The RAC Beta Serine/Threonine Protein Kinase pipeline drugs market research report outlays comprehensive information on the RAC Beta Serine/Threonine Protein Kinase 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 RAC Beta Serine/Threonine Protein Kinase 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, Hematological Disorders, Non Malignant Disorders, and Undisclosed which include the indications Solid Tumor, Endometrial Cancer, Sickle Cell Disease, Proteus Syndrome, and Unspecified Rare Disease. It also reviews key players involved in RAC Beta Serine/Threonine Protein Kinase targeted therapeutics development with respective active and dormant or discontinued products.
The RAC Beta Serine/Threonine Protein Kinase pipeline targets constitutes close to nine molecules. Out of which, approximately seven molecules are developed by companies and the remaining by the universities/institutes. The molecules developed by companies in Pre-Registration, Phase III, Phase II, and Preclinical stages are 1, 1, 3, and 2 respectively. Similarly, the universities portfolio in Phase I, and Preclinical comprises 1, and 1 molecule.
RAC Beta Serine/Threonine Protein Kinase overview
RAC-beta serine/threonine-protein kinase is an enzyme encoded by the AKT2 gene. It plays a role as key modulator of the AKT-mTOR signaling pathway controlling the tempo of the process of newborn neurons integration during adult neurogenesis, including correct neuron positioning, dendritic development and synapse formation. AKT2 is also specifically involved in skeletal muscle differentiation, one of its substrates in this process being ANKRD2.
For a complete picture of RAC Beta Serine/Threonine Protein Kinase’s drug pipeline, buy the report here.
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