EG665562 inhibitors are a class of chemical compounds known for their ability to selectively target and modulate the activity of the enzyme encoded by the EG665562 gene. This enzyme is involved in several cellular pathways, primarily those related to cellular signaling and metabolic regulation. The inhibitors work by binding to the enzyme's active site or allosteric sites, thereby altering its conformation and ultimately inhibiting its activity. Structurally, these inhibitors are characterized by a core scaffold that allows specific interactions with the enzyme, typically featuring aromatic rings, hydrogen bond donors and acceptors, and hydrophobic moieties. These features allow them to form strong, yet selective, interactions with their target enzyme, resulting in effective inhibition without significant off-target effects on other enzymes or proteins within the cell.
The design and development of EG665562 inhibitors are guided by structure-activity relationship (SAR) studies, which explore how modifications to the chemical structure influence the binding affinity and inhibitory potency. The inhibitors are optimized for high specificity, enabling them to effectively disrupt the enzyme's role in its associated pathways. Such specificity often depends on the precise spatial arrangement of functional groups within the inhibitor molecules, which are tailored to complement the enzyme's three-dimensional structure. Because the enzyme encoded by EG665562 is implicated in a variety of cellular processes, studying these inhibitors provides valuable insight into enzyme regulation and the broader biochemical pathways in which they participate. Additionally, understanding the detailed binding mechanisms and structural characteristics of EG665562 inhibitors aids in the exploration of chemical biology, offering a framework for investigating enzyme-ligand interactions and the molecular basis of enzyme inhibition.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Chloramphenicol | 56-75-7 | sc-3594 | 25 g | $53.00 | 10 | |
Binds to the 50S ribosomal subunit and inhibits peptidyl transferase activity. | ||||||
Erythromycin | 114-07-8 | sc-204742 sc-204742A sc-204742B sc-204742C | 5 g 25 g 100 g 1 kg | $56.00 $240.00 $815.00 $1305.00 | 4 | |
Binds to the 50S ribosomal subunit, blocking the exit of the growing peptide chain. | ||||||
Tetracycline | 60-54-8 | sc-205858 sc-205858A sc-205858B sc-205858C sc-205858D | 10 g 25 g 100 g 500 g 1 kg | $62.00 $92.00 $265.00 $409.00 $622.00 | 6 | |
Interacts with the 30S subunit, preventing the attachment of aminoacyl-tRNA to the mRNA-ribosome complex. | ||||||
Streptomycin sulfate | 3810-74-0 | sc-202821 sc-202821A | 10 g 100 g | $90.00 $128.00 | 12 | |
Binds to the 30S subunit, causing misreading of mRNA and inhibition of translocation. | ||||||
Puromycin | 53-79-2 | sc-205821 sc-205821A | 10 mg 25 mg | $163.00 $316.00 | 436 | |
Causes premature chain termination by acting as an analog of aminoacyl-tRNA. | ||||||
Clindamycin | 18323-44-9 | sc-337636A sc-337636B sc-337636C sc-337636 | 25 mg 50 mg 100 mg 1 g | $153.00 $367.00 $561.00 $809.00 | 2 | |
Binds to the 50S ribosomal subunit, inhibiting peptide bond formation. | ||||||
Anisomycin | 22862-76-6 | sc-3524 sc-3524A | 5 mg 50 mg | $97.00 $254.00 | 36 | |
Inhibits peptidyl transferase activity of the 60S ribosomal subunit. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Inhibits translocation step in protein synthesis on 80S ribosomes. | ||||||
Fusidic acid | 6990-06-3 | sc-215065 | 1 g | $292.00 | ||
Prevents the turnover of elongation factor G (EF-G) from the ribosome. | ||||||