Date published: 2025-10-7

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SLIRP Inhibitors

SLIRP inhibitors belong to a class of chemical compounds that have garnered interest in the fields of molecular biology and pharmacology due to modulating specific cellular processes. SLIRP, or SRA stem-loop interacting RNA-binding protein, is a protein known for its interactions with specific types of RNA molecules, including non-coding RNAs. SLIRP is primarily localized within the mitochondria, the cellular organelles responsible for energy production and various metabolic processes. Within the mitochondria, SLIRP plays a crucial role in regulating the expression and stability of mitochondrial-encoded RNA molecules, which are essential for mitochondrial protein synthesis and function. SLIRP inhibitors are designed to interact with the active site or binding domain of the SLIRP protein, effectively inhibiting its function and influencing cellular processes dependent on SLIRP-mediated mitochondrial RNA regulation and mitochondrial function.

Structurally, SLIRP inhibitors are engineered to selectively target the active site or binding domains of SLIRP, ensuring high specificity for this particular RNA-binding protein within the mitochondria. By inhibiting SLIRP, these compounds may disrupt its role in mitochondrial RNA stability and expression, leading to alterations in mitochondrial protein synthesis and mitochondrial function. The study of SLIRP inhibitors is of significant interest to researchers as it provides insights into the regulatory mechanisms governing essential cellular functions related to mitochondrial biogenesis, metabolism, and energy production. This knowledge contributes to our understanding of basic cell biology and may have implications in various research areas, including mitochondrial diseases, cellular bioenergetics, and the molecular basis of conditions associated with mitochondrial dysfunction. However, further research is required to fully explore the extent of their applications and their impact on cellular physiology in the context of SLIRP-mediated mitochondrial RNA regulation.

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