Scitegrity, Sandwich, Kent, UK

Computational Chemist, Drug Discovery Unit, Dundee University, Scotland, UK

Computational ADME Scientist, AstraZeneca, Cambridge UK , Molndal or Waltham

Bioinformatics Scientist, Healx, Cambridge, UK

Postdoctoral Position in Computational Biomedicine, RWTH Aachen

 

 

 

 

 

 

 

 

 

 

Autumn 2015 Newsletter

Autumn 2015 Newsletter

Welcome to the Autumn 2015 Newsletter from CompChem Solutions Limited.

In our autumnal edition we feature a personal perspective on the recent SCI/RSC Medicinal Chemistry Symposium, including an article from Al Dossetter of MedChemica Ltd on their collaborative approach to matched molecular pairs analysis and predictive ADMET which he presented on at the symposium.   With the recent press focus on artificial intelligence and robots potentially replacing humans in the foreseeable future, we take a look at how this might affect us in drug discovery.  With the increasing interest in computational biology across the sector, CCG have contributed an article highlighting how computational approaches can assist in the discovery of biologics, and describe an upcoming (free) course they are offering on this aspect of modelling.   Do check out some upcoming events and jobs which may be of interest to our readers as well as our In Brief section for a brief round-up of news items from CompChem Solutions.

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