Date published: 2026-3-26

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WSCD1 Inhibitors

WSCD1 inhibitors are a class of chemical compounds designed to target and inhibit the activity of the WSCD1 protein, which stands for WSC Domain Containing 1. WSCD1 is involved in metabolic and biosynthetic pathways, particularly those related to lipid metabolism. The protein contains a WSC domain, which is typically involved in carbohydrate binding and is thought to play a role in stabilizing cellular structures or mediating protein-protein interactions. Inhibition of WSCD1 can interfere with the pathways it regulates, potentially leading to alterations in lipid biosynthesis or metabolic functions within the cell. This makes WSCD1 a critical regulatory node in cellular metabolism, influencing processes such as fatty acid synthesis, storage, and transport.

WSCD1 inhibitors are typically designed to block the specific binding sites or catalytic domains of the WSCD1 protein, preventing it from interacting with its molecular targets. These inhibitors may interfere with the protein's ability to engage in metabolic pathways, thus modulating lipid homeostasis. Altering WSCD1 activity can lead to a cascade of effects within cellular lipid networks, influencing not only the synthesis of fats but also their storage and utilization. The inhibition of WSCD1 can also affect the cellular structure, given the involvement of WSC domains in maintaining cell wall integrity or protein interactions. By blocking these interactions, WSCD1 inhibitors provide a deeper understanding of how cells regulate their internal environments, particularly concerning lipid metabolism and associated biosynthetic processes.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

A potent inhibitor of PI3K, LY294002 binds to the ATP-binding site of the enzyme, preventing phosphorylation and activation of downstream targets.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

By inhibiting MEK1/2, PD98059 blocks the MAPK/ERK pathway, which can lead to decreased cell proliferation and differentiation.

SB 431542

301836-41-9sc-204265
sc-204265A
sc-204265B
1 mg
10 mg
25 mg
$82.00
$216.00
$416.00
48
(1)

Targets the TGF-β receptor kinase, SB431542 prevents the phosphorylation of SMAD proteins, thereby inhibiting the TGF-β signaling.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$60.00
$265.00
$1000.00
163
(3)

A proteasome inhibitor, MG132 prevents the degradation of ubiquitinated proteins, affecting various signaling pathways including NF-κB activation.

SP600125

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

As an inhibitor of JNK, SP600125 interferes with transcription factor activation and apoptosis.

ZM-447439

331771-20-1sc-200696
sc-200696A
1 mg
10 mg
$153.00
$356.00
15
(1)

This compound inhibits Aurora kinase activity, which is essential for cell cycle progression, particularly during mitosis.

Gö 6983

133053-19-7sc-203432
sc-203432A
sc-203432B
1 mg
5 mg
10 mg
$105.00
$299.00
$474.00
15
(1)

Gö6983 inhibits protein kinase C (PKC) which is involved in the regulation of cell cycle, apoptosis, and transcription.

PI-103

371935-74-9sc-203193
sc-203193A
1 mg
5 mg
$33.00
$131.00
3
(1)

A dual inhibitor of PI3K and mTOR, PI-103 suppresses the activation of the PI3K/Akt/mTOR signaling axis.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Binds to mTOR complex, Rapamycin inhibits mTORC1, leading to decreased protein synthesis and cell growth.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$186.00
$707.00
88
(1)

An inhibitor of ROCK kinase, Y-27632 disrupts actin cytoskeleton organization and affects cell adhesion and motility.