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1.
Xenobiotica ; 54(5): 257-262, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38178690

RESUMO

1. Challenges, strategies and new technologies in the field of biotransformation were presented and discussed at the fourth European Biotransformation Workshop which was held in collaboration with the joint ISSX/DMDG meeting on June 15, 2023 at the University of Hertfordshire in Hatfield, UK.2. In this meeting report we summarise the presentations and discussions from this workshop.3. The topics covered are listed below: Unusual biotransformation reactionsBiotransformation Workflows in Discovery utilising various softwares for structure elucidationBiotransformation software for the identification of peptide metabolitesAccelerator Mass Spectrometry (AMS) for endogenous and xenobiotic metabolite profilingMetabolite profiling using quantitative Nuclear magnetic resonance (NMR) and liquid chromatography coupled to inductively coupled plasma-mass spectrometry (LC-ICP-MS).


Assuntos
Biotransformação , Xenobióticos , Humanos , Cromatografia Líquida , Europa (Continente) , Espectrometria de Massas , Metabolômica , Xenobióticos/metabolismo
2.
J Med Chem ; 67(15): 13106-13116, 2024 Aug 08.
Artigo em Inglês | MEDLINE | ID: mdl-39078401

RESUMO

Achieving oral bioavailability with Proteolysis Targeting Chimeras (PROTACs) is a key challenge. Here, we report the in vivo pharmacokinetic properties in mouse, rat, and dog of four clinical oral PROTACs and compare with an internally derived data set. We use NMR to determine 3D molecular conformations and structural preorganization free in solution, and we introduce the new experimental descriptors, solvent-exposed H-bond donors (eHBD), and acceptors (eHBA). We derive an upper limit of eHBD ≤ 2 for oral PROTACs in apolar environments and show a greater tolerance for other properties (eHBA, polarity, lipophilicity, and molecular weight) than for Rule-of-5 compliant oral drugs. Within a set of structurally related PROTACs, we show that examples with eHBD > 2 have much lower oral bioavailability than those that have eHBD ≤ 2. We summarize our findings as an experimental "Rule-of-oral-PROTACs" in order to assist medicinal chemists to achieve oral bioavailability in this challenging space.


Assuntos
Disponibilidade Biológica , Proteólise , Animais , Administração Oral , Cães , Camundongos , Ratos , Proteólise/efeitos dos fármacos , Humanos , Masculino , Ligação de Hidrogênio , Quimera de Direcionamento de Proteólise
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