| Literature DB >> 30249495 |
Rita Fuerst1, Jun Yong Choi2, Anna M Knapinska3, Lyndsay Smith3, Michael D Cameron4, Claudia Ruiz4, Gregg B Fields3, William R Roush5.
Abstract
A structure-activity/structure-property relationship study based on the physicochemical as well as in vitro pharmacokinetic properties of a first generation matrix metalloproteinase (MMP)-13 inhibitor (2) was undertaken. After systematic variation of inhibitor 2, compound 31 was identified which exhibited microsomal half-life higher than 20 min, kinetic solubility higher than 20 μM, and a permeability coefficient greater than 20 × 10-6 cm/s. Compound 31 also showed excellent in vivo PK properties after IV dosing (Cmax = 56.8 μM, T1/2 (plasma) = 3.0 h, Cl = 0.23 mL/min/kg) and thus is a suitable candidate for in vivo efficacy studies in an OA animal model.Entities:
Keywords: In vitro and in vivo pharmacokinetics; Matrix metalloproteinase 13; Microsomal stability; Permeability; Solubility; Structure-activity relationship; Structure-property relationship
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Year: 2018 PMID: 30249495 PMCID: PMC6379921 DOI: 10.1016/j.bmc.2018.08.020
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641