Date published: 2026-5-15

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SPINT4 Inhibitors

SPINT4 inhibitors are a class of chemical compounds specifically designed to target and inhibit the activity of SPINT4, a member of the serine protease inhibitor (serpin) family. SPINT4, also known as hepatocyte growth factor activator inhibitor type 2 (HAI-2), plays a significant role in regulating proteolytic activity within tissues by inhibiting serine proteases. This protein is particularly important in controlling the activation of proteases involved in processes such as tissue remodeling, inflammation, and the regulation of cellular signaling pathways. By modulating the activity of these proteases, SPINT4 contributes to maintaining tissue homeostasis and preventing excessive proteolysis that could lead to tissue damage or disease progression. Inhibitors of SPINT4 disrupt its protective function, which can lead to altered protease activity and affect various biological processes.

The mechanism of action of SPINT4 inhibitors typically involves binding to the active site or other functional domains of the SPINT4 protein, preventing it from interacting with its target serine proteases. Some inhibitors may compete directly with serine proteases for binding, thereby blocking the inhibitory effect of SPINT4, while others might induce conformational changes that reduce its effectiveness as an inhibitor. By inhibiting SPINT4, these compounds can disrupt the delicate balance of protease activity in tissues, potentially leading to increased proteolytic activity and subsequent changes in cellular processes such as proliferation, apoptosis, and extracellular matrix remodeling. Research into SPINT4 inhibitors provides insights into the complex regulatory mechanisms governing proteolysis and highlights the critical role of serine protease inhibitors in maintaining physiological balance. Understanding how SPINT4 operates and how its inhibition affects protease regulation enriches our knowledge of cellular homeostasis and the dynamics of protein interactions in various biological contexts.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$218.00
$322.00
$426.00
7
(1)

Alters transcription factor activity by modifying DNA methylation patterns.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

Alters chromatin structure, potentially affecting DNA-binding proteins.

SB 203580

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

Inhibits p38 MAP kinase, which can impact several downstream pathways.

LY 294002

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

Inhibits PI3K, which plays roles in numerous cellular processes.

PD 98059

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

Inhibits the MEK pathway, affecting MAPK/ERK signaling.

Y-27632, free base

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

Inhibits Rho-associated protein kinases (ROCKs), affecting cytoskeletal arrangements.

Rapamycin

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

Influences the mTOR pathway, which controls multiple cellular processes.

Wortmannin

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

Another PI3K inhibitor affecting various cellular processes.

BAPTA/AM

126150-97-8sc-202488
sc-202488A
25 mg
100 mg
$138.00
$458.00
61
(2)

Calcium chelator that can influence cellular calcium signaling.

BAY 11-7082

19542-67-7sc-200615B
sc-200615
sc-200615A
5 mg
10 mg
50 mg
$62.00
$85.00
$356.00
155
(1)

Inhibits the NF-κB pathway by preventing IκBα phosphorylation.