Guiding Principles for Natural Product Drug Discovery
Author(s) -
David Camp,
Rohan A. Davis,
Elizabeth EvansIllidge,
Ronald J. Quinn
Publication year - 2012
Publication title -
future medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.708
H-Index - 69
eISSN - 1756-8927
pISSN - 1756-8919
DOI - 10.4155/fmc.12.55
Subject(s) - drug discovery , natural product , timeline , chemical space , high throughput screening , approved drug , computational biology , biochemical engineering , nanotechnology , drug , computer science , chemistry , biology , pharmacology , bioinformatics , engineering , materials science , stereochemistry , history , archaeology
Natural products (NPs) have historically been a fertile source of new drugs for the pharmaceutical industry. However, this once-popular approach has waned considerably over the past two decades as the high-throughput screening of megalibraries comprised mainly of molecules with non-natural (synthetic) motifs has unfolded. Contemporary high-throughput screening libraries contain molecules compliant with physicochemical profiles considered essential for downstream development. Until recently, there was no strategy that aligned NP screening with the same physicochemical profiles. An approach based on Log P has addressed these concerns and, together with advances in isolation, afforded NP leads in timelines compatible with pure compound screening. Concomitant progress related to access of biological resources has provided long-awaited legal certainty to further facilitate NP drug discovery.
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