Date published: 2025-9-10

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SorCS3 Inhibitors

The chemical class termed SorCS3 Inhibitors represents a group of compounds meticulously designed to selectively target the molecular entity SorCS3. SorCS3, short for Sortilin-Related VPS10p Domain Containing Receptor 3, is a transmembrane protein belonging to the VPS10p domain receptor family. These receptors are involved in cellular processes such as protein trafficking, neurotrophic signaling, and modulation of intracellular pathways. Despite the recognition of SorCS3's significance in these processes, the specific functional roles and detailed interactions associated with SorCS3 remain subjects of active investigation within the field of molecular biology. Inhibitors within the SorCS3 Inhibitors class are intricately engineered molecules with the primary objective of modulating the activity or function of SorCS3, thereby inducing an inhibitory effect. Researchers in this field employ a multifaceted approach, integrating insights from structural biology, medicinal chemistry, and computational modeling to unravel the complex molecular interactions between the inhibitors and the target SorCS3.

Structurally, SorCS3 Inhibitors are characterized by specific molecular features designed to facilitate selective binding to SorCS3. This selectivity is essential to minimize unintended effects on other cellular components, ensuring a focused impact on the intended molecular target. The development of inhibitors within this chemical class involves a comprehensive exploration of structure-activity relationships, optimization of pharmacokinetic properties, and a deep understanding of the molecular mechanisms associated with SorCS3. As researchers delve deeper into the functional aspects of SorCS3 Inhibitors, the knowledge generated contributes not only to deciphering the specific roles of SorCS3 but also to advancing our broader comprehension of cellular processes and molecular regulation. The exploration of SorCS3 Inhibitors stands as a significant avenue for expanding fundamental knowledge in molecular pharmacology and cellular biology.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

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

A cytidine analog that incorporates into DNA and RNA; it inhibits DNA methyltransferases leading to hypomethylation of DNA, which can downregulate gene expression.

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)

A histone deacetylase inhibitor that can alter chromatin structure and gene expression, potentially reducing the transcription of SorCS3.

RG 108

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

A non-nucleoside DNA methyltransferase inhibitor, which may lead to DNA hypomethylation and potentially affect the expression of SorCS3.

MS-275

209783-80-2sc-279455
sc-279455A
sc-279455B
1 mg
5 mg
25 mg
$24.00
$88.00
$208.00
24
(2)

A benzamide histone deacetylase inhibitor that can alter gene expression by changing chromatin accessibility.

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)

An analog of 5-azacytidine that inhibits DNA methyltransferase, leading to DNA hypomethylation and potentially altered gene expression.

Suberoylanilide Hydroxamic Acid

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

Another histone deacetylase inhibitor that can change the expression of many genes, possibly including SorCS3.

Olaparib

763113-22-0sc-302017
sc-302017A
sc-302017B
250 mg
500 mg
1 g
$206.00
$299.00
$485.00
10
(1)

A PARP inhibitor that, while used mainly for its effects on DNA repair, can also influence gene expression profiles.

Nutlin-3

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

Disrupts the interaction between p53 and MDM2, leading to activation of p53 and affecting the expression of genes regulated by this tumor suppressor.

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$226.00
$846.00
1
(0)

A BET bromodomain inhibitor that affects the reading of acetylated histones, potentially downregulating transcription of certain genes.

Mithramycin A

18378-89-7sc-200909
1 mg
$54.00
6
(1)

A chemotherapeutic agent that binds to G-C rich sequences in DNA, interfering with transcription factor binding and potentially downregulating gene expression.