Mike Waring, Editor-in-chief
Newcastle University
ORCID ID: http://orcid.org/0000-0002-9110-8783
Mike Waring is Chair of Medicinal Chemistry at Newcastle University and Head of Chemistry for the Cancer Research UK Newcastle Drug Discovery Unit. He was previously Principal Scientist in Medicinal Chemistry at AstraZeneca. He has worked mainly in the areas of diabetes and oncology and his work has contributed to the discovery of 14 drug candidates, including the marketed EGFR inhibitor osimertinib (Tagrisso™).
He has made significant contributions to the field in many areas, perhaps most notably property-based optimisation, covalent inhibition, novel binding modes and new methods of hit generation. He is a 2018 American Chemical Society Hero of Chemistry and recipient of the 2017 RSC Malcolm Campbell Medal. He is an elected fellow of the Royal Society of Chemistry.
Cynthia Dowd, Associate Editor
George Washington University, USA
Dr. Cynthia Dowd is a Professor of Chemistry at George Washington University. She obtained a BA in Chemistry from the University of Virginia and a PhD in Medicinal Chemistry from Virginia Commonwealth University (with Dr. Richard Glennon). Following a postdoc at the University of Pennsylvania (with Dr. Irwin Chaiken), Cindy was an intramural scientist at the National Institutes of Health (NIH). There, she led a small molecule chemistry group to discover novel agents against tuberculosis.
In 2007, she began her independent career at GWU where her research is focused on the design and synthesis of novel antiinfective therapies, directed primarily against tuberculosis, malaria and the ESKAPE pathogens.
She is the co-author of many peer-reviewed papers, patents, reviews, and book chapters. She is the recipient of the GWU Bender teaching and DREAM mentorship awards, as well as several large research awards from outside institutions.
Maria Duca, Associate Editor
Université Côte d’Azur - CNRS, France
Dr. Maria Duca is head of Targeting of Nucleic Acids research group in the Institute of Chemistry of Nice (Université Côte d’Azur - CNRS). After undergraduate studies in Pharmacy and Medicinal Chemistry (Faculty of Pharmacy, University of Bologna, Italy), she obtained her PhD in Molecular Biochemistry under the supervision of Dr. Paola B. Arimondo (National Natural History Museum, Paris, France) working on topoisomerase II inhibitors. A 2- year post-doctoral training in Sydney Hecht’s lab (Department of Chemistry, University of Virginia, USA) allowed her to pursue the study of nucleic acids working on targeted protein mutagenesis upon chemical modification of tRNAs. After CNRS recruitment as a Research Scientist in 2007, her research activities focus on the targeting of non-coding RNAs using synthetic small molecules toward innovative therapeutic approaches for anticancer, antiviral and antimicrobial applications.
Sally-Ann Poulsen, Associate editor
Griffith University, Queensland, Australia
ORCID: http://orcid.org/0000-0003-4494-3687
Sally-Ann Poulsen is Professor and Deputy Director (acting) at Griffith Institute for Drug Discovery (GRIDD), Griffith University, Brisbane, Australia. She holds a PhD in medicinal chemistry also from Griffith University, receiving a University Medal for academic excellence. Immediately following her PhD she was recipient of a Royal Society & National Health and Medical Research Council (NHMRC) Howard Florey Research Fellowship to undertake research at the University of Cambridge. On returning to Australia, she was awarded an Australian Research Council QEII Fellowship, followed by an Australian Research Council Future Fellowship.
Poulsen works with collaborators in Australia and internationally, both from academia and industry on projects related to development of new chemical probes, medicinal chemistry targeting cancer and infectious disease, and fragment screening using native state mass spectrometry. Her research is defined by the application of chemistry expertise to address complex questions across biology.
Poulsen was appointed as a Fellow, Royal Australian Chemical Institute (RACI) in 2017. She is Chair elect of the RACI Medicinal Chemistry and Chemical Biology Division and is a global council member of the International Chemical Biology Society. She is author of >100 publications in the field of medicinal chemistry and chemical biology.
Jian Zhang, Associate Editor
Shanghai Jiao Tong University School of Medicine, China
Jian Zhang is Distinguished Professor and Head of Medicinal Chemistry & Bioinformatics Center at Shanghai Jiaotong University School of Medicine. In addition, he is also Dean of the School of Pharmacy at Ningxia Medical University, a member of the Academic Degrees Committee of the State Council in China, and founder of Nutshell Therapeutics.
In the last decade, his research is concerned with drug design, medicinal chemistry and chemical biology, especially target identification and first-in-class allosteric drug discovery.
Hayley Binch
Hoffman-La Roche, Switzerland
Dr Hayley Binch is Head of Medicinal Chemistry at Hoffmann-La Roche in Base. She obtained her PhD at University of Bristol, UK in the field of Organic Chemistry, followed by postdoctoral research at University of Hamburg, Germany and King’s College London. In 1998, she joined the Medicinal Chemistry department of Vertex Pharmaceuticals, Oxford, focussing on kinase research in the field of Oncology. In 2006, she moved to Vertex San Diego to work on ion channels for pain and cystic fibrosis. In 2016, she joined as a Section Head within Medicinal Chemistry at Hoffmann-La Roche in Basel and subsequently became Head of Medicinal Chemistry in 2017.
At Roche, the Medicinal Chemistry department supports the design and synthesis of small molecules to identify clinical candidates in the areas of Immunology, Infectious Diseases, Neuroscience, Oncology, Ophthalmology and Rare Diseases.
Paola Castaldi
LifeMine Therapeutics, USA
https://orcid.org/0000-0003-1959-0007
Paola Castaldi is an experienced and passionate chemical biologist with experience in leading multidisciplinary teams supporting programs across several therapeutic areas and stages. Her drive towards embedding state-of-the-art technologies to drug discovery and development, resulted in several contributions to target identification, mechanism of action and safety deconvolution of therapeutics.
