Clb1 inhibitors are a class of chemical compounds that interfere with the function of Clb1, a cyclin protein involved in cell cycle regulation. Clb1, specifically in yeast models like Saccharomyces cerevisiae, is part of the family of B-type cyclins, which partner with cyclin-dependent kinases (CDKs) to drive the cell through different phases of the cell cycle, particularly from the G2 phase into mitosis. These inhibitors act by disrupting the interaction between Clb1 and its associated CDKs, thus preventing the activation of the kinase complex. This inhibition halts the phosphorylation of downstream substrates critical for cell division, effectively interrupting cell cycle progression. The precise mechanism of Clb1 inhibition may vary depending on the structural characteristics of the inhibitor, which could target the protein-binding domain of Clb1 or its interaction interface with CDKs.
The functional role of Clb1 is primarily to ensure proper cell cycle transitions, and its activity is tightly regulated to maintain cellular integrity and genomic stability. Clb1 levels fluctuate throughout the cell cycle, peaking as cells prepare for mitosis. The degradation of Clb1 at the end of mitosis is equally important to reset the cell for subsequent rounds of division. Inhibition of Clb1 disturbs this delicate balance, potentially leading to cell cycle arrest or an inability to properly execute mitotic events. Clb1 inhibitors, by modulating these processes, offer valuable tools for studying cell cycle regulation, helping researchers probe the complex molecular machinery that governs cellular division and proliferation. Understanding the structural interactions between Clb1 and its inhibitors further aids in dissecting the nuances of cell cycle checkpoints and the coordination of various cyclins and CDKs.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rimonabant Hydrochloride | 158681-13-1 | sc-212786 | 10 mg | $166.00 | 1 | |
Rimonabant is a selective CB1 antagonist, blocking the cannabinoid receptor's activation by endocannabinoids, thus reducing the psychoactive effects and appetite stimulation associated with CB1 activation. | ||||||
Org 27569 | 868273-06-7 | sc-204151 sc-204151A | 10 mg 50 mg | $167.00 $703.00 | ||
Org27569 is a CB1 receptor antagonist that competitively inhibits endocannabinoid binding, leading to the suppression of CB1-mediated effects and potential application in obesity and metabolic disorders. | ||||||
(±)-SLV 319 | 362519-49-1 | sc-222317 sc-222317A | 1 mg 5 mg | $30.00 $131.00 | ||
SLV319 is a selective CB1 receptor antagonist that hinders endocannabinoid binding, leading to the attenuation of CB1 receptor activation and suggesting potential use in obesity and related disorders. | ||||||
NESS 0327 | 494844-07-4 | sc-222054 sc-222054A | 1 mg 5 mg | $316.00 $1270.00 | 1 | |
NESS0327 is a CB1 receptor antagonist that interrupts endocannabinoid signaling by competitively inhibiting receptor binding, offering possibilities for managing obesity and metabolic disturbances. | ||||||