Shank2 inhibitors are a theoretical class of chemical compounds designed to specifically target and inhibit the function of the Shank2 protein, a crucial scaffolding protein located in the postsynaptic density of excitatory synapses in the brain. Shank2 plays a vital role in synaptic organization and signal transduction by linking neurotransmitter receptors and other postsynaptic proteins to the actin cytoskeleton. This connection is essential for maintaining synaptic structure and facilitating efficient neuronal communication. By influencing synaptic strength and plasticity, Shank2 is integral to processes such as learning and memory.
Inhibitors of Shank2 would aim to disrupt its interactions with binding partners by targeting specific domains within the protein, such as the PDZ domain, the SH3 domain, or the proline-rich regions. By binding to these domains, these inhibitors could prevent Shank2 from assembling the postsynaptic density complex, thereby modulating synaptic organization and function. Such compounds would be valuable tools for researchers studying the molecular mechanisms underlying synaptic formation and neuronal signaling. By selectively inhibiting Shank2, scientists could dissect its specific contributions to synaptic dynamics without affecting other proteins in the Shank family.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Modulates glycogen synthase kinase 3 (GSK-3) activity, potentially affecting SHANK2's synaptic stability or function. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Histone deacetylase (HDAC) inhibitor, which may influence gene expression, potentially affecting SHANK2 expression. | ||||||
Riluzole | 1744-22-5 | sc-201081 sc-201081A sc-201081B sc-201081C | 20 mg 100 mg 1 g 25 g | $20.00 $189.00 $209.00 $311.00 | 1 | |
Modulates glutamatergic neurotransmission, potentially influencing synaptic function and SHANK2's role in synapses. | ||||||
(±)-Baclofen | 1134-47-0 | sc-200464 sc-200464A | 1 g 5 g | $55.00 $253.00 | ||
GABA_B receptor agonist, potentially modulating synaptic transmission in ways that could indirectly affect SHANK2 activity. | ||||||
Tyrphostin A23 | 118409-57-7 | sc-3554 | 10 mg | $110.00 | 13 | |
A selective antagonist for the mGluR5 receptor, potentially modulating synaptic signaling pathways involving SHANK2. | ||||||
Tianeptine | 66981-73-5 | sc-213044 sc-213044A | 10 mg 50 mg | $250.00 $422.00 | ||
Enhances serotonin uptake, potentially influencing synaptic plasticity and indirectly affecting SHANK2's synaptic role. | ||||||
Lovastatin | 75330-75-5 | sc-200850 sc-200850A sc-200850B | 5 mg 25 mg 100 mg | $28.00 $88.00 $332.00 | 12 | |
Inhibits HMG-CoA reductase, affecting cholesterol biosynthesis; cholesterol plays a role in synaptic membrane composition, potentially influencing SHANK2 function. | ||||||
D-Cycloserine | 68-41-7 | sc-221470 sc-221470A sc-221470B sc-221470C | 200 mg 1 g 5 g 25 g | $27.00 $75.00 $139.00 $520.00 | 4 | |
A partial NMDA receptor agonist, potentially modulating synaptic plasticity in a manner that could affect SHANK2 function. | ||||||
Memantine hydrochloride | 41100-52-1 | sc-203628 | 50 mg | $68.00 | 4 | |
An NMDA receptor antagonist, potentially modulating glutamatergic signaling and synaptic function relevant to SHANK2. | ||||||
FTY720 | 162359-56-0 | sc-202161 sc-202161A sc-202161B | 1 mg 5 mg 25 mg | $32.00 $75.00 $118.00 | 14 | |
Sphingosine 1-phosphate receptor modulator, potentially influencing neuronal survival and synaptic function, indirectly affecting SHANK2 activity. | ||||||