the current limited understanding of the precise functional roles and associated cellular pathways governed by LOC730098, researchers have identified a class of inhibitors dedicated to modulating its activity. The inhibitors within this class are intricately engineered molecules, each with a specific structure aimed at interacting with and influencing the function of LOC730098. The molecular interactions between LOC730098 Inhibitors and the target LOC730098 form the focal point of ongoing scientific investigations, incorporating methodologies from structural biology, medicinal chemistry, and computational modeling to decipher the intricate binding mechanisms and modes of action involved.
Structurally, LOC730098 Inhibitors are characterized by their unique molecular features, carefully designed to facilitate selective binding to LOC730098. This selectivity is crucial to minimize unintended effects on other cellular components, ensuring a targeted impact on the specific molecular entity. The development of inhibitors within this chemical class involves a comprehensive exploration of structure-activity relationships, optimization of pharmacokinetic properties, and a thorough understanding of the molecular mechanisms underlying LOC730098 function. As researchers delve deeper into the functional aspects of LOC730098 Inhibitors, the knowledge gained not only sheds light on the specific roles of LOC730098 but also contributes to the broader understanding of cellular processes and molecular regulation. The exploration of LOC730098 Inhibitors represents a significant avenue for expanding fundamental knowledge in molecular pharmacology and cellular biology.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
Actinomycin D binds to DNA and inhibits RNA polymerase, which can lead to decreased transcription of genes, potentially including LOC730098. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
Triptolide has been shown to inhibit the transcription of a broad range of genes by affecting RNA polymerase II activity, which could reduce LOC730098 levels. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
α-Amanitin binds to RNA polymerase II, blocking mRNA synthesis. This could lead to a decrease in LOC730098 expression if it is transcribed by this polymerase. | ||||||
Cordycepin | 73-03-0 | sc-203902 | 10 mg | $99.00 | 5 | |
Cordycepin (3'-deoxyadenosine) terminates mRNA elongation by inhibiting polyadenylation, potentially reducing LOC730098 mRNA levels. | ||||||
DRB | 53-85-0 | sc-200581 sc-200581A sc-200581B sc-200581C | 10 mg 50 mg 100 mg 250 mg | $42.00 $185.00 $310.00 $650.00 | 6 | |
DRB inhibits transcription elongation by RNA polymerase II, potentially leading to reduced expression of genes like LOC730098. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide inhibits eukaryotic protein synthesis by preventing ribosomal translocation, which could indirectly affect LOC730098 levels. | ||||||
Puromycin dihydrochloride | 58-58-2 | sc-108071 sc-108071B sc-108071C sc-108071A | 25 mg 250 mg 1 g 50 mg | $40.00 $210.00 $816.00 $65.00 | 394 | |
Puromycin causes premature chain termination during protein synthesis, potentially leading to reduced expression of proteins such as LOC730098. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Flavopiridol inhibits cyclin-dependent kinases, which may lead to downregulation of genes through affecting cell cycle-regulated transcription. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $226.00 $846.00 | 1 | |
JQ1 inhibits BET bromodomains, which can alter chromatin structure and reduce transcription of certain genes, possibly including LOC730098. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A is an inhibitor of histone deacetylases (HDACs) which can alter chromatin structure and downregulate gene expression. | ||||||