Date published: 2026-1-21

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Shank 3 Inhibitors

Shank 3 inhibitors belong to a distinct chemical class that has garnered significant attention within the realm of neurological research. This class of compounds interacts with a specific protein known as Shank 3, which plays a crucial role in synaptic function and neuronal connectivity. Shank 3 is a postsynaptic scaffold protein located in the excitatory synapses of neurons in the central nervous system. It acts as a molecular scaffold, facilitating the assembly and stabilization of various proteins within the synapse, thereby influencing synaptic structure and transmission. Shank 3 inhibitors are designed to modulate the activity of Shank 3 by binding to its functional domains and altering its interaction with other synaptic proteins. By doing so, these inhibitors have the potential to modulate the molecular architecture of synapses, leading to downstream effects on synaptic strength and plasticity. Researchers are particularly interested in understanding the impact of Shank 3 inhibitors on the synapse, as aberrant synaptic function has been implicated in a range of neurological disorders. The inhibition of Shank 3 may provide a unique way to study the intricate mechanisms of synapse formation, maintenance, and plasticity, shedding light on fundamental processes that govern normal brain function and dysfunction.

In conclusion, Shank 3 inhibitors represent a notable chemical class that holds promise in unraveling the complexities of synaptic biology. Through their ability to modulate the function of the Shank 3 protein, these inhibitors offer a unique tool for researchers to dissect the molecular underpinnings of synapse dynamics. As investigations into the role of Shank 3 and its inhibitors continue, a deeper understanding of synaptic function and potential insights into neurological conditions could emerge, paving the way for future scientific advancements in the field.

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Ibrutinib

936563-96-1sc-483194
10 mg
$156.00
5
(0)

Covalently binds to Bruton's tyrosine kinase (BTK), preventing B-cell receptor signaling and B-cell activation.

CAL-101

870281-82-6sc-364453
10 mg
$193.00
4
(1)

Selectively inhibits phosphoinositide 3-kinase delta (PI3Kδ), disrupting the PI3K signaling pathway in B-cells.

Acalabrutinib

1420477-60-6sc-507392
250 mg
$255.00
(0)

Irreversibly inhibits BTK, hindering B-cell receptor signaling and reducing B-cell activation.

IPI 145

1201438-56-3sc-488318
5 mg
$317.00
(0)

Targets both PI3Kδ and PI3Kγ isoforms, disrupting PI3K-mediated signaling in B-cells and T-cells.

Tirabrutinib

1351636-18-4sc-507435
10 mg
$138.00
(0)

Covalently binds to BTK, impeding B-cell receptor signaling and suppressing malignant B-cell proliferation.