| Literature DB >> 26241578 |
Mijoon Lee, Zhenzhou Chen1, Brittany N Tomlinson1, Major Gooyit, Dusan Hesek, María Raquel Juárez1, Rasheeq Nizam1, Bill Boggess, Elena Lastochkin, Valerie A Schroeder, William R Wolter, Mark A Suckow, Jiancun Cui1, Shahriar Mobashery, Zezong Gu1, Mayland Chang.
Abstract
SB-3CT is a potent and selective inhibitor of matrix metalloproteinase (MMP)-2 and -9, which has shown efficacy in an animal model of severe traumatic brain injury (TBI). However, SB-3CT is poorly water-soluble and is metabolized primarily to p-hydroxy SB-3CT (2), a more potent inhibitor than SB-3CT. We synthesized the O-phosphate prodrug (3) of compound 2 to enhance its water solubility by more than 2000-fold. The prodrug 3 was a poor MMP inhibitor, but readily hydrolyzed to the active 2 in human blood. Pharmacokinetics and brain distribution studies in mice showed that 2 crossed the blood-brain barrier (BBB) and achieved therapeutic concentrations in the brain. The prodrug 3/compound 2 was evaluated in a mouse model of severe TBI and found to significantly decrease the brain lesion volume and improve neurological outcomes. MMP-9 inhibition by a water-soluble thiirane inhibitor is a promising therapy for treatment of TBI.Entities:
Keywords: MMP-9; brain distribution; prodrug; traumatic brain injury
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Year: 2015 PMID: 26241578 PMCID: PMC5800744 DOI: 10.1021/acschemneuro.5b00140
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418