cyclin A Inhibitors
Santa Cruz Biotechnology now offers a broad range of cyclin A Inhibitors. Drosophila cyclin A and B both regulate the cyclin dependent kinase cdc2 with cyclin A expression peaking in prophase, while cyclin B expression peaks until metaphase. cyclin A Inhibitors offered by Santa Cruz inhibit cyclin A and, in some cases, other cell cycle and cyclin dependent kinase related proteins. View detailed cyclin A Inhibitor specifications, including cyclin A Inhibitor CAS number, molecular weight, molecular formula and chemical structure, by clicking on the product name.
Items 1 to 10 of 23 total
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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 | |
Roscovitine is a selective inhibitor of cyclin-dependent kinases (CDKs), including CDK1 and CDK2. It competes with ATP for binding to the kinase's active site, leading to cell cycle arrest and inhibition of cell proliferation. | ||||||
RO-3306 | 872573-93-8 | sc-358700 sc-358700A sc-358700B | 1 mg 5 mg 25 mg | $65.00 $160.00 $320.00 | 37 | |
RO-3306 (CAS 872573-93-8) is a chemical compound known for its ability to inhibit cyclin A, a key protein involved in cell cycle regulation. This inhibition hampers the progression of the cell cycle, thereby affecting cellular processes without venturing into clinical applications. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
Staurosporine (CAS 62996-74-1) is a chemical compound that functions as a potent inhibitor of cyclin A, a key protein involved in cell cycle regulation. It has significant interactions with cellular processes, influencing cyclin A activity. | ||||||
Ro 31-8220 | 138489-18-6 | sc-200619 sc-200619A | 1 mg 5 mg | $90.00 $240.00 | 17 | |
Ro 31-8220 (CAS 138489-18-6) is a chemical compound that functions as a cyclin A inhibitor. It modulates cyclin A activity, impacting cell cycle processes. The compound's mechanism involves interaction with cyclin A, influencing cellular functions. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Flavopiridol inhibits CDKs, particularly CDK1, CDK2, CDK4, and CDK6. By binding to the ATP-binding site, it disrupts phosphorylation of key substrates involved in cell cycle progression, ultimately causing cell cycle arrest and apoptosis. | ||||||
Kenpaullone | 142273-20-9 | sc-200643 sc-200643A sc-200643B sc-200643C | 1 mg 5 mg 10 mg 25 mg | $60.00 $150.00 $226.00 $495.00 | 1 | |
Kenpaullone (CAS 142273-20-9) is a chemical compound that acts as a potent inhibitor of cyclin A. It interacts with key cellular processes, modulating cell cycle progression. Its mechanism of action influences cell behavior, making it a subject of scientific interest. | ||||||
SU 9516 | 377090-84-1 | sc-222330 sc-222330A | 5 mg 25 mg | $122.00 $383.00 | 3 | |
SU 9516 (CAS 377090-84-1) is a chemical compound known for its role as a cyclin A inhibitor. It affects cyclin A's function without involvement in clinical applications or therapeutic implications. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
Dexamethasone (CAS 50-02-2) is a chemical compound known for its role as an inhibitor of cyclin A, which is involved in cell cycle regulation. It influences cellular processes through its specific mechanism of action. | ||||||
10Z-Hymenialdisine | 82005-12-7 | sc-360987 | 500 µg | $210.00 | ||
10Z-Hymenialdisine (CAS 82005-12-7) is a chemical compound known for its role as an inhibitor of cyclin A, a crucial protein involved in cell cycle regulation. This compound's interaction with cyclin A interferes with certain cellular processes. | ||||||
AT7519 | 844442-38-2 | sc-364416 sc-364416A sc-364416B sc-364416C | 5 mg 10 mg 100 mg 1 g | $207.00 $246.00 $1025.00 $3065.00 | 1 | |
AT7519 is a multi-CDK inhibitor that targets CDK1, CDK2, CDK4, CDK5, and CDK9. By disrupting CDK-mediated phosphorylation, it halts cell cycle progression and impedes transcription, ultimately inducing cell cycle arrest and apoptosis. | ||||||