Date published: 2026-4-1

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C4ST-3 Inhibitors

C4ST-3 inhibitors are a class of chemical compounds that specifically target the activity of the carbohydrate sulfotransferase enzyme known as C4ST-3, which is responsible for catalyzing the sulfation of chondroitin, a type of glycosaminoglycan. C4ST-3 plays a key role in the biosynthesis of sulfated chondroitin, transferring sulfate groups to the 4-position of N-acetylgalactosamine residues within the chondroitin sulfate chains. This modification is critical for the structural integrity and function of extracellular matrix components, which are involved in cellular signaling, structural support, and molecular interactions within tissues. Inhibiting C4ST-3 interferes with this sulfation process, potentially altering the biochemical properties of chondroitin sulfate and its ability to participate in key cellular processes.

The development of C4ST-3 inhibitors typically focuses on identifying and blocking the active site of the enzyme or its substrate-binding regions, preventing the transfer of sulfate groups. These inhibitors are usually designed as small molecules or peptide-based compounds with high specificity for C4ST-3 to minimize cross-reactivity with other sulfotransferases that act on different substrates. By inhibiting C4ST-3, researchers can explore the impact of altered chondroitin sulfation on the structure and function of extracellular matrices, as well as the downstream effects on cellular communication, migration, and tissue organization. C4ST-3 inhibitors are valuable tools for studying the enzymatic mechanisms involved in sulfation and for gaining insights into the role of sulfated glycosaminoglycans in the regulation of complex biological systems.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

By disrupting DNA methylation, 5-Azacytidine can downregulate gene expression, potentially leading to decreased levels of C4ST-3.

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)

Trichostatin A may induce hyperacetylation of histones, which could result in the repression of C4ST-3 transcription.

Retinoic Acid, all trans

302-79-4sc-200898
sc-200898A
sc-200898B
sc-200898C
500 mg
5 g
10 g
100 g
$66.00
$325.00
$587.00
$1018.00
28
(1)

Retinoic acid can bind to retinoic acid receptors, altering the transcription of genes, which may include a reduction in C4ST-3 synthesis.

Forskolin

66575-29-9sc-3562
sc-3562A
sc-3562B
sc-3562C
sc-3562D
5 mg
50 mg
1 g
2 g
5 g
$78.00
$153.00
$740.00
$1413.00
$2091.00
73
(3)

Forskolin increases intracellular cAMP levels, which may lead to a reduction in C4ST-3 expression through cAMP-dependent pathways.

Rapamycin

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

Rapamycin inhibits the mTOR pathway, which is crucial for protein synthesis, potentially leading to decreased synthesis of C4ST-3.

Sodium Butyrate

156-54-7sc-202341
sc-202341B
sc-202341A
sc-202341C
250 mg
5 g
25 g
500 g
$31.00
$47.00
$84.00
$222.00
19
(3)

Sodium butyrate may cause increased histone acetylation, which could repress the transcription of the C4ST-3 gene.

PD 98059

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

By inhibiting MEK, PD 98059 could lead to a downregulation in the expression of C4ST-3 via the ERK/MAPK signaling pathway.

SP600125

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

SP600125 inhibits JNK activity, which may lead to the suppression of C4ST-3 expression by altering JNK-mediated transcriptional control.

LY 294002

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

LY 294002, as a PI3K inhibitor, could decrease C4ST-3 expression by hindering the PI3K/AKT signaling pathway.

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$37.00
$69.00
$109.00
$218.00
$239.00
$879.00
$1968.00
47
(1)

Curcumin may decrease the transcriptional activation of the C4ST-3 gene by hindering NF-κB signaling.