Recent advances in fluorination techniques and their anticipated impact on drug metabolism and toxicity
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|Title:||Recent advances in fluorination techniques and their anticipated impact on drug metabolism and toxicity||Authors:||Murphy, Cormac D.
|Permanent link:||http://hdl.handle.net/10197/7885||Date:||2-Mar-2015||Online since:||2016-09-06T15:55:31Z||Abstract:||Introduction: Fluorine’s unique physicochemical properties make it a key element for incorporation into pharmacologically active compounds. Its presence in a drug can alter a number of characteristics that affect ADME-Tox, which has prompted efforts at improving synthetic fluorination procedures. Areas covered: This review describes the influence of fluorine on attributes such as potency, lipophilicity, metabolic stability and bioavailablility and how the effects observed are related to the physicochemical characteristics of the element. Examples of more recently used larger scale synthetic methods for introduction of fluorine into drug leads are detailed and the potential for using biological systems for fluorinated drug production is discussed. Expert opinion: The synthetic procedures for carbon-fluorine bond formation largely still rely on decades-old technology for the manufacturing scale and new reagents and methods are required to meet the demands for the preparation of structurally more complex drugs. The improvement of in vitro and computational methods should make fluorinated drug design more efficient and place less emphasis on approaches such as fluorine scanning and animal studies. The introduction of new fluorinated drugs, and in particular those that have novel fluorinated functional groups, should be accompanied by rigorous environmental assessment to determine the nature of transformation products that may cause ecological damage.||Type of material:||Journal Article||Publisher:||Taylor and Francis||Journal:||Expert Opinion on Drug Metabolism and Toxicology||Volume:||11||Issue:||4||Start page:||589||End page:||599||Copyright (published version):||2015 Informa UK, Ltd.||Keywords:||Biotransformation; Fluorinating reagent; Organofluorine; Synthesis||DOI:||10.1517/17425255.2015.1020295||Language:||en||Status of Item:||Peer reviewed|
|Appears in Collections:||Biomolecular and Biomedical Science Research Collection|
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