On the Metabolic Stability of Fluorinated Small Molecules;A Physical Organic Chemistry Perspective

The incorporation of fluorine and fluorinated motifs into medicinally relevant scaffolds can improve the metabolic and pharmacokinetic properties (DMPK) of drug molecules. Typically, this phenomenon is attributed to differences in C–H vs. C–F bond strengths, though such an explanation ignores accepted mechanisms of drug metabolism and how fluorine and fluorinated substituents perturb physicochemical properties of small molecules. Instead of relying on bond strengths, this perspective will review established mechanisms of drug metabolism and provide mechanistic rationale for the improved metabolic profiles achieved by fluorinating drug candidates. This discussion will connect observed trends in structure-metabolism-relationships with known mechanistic features of relevant drug-metabolizing enzymes, with the ultimate goal of improving medicinal chemistry decision-making.

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Publication Details

Journal
ChemRxiv
Published
2025-08-25
DOI
https://doi.org/10.26434/chemrxiv-2025-mtqbs
Primary Topic
Eicosanoids and Hypertension Pharmacology
Type
article
Field-Weighted Citation Impact
0.00

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article

On the Metabolic Stability of Fluorinated Small Molecules;A Physical Organic Chemistry Perspective

Trevor A. Trombley, Ryan A. Altman, Pankaj Bhattarai
ChemRxiv
Eicosanoids and Hypertension Pharmacology
article

On the Metabolic Stability of Fluorinated Small Molecules;A Physical Organic Chemistry Perspective

Trevor A. Trombley, Ryan A. Altman, Pankaj Bhattarai
article en

Abstract

The incorporation of fluorine and fluorinated motifs into medicinally relevant scaffolds can improve the metabolic and pharmacokinetic properties (DMPK) of drug molecules. Typically, this phenomenon is attributed to differences in C–H vs. C–F bond strengths, though such an explanation ignores accepted mechanisms of drug metabolism and how fluorine and fluorinated substituents perturb physicochemical properties of small molecules. Instead of relying on bond strengths, this perspective will review established mechanisms of drug metabolism and provide mechanistic rationale for the improved metabolic profiles achieved by fluorinating drug candidates. This discussion will connect observed trends in structure-metabolism-relationships with known mechanistic features of relevant drug-metabolizing enzymes, with the ultimate goal of improving medicinal chemistry decision-making.

ChemRxiv
Purdue University West Lafayette (US)
National Institute of General Medical Sciences
Openalex Percentile: Top 79%
Eicosanoids and Hypertension Pharmacology
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