Date published: 2026-4-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

Krs Activators

Santa Cruz Biotechnology now offers a broad range of Krs Activators for use in various applications. Kinase-related serine/threonine kinases (Krs) are a subset of protein kinases that play a crucial role in regulating various cellular processes, including cell growth, differentiation, apoptosis, and response to external stimuli. These kinases are integral to many signaling pathways, influencing cellular behavior by phosphorylating specific substrates that drive downstream biological effects. Krs Activators are essential tools in scientific research, enabling researchers to selectively enhance the activity of these kinases to study their roles in cellular signaling networks. By activating Krs, scientists can investigate how these kinases modulate critical pathways involved in cell cycle control, stress responses, and developmental processes. These activators are widely used in molecular biology, biochemistry, and cell biology to dissect the mechanisms by which Krs influence cellular function and to explore their potential roles in disease states such as cancer and neurodegenerative disorders. Additionally, Krs Activators are valuable in drug discovery and development, providing insights into how modulating kinase activity could lead to novel scientific approaches for diseases characterized by dysregulated kinase signaling. The availability of these activators has significantly advanced research in various fields, offering critical tools for understanding the complex dynamics of kinase-mediated regulation in both health and disease. View detailed information on our available Krs Activators by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

MT-21

186379-49-7sc-221959
sc-221959A
10 mg
50 mg
$245.00
$872.00
(0)

MT-21 acts as a potent kappa opioid receptor (KOR) modulator, exhibiting a unique ability to engage in π-π stacking interactions with aromatic residues within the receptor binding site. This interaction stabilizes the ligand-receptor complex, leading to enhanced affinity and selectivity. The compound's rigid molecular framework contributes to its distinct binding kinetics, allowing for rapid receptor activation and subsequent downstream signaling cascades. Its amphiphilic nature may also affect membrane permeability and cellular uptake.