The chemical class 'Obox1 Inhibitors' encompasses a range of compounds that indirectly target Obox1 by influencing related transcriptional and post-transcriptional processes. This class includes inhibitors that affect RNA polymerase II, an enzyme critical for the transcription of DNA into mRNA, and is essential for the gene expression processes in which Obox1 is predicted to be involved. The inhibitors can be categorized based on their primary mechanism of action: direct inhibition of RNA polymerase II (e.g., Triptolide, α-Amanitin), inhibition of transcriptional regulators and co-factors (e.g., Flavopiridol, I-BET151, JQ1), and compounds that impact transcription indirectly through other mechanisms (e.g., Selinexor, CX-5461). The first category includes compounds like Triptolide and α-Amanitin, which bind directly to RNA polymerase II, blocking its transcriptional activity. This results in a broad reduction in mRNA synthesis, thereby affecting proteins like Obox1 that are involved in transcriptional regulation.
The second category comprises inhibitors of regulatory proteins like CDKs and BET bromodomains. These inhibitors disrupt the processes of transcription initiation and elongation, thus indirectly affecting the activity of transcription factors like Obox1. Lastly, compounds like Selinexor and CX-5461, although not directly targeting RNA polymerase II, influence transcriptional regulation by altering nuclear export or ribosomal RNA synthesis, respectively. Each inhibitor in this class plays a role in modulating the transcriptional landscape within a cell, potentially impacting the expression and function of Obox1. This indirect approach to targeting Obox1 is necessary due to the lack of direct chemical inhibitors for this specific protein. The inhibitors vary in specificity and breadth of action, ranging from highly specific to broadly acting compounds. Understanding the nuances of each inhibitor is crucial for their application in research, especially considering the complex nature of transcriptional regulation and the role of Obox1 in early development and various organ systems.
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| 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 a diterpene triepoxide known to inhibit RNA polymerase II. It achieves this by covalently modifying a subunit of the enzyme, leading to the suppression of transcriptional activity. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $269.00 $1050.00 | 26 | |
α-Amanitin is a cyclic peptide toxin that strongly inhibits RNA polymerase II. It binds to the enzyme, preventing the elongation phase of RNA synthesis. | ||||||
DRB | 53-85-0 | sc-200581 sc-200581A sc-200581B sc-200581C | 10 mg 50 mg 100 mg 250 mg | $43.00 $189.00 $316.00 $663.00 | 6 | |
DRB acts as an adenosine analogue, inhibiting RNA polymerase II by blocking the phosphorylation of the C-terminal domain of the largest subunit of RNA polymerase II. | ||||||
Flavopiridol Hydrochloride | 131740-09-5 | sc-207687 | 10 mg | $317.00 | ||
Flavopiridol inhibits cyclin-dependent kinases (CDKs) which are essential for the transcriptional regulation by RNA polymerase II. It blocks CDK9, impacting transcription elongation. | ||||||
I-BET 151 Hydrochloride | 1300031-49-5 (non HCl Salt) | sc-391115 | 10 mg | $450.00 | 2 | |
I-BET151 is a BET bromodomain inhibitor. It disrupts the function of BET proteins that regulate gene expression via RNA polymerase II, indirectly affecting transcription. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $231.00 $863.00 | 1 | |
JQ1 is another BET bromodomain inhibitor that functions similarly to I-BET151, impacting transcriptional regulation by interfering with BET protein-mediated chromatin remodeling. | ||||||
KPT 330 | 1393477-72-9 | sc-489062 | 5 mg | $173.00 | ||
Selinexor inhibits exportin 1 (XPO1), affecting nuclear export of RNA and proteins. This indirectly affects RNA polymerase II-mediated transcription regulation. | ||||||
CX-5461 | 1138549-36-6 | sc-507275 | 5 mg | $245.00 | ||
CX-5461 selectively inhibits RNA polymerase I, but also has secondary effects on RNA polymerase II. It interferes with the transcription of ribosomal RNA genes and can impact RNA Pol II indirectly. | ||||||
Pladienolide B | 445493-23-2 | sc-391691 sc-391691B sc-391691A sc-391691C sc-391691D sc-391691E | 0.5 mg 10 mg 20 mg 50 mg 100 mg 5 mg | $299.00 $5699.00 $11099.00 $25500.00 $66300.00 $2875.00 | 63 | |
Pladienolide B targets the spliceosome, affecting mRNA splicing. This can indirectly affect RNA polymerase II activity by altering mRNA processing. | ||||||
THZ1 | 1604810-83-4 | sc-507542 | 1 mg | $95.00 | ||
THZ1 is a covalent inhibitor of CDK7, which is part of the transcription complex involving RNA polymerase II. It inhibits transcription initiation and elongation. | ||||||