Bone Morphogenetic Proteins (BMPs) are a group of growth factors originally identified by their ability to induce bone formation, and they belong to the Transforming Growth Factor-beta (TGF-β) superfamily. Among BMPs, BMP2 is a critical member known to play vital roles in various biological processes. It mediates a multitude of cellular activities, from cell differentiation to apoptosis, largely depending on the cellular context and its interaction with other molecules. However, the activities of BMP2, like many other proteins, need to be precisely regulated to ensure proper cellular function and to prevent aberrant signaling pathways that could lead to undesired outcomes. This is where BMP2 inhibitors come into play.
BMP2 inhibitors are molecules that specifically prevent or reduce the activity of BMP2. The inhibition can be achieved through various mechanisms, such as blocking the binding of BMP2 to its receptors, interfering with its interaction with other proteins, or inhibiting its downstream signaling pathways. These inhibitors can be naturally occurring proteins or synthetic molecules. Some well-known natural BMP2 inhibitors include Noggin, Chordin, and Follistatin. These proteins can bind directly to BMP2, thereby preventing it from interacting with its receptors and executing its biological functions. On the molecular front, understanding the intricate mechanisms by which these inhibitors regulate BMP2 is crucial for comprehending the broader BMP signaling network and its roles in various biological processes. The study of BMP2 inhibitors not only adds layers to our knowledge of cellular regulation but also uncovers the intricacies of molecular interactions within the cell.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-(6-(4-(Piperazin-1-yl)phenyl)pyrazolo[1,5-a]pyrimidin-3-yl)quinoline | 1062368-24-4 | sc-476297 | 5 mg | $240.00 | ||
Potent and selective BMP type I receptor inhibitor targeting ALK2, ALK3, and ALK6, preventing downstream phosphorylation of SMAD proteins, disrupting BMP signal transduction. | ||||||
BML-275 | 866405-64-3 | sc-200689 sc-200689A | 5 mg 25 mg | $96.00 $355.00 | 69 | |
Initially identified as an AMPK inhibitor; inhibits BMP type I receptors ALK2, ALK3, and ALK6, preventing BMP-induced SMAD1/5/8 phosphorylation. | ||||||
LDN-214117 | 1627503-67-6 | sc-507451 | 5 mg | $165.00 | ||
Closely related to LDN-193189, selectively inhibits ALK2, impeding the BMP signaling pathway. | ||||||
DMH-1 | 1206711-16-1 | sc-361171 sc-361171B sc-361171A sc-361171C | 10 mg 25 mg 50 mg 100 mg | $213.00 $318.00 $632.00 $1047.00 | 2 | |
Selectively targets BMP type I receptors, particularly ALK2, preventing the phosphorylation of downstream SMAD proteins. | ||||||
K02288 | 1431985-92-0 | sc-488981 | 5 mg | $330.00 | ||
ATP-competitive inhibitor targeting ALK1, ALK2, and ALK3, disrupting BMP-mediated SMAD1/5/8 phosphorylation. | ||||||
LDN 193719 | 1062368-49-3 | sc-489383 | 10 mg | $189.00 | ||
Selective BMP type I receptor inhibitor, particularly targeting ALK1 and ALK2, suppressing BMP2 signaling. | ||||||
EW-7197 | 1352608-82-2 | sc-507465 | 5 mg | $345.00 | ||
Primarily an ALK5 inhibitor but also inhibits ALK2, blocking BMP2 signaling alongside TGF-β signaling. | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $82.00 $216.00 $416.00 | 48 | |
Primarily an inhibitor of the TGF-β type I receptor ALK5, but also influences BMP signaling. | ||||||