"Doc 4 Inhibitors," short for "Downstream of C kinase 4 Inhibitors," constitute a distinctive class of chemical compounds that have garnered significant attention in the field of molecular pharmacology. These inhibitors are specifically designed to target and modulate the activity of the Downstream of C kinase 4 (Doc 4) enzyme. Doc 4, an integral component of cellular signaling pathways, plays a pivotal role in the regulation of various cellular processes and functions. The inhibitors belonging to this class interact with the active site of the Doc 4 enzyme, impeding its enzymatic activity and subsequent downstream signaling cascades. Structurally, Doc 4 Inhibitors encompass a diverse array of chemical entities, each exhibiting unique interactions with the active site of the Doc 4 enzyme. Through intensive structure-activity relationship studies, researchers have elucidated the key structural motifs necessary for effective binding and inhibition.
The binding interaction between the inhibitor and the active site of the Doc 4 enzyme often involves hydrogen bonding, hydrophobic interactions, and electrostatic forces, thereby ensuring the specificity and potency of the inhibition. Given the centrality of the Doc 4 enzyme in several vital signaling pathways, the development of inhibitors targeting this enzyme class has generated considerable interest for their potential in modulating cellular responses. Research efforts have been directed towards optimizing the pharmacokinetic and pharmacodynamic properties of Doc 4 Inhibitors, aiming to enhance their bioavailability, metabolic stability, and target selectivity. Ongoing studies continue to explore the potential applications of Doc 4 Inhibitors in various contexts, harnessing their inhibitory prowess to dissect cellular processes and uncover novel avenues for modulation.
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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 | |
Irreversible inhibition of COX enzymes, reducing prostaglandin production and inhibiting platelet aggregation. | ||||||
Omeprazole | 73590-58-6 | sc-202265 | 50 mg | $67.00 | 4 | |
Proton pump inhibitor that covalently binds to the H+/K+ ATPase in gastric parietal cells, reducing acid secretion. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
BCR-ABL tyrosine kinase inhibitor. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Inhibits multiple kinases including RAF and VEGFR, blocking cell proliferation and angiogenesis in cancer. | ||||||
Allopurinol | 315-30-0 | sc-207272 | 25 g | $131.00 | ||
Xanthine oxidase inhibitor, decreasing uric acid production. | ||||||
Donepezil | 120014-06-4 | sc-279006 | 10 mg | $74.00 | 3 | |
Acetylcholinesterase inhibitor, raising acetylcholine levels to improve cognitive function in Alzheimer's disease. | ||||||
Ritonavir | 155213-67-5 | sc-208310 | 10 mg | $124.00 | 7 | |
Protease inhibitor preventing viral maturation in HIV by inhibiting the viral protease enzyme. | ||||||
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $156.00 | 5 | |
BTK kinase inhibitor, disrupting B-cell receptor signaling. | ||||||