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A New Straightforward Method for Lipophilicity logP Measurement using 19F NMR Spectroscopy
Published on: January 30, 2019
Lipophilicity in Drug Development: Too Much or Not Enough?
Christel A S Bergström1, Mehran Yazdanian2
1Department of Pharmacy, Uppsala University, Uppsala Biomedical Centre, P.O. Box 580, SE-751 23, Uppsala, Sweden. christel.bergstrom@farmaci.uu.se.
Drug development needs more discussion on lipophilicity. Diverse strategies exist for selecting drug candidates, impacting disease treatment efficiency.
Area of Science:
- Pharmaceutical Sciences
- Medicinal Chemistry
Background:
- A round table discussion at the AAPS Annual Meeting (October 27, 2015) addressed the role of lipophilic compounds in drug development.
- The session fostered idea exchange between academic and industry scientists, attracting over 250 participants.
Framework:
- The core debate centered on whether an increase or decrease in lipophilic compounds is beneficial for drug discovery.
- Key discussion points included the varying approaches to compound selection and development strategies across different organizations.
Implementation:
- The round table served as a platform for scientists to share diverse perspectives on optimizing drug development pipelines.
- Feedback indicated the session was highly valuable for its interactive and informative nature.
Implications:
- The dialogue underscored the critical need for continued debate on selecting optimal drug development candidates.
- Effective candidate selection is crucial for enabling efficient drug delivery and successful disease treatment.
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