Date published: 2025-10-16

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DCAMKL2 Inhibitors

DCAMKL2 inhibitors are a class of chemical compounds specifically designed to target and inhibit the activity of the DCAMKL2 protein, also known as doublecortin-like kinase 2. DCAMKL2 is a serine/threonine kinase that belongs to the family of doublecortin-like kinases, which are known for their roles in regulating microtubule dynamics and neuronal development. This protein is involved in various cellular processes, including the stabilization and organization of the microtubule network, which is essential for maintaining the structure and function of cells, particularly in the nervous system. DCAMKL2 plays a critical role in the migration and differentiation of neurons during development, as well as in maintaining the structural integrity of microtubules in mature cells. The inhibition of DCAMKL2 by specific inhibitors typically involves the binding of these compounds to the kinase domain of the protein, preventing its catalytic activity. This inhibition can disrupt the protein's ability to phosphorylate target substrates, which is essential for its role in regulating microtubule dynamics. By blocking DCAMKL2 activity, these inhibitors can lead to alterations in the microtubule network, potentially affecting cellular processes such as cell division, intracellular transport, and cell motility. In neurons, where microtubule organization is crucial for axon guidance, synaptic function, and overall neuronal connectivity, DCAMKL2 inhibition may result in significant changes in neuronal morphology and function. Additionally, the inhibition of DCAMKL2 could impact other signaling pathways and protein interactions that rely on its kinase activity, further influencing cellular behavior and response to environmental cues. Understanding the effects of DCAMKL2 inhibition provides valuable insights into the role of this kinase in cellular physiology, particularly in the context of microtubule regulation and its broader implications for cellular structure and function. This knowledge is essential for advancing our understanding of the molecular mechanisms that govern cytoskeletal dynamics and the maintenance of cellular architecture.

Items 1 to 10 of 13 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

XMD 8-92 (free base)

1234480-50-2sc-364068
sc-364068A
sc-364068B
sc-364068C
5 mg
10 mg
100 mg
1 g
$235.00
$340.00
$1700.00
$10330.00
10
(0)

XMD 8-92 (free base) exhibits intriguing properties as a DCAMKL2 modulator, characterized by its ability to engage in specific hydrogen bonding interactions with target proteins. This compound's unique structural features enable it to influence intracellular signaling pathways, promoting distinct conformational changes in protein targets. Its hydrophobic regions enhance membrane permeability, while its electronic characteristics contribute to unique fluorescence properties, allowing for advanced analytical applications.

5-Azacytidine

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

This DNA methyltransferase inhibitor could induce hypomethylation of the DCAMKL2 gene promoter, potentially leading to a decrease in gene transcription and subsequent protein synthesis.

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$130.00
$270.00
37
(2)

Suberoylanilide Hydroxamic Acid, a histone deacetylase inhibitor, may enhance histone acetylation near the DCAMKL2 gene, potentially resulting in chromatin remodeling and decreased transcriptional activity of the DCAMKL2 gene.

RG 108

48208-26-0sc-204235
sc-204235A
10 mg
50 mg
$128.00
$505.00
2
(1)

By inhibiting DNA methyltransferases, RG 108 could specifically prevent the methylation of CpG islands within the DCAMKL2 promoter, possibly resulting in reduced transcriptional initiation and lower protein levels.

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$214.00
$316.00
$418.00
7
(1)

5-Aza-2′-Deoxycytidine may lead to the demethylation of the DCAMKL2 gene promoter, potentially causing a reduction in transcriptional activity and a subsequent decrease in DCAMKL2 protein levels.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$149.00
$470.00
$620.00
$1199.00
$2090.00
33
(3)

This inhibitor may prevent deacetylation of histones associated with the DCAMKL2 gene, possibly leading to a less compact chromatin structure and a downregulation of gene expression.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

By inhibiting the mTOR pathway, Rapamycin could potentially reduce the translation of many mRNAs, which may include the mRNA of DCAMKL2, leading to lower levels of the protein.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

Inhibiting the PI3K/AKT signaling cascade with LY 294002 could lead to a decrease in the transcriptional activity of genes controlled by this pathway, which might include DCAMKL2.

Nutlin-3

548472-68-0sc-45061
sc-45061A
sc-45061B
1 mg
5 mg
25 mg
$56.00
$212.00
$764.00
24
(1)

Nutlin-3 could stabilize p53, leading to an increased expression of p53-responsive genes that could indirectly lead to the downregulation of the DCAMKL2 gene.

SP600125

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

As a JNK inhibitor, Sp600125 could reduce the activity of transcription factors activated by the JNK pathway, potentially leading to a decrease in DCAMKL2 gene transcription.