MCC inhibitors refer to compounds that target and inhibit the activity of the mitotic checkpoint complex (MCC), a crucial component involved in regulating the cell cycle during mitosis. The MCC functions as a safeguard to ensure accurate chromosome segregation by preventing the premature progression from metaphase to anaphase until all chromosomes are correctly aligned on the mitotic spindle. It achieves this by inhibiting the anaphase-promoting complex/cyclosome (APC/C), a key ubiquitin ligase responsible for marking specific proteins for degradation, thereby controlling the metaphase-anaphase transition. MCC is composed of several key proteins, including Mad2, BubR1 (or Bub1), Bub3, and Cdc20, which together form a regulatory network ensuring the proper timing of anaphase onset. When MCC is active, it binds to and inhibits APC/C, thus delaying cell cycle progression until chromosomal alignment is achieved.
The inhibition of MCC activity is of interest due to its potential to disrupt the precise timing mechanisms involved in cell cycle control, particularly in mitosis. By inhibiting MCC, the checkpoint that halts the transition to anaphase is disabled, allowing premature progression through mitosis even if the chromosomes are not properly aligned. This can lead to aneuploidy, where cells have abnormal numbers of chromosomes, a phenomenon closely linked to genomic instability. MCC inhibitors typically function by interfering with the formation of the MCC complex or by preventing its interaction with APC/C, which disturbs the regulatory control of mitosis. These inhibitors are also of interest to researchers studying cell cycle regulation and the mechanisms that ensure genetic fidelity during cell division, as perturbations in these processes can illuminate key aspects of mitotic control and checkpoint signaling pathways.
VEJA TAMBÉM
Nome do Produto | CAS # | Numero de Catalogo | Quantidade | Preco | Uso e aplicacao | NOTAS |
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Doxycycline-d6 | 564-25-0 unlabeled | sc-218274 | 1 mg | $16500.00 | ||
As tetraciclinas podem inibir algumas MMPs e são por vezes utilizadas como inibidores de MCC de largo espetro. | ||||||
Marimastat | 154039-60-8 | sc-202223 sc-202223A sc-202223B sc-202223C sc-202223E | 5 mg 10 mg 25 mg 50 mg 400 mg | $165.00 $214.00 $396.00 $617.00 $4804.00 | 19 | |
Um inibidor sintético da MCC que foi um dos primeiros a ser desenvolvido para utilização clínica. Inibe múltiplas MMPs e tem sido estudado na terapia do cancro. | ||||||
Batimastat | 130370-60-4 | sc-203833 sc-203833A | 1 mg 10 mg | $175.00 $370.00 | 24 | |
Outro inibidor sintético precoce da MCC, que tem sido investigado pelo seu potencial na investigação do cancro. | ||||||
GM 6001 | 142880-36-2 | sc-203979 sc-203979A | 1 mg 5 mg | $75.00 $265.00 | 55 | |
Um inibidor de MCC de largo espetro que pode inibir várias MMPs e é utilizado em contextos de investigação. | ||||||
Prinomastat | 192329-42-3 | sc-507449 | 5 mg | $190.00 | ||
Um inibidor da MCC com seletividade para MMPs específicas, incluindo MMP-2 e MMP-9. | ||||||
PD166793 | 199850-67-4 | sc-202709 | 5 mg | $147.00 | 6 | |
Um inibidor seletivo da MMP-2. | ||||||
ARP 100 | 704888-90-4 | sc-203522 | 5 mg | $121.00 | 26 | |
Um inibidor com seletividade para MMP-2 e MMP-9. | ||||||
SB-3CT | 292605-14-2 | sc-205847 sc-205847A | 1 mg 5 mg | $100.00 $380.00 | 15 | |
Seletivo para MMP-2 e MMP-9, com potenciais aplicações no cancro e em doenças inflamatórias. | ||||||
MMP Inhibitor V | 223472-31-9 | sc-203139 | 2 mg | $216.00 | 2 | |
Um inibidor seletivo da MMP-9, que tem sido explorado pelo seu potencial em doenças que envolvem remodelação de tecidos e inflamação. |