Date published: 2026-1-11

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She Inhibitors

She inhibitors is a reference to a class of chemical compounds designed for the specific purpose of inhibiting the activity of a molecular target referred to as "She." The identity and function of this target are not provided in the query, but it is assumed that She is a biologically relevant protein or molecule involved in cellular processes. These inhibitors are carefully designed to interact with She in a manner that disrupts its normal function or activity. The molecular design of She inhibitors typically involves structures that can specifically bind to She, altering its role within cellular processes. These inhibitors may incorporate various chemical features, including ring structures, hydrophobic chains, and hydrogen bond donors or acceptors, depending on the specific interactions required for effective inhibition.

The development of She inhibitors is a multifaceted process that encompasses principles of medicinal chemistry, structural biology, and computational drug design. Structural studies of She, using advanced techniques like X-ray crystallography or NMR spectroscopy, are essential for gaining insights into the protein's three-dimensional structure and its mechanism of action. This structural knowledge is crucial for the rational design of molecules that can effectively target and inhibit She. In the realm of synthetic chemistry, a variety of compounds are synthesized and evaluated for their ability to interact with She. These compounds undergo iterative modifications to optimize their binding efficiency, specificity, and overall stability. Computational modeling plays a significant role in this development process, allowing for the prediction of how different chemical structures might interact with She and aiding in the identification of promising candidates for further development. Additionally, the physicochemical properties of She inhibitors, such as solubility, stability, and bioavailability, are carefully considered to ensure their suitability for use in diverse biological systems. The development of She inhibitors highlights the intricate interplay between chemical structure and biological function, even in cases where the precise nature of the target remains undisclosed.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$74.00
$243.00
$731.00
$2572.00
$21848.00
53
(3)

Interferes with DNA-dependent RNA synthesis, potentially reducing SHB mRNA transcription.

Triptolide

38748-32-2sc-200122
sc-200122A
1 mg
5 mg
$90.00
$204.00
13
(1)

Inhibits transcription by affecting RNA polymerase activity, possibly lowering SHB expression.

α-Amanitin

23109-05-9sc-202440
sc-202440A
1 mg
5 mg
$269.00
$1050.00
26
(2)

Specifically inhibits RNA polymerase II, potentially decreasing mRNA synthesis for SHB.

Cordycepin

73-03-0sc-203902
10 mg
$101.00
5
(1)

Shortens mRNA poly(A) tail, which could destabilize SHB mRNA and lower protein levels.

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$41.00
$84.00
$275.00
127
(6)

Inhibits eukaryotic protein synthesis, potentially reducing SHB protein levels.

Puromycin

53-79-2sc-205821
sc-205821A
10 mg
25 mg
$166.00
$322.00
436
(1)

Causes premature chain termination during translation, possibly decreasing SHB protein synthesis.

Anisomycin

22862-76-6sc-3524
sc-3524A
5 mg
50 mg
$99.00
$259.00
36
(2)

Inhibits peptide elongation during translation, which could lead to reduced SHB protein.

DRB

53-85-0sc-200581
sc-200581A
sc-200581B
sc-200581C
10 mg
50 mg
100 mg
250 mg
$43.00
$189.00
$316.00
$663.00
6
(1)

Inhibits RNA synthesis, potentially downregulating SHB expression.

Flavopiridol

146426-40-6sc-202157
sc-202157A
5 mg
25 mg
$78.00
$259.00
41
(3)

Inhibits cyclin-dependent kinases, possibly reducing transcription of SHB.

Chloroquine

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

Elevates endosomal pH, possibly affecting SHB mRNA transport/stability.