Topical BET PROTACs for locally restricted protein degradation in the lung

Proteolysis targeting chimeras (PROTACs) have been studied extensively to optimize their oral bioavailability. Based on Lipinski's and Veber's rules, molecular weight, log <i>P</i>, log <i>D</i>, the number of hydrogen bond donors and acceptors, the polar surface area and the number of rotatable bonds play a critical role for the oral bioavailability of any given PROTAC. Multiple analyses of the published PROTAC chemical space show that the overall guidelines for obtaining orally available PROTACs are broadly in line with those of the bRo5 space established for oral drugs. In contrast to the significant knowledge that has been generated for the design of oral PROTACs, there is little expertise regarding inhaled and generally topically administered PROTACs. In this work we (1) introduce parameters influencing the inhaled route of administration of PROTACs and (2) describe the first examples of inhaled bromodomain and extra terminal domain (BET) PROTACs which were designed for inhaled delivery and characterized <i>in vitro</i> and <i>in vivo</i>.

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Publication Details

Journal
RSC Medicinal Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5md00173k
Citations
1
Primary Topic
Peptidase Inhibition and Analysis
Type
article
Field-Weighted Citation Impact
1.05
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article

Topical BET PROTACs for locally restricted protein degradation in the lung

Ulf Hedström, Bernardo Ranieri, Karolina Kwapień, Frederik Eisele et al.
1 citations
RSC Medicinal Chemistry
Peptidase Inhibition and Analysis
1.05
article

Topical BET PROTACs for locally restricted protein degradation in the lung

Ulf Hedström, Bernardo Ranieri, Karolina Kwapień, Frederik Eisele, Stefan Schießer, Madeleine Engsevi, Jesper Malmberg, Pia Hansson, Anna Novén, Johan Jirholt, Martin Hemmerling, Antonio Piras, Rikard Pehrson, Lena Ripa, Annica Jarke, Lisa‐Catherine Rosenbaum, Werngard Czechtizky, Markus Nordberg, Jianming Liu, Hyunsoo Park, Annika Borde, Mei Ding, Cecilia Forss, Oliwia Slettengren, Lassina Badolo, Perla Breccia, Carlo Cassani, Karin Ribbing
article en
1 citations

Abstract

Proteolysis targeting chimeras (PROTACs) have been studied extensively to optimize their oral bioavailability. Based on Lipinski's and Veber's rules, molecular weight, log <i>P</i>, log <i>D</i>, the number of hydrogen bond donors and acceptors, the polar surface area and the number of rotatable bonds play a critical role for the oral bioavailability of any given PROTAC. Multiple analyses of the published PROTAC chemical space show that the overall guidelines for obtaining orally available PROTACs are broadly in line with those of the bRo5 space established for oral drugs. In contrast to the significant knowledge that has been generated for the design of oral PROTACs, there is little expertise regarding inhaled and generally topically administered PROTACs. In this work we (1) introduce parameters influencing the inhaled route of administration of PROTACs and (2) describe the first examples of inhaled bromodomain and extra terminal domain (BET) PROTACs which were designed for inhaled delivery and characterized <i>in vitro</i> and <i>in vivo</i>.

RSC Medicinal ChemistryVol. 16(9)
AstraZeneca (France) (FR), AstraZeneca (Netherlands) (NL), AstraZeneca (Japan) (JP), AstraZeneca (Finland) (FI), AstraZeneca (Italy) (IT), AstraZeneca (Sweden) (SE), AstraZeneca (Spain) (ES)
Openalex Percentile: Top 23%
Peptidase Inhibition and Analysis
1.05
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