From Nutraceuticals to Pharmaceuticals – Common Challenges and Approaches
Joint Conference between the International Conference on the Mechanism of Action of Nutraceutical (ICMAN)
International Union of Pharmacology (IUPHAR) Natural Products Section
27 – 29 SEPTEMBER 2017, AECC, ABERDEEN, SCOTLAND
Thanks to generous sponsorship from Opportunity North East (ONE) Life Sciences there will be a Life Sciences Pavilion for companies and academic service providers , with subsidies for SME’s
Contact email@example.com for more details
Keynote Speakers include:Professor Michael Fenech – CSIRO, Adelaide Professor
Raymond Anderson – UBC, Canada Professor Jeremy
Spencer – University of Reading, UK Professor
Rudolph Bauer – University of Graz, Austria Professor
Junji Terao – Kobe City, Japan
- Novel sources of nutraceuticals and natural product pharmaceuticals
- Bioavailability / pharmacokinetics of nutraceuticals and natural product pharmaceuticals
- Translating novel pathways and mechanisms of action into the clinical use of nutraceuticals and natural product pharmaceuticals
- Personalized nutrition and natural product medicine: therapeutic evidence and regulatory requirements
- Two different worlds? Addressing the convergence between nutraceuticals, TCM and Western medicine
- Drug / nutrient / microbiome / lifestyle interactions
Poster Presentations still being accepted up to 31st August!
Visit the conference website for full details of the conference programme
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ICMAN / IUPHAR-NP 2017
“From Nutraceuticals to Pharmaceuticals – Common Challenges and Approaches”
27 – 29 SEPTEMBER 2017, AECC, ABERDEEN, SCOTLAND
Thanks to generous sponsorship from Opportunity North East (ONE) Life Sciences there will be a Life Sciences Pavilion for companies to showcase their activities
This joint conference brings together a global audience to listen to invited speakers from both academia and industry in the areas of Nutraceuticals and Pharmaceuticals derived from Natural Products. In addition to three days of keynote lectures, free oral communications and poster presentations, the programme includes:
- Dedicated industry sessions, including speakers from Pierre Fabré, Nestlé and Neem Biotech
- Interactive lunchtime workshops focusing on key challenges facing the natural product drug discovery and nutraceutical industries, including:
- Biotechnology/upscaling of production
- Regulation & Health Claims
- Creating Natural Product Databases
- Sustainability & Social Responsibility of exploiting natural resources
- Opportunity to contribute to discussions on development of:
- IUPHAR recommendations for testing natural products
- Internationally accepted protocols for worldwide screening
Take part as an industrial participant, sponsor or exhibitor!
Industrial participants are offered the opportunity to take up one of the following options:
– Attend as a registered delegate and give an oral presentation – day rates are available (register here)
– Exhibit alongside other companies in the Life Sciences Pavilion to showcase your company’s activities in Natural Products/Nutraceutical Research.
Rates (1 person exhibiting – £550 + VAT; 2 persons exhibiting – £715 + VAT) include:
– Full delegate pass for exhibitors
– Company “pitch” opportunity in industry session
***SME’s/Academic service providers are eligible to apply for a £200 subsidy towards the exhibition rates***
– Sponsor the event. Platinum, Gold, Silver and Bronze options are available including the opportunity to sponsor the conference dinner, drinks reception or delegate pack.
For more detailed information visit our website or contact firstname.lastname@example.org
Industry Sessions : Natural Product Research and IUPHAR
- IUPHAR can play a major role in bringing together two different worlds by creating synergies between them, rather than independent research:
|Natural/traditional products (NPs)
||New Molecular Chemical Entities (NMEs)
|– Plant, Microbial, Animal, Marine‐based
||– Synthetic chemistry‐based
|– Sometimes Mixtures
||– Frequently multiple metabolites
|– Chinese, Indian, African ‐based research
||– USA and European‐based research
|– Benefits from centuries of natural practice
||– Benefits from molecular research
|– Biological Synthesis
||– Organic/Aqueous phase separation
|– Novel ?
||– NPs Starting points for NMEs
Nobel prize for Artemesin, Youyou Tu.
