The term LOC642361 Inhibitors designates a specialized class of chemical compounds engineered to modulate the activity of LOC642361, a molecular target currently under investigation in scientific research. These inhibitors are intricately designed through the principles of medicinal chemistry, focusing on selectively interfering with the normal functions of LOC642361 within cellular processes. The structural features of LOC642361 Inhibitors undergo a meticulous optimization process, involving computational modeling and structure-activity relationship studies, to refine their molecular configurations for precise binding to the target.
The significance of LOC642361 Inhibitors lies in their potential to disrupt the biochemical activities associated with LOC642361, a molecular entity believed to be involved in various biological pathways. Researchers in this field delve into the three-dimensional structure of LOC642361 and its binding interactions with inhibitors, aiming to unravel the intricate molecular mechanisms underlying inhibition. The study of LOC642361 Inhibitors contributes to a broader understanding of cellular processes, offering insights into the roles played by LOC642361 in diverse biological pathways and expanding our knowledge of the regulatory networks governing cellular activities. This research not only advances our comprehension of the molecular intricacies surrounding LOC642361 but also contributes to the broader scientific understanding of molecular targets and their involvement in fundamental cellular functions.
Items 1 to 10 of 12 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $90.00 $204.00 | 13 | |
Triptolide is known to inhibit the transcription of a wide range of genes by affecting RNA polymerase activity. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $58.00 $186.00 $94.00 | 21 | |
Camptothecin inhibits DNA topoisomerase I, which is necessary for DNA replication and transcription processes. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine is incorporated into RNA and DNA which can disrupt nucleic acid function and methylation patterns. | ||||||
Oxaliplatin | 61825-94-3 | sc-202270 sc-202270A | 5 mg 25 mg | $112.00 $394.00 | 8 | |
Oxaliplatin forms DNA adducts, which can interfere with DNA replication and transcription. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $51.00 $231.00 $523.00 | 63 | |
Etoposide inhibits DNA topoisomerase II, leading to DNA damage and potentially affecting transcription. | ||||||
Ellipticine | 519-23-3 | sc-200878 sc-200878A | 10 mg 50 mg | $145.00 $569.00 | 4 | |
Ellipticine intercalates into DNA and can inhibit various DNA-processing enzymes, affecting gene expression. | ||||||
Chetomin | 1403-36-7 | sc-202535 sc-202535A | 1 mg 5 mg | $186.00 $674.00 | 10 | |
Chetomin disrupts the structure of chromatin by binding to the chromatin remodeling factor, affecting transcription. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $218.00 $322.00 $426.00 | 7 | |
Decitabine is a DNA methyltransferase inhibitor, which can result in gene reactivation by hypomethylation. | ||||||
Harringtonin | 26833-85-2 | sc-204771 sc-204771A sc-204771B sc-204771C sc-204771D | 5 mg 10 mg 25 mg 50 mg 100 mg | $250.00 $367.00 $548.00 $730.00 $980.00 | 30 | |
Homoharringtonine inhibits protein synthesis at the initiation step, which can indirectly affect gene expression. | ||||||
Cyclopamine | 4449-51-8 | sc-200929 sc-200929A | 1 mg 5 mg | $94.00 $208.00 | 19 | |
Cyclopamine inhibits the Hedgehog signaling pathway, which could downregulate genes that are downstream targets. | ||||||