PHAX inhibitors belong to a class of chemical compounds that have garnered significant attention in the realm of molecular biology and cellular research. These inhibitors are specifically designed to target and modulate the activity of a protein known as PHAX, short for "Phosphorylated Adaptor for RNA Export." PHAX is a crucial component of the intricate machinery responsible for the transport of certain RNA molecules, such as small nuclear RNAs (snRNAs) and small nucleolar RNAs (snoRNAs), from the nucleus to the cytoplasm within eukaryotic cells. This transport process is essential for the proper functioning of various cellular activities, including the maturation and processing of ribosomal RNA and the splicing of pre-messenger RNAs.
The primary mode of action of PHAX inhibitors involves their interaction with PHAX, either directly or indirectly, to disrupt its normal function. By doing so, these inhibitors can interfere with the export of specific RNA molecules and consequently impact various cellular processes that rely on the timely and precise delivery of these RNAs. Researchers have been investigating PHAX inhibitors to gain insights into the fundamental mechanisms governing RNA export and processing within cells. Moreover, these compounds serve as valuable tools for dissecting the roles of PHAX and related proteins in cellular biology.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Imatinib mesylate | 220127-57-1 | sc-202180 sc-202180A | 25 mg 100 mg | $45.00 $111.00 | 61 | |
Inhibits BCR-ABL tyrosine kinase, blocking signaling in chronic myeloid leukemia. | ||||||
MDV3100 | 915087-33-1 | sc-364354 sc-364354A | 5 mg 50 mg | $245.00 $1051.00 | 7 | |
Blocks androgen receptor (AR) activation. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Targets RAF kinases and VEGFR/PDGFR, inhibiting angiogenesis in cancer. | ||||||
Raltegravir | 518048-05-0 | sc-364600 sc-364600A sc-364600B sc-364600C sc-364600D | 5 mg 50 mg 100 mg 500 mg 1 g | $100.00 $821.00 $1229.00 $2861.00 $4085.00 | 21 | |
Inhibits HIV-1 integrase, blocking viral DNA integration into the host genome. | ||||||
Allopurinol | 315-30-0 | sc-207272 | 25 g | $131.00 | ||
Decreases uric acid production by inhibiting xanthine oxidase, used in gout and hyperuricemia. | ||||||
Omeprazole | 73590-58-6 | sc-202265 | 50 mg | $67.00 | 4 | |
Proton pump inhibitor that reduces gastric acid production. | ||||||
Donepezil hydrochloride | 120011-70-3 | sc-218265 sc-218265A | 10 mg 100 mg | $97.00 $202.00 | 9 | |
Acetylcholinesterase inhibitor, increases acetylcholine levels in Alzheimer's disease therapy. | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $59.00 $173.00 | 15 | |
Calcium channel blocker that reduces calcium influx in cardiac muscle, used in hypertension and angina. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
Proteasome inhibitor, blocking protein degradation, employed in multiple myeloma and mantle cell lymphoma. | ||||||
Temozolomide | 85622-93-1 | sc-203292 sc-203292A | 25 mg 100 mg | $91.00 $255.00 | 32 | |
Alkylating agent that damages DNA, inhibiting cell division associated with glioblastoma multiforme. | ||||||