The chemical class called NLK Inhibitors comprises a diverse group of compounds that can either directly inhibit NLK or indirectly influence its activity by targeting various pathways and cellular processes. NLK is involved in multiple signaling cascades, particularly the Wnt pathway, and these inhibitors play a crucial role in regulating NLK function. Direct NLK inhibitors, such as VU 0364439, specifically target NLK's kinase activity by binding to its ATP-binding site, thereby blocking its function. On the other hand, indirect inhibitors like XAV939, IWP-2, and IWR-1-endo primarily impact NLK through the inhibition of the Wnt pathway. They disrupt Wnt signaling by destabilizing β-catenin or inhibiting Wnt ligand secretion, ultimately leading to reduced NLK activation. Other indirect inhibitors like SB-216763, an upstream regulator of NLK, inhibits its activity and subsequently affecting NLK activation.
Furthermore, LDN-193189 indirectly inhibits NLK by targeting the BMP receptor, which can cross-talk with NLK pathways in certain cellular contexts. PKF115-584 and IC261 indirectly inhibit NLK by targeting CK1, a kinase that phosphorylates NLK, thereby modulating NLK activity. Additionally, epigenetic modifiers like BIX 01294 and UNC0642 can indirectly influence NLK by altering chromatin structure and gene expression patterns related to NLK activity. In summary, NLK inhibitors encompass a diverse range of chemicals that can directly or indirectly modulate NLK function. These compounds are instrumental in elucidating the intricate roles of NLK in various signaling pathways and cellular processes, contributing to a better understanding of its regulatory mechanisms within cellular contexts.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
XAV939 | 284028-89-3 | sc-296704 sc-296704A sc-296704B | 1 mg 5 mg 50 mg | $35.00 $115.00 $515.00 | 26 | |
XAV939 is a potent inhibitor of the Wnt signaling pathway, indirectly inhibiting NLK. It promotes the degradation of β-catenin, a key component of the Wnt pathway, which is involved in NLK activation. | ||||||
IWP-2 | 686770-61-6 | sc-252928 sc-252928A | 5 mg 25 mg | $94.00 $286.00 | 27 | |
IWP-2 is another Wnt pathway inhibitor that indirectly impacts NLK. It inhibits Wnt ligand secretion, reducing Wnt pathway activity and, consequently, NLK activation. | ||||||
IWR-1-endo | 1127442-82-3 | sc-295215 sc-295215A | 5 mg 10 mg | $82.00 $132.00 | 19 | |
IWR-1-endo is a small molecule that antagonizes Wnt signaling by destabilizing β-catenin. This disruption of the Wnt pathway indirectly inhibits NLK, which is downstream of Wnt signaling. | ||||||
SB-216763 | 280744-09-4 | sc-200646 sc-200646A | 1 mg 5 mg | $70.00 $198.00 | 18 | |
SB-216763 is a selective inhibitor of GSK-3 (Glycogen Synthase Kinase-3), a kinase upstream of NLK in the Wnt pathway. Inhibition of GSK-3 can lead to reduced NLK activation. | ||||||
GSK-3 Inhibitor IX | 667463-62-9 | sc-202634 sc-202634A sc-202634B | 1 mg 10 mg 50 mg | $57.00 $184.00 $867.00 | 10 | |
GSK-3 Inhibitor IX indirectly inhibits NLK by suppressing GSK-3 activity, which is involved in the regulation of NLK. | ||||||
4-(6-(4-(Piperazin-1-yl)phenyl)pyrazolo[1,5-a]pyrimidin-3-yl)quinoline | 1062368-24-4 | sc-476297 | 5 mg | $240.00 | ||
This compound, also called LDN-193189, is a Bone Morphogenetic Protein receptor inhibitor. It indirectly inhibits NLK by affecting BMP signaling, which can cross-talk with NLK pathways in certain contexts. | ||||||
Wnt-C59 | 1243243-89-1 | sc-475634 sc-475634A sc-475634B | 5 mg 10 mg 50 mg | $210.00 $320.00 $1250.00 | 1 | |
Wnt-C59 is a potent Wnt signaling inhibitor that indirectly suppresses NLK activity by disrupting the Wnt pathway upstream of NLK. It prevents the binding of Wnt ligands to their receptors. | ||||||
Calphostin C | 121263-19-2 | sc-3545 sc-3545A | 100 µg 1 mg | $336.00 $1642.00 | 20 | |
Calphostin C is an inhibitor of CK1, a kinase that phosphorylates NLK. By inhibiting CK1, PKF115-584 indirectly reduces NLK activity. | ||||||
IC261 | 186611-52-9 | sc-3561 | 5 mg | $137.00 | 11 | |
IC261 is a small molecule that inhibits CK1, indirectly affecting NLK by preventing its phosphorylation by CK1, which is necessary for NLK activation. | ||||||
Histone Lysine Methyltransferase Inhibitor Inhibitor | 935693-62-2 (free base) | sc-202651 | 5 mg | $148.00 | 4 | |
BIX 01294 inhibits G9a, a histone methyltransferase. It indirectly influences NLK by modulating chromatin structure, potentially affecting the transcription of genes related to NLK activity. | ||||||