OMG inhibitors, short for Oligosaccharyltransferase (OST) Modulating Glycosylation inhibitors, represent a distinctive class of compounds within the realm of biochemistry and molecular biology. Central to their mechanism of action is the interference with the process of protein glycosylation, a crucial post-translational modification that involves the attachment of complex sugar moieties to nascent proteins in the endoplasmic reticulum.
Specifically, OMG inhibitors target the oligosaccharyltransferase enzyme complex, a key player in the glycosylation pathway responsible for transferring preassembled oligosaccharide chains onto target proteins. By modulating this enzymatic activity, OMG inhibitors exert a pronounced impact on the glycosylation status of proteins, influencing their folding, stability, and cellular functions.OMG inhibitors is rooted in the fundamental understanding of the intricate interplay between glycosylation and cellular processes. These inhibitors, through their targeted disruption of oligosaccharyltransferase function, hold the potential to unveil new insights into the regulation of protein maturation and trafficking. Moreover, the chemical class of OMG inhibitors serves as a valuable tool for researchers exploring the diverse roles of glycosylation in cellular physiology. As the scientific community continues to unravel the complexities of post-translational modifications, OMG inhibitors contribute to the expanding toolkit available for investigating the molecular intricacies that underlie cellular function and homeostasis.
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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 | |
Inhibits cyclooxygenase (COX) enzymes, reducing prostaglandin synthesis, and thus, inflammation and pain. | ||||||
Omeprazole | 73590-58-6 | sc-202265 | 50 mg | $67.00 | 4 | |
Proton pump inhibitor that reduces gastric acid secretion by inhibiting the H+/K+ ATPase pump in stomach parietal cells. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $94.00 $213.00 | 33 | |
Inhibits dihydrofolate reductase, blocking the synthesis of DNA, RNA, and proteins. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
Tyrosine kinase inhibitor targeting BCR-ABL. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $272.00 | 18 | |
Selective estrogen receptor modulator (SERM), competes with estrogen for binding to estrogen receptors in breast tissue. | ||||||
Captopril | 62571-86-2 | sc-200566 sc-200566A | 1 g 5 g | $49.00 $91.00 | 21 | |
Angiotensin-converting enzyme (ACE) inhibitor, blocks the conversion of angiotensin I to angiotensin II. | ||||||
Allopurinol | 315-30-0 | sc-207272 | 25 g | $131.00 | ||
Inhibits xanthine oxidase, reducing the conversion of purines to uric acid. | ||||||
Acyclovir | 59277-89-3 | sc-202906 sc-202906A | 50 mg 500 mg | $150.00 $940.00 | 2 | |
Guanosine analogue that inhibits viral DNA polymerase. | ||||||
Warfarin | 81-81-2 | sc-205888 sc-205888A | 1 g 10 g | $73.00 $246.00 | 7 | |
Vitamin K antagonist, interferes with the blood clotting process by inhibiting the activation of vitamin K-dependent clotting factors. | ||||||
Donepezil hydrochloride | 120011-70-3 | sc-218265 sc-218265A | 10 mg 100 mg | $97.00 $202.00 | 9 | |
Acetylcholinesterase inhibitor, increases acetylcholine levels in the brain. | ||||||