MELK inhibitors belong to a class of small-molecule compounds that specifically target the Maternal Embryonic Leucine Zipper Kinase (MELK) enzyme. MELK is a serine/threonine protein kinase that plays a significant role in various cellular processes, including cell cycle regulation, proliferation, and survival. Inhibitors of MELK have been developed to modulate its activity and investigate its function in cellular signaling pathways.
These inhibitors work by binding to the active site of the MELK enzyme, thereby interfering with its catalytic function and disrupting downstream signaling cascades that are regulated by MELK. By selectively inhibiting MELK, researchers aim to gain a better understanding of its physiological and pathological roles in different cellular contexts. The study of MELK inhibitors has contributed to advancements in the field of molecular biology and has shed light on the significance of MELK as a target in various diseases. Continued research in this area may lead to a deeper understanding of MELK's role in cellular biology and may uncover novel avenues for drug development and scientific exploration.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
BI6727 | 755038-65-4 | sc-364432 sc-364432A sc-364432B sc-364432C sc-364432D | 5 mg 50 mg 100 mg 500 mg 1 g | $150.00 $1050.00 $1665.00 $3329.00 $4382.00 | 1 | |
Volasertib is a potent inhibitor of Melk and other kinases involved in cell cycle regulation. It has shown activity against a broad range of cancer types and has been evaluated for acute myeloid leukemia (AML). | ||||||
CGP-60474 | 164658-13-3 | sc-507525 | 5 mg | $165.00 | ||
CGP60474 is a small molecule inhibitor of Melk. It has exhibited anticancer activity in research studies, particularly in combination with other anticancer agents. | ||||||
EHT 1864 | 754240-09-0 | sc-361175 sc-361175A | 10 mg 50 mg | $213.00 $889.00 | 12 | |
EHT 1864 is a selective inhibitor of Melk with potential anticancer activity. It has been shown to induce apoptosis and inhibit tumor growth in research models. | ||||||