Date published: 2026-4-1

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LENG4 Inhibitors

LENG4 inhibitors comprise a class of compounds that specifically target and reduce the activity of the LENG4 protein. LENG4, short for Leukocyte Receptor Cluster (LRC) Member 4, is a protein that may be involved in cellular functions that are yet to be fully elucidated. Inhibitors in this category are designed to bind to LENG4 in a manner that prevents it from performing its normal cellular roles. These roles could include interactions with other proteins or involvement in signaling pathways. The inhibitors might function through several possible mechanisms, such as directly binding to the active site of LENG4, altering its conformation, interfering with substrate binding, or preventing its interaction with other regulatory proteins. The specific design of LENG4 inhibitors takes into account the unique structural features of the protein, aiming to achieve a high degree of selectivity to ensure that the inhibition is specific to LENG4 without affecting similar proteins.

The process of developing LENG4 inhibitors begins with a comprehensive understanding of the protein's structure and function. Structural studies, including methods like X-ray crystallography or cryo-electron microscopy, provide insights into the molecular architecture of LENG4, identifying potential druggable sites where inhibitors could effectively bind. Once potential binding sites are identified, a variety of chemical compounds are synthesized and screened for their ability to interact with and inhibit LENG4. During this phase, the interaction between LENG4 and the inhibitors is evaluated using biochemical assays to determine the affinity and specificity of binding. The inhibitors are then further optimized through an iterative process of structural modification and activity measurement. The goal of this optimization is to refine the compounds to enhance their inhibitory activity against LENG4 while minimizing any off-target effects that could disrupt the function of other proteins.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Arachidonic Acid (20:4, n-6)

506-32-1sc-200770
sc-200770A
sc-200770B
100 mg
1 g
25 g
$92.00
$240.00
$4328.00
9
(1)

By serving as a substrate for MBOAT7, excessive arachidonic acid can saturate and indirectly inhibit MBOAT7 enzymatic action on other substrates.

Triacsin C Solution in DMSO

76896-80-5sc-200574
sc-200574A
100 µg
1 mg
$187.00
$843.00
14
(1)

This compound inhibits acyl-CoA synthetases, thereby potentially decreasing the available substrates for MBOAT7's acyltransferase activity.

Lipase Inhibitor, THL

96829-58-2sc-203108
50 mg
$52.00
7
(1)

Known as a lipase inhibitor, orlistat can disrupt lipid metabolism, potentially influencing the substrate availability for MBOAT7.

N-Ethylmaleimide

128-53-0sc-202719A
sc-202719
sc-202719B
sc-202719C
sc-202719D
1 g
5 g
25 g
100 g
250 g
$22.00
$69.00
$214.00
$796.00
$1918.00
19
(1)

Can modify cysteine residues, and if MBOAT7 possesses crucial cysteine residues for its function, NEM can inhibit its activity.

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$37.00
$69.00
$109.00
$218.00
$239.00
$879.00
$1968.00
47
(1)

Influences lipid metabolism and potentially affects lipid substrates available for MBOAT7's enzymatic function.

rac Perhexiline Maleate

6724-53-4sc-460183
10 mg
$188.00
(0)

Alters lipid metabolism, potentially affecting the substrates and consequently MBOAT7 activity.

Fumonisin B1

116355-83-0sc-201395
sc-201395A
1 mg
5 mg
$200.00
$680.00
18
(1)

It's a ceramide synthase inhibitor, and by modulating sphingolipid metabolism, can indirectly affect MBOAT7's lipid transferase activity.

D609

83373-60-8sc-201403
sc-201403A
5 mg
25 mg
$189.00
$575.00
7
(1)

Inhibits phosphatidylcholine-specific phospholipase C, potentially altering the lipid substrate pool for MBOAT7.

C75 (racemic)

191282-48-1sc-202511
sc-202511A
sc-202511B
1 mg
5 mg
10 mg
$72.00
$206.00
$290.00
9
(1)

As a fatty acid synthase inhibitor, C75 can modify lipid profiles, potentially affecting MBOAT7's substrate availability.