Date published: 2026-2-14

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NAG6 Inhibitors

NAG6 inhibitors, belonging to the class of small molecules, are compounds designed to modulate a specific biochemical pathway by selectively inhibiting the activity of N-acetylglucosaminyltransferase 6 (NAG6). NAG6 is an essential enzyme involved in glycosylation processes within cells, particularly in the Golgi apparatus, where it catalyzes the transfer of N-acetylglucosamine (GlcNAc) residues to target substrates. The inhibition of NAG6 by these molecules disrupts the glycosylation pattern of proteins, impacting various cellular functions and signaling pathways.

The structural diversity of NAG6 inhibitors allows for versatile interactions with the enzyme, targeting specific binding sites crucial for its catalytic activity. Researchers have explored the synthesis of novel NAG6 inhibitors with the aim of elucidating the molecular mechanisms underlying glycosylation and its implications in cellular processes. Understanding the structural nuances of these inhibitors provides valuable insights into the intricate network of glycosylation pathways and offers potential avenues for modulating cellular functions.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Rapamycin

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

Rapamycin acts by directly binding to FKBP12 and then targeting mTOR complex 1 (mTORC1), leading to the inhibition of mTOR signaling. Since mTOR can regulate protein synthesis, its inhibition can decrease the functional activity of NAG6 if NAG6 synthesis is mTOR-dependent.

LY 294002

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

A potent inhibitor of phosphatidylinositol 3-kinase (PI3K), LY294002 impedes the PI3K/Akt/mTOR pathway. By doing so, it prevents the phosphorylation and activation of mTOR, which could indirectly decrease NAG6 synthesis if it is under the control of this signaling pathway.

Wortmannin

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

Wortmannin is another potent inhibitor of PI3K. Similar to LY294002, it inhibits the PI3K/Akt/mTOR cascade, which can result in reduced activity of downstream proteins, potentially including NAG6 if its expression is regulated by this pathway.

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
$64.00
$246.00
136
(2)

U0126 is an inhibitor of MEK1/2, effectively blocking the MAPK/ERK pathway. If NAG6 activity or stability is modulated by ERK signaling, the inhibition of this pathway by U0126 could lead to reduced function of NAG6.

PD 98059

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

PD98059 selectively inhibits MEK, which in turn prevents the activation of ERK. This compound can decrease NAG6 functional activity by inhibiting the MAPK/ERK pathway if NAG6 is downstream of this signaling cascade.

SB 203580

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

SB203580 is a selective inhibitor of p38 MAPK. The p38 MAPK pathway is involved in the stress response and inflammation. Inhibition of this pathway by SB203580 could result in decreased activation of NAG6 if it is implicated in the same cellular responses.

SP600125

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

This compound is an inhibitor of JNK, which plays a role in stress response, apoptosis, and transcriptional regulation. If NAG6 is regulated by JNK signaling, SP600125 could indirectly reduce its activity.

Brefeldin A

20350-15-6sc-200861C
sc-200861
sc-200861A
sc-200861B
1 mg
5 mg
25 mg
100 mg
$31.00
$53.00
$124.00
$374.00
25
(3)

Brefeldin A disrupts protein transport by inhibiting ADP-ribosylation factor (Arf). If the transport and proper localization of NAG6 are essential for its activity, Brefeldin A could decrease its functional activity by disrupting these processes.

Cyclosporin A

59865-13-3sc-3503
sc-3503-CW
sc-3503A
sc-3503B
sc-3503C
sc-3503D
100 mg
100 mg
500 mg
10 g
25 g
100 g
$63.00
$92.00
$250.00
$485.00
$1035.00
$2141.00
69
(5)

Cyclosporin A binds to cyclophilins and inhibits calcineurin, thereby blocking NFAT (nuclear factor of activated T-cells) translocation to the nucleus. If NAG6 activity is modulated by NFAT-mediated signaling, this inhibition could lead to a decrease in NAG6 function.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$60.00
$265.00
$1000.00
163
(3)

MG132 is a proteasome inhibitor that can prevent the degradation of ubiquitinated proteins. If NAG6 is regulated through proteasomal degradation, MG132 could indirectly affect its functional activity by stabilizing regulatory proteins that inhibit NAG6.