SmarcAL1 inhibitors represent a distinctive class of chemical compounds designed to target the SWI/SNF (switch/sucrose non-fermentable) chromatin remodeling complex. The SWI/SNF complex plays a pivotal role in regulating gene expression by modulating chromatin structure, making it a critical determinant in cellular processes such as proliferation, differentiation, and DNA repair. SmarcAL1, a specific subunit of the SWI/SNF complex, has garnered attention as a potential target for intervention due to its involvement in the maintenance of chromatin architecture and gene transcription.
SmarcAL1 inhibitors are characterized by their ability to selectively bind to the SmarcAL1 subunit, impeding its function within the SWI/SNF complex. This inhibition results in the modulation of chromatin remodeling activities, ultimately influencing the expression of genes associated with various cellular functions. The development of SmarcAL1 inhibitors involves a meticulous design process, aiming to achieve high specificity and affinity for the target subunit while minimizing off-target effects. Researchers utilize structural biology techniques, medicinal chemistry principles, and computational modeling to optimize the chemical structures of these inhibitors, ensuring their efficacy in disrupting SmarcAL1-mediated chromatin remodeling. As a burgeoning field within chemical biology, the study of SmarcAL1 inhibitors holds promise for unraveling the intricacies of chromatin dynamics and may pave the way for innovative strategies in the modulation of gene expression for future scientific investigations.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ceralasertib | 1352226-88-0 | sc-507439 | 10 mg | $573.00 | ||
AZD6738 inhibits ATR kinase which is involved in the DNA damage response and can modulate the activity of proteins related to DNA repair, including SmarcAL1. | ||||||
VE 821 | 1232410-49-9 | sc-475878 | 10 mg | $360.00 | ||
VE-821 is another ATR inhibitor that can perturb the DNA damage response pathway, thereby influencing the functional context of SmarcAL1. | ||||||
NU 7441 | 503468-95-9 | sc-208107 | 5 mg | $357.00 | 10 | |
NU7441 is a DNA-dependent protein kinase (DNA-PK) inhibitor, which can disrupt DNA repair mechanisms where SmarcAL1 is operative. | ||||||
ATM Kinase Inhibitor | 587871-26-9 | sc-202963 | 2 mg | $110.00 | 28 | |
This ATM Kinase Inhibitor affects the DNA damage repair pathway, potentially altering the cellular environment of SmarcAL1. | ||||||
MRN-ATM Pathway Inhibitor, Mirin | 299953-00-7 | sc-203144 | 10 mg | $141.00 | 4 | |
Mirin inhibits the Mre11-Rad50-Nbs1 (MRN) complex, which is involved in DNA repair processes and therefore can affect the functional landscape of SmarcAL1. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Wortmannin is a PI3K inhibitor that also inhibits DNA-PK and ATM, all of which are integral to pathways SmarcAL1 is associated with. | ||||||
ETP-46464 | 1345675-02-6 | sc-497432 | 10 mg | $550.00 | ||
ETP-46464 is a small molecule inhibitor of the MRN complex, similar to Mirin, and can indirectly alter SmarcAL1 activities by affecting its associated DNA repair pathways. | ||||||
ATM/ATR Kinase Inhibitor Inhibitor | 905973-89-9 | sc-202964 | 5 mg | $106.00 | 8 | |
CGK733 inhibits both ATM and ATR kinases, possibly changing the conditions that influence SmarcAL1 activity. | ||||||
PF 477736 | 952021-60-2 | sc-362781 sc-362781A | 5 mg 25 mg | $115.00 $431.00 | ||
This compound is a checkpoint kinase inhibitor, affecting the cell cycle checkpoint machinery and potentially the role of SmarcAL1 within it. | ||||||
BML-277 | 516480-79-8 | sc-200700 sc-200700A | 10 mg 50 mg | $132.00 $492.00 | 2 | |
By inhibiting Chk2, this chemical can impact the DNA damage signaling cascade that may modulate SmarcAL1's function. | ||||||