The global market for protein kinase c beta (PKC-Beta) Inhibitors is increasing significantly. This increase in the market is majorly due to high efficacy of treatment for diabetes, cardiac disorder, cancer, and others has increased the scope for protein kinase c beta inhibitors. The advantage of long acting, specific and effective treatment of the diseases has increased the preference for protein kinase c beta inhibitors market.
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The protein kinase c beta molecules are serine/threonine protein kinases, that perform a significant function in numerous cellular functions such as gene expression, hormone secretion, and cell growth and differentiation. The protein kinase – C (PKC) molecules are integrated into several important signal transduction pathways stimulated by a wide range of growth factors like GPCRs. These PKC enzyme are calcium and lipid sensitive. The phospholipase C enzymes hydrolyze phosphatidylinositol 4, 5-bisphosphate (PIP2) to produce membrane bound Di-acyl glycerol (DAG), which in turn activates inositol trisphosphate (IP3) and protein kinase c (PKC), which leads to mobilization of intracellular calcium. Protein kinase c (PKC) is expressed in most of the tissues and various protein kinase c (PKC) sub-families are expressed in the single cell.
The protein kinase c (PKC) beta inhibitors are available in two conventional isoforms, PKC-beta I and PKC-beta II with C1 domain. PKCβ1 (PRKCB) situated on chromosome 16p11.2. It comprises 17 exons. The PKCβ1 isoform is comparatively short amongst the two isoforms. It included two alternatively spliced mRNAs and it results from use of an alternating splice site at the 5′-end of the terminal exon. Both the PKCβ1 and PKCβ2 isoform has different C-terminus. It includes 671 amino acid proteins and is involved in B cell activation, endothelial cell proliferation, and endothelial cell proliferation. It also includes intestinal carbohydrate absorption, immediate stress. The protein kinase c PKCβ2/ PRKCB are situated on chromosome 16p11.2 which is composed of 17 exons, 673 amino acid proteins and with two alternatively spliced mRNAs. The PKCβ2 isoform is comparatively the longer isoform.
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The Protein Kinase C Beta (PKC-Beta) Inhibitors market can be segmented into by therapy, by route of administration, by drug class and by geography. In the terms of therapy, the Protein Kinase C Beta (PKC-Beta) Inhibitors is classified into monotherapy and combination therapy. The combination therapy offers a wide therapeutic range, thus the segment is showing high acceptance. Several protein kinase C beta (PKC-Beta) inhibitors are still in drug pipeline. However, few drugs in phase 3 clinical trials has shown a promising results against the diabetes indication.
Based on specificity and selectivity of drug action, the protein kinase C beta (PKC-Beta) inhibitors are classified. According to drug class, protein kinase C beta (PKC-Beta) inhibitors can be classified as Phorbol esters, Indolocarbazole, Macrocyclic lactones, Nonsteroidal anti-oestrogen and others.
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Based on the route of administration, several protein kinase C beta (PKC-Beta) inhibitors market is classified into intravenous, oral and others. Due to high safety, oral administration has been the preferred choice of option for the patient.
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