PAMR1 inhibitors are a class of chemical compounds designed to specifically target and modulate the activity of the PAMR1 protein, which stands for Peptidase Domain Containing Associated with Muscle Regeneration 1. PAMR1 is involved in various biological processes, including cell differentiation and muscle regeneration. It is predominantly expressed in skeletal muscle tissues and is thought to play a role in the regulation of extracellular matrix remodeling, particularly in tissues undergoing repair or regeneration. By inhibiting PAMR1, these compounds affect the protein's ability to mediate cellular and extracellular interactions that are critical for maintaining tissue integrity and regulating the regeneration processes.
The mechanisms through which PAMR1 inhibitors exert their effects can vary. These compounds may bind directly to the peptidase domain of PAMR1, thereby preventing its enzymatic activity, or they might interfere with the protein's interaction with other regulatory molecules in the muscle regeneration pathway. By modulating PAMR1 activity, researchers are able to investigate its precise role in cellular mechanisms, particularly those related to muscle tissue organization, growth, and regeneration. PAMR1 inhibitors also offer insights into how extracellular matrix components influence cell behavior, allowing for a deeper understanding of the molecular signals involved in tissue repair and maintenance. These inhibitors are valuable tools in basic research for dissecting the complex regulatory networks involved in cellular differentiation and tissue homeostasis, particularly within the context of muscle biology.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Olaparib | 763113-22-0 | sc-302017 sc-302017A sc-302017B | 250 mg 500 mg 1 g | $206.00 $299.00 $485.00 | 10 | |
Olaparib is a potent PARP1 inhibitor that binds to the catalytic site of PARP1, blocking the enzyme from repairing DNA damage, leading to synthetic lethality in BRCA-mutated cancer cells. It traps PARP1 on damaged DNA, hindering DNA repair. | ||||||
Rucaparib | 283173-50-2 | sc-507419 | 5 mg | $150.00 | ||
Rucaparib inhibits PARP1 by competitively binding to its catalytic domain, disrupting DNA repair. This can lead to the accumulation of DNA damage and cell death, particularly in cancer cells with BRCA mutations. | ||||||
Niraparib | 1038915-60-4 | sc-507492 | 10 mg | $150.00 | ||
Niraparib inhibits PARP1 by trapping it on DNA at sites of damage, blocking DNA repair. This mechanism selectively targets cancer cells with DNA repair deficiencies, such as BRCA-mutated cells. | ||||||
Talazoparib | 1207456-01-6 | sc-507440 | 10 mg | $795.00 | ||
Talazoparib inhibits PARP1 by trapping it on damaged DNA, preventing the repair of single-strand DNA breaks. This leads to the accumulation of DNA damage and cell death in cancer cells. | ||||||
Veliparib | 912444-00-9 | sc-394457A sc-394457 sc-394457B | 5 mg 10 mg 50 mg | $178.00 $270.00 $712.00 | 3 | |
Veliparib inhibits PARP1 by binding to its catalytic domain, impairing DNA repair in cancer cells. It is used in combination with chemotherapy to enhance the efficacy of therapy | ||||||