Encourage mechanism of action studies and clear effects in clinical pharmacology.
Multiple compounds with small structural similarities are also found in classical medicinal chemistry. Cross‐over technologies, increase database access, define mechanism of action?
Can we synthesise them in sufficient quantity? Eg Abolis technology
How do we get out of the mechanistic ‘soup’ of poorly defined redox, antinflammatory, immunological, antiaging effects claimed for some NPs.
Challenges of Natural Products in drug discovery programs: a future to reinvent ?
Plant and microbial biodiversity still represents a huge reservoir of chemically diversified and bioactive molecules, but the pharmaceutical industry and Natural Products seem divorced today : a stop or at least strong reduction in many companies.
- Drawbacks of NP for a lot of companies:
- The access to biodiversity and associated legal uncertainty adds risk, how to manage? Are WHO guidelines compatible?
- Mixtures are problematic : dereplication and isolation steps, up to date technologies (profiling of new compounds)
- Hits are easy to discover, leads and candidates more rare : are most NP druggable? (e.g. curcumin, Nelson et al, 2016) Recollection and scaling up are challenging. Is redox critical to many NPs? What are the best ways to prevent issues such as those raised about curcumin developability?
- Many new chemical entities have been derived from natural products – have we taken the ‘low hanging fruits’ ?
Theoretically, a very huge numbers of underexplored NP and large chemical diversity : let us be sure of it. How to conclude ?
- New screening technologies, new targets?
- Phenotypic and uncommon assays ? in vivo (systemic effect)?
- Rare samples/products ? Special attention to minor compounds?
- Virtual screening?
Is the road for success comes with the evolution/progress of platforms and translational medicines strategies?
- “omics” technologies?
- Repositioning of known compounds?
- Valorization of complex mixtures as herbal drugs?
Challenges of Natural Products in drug discovery/development programs: a future to reinvent?
- Development of NPs and NCEs for use as medicines are well defined (and expensive), yet NPs are used everywhere – how can we navigate between the two worlds, Or do we just leave them separate ?
- There is an immunopharmacology revolution and reactivating the immune system, or suppressing it, can have immense impact. There thousands of papers about NPs affecting inflammation, but with little mechanistic or clinical follow‐up.
- IUIS and IUPHAR have agreed to collaborate on delineating immunopharmacology drug targets and prepare common databases of validated targets. Furthermore, simple lists of human biomarkers are validated by IUIS/SITC and these could be rapidly applied to human NP research.
So is it worth keeping searching ? Are we prepared to invest again in a new maturity of NP research in Pharma/Biotech/Academic drug discovery? If so we need clear recommendations.
This is the last meeting of a series of strategic events to propose recommendations.
Industry Sessions: IUPHAR and Natural Products
- We encourage clear definition of the chemical substance and molecular targets
- We already have a very good database tool to encourage worldwide access and establish guidelines
- The clinical group are implicated in guidelines for registration cf FDA and EMEA.
- Worldwide discussions, Africa (PharfA), India, China, Brazil, US FDA centre.
- Real recommendations from the IUPHAR Natural Products meeting at Aberdeen, with the possibility of a Nature Drug Discovery article.
- Define differences and synergies between Food – Dietary Supplement – Drug. Must be Oral – if skin application then a cosmetic. A new category is ‘New Dietary Ingredient’ (DTI).
- Chemical NP libraries for screening
- Deep metabolomics for defining mixtures – centralised facilities.
- Breakthroughs in biological synthesis.
- Phenotypical screening.
- Clear recommendations of testing NPs.
- We recommend mixtures be tested for rare/orphan diseases (FDA route)
- We propose protocols for worldwide screening, especially in immunology.
- YOUR input is necessary. 4