Date published: 2026-5-16

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BMPR-II Inhibitors

BMPR-II inhibitors, short for Bone Morphogenetic Protein Receptor Type II inhibitors, belong to a class of small molecules or biologics designed to modulate the activity of the BMPR-II receptor. BMPR-II, a transmembrane serine/threonine kinase receptor, plays a crucial role in the regulation of various cellular processes, particularly in embryonic development, tissue homeostasis, and cell differentiation. BMPR-II is a part of the bone morphogenetic protein (BMP) signaling pathway, which is essential for the growth and maintenance of bone, cartilage, and various other tissues in the body.

BMPR-II inhibitors exert their effects by interfering with the normal activation and signaling cascades initiated by BMPR-II upon binding to its ligands. These ligands, including BMPs, initiate intracellular signaling pathways that ultimately regulate gene expression and cellular responses. BMPR-II inhibitors can disrupt this signaling, either by directly binding to the receptor and preventing ligand-receptor interaction or by modulating downstream signaling molecules. This disruption can lead to a range of cellular outcomes, depending on the specific context, including alterations in cell fate determination, proliferation, migration, and apoptosis. The development and study of BMPR-II inhibitors have provided valuable insights into the fundamental mechanisms of BMP signaling, offering avenues for research and drug discovery in various fields, including regenerative medicine, tissue engineering, and developmental biology. Understanding the precise mechanisms and effects of BMPR-II inhibitors can illuminate their roles in cellular and tissue biology, aiding in the broader understanding of how BMP signaling contributes to both normal physiological processes and pathological conditions.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

SB 431542

301836-41-9sc-204265
sc-204265A
sc-204265B
1 mg
10 mg
25 mg
$82.00
$216.00
$416.00
48
(1)

SB-431542 is a selective TGF-β type I receptor (ALK4/ALK5/ALK7) inhibitor. It indirectly inhibits BMPR-II signaling by preventing TGF-β from activating downstream Smad proteins, which regulate gene expression and cell proliferation.

4-(6-(4-(Piperazin-1-yl)phenyl)pyrazolo[1,5-a]pyrimidin-3-yl)quinoline

1062368-24-4sc-476297
5 mg
$240.00
(0)

LDN-193189 inhibits BMP type I receptors (ALK2/ALK3) by binding to their ATP-binding pockets, blocking the phosphorylation of Smad1/5/8. This prevents BMP signaling, crucial for bone and cartilage development.

BML-275

866405-64-3sc-200689
sc-200689A
5 mg
25 mg
$96.00
$355.00
69
(1)

Dorsomorphin, also known as Compound C, inhibits BMP type I receptors (ALK2/ALK3) and AMP-activated protein kinase (AMPK). It prevents Smad1/5/8 phosphorylation, disrupting BMPR-II signaling.

DMH-1

1206711-16-1sc-361171
sc-361171B
sc-361171A
sc-361171C
10 mg
25 mg
50 mg
100 mg
$213.00
$318.00
$632.00
$1047.00
2
(0)

DMH1 is a selective inhibitor of BMP type I receptor ALK2. It competes with ATP for binding to ALK2's kinase domain, effectively blocking BMP signaling in various cellular processes.

5-[6-[4-(1-Piperazinyl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]quinoline

1432597-26-6sc-476318
5 mg
$380.00
(0)

LDN-212854 is an ALK2-specific inhibitor, impeding BMP signaling by binding to the ATP-binding pocket of ALK2.

LDN-214117

1627503-67-6sc-507451
5 mg
$165.00
(0)

LDN-214117 is a selective ALK2 inhibitor, similar to LDN-193189. It impedes BMP signaling by blocking ALK2 kinase activity, influencing bone formation and repair processes.

K02288

1431985-92-0sc-488981
5 mg
$330.00
(0)

K02288 targets BMP type I receptor ALK2, disrupting BMPR-II signaling pathways. By binding to ALK2's ATP-binding site, it prevents phosphorylation of Smad1/5/8 and downstream effects.

A 83-01

909910-43-6sc-203791
sc-203791A
10 mg
50 mg
$202.00
$811.00
16
(1)

A83-01 inhibits both TGF-β type I receptor (ALK4/ALK5/ALK7) and ALK2. It disrupts TGF-β and BMP signaling, affecting cell differentiation and proliferation in various contexts.

LY2157299

700874-72-2sc-391123
sc-391123A
5 mg
10 mg
$213.00
$359.00
3
(1)

LY2157299 is a TGF-β type I receptor inhibitor that indirectly impacts BMPR-II signaling by blocking TGF-β signaling pathways. It is being investigated for its anti-fibrotic and anti-tumor properties.