Small molecule E (Sm E) inhibitors represent a diverse and essential class of chemical compounds utilized in biomedical research and drug discovery. These small molecules, characterized by their relatively low molecular weight, typically ranging from hundreds to a few thousand Daltons, play a pivotal role in the modulation of cellular processes. Sm E inhibitors achieve this by precisely interacting with and influencing the activities of specific enzymes or proteins within cells. The mechanisms of action employed by Sm E inhibitors vary widely, depending on their target. Some function as competitive inhibitors, binding to the active sites of enzymes and effectively obstructing their catalytic function by competing with the substrate. Others act as allosteric inhibitors, binding to regulatory sites on the enzyme and causing conformational changes that disrupt their activity.
Additionally, certain Sm E inhibitors may modify the enzyme's structure or function covalently, resulting in irreversible inhibition. This diversity in mechanisms allows Sm E inhibitors to be versatile tools, capable of targeting an array of cellular processes such as signal transduction pathways, metabolic pathways, and DNA replication or repair mechanisms. Researchers rely heavily on Sm E inhibitors in laboratory investigations. Their capacity to selectively modulate specific cellular targets provides invaluable insights into the fundamental biological processes underlying various diseases. Furthermore, their compact size and relative ease of synthesis make Sm E inhibitors essential for probing cellular functions and exploring new avenues for drug development.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
Inhibits tyrosine kinase activity, targeting the BCR-ABL fusion protein, studied in the research of leukemia. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $272.00 | 18 | |
Selective estrogen receptor modulator (SERM) that competes with estrogen for binding to estrogen receptors. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Multikinase inhibitor that targets Raf kinases and VEGFR. | ||||||
Aspirin | 50-78-2 | sc-202471 sc-202471A | 5 g 50 g | $20.00 $42.00 | 4 | |
Irreversibly inhibits cyclooxygenase (COX) enzymes, reducing prostaglandin production. | ||||||
Metformin | 657-24-9 | sc-507370 | 10 mg | $79.00 | 2 | |
Activates AMP-activated protein kinase (AMPK) to improve insulin sensitivity. | ||||||
Omeprazole | 73590-58-6 | sc-202265 | 50 mg | $67.00 | 4 | |
Proton pump inhibitor (PPI) that reduces gastric acid production by inhibiting the H+/K+ ATPase pump. | ||||||
Allopurinol | 315-30-0 | sc-207272 | 25 g | $131.00 | ||
Inhibits xanthine oxidase, reducing uric acid production. | ||||||
Warfarin | 81-81-2 | sc-205888 sc-205888A | 1 g 10 g | $73.00 $246.00 | 7 | |
Anticoagulant that interferes with vitamin K-dependent clotting factors, preventing blood clot formation. | ||||||
Ciprofloxacin | 85721-33-1 | sc-217900 | 1 g | $43.00 | 8 | |
Inhibits bacterial DNA gyrase, disrupting DNA replication and repair. | ||||||
Fluconazole | 86386-73-4 | sc-205698 sc-205698A | 500 mg 1 g | $54.00 $84.00 | 14 | |
Inhibits fungal cytochrome P450 enzymes, disrupting ergosterol synthesis. | ||||||