Transporters in drug discovery and development: Detailed by Yurong Lai

By Yurong Lai

Written through a number one researcher within the box, Transporters in drug discovery and improvement presents a complete and useful consultant to drug transporter households which are an important for drug discovery and improvement. It covers: an summary of transporter households and organ distribution; scientific suitable drug-drug interplay; scientific suitable polymorphism; drug transporter comparable pharmacokinetic, pharmacodynamics and toxicity; in vitro/in vivo probes of drug delivery stories; the sensible methodologies of business transporter screening and translational point in drug discovery and advancements.

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By Yurong Lai

Written through a number one researcher within the box, Transporters in drug discovery and improvement presents a complete and useful consultant to drug transporter households which are an important for drug discovery and improvement. It covers: an summary of transporter households and organ distribution; scientific suitable drug-drug interplay; scientific suitable polymorphism; drug transporter comparable pharmacokinetic, pharmacodynamics and toxicity; in vitro/in vivo probes of drug delivery stories; the sensible methodologies of business transporter screening and translational point in drug discovery and advancements.

Show description

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Corneal dystrophy associated with teenage perceptive deafness 2. Congenital hereditary endothelial dystrophy of the cornea 2 3.

Mrp2/Abcc2. , 2005). These proteins function in the transport of a wide variety of substrates, such as metabolic products, lipids, sterols and drugs, across biological membranes. Although the homeostatic function usually results in the protection of the body against harmful cytotoxic and xenobiotic compounds, this process is usually counterproductive when drug treatment is pursued to treat disease. For example, during chemotherapy, efflux transporters such as MRP1 or P-gp can be an obstacle to drug exposure if the given drugs are substrates for the protein.

1993). The very long-chain fatty acids that accumulate in the body are toxic to the adrenal cortex and the myelin membranes that protect the nerves in the brain and spinal cord. , 2010). , 1986). , 1996). Belonging to ABC subfamily D, the ABCD1, 2 and 3 genes encode half transporters that require a partner half transporter to form a functional homodimeric or heterodimeric protein. , 1996). , 2011). , 2005; Van Veldhoven, 2010). ABCG5 and ABCG8: sitosterolemia Sitosterolemia, also called phytosterolemia, is a rare autosomal recessive lipid metabolic disorder.

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