ST8Sia V Inhibitors are a class of chemical compounds engineered to interact with and modulate the activity of Sialyltransferase 8B (ST8Sia V), an enzyme critical in the biosynthesis of sialic acid-containing glycans. Sialic acids are a family of nine-carbon monosaccharides found on the terminal ends of glycan chains, which are essential components of cell surface glycoconjugates. ST8Sia V is specifically responsible for catalyzing the transfer of sialic acid to glycan structures in a highly regulated manner, contributing to the molecular diversity and functional complexity of cell surface molecules. Inhibitors developed to target ST8Sia V are designed with precision to selectively interact with this enzyme, allowing researchers to dissect the intricacies of glycan biosynthesis and uncover the specific roles played by sialic acids in cell-cell interactions and signaling.
The design of ST8Sia V inhibitors emphasizes their selectivity, ensuring that they interact exclusively with ST8Sia V and do not interfere with other enzymes or glycan biosynthetic processes. This selectivity is crucial in the realm of scientific research, as it enables scientists to investigate the distinct contributions of ST8Sia V in shaping the structural and functional properties of cell surface glycans. By employing ST8Sia V inhibitors, researchers can gain deeper insights into the molecular and cellular mechanisms underpinning glycan diversity and its implications for various biological processes, ranging from immune response modulation to cell adhesion and signaling. Understanding the intricacies of ST8Sia V's function and its control over sialic acid addition to glycans has far-reaching implications for our comprehension of cellular biology and its relevance to numerous physiological and pathological processes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Aspirin | 50-78-2 | sc-202471 sc-202471A | 5 g 50 g | $20.00 $42.00 | 4 | |
Irreversibly inhibits cyclooxygenase (COX) enzymes, reducing prostaglandin synthesis, thereby decreasing pain, inflammation, and fever. | ||||||
Omeprazole | 73590-58-6 | sc-202265 | 50 mg | $67.00 | 4 | |
Proton pump inhibitor that suppresses gastric acid production by inhibiting the H+/K+ ATPase enzyme in the stomach. | ||||||
Allopurinol | 315-30-0 | sc-207272 | 25 g | $131.00 | ||
Inhibits xanthine oxidase, reducing the production of uric acid, used in the management of gout and hyperuricemia. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
Selectively targets BCR-ABL tyrosine kinase, blocking the abnormal signaling pathway in chronic myeloid leukemia (CML) cells. | ||||||
Metformin | 657-24-9 | sc-507370 | 10 mg | $79.00 | 2 | |
Activates AMP-activated protein kinase (AMPK), which improves insulin sensitivity, lowers blood glucose, and is used to manage type 2 diabetes. | ||||||
Losartan | 114798-26-4 | sc-353662 | 100 mg | $130.00 | 18 | |
Blocks angiotensin II type 1 receptors, reducing blood vessel constriction and blood pressure, commonly prescribed for hypertension. | ||||||
Warfarin | 81-81-2 | sc-205888 sc-205888A | 1 g 10 g | $73.00 $246.00 | 7 | |
Inhibits vitamin K epoxide reductase, thus interfering with blood clotting by reducing the activation of vitamin K-dependent clotting factors. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $272.00 | 18 | |
An estrogen receptor antagonist, used for hormone-sensitive breast cancers by blocking the growth-promoting effects of estrogen. | ||||||
Donepezil | 120014-06-4 | sc-279006 | 10 mg | $74.00 | 3 | |
Enhances cholinergic neurotransmission by inhibiting acetylcholinesterase, improving cognitive function in Alzheimer's disease. | ||||||
Cimetidine | 51481-61-9 | sc-202996 sc-202996A | 5 g 10 g | $62.00 $86.00 | 1 | |
Blocks H2 histamine receptors in the stomach, reducing gastric acid secretion. | ||||||