Date published: 2026-4-1

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Lce1a1 Inhibitors

Lce1a1 inhibitors are a class of chemical compounds that specifically target the Lce1a1 protein, a part of a larger family of proteins known for their unique structures and functions within cellular biology. The Lce1a1 protein, belonging to the Lce (Late Cornified Envelope) protein family, plays a significant role in various biological processes. This protein family is characterized by its involvement in the formation of the cornified envelope, a structure that is critical in the outermost layer of the skin. The Lce proteins, including Lce1a1, are noted for their specific expression patterns and are typically localized in the epidermal layers of the skin. The inhibitors designed to target Lce1a1 are crafted through a meticulous process of molecular engineering, ensuring specificity and efficacy in their interaction with the protein.

The development of Lce1a1 inhibitors involves advanced techniques in medicinal chemistry and molecular biology. Researchers focus on understanding the precise molecular structure of the Lce1a1 protein, which is crucial for the design of effective inhibitors. The binding interaction between these inhibitors and the Lce1a1 protein is a key area of study, as it determines the inhibitor's efficiency and specificity. This interaction is often characterized by the formation of a complex between the inhibitor and specific sites on the protein, a process that requires precise alignment of molecular structures and often involves the formation of hydrogen bonds and other types of molecular interactions. The design of Lce1a1 inhibitors also takes into account factors such as the compound's stability, solubility, and its ability to reach the target site within biological systems. This involves a careful balance of hydrophobic and hydrophilic properties, as well as considerations for the compound's overall molecular size and shape. The intricate process of designing these inhibitors reflects the complexity and specificity required to effectively target the Lce1a1 protein, highlighting the advanced state of current biochemical and pharmacological research techniques.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

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

This compound is a DNA methyltransferase inhibitor, which can lead to hypomethylation of DNA and potentially upregulate or 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
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

TSA is a histone deacetylase inhibitor that can change chromatin structure and thereby influence gene expression.

Sodium Butyrate

156-54-7sc-202341
sc-202341B
sc-202341A
sc-202341C
250 mg
5 g
25 g
500 g
$31.00
$47.00
$84.00
$222.00
19
(3)

Sodium butyrate also acts as a histone deacetylase inhibitor, modifying chromatin and affecting transcription.

RG 108

48208-26-0sc-204235
sc-204235A
10 mg
50 mg
$131.00
$515.00
2
(1)

RG108 is another DNA methyltransferase inhibitor, preventing DNA methylation and potentially altering gene expression.

Mithramycin A

18378-89-7sc-200909
1 mg
$55.00
6
(1)

This compound binds to DNA and inhibits RNA synthesis, which could affect the expression of several genes.

Chloroquine

54-05-7sc-507304
250 mg
$69.00
2
(0)

Chloroquine affects DNA and RNA polymerase activity and can alter the expression of genes and protein production.

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$231.00
$863.00
1
(0)

JQ1 is a bromodomain inhibitor that can affect transcriptional regulation and thereby potentially downregulate gene expression.

MS-275

209783-80-2sc-279455
sc-279455A
sc-279455B
1 mg
5 mg
25 mg
$24.00
$90.00
$212.00
24
(2)

A selective histone deacetylase inhibitor that can modify chromatin structure and gene expression.

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$218.00
$322.00
$426.00
7
(1)

Decitabine is used to induce DNA hypomethylation and may alter the expression of genes.

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$133.00
$275.00
37
(2)

Vorinostat is a histone deacetylase inhibitor, which can lead to chromatin remodeling and changes in gene expression.