Date published: 2026-4-1

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SOLO Inhibitors

SOLO inhibitors represent a distinct class of compounds designed to target a specific biological process within cells. The term "SOLO" itself is an acronym that stands for "Suppressor of lkb1 One." These inhibitors are designed to modulate the activity of the LKB1 (Liver Kinase B1) pathway, a crucial signaling cascade involved in cellular processes such as energy homeostasis, cell polarity, and cell growth. LKB1, also known as serine/threonine kinase 11, is a tumor suppressor protein that plays a central role in regulating cell metabolism and proliferation. The development of SOLO inhibitors is rooted in the understanding that dysregulation of the LKB1 pathway is implicated in various diseases, particularly cancer.

The chemical structure of SOLO inhibitors is meticulously designed to interact with key components of the LKB1 pathway, inhibiting specific enzymatic activities or disrupting protein-protein interactions critical for downstream signaling. These small molecules often possess a unique combination of functional groups and structural motifs that enable them to selectively bind to the target proteins associated with the LKB1 pathway. The rationale behind SOLO inhibitors lies in their ability to modulate cellular processes by intervening at the molecular level, thereby offering a novel avenue for exploring the underlying mechanisms of diseases associated with LKB1 dysregulation. As research in this field progresses, the development and refinement of SOLO inhibitors may contribute valuable insights into the intricacies of cellular signaling pathways, opening up new possibilities for understanding and addressing diseases linked to aberrant LKB1 pathway activity.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

A potent inhibitor of phosphoinositide 3-kinases (PI3K) which may indirectly affect SESTD1-related signaling pathways by altering lipid signaling dynamics.

LY 294002

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

Another PI3K inhibitor that could alter the phosphatidylinositol signaling SESTD1 is potentially involved with.

Staurosporine

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

A broad-spectrum protein kinase inhibitor that could affect various kinases within SESTD1-related signaling cascades.

Gö 6983

133053-19-7sc-203432
sc-203432A
sc-203432B
1 mg
5 mg
10 mg
$105.00
$299.00
$474.00
15
(1)

A protein kinase C inhibitor that could alter signaling pathways influencing SESTD1's function or localization.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

An mTOR inhibitor which may have an impact on SESTD1 function by modulating downstream signaling pathways that SESTD1 might interact with.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$90.00
$349.00
284
(5)

A p38 MAPK inhibitor which might influence stress response pathways and potentially affect SESTD1's role in signaling.

SP600125

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

An inhibitor of c-Jun N-terminal kinase (JNK) signaling, potentially modifying pathways that SESTD1 is involved in.

PD 98059

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

An ERK pathway inhibitor that might have an impact on SESTD1's role in cell signaling by altering the MAPK pathway.

BAPTA, Free Acid

85233-19-8sc-201508
sc-201508A
100 mg
500 mg
$68.00
$267.00
10
(1)

A calcium chelator that could indirectly affect SESTD1 by disrupting calcium-dependent signaling pathways.

2-APB

524-95-8sc-201487
sc-201487A
20 mg
100 mg
$28.00
$53.00
37
(1)

An inositol trisphosphate receptor antagonist that could influence calcium signaling and thus SESTD1's function.