12 October - 13 October 2021

RNA as a target for the life sciences

Organised by:

SCI’s Fine Chemicals Group

Online webinar (2 consecutive afternoons): 14:00-17:00 BST

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Prices start from £80.00

Early bird offer ends 8 September 2021

Synopsis

RNA as a target for small molecules is a rapidly evolving topic of major relevance to modern drug discovery and agrochemical science. Moving beyond the established targets of proteins and DNA, it is increasingly clear that RNA is also adept at binding potential pharmacophores and this contemporary topic is the primary focus of our event.  

 

With the isolation of reverse transcriptases it became apparent that RNA was not simply a passive intermediate in biological function, and its relevance for the treatment of disease has since become clear. The first antisense oligonucleotide that modified mRNA expression was approved in 1998 and since the 2006 Nobel prize in Physiology or Medicine was awarded for discovering the mechanism of RNA interference only three years earlier, interest in small interfering RNA as a treatment has been a major field of research with the first drug approval in 2018. It is also now increasingly clear it is feasible to target RNA with small molecules, with numerous start-ups established and a plethora of collaborations with global leaders in the Life Sciences announced in recent years. Here, we are inviting leading experts from these organisations to discuss current and future aspects of this field. 


Attendees

Bringing together contemporary chemical biology and established small molecule research, this event is of significant interest to students and academics in chemistry, biology and pharmacy as well as the established pharmaceutical and agrochemical sectors and the broader biotech community. 


Speakers

Dr Beth Thomas

Storm Therapeutics

Beth has over 20 years of experience in medicinal and computational chemistry. She is currently working at STORM Therapeutics as Director, Medicinal Chemistry where she been since its inception. STORM Therapeutics is the first company to target the entirely new area of RNA modifying enzymes and has recently announced a first-in-class clinical candidate targeting METTL3.
Beth has also worked at Celltech, UCB, BioFocus, University of Cambridge and the Cambridge Crystallogarphic Data Centre. She completed her B.Sc. in Chemistry at the University of St Andrews followed by a Ph.D. in polyketide biosynthesis with Profs. Staunton and Leadlay at the University of Cambridge.

Dr Daniel Palacios

Novartis

Daniel Palacios obtained his B.S. from the University of California at San Diego (2005) and his Ph.D. from the University of Illinois at Urbana Champaign with Prof. Marty Burke (2011). Subsequently, he joined the Global Discovery Chemistry organization at the Novartis Institute for Biomedical Research where he has worked in chemical biology and medicinal chemistry groups, leading projects ranging from hit and target identification to lead optimization and clinical candidate selection. He is currently a Senior Principal Scientist investigating novel therapeutic modalities for neurological diseases.

Dr Kamal Azzaoui

Saverna Therapeutics

Kamal Azzaoui received his PhD in computational chemistry from the University of Orléans followed by two postdocs at McGill University and Georgetown University. He also holds a Master for Advanced Science (MAS) from the Swiss Institute for Translational and Entrepreneurial Medicine (sitem-insel, university of Bern). He worked for more than 15 years in pharmaceutical industry in charge of data analysis, data modeling, drug design using machine learning, cheminformatics and molecular modeling tools. Since 2017, he is the CEO and co-founder of Saverna Therapeutics, a Swiss start-up aiming to discover drugs for non-coding RNAs targets.

Dr Iris Alroy

Animabiotech

AnimaBiotech

Dr Iris Alroy has broad background and more than 20 years of experience in small molecule drug discovery, preclinical development, and development of IND-enabling studies. Dr. Alroy was VP of Discovery at Proteologics, where she established several research programs for the identification of small molecules inhibiting the activity of E3 ubiquitin ligases in HIV-1 and Cancer. Subsequently, she was VP R&D at Pharmos Corp., in which she managed organic and medicinal chemistry, biology and pharmacology groups. Dr. Alroy was also entrepreneur and CEO of startup biotech companies, Fusimab, Ltd., ProMining Therapeutics Ltd., developing bispecific antibodies and small molecules, respectively.

Dr Kevin Weeks

University of North Carolina / Ribometrix

Dr Kevin Weeks is a Kenan Distinguished Professor of Chemistry at the University of North Carolina at Chapel Hill. The vision of his laboratory is to use chemical principles to explore the central role of RNA in biology with a focus on real-world problems and understanding human disease. RNA SHAPE and single-molecule RING technologies, invented in his laboratory, are used worldwide. Dr Weeks is a Fulbright and a Searle Scholar, an NIH EUREKA awardee, a Fellow of American Association for the Advancement of Science, the founder of Ribometrix, and has taught many hundreds of undergraduates first year chemistry.

Prof Matt Disney

Scripps Research

Matt Disney is currently Professor in the Department of Chemistry at Scripps Research on the Florida Campus. His laboratory works in the area of small molecule targeting of RNA. The lab studies regarding molecular recognition events between RNA folds and small molecules to attempt to solve problems of biomedical importance. The lab’s research has garnered various awards including the Sackler Prize in the Physical Sciences, Barry Cohen Award in Medicinal Chemistry, NIH Director’s Pioneer Award, the Tetrahedron Young Investigator Award, the Eli Lily Award in Biological Chemistry, the David W. Robertson Award in Medicinal Chemistry, and others.


Programme

Tuesday 12 October

14:00
Welcome & Introduction
14:10
Structure-based discovery of new functions in large RNAs
Prof Kevin Weeks, UNC-Chapel Hill and Ribometrix
14:55
Break
15:05
Prof Jon Hall, ETH Zürich – Pharmaceutical Chemistry
15:40
Small molecule mRNA splice modulators in neurological diseases
Daniel Palacios, Novartis
16:10
Break
16:25
Drugging RNA modifying enzymes
Dr Beth Thomas, Storm Therapeutics
17:00
Panel discussion
17:30
Closing remarks

Wednesday 13 October

14:00
Welcome
14:05
mRNA translation modulators binding to novel targets: from mRNA processing to mRNA translation
Dr Iris Alroy, Anima Biotech
14:40
Targeting microRNAs for therapy - lessons learned
Dr Kamal Azzaoui, Saverna Therapeutics AG
15:10
Break
15:25
Speaker tbc
16:00
Sequence-based design of bioactive small molecules targeting RNA
Prof Matthew Disney, Scripps Research and Expansion Therapeutics
16:45
Break
16:55
Panel discussion
17:20
Closing remarks


 


Fees
Before early bird – Ends 8 September 2021
SCI member - £80
Non-member - £155
SCI student member - £40
After early bird
SCI member - £135
Non-member - £210
SCI student member - £40

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Organising committee

Karl Collins, SCI / Bayer
Fred Hancock, SCI
Silvia Bonomo, Charles River Laboratories
Daniel Jones, SCI / Charles River Laboratories
Fiona Laraman, SCI / AstraZeneca
Caroline Low, SCI / Google DeepMind
Jason Tierney, SCI / Anima Biotech 


Contact
Conference team
Tel: +44 (0)20 7598 1561
Email: conferences@soci.org