DBC1 Activators encompass a diverse group of chemical compounds known for their ability to directly enhance the functional activity of the DBC1 protein. DBC1, or Deleted in Breast Cancer 1, is a crucial player in cellular processes involving DNA repair, apoptosis, and gene expression regulation. One notable activator within this class is Resveratrol, a natural polyphenol. Resveratrol acts by modulating the SIRT1 pathway. It effectively activates SIRT1, a deacetylase enzyme that targets DBC1. As a result of this activation, SIRT1 deacetylates DBC1, increasing its binding affinity for various protein partners. This enhanced interaction amplifies DBC1's role in DNA repair mechanisms and apoptotic pathways. Quercetin, a flavonoid, indirectly activates DBC1 by inhibiting CD38, an enzyme that consumes NAD+. This inhibition leads to elevated cellular NAD+ levels, further stimulating SIRT1, which promotes DBC1 deacetylation, strengthening its participation in DNA damage repair and gene expression control.
Another member of the DBC1 Activators is Nicotinamide, which has a unique mechanism. Nicotinamide inhibits SIRT1, causing an accumulation of acetylated DBC1. Surprisingly, this acetylation increase makes DBC1 a more effective inhibitor of other proteins like PARP1 involved in DNA repair processes. These DBC1 Activators, by influencing DBC1's interactions within specific cellular pathways, offer valuable tools to enhance DBC1's functional activity. They play a pivotal role in maintaining genomic integrity, regulating gene expression, and promoting efficient DNA repair, all of which are essential processes for cellular health and survival.
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