Assay Service for assessing ADME properties and in vivo PK properties with the selected vendor. ENAMINE US INC
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The Section on Medicinal Chemistry within the National Institutes of Health is seeking chemical reagent assay development and laboratory testing services from Enamine US Inc. This contract focuses on the development of grouped ADME assays and pharmacokinetic studies in C57BL6 mice to evaluate the translational potential of new molecular entities targeting metabolic and alcohol associated diseases. A primary component of this request is the Caco-2 Permeability Assay, which will be used to predict oral absorption potential by mimicking the human intestinal epithelium and analyzing passive diffusion, active transport, and efflux processes. The data generated from these services will inform structure-activity relationship optimization and help reduce transporter-related liabilities to improve bioavailability. This procurement is managed by the Department of Health and Human Services in Bethesda, Maryland, under solicitation number 75N98026Q01193ENAMINEUSINCPCANIAAA08396.
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Bethesda, MD, 20892, USASet-Aside
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Full Description
The Section on Medicinal Chemistry (SMC) develops new molecular entities with implications in improving health and treatment for various metabolic and alcohol associated diseases. To assess the translational potential of novel molecular entities, which would allow us to make decisions to proceed the compounds for further development we utilize multiple derisking assays. These assays comprise of both cell-based (in vitro) testing and then eventually in mice to assess pharmacokinetic parameters to see if the drug is orally available.
Request to procure Chemical Reagent (Assay) Development & Laboratory Testing Service SMC to produce grouped ADME assays and perform a Pharmacokinetic study in C57BL6 mice. By including the Caco-2 Permeability Assay in our ADME evaluation it'll accurately predict the oral absorption potential of our compounds. This well-established in vitro model closely mimics the human intestinal epithelium, providing critical insights into a compound’s passive diffusion, active transport, and efflux processes, such as those mediated by P-glycoprotein (P-gp). The data generated from this assay are vital for informing structure-activity relationship (SAR) optimization, improving compound permeability, and reducing transporter-related liabilities that could hinder bioavailability
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