Date published: 2025-10-15

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Calcitonin Inhibitors

Santa Cruz Biotechnology now offers a broad range of Calcitonin Inhibitors for use in various applications. Calcitonin Inhibitors are essential tools for studying the function and regulation of calcitonin, a hormone known for its role in calcium and bone metabolism. By specifically inhibiting calcitonin activity, researchers can investigate its effects on calcium homeostasis and bone resorption, providing insights into the complex regulatory mechanisms involved. In scientific research, Calcitonin Inhibitors are used to explore the downstream effects of calcitonin inhibition on cellular processes such as osteoclast activity, bone formation, and calcium signaling pathways. Researchers employ these inhibitors to study the molecular mechanisms by which calcitonin interacts with its receptor and influences various signaling cascades. Additionally, Calcitonin Inhibitors are valuable in high-throughput screening assays aimed at identifying new modulators of calcitonin activity, facilitating the discovery of novel regulatory pathways and potential research targets. The use of Calcitonin Inhibitors supports the development of experimental models to dissect the intricate interactions between calcitonin and other hormones or signaling molecules involved in bone and calcium metabolism. By enabling precise control over calcitonin activity, these inhibitors facilitate detailed studies of calcitonin's role in cellular physiology. View detailed information on our available Calcitonin Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

SB 268262

217438-17-0sc-362793
sc-362793A
10 mg
50 mg
$199.00
$849.00
(0)

SB 268262 functions as a calcitonin analog, showcasing unique interactions with calcitonin receptors through specific conformational changes that enhance binding affinity. Its structural design promotes effective dimerization, influencing downstream signaling pathways. The compound's hydrophilic regions facilitate solvation, while its distinct stereochemistry allows for selective engagement with target proteins, modulating physiological responses. This specificity in receptor interaction underscores its potential for nuanced biological activity.