The Cystine/Glutamate Transporter pipeline drugs market research report outlays comprehensive information on the Cystine/Glutamate Transporter targeted therapeutics, complete with analysis by indications, stage of development, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses the drugs in the Cystine/Glutamate Transporter pipeline by therapy areas, indications, stages, MoA, RoA, molecule type and the key players in the development pipeline. Buy the report here.
The report also covers products from therapy areas such as Oncology, and Central Nervous System which include the indications Breast Cancer, Lung Cancer, Substance (Drug) Abuse, and Trichotillomania. It also reviews key players involved in Cystine/Glutamate Transporter targeted therapeutics development with respective active and dormant or discontinued products.
The Cystine/Glutamate Transporter pipeline targets constitutes close to seven molecules. Out of which, approximately four molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Phase II, Preclinical, and Discovery stages are 1, 1, and 2 respectively. Similarly, the universities portfolio in Preclinical, and Discovery comprises 1, and 1 molecule.
Cystine/Glutamate Transporter overview
Cystine/glutamate transporter (SLC7A11) is a member of a heteromeric, sodium-independent, anionic amino acid transport system that is highly specific for cysteine and glutamate. SLC7A11 functions as an antiporter by mediating the exchange of extracellular anionic L-cystine and intracellular L-glutamate across the cellular plasma membrane. Also, provides L-cystine for the maintenance of the redox balance between extracellular L-cystine and L-cysteine and for the maintenance of the intracellular levels of glutathione that is essential for cells protection from oxidative stress.
For a complete picture of Cystine/Glutamate Transporter’s drug pipeline, buy the report here.
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