Date published: 2026-3-18

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SH3BGRL Inhibitors

SH3BGRL inhibitors represent a class of chemical compounds that specifically target and inhibit the activity of the SH3-binding glutamic acid-rich-like protein (SH3BGRL). SH3BGRL is a member of the SH3BGR family, which is known to play a role in various cellular processes, including cell signaling, proliferation, and differentiation. The SH3 domain is a conserved protein interaction module that mediates the binding of proteins to proline-rich sequences, thereby influencing protein-protein interactions and signal transduction pathways. The inhibition of SH3BGRL is of particular interest in research as it provides insights into the modulation of these critical cellular pathways. By binding to SH3BGRL, inhibitors can disrupt its interaction with other proteins, leading to alterations in signaling cascades and the potential to modulate cellular behaviors, such as growth and development. Structurally, SH3BGRL inhibitors are designed to interact with the SH3 domain-binding site, typically through high-affinity binding that mimics the natural ligands of SH3BGRL. These inhibitors often contain chemical moieties that enhance their binding specificity and stability within the cellular environment. The development and study of these inhibitors involve a comprehensive understanding of the SH3BGRL protein structure, including the key amino acids involved in ligand binding and the conformational changes that occur upon inhibitor binding. Research into SH3BGRL inhibitors also explores the downstream effects of SH3BGRL inhibition on various signaling pathways, which can reveal new aspects of cellular regulation and the role of SH3BGRL in maintaining cellular homeostasis. Through this research, SH3BGRL inhibitors contribute to the broader understanding of protein-protein interactions and the complex network of signals that govern cellular function.

Items 1 to 10 of 17 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Staurosporine

62996-74-1sc-3510
sc-3510A
sc-3510B
100 µg
1 mg
5 mg
$82.00
$153.00
$396.00
113
(4)

Staurosporine is a potent inhibitor of protein kinases, including PKC. SH3BGR, as part of the SH3 domain-containing proteins, can interact with proline-rich motifs of proteins involved in signaling pathways, such as those activated by PKC. Inhibition of PKC by Staurosporine can, therefore, prevent the activation of proteins bound by SH3BGR, leading to its functional inhibition.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

LY294002 is a potent inhibitor of PI3K, which is involved in multiple signaling pathways. Considering that SH3BGR can bind to proteins that are downstream targets of PI3K, inhibition of this kinase can indirectly lead to decreased functional activity of SH3BGR.

SU6656

330161-87-0sc-203286
sc-203286A
1 mg
5 mg
$57.00
$133.00
27
(1)

Src family kinase inhibitor, similar to PP2, potentially altering SH3 domain-mediated signaling.

Dasatinib

302962-49-8sc-358114
sc-358114A
25 mg
1 g
$70.00
$145.00
51
(1)

A tyrosine kinase inhibitor that can inhibit Src kinases and may affect SH3 domain interactions.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

PD98059 is a selective inhibitor of MEK, which is upstream of ERK in the MAPK pathway. Since SH3BGR can bind to proteins in the MAPK pathway, inhibiting MEK and thus reducing ERK activation can lead to decreased functional activity of SH3BGR.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$186.00
$707.00
88
(1)

Y-27632 is a selective inhibitor of ROCK, which is involved in actin cytoskeleton reorganization. Given that SH3BGR binds to proteins involved in actin remodeling, inhibition of ROCK can indirectly lead to decreased functional activity of SH3BGR.

Herbimycin A

70563-58-5sc-3516
sc-3516A
100 µg
1 mg
$277.00
$1532.00
13
(1)

Tyrosine kinase inhibitor that may disrupt interactions with SH3 domain-containing proteins.

PP 2

172889-27-9sc-202769
sc-202769A
1 mg
5 mg
$94.00
$227.00
30
(1)

PP2 is an inhibitor of Src family kinases, which are known to interact with SH3 domain-containing proteins. PP2 can inhibit the functional activity of SH3BGR by preventing the activation of proteins that interact with SH3BGR.

PIK-75, hydrochloride

372196-77-5sc-296089
sc-296089A
1 mg
5 mg
$29.00
$124.00
(1)

PI3K inhibitor that could influence downstream signaling pathways associated with SH3 domain interactions.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

SP600125 is an inhibitor of JNK, a kinase involved in various signaling pathways. Since SH3BGR can bind to proteins that are downstream targets of JNK, inhibiting this kinase can indirectly lead to decreased functional activity of SH3BGR.