Cyclin M2 inhibitors are a category of chemical agents specifically designed to interact with and inhibit the function of cyclin M2, a protein that belongs to the cyclin family. Cyclins are a group of regulatory proteins that control the progression of cells through the cell cycle by activating cyclin-dependent kinases (CDKs), and cyclin M2 is presumed to be involved in these regulatory processes. The role of cyclin M2 is less characterized compared to other cyclins, but like its counterparts, it is believed to play a role in the complex orchestration of cellular proliferation. Inhibitors of cyclin M2 would bind to the protein, impeding its ability to associate with its CDK partners or inhibit its function by other mechanisms. This interference with the normal function of cyclin M2 can affect the progression of the cell cycle and the subsequent cellular functions that depend on the precise timing and regulation of cell division and growth.
The development of inhibitors targeting cyclin M2 involves intricate chemical design to ensure specificity and efficacy. Cyclin M2 inhibitors must be able to discriminate between the targeted cyclin and other members of the cyclin family to minimize off-target effects and maximize the desired interaction. This is challenging due to the conserved nature of the cyclin family's structure and function. The inhibitors may be small molecules or larger peptide-based entities that are capable of interacting with cyclin M2 with high affinity. The mode of action of these inhibitors can vary; some may block the interaction sites between cyclin M2 and its CDK partners, while others might allosterically modulate the cyclin's structure, rendering it inactive.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Roscovitine | 186692-46-6 | sc-24002 sc-24002A | 1 mg 5 mg | $92.00 $260.00 | 42 | |
Inhibits cyclin-dependent kinases (CDKs), which can prevent activation of cyclin/CDK complexes that may include cyclin M2. | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $315.00 | ||
Selectively inhibits CDK4/6, potentially altering the activity of cyclin M2 if it interacts with these CDKs. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Inhibits CDKs broadly, which could affect cyclin M2 function if it is dependent on CDK interaction for its activity. | ||||||
AG14361 | 328543-09-5 | sc-483192 | 5 mg | $255.00 | ||
Inhibits CDK9, potentially impacting transcription regulation that cyclin M2 may be involved in. | ||||||
Dinaciclib | 779353-01-4 | sc-364483 sc-364483A | 5 mg 25 mg | $242.00 $871.00 | 1 | |
Inhibits multiple CDKs, which could alter cyclin M2's role in cell cycle regulation if it is part of CDK complexes. | ||||||
SNS-032 | 345627-80-7 | sc-364621 sc-364621A | 5 mg 10 mg | $169.00 $262.00 | ||
Targets CDKs 2, 7, and 9, which can affect cyclin M2 if it is involved in signaling pathways regulated by these kinases. | ||||||
AZD 5438 | 602306-29-6 | sc-361115 sc-361115A | 10 mg 50 mg | $205.00 $865.00 | ||
Inhibits CDKs 1, 2, and 9, potentially affecting cyclin M2 activity in cell cycle progression and transcription regulation. | ||||||
Purvalanol B | 212844-54-7 | sc-361300 sc-361300A | 10 mg 50 mg | $199.00 $846.00 | ||
Inhibits CDK1, 2, and 5, which could influence cyclin M2 activity if it is associated with these kinases in cell cycle control. | ||||||
AT-7519 Hydrochloride | 902135-91-5 | sc-482715 | 5 mg | $125.00 | ||
Inhibits multiple CDKs, which can affect cyclin M2 activity in various phases of the cell cycle. | ||||||
Olomoucine | 101622-51-9 | sc-3509 sc-3509A | 5 mg 25 mg | $72.00 $274.00 | 12 | |
Inhibits CDK1, 2, and 5, which could affect cyclin M2 if it is involved in cell cycle regulation mediated by these kinases. | ||||||