Before joining LifeMine Therapeutics, Paola headed the Chemical Biology & Proteomics department at AstraZeneca. Over the years Paola was responsible for the build of a state-of-the-art chemical biology and mass spectrometry hub with global impact across all therapeutic areas and platforms. Notably she played a critical role to the establishment of the protein degradation and the multiomics initiatives.
Before AstraZeneca, Paola was a key contributor of the Chemical Genetics group at Sanofi Oncology, Cambridge, MA with a focus on phenotypic drug discovery projects for the Wnt and KRAS oncogenic pathways.
Between other responsibilities, Paola is part of the SAB for the Chemical Biology Doctorate Program at Imperial College London and has authored more than 25 peer-reviewed articles.
Paola completed her undergraduate studies in pharmaceutical chemistry and received her Laurea (MSc) at University of Padova, Italy. She then went on to conduct graduate research studies at Imperial College London, UK and postdoctoral studies at UCSD and Boston University.
Matthew Fuchter
Imperial College London, UK
ORCID: http://orcid.org/0000-0002-1767-7072
Matthew Fuchter is a Reader in Chemistry at the Department of Chemistry, Imperial College London. In addition, he is working group lead within the new therapeutics Theme of the Imperial College Cancer Research UK Centre. He is a research board member of the Institute of Chemical Biology, co-director of the Imperial MRes in Drug Discovery, a panel member of the Cancer Research UK Multidisciplinary Award, and an appointed member of the Royal Society of Chemistry Organic Division. He is heavily involved in medicinal chemistry, chemical biology and translational activities at Imperial and externally.
His primary research interests concern the misregulation of epigenetic events in disease, although he has made a number of contributions to other disease areas/targets.
Jayanta Haldar
Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, India
Jayanta Haldar completed his undergraduate training at the Presidency College, University of Calcutta and he received his Master of Science and PhD from the Indian Institute of Science, Bangalore in 2005. He then pursued his Postdoctoral Research at the Department of Chemistry, Massachusetts Institute of Technology, USA till 2009. He then joined New Chemistry Unit at JNCASR as Assistant Professor (Faculty Fellow) in 2009 and currently he is an Associate Professor. He is also associated with the School of Advanced Materials (SAMat) at JNCASR.
Jayanta has received several awards and honours such as the Ramanujan Fellowship Govt. of India, CDRI Excellence in Drug Research Award in Chemistry, Chemical Research Society of India (CRSI) Bronze Medal, Sheik Saqr Career Award Fellowship, etc.
Over the past decade, his lab has been persistently undertaking a diverse set of projects in the field of Medicinal Chemistry and Chemical Biology, with the aim of tackling and preventing antimicrobial resistance and infections. His group has established various chemical strategies and invented several antimicrobial solutions through rationally designed semi-synthetic antibiotics and new synthetic drug-candidates with novel mechanisms of action. Haldar group has adopted innovative approaches to target drug-resistant bacteria through development of new class of glycopeptide-antibiotics and metallo-β-lactamase inhibitors.
Recently, his group has also developed antimicrobial peptide (AMP) mimics which can cure complex biofilm-related infections and engineered small-molecular antibiotic adjuvants which can, in combination, resensitize multiple classes of obsolete antibiotics ubiquitously, for tackling the most critical drug-resistant Gram-negative superbugs. As a part of the preventive strategy, Dr. Haldar’s group has engineered antimicrobial paints that prevent catheters/implant-associated infection and surgical-sealants that prevent/cure eye infections and promote wound-healing. The group has also developed antimicrobial coatings on Personal Protective Equipment (PPE) which can prevent the spread of bacterial, fungal and respiratory viral infections.
Lyn Jones
Dana-Farber Cancer Institute, Boston, USA
Lyn Jones completed PhD studies in synthetic organic chemistry at the University of Nottingham, before starting his post-doctorate research at The Scripps Research Institute, California in the area of chemical biology. He joined Pfizer (Sandwich, UK) as a medicinal chemistry team leader, eventually becoming Director of Chemical Biology and Lead Discovery Technologies. He transferred to Pfizer Cambridge, MA to become Head of Rare Disease Chemistry and Head of Chemical Biology, before joining Jnana Therapeutics as Vice President of Chemistry and Chemical Biology. He is currently Chief Scientist at the Center for Protein Degradation at the Dana-Farber Cancer Institute.
He has been recognized with Royal Society of Chemistry awards for his contributions to HIV, COPD and rare genetic disease research. He has considerable experience working in many other disease areas, including cancer, inflammation, and pain. He is also an elected Fellow of the Royal Society of Chemistry, the Royal Society of Biology, and the Linnean Society, and was most recently recognized as a Fellow of the American Association for the Advancement of Science for his contributions to the field of medicinal chemistry.
Jean-Louis Reymond
University of Bern, Switzerland
ORCID:https://orcid.org/0000-0003-2724-2942
Jean-Louis Reymond is a Professor of Chemistry at the University of Bern, Switzerland. He studied Chemistry and Biochemistry at the ETH Zürich and obtained his Ph.D. at the University of Lausanne on natural products synthesis (1989). After a Post-Doc and Assistant Professorship at the Scripps Research Institute, he joined the University of Bern (1997). His research focuses on the enumeration and visualization of chemical space for small molecule drug discovery, the synthesis of new molecules from GDB (http://gdb.unibe.ch), and the design and synthesis of peptide dendrimers and polycyclic peptides as antimicrobials and for nucleic acids delivery. He is the author of > 300 scientific publications and reviews.
